Literature DB >> 14584524

Solid dispersions: revival with greater possibilities and applications in oral drug delivery.

Sundeep Sethia1, Emilio Squillante.   

Abstract

Improvement of oral bioavailability of poorly water-soluble drugs remains one of the most challenging aspects of drug development. Solid dispersions seem to be a viable technique for overcoming this problem. However, the practical applicability of these systems has remained limited because of difficulties in conventional methods of preparation, poor reproducibility of physicochemical properties, difficulties in dosage form development, and lack of feasibility for scale-up of manufacturing processes. This review addresses various aspects of solid dispersions and compiles some of the recent technology transfers from various fields such as the chemical, food, and polymer industries for the preparation of solid dispersions that can lead to highly efficient and controlled large-scale manufacturing. Some of the practical aspects to be considered for the preparation of solid dispersions, such as selection of carrier and methods of physicochemical characterization, along with an insight into the release mechanism of drugs are also discussed. Finally, an in-depth rationale for limited commercialization of solid dispersions and recent revival has been considered.

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Year:  2003        PMID: 14584524     DOI: 10.1615/critrevtherdrugcarriersyst.v20.i23.40

Source DB:  PubMed          Journal:  Crit Rev Ther Drug Carrier Syst        ISSN: 0743-4863            Impact factor:   4.889


  9 in total

1.  Microparticles Containing Curcumin Solid Dispersion: Stability, Bioavailability and Anti-Inflammatory Activity.

Authors:  C C C Teixeira; L M Mendonça; M M Bergamaschi; R H C Queiroz; G E P Souza; L M G Antunes; L A P Freitas
Journal:  AAPS PharmSciTech       Date:  2015-06-04       Impact factor: 3.246

2.  Dissolution enhancement of atorvastatin calcium by co-grinding technique.

Authors:  Priyanka Prabhu; Vandana Patravale
Journal:  Drug Deliv Transl Res       Date:  2016-08       Impact factor: 4.617

3.  A comparison of the physical stability of amorphous felodipine and nifedipine systems.

Authors:  Patrick J Marsac; Hajime Konno; Lynne S Taylor
Journal:  Pharm Res       Date:  2006-08-23       Impact factor: 4.200

4.  Mechanistic investigation of Pluronic based nano-crystalline drug-polymer solid dispersions.

Authors:  Feng Qian; Jing Tao; Sridhar Desikan; Munir Hussain; Ronald L Smith
Journal:  Pharm Res       Date:  2007-03-23       Impact factor: 4.200

5.  Characterization of a cyclosporine solid dispersion for inhalation.

Authors:  Gerrit S Zijlstra; Michiel Rijkeboer; Dirk Jan van Drooge; Marc Sutter; Wim Jiskoot; Marco van de Weert; Wouter L J Hinrichs; Henderik W Frijlink
Journal:  AAPS J       Date:  2007-06-15       Impact factor: 4.009

6.  Estimation of drug-polymer miscibility and solubility in amorphous solid dispersions using experimentally determined interaction parameters.

Authors:  Patrick J Marsac; Tonglei Li; Lynne S Taylor
Journal:  Pharm Res       Date:  2008-09-09       Impact factor: 4.200

7.  Formation and Characterization of Beclomethasone Dipropionate Nanoparticles Using Rapid Expansion of Supercritical Solution.

Authors:  Mohsen Hosseinpour; Alireza Vatanara; Reza Zarghami
Journal:  Adv Pharm Bull       Date:  2015-09-19

8.  Nanocrystals for the parenteral delivery of poorly water-soluble drugs.

Authors:  Bo Sun; Yoon Yeo
Journal:  Curr Opin Solid State Mater Sci       Date:  2012-12-01       Impact factor: 11.354

Review 9.  Formulation strategies to improve the bioavailability of poorly absorbed drugs with special emphasis on self-emulsifying systems.

Authors:  Shweta Gupta; Rajesh Kesarla; Abdelwahab Omri
Journal:  ISRN Pharm       Date:  2013-12-26
  9 in total

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