Analytical quality by design in the development of a solvent-modified micellar electrokinetic chromatography method for the determination of sitagliptin and its related compounds.

Capillary electrophoresis Experimental design Impurities Method operable design region Quality by design Sitagliptin

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 Aug 2021
Historique:
received: 12 04 2021
revised: 19 05 2021
accepted: 20 05 2021
pubmed: 31 5 2021
medline: 22 6 2021
entrez: 30 5 2021
Statut: ppublish

Résumé

A solvent-modified micellar electrokinetic chromatography method was developed following the Quality by Design approach for the simultaneous determination of sitagliptin (SIT), an oral antihyperglycemic drug, and its main impurities derived from the synthesis process. The separation system was identified in the scouting phase and was made by sodium dodecyl sulphate (SDS) micelles with the addition of n-butanol and methanol. The knowledge space was investigated through an asymmetric screening matrix, taking into consideration eight critical method parameters (CMPs) involving the composition of the background electrolyte in terms of buffer concentration and pH, the concentration of surfactants and organic modifiers, and voltage. The critical method attributes (CMAs) were identified as analysis time and the distance between the tail of the electroosmotic flow system peak and the front edge of impurity I

Identifiants

pubmed: 34052552
pii: S0731-7085(21)00274-0
doi: 10.1016/j.jpba.2021.114163
pii:
doi:

Substances chimiques

Micelles 0
Solvents 0
Sodium Dodecyl Sulfate 368GB5141J
Sitagliptin Phosphate TS63EW8X6F

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114163

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors report no declarations of interest.

Auteurs

Benedetta Pasquini (B)

Department of Chemistry "U. Schiff", University of Florence, Via U. Schiff 6, Via della Lastruccia 3-13, 50019, Sesto Fiorentino, Florence, Italy. Electronic address: benedetta.pasquini@me.com.

Roberto Gotti (R)

Department of Pharmacy and Biotechnology, University of Bologna, Via Belmeloro 6, 40126, Bologna, Italy. Electronic address: roberto.gotti@unibo.it.

Mercedes Villar-Navarro (M)

Department of Analytical Chemistry, University of Seville, c/Prof. García González, s/n., 41012, Seville, Spain. Electronic address: mvn@us.es.

Michal Douša (M)

Zentiva, k.s. Praha, a Sanofi Company, U Kabelovny 130, 102 37, Praha 10, Czech Republic. Electronic address: michal.dousa@seznam.cz.

Lapo Renai (L)

Department of Chemistry "U. Schiff", University of Florence, Via U. Schiff 6, Via della Lastruccia 3-13, 50019, Sesto Fiorentino, Florence, Italy. Electronic address: lapo.renai@unifi.it.

Massimo Del Bubba (M)

Department of Chemistry "U. Schiff", University of Florence, Via U. Schiff 6, Via della Lastruccia 3-13, 50019, Sesto Fiorentino, Florence, Italy. Electronic address: massimo.delbubba@unifi.it.

Serena Orlandini (S)

Department of Chemistry "U. Schiff", University of Florence, Via U. Schiff 6, Via della Lastruccia 3-13, 50019, Sesto Fiorentino, Florence, Italy. Electronic address: serena.orlandini@unifi.it.

Sandra Furlanetto (S)

Department of Chemistry "U. Schiff", University of Florence, Via U. Schiff 6, Via della Lastruccia 3-13, 50019, Sesto Fiorentino, Florence, Italy. Electronic address: sandra.furlanetto@unifi.it.

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