Rapid detection of active pharmaceutical ingredients in drug products collected at an international mail facility by a satellite laboratory using a "toolkit" consisting of a handheld Raman spectrometer, portable mass spectrometer and portable FT-IR spectrometer.


Journal

Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336

Informations de publication

Date de publication:
05 Feb 2023
Historique:
received: 28 09 2022
revised: 07 11 2022
accepted: 08 11 2022
pubmed: 25 11 2022
medline: 7 1 2023
entrez: 24 11 2022
Statut: ppublish

Résumé

A satellite laboratory "toolkit" consisting of a handheld Raman spectrometer, portable direct analysis in real-time mass spectrometer (DART-MS) and portable Fourier transform infrared (FT-IR) spectrometer was employed to examine 926 pharmaceutical, unknown and dietary supplement products collected at an international mail facility (IMF) for the presence of declared and undeclared active pharmaceutical ingredients (APIs) over the course of 68 working days. The toolkit successfully identified over 650 APIs, including over 200 unique APIs, using two or more devices. The performance of each individual device, and toolkit as a whole, were evaluated on all products and a subset of the products was forwarded to full-service laboratories for confirmatory analysis to determine false positive and false negative rates of the toolkit. The subset consisted of seven negative items (those not found to contain APIs using the toolkit) and 124 positive items (those found to contain at least one API using the toolkit). Overall, no false positives were detected in the negative items and only four false negatives and five false positives were detected in the positive items. Regarding the positive items, 119 of the 124 items were found to contain at least one API using at least two toolkit devices; each of these APIs were confirmed by a full-service laboratory. Furthermore, 90.2% of the APIs found by confirmatory laboratory analysis were detected by at least two toolkit devices. Based on these metrics and the fact that no false positives were detected by more than one device, it was concluded that when the toolkit detects and subsequently verifies/confirms an API using two or more devices, the results are as reliable as those generated by a full-service laboratory.

Identifiants

pubmed: 36423496
pii: S0731-7085(22)00574-X
doi: 10.1016/j.jpba.2022.115153
pii:
doi:

Substances chimiques

Pharmaceutical Preparations 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115153

Informations de copyright

Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Adam Lanzarotta (A)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA. Electronic address: adam.lanzarotta@fda.hhs.gov.

Sara Kern (S)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

JaCinta Batson (J)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Brian Boyd (B)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Martin M Kimani (MM)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Weiwei Kuo (W)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Donna LaGarde (D)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Mark Loh (M)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Laurenee L Adeoshun (LL)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Lisa Lorenz (L)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Rebeca Melendez (R)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Flavia Morales-Garcia (F)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Michael Thatcher (M)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Anthony E Wetherby (AE)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

Mark R Witkowski (MR)

Forensic Chemistry Center, Office of Regulatory Science, Office of Regulatory Affairs, US Food & Drug Administration, Cincinnati, OH 45237, USA.

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Classifications MeSH