In situ gastric floating gel of atazanavir sulphate for sustained release : formulation, optimization and evaluation

Aim: Atazanavir sulphate belongs to BCS class II drug, its oral bioavailability is limited due to its rapid first-pass metabolism and P-gp efflux. Materials & methods: The in situ floating gel using the complexed drug was prepared by ion gelation method and optimized the formulation as per 32 full factorial design. Results: Floating lag time of optimized formulation was found to be 18 s and percentage drug release of 94.18 ± 0.18 % at the end of 16 h. The concentration of gelling polymer affects drug release and a floating lag time and vice versa. Conclusion: In situ floating gel of atazanavir sulphate was found promising to sustain drug release due to an increased gastric residence time, which leads to enhanced potential therapy.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:14

Enthalten in:

Therapeutic delivery - 14(2023), 10 vom: 01. Okt., Seite 619-633

Sprache:

Englisch

Beteiligte Personen:

Masareddy, Rajashree [VerfasserIn]
Sandure, Pradnya [VerfasserIn]
Patil, Archana [VerfasserIn]
Gaude, Yadishma [VerfasserIn]
Patil, Arpana [VerfasserIn]

Links:

Volltext

Themen:

β-cyclodextrin complex
4MT4VIE29P
Atazanavir Sulfate
Atazanavir sulphate
Bioavailability
Delayed-Action Preparations
Gels
In situ floating gel
Journal Article
Sustained drug delivery
Tablets

Anmerkungen:

Date Completed 11.12.2023

Date Revised 09.02.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.4155/tde-2023-0037

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM365451606