key: cord-0055048-6swsfztl authors: Mohamad, Nur Syamimi; Zakaria, Nur Hanis; Daud, Nurulhaidah; Tan, Ling Ling; Ta, Goh Choo; Heng, Lee Yook; Hassan, Nurul Izzaty title: The Role of 8-Amidoquinoline Derivatives as Fluorescent Probes for Zinc Ion Determination date: 2021-01-05 journal: Sensors (Basel) DOI: 10.3390/s21010311 sha: 5040745a1c3b85c57b0c188ae67b3de4de3c7622 doc_id: 55048 cord_uid: 6swsfztl Mass-spectrometry-based and X-ray fluorescence-based techniques have allowed the study of the distribution of Zn(2+) ions at extracellular and intracellular levels over the past few years. However, there are some issues during purification steps, sample preparation, suitability for quantification, and the instruments’ availability. Therefore, work on fluorescent sensors based on 8-aminoquinoline as tools to detect Zn(2+) ions in environmental and biological applications has been popular. Introducing various carboxamide groups into an 8-aminoquinoline molecule to create 8-amidoquinoline derivatives to improve water solubility and cell membrane permeability is also a recent trend. This review aims to present a general overview of the fluorophore 8-aminoquinoline and its derivatives as Zn(2+) receptors for zinc sensor probes. Various fluorescent chemosensor designs based on 8-amidoquinoline and their effectiveness and potential as a recognition probe for zinc analysis were discussed. Based on this review, it can be concluded that derivatives of 8-amidoquinoline have vast potential as functional receptors for zinc ions primarily because of their fast reactivity, good selectivity, and bio-compatibility, especially for biological applications. To better understand the Zn(2+) ion fluorophores’ function, diversity of the coordination complex and geometries need further studies. This review provides information in elucidating, designing, and exploring new 8-amidoquinoline derivatives for future studies for the improvement of chemosensors that are selective and sensitive to Zn(2+). Zinc ion plays a significant role in biological and pathological processes [1] [2] [3] . The past decade has seen many excellent metal-ion sensors detect transition and heavy metal ions such as zinc ions Zn 2+ . Zn 2+ , as an essential element in the human body, is actively involved in various biochemical processes such as neuronal signal transmission, DNA binding, enzyme regulators, and catalytic centers. Zn 2+ deficiency and imbalance distribution then lead towards a much broad range of pathologies in parts of body systems [4, 5] . The deficiency of Zn 2+ in the human body can lead to severe neurological disorders like Alzheimer's. In contrast, an excess of Zn 2+ reported as an effect of excessive consumption in time can lead to Parkinson's disease [6] [7] [8] . According to the US Food and Nutritional Board, the human body can receive a safe amount of Zn 2+ in a range of 2 mg (0-5 years) to 15 mg (adults) [9] . Derivatives of 8-hydroxyquinoline and 8-aminoquinoline are common fluorogenic chelators for Zn 2+ ions [40] . Mummidivarapu and co-workers synthesized 8-amino quinoline and 8-amino naphthalene moiety 1,3,5-triderivatives of calix [6] arene and studied their binding ability toward biologically essential metal ions. They observed a stronger binding of Zn 2+ from the absorption study, along with the complexation energies computed from the computational data [44] . A susceptible sensor was also reported by using amidoquino-Sensors 2021, 21, 311 5 of 29 line as part of the recognition element towards glucosamine in living Caco-2 cells, resulted in the enhancement of fluorescence quantum yields by 14 folds [45] . Another highly selective probe by Xia and co-workers used the diarylethene compound with a piperazine-linked amidoquinoline unit as a binder for zinc ions [46] . They reported a higher binding affinity of the complex with the targeted analyte in fluorescence intensity. These showed the derivatives of 8-aminoquinoline in the presence of amide gradually to be acknowledged. Several studies focusing on improving and increasing the sensitivity and selectivity of fluorescent probes for Zn 2+ based on 8-amidoquinoline and its derivatives are widely developed [47, 48] . Further, 8-amidoquinoline derivatives exhibit fluorescence properties for sensing Zn 2+ based on important signaling mechanisms and internal charge transfer (ICT) [48, 52] . Therefore, this review aims to assess collected studies related to 8-amidoquinoline derivatives as fluorophores of zinc chemosensor. The global focus has recently been devoted to developing and synthesizing highly sensitive fluorescent probes for the selective recognition of Zn 2+ ions as a concern for human health and environmental safety. In total, 41 titles and abstracts were screened independently based on the criteria "practices of 8-aminoquinoline derivatives in the detection of zinc only". Next, the left articles were evaluated for inclusion or exclusion based on 8-aminoquinoline with amide structure, or we might be called it 8-amidoquinoline or N-(quinolin-8-yl) formamide. The addition of the carboxamide group, followed by intramolecular hydrogen bond breaking of 8-aminoquinoline, inhibits intramolecular electron-transfer, which in turn enhanced the ICT process as pronounced in the Zhang [53] and Xu [54] study. This observation would enhance fluorescence emission. The devotion to the spectroscopically silent behavior of the Zn 2+ ion leads to interferences from the other metal ions. Aside from these interferences, the sensing results were influenced by the other factors such as the environment of the system including solvent used, type and pH of the buffer, the concentration of Zn 2+ ions present compared to the other ions, solubility properties, and of course, the characteristic and behavior of the probe itself. They are so many receptors used as fluorophore as binding sites such as di-2-picolylamine (DPA) [55, 56] quinoline [57, 58] , bipyridine [59] [60] [61] [62] , acyclic and cyclic polyamines [63, 64] , iminodiacetic acid [65, 66] , triazole [67] [68] [69] , and Schiff-base receptors [70] (Figure 1 ). Derivatives of 8-hydroxyquinoline and 8-aminoquinoline are common fluorogenic chelators for Zn 2+ ions [40] . Mummidivarapu and co-workers synthesized 8-amino quinoline and 8-amino naphthalene moiety 1,3,5-triderivatives of calix [6] arene and studied their binding ability toward biologically essential metal ions. They observed a stronger binding of Zn 2+ from the absorption study, along with the complexation energies computed from the computational data [44] . A susceptible sensor was also reported by using amidoquinoline as part of the recognition element towards glucosamine in living Caco-2 cells, resulted in the enhancement of fluorescence quantum yields by 14 folds [45] . Another highly selective probe by Xia and co-workers used the diarylethene compound with a piperazine-linked amidoquinoline unit as a binder for zinc ions [46] . They reported a higher binding affinity of the complex with the targeted analyte in fluorescence intensity. These showed the derivatives of 8-aminoquinoline in the presence of amide gradually to be acknowledged. Several studies focusing on improving and increasing the sensitivity and selectivity of fluorescent probes for Zn 2+ based on 8-amidoquinoline and its derivatives are widely developed [47, 48] . Further, 8-amidoquinoline derivatives exhibit fluorescence properties for sensing Zn 2+ based on important signaling mechanisms and internal charge transfer (ICT) [48, 52] . Therefore, this review aims to assess collected studies related to 8-amidoquinoline derivatives as fluorophores of zinc chemosensor. The global focus has recently been devoted to developing and synthesizing highly sensitive fluorescent probes for the selective recognition of Zn 2+ ions as a concern for human health and environmental safety. In total, 41 titles and abstracts were screened independently based on the criteria "practices of 8-aminoquinoline derivatives in the detection of zinc only". Next, the left articles were evaluated for inclusion or exclusion based on 8aminoquinoline with amide structure, or we might be called it 8-amidoquinoline or N-(quinolin-8-yl) formamide. The addition of the carboxamide group, followed by intramolecular hydrogen bond breaking of 8-aminoquinoline, inhibits intramolecular electrontransfer, which in turn enhanced the ICT process as pronounced in the Zhang [53] and Xu [54] study. This observation would enhance fluorescence emission. The devotion to the spectroscopically silent behavior of the Zn 2+ ion leads to interferences from the other metal ions. Aside from these interferences, the sensing results were influenced by the other factors such as the environment of the system including solvent used, type and pH of the buffer, the concentration of Zn 2+ ions present compared to the other ions, solubility properties, and of course, the characteristic and behavior of the probe itself. They are so many receptors used as fluorophore as binding sites such as di-2picolylamine (DPA) [55, 56] quinoline [57, 58] , bipyridine [59] [60] [61] [62] , acyclic and cyclic polyamines [63, 64] , iminodiacetic acid [65, 66] , triazole [67] [68] [69] , and Schiff-base receptors [70] ( Figure 1 ). However, it is necessary to notice that few compounds fluoresce by itself or fluoresce after the interaction with the target. The behavior of the compounds usually can electronically go to an excited and ground state during inter-intramolecular transfer. Thus, the most intense and valuable fluorescence is generally seen in compounds that comprise aromatic functional groups since they have a π system orbital [71] . Therefore, the earliest probes for zinc (II) detection are derivatives of zinquin [72] , Zinbo-5 [73] , Zinpyr [74] , aminoquinoline [75] , and coumarin families [76] (Figure 2 ). However, it is necessary to notice that few compounds fluoresce by itself or fluoresce after the interaction with the target. The behavior of the compounds usually can