Oral Bioavailability Enhancement of Exemestane from Self-Microemulsifying Drug Delivery System (SMEDDS)-Reference-Cited by-同舟云学术

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Oral Bioavailability Enhancement of Exemestane from Self-Microemulsifying Drug Delivery System (SMEDDS)

Published:2009-07-17 Issue:3 Volume:10 Page:906-916
ISSN:1530-9932
Container-title:AAPS PharmSciTech
language:en
Short-container-title:AAPS PharmSciTech

Author:

Singh Ajeet K.,Chaurasiya Akash,Awasthi Anshumali,Mishra Gautam,Asati Dinesh,Khar Roop K.,Mukherjee Rama

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmaceutical Science,Agronomy and Crop Science,Ecology,Aquatic Science,General Medicine,Ecology, Evolution, Behavior and Systematics

Link

http://link.springer.com/content/pdf/10.1208/s12249-009-9281-7.pdf

Reference37 articles.

1. Robinson JR. Introduction: semi-solid formulations for oral drug delivery. Buletin Technique Gatefosse. 1996;89:3–11.

2. Lipinski CA. Drug-like properties and the causes of poor solubility and poor permeability. J Pharmacol Toxicol Methods. 2000;44:235–49.

3. Lipinski CA, Lombardo F, Dominy BW, Feeney PJ. Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv Drug Deliv Rev. 1997;23:3–25.

4. Gursoy RN, Benita S. Self-emulsifying drug delivery systems (SEDDS) for improved oral delivery of lipophilic drugs. Biomed Pharmacother. 2004;58:173–82.

5. Lonning PE. Pharmacological profiles of exemestane and formestane, steroidal aromatase inhibitors used for the treatment of post-menopausal breast cancer. Breast Can Res Treat. 1998;49:S45–52.

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