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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2976899/
Jan 18, 2008 · Microemulsion based delivery of amphotericin B investigated in this paper results in an equi-efficacious formulation but with lesser extent of some undesirable features of Fungizone® such as its hemolytic potential when examined in vitro.Author: Pradnya S. Darole, Darshana D. Hegde, Hema A. Nair
https://www.ncbi.nlm.nih.gov/pubmed/18446472
Formulation and evaluation of microemulsion based delivery system for amphotericin B. Darole PS(1), Hegde DD, Nair HA. Author information: (1)Department of Pharmaceutics, Bombay College of Pharmacy, Kalina, Santacruz (E.), Mumbai 400098, Maharashtra, India.Author: Pradnya S. Darole, Darshana D. Hegde, Hema A. Nair
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555009/
The developed microemulsion formulation was evaluated for the responses and the experimental values obtained were compared with those predicted by the mathematical models. On the basis of globule size, zeta potential, % drug release, and % permeability, formulation 5 (F5) was selected for the further study.
https://pdfs.semanticscholar.org/bcf6/78c7e94306899ac239a5a404e6a5e202895a.pdf
microemulsion drug delivery system designed for intranasal administration of a hydrophobic model drug Olanzapine. Drug-loaded microemulsions were successfully prepared by a water titration method.
https://link.springer.com/article/10.1208%2Fs12249-007-9022-8
Jan 18, 2008 · The present studies were designed to develop a formulation of amphotericin B in a lipid-based preparation as a microemulsion and to compare its toxicity with the commercial formulation Fungizone®. The final product developed is a lyophilized amphotericin B, oil and surfactant blend for reconstitution in water to yield a microemulsion containing 5 mg/ml of the drug.Author: Pradnya S. Darole, Darshana D. Hegde, Hema A. Nair
https://www.ijper.org/article/1135
Results and Discussion: Two microemulsion were selected based on the globule area, PDI and physical stability and incorporated into the gel base of sodium alginate. The optimized microemulgel (F1) showed acceptable physical properties with lowest viscosity value (2325 cps) and showed pseudoplastic behaviour, highest spreadability value (3.7 gm.cm/sec), Highest drug permeation (63.50%) after 5 hr. …Author: Panchaxari Mallappa Dandagi, Pratibha Pandey, Anand Panchakshari Gadad, Vinayak Shivamurthy Mastihol...
http://europepmc.org/articles/PMC2976899/
Dec 01, 2007 · Formulation and Evaluation of Microemulsion Based Delivery System for Amphotericin B Pradnya S. Darole , Darshana D. Hegde , and Hema A. Nair Department of Pharmaceutics, Bombay College of Pharmacy, Kalina, Santacruz …
https://www.researchgate.net/publication/5406911_Formulation_and_Evaluation_of_Microemulsion_Based_Delivery_System_for_Amphotericin_B
Formulation and Evaluation of Microemulsion Based Delivery System for Amphotericin B Article in AAPS PharmSciTech 9(1):122-8 · February 2008 with 47 Reads How we measure 'reads'
https://www.researchgate.net/publication/235393682_Formulation_and_evaluation_of_microemulsion-based_hydrogel_for_topical_delivery
The optimized microemulsion-based hydrogel was evaluated for viscosity, spreadability, skin irritancy, skin permeability, stability, and antifungal activity by comparing it with marketed bifonazole cream. Results: The mechanism of drug release from microemulsion-based...
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