electronically go to an excited and ground state during inter-intramolecular transfer. Thus, the most intense and valuable fluorescence is generally seen in compounds that comprise aromatic functional groups since they have a π system orbital [71] . Therefore, the earliest probes for zinc (II) detection are derivatives of zinquin [72] , Zinbo-5 [73] , Zinpyr [74] , aminoquinoline [75] , and coumarin families [76] (Figure 2 ). An aryl sulfonamide derivative of 8-aminoquinoline, 6-methoxy-(8-p-toluenesulfonam -ido)quinoline (TSQ) is amongst the most efficient used as fluorophore in zinc sensor, especially in the biological field [21] . This TSQ was first published in the early seventies by Toroptsey and Eshchenko [77] . Then, referring to Meeusen and co-workers, TSQ acts as a chelating ligand to Zn 2+ by a ratio of 2 to 1 ((TSQ)2Zn), which will form a metal complex. TSQ-Zn will increase the fluorescence intensity of TSQ by 4-fold (excitation maximum: 360 nm, emission maximum: 490 nm). They also indicate a blue-shifted emission spectrum as a ternary TSQ-Zn-protein adduct ( Figure 3 ) [78] . Moreover, this TSQ has been used as a stain to recognized Zn 2+ ions for biological purposes since it still provides selectivity over concentrations of Ca 2+ and Mg 2+ ions [43, 79] . An aryl sulfonamide derivative of 8-aminoquinoline, 6-methoxy-(8-p-toluenesulfonam -ido)quinoline (TSQ) is amongst the most efficient used as fluorophore in zinc sensor, especially in the biological field [21] . This TSQ was first published in the early seventies by Toroptsey and Eshchenko [77] . Then, referring to Meeusen and co-workers, TSQ acts as a chelating ligand to Zn 2+ by a ratio of 2 to 1 ((TSQ) 2 Zn), which will form a metal complex. TSQ-Zn will increase the fluorescence intensity of TSQ by 4-fold (excitation maximum: 360 nm, emission maximum: 490 nm). They also indicate a blue-shifted emission spectrum as a ternary TSQ-Zn-protein adduct ( Figure 3 ) [78] . Moreover, this TSQ has been used as a stain to recognized Zn 2+ ions for biological purposes since it still provides selectivity over concentrations of Ca 2+ and Mg 2+ ions [43, 79] . TSQ derivatives are extensively used as fluorogenic chelators in the detection of zinc in biological samples. However, these derivatives have low water solubility, poor membrane penetrability, and complicating free zinc ion measuring in cells quantitatively [41] . Therefore, to overcome those problems, developing on the quinoline-based derivatives still ongoing until now. This is due to their behavior high soluble in water and showed excellent selectivity for Zn 2+ ion [80] as we can say that the importance of zinc detection almost in biological and environmental applications. Therefore, among other fluorophores, quinoline-based derivatives are studied extensively. As confirmation, the characteristic of quinoline on the zinc detection, Mikata, and coworkers substituted pyridine ring with quinoline group in N, N, N, N-tetrakis(2-pyridylmethyl) -ethylenediamine, (TPEN) to form N, N, N, N-tetrakis(2-quinolylmethyl) ethylenediamine (TQEN) compound ( Figure 4a ). Then, they modified the combination with the addition of the methoxy group. Those compounds are selective to Zn 2+ by photoin- TSQ derivatives are extensively used as fluorogenic chelators in the detection of zinc in biological samples. However, these derivatives have low water solubility, poor membrane penetrability, and complicating free zinc ion measuring in cells quantitatively [41] . Therefore, to overcome those problems, developing on the quinoline-based derivatives still ongoing until now. This is due to their behavior high soluble in water and showed excellent selectivity for Zn 2+ ion [80] as we can say that the importance of zinc detection almost in biological and environmental applications. Therefore, among other fluorophores, quinoline-based derivatives are studied extensively. As confirmation, the characteristic of quinoline on the zinc detection, Mikata, and co-workers substituted pyridine ring with quinoline group in N, N, N, N-tetrakis(2pyridylmethyl) -ethylenediamine, (TPEN) to form N, N, N, N-tetrakis(2-quinolylmethyl) ethylenediamine (TQEN) compound ( Figure 4a ). Then, they modified the combination with the addition of the methoxy group. Those compounds are selective to Zn 2+ by photoinduced electron-transfer (PET) and chelation enhanced fluorescence (CHEF). The modified combination of TQEN showed strong fluorescence upon binding with Zn 2+ compared to the weak fluorescence of TPEN [81] . Steric and stereochemical effects are the key factors of metal-binding affinity. The aromatic ring of quinoline can be versatile and exhibit different affinities to the other metal-ligand binding. In the development of Zn 2+ chelators, N-containing ligands like quinoline have been developed and investigated [82] . stronger metal bonding affinity, the sensor has higher selectivity towards Zn 2+ detection [84] . It is crucial to keep in mind that fluorescent groups with lone pairs of electrons like nitrogen will be quenching the emission. However, the coordinate bond formed between that lone pairs of electrons and metal ions like Zn 2+ ion can prevent fluorescence from quenching. Hence, those nitrogen-containing heterocyclic chromophores whose nitrogen will form a chelate ring with metal ions will give a CHEF effect [71] . Upon excitation, the electron donor from the chelator to the acceptor will permit intramolecular charge transfer (ICT), preceded by a large Stokes' shift [41] . This chemosensor design would be valued as a wavelength-shifted fluorescence intensity enhancement that will amplify the recognition event. Compared to quinoline isomer TQEN, isoquinoline derivates of TQEN exhibited strong fluorescence upon binding with Zn 2+ , and the isoquinoline (benzene ring position) showed higher metal binding affinity [83] . Next, hybrids of (N, N-bis(2-quinolylmethyl) ethylenediamine-N', N'-diacetic acid (N, N-BQENDA) (Figure 4b) , shows a 32-fold emission enhancement at 456 nm in buffer 4-(2-Hydroxyethyl)piperazine-1-ethane sulfonic acid, HEPES (pH = 7.5). The substitution of carboxylate groups into two quinolines in TQEN reduced the steric hindrance in forming metal ligands binding between Zn 2+ and remaining N-atoms of quinolines. Figure 4c showed, under the same condition, the emission of N, N-BQENDA-Zn is more enhanced than the emission of TQEN-Zn. With the stronger metal bonding affinity, the sensor has higher selectivity towards Zn 2+ detection [84] . Another study using quinolines scaffold as zinc's receptor was reported by Wang and co-workers [85] . They develop a new small molecular organic compound with excellent bonding affinity and high selectivity towards Zn 2+ ions compared to other divalent metals. They combined 8-hydroxy-2-methyl quinoline (Oxn) that had a building block for the CHEF process to take place once binding with metals with potent chelators like di-2-picolylamine (DPA) moiety at the 2-position (1) (Figure 5a ). Then, further saponification is conducted to get a carboxylic moiety for increasing the solubility of the compound in water. UV-Vis, fluorescent, and NMR titrations indicated tight binding between the compound and Zn 2+ ion. Figure 5b showed three isosbestic's points at 245, 250, and 312 nm, suggesting forming only one UV active zinc complex. Moreover, X-ray diffraction revealed zinc coordinated with quinoline, carboxylic moiety, and two pyridyl moieties. Bond lengths of Zn-N are reported, like the bond lengths of other Zn-DPA complexes [86] [87] [88] . Ligand 8-hydroxyquinoline (8-HQ), an established chromophore for zinc chelation, became the starting material as three tripodal ligands for zinc detection in research studied by Royzen and co-workers. All these three ligands were reported bound with Zn at a ratio of one to one. Strong fluorescent emission for all ligands (λmax 1 = 526 nm, λmax 2 = 513 nm, λmax 3 = 486 nm). Moreover, enhancement for ligands 2 and 3 showed 13.1 folds and 11.3 folds, respectively. X-ray crystallographic of these ligands indicated different molecular geometries of Zn-complex formation might influence their spectroscopic interactions of metal-ligands [89] . As TSQ had low solubility in water, several attempts had been made to overcome those properties, including diverting to quinoline-based derivatives, introducing carboxylic acid or ester to the extent of replacing methyl in benzene with a carboxylate group, and adding hydroxyl group as mentioned above. Other research groups take the initiative to covalently linked 6-deoxy-6-formyl-ß-cyclodextrin (CD) into an analog of TSQ, N-(8quinolyl)-p-aminobenzene -sulfonamide (HQAS) ( Figure 5c ). As we can see, Figure 5d , there was two bands wavelength for excitation (285 nm and 362 nm) while the emission was emitted at 507 nm. For both situations (with/out the existence of Zn), the peak appeared at the same wavelength. The only difference just the intensities. The fluorescence intensity is enhanced because the electron-process was forbidden as per binding, and the π-electron conjugation system was involved in ICT from donor to acceptor [90] . This process will lead from weak fluorescence to strong fluorescence. They reported slight interferences of several metal ions ordinarily present in a physiological environment, such as Na + , K + , Ca 2+ , Mg 2+ , Mn 2+ , Fe 2+ , and Co 2+ . However, this fluorescence sensor still satisfies Zn 2+ fluorescence response in a wide range of pH, between pH 4 and 10. The development of an aminoquinoline-based fluorophore for zinc sensors has been explored extensively. The combination of carboxamidoquinoline (2-hydroxy-3-hydroxymethyl) -5-methylbenzaldehyde ( Figure 6a ) was found to improve water solubility. Simultaneously, the sensor displayed remarkable selectivity for Zn 2+ ions in the existence of other cations in an aqueous solution [4] . A notable 81-nm red-shift of fluorescence emission and enhancement on the fluorescence intensity at 489 nm upon titration between ligands and Zn 2+ solution (0-20 eq.). A distinct isoemission point at 427 nm was noticeable (Figure 6b ). High yield of synthesized Py2 by the reaction of pyrene-1-carbaldehyde with quinoline derivative (Figure 6c ) was selective to Zn 2+ ion in ethanol: water solution (95:5 v/v). Based on the Benesi-Hildebrand equation [91] , the binding constant, Ka, of Py2 with Zn 2+ was calculated to be 5.1 × 10 −4 M −1 with a ratio of one metal-ligand. Moreover, the reversibility of the sensor occurred over EDTA. Both enhancing (500 nm) and quenching (420 nm) fluorescence response of Py2 (10 μM) upon addition of increasing Zn 2+ (0-30 eq.) in ethanol-water solution (Figure 6d ). Regarding interferences studied, no other transition metals interfered at all except for Cu 2+ [92] . The development of an aminoquinoline-based fluorophore for zinc sensors has been explored extensively. The combination of carboxamidoquinoline (2-hydroxy-3-hydroxymethyl) -5-methylbenzaldehyde ( Figure 6a ) was found to improve water solubility. Simultaneously, the sensor displayed remarkable selectivity for Zn 2+ ions in the existence of other cations in an aqueous solution [4] . A notable 81-nm red-shift of fluorescence emission and enhancement on the fluorescence intensity at 489 nm upon titration between ligands and Zn 2+ solution (0-20 eq.). A distinct isoemission point at 427 nm was noticeable (Figure 6b ). High yield of synthesized Py2 by the reaction of pyrene-1-carbaldehyde with quinoline derivative (Figure 6c ) was selective to Zn 2+ ion in ethanol: water solution (95:5 v/v). Based on the Benesi-Hildebrand equation [91] , the binding constant, Ka, of Py2 with Zn 2+ was calculated to be 5.1 × 10 −4 M −1 with a ratio of one metal-ligand. Moreover, the reversibility of the sensor occurred over EDTA. Both enhancing (500 nm) and quenching (420 nm) fluorescence response of Py2 (10 µM) upon addition of increasing Zn 2+ (0-30 eq.) in ethanol-water solution ( Figure 6d ). Regarding interferences studied, no other transition metals interfered at all except for Cu 2+ [92] . A series highly soluble of the carboxamidoquinoline-based fluorophore on the recognition of Zn 2+ ion in aqueous buffer was investigated (Figure 7 ) [93] . They reported the affinity's influences of four different substituents and three various sites on the quinoline ring. As reported by Jiang and co-workers, chelation of Zn 2+ ion with two N-atoms carboxamidoquinoline produces a five-membered ring due to conjugation increases, and the energy gap between HOMO-LUMO decreases [94] . The coordinated binding still the same as the parent compound similar. However, absorption and fluorescence response varied with a different substituent. These related to the substituent's behavior, whether it enhanced or prevented the ICT of AQZ upon binding with increasing Zn 2+ . As the position of the same substituent, there is not so much difference in the fluorescence response between 2-position and 4-position. In contrast, 5-position showed no emission with or without Zn 2+ ion presence due to the carboxamide group [93] . The carboxamide group is deprotonated after Zn 2+ binding, and the 8-aminoquinoline intramolecular hydrogen bond is broken to inhibit the electron-transfer process, which quenches the fluorescence of quinoline [95] . As reported, this carboxamidoquinoline affords two coordination sites for Zn 2+ ions to bind [96] . Aside from these two sites, A series highly soluble of the carboxamidoquinoline-based fluorophore on the recognition of Zn 2+ ion in aqueous buffer was investigated (Figure 7 ) [93] . They reported the affinity's influences of four different substituents and three various sites on the quinoline ring. As reported by Jiang and co-workers, chelation of Zn 2+ ion with two N-atoms carboxamidoquinoline produces a five-membered ring due to conjugation increases, and the energy gap between HOMO-LUMO decreases [94] . The coordinated binding still the same as the parent compound similar. However, absorption and fluorescence response varied with a different substituent. These related to the substituent's behavior, whether it enhanced or prevented the ICT of AQZ upon binding with increasing Zn 2+ . As the position of the same substituent, there is not so much difference in the fluorescence response between 2-position and 4-position. In contrast, 5-position showed no emission with or without Zn 2+ ion presence due to the carboxamide group [93] . ure 8) gave dissimilar coordination upon binding with Zn 2+ even though all the receptors were almost similar, which contained 8-carboxamidoquinoline and dipicolylamine (DPA). Generally, Zn 2+ favored nitrogen of quinoline and nitrogen or oxygen from the amide group and nitrogen from DPA [97] . These results proved to add an amide group into 8-aminoquinoline to improve chemosensor Zn(II). As mentioned before, aside from increasing the water solubility and membrane permeability, the amide group also helps the sensor to be more selective and efficient by growing the binding tendency. Subsequently, 8-carboxamidoquinoline derivatives started to get attention as fluorophore to detect Zn 2+ ion, especially in biological fields due to more reports related to carboxamidoquinoline focused on introduction various receptor [98] [99] [100] [101] and the use of it [102, 103] and nanoparticle functionalize onto carboxamidoquinoline [104] [105] [106] . Therefore, a systematic search is needed to better understand the development of 8-carboxamidoquinoline as receptors of the Zn(II) sensor with all due respect to enhanced sensitivity and selectivity for future biological studies application. The interaction and coordination of Zn 2+ with existing 8-carboxamidoquinoline derivatives differed, requiring many factors to be considered. The carboxamide group is deprotonated after Zn 2+ binding, and the 8-aminoquinoline intramolecular hydrogen bond is broken to inhibit the electron-transfer process, which quenches the fluorescence of quinoline [95] . As reported, this carboxamidoquinoline affords two coordination sites for Zn 2+ ions to bind [96] . Aside from these two sites, introducing a 2-(2-hydroxyethoxy)-ethylamino group recorded an eight-fold rise in quantum fluorescence yield and a red-shift of 75 nm in fluorescence emission when Zn 2+ was bound in an aqueous buffer solution. A research study by Lee and co-workers demonstrated the binding complex formation between Zn 2+ and receptors are versatile. It depended on the receptor itself and the environment of the binding. They proved three different receptors (QP, NA, QA) ( Figure 8 ) gave dissimilar coordination upon binding with Zn 2+ even though all the receptors were almost similar, which contained 8-carboxamidoquinoline and dipicolylamine (DPA). Generally, Zn 2+ favored nitrogen of quinoline and nitrogen or oxygen from the amide group and nitrogen from DPA [97] . These results proved to add an amide group into 8-aminoquinoline to improve chemosensor Zn(II). As mentioned before, aside from increasing the water solubility and membrane permeability, the amide group also helps the sensor to be more selective and efficient by growing the binding tendency. A research study by Lee and co-workers demonstrated the binding complex formation between Zn 2+ and receptors are versatile. It depended on the receptor itself and the environment of the binding. They proved three different receptors (QP, NA, QA) (Figure 8 ) gave dissimilar coordination upon binding with Zn 2+ even though all the receptors were almost similar, which contained 8-carboxamidoquinoline and dipicolylamine (DPA). Generally, Zn 2+ favored nitrogen of quinoline and nitrogen or oxygen from the amide group and nitrogen from DPA [97] . These results proved to add an amide group into 8-aminoquinoline to improve chemosensor Zn(II). As mentioned before, aside from increasing the water solubility and membrane permeability, the amide group also helps the sensor to be more selective and efficient by growing the binding tendency. Subsequently, 8-carboxamidoquinoline derivatives started to get attention as fluorophore to detect Zn 2+ ion, especially in biological fields due to more reports related to carboxamidoquinoline focused on introduction various receptor [98] [99] [100] [101] and the use of it [102, 103] and nanoparticle functionalize onto carboxamidoquinoline [104] [105] [106] . Therefore, a systematic search is needed to better understand the development of 8-carboxamidoquinoline as receptors of the Zn(II) sensor with all due respect to enhanced sensitivity and selectivity for future biological studies application. The interaction and coordination of Zn 2+ with existing 8-carboxamidoquinoline derivatives differed, requiring many factors to be considered. Subsequently, 8-carboxamidoquinoline derivatives started to get attention as fluorophore to detect Zn 2+ ion, especially in biological fields due to more reports related to carboxamidoquinoline focused on introduction various receptor [98] [99] [100] [101] and the use of it [102, 103] and nanoparticle functionalize onto carboxamidoquinoline [104] [105] [106] . Therefore, a systematic search is needed to better understand the development of 8-carboxamidoquinoline as receptors of the Zn(II) sensor with all due respect to enhanced sensitivity and selectivity for future biological studies application. The interaction and coordination of Zn 2+ with existing 8-carboxamidoquinoline derivatives differed, requiring many factors to be considered. All the articles reviewed were cross-sectional studies with four sections-first, the function of synthesized, second, titration analysis between probe and zinc ion (fluorescence titration or UV-Vis titration or both), third, the selectivity of the probe sensor with other competitive metal cations, and finally, the limit of detection and reliability of the assessment according to the real sample applications. Most of the papers, starting with the synthesizing 8-amidoquinoline derivatives, then proceed with solution works that are involved titration of the compound with