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
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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
Lawsonia
inermis. It has antibacterial, antifungal, antiviral, wound healing, antiparasitic,
tuberculostatic, anti-fertility, analgesic, anti-inflammatory, enzyme inhibitory,
nematicidal, anticoagulant, and protein glycation inhibitory activities. It has poor water
solubility (hydrophobic), poor bioavailability, and poor dissolution characteristics.
Aim: The purpose of this research is to improve the aqueous solubility of Lawsone
by preparing the inclusion complexes of Lawsone with beta-cyclodextrin. Materials and
Methods: Inclusion complexes of Lawsone were prepared by different methods such as
physical mixture, kneading method and co-precipitation method. Characterization of the
complexes were done by Fourier Transform Infrared (FTIR) spectroscopy and
in vitro
dissolution study. Differential scanning calorimetry (DSC), Nuclear Magnetic Resonance
spectroscopy (NMR), and Powder X-Ray Diffraction (PXRD). were used to evaluate
the co-precipitation technique inclusion complexes. Antimicrobial studies of complexes
against
Escherichia coli
(E. coli),
Staphylococcus aureus
(S. aureus)
, Bacillus subtilis
(B. subtilis), and
Pseudomonas aeruginosa
(P. aeruginosa ) were done by colony counting
method. Results: Phase solubility study revealed the molar ratio of Lawsone to beta-
cyclodextrin in the complex is 1:1. At the third hour, the drug release was 64%, 78%,
93%, and 97% for pure drug, physical mixture, inclusion complexes formed by kneading
technique and co-precipitation technique respectively. DSC, NMR, and PXRD confirmed
the formation of complexes of Lawsone. The order of antibacterial activity of inclusion
complexes was
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
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2022-08-25 2022-1377 2022-08-25 2022-08-25 Articles Abstract Database
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