Literature DB >> 12594003

Nanosizing: a formulation approach for poorly-water-soluble compounds.

Elaine Merisko-Liversidge1, Gary G Liversidge, Eugene R Cooper.   

Abstract

Poorly-water-soluble compounds are difficult to develop as drug products using conventional formulation techniques and are frequently abandoned early in discovery. The use of media milling technology to formulate poorly-water-soluble drugs as nanocrystalline particles offers the opportunity to address many of the deficiencies associated with this class of molecules. NanoCrystal Technology is an attrition process wherein large micron size drug crystals are media milled in a water-based stabilizer solution. The process generates physically stable dispersions consisting of nanometer-sized drug crystals. Nanocrystalline particles are a suitable delivery system for all commonly used routes of administration, i.e. oral, injectable (IV, SC, and IM) and topical applications. In addition, aqueous dispersions of nanoparticles can be post-processed into tablets, capsules, fast-melts and lyophilized for sterile product applications. The technology has been successfully incorporated into all phases of the drug development cycle from identification of new chemical entities to refurbishing marketed products for improving their performance and value.

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Year:  2003        PMID: 12594003     DOI: 10.1016/s0928-0987(02)00251-8

Source DB:  PubMed          Journal:  Eur J Pharm Sci        ISSN: 0928-0987            Impact factor:   4.384


  146 in total

Review 1.  Crystalline nanosuspensions as potential toxicology and clinical oral formulations for BCS II/IV compounds.

Authors:  Filippos Kesisoglou; Amitava Mitra
Journal:  AAPS J       Date:  2012-06-27       Impact factor: 4.009

2.  Multicomponent amorphous nanofibers electrospun from hot aqueous solutions of a poorly soluble drug.

Authors:  Deng-Guang Yu; Li-Dong Gao; Kenneth White; Christopher Branford-White; Wei-Yue Lu; Li-Min Zhu
Journal:  Pharm Res       Date:  2010-08-19       Impact factor: 4.200

3.  Flocculated amorphous nanoparticles for highly supersaturated solutions.

Authors:  Michal E Matteucci; Joseph C Paguio; Maria A Miller; Robert O Williams Iii; Keith P Johnston
Journal:  Pharm Res       Date:  2008-08-15       Impact factor: 4.200

4.  Evaluation of nanosuspensions for absorption enhancement of poorly soluble drugs: in vitro transport studies across intestinal epithelial monolayers.

Authors:  T Lenhardt; G Vergnault; P Grenier; D Scherer; P Langguth
Journal:  AAPS J       Date:  2008-08-09       Impact factor: 4.009

5.  The preparation and evaluation of water-soluble SKLB610 nanosuspensions with improved bioavailability.

Authors:  Yunchuang Huang; Xun Luo; Xinyu You; Yong Xia; Xuejiao Song; Luoting Yu
Journal:  AAPS PharmSciTech       Date:  2013-08-10       Impact factor: 3.246

6.  Ordered nanoporous silica as carriers for improved delivery of water insoluble drugs: a comparative study between three dimensional and two dimensional macroporous silica.

Authors:  Ying Wang; Qinfu Zhao; Yanchen Hu; Lizhang Sun; Ling Bai; Tongying Jiang; Siling Wang
Journal:  Int J Nanomedicine       Date:  2013-10-22

7.  Using USP I and USP IV for discriminating dissolution rates of nano- and microparticle-loaded pharmaceutical strip-films.

Authors:  Lucas Sievens-Figueroa; Natasha Pandya; Anagha Bhakay; Golshid Keyvan; Bozena Michniak-Kohn; Ecevit Bilgili; Rajesh N Davé
Journal:  AAPS PharmSciTech       Date:  2012-10-23       Impact factor: 3.246

8.  Application of a four-fluid nozzle spray drier to prepare inhalable rifampicin-containing mannitol microparticles.

Authors:  Takuto Mizoe; Tetsuya Ozeki; Hiroaki Okada
Journal:  AAPS PharmSciTech       Date:  2008-06-18       Impact factor: 3.246

9.  Interaction of selegiline-loaded PLGA-b-PEG nanoparticles with beta-amyloid fibrils.

Authors:  Ipek Baysal; Samiye Yabanoglu-Ciftci; Yeliz Tunc-Sarisozen; Kezban Ulubayram; Gulberk Ucar
Journal:  J Neural Transm (Vienna)       Date:  2013-02-19       Impact factor: 3.575

Review 10.  Nanovehicular intracellular delivery systems.

Authors:  Ales Prokop; Jeffrey M Davidson
Journal:  J Pharm Sci       Date:  2008-09       Impact factor: 3.534

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