a zinc ion. They continued with certain optimization before undergoes selectivity test with other transition metals such as cadmium (Cd 2+ ), copper (Cu 2+ ), cobalt (Co 2+ ), nickel (Ni 2+ ), chromium (Cr 3+ ), silver (Ag 2+ ), ferum (Fe 2+ ), lead (Pb 2+ ), and mercury (Hg 2+ ). Latterly, they tested the sensor with real samples either from biological or environmental samples that involved requirement detection of zinc as per validation status. However, out of 13 articles, one research does not validate with real sample(s), only three articles tested with water, one article tested with cabbage, and the rest tested with biological samples ( Table 2 ). Most of the researchers started and trying to develop sensors specifically for the detection of zinc intensively. Among various conventional probes for zinc (II) are derivatives of zinquin [72] , Zinbo-5 [73] , Zinpyr [74] , aminoquinoline [75] and coumarin families [76] . Meanwhile, 8-aminoquinoline and its derivatives [115] were among the first probes devel- oped for zinc (II) detection. They exhibited excellent stability, high affinity to metal ions, and good membrane permeability [41] . However, this zinc (II) chemosensor developed had suffered to differentiate between zinc ion and other competitive cation metals, such as Cd 2+ , Cu 2+ , Co 2+ , Ni 2+ , Hg 2+ , and its 3d 10 electronic configurations [44, 111] . An ideal chemosensor contains a receptor with the most robust affinity binding towards Zn 2+ ion without interferences (signal-selectivity) of other heavy metals. It has a broad linear responsive range that is highly explored. By inserting a functional group of amide into a conjugated molecule of 8-aminoquinoline, Zn 2+ ion (borderline acid) is coordinated favorably with aromatic nitrogen atoms (borderline bases), N-amide, and O-amide. Based on this HSAB theory, some researchers [116, 117] , including us thinking of adding some more nitrogen and oxygen atoms into the 8-aminoquinoline molecule. We believed it could increase the binding affinity towards Zn(II) ion so that it will help to null out the competitive metals that have the same electronic configuration, 3d 10 . In determining the binding studies between receptor 8-amidoquinoline compounds, all the papers reviewed were reported on characterization spectroscopy, fluorescence titration, and UV-Vis titration [42, 112, 118] . They seek binding mode via job plot method and binding constant (K d ) or association constant (K a ). However, not all papers were recorded for job plot data. The binding modes were summarized in Table 2 . Out of 13 papers, six of them do not conduct the job plot analysis. The left articles stated binding mode between probes and zinc ion was one to one ratio except for research studied by Zhang and co-workers [107] , with a ratio of 2:1. Other than fluorescence and UV-Vis titration, some researchers reported on NMR titration and X-ray crystallography as methods for binding studies between the ligands and Zn 2+ ion. Both of these studies could help in proposing and determining the binding modes of coordination of metal complexes. As in 8-amidoquinoline derivatives reported, which atom(s) or position(s) had interaction (directly or indirectly) upon binding with Zn 2+ ion. Therefore, these methods also crucial in metal-ligand binding characterization methods as fluorescence and UV-Vis titration. The combination of fluorescence and UV-Vis titration (gave information on the changes in absorption, emission, and wavelength, provide binding constant and binding ratio) and NMR titration and X-ray crystallography (supported in understanding on how and where they bind) necessitating to get a better experience in determining the interaction between receptors and analytes. Molecules containing bonding and non-bonding electrons (n-electrons) can absorb energy in the form of ultraviolet or visible light to excite these electrons to higher antibonding molecular orbitals [119] . The more quickly the electrons are excited (i.e., the lower the energy difference between HOMO and LUMO), the longer the light wavelength they can absorb. This is the basic principle of UV-Vis spectroscopy, and it is also applied to the UV-Vis titration method for host-guest complexations [120] . The titration method of UV absorbance has the advantages of quick determination and effortless efficiency. It is likely to become the latest approach to studying interactions between ligands and trace metal ions [121] . Much information could gain from this UV-Vis titration method, such as molar absorptivity or extinction coefficient, changes of absorption (increase or decrease), binding constant, constant rate, job's plot result (binding ratio), and isobestic's point in kinetic measurement [122] . As fluorescence titration, the purposes are just as same as UV-Vis titration, except it reads the solution's emission when comparing. Therefore, fluorescence titration could obtain binding interaction of ionophore towards metal [123] . As mentioned by Tamayo and co-workers, spectrophotometric and spectrofluorimetric titration was prepared by the same methods [124] . The stock solutions of ligand and metal were prepared separately by diluting the same concentration. The ligands and metal titration were done by adding the metal ions before proceeded with absorbances and emission reading. NMR provides specific abilities to characterize ligand molecules that bind enough to be rapidly exchanged between attached and independent state binding modes [125] . Within spectroscopy, NMR spectroscopy plays a vital role in many areas of chemistry and related sciences. The reason for this is that the spectra can be very easily interpreted. In theory, the number of peaks in that spectra could analyze the number of atoms present in the solution. Sometimes, the position of those atoms can be predicted by running a variety of NMR methods. Other than that, NMR also plays a dominant role in studying complex coordination [126] . As we can see, many researchers reported on NMR binding studies of metal-ligands by analyzing the chemical Shift's change of the presented peaks in ligand upon binding with increasing metal. They proposed that the interaction happened at the peaks that shifted more downfield or upfield once the proportion of the metal increased [42, 97, 110, 111] . As in 1 H NMR titration of the ligand's stock solution with various of the equivalent of stock solution of Zn 2+ ion (0-1.0 eq.), NMR spectra showed NH proton at 11.34 ppm gradually absent upon increase the equivalent of Zn 2+ ions. Another noticeable change, a new peak of OH, appeared at 10.01 ppm as pile up the volume of Zn 2+ . They suggested that the ligand (Probe 1) probably coordinated with the Zn 2+ ion in the imidic acid form resulted from tautomerization in acetonitrile. The benefit of Probe 1 (Figure 9 ) was demonstrated with good selectivity to differentiate between Zn 2+ and Cd 2+ through two tautomers, amide and imidic acid [53] . The resonance of amide that was inserted into 8-aminoquinoline offered different binding modes and coordination complex. Therefore, the fluorescence response signal varied according to the introduced metal or Zn 2+ . In Song and co-worker's case, other cations could have different binding behavior. Aside from that, the solvent also significantly affected the fluorescence response where Zn 2+ in water, THF, DMSO, ethanol, and Cd 2+ only in CH 3 CN [110] . Table 2 . As per the development of any analytical methods like fluorescence sensor, it will require some validation assessments and testing with real samples to ensure consistency, accuracy, and applicability. By definition, validation is to verify that the analytical method is appropriate for its intended purpose. The analyte can be tested correctly, clearly, and precisely over the specified range [134] . After the sensor's optimization, performances of the sensors that comprise among these parameters (calibration curve, linear range, detection limits, selectivity, specificity, repeatability, reproducibility, reversibility, stability, Research by Boonkitpatarakul and co-workers also focused on distinguished between Zn 2+ and Cd 2+ by using Compound 1 (Figure 9 ) that contained amidic acid. Deprotonation of amidic proton of Compound 1 upon binding with Zn 2+ resulted in a large bathochromic shift of UV-Vis absorption from 300 nm to 344 nm. This indicated greater electron delocalization. Zn-Compound 1 binding gave a substantial fluorescent enhancement and shifted from 420 nm and 504 nm. The binding involved strong CHEF, PET of the quinoline's amino group, and excited-state intramolecular proton transfer (ESIPT) from the amidic proton to N atom of quinoline. The coordination geometry of the Zn 2+ complex was distorted square pyramidal by three chelating nitrogen from one ligand, one oxygen from another ligand, and one more oxygen of NO 3− anion [42] . Proton chemical shift changes on methylene of DPA and amide N verified Zn 2+ ions bound to QP (Figure 9 ) by coordinating with carbonyl oxygen (C=O). The peak of methylene protons of DPA split into doublets and more deshielded upon addition of Zn 2+ ion equivalent. These methods were tried in various solvents like methanol, acetonitrile, DMSO, and acetonitrile/water mixture. The result was different since the N-H proton moves towards the downfield in DMSO while vice versa when in acetonitrile. However, once over two equivalent of Zn 2+ proton of amide (N-H) shifted upfield. Therefore, the binding position suggested taking place was carbonyl O since the proton changes recorded at neighbour proton (methylene DPA and N-H amide) [97] . 