Simultaneous determination of praziquantel, fipronil, eprinomectin, (S)-methoprene, their key related substances and butylated hydroxytoluene (BHT) in a topical veterinary drug product by a single stability indicating high performance liquid chromatography method.


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:
20 Jan 2024
Historique:
received: 26 07 2023
revised: 14 10 2023
accepted: 17 10 2023
medline: 6 12 2023
pubmed: 10 11 2023
entrez: 10 11 2023
Statut: ppublish

Résumé

A simple, robust and QC (quality control) friendly high performance liquid chromatography (HPLC) method was developed and validated for simultaneous determination of four active pharmaceutical ingredient [namely fipronil, (S)-methoprene, eprinomectin, and praziquantel] and their key degradation products in a broad-spectrum topical finished product. Typical sample of the finished product contains a total of 30-plus peaks of interest. Analytes were separated on a HALO C18 column (150 mm × 4.6 mm i.d., 2.7 µm particle size) with a gradient elution at 50 °C column temperature and 0.6 mL/min flow rate. Detection wavelength of 245 nm is used for praziquantel, eprinomectin and their degradation products, 265 nm for (S)-methoprene and its degradation products and 280 nm for fipronil and its degradation products and for the antioxidant, BHT. Mobile phase of the method is composed of 10 mM potassium phosphate buffer and 1,4- Dioxane (98/2, v/v, pH 5.0) as mobile phase-A, and EtOH/MeOH/MeCN/IPA (86/4/6/4, v/v/v/v) as mobile phase-B. All analytes of interest were adequately separated by this single HPLC method. The stability-indicating capability of the method has been demonstrated by successfully separating the degradation products in the stressed degraded samples of the finished product. Limit of quantitation (LOQ) and limit of detection (LOD) of the method is 0.3% and 0.1% of target analytical concentration for each individual API in the finished product. This method has been demonstrated to be sensitive, robust, specific, accurate and stability-indicating for analysis of the topical drug product containing praziquantel, fipronil, eprinomectin and (S)-methoprene.

Identifiants

pubmed: 37948779
pii: S0731-7085(23)00574-5
doi: 10.1016/j.jpba.2023.115805
pii:
doi:

Substances chimiques

eprinomectin 75KP30FD8O
Praziquantel 6490C9U457
Antiparasitic Agents 0
Methoprene 8B830OJ2UX
fipronil QGH063955F
Butylated Hydroxytoluene 1P9D0Z171K
Veterinary Drugs 0
Drug Combinations 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

115805

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

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

Renuka P Rathnasekara (RP)

Global Pharmaceutical Technical Support (GPTS), Boehringer Ingelheim Animal Health USA Inc., 631 Route 1 South, North Brunswick, NJ 08902, USA. Electronic address: renuka.rathnasekara@boehringer-ingelheim.com.

Abu M Rustum (AM)

Global Pharmaceutical Technical Support (GPTS), Boehringer Ingelheim Animal Health USA Inc., 631 Route 1 South, North Brunswick, NJ 08902, USA.

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Classifications MeSH