Literature DB >> 16920290

A century of dissolution research: from Noyes and Whitney to the biopharmaceutics classification system.

Aristides Dokoumetzidis1, Panos Macheras.   

Abstract

Dissolution research started to develop about 100 years ago as a field of physical chemistry and since then important progress has been made. However, explicit interest in drug related dissolution has grown only since the realisation that dissolution is an important factor of drug bioavailability in the 1950s. This review attempts to account the most important developments in the field, from a historical point of view. It is structured in a chronological order, from the theoretical foundations of dissolution, developed in the first half of the 20th century, and the development of a relationship between dissolution and bioavailability in the 1950s, going to the more recent developments in the framework of the Biopharmaceutics Classification System (BCS). Research on relevant fields of pharmaceutical technology, like sustained release formulations, where drug dissolution plays an important role, is reviewed. The review concludes with the modern trends on drug dissolution research and their regulatory implications.

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Year:  2006        PMID: 16920290     DOI: 10.1016/j.ijpharm.2006.07.011

Source DB:  PubMed          Journal:  Int J Pharm        ISSN: 0378-5173            Impact factor:   5.875


  74 in total

1.  Pharmacokinetic evaluation of intranasally administered vinyl polymer-coated lorazepam microparticles in rabbits.

Authors:  Yanjun Zhao; Marc B Brown; Rajeshree H Khengar; Matthew J Traynor; Pedro Barata; Stuart A Jones
Journal:  AAPS J       Date:  2012-03-01       Impact factor: 4.009

Review 2.  Challenges and opportunities in achieving bioequivalence for fixed-dose combination products.

Authors:  Amitava Mitra; Yunhui Wu
Journal:  AAPS J       Date:  2012-06-09       Impact factor: 4.009

3.  The role of mass balance equations in growth mechanics illustrated in surface and volume dissolutions.

Authors:  Gerard A Ateshian
Journal:  J Biomech Eng       Date:  2011-01       Impact factor: 2.097

4.  What is a suitable dissolution method for drug nanoparticles?

Authors:  Desmond Heng; David J Cutler; Hak-Kim Chan; Jimmy Yun; Judy A Raper
Journal:  Pharm Res       Date:  2008-03-05       Impact factor: 4.200

5.  Fractional kinetics in drug absorption and disposition processes.

Authors:  Aristides Dokoumetzidis; Panos Macheras
Journal:  J Pharmacokinet Pharmacodyn       Date:  2009-04-02       Impact factor: 2.745

Review 6.  The science of USP 1 and 2 dissolution: present challenges and future relevance.

Authors:  Vivian Gray; Gregg Kelly; Min Xia; Chris Butler; Saji Thomas; Stephen Mayock
Journal:  Pharm Res       Date:  2009-01-23       Impact factor: 4.200

7.  A new approach to the compartmental analysis in pharmacokinetics: fractional time evolution of diclofenac.

Authors:  Jovan K Popović; Milica T Atanacković; Ana S Pilipović; Milan R Rapaić; Stevan Pilipović; Teodor M Atanacković
Journal:  J Pharmacokinet Pharmacodyn       Date:  2010-01-14       Impact factor: 2.745

8.  Powder dissolution method for estimating rotating disk intrinsic dissolution rates of low solubility drugs.

Authors:  Konstantin Tsinman; Alex Avdeef; Oksana Tsinman; Dmytro Voloboy
Journal:  Pharm Res       Date:  2009-06-19       Impact factor: 4.200

9.  Engineering cells with intracellular agent-loaded microparticles to control cell phenotype.

Authors:  James A Ankrum; Oscar R Miranda; Kelvin S Ng; Debanjan Sarkar; Chenjie Xu; Jeffrey M Karp
Journal:  Nat Protoc       Date:  2014-01-09       Impact factor: 13.491

Review 10.  Lipid-associated oral delivery: Mechanisms and analysis of oral absorption enhancement.

Authors:  Oljora Rezhdo; Lauren Speciner; Rebecca Carrier
Journal:  J Control Release       Date:  2016-08-09       Impact factor: 9.776

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