1 H NMR titrations in CD 3 CN suggesting three N atoms of amino groups of QLNYP ( Figure 9 ) were coordinate with Zn 2+ ions since the chemical Shift of secondary amine's proton were shifted and gradually missing by increasing Zn 2+ ion equivalent up to 2.0 eq. In the meantime, protons of quinoline, pyridine, and methylene group showed downshift. The peak changes in the position of -CH 2 deduced the neighbour of the methylene group might be the one that coordinated with Zn 2+ ions [108] . This suggestion is like a deduction of proton chemical shift changes on DPA from research done by [97] . Given the advantage of fully water-soluble AQZ-2COOH ( Figure 9 ) due to carboxyl groups' insertion, make it a promising receptor for testing Zn 2+ in aqueous solution [111] . Crystallography result of binding between Zn 2+ and AQZ-2COOH confirmed Zn 2+ formed five-coordinated with three N atoms of pyridine, amide, and amine and another two O atoms of carboxyl groups. These five-membered chelation rings made the Zn-complex more stable. The strong and red-shift of UV-Vis absorption explained the deprotonation of amide moiety, reducing the HOMO-LUMO energy gap and the electron transfer reaction of heterocyclic ligand-metal [111] . Fluorescence enhancement of HAQT ( Figure 9 ) increased proportionally with the increasing zinc concentration up to 10 µM by five-fold at 488 nm, and further addition did not record any further enhancement. Zn 2+ was proved coordinated with the HAQT via infrared spectroscopy. It noted the disappearance of OH group at 3419 cm −1 , amide carbonyl absorption slightly shifted to 1656 cm −1 , and significant difference of N atom of pyridine group at 1300 cm −1 and 755 cm −1 characteristic hydroxyls [42] . Thus, the plausible reaction between HAQT-Zn involved the deprotonation process that increases electron-donating from N atom of 8-amino to quinoline ring and ICT process that transfers an electron from N atom of the pyridyl group to the metal ion. Deprotonation and ICT process of L1-Zn (Figure 9 ) also like the plausible interaction of HAQT-Zn. Fluorescence intensity remarkably shifted from 408 to 489 nm with a quantum yield of 0.138. As in, the isoemissive point was observed at 427 nm. L1 exhibited weak fluorescence, while the coordination of L1 as a ligand to metal gave strong fluorescence [75] . Slightly different from the QPA receptor, other than the transferred electron of N-atom from quinoline, it is also involved in breaking an intramolecular hydrogen bond. The chelation ring formed is more firmed and rigid. Therefore, the fluorescence emission spectrum showed a new emission at 500 nm with a 106-fold rise [73] . Surprisingly, the crystal structure of PMQA-Zn shown uncommon evidence of binding between 8-aminoquinoline and Zn 2+ . Neither N atom of 8-aminoquinoline was bound to zinc even though PMQA (Figure 9 ) formed a hexadentate chelate ring with Zn 2+ . Those N atoms are critically coordinated to Cu 2+ perfectly. PMQA-Cu complexes are more stable than PMQA-Zn because ligands containing nitrogen ligands usually have a higher affinity with Zn 2+ , Cd 2+, and Cu 2+ . Even though the fluorescence emission quenching when introduced to Cu 2+ , this PMQA also provides information for elucidating zinc probes to prevent Cu 2+ interferences [107] . A novel and simple turn-on fluorescent were developed by embedded modified 8amiquinoline ( Figure 9 ) and on the surface of semiconductor nanocrystal quantum dots (QDs), QDs-carboxylic groups. Covalent bonds linked the carboxylic groups of CuInS2 QDs and 8-aminoquinoline at NH 2 groups to form the CuInS2 QDs/8-aminoquinoline conjugate. Next, upon introducing of Zn 2+ ions into CuInS2 QDs/8-aminoquinoline conjugate system, the lone pair of electrons of N atoms makes the hole-transfer mechanism inhibit and enhanced the fluorescent of CuInS2 QDs/8-aminoquinoline [113] . Therefore, the fluorescence intensity of CuInS2 QDs/8-aminoquinoline conjugate in the total concentrations of Zn(II) was enhanced with the addition of Zn 2+ ions. The ligand added for 8-carboxamidoquinoline consisted of either nitrogen, oxygen, and/or sulfur due to existing of lone pairs of electrons for each atom (Figure 9 ). These three atoms may react as electron-donating during the coordination binding with Zn 2+ . However, Zn 2+ does not behave reliably either as a soft or as a hard Lewis acid. It poses a borderline case with no particular fondness for oxygen, nitrogen, or sulfur-donor ligands to be coordinated. The results of the concluded binding coordination sites to form complexes were different. Roughly, we reviewed all of them as there were no fixed preferences and they differ based on derivative, atoms presenting, molecular geometry, medium, and environment. Therefore, the results might contradict. Nevertheless, the importance of development in sensing Zn 2+ was successful since the different enhancement for fluorescence upon binding with Zn 2+ was recognized. In analytical chemistry, the detection limit or, in other terms, is the limit of detection (LOD), defined as the lowest concentration of target substance reliably distinguished from the blank [127] [128] [129] . As we mentioned earlier, the purpose of this systematic review was to summarize the research design and outcomes of the recognition of zinc ions by 8amidoquinoline. Herein, the lowest concentration of analyte zinc ion detected was reported. Based on our review, the LOD range of the included articles was between 3.36 × 10 −8 M to 445 × 10 −8 M. Therefore, the detection limit of 8-amidoquinoline-based zinc chemosensor was in nanomolar proven these derivatives are highly sensitive to recognized Zn(II) ion. There are potential interferences of transition metals, especially metals that belong to the same group (Group 12) or same period (Period 4) as Zn(II) ion in the periodic table. They showed almost similar characteristics to Zn(II), 3d 10 configuration. Therefore, Zn(II) detection had suffered from the cross-interference of Cd 2+ , Cu 2+ , Co 2+ , Ni 2+ , and Hg 2+ [130] [131] [132] . Based on [71] , when the chelation of a metal-ligand complex coordinated from a five-membered to a six-membered ring, ligands usually selective for the smaller metal ions compared to the larger metal ions. For example, TQA ligands are more selective to metal Zn 2+ (smaller radius) than Cd 2+ (larger radius). In this research, they demonstrated the selectivity of the ligand to the metal ion radius. They concluded, good metal-ligand binding depends on two factors that are the size of metals ion and the size of chelate rings. Thus, all the included articles performed a screening and analysis of 8-amidoquinoline derivatives on the study of the interference of the other heavy metals towards zinc detection-evaluations between those studies on the interference of the transition metals are documented in Table 2 . All of the studies recorded interference. Trace metals like Cd 2+ , Cu 2+ , Co 2+ , Ni 2+ , Hg 2+ , Fe 2+ , Pb 2+ , and Cr 3+ interfered in the detection of zinc using 8amidoquinoline derivatives. The only difference in those studies is the interference metals and the metal ratio to zinc used. Nevertheless, certain studies [53, 72, 96, 109, 110, 112, 113, 133] demonstrated that the sensing probe could be used in a real sample due to the metals involved not present or least in biological applications. These exhibited 8-amidoquinoline derivatives are selective to zinc detection due to minor interferences issues. As per the development of any analytical methods like fluorescence sensor, it will require some validation assessments and testing with real samples to ensure consistency, accuracy, and applicability. By definition, validation is to verify that the analytical method is appropriate for its intended purpose. The analyte can be tested correctly, clearly, and precisely over the specified range [134] . After the sensor's optimization, performances of the sensors that comprise among these parameters (calibration curve, linear range, detection limits, selectivity, specificity, repeatability, reproducibility, reversibility, stability, analysis time, response time, and others) needed to be done as validation [135] . As for the chosen papers, validation for specific parameters was done after each optimization step. They also test the fabricated sensor with a real sample that has been selected, as mentioned before, in Table 2 . As the detection of Zn 2+ ions is crucial for biological purposes, eight of 13 articles were tested with biological samples involving cells. The remaining papers were tested with river or tap water and cabbage. Fluorescence occurs when a substance can absorb energy from photons and emit the energy as fluorescence by internal conversion mechanisms and losing the energy from an excited state to ground state level. It is indicated for better visualization and explanation on a simplified Jablonski diagram (Figure 10a) . The diagram showed the increasing energy level from the ground state (S 0 ) to the excited state (S 1 ) and an excited singlet state (S 2 ). The excitation from S 0 to S 1 or S 2 depends on the photons' energy given during the excitation and absorption process. The energy absorbed will then undergo vibrational relaxation by dissipating energy into the surrounding medium before released to S 0 . The losing energy involved the transition of higher to lower electrical energy and lower to higher vibrational energy. These changes made the substance fluoresce [136, 137] . From Jabslonki's diagram, we can say that the longer the wavelength, the lower the energy, and vice versa. Stokes shift is a difference between absorbance maximum and emission maximum. The calculation of this may present in wavelength or wavenumber (Figure 10b ). In some instances, it is essential in determining the value of the Stokes shift, especially in the biological application. The smaller distance between excitation and emission wavelength can hardly distinguish the wavelength, and the spectral will significantly overlap. As we can see in Figure 10c , the table showed the difference between the two wavelengths were in the range of 65-204. It is considered wide Stokes shift for all the probes, and therefore, they were suitable in testing the bio-real samples. Those are the basic principle of interactions in fluorescence spectroscopy. Next, the photophysical mechanisms for the fluorescent probe of 8-amidoquinoline for