Chem. J. Chinese Universities ›› 2019, Vol. 40 ›› Issue (11): 2294.doi: 10.7503/cjcu20190379
• Analytical Chemistry • Previous Articles Next Articles
YANG Weiqiang1,ZHANG Guiyun2,LIN Hua1,NI Jiancong1,*(),HUANG Lingfeng1
Received:
2019-07-07
Online:
2019-11-10
Published:
2019-10-15
Contact:
NI Jiancong
E-mail:nijiancong@foxmail.com
Supported by:
CLC Number:
TrendMD:
YANG Weiqiang, ZHANG Guiyun, LIN Hua, NI Jiancong, HUANG Lingfeng. Ratiometric Fluorescence Assay for Visual Detection of Tetracycline Residues based on the Complex of Carbon Dots and Europium †[J]. Chem. J. Chinese Universities, 2019, 40(11): 2294.
Fig.1 Fluorescence quenching effect of tetracycline on CDs(A) and fluorescence enhancement effect of tetracycline on Eu3+ (B) c(Tetracycline)/(nmol·L-1): a. 0; b. 20; c. 40; d. 60; e. 80; f. 100. ρ(CDs)=1 μg/mL, c(Eu3+)=20 μmol/L. The NaOH-H3BO3 buffer solution concentration was 20 mmol/L with pH=9.0. Insets are the linear relationships between the fluorescence intensities of CDs(A) and Eu-TC(B) and the concentration of tetracycline, respectively.
Fig.3 Effect of mass concentration ratio of CDs/Eu3+ on the fluorescence assay(A) and effect of pH on the fluorescence of CDs and Eu-TC(B) (A) c(Tetracycline)=50 nmol/L, ρ(CDs)=1—3 μg/mL, c(Eu3+)=6—60 μmol/L. The NaOH-H3BO3 buffer solution concentration was 20 mmol/L(pH=9.0); (B) c(tetracycline)=100 nmol/L, ρ(CDs)=1 μg/mL, c(Eu3+)=20 μmol/L. The NaOH-H3BO3 buffer solution concentration was 20 mmol/L.
Fig.4 Fluorescence spectrum of CDs-Eu3+ probe varying with the concentration of tetracycline(A) and linear relationship between the lg(I618/I440) and the concentration of tetracycline(B) (A) The inset was the fluorescence color change of the solution. c(Tetracycline)/(nmol·L-1): a. 0; b. 20; c. 40; d. 60; e. 80; f. 100. ρ(CDs)=1 μg/mL; ρ(Eu3+)=20 μmol/L. The NaOH-H3BO3 buffer solution concentration was 20 mmol/L with pH=9.0.
Fig.5 Fluorescence response of CDs-Eu3+ probe to different antibiotics The concentration of tetracycline(TC), oxytetracycline(OTC), chlorotetracycline(CTC) and doxycycline(DOX) were 100 nmol/L; and the concentration of penicillin(PCN), erythromycin(ERY), ciprofloxacin(CIP), sulfadiazine(SD) and chloramphenicol(CAP) were 1 μmol/L.
Interference | Concentration of interference/(μmol·L-1) | Error(%) | Interference | Concentration of interference/(μmol·L-1) | Error(%) |
---|---|---|---|---|---|
LAS | 50.0 | 3.58 | Al3+ | 5.0 | -2.67 |
CPC | 50.0 | 2.89 | Fe3+ | 5.0 | 3.16 |
Tween-80 | 20.0 | 3.77 | Cu2+ | 10.0 | 2.53 |
Ca2+ | 50.0 | -0.83 | Zn2+ | 50.0 | 1.12 |
Mg2+ | 50.0 | -0.15 | Pb2+ | 20.0 | 0.45 |
Interference | Concentration of interference/(μmol·L-1) | Error(%) | Interference | Concentration of interference/(μmol·L-1) | Error(%) |
---|---|---|---|---|---|
LAS | 50.0 | 3.58 | Al3+ | 5.0 | -2.67 |
CPC | 50.0 | 2.89 | Fe3+ | 5.0 | 3.16 |
Tween-80 | 20.0 | 3.77 | Cu2+ | 10.0 | 2.53 |
Ca2+ | 50.0 | -0.83 | Zn2+ | 50.0 | 1.12 |
Mg2+ | 50.0 | -0.15 | Pb2+ | 20.0 | 0.45 |
Sample | Add/(nmol·L-1) | Found*/(nmol·L-1) | Recovery(%) | RSD(%, n=3) |
---|---|---|---|---|
1 | 5.0 | 5.33 | 106.6 | 4.7 |
2 | 20.0 | 20.33 | 101.7 | 3.9 |
3 | 80.0 | 78.21 | 97.8 | 2.5 |
Sample | Add/(nmol·L-1) | Found*/(nmol·L-1) | Recovery(%) | RSD(%, n=3) |
