1. Guidance for Industry. Dissolution Testing of Immediate Release Solid Oral Dosage Forms;FDA,1997
2. Dissolution testing for generic drugs: an FDA perspective;Anand;AAPS J.,2011
3. The United States Pharmacopeia, USP35-NF30, Chapter <1092>. Dissolution Procedure: Development and Validation,2011
4. Note for Guidance on the Investigation of Bioavailability and Bioequivalence,2001
5. The United States Pharmacopeia,2011