Zn 2+ ions involve CHEF, ICT, PET, ESIPT, and FRET signals. Among the chosen articles, some probes used multi-signal mechanisms, and others using conventional mechanisms (only one). It should be noted that a combination of two or more mechanisms sensors produces much better results. Figure 10c shows that the largest Stokess shift was Compound 1 by Boonkitpatarakul and co-workers [42] . The more significant difference may be due to the (1) strong CHEF signal upon binding with Zn 2+ , (2) PET process of N-atoms from amino group to the fluorophore, (3) ESIPT mechanism of H-amidic to N-quinoline, and ICT of the complex Zn-1 ( Figure 11 ). Table 2 ; Stoke's Shift calculated from the difference between emission and absorbance wavelength. Those are the basic principle of interactions in fluorescence spectroscopy. Next, the photophysical mechanisms for the fluorescent probe of 8-amidoquinoline for Zn 2+ ions involve CHEF, ICT, PET, ESIPT, and FRET signals. Among the chosen articles, some probes used multi-signal mechanisms, and others using conventional mechanisms (only one). It should be noted that a combination of two or more mechanisms sensors produces much better results. Figure 10c shows that the largest Stokess shift was Compound 1 by Boonkitpatarakul and co-workers [42] . The more significant difference may be due to the (1) strong CHEF signal upon binding with Zn 2+ , (2) PET process of N-atoms from amino Table 2 ; Stoke's Shift calculated from the difference between emission and absorbance wavelength. while quinoline became an acceptor. Figure 11 , probes L1, AQZ-2COOH, and HAQT showed dual signal mechanisms, CHEF and ICT [96, 111, 112] . Upon binding with Zn 2+ , intramolecular hydrogen bonding of 8-amino broken. It leads to the intramolecular transfer of electrons of N-atom of the amide to quinoline (CHEF). Other than that, ICT mechanisms were involved between N-quinoline to Zn. These will enhance the intensity of the fluorescence. The mechanisms involved between 8-amidoquinoline derivatives upon binding with Zn almost have the same signals and more than one signal. Figure 11 . Possible mechanisms and interactions involved 8-amidoquinoline derivatives upon binding with Zn 2+. Figure 11 . Possible mechanisms and interactions involved 8-amidoquinoline derivatives upon binding with Zn 2+ . As for QA-Zn, we believed the FRET mechanism occurred. It was between fluorophore anthracene and fluorophore quinoline due to the spectral of anthracene (emission) was overlapped with quinoline (excitation) [109] . In this case, anthracene became a donor while quinoline became an acceptor. Figure 11 , probes L1, AQZ-2COOH, and HAQT showed dual signal mechanisms, CHEF and ICT [96, 111, 112] . Upon binding with Zn 2+ , intramolecular hydrogen bonding of 8-amino broken. It leads to the intramolecular transfer of electrons of N-atom of the amide to quinoline (CHEF). Other than that, ICT mechanisms were involved between N-quinoline to Zn. These will enhance the intensity of the fluorescence. The mechanisms involved between 8-amidoquinoline derivatives upon binding with Zn almost have the same signals and more than one signal. Zn 2+ sensors based on fundamental carboxamidoquinoline have rapidly developed because of simple synthesis, binding ratio, and ratio detection. Zebin and co-workers linked functional magnetic core-shell fibrous silica material (AQ-Fe 3 O 4 @SiO 2 @KCC-1) and amidoquinoline group with piperazine to get high selectivity and enhanced the fluorescence intensity in aqueous solution [138] . As for combination of diarylethene based sensors with carboxamidoquinoline unit were reported by three groups, (1) Diarylethenebased sensor with a carboxamidoquinoline unit (linker-piperazine) that can differentiate Zn 2+ and Cu 2+ [46] , (2) Consist of diarylethene with a benzyl-linked 8-aminoquinoline-2 -aminomethyl pyridine reported naked eye Zn fluorescent chemosensor [139] , (3) Ratiometric and reversible of fluorescence Zn sensor based on diarylethene and carboxamidoquinoline unit [140] . Hydrogen bonds are readily formed by the nitrogen center in quinolines, rendering those derivatives weak in fluorescent intensity in protic polar solvents. However, as mentioned above, the coordination between NH-amide and Zn would induce ICT and ESIPT mechanisms and inhibit the PET process resulting in enhanced fluorescence intensity (CHEF). Other than that, a metal complex coordination in the presence of an amidecontaining ligand along with a carboxylate ligand will boost the self-assembly required for an emission induced by aggregation. This mechanism is also known as aggregationinduced emission (AIE) [141] . Simple chemosensor 1 (2-(N-(2-hydroxyethyl)-N-((pyridin-2-yl) methyl)amino)-N-(quinoline-8 -yl) acetamide) (Figure 12a) consists of both the binding site and the watersoluble functional group of quinoline as fluorophore and 2-((pyridin-2-yl)methylamino) ethanol. The probe showed changes from weak fluorescence to strong fluorescence upon binding with Zn 2+ (Figure 12a,b) . In Figure 12c , we can see that other than Zn 2+ , Cd 2+ also showed the enhancement of fluorescence intensity at wavelength 500 nm. However, both intensities could be compared. Therefore, this chemosensor demonstrated its potential in monitoring Zn 2+ in human dermal fibroblasts. We could see that the fluorescence imaging of the cells with 1 at different concentrations of Zn 2+ was significantly enhanced (Figure 12d-f) [142] . A novel fluorescent sensor of AQTF1-Zn (Figure 13a ) made up of N-(quinolin-8-yl) tetrahydrofuran-2-carboxamide moiety demonstrated color changes under a UV lamp long-wavelength. The color was enhanced upon adding the Zn. Therefore, the fluorescence intensity of AQTF1 lower compared to AQTF1-Zn (Figure 13b ). The probe was tested at fluorescence emission at 511nm in solvent DMSO-water at pH 7.4, 1:1. This condition makes this sensor suitable for the Zn testing cell imaging in vivo. Du and co-workers also stated this sensor produced high selectivity to Zn 2+ ions without interference from Cd 2+ ions. [143] . Followed by AQTF1-Zn as a type of fluorescent chemosensor for the relay recognition of Zn 2+ and H 2 PO 4 − , Kumar and co-workers explored "Off-On-Off" fluorescent chemosensor based on the receptor 2-(diethylamino)-N-(quinolin-8-yl) acetamide (L) for the same relay's detection (Figure 14a ) [144] . Zn 2+ ions and phosphate are two necessary biomolecular involved in DNA and RNA, pharmaceutical drugs, and therapeutic [145] . Other than that, excessive H 2 PO 4 − in the environment will cause algal growth that will lead to decomposition and reduce the dissolved oxygen levels and lower the water quality [146] . Upon interaction with Zn 2+ , three N-atom formed complexation with Zn 2+ , led to PET's inhibition, and promoted ICT and CHEF. Therefore, the color intensity was changed from blue to cyan under visible fluorescence change by the naked eye (Figure 14a,b) . The metal complex may then turn off fluorescent upon binding with H 2 PO 4 − (visible under UV light-colourless) (Figure 14c ). A novel fluorescent sensor of AQTF1-Zn (Figure 13a ) made up of N-(quinolin-8-yl) tetrahydrofuran-2-carboxamide moiety demonstrated color changes under a UV lamp long-wavelength. The color was enhanced upon adding the Zn. Therefore, the fluorescence intensity of AQTF1 lower compared to AQTF1-Zn (Figure 13b ). The probe was tested at fluorescence emission at 511nm in solvent DMSO-water at pH 7.4, 1:1. This condition makes this sensor suitable for the Zn testing cell imaging in vivo. Du and co-workers also stated this sensor produced high selectivity to Zn 2+ ions without interference from Cd 2+ ions. [143] . Followed by AQTF1-Zn as a type of fluorescent chemosensor for the relay recognition of Zn 2+ and H2PO4 -, Kumar and co-workers explored "Off-On-Off" fluorescent chemosensor based on the receptor 2-(diethylamino)-N-(quinolin-8-yl) acetamide (L) for the same relay's detection (Figure 14a ) [144] . Zn 2+ ions and phosphate are two necessary biomolecular involved in DNA and RNA, pharmaceutical drugs, and therapeutic [145] . Other than that, excessive H2PO4 -in the environment will cause algal growth that will lead to decomposition and reduce the dissolved oxygen levels and lower the water quality [146] . Upon interaction with Zn 2+ , three N-atom formed complexation with Zn 2+ , led to Other than that, excessive H2PO4in the environment will cause algal growth that will lead to decomposition and reduce the dissolved oxygen levels and lower the water quality [146] . Upon interaction with Zn 2+ , three N-atom formed complexation with Zn 2+ , led to PET's inhibition, and promoted ICT and CHEF. Therefore, the color intensity was changed from blue to cyan under visible fluorescence change by the naked eye (Figure 14a,b) . The metal complex may then turn off fluorescent upon binding with H2PO4 -(visible under UV light-colourless) (Figure 14c ). Vongnam and co-workers proved that emissions' impacts depended on the structure; even the structure consisting of 8-amidoquinoline and salicylaldimine moieties, slightly different in structure, will produce different results (Figure 15a ). These salicylaldimine group 1) lowered the fluorescence intensity by isomerization of C=N and PET, 2) Formed pentacoordinate complex with Zn 2+ via chelation. The range of detection limits for the four sensors was recorded from 0.024 to 0.431 mM, and among the four sensors, only sensor 1 could be fabricated as a paper-strip fluorescent chemosensor. Sensor 1 showed changes in intensity upon binding with Al 3+ ions ( Figure 15a ). However, the emission was at different wavelength (Al 3+ = 439 nm, Zn 2+ = 550 nm). Figure 15b ) displayed fluorescence enhancement ratios of sensors 1-4 in 9 EtOH: 1 H 2 O in the presence of different metal ions, respectively [147] . This review has made an effort to systematically analyze the existing literature on the 8-amidoquinoline derivatives as fluorophore in detecting Zn 2+ ions (2010-Jan 2020). As a result, 13 articles were analyzed