Development and validation of ion-pairing HPLC-CAD chromatography for measurement of Islatravir's phosphorylated intermediates.


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:
10 May 2022
Historique:
received: 05 01 2022
revised: 17 02 2022
accepted: 18 02 2022
pubmed: 28 2 2022
medline: 6 4 2022
entrez: 27 2 2022
Statut: ppublish

Résumé

Biocatalytic processes have become more prevalent in the pharmaceutical industry, leading to analytical challenges not faced when characterizing more traditional synthetic routes. A novel one-pot biocatalytic process has been established for Islatravir, an HIV reverse transcriptase translocation inhibitor for the treatment and prevention of HIV-1. As a one-pot reaction, the Islatravir chemistry contains multiple intermediates that are not isolated. Additionally, these unisolated intermediates have no chromophores, making traditional LC-UV techniques ineffective for characterization. A hydrophilic interaction chromatography (HILIC) method with a charged aerosol detector (CAD) was initially developed, however numerous inorganic species present in the one-pot reaction were retained; this led to co-elution of compounds and poor peak shapes. An innovative ion-pairing LC method was developed in order to resolve inorganic species, intermediates, and the API, for use during in-process control of the Islatravir biocatalytic reaction. Aided by a volatile ion-pairing reagent compatible with the CAD, this method successfully retains and resolves the highly polar intermediates of interest and Islatravir API. This novel method was successfully validated and has allowed the Islatravir biocatalytic process to be fully characterized from the early intermediates through the final API within the one-pot reaction without the need for isolations. This novel ion-pairing HPLC-CAD technique lays the groundwork for method development on current and future biocatalytic-produced drug substances.

Identifiants

pubmed: 35220202
pii: S0731-7085(22)00105-4
doi: 10.1016/j.jpba.2022.114684
pii:
doi:

Substances chimiques

Aerosols 0
Deoxyadenosines 0
islatravir QPQ082R25D

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114684

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Auteurs

Matthew J Gunsch (MJ)

Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, NJ 07065, USA. Electronic address: matthew.gunsch@merck.com.

Erica L Schwalm (EL)

Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, NJ 07065, USA.

Claire M Ouimet (CM)

Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, NJ 07065, USA.

Holst M Halsey (HM)

Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, NJ 07065, USA.

Simon E Hamilton (SE)

Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, NJ 07065, USA.

Frank Bernardoni (F)

Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, NJ 07065, USA.

Junyong Jo (J)

Analytical Research and Development, MRL, Merck & Co., Inc., Rahway, NJ 07065, USA.

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Classifications MeSH