---|---|---|---|---|
1 | 5.0 | 5.33 | 106.6 | 4.7 |
2 | 20.0 | 20.33 | 101.7 | 3.9 |
3 | 80.0 | 78.21 | 97.8 | 2.5 |
[1] | Chopra I., Roberts M., Microbiol. Mol.Biol.Rev., 2001,65, 232— 260 |
[2] | Zhang X., Chen Z., Deng H., Yang K., Gong S., Lu W., Lan H., Asian J . Ecotoxicol., 2016,11, 44— 52 |
[3] | Liu X., Huang D., Lai C., Zeng G., Qin L., Zhang C., Yi H., Li B., Deng R., Liu S., Zhang Y., Trends Anal.Chem., 2018,109, 260— 274 |
[4] | Virolainen N. E., Pikkemaat M. G., Elferink J. W. A., Karp M. T., J. Agric. Food Chem., 2008,56, 11065— 11070 |
[5] | Chen Y., Kong D., Liu L., Song S., Hua K., Xu C., Food Anal. Method, 2015,9, 1— 10 |
[6] | Önal A., ., Food Chem 2011,127, 197— 203 |
[7] | Yang X., Zhu S., Dou Y., Zhuo Y., Luo Y., Feng Y ., Talanta, 2014,122, 36— 42 |
[8] | Sun X., Lei Y., Trends Anal.Chem., 2017,89, 163— 180 |
[9] | Gao X., Du C., Zhuang Z., Chen W ., J. Mater. Chem. C, 2016,4, 6927— 6945 |
[10] | Li Y. K., Yang T., Chen M. L., Wang J. H ., Talanta, 2018,180, 18— 24 |
[11] | Shamsipur M., Molaei K., Molaabasi F., Hosseinkhani S., Alizadeh N., Alipour M., Moassess S ., . Sens Actuators B, 2018,257, 772— 782 |
[12] | Jin H., Gui R., Sun J., Wang Y ., Talanta, 2018,176, 277— 283 |
[13] | Yan X., Song Y., Zhu C., Li H., Du D., Su X., Lin Y., Anal.Chem., 2018,90, 2618— 2624 |
[14] | Shi X., Wei W., Fu Z., Gao W., Zhang C., Zhao Q., Deng F., Lu X ., Talanta, 2019,194, 809— 821 |
[15] | Chen C., Zhao J., Lu Y., Sun J., Yang X., Anal. Chem., 2018,90, 3505— 3511 |
[16] | Zhong D., Yang K., Wang Y., Yang X ., Talanta, 2017,175, 217— 223 |
[17] | Ruiz-Palomero C., Benitez-Martinez S., Soriano M. L., Valcarcel M., . Anal. Chim. Acta, 2017,974, 93— 99 |
[18] | Feng Y., Zhong D., Miao H., Yang X ., Talanta, 2015,140, 128— 133 |
[19] | Shi W., Guo F., Han M., Yuan S., Guan W., Li H., Huang H., Liu Y., Kang Z ., J. Mater. Chem. B, 2017,5, 3293— 3299 |
[20] | Qian S Qiao L. n., Xu W., Jiang K., Wang Y., Lin H., ., Talanta, 2019,194, 598— 603 |
[21] | Heffern M. C., Matosziuk L. M., Meade T. J., Chem. Rev., 2014,114, 4496— 4539 |
[22] | Tan H., Ma C., Song Y., Xu F., Chen S., Wang L., Biosens. Bioelectron., 2013,50, 447— 452 |
[23] | Zhou Z., Li X., Gao J., Tang Y., Wang Q ., J. Agric. Food Chem., 2019,67, 3871— 3878 |
[24] | Li X., Ma H., Deng M., Iqbal A., Liu X., Li B., Liu W., Li J., Qin W ., J. Mater. Chem. C, 2017,5, 2149— 2152 |
[25] | Shen Z., Zhang C., Yu X., Li J., Wang Z., Zhang Z., Liu B ., J. Mater. Chem. C, 2018,6, 9636— 9641 |
[26] | Xu J., Shen X., Jia L., Zhou T., Ma T., Xu Z., Cao J., Ge Z., Bi N., Zhu T., Guo S., Li X ., J. Hazard. Mater., 2018,342, 158— 165 |
[27] | Gui R., Jin H., Bu X., Fu Y., Wang Z., Liu Q., ., Coord. Chem. Rev 2019,383, 82— 103 |
[28] | Zhou Y., Huang X., Liu C., Zhang R., Gu X., Guan G., Jiang C., Zhang L., Du S., Liu B., Han M. Y., Zhang Z ., Anal. Chem., 2016,88, 6105— 6109 |
[29] | He W., Gui R., Jin H., Wang B., Bu X., Fu Y ., Talanta, 2018,178, 109— 115 |
[30] | Li J. Y., Liu Y., Shu Q. W., Liang J. M., Zhang F., Chen X. P., Deng X. Y., Swihart M. T., Tan K. J., Langmuir., 2017,33, 1043— 1050 |
[31] | Tan H., Chen Y ., Sens. Actuators B, 2012,173, 262— 267 |
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