Literature DB >> 18320295

What is a suitable dissolution method for drug nanoparticles?

Desmond Heng1, David J Cutler, Hak-Kim Chan, Jimmy Yun, Judy A Raper.   

Abstract

PURPOSE: Many existing and new drugs fail to be fully utilized because of their limited bioavailability due to poor solubility in aqueous media. Given the emerging importance of using nanoparticles as a promising way to enhance the dissolution rate of these drugs, a method must be developed to adequately reflect the rate-change due to size reduction. At present, there is little published work examining the suitability of different dissolution apparatus for nanoparticles.
METHODS: Four commonly-used methods (the paddle, rotating basket and flow-through cell from the US Pharmacopia, and a dialysis method) were employed to measure the dissolution rates of cefuroxime axetil as a model for nanodrug particles.
RESULTS: Experimental rate ratios between the nanoparticles and their unprocessed form were 6.95, 1.57 and 1.00 for the flow-through, basket and paddle apparatus respectively. In comparison, the model-predicted value was 7.97. Dissolution via dialysis was rate-limited by the membrane.
CONCLUSIONS: The data showed the flow-through cell to be unequivocally the most robust dissolution method for the nanoparticulate system. Furthermore, the dissolution profiles conform closely to the classic Noyes-Whitney model, indicating that the increase in dissolution rate as particles become smaller results from the increase in surface area and solubility of the nanoparticles.

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Year:  2008        PMID: 18320295     DOI: 10.1007/s11095-008-9560-0

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  15 in total

1.  Microcrystals for dissolution rate enhancement of poorly water-soluble drugs.

Authors:  Norbert Rasenack; Helge Hartenhauer; Bernd W Müller
Journal:  Int J Pharm       Date:  2003-03-26       Impact factor: 5.875

2.  Organic Nanoparticles in the Aqueous Phase-Theory, Experiment, and Use.

Authors:  Dieter Horn; Jens Rieger
Journal:  Angew Chem Int Ed Engl       Date:  2001-12-03       Impact factor: 15.336

3.  Aerosol flow reactor method for synthesis of drug nanoparticles.

Authors:  Hannele Eerikäinen; Wiwik Watanabe; Esko I Kauppinen; P Petri Ahonen
Journal:  Eur J Pharm Biopharm       Date:  2003-05       Impact factor: 5.571

4.  Reexamination of convective diffusion/drug dissolution in a laminar flow channel: accurate prediction of dissolution rate.

Authors:  Paul J Missel; Larry E Stevens; John W Mauger
Journal:  Pharm Res       Date:  2004-12       Impact factor: 4.200

5.  Shear-induced variability in the United States Pharmacopeia Apparatus 2: modifications to the existing system.

Authors:  Jennifer L Baxter; Joseph Kukura; Fernando J Muzzio
Journal:  AAPS J       Date:  2006-01-03       Impact factor: 4.009

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

Authors:  Aristides Dokoumetzidis; Panos Macheras
Journal:  Int J Pharm       Date:  2006-07-15       Impact factor: 5.875

7.  Nanoparticles of poorly water-soluble drugs prepared by supercritical fluid extraction of emulsions.

Authors:  Boris Y Shekunov; Pratibhash Chattopadhyay; Jeff Seitzinger; Robert Huff
Journal:  Pharm Res       Date:  2006-11-30       Impact factor: 4.200

8.  Experimental evaluation of three single-particle dissolution models.

Authors:  P V Pedersen; K F Brown
Journal:  J Pharm Sci       Date:  1976-10       Impact factor: 3.534

9.  Dynamic dialysis for the drug release evaluation from doxorubicin-gelatin nanoparticle conjugates.

Authors:  E Leo; R Cameroni; F Forni
Journal:  Int J Pharm       Date:  1999-03-25       Impact factor: 5.875

10.  Oral cefuroxime axetil: clinical pharmacology and comparative dose studies in urinary tract infection.

Authors:  D H Adams; M J Wood; I D Farrell; C Fox; A P Ball
Journal:  J Antimicrob Chemother       Date:  1985-09       Impact factor: 5.790

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  20 in total

1.  Development of a new method to assess nanocrystal dissolution based on light scattering.

Authors:  Katharina Anhalt; Simon Geissler; Meike Harms; Markus Weigandt; Gert Fricker
Journal:  Pharm Res       Date:  2012-06-12       Impact factor: 4.200

2.  Dissolution studies of poorly soluble drug nanosuspensions in non-sink conditions.

Authors:  Peng Liu; Odile De Wulf; Johanna Laru; Teemu Heikkilä; Bert van Veen; Juha Kiesvaara; Jouni Hirvonen; Leena Peltonen; Timo Laaksonen
Journal:  AAPS PharmSciTech       Date:  2013-04-25       Impact factor: 3.246

3.  Porous mannitol carrier for pulmonary delivery of cyclosporine A nanoparticles.

Authors:  Sharon Shui Yee Leung; Jennifer Wong; Heloisa Victorino Guerra; Kevin Samnick; Robert K Prud'homme; Hak-Kim Chan
Journal:  AAPS J       Date:  2017-01-09       Impact factor: 4.009

Review 4.  Improved delivery of poorly soluble compounds using nanoparticle technology: a review.

Authors:  Sandeep Kalepu; Vijaykumar Nekkanti
Journal:  Drug Deliv Transl Res       Date:  2016-06       Impact factor: 4.617

Review 5.  Development Considerations for Nanocrystal Drug Products.

Authors:  Mei-Ling Chen; Mathew John; Sau L Lee; Katherine M Tyner
Journal:  AAPS J       Date:  2017-03-09       Impact factor: 4.009

6.  Preparation of Nanocrystals for Insoluble Drugs by Top-Down Nanotechnology with Improved Solubility and Bioavailability.

Authors:  Xun Zhang; Zhiguo Li; Jing Gao; Zengming Wang; Xiang Gao; Nan Liu; Meng Li; Hui Zhang; Aiping Zheng
Journal:  Molecules       Date:  2020-02-28       Impact factor: 4.411

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.  In Vitro Dissolution Testing Strategies for Nanoparticulate Drug Delivery Systems: Recent Developments and Challenges.

Authors:  Jie Shen; Diane J Burgess
Journal:  Drug Deliv Transl Res       Date:  2013-10-01       Impact factor: 4.617

9.  Determining drug release rates of hydrophobic compounds from nanocarriers.

Authors:  Suzanne M D'Addio; Abdallah A Bukari; Mohammed Dawoud; Heike Bunjes; Carlos Rinaldi; Robert K Prud'homme
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-07-28       Impact factor: 4.226

10.  Effects of Surface Composition on the Aerosolisation and Dissolution of Inhaled Antibiotic Combination Powders Consisting of Colistin and Rifampicin.

Authors:  Wenbo Wang; Qi Tony Zhou; Si-Ping Sun; John A Denman; Thomas R Gengenbach; Nicolas Barraud; Scott A Rice; Jian Li; Mingshi Yang; Hak-Kim Chan
Journal:  AAPS J       Date:  2015-11-24       Impact factor: 4.009

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