Quantitative Solubility Relationships and the Effect of Water Uptake in Triglyceride/Monoglyceride Microemulsions

Author:

Rane Sagar S.,Cao Yichen,Anderson Bradley D.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology

Reference72 articles.

1. L. V. Allen Jr., N. G. Popovich, and H. C. Ansel. Pharmaceutical Dosage Forms and Drug Delivery Systems, 8th ed. Lippincott Williams & Wilkins, (2004).

2. C. Lipinski. Physicochemical properties in drug design/development. 2nd International Drug Discovery and Development Summit: Novel Concepts and Technologies to Accelerate Drug Development: Honolulu, HI, (2003).

3. N. A. Armstrong, and K. C. James. Drug release from lipid-based dosage forms. I. Int. J. Pharm 6:185–193 (1980).

4. A. J. Humberstone, and W. N. Charman. Lipid-based vehicles for the oral delivery of poorly water soluble drugs. Adv. Drug Delivery Rev. 25:103–128 (1997).

5. R. A. Myers, and V. J. Stella. Systemic bioavailability of penclomedine (NSC 338720) from oil-in-water emulsions administered intraduodenally to rats. Int. J. Pharm. 78:217–226 (1992).

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