• Media type: E-Article
  • Title: Development of a point‐of‐care test for the detection of MDMA in latent fingerprints using surface plasmon resonance and lateral flow technology
  • Contributor: Pollard, Caroline; Hudson, Mark; McDonnell, James M.; Royall, Paul G.; Wolff, Kim
  • imprint: Wiley, 2022
  • Published in: Drug Testing and Analysis
  • Language: English
  • DOI: 10.1002/dta.3196
  • ISSN: 1942-7603; 1942-7611
  • Keywords: Spectroscopy ; Pharmaceutical Science ; Environmental Chemistry ; Analytical Chemistry
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>To date, a specific point‐of‐care test (POCT) for 3,4‐methylenedioxymethamphetamine (MDMA, ecstasy, ‘E’) in latent fingerprints (LFPs) has not been explored. Other POCTs identify MDMA in sweat by detecting the drug as a cross‐reactant rather than target analyte, thus decreasing the test's sensitivity. The study's aim was to design a sensitive POCT for the detection of MDMA in LFPs using surface plasmon resonance (SPR) and lateral flow immunoassay (LFA) technology. A high‐affinity antibody binding pair was identified using the former technique, deeming the pair suitable for a LFA. Titrations of fluorescently labelled antibody and antigen concentrations were tested to identify a sharp drop‐in signal upon the addition of MDMA to allow a clear distinction between negative and positive outcomes. We trialled the LFA by producing dose response curves with MDMA and a group of drugs that share a similar chemical structure to MDMA. These were generated through spiking the LFA with increasing levels of drug (0–400 pg/10 μl of MDMA; 0–10,000 pg/10 μl of cross‐reactant). Fluorescent test signals were measured using a cartridge reader. The cut‐off (threshold) 60 pg/10 μl calculated better cartridge performance (1.00 sensitivity, 0.95 specificity and 0.98 accuracy), when compared with 40 pg/10 μl. The biggest cross‐reactant was PMMA (250%), followed by MDEA (183%), MBDB (167%), MDA (16%) and methamphetamine (16%). A sensitive LFP screening tool requiring no sample preparation was successfully designed.</jats:p>