Author:
Laitinen Riikka,Lahtinen Jani,Silfsten Pertti,Vartiainen Erik,Jarho Pekka,Ketolainen Jarkko
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference27 articles.
1. High throughput solubility measurement in drug discovery and development;Alsenz;Adv. Drug Deliv. Rev.,2007
2. Impact of solid state properties on developability assessment of drug candidates;Huang;Adv. Drug Deliv. Rev.,2004
3. United States Pharmacopoeia and National Formulary USP 32 NF27, The United States Pharmacopoeial Convention, Inc., Rockville, 2009.
4. J. Dressman, Dissolution testing of Immediate-Release Products and Its Application to Forecasting In Vivo Performance, in: J. Dressman (Ed.), Oral Drug Absorption: Prediction and Assessment, Marcel Dekker Inc., New York, 2000, pp. 155–181.
5. Commentary on AAPS Workshop. Dissolution testing for the twenty-first century: linking critical quality attributes and critical process parameters to clinically relevant dissolution;Tong;Pharm. Res.,2007
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