Development of tapentadol hydrochloride loaded proniosomal gel using main effects screening design and in silico verification using parameter sensitivity analysis (Record no. 17597)

MARC details
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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220922120051.0
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) 18031
Author Sangeetha G.
245 ## - TITLE STATEMENT
Title Development of tapentadol hydrochloride loaded proniosomal gel using main effects screening design and in silico verification using parameter sensitivity analysis
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 65-76p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim: Tapentadol Hydrochloride is a centrally acting opioid analgesic of biopharmaceutical<br/>classification system class I drug. Oral administration of tapentadol hydrochloride<br/>undergoes extensive first-pass metabolism leads to poor bioavailability. The present study<br/>was aimed to screen the critical material attributes to deliver the tapentadol hydrochloride<br/>through the transdermal route using a carrier proniosomal gel. Methodology: Main effect<br/>screening design has been constructed to screen the choice of surfactant used for the<br/>formulation of tapentadol hydrochloride proniosomal gel. The critical material attributes<br/>selected were surfactant, cholesterol, and soya lecithin, with responses entrapment<br/>efficiency (%), vesicle size (nm), and zeta potential (mV). All 24 runs of experiments were<br/>performed and evaluated to check the model fit. The<br/>in silico verification was analyzed<br/>using parameter sensitivity analysis. Results: The prediction profiler showed maximum<br/>desirability for Kolliphore RH 40 against the set goals. The design diagnostic efficiency<br/>was measured better for the constructed MESD. Also, parameter sensitivity analysis<br/>confirms that the vesicle size would play a principal role in the permeation of tapentadol<br/>hydrochloride proniosomal gel. Conclusion: Hence, Kolliphore RH 40 was considered for<br/>the further optimization process. The tapentadol hydrochloride proniosomal gel would be<br/>a better alternative to oral therapy.
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) 18032
Co-Author Swamivel Manickam, M.
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-56-1-65_0.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   2022-1699 22/09/2022 22/09/2022 Articles Abstract Database
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