Preparation and in-vitro / in-vivo characterization of transdermal amphiphilogel loaded with biodegradable polymeric submicron carriers of meloxicam for treatment of inflammation (Record no. 17613)

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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 18050
Author Singhavi, Dilesh Jagdish
245 ## - TITLE STATEMENT
Title Preparation and in-vitro / in-vivo characterization of transdermal amphiphilogel loaded with biodegradable polymeric submicron carriers of meloxicam for treatment of inflammation
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(1), Jan-Mar
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Karnataka
Name of publisher, distributor, etc. Association of Pharmaceutical Teachers of India (APTI)
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 133-143p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim: The main purpose for this study was to develop and evaluate amphiphilogels loaded<br/>with meloxicam-submicron particles considering the benefits of the transdermal route of<br/>administration of anti-inflammatory drugs (nonsteroidal). Materials and Methods: Glyceryl<br/>monostearate (7%, 9% and 11% w/w) and sorbiton monostearate (span 60; 21%, 23%<br/>and 25% w/w) amphiphilogels containing meloxicam-submicron particles equivalent to<br/>0.5% w/w drug were formulated. Then these were evaluated through rheological,<br/>in-vitro<br/>permeation,<br/>in-vitro release, pharmacokinetics, pharmacodynamics and skin irritation<br/>studies. The rodents were chosen as subjects to conduct the pharmacokinetics study of<br/>meloxicam via oral administration and transdermally as solutions and gels, respectively.<br/>Results: It was observed that the Cmax value of drug obtained from meloxicam solution<br/>and a marketable piroxicam gel formulation were radically lower than that obtained<br/>from an amphiphilogel (FM4, containing 7% w/w glyceryl monostearate). It was also<br/>observed that when applied transdermally, the bioavailability of meloxicam from FM4<br/>was higher (<br/>n = 3,<br/>p< 0.001) than 2.5 times the bioavailability of meloxicam from a<br/>solution which was orally administered. The anti-inflammatory property of FM4 was<br/>comparatively much greater than the commercially available formulations in carrageenan-<br/>induced edema in rat’s paw. Conclusion: It can be concluded that the amphiphilogels<br/>loaded with meloxicam-submicron particles was found to be a safe and efficient drug<br/>delivery system for enhanced transdermal delivery of meloxicam.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4774
Topical term or geographic name entry element PHARMACOLOGY
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 18051
Co-Author Yeole, Pramod
773 0# - HOST ITEM ENTRY
International Standard Serial Number 0019-5464
Title Indian journal of pharmaceutical education and research
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-1-133.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 22/09/2022   2022-1709 22/09/2022 22/09/2022 Articles Abstract Database
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