Formulation and evaluation of film forming solution of diphenhydramine hydrochloride for transdermal delivery (Record no. 17594)

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003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220922111327.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220922b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 18024
Author Akhil Baby
245 ## - TITLE STATEMENT
Title Formulation and evaluation of film forming solution of diphenhydramine hydrochloride for transdermal delivery
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 43-49p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim: The present work intends to formulate and evaluate film forming solution of<br/>diphenhydramine. Materials and Methods: Film forming solutions (FFS) for transdermal<br/>delivery of Diphenhydramine HCl were prepared using different polymers (hydroxypropyl<br/>cellulose, Eudragit L 100, polyvinylpyrollidone K30 and polyvinylpyrollidone K90), PEG<br/>400 as plasticizer and ethyl alcohol as solvent. Results: The film forming solutions were<br/>found to display an acceptable drying time ranging from 2 to 5 min.<br/>In-vitro release<br/>studies indicated percentage drug released by the end of 8 h from FFS of HPC-EF,<br/>Eudragit L 100 and PVP K 30 was found to be 41.31 ± 2.1%, 14.81 ± 1.2 % and<br/>25.7 ± 1.9 % respectively. FFS of HPC-EF that readily released drug were considered<br/>for further development by incorporating penetration enhancers like azone, isopropyl<br/>myristate and oleic acid. Steady state flux of drug across shed snake skin used as a<br/>barrier in vertical Franz diffusion cell was found to be 42.27 ±3.5 mg/cm2/hr, 51.18<br/>±4.9 mg/cm2/hr and 57.91 ± 7.2 mg/cm2/hr for FFS containing isopropyl myristate,<br/>oleic acid and azone as permeation enhancers respectively. Conclusion: Considering the<br/>plasma clearance of the drug and transdermal steady state flux, it can be inferred that<br/>FFS containing azone as enhancer needs to be spread across an application area of<br/>0.5 cm2 to elicit a therapeutic response.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 18025
Co-Author Hagalavadi, Nanjappa Shivakumar
773 0# - HOST ITEM ENTRY
Title Indian journal of pharmaceutical education and research
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
International Standard Serial Number 0019-5464
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-1-43_0.pdf
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 22/09/2022   2022-1696 22/09/2022 22/09/2022 Articles Abstract Database
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