[Application of high-throughput technologies in pharmaceutics].

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超能文献

作者信息

Bai Xue-Lian, Gao Yong-Liang

机构信息

Institute of Pharmacology and Toxicology, Academy of Military Medical Sciences, Beijing 100850, China.

出版信息

Yao Xue Xue Bao. 2006 Jun;41(6):487-92.

PMID:16927820

Abstract

摘要

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相似文献

[Application of high-throughput technologies in pharmaceutics].

Yao Xue Xue Bao. 2006 Jun;41(6):487-92.

High-throughput crystallization: polymorphs, salts, co-crystals and solvates of pharmaceutical solids.

Adv Drug Deliv Rev. 2004 Feb 23;56(3):275-300. doi: 10.1016/j.addr.2003.10.020.

New QSPR study for the prediction of aqueous solubility of drug-like compounds.

Bioorg Med Chem. 2008 Sep 1;16(17):7944-55. doi: 10.1016/j.bmc.2008.07.067. Epub 2008 Jul 29.

Future perspectives in pharmaceutics: contributions from younger scientists. Preface.

Int J Pharm. 2008 Dec 8;364(2):157-8. doi: 10.1016/j.ijpharm.2008.09.026. Epub 2008 Sep 25.

Solid form screening--a review.

Eur J Pharm Biopharm. 2009 Jan;71(1):23-37. doi: 10.1016/j.ejpb.2008.07.014. Epub 2008 Jul 31.

[Application of supercritical solution rapid expansion technology in preparation of fine pharmacal particles].

Zhongguo Zhong Yao Za Zhi. 2006 Dec;31(23):1933-6.

Theme issue "Solid state and solid dosage forms".

Eur J Pharm Biopharm. 2009 Jan;71(1):1. doi: 10.1016/j.ejpb.2008.08.022. Epub 2008 Sep 9.

Assessing drug-likeness--what are we missing?

Drug Discov Today. 2008 Apr;13(7-8):285-94. doi: 10.1016/j.drudis.2007.11.007. Epub 2008 Jan 16.

Achieving polymorph selectivity in the crystallization of pharmaceutical solids: basic considerations and recent advances.

Curr Opin Drug Discov Devel. 2006 Nov;9(6):806-15.

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Int J Pharm. 2007 Aug 16;341(1-2):1-19. doi: 10.1016/j.ijpharm.2007.05.049. Epub 2007 May 26.