and discussed in this review. The developing and synthesizing of highly sensitive fluorescent probes for zinc recognition, especially in the biological field, is expected to be ongoing. Based on the recent exploration on the 8amidoquinoline to improve cell permeability and HSAB theory's rule, we believed N-atom and O-atom in 8-amidoquinoline derivatives could be an excellent probe in detecting Zn. The identification of 8-amidoquinoline derivatives conducted for decades may help to elucidate and plan future studies. According to HSAB theory's rule, as borderline acid, zinc will be preferred to bind to borderline bases like aniline, pyridine, N 3− , Br − , NO 2− , SO 3 2− , N 2 . As in Figure 9 , at least one of these borderline bases is added to the 8-amidoquinoline combination structure. We summarized that fluorescent chemosensors of Zn 2+ based on 8-amidoquinoline succeed in improved water solubility and membrane permeability as most of the applications were tested with biological samples. Nevertheless, some of these sensors showed that Zn 2+ could be distinguished with Cd 2+ , the most competitive metal ions, since it is in the same group as Zn 2+ . Development of these sensors also provides visibility by naked-eye on color changes before and after binding with Zn 2+ under long-wavelength (365 nm). The apparent color changes would help in determining the presence of Zn 2+ ions without using the instrument. It also could be used as preliminary results before proceeding to the next steps. pentacoordinate complex with Zn 2+ via chelation. The range of detection limits for the four sensors was recorded from 0.024 to 0.431 mM, and among the four sensors, only sensor 1 could be fabricated as a paper-strip fluorescent chemosensor. Sensor 1 showed changes in intensity upon binding with Al 3+ ions (Figure 15a) . However, the emission was at different wavelength (Al 3+ = 439 nm, Zn 2+ = 550 nm). Figure 15b ) displayed fluorescence enhancement ratios of sensors 1-4 in 9 EtOH: 1 H2O in the presence of different metal ions, respectively [147] . However, some limitations still exist for these compounds as Zn fluorophores. All of the fluorophores suffered some interferences, especially in higher concentrations of the interfering ions. Thus, some of the binding mechanisms were not as expected, probably attributed to the ligand and steric hindrance position in forming five chelation with zinc. Some studies showed the most affected on the fluorophore changes were environments like the type of solvent and environment of the target ions. These fluorescent probes may be explored more by changing the chemical structure. We can also confirm from this analysis that it does not mean that a probe with a rich borderline base will offer the best zinc detection performance. Fluorescence is best known for its high sensitivity, repeatability, low detection limits, simplicity, and potential to allow real-time monitoring due to their quick response times. These characteristics made fluorescence sensing of metal ions one of the most potent detection tools to be explored. In this review, we covered tremendous interest in 8-amidoquinoline as Zn 2+ probes in fluorescent sensor design reported in the last few years, and the output of their research was discussed. Zinc sensors were involved via various binding modes and different fluorescence response mechanisms based on the system and experimental conditions such as the type of metal salt used, type of pH, type of buffer, and solvent used, and the analyte's concentrations. However, all the selected sensors were stilled, allowing the selective detection of Zn 2+ ions in various environmental or/and biological samples. Most of the receptors use nitrogen as the binding site as it is favorable and form relatively simple geometries with Zn 2+ . Based on this review, there is still much to improve regarding the derivative of 8-amidoquinoline as a receptor, such as fast response and bio-compatibility, especially for biological applications. Further studies are suggested for a better understanding of the diversity of the coordination complexes and geometries. This review could help to elucidate, design, and explore new 8-amidoquinoline derivatives for future chemosensor applications that are more selective and sensitive to zinc ions. No new data were created or analyzed in this study. Data saharing is not applicable to this article. Design of fluorescent materials for chemical sensing Introduction to Sensors Chemical sensors and biosensors in Italy: A review of the 2015 literature An "off-on-off" fluorescent probe for the sequential detection of Zn 2+ and hydrogen sulfide in aqueous solution Fluorescent chemosensors for various analytes including reactive oxygen species, biothiol, metal ions, and toxic gases Zinc metabolism in the brain: Relevance to human neurodegenerative disorders Identification of SLC39A4, a gene involved in acrodermatitis enteropathica The role of zinc in selective neuronal death after transient global cerebral ischemia Review on Recent Advances in Metal Ions Sensing Using Different Fluorescent Probes Techniques for measuring cellular zinc High precision zinc isotopic measurements applied to mouse organs The neurobiology of zinc in health and disease Zinc isotope ratio imaging of rat brain thin sections from stable isotope tracer studies by LA-MC-ICP-MS Elemental bio-imaging of melanoma in lymph node biopsies Novel bioimaging techniques of metals by laser ablation inductively coupled plasma mass spectrometry for diagnosis of fibrotic and cirrhotic liver disorders Zinc and cadmium mapping in the apical shoot and hypocotyl tissues of radish by high-resolution secondary ion mass spectrometry (NanoSIMS) after short-term exposure to metal contamination Cadmium and zinc localization by SIMS in leaves of Populus deltoides (cv. Lena) grown in a metal polluted soil Subcellular redistribution and mitotic inheritance of transition metals in proliferating mouse fibroblast cells Quantitative mapping of zinc fluxes in the mammalian egg reveals the origin of fertilization-induced zinc sparks Zinc sparks are triggered by fertilization and facilitate cell cycle resumption in mammalian eggs Importance of measuring free zinc in cells Chemically diverse small molecule fluorescent chemosensors for copper ion Selective chemosensor capable of sensing both CN − and Zn 2+ : Its application to zebrafish Recent Advances in the Development of Chromophore-Based Chemosensors for Nerve Agents and Phosgene Supramolecular Luminescent Sensors Development of Ion Chemosensors Based on Porphyrin Analogues Development and Clinical Application of A Rapid IgM-IgG Combined Antibody Test for SARS-CoV-2 Infection Diagnosis Fluorescent chemosensors: The past, present, and future Chemosensors for Hg Ions: A Review of Literature Colorimetric Fluorescent Sensors for Hemoglobin Based on BODIPY Dyes Single Chemosensor for Double Analytes: Spectrophotometric Sensing of Cu 2+ and Fluorogenic Sensing of Al 3+ Under Aqueous Conditions Fluorescent Chemosensors for Toxic Organophosphorus Pesticides: A Review Coumarin-hydrazone based high selective fluorescence sensor for copper (II) detection in aqueous solution Substitutional group dependent colori/fluorimetric sensing of Mn 2+ , Fe 3+ and Zn 2+ ions by simple Schiff base chemosensor turn-on" fluorimetric chemosensor for the selective detection of cyanide and its application in food samples Synthesis of new colori/fluorimetric chemosensor for selective sensing of biologically important Fe 3+ , Cu 2+ , and Zn 2+ metal ions A new multifunctional Schiff-based chemosensor for mask-free fluorimetric and colorimetric sensing of F − and CN − A new thiophene-based dual functional chemosensor for ultrasensitive colorimetric detection of Cu 2+ in aqueous solution and highly selective fluorimetric detection of Al 3+ in living cells BODIPY-derived multi-channel polymeric chemosensor with pH-tunable sensitivity: Selective colorimetric and fluorimetric detection of Hg 2+ and HSO 4 − in aqueous media Fluorescent chemosensors for Zn 2+ A simple quinolone Schiff-base containing CHEF based fluorescence "turn-on" chemosensor for distinguishing Zn 2+ and Hg 2+ with high sensitivity, selectivity, and reversibility An 8-aminoquinoline derivative as a molecular platform for fluorescent sensors for Zn(II) and Cd(II) ions Quinoline fluorescent probes for zinc-From diagnostic to therapeutic molecules in treating neurodegenerative diseases Binding and ratiometric dual ion recognition of Zn 2+ and Cu 2+ by 1,3,5-tris-amidoquinoline conjugate of calix[6]arene by spectroscopy and its supramolecular features by microscopy A highly selective turn-on fluorescent sensor for glucosamine from amidoquinoline-napthalimide dyads A highly selective fluorescence sensor for Zn 2+ and Cu 2+ based on diarylethene with a piperazine-linked amidoquinoline unit A new fluorescence sensor based on diarylethene with a N'-(quinolin-8-ylmethylene)benzohydrazide group for Zn 2+ detection An efficient sensor for Zn 2+ and Cu 2+ based on different binding modes 4-Amino-1,8-naphthalimide-based fluorescent sensor with high selectivity and sensitivity for Zn 2+ imaging in living cells Selective fluorescence sensing of Cu(II) and Zn(II) using a simple Schiff base ligand: Naked eye detection and elucidation of photoinduced electron transfer (PET) mechanism A Schiff base ligand of coumarin derivative as an ICT-Based fluorescence chemosensor for Al 3+ An ICT based "turn on/off" quinoline armed calix[4]arene fluoroionophore: Its sensing efficiency towards fluoride from wastewater and Zn 2+ from blood serum A selective and sensitive fluorescence probe for imaging endogenous zinc in living cells Zn 2+ -triggered amide tautomerization produces a highly Zn 2+ -selective, cell-permeable, and ratiometric fluorescent sensor Responsive mechanism and molecular design of di-2-picolylamine-based two-photon fluorescent probes for zinc ions Novel 1,10-phenanthroline-Di-2-picolylamine scaffold as a selective chemosensor for copper and