*Five Years Citation in Google scholar (2016 - 2020) is. 1451*   *    IJPR IS INDEXED IN ELSEVIER EMBASE & EBSCO *       

logo

INTERNATIONAL JOURNAL OF PHARMACEUTICAL RESEARCH

A Step Towards Excellence
Published by : Advanced Scientific Research
ISSN
0975-2366
Current Issue
No Data found.
Article In Press
No Data found.
ADOBE READER

(Require Adobe Acrobat Reader to open, If you don't have Adobe Acrobat Reader)

Index Page 1
Click here to Download
IJPR 9[3] July - September 2017 Special Issue

July - September 9[3] 2017

Click to download
 

Article Detail

Label
Label
Design and Characterization Of Miconazole Niosomal Gel

Author: YENUMULA NETTEKALLU, SAMPATH KUMAR RAMALA, HAREESH DARA, LYAKAT S. ALI, BHARGAV BHONGIRI, GAJULA NAGARAJU, G.JAGADISH
Abstract: Miconazole, a macrolide antibiotic, is employed to treat certain susceptible bacteria. Niosomes play a significant role in drug delivery since they can alter pharmacokinetics and bioavailability characteristics, as well as minimise toxicity. Niosomes are becoming more and more crucial in the administration of drugs. While decreasing the drug's systemic absorption, topically administered niosomes can lengthen the duration that medications remain in the stratum corneum and epidermis. Miconazole-loaded topical gel niosomes are intended to be developed and evaluated in this study. Span 20, 40, 60 (as a non-ionic surfactant) and cholesterol were used to create niosomes by the thin film hydration method (as stable vesicle forming agent). Different dosages of the drugs, surfactants, and cholesterol were used to make niosomes (0.30:1:0.6, 0.6:1:0.6, 0.9:1:0.6). The vesicle size, surface shape, % entrapment effectiveness, drug content, and in vitro drug release of the niosomal dispersion were examined. Using a UV spectrophotometer, the drug concentration and entrapment efficiency were determined at 262 nm. A range of 77.650.25 to 94.120.48 was discovered for the entrapment efficiency. A maximum entrapment efficiency of 94.12 ± 0.48 was shown for Formulation FS5, which contains Span 60, and 93.900.70 was shown for Formulation FT4, which contains Tween 60. Carbopol 940, glycerol, triethanolamine, and distilled water were used to make Miconazole niosomal gel. Niosomal gel's evaluation was based on its outward appearance, pH, viscosity, drug content, entrapment effectiveness, and in-vitro permeation investigations. The amount of medication released from the niosomal gel was discovered to be 80.76%. The aforementioned data show that encapsulating a Miconazole-loaded niosomal topical gel lengthens drug release, increases drug retention in skin, and enhances cellular permeability.
Keyword: Niosomes; Miconazole; carbopol 934,fungal infection
DOI: https://doi.org/10.31838/ijpr/2020.12.01.421
Download: Request For Article
 
Clients

Clients

Clients

Clients

Clients
ONLINE SUBMISSION
USER LOGIN
Username
Password
Login | Register
News & Events
SCImago Journal & Country Rank

Terms and Conditions
Disclaimer
Refund Policy
Instrucations for Subscribers
Privacy Policy

Copyrights Form

0.12
2018CiteScore
 
8th percentile
Powered by  Scopus
Google Scholar

hit counters free