Deconvolution and IVIVC: Exploring the Role of Rate-Limiting Conditions

Author:

Margolskee Alison,Darwich Adam S.,Galetin Aleksandra,Rostami-Hodjegan Amin,Aarons Leon

Publisher

Springer Science and Business Media LLC

Subject

Pharmaceutical Science

Reference26 articles.

1. U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Guidance for Industry: SUPAC-MR: Modified Release Solid Oral Dosage Forms. http://www.fda.gov/downloads/Drugs/Guidances/UCM070640.pdf (1997). Accessed Dec 3 2014.

2. U.S. Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER). Guidance for industry: extended release oral dosage forms: development, evaluation, and application of in vitro/in vivo correlations. http://www.fda.gov/downloads/drugs/GuidanceComplianceRegulatoryInformation/Guidances/ ucm070239.pdf (1997). Accessed Dec 3 2014.

3. Loo JCK, Riegelman S. New method for calculating the intrinsic absorption rate of drugs. J Pharm Sci. 1968;57(6):918–28.

4. Wagner JG, Nelson E. Kinetic analysis of blood levels and urinary excretion in the absorptive phase after single doses of drug. J Pharm Sci. 1964;53:1392–403.

5. Cutler DJ. Numerical deconvolution by least squares: use of prescribed input functions. J Pharmacokinet Biopharm. 1978;6(3):227–41.

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