Identification, isolation, and structural characterization of novel forced degradation products of Ertugliflozin using advanced analytical techniques.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
10 Jun 2023
Historique:
received: 15 01 2023
accepted: 31 05 2023
medline: 12 6 2023
pubmed: 11 6 2023
entrez: 10 6 2023
Statut: epublish

Résumé

The research elucidates the stress degradation behavior of Ertugliflozin, which is used for the treatment of type-2 diabetics. The degradation was conducted as per ICH guidelines and Ertugliflozin is relatively stable in thermal, photolytic, neutral, and alkaline hydrolysis conditions; however, considerable degradation was detected in acid hydrolysis and oxidative hydrolysis. Degradation products were identified by ultra-high-performance liquid chromatography-mass spectrometry, isolated by semi-preparative high-performance liquid chromatography, and structural characterization using high-resolution mass spectrometry and nuclear magnetic resonance spectroscopy. Total four degradation products were identified and isolated in acid degradation, which are degradation products 1, 2, 3, and 4. Whereas in oxidative conditions, degradation product 5 was identified. All the five degradation products formed are novel, which was not reported earlier. This is the first time documented complete structural characterization of all five degradation products by using a hyphenated analytical technique. High-resolution mass, and nuclear magnetic resonance spectroscopy were used in the present study to get concrete confirmation of degradation products structures. The current method is also used to identify degradation products with shorter runtime in the future.

Identifiants

pubmed: 37301855
doi: 10.1038/s41598-023-36289-9
pii: 10.1038/s41598-023-36289-9
pmc: PMC10257675
doi:

Substances chimiques

ertugliflozin 6C282481IP

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

9472

Informations de copyright

© 2023. The Author(s).

Références

Anal Biochem. 2019 Feb 15;567:112-116
pubmed: 30578763
Clin Pharmacol Drug Dev. 2019 Jul;8(5):619-627
pubmed: 30427588
Drug Metab Dispos. 2013 Feb;41(2):445-56
pubmed: 23169609
Front Endocrinol (Lausanne). 2017 Jan 24;8:6
pubmed: 28167928
Drug Des Devel Ther. 2017 Oct 03;11:2905-2919
pubmed: 29042751

Auteurs

Suresh Salakolusu (S)

Analytical Discovery Chemistry, Aragen Life Sciences Pvt. Ltd., IDA Nacharam, Hyderabad, 500076, India.
Department of Chemistry, GITAM School of Science, GITAM Deemed to be University, Visakhapatnam, 530045, Andhra Pradesh, India.

Naresh Kumar Katari (NK)

Department of Chemistry, GITAM School of Science, GITAM Deemed to be University, Hyderabad, 502329, Telangana, India. nkatari@gitam.edu.
School of Chemistry and Physics, College of Agriculture, Engineering and Science, Westville Campus, University of KwaZulu-Natal, P Bag X 54001, Durban, 4000, South Africa. nkatari@gitam.edu.

Ganapavarapu Veera Raghava Sharma (GVR)

Department of Chemistry, GITAM School of Science, GITAM Deemed to be University, Visakhapatnam, 530045, Andhra Pradesh, India. sganapav@gitam.edu.

Muralidharan Kaliyaperumal (M)

Analytical Discovery Chemistry, Aragen Life Sciences Pvt. Ltd., IDA Nacharam, Hyderabad, 500076, India.

Umamaheshwar Puppala (U)

Analytical Discovery Chemistry, Aragen Life Sciences Pvt. Ltd., IDA Nacharam, Hyderabad, 500076, India.

Mahesh Ranga (M)

Analytical Discovery Chemistry, Aragen Life Sciences Pvt. Ltd., IDA Nacharam, Hyderabad, 500076, India.

Sreekantha Babu Jonnalagadda (SB)

School of Chemistry and Physics, College of Agriculture, Engineering and Science, Westville Campus, University of KwaZulu-Natal, P Bag X 54001, Durban, 4000, South Africa.

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Classifications MeSH