Impact of Apparatus and Adapter on In vitro Drug Release of Ophthalmic Semisolid Drug Products
Author:
Funder
U.S. Food and Drug Administration
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology
Link
https://link.springer.com/content/pdf/10.1007/s11095-023-03586-x.pdf
Reference22 articles.
1. Xu X, et al. Kinetics of drug release from ointments: role of transient-boundary layer. Int J Pharm. 2015;494(1):31–9.
2. SUPAC-SS: Nonsterile Semisolid Dosage Forms; Scale-Up and Post-Approval Changes: Chemistry, Manufacturing and Controls; In Vitro Release Testing and In Vivo Bioequivalence Documentation. In: FDA Guidance Documents for Industry. 1997. https://www.fda.gov/regulatory-information/search-fda-guidance-documents/supac-ss-nonsterile-semisolid-dosage-forms-scale-and-post-approval-changes-chemistrymanufacturing. Accessed 15 Aug 2023.
3. Sripetch S, Loftsson T. Topical drug delivery to the posterior segment of the eye: thermodynamic considerations. Int J Pharm. 2021;597:120332.
4. Mazet R, et al. Recent advances in the design of topical ophthalmic delivery systems in the treatment of ocular surface inflammation and their biopharmaceutical evaluation. Pharmaceutics. 2020;12(6):570.
5. Hardberger R, Hanna C, Boyd CM. Effects of drug vehicles on ocular contact time. Arch Ophthalmol. 1975;93(1):42–5.
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