Utility of different lipids and effect of soya lecithin on sustained delivery of zidovudine via biodegradable solid lipid microparticles: formulation and in-vitro characterization (Record no. 17324)

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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220825142217.0
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fixed length control field 220825b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17591
Author Sathyamoorthy, Nandhakumar
245 ## - TITLE STATEMENT
Title Utility of different lipids and effect of soya lecithin on sustained delivery of zidovudine via biodegradable solid lipid microparticles: formulation and in-vitro characterization
250 ## - EDITION STATEMENT
Volume, Issue number Vol.56(3), Jul-Sep
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 689-696p.
520 ## - SUMMARY, ETC.
Summary, etc. Background: Zidovudine (Azidothymidine, AZT) is widely used in the treatment of<br/>Acquired Immuno Deficiency Syndrome (AIDS) and related conditions, either alone or<br/>in combination with other antiviral agents to combat HIV. AZT is a Biopharmaceutical<br/>Classification System (BCS) class III drug and has various disadvantages. Thus, AZT<br/>is a potential candidate for delivery<br/>via lipid-based drug delivery system. Materials<br/>and Methods: In the present work, solid lipid microparticles (SLMs) of Zidovudine<br/>were developed for sustaining the drug release, to overcome or to reduce the hepatic<br/>metabolism and to ensure optimal bioavailability. A total of sixteen formulations of<br/>Zidovudine loaded solid lipid microparticles in two groups viz., one with tripalmitin<br/>and another with trimyristin were prepared by emulsion-solvent evaporation method.<br/>Results: The average particle size and entrapment efficiency of the prepared SLM varied<br/>between 5.48 μm-10.64 μm and 46.92 % and 58.39% respectively. The release of<br/>zidovudine from the SLM varied between 70.47% and 100% at the end of 24 hrs. 80%<br/>of the drug release which is required for obtaining the optimal therapeutic concentration<br/>was achieved by SLM 8. Conclusion: Formulation SLM 8 was considered best with<br/>maximum sustainability in the drug release along with maintaining therapeutic optimum.<br/>The formulation was found stable under stressed conditions.
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) 17592
Co-Author Vankayala, Devendiran Sundar
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
Title Indian journal of pharmaceutical education and research
International Standard Serial Number 0019-5464
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-3-689.pdf
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 25/08/2022   2022-1374 25/08/2022 25/08/2022 Articles Abstract Database
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