Development of a Clinically Relevant Dissolution Approach to Simulate Physiological Forces with a USP 2 Apparatus: “Peristaltic Dissolution”
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmaceutical Science
Link
https://link.springer.com/content/pdf/10.1007/s12247-020-09485-7.pdf
Reference39 articles.
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2. Reppas C, Vertzoni M. Biorelevant in-vitro performance testing of orally administered dosage forms. J Pharm Pharmacol. 2012;64:919–30.
3. Garbacz G, Klein S. Dissolution testing of oral modified-release dosage forms. J Pharm Pharmacol. 2012;64:944–68.
4. Cassilly D, Kantor S, Knight LC, Maurer AH, Fisher RS, Semler J, et al. Gastric emptying of a non-digestible solid: assessment with simultaneous SmartPill pH and pressure capsule, antroduodenal manometry, gastric emptying scintigraphy. Neurogastroenterol Motil. 2008;20:311–9.
5. Simmons DL, Legore AA, Picotte P, Lee KS, Joshi NN. A dissolution rate apparatus for the prediction of initial drug absorption patterns in beagles: tolbutamide tablets. J Pharmacokinet Biopharm. 1975;3:39–49.
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