Citations (10)
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Saroj Vangani, Xiaoling Li, Peter Zhou, Mary-Anne Del-Barrio, Rick Chiu, Nina Cauchon, Ping Gao, Cesar Medina & Bhaskara Jasti. (2009) Dissolution of poorly water-soluble drugs in biphasic media using USP 4 and fiber optic system. Clinical Research and Regulatory Affairs 26:1-2, pages 8-19.
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Larry E. Stevens, Paul J. Missel & Alan L. Weiner. (2008) Controlled Flow-Through Dissolution Methodology: A High-Performance System. Pharmaceutical Development and Technology 13:2, pages 135-153.
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G. H. Zhang, W. A. Vadino, T. T. Yang, W. P. Cho & I. A. Chaudry. (1994) Evaluation of the Flow-Through Cell Dissolution Apparatus: Effects of Flow Rate, Glass Beads and Tablet Position on Drug Release from Different Type of Tablets. Drug Development and Industrial Pharmacy 20:13, pages 2063-2078.
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M. K. Kottke & C. T. Rhodes. (1991) Limitations of Presently Available In Vitro Release Data for the Prediction of In Vivo Performance. Drug Development and Industrial Pharmacy 17:9, pages 1157-1176.
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Articles from other publishers (6)
Rajan Jog, Geoffrey N. Grove & Diane J. Burgess. 2017. Poorly Soluble Drugs. Poorly Soluble Drugs
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Deirdre M. D’Arcy, Bo Liu & Owen I. Corrigan. (2011) Investigating the effect of solubility and density gradients on local hydrodynamics and drug dissolution in the USP 4 dissolution apparatus. International Journal of Pharmaceutics 419:1-2, pages 175-185.
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Wei-Guo Dai. (2010) In vitro methods to assess drug precipitation. International Journal of Pharmaceutics 393:1-2, pages 1-16.
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Deirdre M. D’Arcy, Bo Liu, Geoff Bradley, Anne Marie Healy & Owen I. Corrigan. (2009) Hydrodynamic and Species Transfer Simulations in the USP 4 Dissolution Apparatus: Considerations for Dissolution in a Low Velocity Pulsing Flow. Pharmaceutical Research 27:2, pages 246-258.
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Cherng-Yih Perng, Albert S Kearney, Nagesh R Palepu, Brian R Smith & Leonard M Azzarano. (2003) Assessment of oral bioavailability enhancing approaches for SB-247083 using flow-through cell dissolution testing as one of the screens. International Journal of Pharmaceutics 250:1, pages 147-156.
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W.C.G Butler & S.R Bateman. (1998) A flow-through dissolution method for a two component drug formulation where the actives have markedly differing solubility properties. International Journal of Pharmaceutics 173:1-2, pages 211-219.
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