Preparation and Physicochemical Characterization of Acyclovir Cocrystals with Improved Dissolution Properties
- 1 November 2013
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 102 (11) , 4079-4086
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Cocrystallization and amorphization induced by drug–excipient interaction improves the physical properties of acyclovirInternational Journal of Pharmaceutics, 2011
- Preparation and characterization of carprofen co-crystalsCrystEngComm, 2011
- Pharmaceutical Cocrystals and Their Physicochemical PropertiesCrystal Growth & Design, 2009
- Biowaiver Monographs for Immediate Release Solid Oral Dosage Forms: AciclovirJournal of Pharmaceutical Sciences, 2008
- The Co‐Crystal Approach to Improve the Exposure of a Water‐Insoluble Compound: AMG 517 Sorbic Acid Co‐Crystal Characterization and PharmacokineticsJournal of Pharmaceutical Sciences, 2008
- Sulfa Drugs as Model Cocrystal FormersMolecular Pharmaceutics, 2007
- Pharmaceutical Co-CrystalsJournal of Pharmaceutical Sciences, 2006
- Antiviral prodrugs – the development of successful prodrug strategies for antiviral chemotherapyBritish Journal of Pharmacology, 2006
- Current Treatments of Muco-Cutaneous Herpes Simplex Virus InfectionsCurrent Medicinal Chemistry - Anti-Infective Agents, 2002
- Antiviral DrugsNew England Journal of Medicine, 1999