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WHY FALSE POSITIVES ARE PROBLEMATIC FOR OPIOID TESTING

January 20, 2019

Testing for Opioid Use

It’s no wonder so many businesses, governmental entities, and organizations are vested in more accurate testing for opioid use. The trouble with opioids is that they can be used both legally and illegally; for many, prescription painkillers act as a gateway to other, harder opioids like heroin. In 2015, nearly half of all opioid overdoses involved synthetic or semisynthetic drugs such as morphine, oxycodone, or fentanyl.

Opiates belong to a class of compounds noted for the way in which they interact with their endogenous opiate receptors. Synthetic opioids are notoriously difficult to detect and typically require separate immunoassays for screening.

Image of a spilled pill bottle with red and white pills

False Positives in Opiate Testing

The primary toxicology tests used for opioid testing are antibody-based immunoassays and specific drug identification tests. The former is cost-effective and typically quite sensitive, but its specificity is limited by cross-reactivity. False positives can result due to cross-reactivity through direct binding of the antibody, either from ingestion of a common opiate (such as poppy seeds) or even some common medications (such as quinolone antibiotics.)

It is particularly difficult to detect opioid abuse in patients who are already taking legally prescribed opiates. Prescription codeine, for example, can result in a false positive for heroin use as both codeine and heroin share morphine as their metabolite. Likewise, patients being treated for the avoidance of opiates may be given buprenorphine; in some cases, actual heroin use has presented as a false-positive for buprenorphine, failing to alert medical professionals of continued illicit drug use.

RELATED WEBINAR: How Enzymes Fail: The Hidden Secrets of Urine-Induced Inhibition Are urine samples destroying your β-glucuronidase enzyme? Why do some enzymes work beautifully with reference materials and eventually fail when challenged with real human samples? Join us as we walk you through this phenomenon. Learn how you can prevent your difficult urine samples from compromising your confirmatory tests and prevent the likelihood of false negatives. WATCH NOW

Solving the Problem of False Positives

Urine analysis for the presence of specific opioids is a more complicated process than traditional urine drug testing. Most synthetic and semisynthetic opioids have their own EIAs; a full roster of EIAs should be on-hand in any laboratory or clinical setting. The concentration of urine can also prove problematic, particularly when the sample has been tampered with or diluted in any way.

IMCSzyme is advancing the science of drug testing through faster, more comprehensive hydrolysis. In less than 15 minutes, the enzyme can reach over 90% hydrolysis for a wide array of opiates including codeine-6, benzodiazepine, and morphine-3. By reducing the incubation period for the testing of commonly prescribed/abused opiates, IMCSzyme expedites the process of any follow-up specificity testing that might ensue.

Are you interested in a better, more reliable solution for drugs of abuse testing in your lab or clinic? Find  more information on IMCSzyme’s technical specifications here, or reach out to an IMCS team member today to talk further.

Category: BLOG, LATEST NEWS
Next Post:3 CHANGES ON THE HORIZON FOR PRECISION MEDICINE

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ABOUT IMCS

INTEGRATED MICRO-CHROMATOGRAPHY SYSTEMS, INC. (IMCS) IS A BIOTECHNOLOGY COMPANY FOCUSED ON DELIVERING TOOLS AND SERVICES THAT HELP PAVE THE WAY FOR THE FUTURE OF PRECISION MEDICINE. WE STRIVE TO ADDRESS THE GROWING NEEDS OF CLINICAL AND RESEARCH LABORATORIES THROUGH ADVANCED TECHNOLOGIES THAT INCREASE TESTING EFFICIENCY AND ACCURACY.

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Caleb-Schlachter-for-web

Caleb R. Schlachter, Ph.D.

Principal Scientist
Caleb R. Schlachter, Ph.D., as the Principal Scientist at IMCS, leads and provides guidance for several research and development projects that involve proteins, including enzymes for glycan hydrolysis and glycan synthesis. He has co-authored multiple patents, posters, and peer-reviewed articles on β-glucuronidases and sulfatases.
Gray Amick for web

Gray D. Amick, Ph.D.

Director of Operations
Gray D. Amick, Ph.D., is the Director of Operations at IMCS with over 26 years of experience in forensic DNA analysis and toxicology. Prior to joining IMCS, he led forensic DNA testing for the Richland County Sheriff’s Department as technical leader and lab director. He has been court-qualified as an expert over 100 times and has authored and co-authored multiple posters and peer-reviewed articles.
Amanda M Headshot

Amanda C. McGee

Research Scientist
Amanda C. McGee is a Research Scientist at IMCS involved with enzyme characterizations, new analytical method developments, and advanced technical support. She joined IMCS with several years of experience in analytical testing for active pharmaceutical ingredients as per cGMP, USP and ICH guidelines. She has co-authored peer reviewed articles in the Journal of Analytical Toxicology and presented research at national and international conferences.
Andrew_Headshot

L. Andrew Lee, Ph.D.

Co-Founder and Chief Scientific Officer
L. Andrew Lee, Ph.D. co-founded IMCS and leads research and development efforts in enzyme engineering and automated micro-chromatography workflows. He directs new market efforts in glycan synthesis, supported by three NIH Fast-Track awards.

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