Solubility enhancement of lawsone by complexation with beta cyclodextrin (Record no. 17327)

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003 - CONTROL NUMBER IDENTIFIER
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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220825150639.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
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) 17596
Author Francis, Shincy Mariya
245 ## - TITLE STATEMENT
Title Solubility enhancement of lawsone by complexation with beta cyclodextrin
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 706-715p.
520 ## - SUMMARY, ETC.
Summary, etc. Introduction: Lawsone is a phyto-constituent obtained from the leaves of the<br/>Lawsonia<br/>inermis. It has antibacterial, antifungal, antiviral, wound healing, antiparasitic,<br/>tuberculostatic, anti-fertility, analgesic, anti-inflammatory, enzyme inhibitory,<br/>nematicidal, anticoagulant, and protein glycation inhibitory activities. It has poor water<br/>solubility (hydrophobic), poor bioavailability, and poor dissolution characteristics.<br/>Aim: The purpose of this research is to improve the aqueous solubility of Lawsone<br/>by preparing the inclusion complexes of Lawsone with beta-cyclodextrin. Materials and<br/>Methods: Inclusion complexes of Lawsone were prepared by different methods such as<br/>physical mixture, kneading method and co-precipitation method. Characterization of the<br/>complexes were done by Fourier Transform Infrared (FTIR) spectroscopy and<br/>in vitro<br/>dissolution study. Differential scanning calorimetry (DSC), Nuclear Magnetic Resonance<br/>spectroscopy (NMR), and Powder X-Ray Diffraction (PXRD). were used to evaluate<br/>the co-precipitation technique inclusion complexes. Antimicrobial studies of complexes<br/>against<br/>Escherichia coli<br/>(E. coli),<br/>Staphylococcus aureus<br/>(S. aureus)<br/>, Bacillus subtilis<br/>(B. subtilis), and<br/>Pseudomonas aeruginosa<br/>(P. aeruginosa ) were done by colony counting<br/>method. Results: Phase solubility study revealed the molar ratio of Lawsone to beta-<br/>cyclodextrin in the complex is 1:1. At the third hour, the drug release was 64%, 78%,<br/>93%, and 97% for pure drug, physical mixture, inclusion complexes formed by kneading<br/>technique and co-precipitation technique respectively. DSC, NMR, and PXRD confirmed<br/>the formation of complexes of Lawsone. The order of antibacterial activity of inclusion<br/>complexes was<br/>E. coli > B. subtilis > P. aeruginosa > S. aureus.
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) 17597
Co-Author Xavier, Elizabeth N.
773 0# - HOST ITEM ENTRY
Title Indian journal of pharmaceutical education and research
International Standard Serial Number 0019-5464
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-56-3-706.pdf
Link text Click here
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Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Shelving location Date acquired Total Checkouts Barcode Date last seen Price effective from Koha item type
    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 25/08/2022   2022-1377 25/08/2022 25/08/2022 Articles Abstract Database
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