Formulation and characterization of a paediatric nanoemulsion dosage form with modified oral drug delivery system for improved dissolution rate of nevirapine-Reference-Cited by-同舟云学术

Formulation and characterization of a paediatric nanoemulsion dosage form with modified oral drug delivery system for improved dissolution rate of nevirapine

Published:2018-04-02 Issue:37 Volume:3 Page:2203-2219
ISSN:2059-8521
Container-title:MRS Advances
language:en
Short-container-title:MRS Advances

Author:

Manyarara Tapiwa E.,Khoza Star,Dube Admire,Maponga Chiedza C.

Publisher

Springer Science and Business Media LLC

Subject

Mechanical Engineering,Mechanics of Materials,Condensed Matter Physics,General Materials Science

Link

http://link.springer.com/content/pdf/10.1557/adv.2018.320.pdf

Reference37 articles.

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2. Shegokar R, Singh KK. Nevirapine nanosuspensions for HIV reservoir targeting. Pharmazie. 2010 Nov 16;66:408–15.

3. Holm R. FORMULATION STRATEGIES FOR LOW SOLUBLE DRUGS- AN OVERVIEW [Internet] http://rbbbd.com/pdf/presentations/Ren%E9%20Holm/Amman_sep_2013_reneholm.pdf Date Accessed: 14/05/2015

4. Nanjwade BK, Patel DJ, Udhani RA. Functions of Lipids for Enhancement of Oral Bioavailability of Poorly Water-Soluble Drugs. Sci Pharm. 2011;79:705–27.

5. Yadollahi R, Vasilev K, Simovic S. Nanosuspension Technologies for Delivery of Poorly Soluble Drugs. 2014 Oct 15;2015 (2015):13.

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