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Lateral flow immunoassay and enzyme linked immunosorbent assay as effective immunomethods for the detection of synthetic cannabinoid JWH-200 based on the newly synthesized hapten

. 2018 ; 5 () : 65-75. [epub] 20171206

Status PubMed-not-MEDLINE Language English Country Ireland Media electronic-ecollection

Document type Journal Article

Links

PubMed 29276691
PubMed Central PMC5738196
DOI 10.1016/j.toxrep.2017.12.004
PII: S2214-7500(17)30109-9
Knihovny.cz E-resources

In recent years, the use of synthetic cannabinoids (SCs) as drugs of abuse has greatly increased. SCs are associated with a risk of severe poisoning or even death. Therefore, more rapid, cost effective and reliable methods are needed, especially for the screening of drivers after traffic accidents and for detailed toxicological analysis in forensic laboratories. In this study, we developed a lateral flow immunoassay (LFIA) and an enzyme linked immunosorbent assay (ELISA) for the detection of JWH-200 in oral fluids. For this purpose a new hapten was prepared using a ten-step synthetic route. The developed immuno methods are based on antibodies obtained from rabbit immunized with synthesized hapten conjugated to carrier protein. The proposed methods are highly sensitive (LODLFIA = 0.08 ± 0.04 ng mL-1; LODELISA = 0.04 ± 0.02 ng mL-1). They were applied to the quantification of JHW-200 in spiked oral fluids. The recoveries ranged from 82 to 134% for both methods. The results correlated excellently with results obtained using UHPLC-MS/MS (R2LFIA = 0.99; R2ELISA = 0.99). Our developed methods could be an important tool for analyses of JWH-200 in human oral fluids. The one-step LFIA is particularly suitable for roadside and on-site monitoring due to the rapid qualitative results it delivers, while the ELISA is especially useful for laboratory quantitative analyses of positive samples captured by LFIA.

See more in PubMed

EMCDDA . Strategic Overview. 2016. EU drug markets report; pp. 28–29.

EMCDDA . Synthetic Cannabinoids in Europe. 2016. Perspectives on drugs.

Yeakel J.K., Logan B.K. Blood synthetic cannabinoid concentrations in cases of suspected impaired driving. J. Anal. Toxicol. 2013;37(8):547–551. PubMed

McGuinness T.M., Newell D. RISKY RECREATION synthetic cannabinoids have dangerous effects. J. Psychosoc. Nurs. Ment. Health Serv. 2012;50(8):16–18. PubMed

Logan B.K. Identification of synthetic cannabinoids in herbal incense blends in the United States. J. Forensic Sci. 2012;57(5):1168–1180. PubMed

Harris C.R., Brown A. Synthetic cannabinoid intoxication: a case series and review. J. Emerg. Med. 2013;44(2):360–366. PubMed

Uchiyama N. Identification and quantitation of two cannabimimetic phenylacetylindoles JWH-251 and JWH-250: and four cannabimimetic naphthoylindoles JWH-081, JWH-015, JWH-200, and JWH-073 as designer drugs in illegal products. Forensic Toxicol. 2010;29(1):25–37.

Wohlfarth A. Qualitative confirmation of 9 synthetic cannabinoids and 20 metabolites in human urine using LC-MS/MS and library search. Anal. Chem. 2013;85(7):3730–3738. PubMed PMC

Rodrigues W.C. Detection of synthetic cannabinoids in oral fluid using ELISA and LC-MS-MS. J. Anal. Toxicol. 2013;37(8):526–533. PubMed

Barnes A.J. Evaluation of a homogenous enzyme immunoassay for the detection of synthetic cannabinoids in urine. Forensic Sci. Int. 2014;241:27–34. PubMed PMC

Barnes A.J. Validation of an ELISA synthetic cannabinoids urine assay. Ther. Drug Monit. 2015;37(5):661–669. PubMed PMC

Arntson A. Validation of a novel immunoassay for the detection of synthetic cannabinoids and metabolites in urine specimens. J. Anal. Toxicol. 2013;37(5):284–290. PubMed

Spinelli E. Performance characteristics of an ELISA screening assay for urinary synthetic cannabinoids. Drug Test. Anal. 2015;7(6):467–474. PubMed

Mohr A.L. Enzyme-linked immunosorbent assay (ELISA) for the detection of use of the synthetic cannabinoid agonists UR-144 and XLR-11 in human urine. J. Anal. Toxicol. 2014;38(7):427–431. PubMed

Wang K. The application of lateral flow immunoassay in point of care testing: a review. Nano Biomed. Eng. 2016;8(3):172–183.

