Oral controlled release dosage forms: dissolution versus diffusion

Author:

Bermejo Marival1,Sanchez-Dengra Barbara1,Gonzalez-Alvarez Marta1,Gonzalez-Alvarez Isabel1

Affiliation:

1. Department of Engineering, Pharmacokinetics and Pharmaceutical Technology Area, Miguel Hernandez University, Elche, Spain

Funder

Ministry of Science, Innovation and Universities of Spain

Agencia Estatal de Investigación and European Union

Publisher

Informa UK Limited

Subject

Pharmaceutical Science

Reference146 articles.

1. EMA - Committee for Medicinal Products for Human Use (CHMP). Guideline on the pharmacokinetic and clinical evaluation of modified release dosage forms (EMA/CPMP/EWP/280/96 Corr1) [Internet]. 2014 [cited 2020 Jan 16]. Available from: www.ema.europa.eu/contact.

2. Fda. Bioavailability studies submitted in NDAs or INDs-general considerations guidance for industry [Internet]. 2019 [cited 2020 Jan 28]. Available from: http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/default.htm.

3. Taylor K, Aulton M Aulton’s pharmaceutics - 4th edition [Internet]. 2013 [cited 2020 Jan 28]. Available from: https://www.elsevier.com/books/aultons-pharmaceutics/aulton/978-0-7020-4290-4.

4. Critical factors in the release of drugs from sustained release hydrophilic matrices

5. Methodology of oral formulation selection in the pharmaceutical industry

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