Development of Immunochromatographic Assay for Determination of Tetracycline in Human Serum
Determining antibiotic concentration in human blood provides useful pharmacokinetic information. Commonly used methods such as ELISA require a long time to obtain results and thus cannot be applied when information is needed immediately. In this study, a novel antibody-based lateral flow technique w...
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doaj-c400fbb3f2ad4df68326f9fabbcfeb9a2020-11-25T00:33:28ZengMDPI AGAntibiotics2079-63822018-11-01749910.3390/antibiotics7040099antibiotics7040099Development of Immunochromatographic Assay for Determination of Tetracycline in Human SerumAnna N. Berlina0Anastasia V. Bartosh1Anatoly V. Zherdev2Chuanlai Xu3Boris B. Dzantiev4A.N. Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, Moscow 119071, RussianA.N. Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, Moscow 119071, RussianA.N. Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, Moscow 119071, RussianSchool of Food Science and Technology, Jiangnan University, Wuxi 214122, ChinaA.N. Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, Moscow 119071, RussianDetermining antibiotic concentration in human blood provides useful pharmacokinetic information. Commonly used methods such as ELISA require a long time to obtain results and thus cannot be applied when information is needed immediately. In this study, a novel antibody-based lateral flow technique was developed for tetracycline detection in human serum. Contrary to tests developed to analyze food samples, the features of work with serum as analyzed probe were studied for the first time here. The application of labeled and unlabeled specific antibodies was compared. For this purpose, specific and anti-species antibodies were labeled with gold nanoparticles and used for antigen⁻antibody interaction on the membrane surface with observed staining in the test zone. For both schemes, optimal conditions were established to provide the best sensitivity. The developed assay has a limit of visual detection as low as 35 and 11 ng/mL for the direct and indirect labeled antibodies, respectively. The limit of instrumental detection is from 0.4 to 3.5 ng/mL for diluted and undiluted sera. The use of indirect antibody labeling showed a small increase in sensitivity compared to traditional direct antibody labeling. The developed method showed no cross-reactivity with antibiotics of other classes. The method was used to test samples of serum. The results showed high correlation with the data obtained by ELISA (R<sup>2</sup> = 0.98968). The assay provides a quick assessment of the amount of antibiotics in the blood and keeps them under control throughout the duration of therapy.https://www.mdpi.com/2079-6382/7/4/99tetracyclinehuman serumlateral flowantibiotics detectionimmunoassaygold nanoparticles |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anna N. Berlina Anastasia V. Bartosh Anatoly V. Zherdev Chuanlai Xu Boris B. Dzantiev |
spellingShingle |
Anna N. Berlina Anastasia V. Bartosh Anatoly V. Zherdev Chuanlai Xu Boris B. Dzantiev Development of Immunochromatographic Assay for Determination of Tetracycline in Human Serum Antibiotics tetracycline human serum lateral flow antibiotics detection immunoassay gold nanoparticles |
author_facet |
Anna N. Berlina Anastasia V. Bartosh Anatoly V. Zherdev Chuanlai Xu Boris B. Dzantiev |
author_sort |
Anna N. Berlina |
title |
Development of Immunochromatographic Assay for Determination of Tetracycline in Human Serum |
title_short |
Development of Immunochromatographic Assay for Determination of Tetracycline in Human Serum |
title_full |
Development of Immunochromatographic Assay for Determination of Tetracycline in Human Serum |
title_fullStr |
Development of Immunochromatographic Assay for Determination of Tetracycline in Human Serum |
title_full_unstemmed |
Development of Immunochromatographic Assay for Determination of Tetracycline in Human Serum |
title_sort |
development of immunochromatographic assay for determination of tetracycline in human serum |
publisher |
MDPI AG |
series |
Antibiotics |
issn |
2079-6382 |
publishDate |
2018-11-01 |
description |
Determining antibiotic concentration in human blood provides useful pharmacokinetic information. Commonly used methods such as ELISA require a long time to obtain results and thus cannot be applied when information is needed immediately. In this study, a novel antibody-based lateral flow technique was developed for tetracycline detection in human serum. Contrary to tests developed to analyze food samples, the features of work with serum as analyzed probe were studied for the first time here. The application of labeled and unlabeled specific antibodies was compared. For this purpose, specific and anti-species antibodies were labeled with gold nanoparticles and used for antigen⁻antibody interaction on the membrane surface with observed staining in the test zone. For both schemes, optimal conditions were established to provide the best sensitivity. The developed assay has a limit of visual detection as low as 35 and 11 ng/mL for the direct and indirect labeled antibodies, respectively. The limit of instrumental detection is from 0.4 to 3.5 ng/mL for diluted and undiluted sera. The use of indirect antibody labeling showed a small increase in sensitivity compared to traditional direct antibody labeling. The developed method showed no cross-reactivity with antibiotics of other classes. The method was used to test samples of serum. The results showed high correlation with the data obtained by ELISA (R<sup>2</sup> = 0.98968). The assay provides a quick assessment of the amount of antibiotics in the blood and keeps them under control throughout the duration of therapy. |
topic |
tetracycline human serum lateral flow antibiotics detection immunoassay gold nanoparticles |
url |
https://www.mdpi.com/2079-6382/7/4/99 |
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