Sajid M., Kawde A.-N., Daud M. Designs, formats and applications of lateral flow assay: a literature review. J. Saudi Chem. Soc. 2015;19(6):689–705.

Blažková M., Rauch P., Fukal L. Strip-based immunoassay for rapid detection of thiabendazole. Biosens. Bioelectron. 2010;25(9):2122–2128. PubMed

Velasco R., Feberero C., Sanz R. α-Lithiated aryl benzyl ethers: inhibition of [1,2]-wittig rearrangement and application to the synthesis of benzo[b]furan derivatives. Org. Lett. 2015;17(18):4416–4419. PubMed

Willis P.G. Synthesis and structure-activity relationship of a novel series of aminoalkylindoles with potential for imaging the neuronal cannabinoid receptor by positron emission tomography. J. Med. Chem. 2005;48(18):5813–5822. PubMed

Upender V. The synthesis and biological activity of two analogs of the anti-HIV alkaloid michellamine B. J. Heterocycl. Chem. 1996;33(4):1371–1384.

Cai L. Efficient microwave-assisted cyanation of aryl bromide. Synth. Commun. 2004;34(7):1215–1221.

Ghaffarzadeh M., Bolourtchian M., Halvagar M.M.R. High yield synthesis of aryl cyanides under microwave irradiation. J. Chem. Res. 2003;2003(12):814.

Zhang Q., Botting N.P. The synthesis of [2,3,4-13C3]glycitein. Tetrahedron. 2004;60(52):12211–12216.

Cavill G.W.K., Tetaz J.R. 696. The hydroxynaphthoate series. Part I. A synthesis of 4-hydroxynaphthoic acid and its simple esters. J. Chem. Soc. 1952;0:3634–3636.

Frost J.M. Indol-3-ylcycloalkyl ketones: effects of N1 substituted indole side chain variations on CB2 cannabinoid receptor activity. J. Med. Chem. 2009;53(1):295–315. PubMed

Guchhait S.K., Kashyap M., Kamble H. ZrCl4-mediated regio- and chemoselective Friedel-Crafts acylation of indole. J. Org. Chem. 2011;76(11):4753–4758. PubMed

Yatsimirskaya E.A. Preparation of conjugates of progesterone with bovine serum albumin in the reversed micellar medium. Steroids. 1993;58(11):547–550. PubMed

Lapcik O. Immunoassay for biochanin a. J. Immunol. Methods. 2004;294(1–2):155–163. PubMed

Holubova-Mickova B. Development of colloidal carbon-based immunochromatographic strip for rapid detection of carbaryl in fruit juices. Eur. Food Res. Technol. 2010;231(3):467–473.

Fojtíková L. Development of enzyme-linked immunosorbent assay for determination of boldenone in dietary supplements. Food Anal. Methods. 2016;9(11):3179–3186.

Goodrow M.H. Strategies for immunoassay hapten design, in immunoanalysis of agrochemicals. Am. Chem. Soc. 1995:119–139.

Marco M.-P., Gee S., Hammock B.D. Immunochemical techniques for environmental analysis II: Antibody production and immunoassay development. TrAC Trends Anal. Chem. 1995;14(8):415–425.

Urusov A.E. Multistage in one touch design with a universal labelling conjugate for high-sensitive lateral flow immunoassays. Biosens. Bioelectron. 2016;86:575–579. (Supplement C) PubMed

Posthuma-Trumpie G.A., Korf J., van Amerongen A. Lateral flow (immuno) assay: its strengths, weaknesses, opportunities and threats. A literature survey. Anal. Bioanal. Chem. 2009;393(2):569–582. PubMed

Coulter C., Garnier M., Moore C. Synthetic cannabinoids in oral fluid. J. Anal. Toxicol. 2011;35(7):424–430. PubMed

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