cyanide ions Quinoline-based "on-off" fluorescent sensor for acetate: Effect of link mode between binding sites and fluorophore on fluorescence changes A Quinoline-Appended Cyclodextrin Derivative as a Highly Selective Receptor and Colorimetric Probe for Nucleotides Fluorescent anion sensing by bisquinolinium pyridine-2,6-dicarboxamide receptors in water Ratiometric fluorescent probe based on symmetric peptidyl receptor with picomolar affinity for Zn 2+ in aqueous solution Chupakhin, O.N. π-Extended fluorophores based on 5-aryl-2,2'-bipyridines: Synthesis and photophysical studies Direct C[sbnd]H/C[sbnd]Li coupling of 1,2,4-triazines with C 6 F 5 Li followed by aza-Diels-Alder reaction as a pot, atom, and step economy (PASE) approach towards novel fluorinated 2,2 -bipyridine fluorophores Probing biologically and environmentally important metal ions with fluorescent chemosensors: Thermodynamic versus optical response selectivity in some study cases BODIPY Dyes Functionalized with Pendant Cyclic and Acyclic Polyamines A simple and selective fluorometric assay for dopamine using a calcein blue-Fe 2+ complex fluorophore Design of a binuclear Ni(II)-iminodiacetic acid (IDA) complex for selective recognition and covalent labeling of His-tag fused proteins A indole-trizole-rhodamine triad as ratiometric fluorescent probe for nanomolar-concentration level Hg 2+ sensing with high selectivity The binding behavior of itraconazole with hemoglobin: Studies from multi-spectroscopic techniques Synthesis of Novel Triazole-Linked Schiff Base Derivative A Schiff-base receptor based naphthalimide derivative: Highly selective and colorimetric fluorescent turn-on sensor for Al 3+ Synthesis and Design of Fluorescence Ligands to Act as Sensor for Zinc A highly selective ratiometric fluorescent chemosensor for Cu(II) based on dansyl-functionalized thiol stabilized silver nanoparticles A quinolinyl antipyrine based fluorescence sensor for Zn 2+ and its application in bioimaging Evolution of fluorescein as a platform for finely tunable fluorescence probes A new Zn 2+ -selective potentiometric sensor based on dithizone-PVC membrane A Schiff base complex of Zn(II) as a neutral carrier for highly selective PVC membrane sensors for the sulfate ion Histochemically-reactive zinc in amyloid plaques, angiopathy, and degenerating neurons of Alzheimer's diseased brains -methoxy-8-p-toluenesulfonamido-quinoline), a common fluorescent sensor for cellular zinc, images zinc proteins Chemistry of zinc(II) fluorophore sensors Development of fluorescent zinc chemosensors based on various fluorophores and their applications in zinc recognition Methoxy-Substituted TQEN Family of Fluorescent Zinc Sensors Steric and Stereochemical Modulation in Pyridyl-and Quinolyl-Containing Ligands Isoquinoline-Based TQEN Family as TPEN-Derived Fluorescent Zinc Sensors Bis(2-quinolylmethyl)ethylenediaminediacetic acids (BQENDAs), TQEN-EDTA hybrid molecules as fluorescent zinc sensors Small Molecular Fluorescent Sensor with Femtomolar Sensitivity for Zinc Ion Fluorescent Sensors for Zn 2+ Based on a Fluorescein Platform: Synthesis, Properties, and Intracellular Distribution ZP4, an Improved Neuronal Zn 2+ Sensor of the Zinpyr Family A Sensitive Probe for the Detection of Zn(II) by Time-Resolved Fluorescence Structural parameters of Zn(II) complexes of 8-hydroxyquinoline-based tripodal ligands affect fluorescence quantum yield Fluorescence Sensing and Binding Behavior of Aminobenzenesulfonamido-quinolinoβcyclodextrin to Zn 2+ Fluorometric study of the inclusion interaction of b-cyclodextrin derivatives with tetraphenylporphyrin and its analytical application Synthesis and Characterization of Pyrene/Quinoline Based Zn 2+ Selective Fluorescent Sensor Substituent-dependent fluorescent sensors for zinc ions based on carboxamidoquinoline Novel zinc fluorescent probe bearing dansyl and aminoquinoline groups Ratiometric and water-soluble fluorescent zinc sensor of carboxamidoquinoline with an alkoxyethylamino chain as receptor A highly selective fluorescent and colorimetric chemosensor for Zn II and its application in cell imaging Zinc selective chemosensors based on the flexible dipicolylamine and quinoline Highly sensitive and selective fluorescent sensor for distinguishing cadmium from zinc ions in aqueous media The quinoline derivative of ratiometric and sensitive fluorescent zinc probe based on deprotonation A ratiometric fluorescent probe for zinc ions based on the quinoline fluorophore A highly zinc(II) -selective fluorescent sensor based on 8-aminoquinoline and its application in biological imaging A colorimetric and fluorescent turn-on chemosensor operative in aqueous media for Zn 2+ based on a multi functionalized spirobenzopyran derivative A new rhodamine based colorimetric 'off-on' fluorescence sensor selective for Pd 2+ along with the first bound X-ray crystal structure A quinoline group modified SBA-15 inhibit logic gate with [Cu 2+ and Zn 2+ ] or [Cu 2+ and Cd 2+ ] as inputs. Micropor Mesopor Mat Ratiometric and reusable fluorescent nanoparticles for Zn 2+ and H 2 PO 4 . A detection in aqueous solution and living cells Sensing of Zinc (II) Using Ordered Mesoporous Silica Material (MCM-41) Functionalized with N-(Quinolin-8-yl)-2-[3-(triethoxysilyl) propylamino] acetamide 8-Aminoquinoline-based ratiometric zinc probe: Unexpected binding mode and its application in living cells A quinoline-based selective 'turn on' chemosensor for zinc(II) via quad-core complex, and its application in live cell imaging A highly sensitive and selective ratiometric fluorescent sensor for Zn 2+ ion based on ICT and FRET A quinoline-based ratiometric fluorescent probe for discriminative detection of Zn 2+ and Cd 2+ with different binding modes, and its Zn 2+ complex for relay sensing of pyrophosphate and adenosine triphosphate A water-soluble fluorescent chemosensor having a high affinity and sensitivity for Zn 2+ and its biological application A highly selective "turn-on" fluorescent chemosensor based on 8-aminoquinoline for detection of Zn 2+ A near-infrared turn-on fluorescent nanosensor for zinc(II) based on CuInS2 quantum dots modified with 8-aminoquinoline 8-aminoquinoline functionalized silica nanoparticles: A fluorescent nanosensor for detection of divalent zinc in aqueous and in yeast cell suspension Flipping the light switch 'ON'-the design of sensor molecules that show cation-induced fluorescence enhancement with heavy and transition metal ions Estimation of stability constants for metal-ligand complexes containing neutral nitrogen donor atoms with applications to natural organic matter The development of two fluorescent chemosensors for the selective detection of Zn 2+ and Al 3+ ions in a quinoline platform by tuning the substituents in the receptor part: Elucidation of the structures of the metal-bound chemosensors and biological studies Synthesis and characterization of 8-aminoquinolines, substituted by electron-donating groups, as high-affinity copper chelators for the treatment of Alzheimer's disease Optical and Electrical Properties of Eggshell Determination of Binding Constants Ultraviolet absorbance titration for the determination of conditional stability constants of Hg (II) and dissolved organic matter Spectroscopic Study on the Interaction between Methylene Blue and Chondroitin 4-Sulfate and Its Analytical Application Interaction of. delta.-and. lambda.-[Ru (phen) 2DPPZ] 2+ with DNA: A calorimetric and equilibrium binding study New Fluorescence PET Systems Based on N 2 S 2 Pyridine-Anthracene-Containing Macrocyclic Ligands. Spectrophotometric, Spectrofluorimetric, and Metal Ion Binding Studies Ba nyai, I. Dynamic NMR for coordination chemistry Detection limits of chemical sensors: Applications and misapplications Methodologies for assessment of limit of detection and limit of identification using surface-enhanced Raman spectroscopy IUPAC-consistent approach to the limit of detection in partial least-squares calibration Simultaneous Determination of Zn(II), Cd(II), Pb(II), and Cu(II) Using Differential Pulse Anodic Stripping Voltammetry at a Bismuth Film-Modified Electrode Quinoline-based hydrazone for colorimetric detection of Co 2+ and fluorescence turn-on response of Zn 2+ Selective and differential detection of Hg 2+ and Cu 2+ with use of a single rhodamine hydrazone-type probe in the absence and presence of UV irradiation Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement Analytical methods development and validation Validation of Analytical Methods Based on Chromatographic Techniques: An Overview Basic Principles of Fluorescence Microscopy Fluorescence spectroscopy in biochemistry: Teaching basic principles with visual demonstrations Multifunctional magnetic core-shell fibrous silica sensing probe for highly sensitive detection and removal of Zn 2+ in aqueous solution A highly selective and sensitive ratiometric fluorescent chemosensor for Zn 2+ based on diarylethene with a benzyl-linked 8-aminoquinoline-2-aminomethylpyridine unit A novel diarylethene-based fluorescent switch with a carboxamidoquinoline unit for sensing of Zn(II) ion Self-assemblies of zinc complexes for aggregation-induced emission luminogen precursors A highly selective turn-on chemosensor capable of monitoring Zn 2+ concentrations in living cells and aqueous solution A novel highly selective ratiometric fluorescent sensor for relay recognition of Zn 2+ and H 2 PO 4 − Off-On-Off" type fluorescent chemosensor for the relay detection of Zn 2+ and H 2 PO 4 − in aqueous environment Molecular recognition and fluorescence sensing of monophosphorylated peptides in aqueous solution by bis (zinc(II)-Dipicolylamine) -based artificial receptors Amidopyrroles: From anion receptors to membrane transport agents Aminoquinoline-salicylaldimine dyads as highly selective turn-on fluorescent sensors for zinc(II) ions The authors appreciate and acknowledge the support from Centre of Research and Instrumentation, Universiti Kebangsaan Malaysia. The authors declare no conflict of interest.