Solid dispersion of lumefantrine using soluplus® by solvent evaporation method: formulation, characterization and in-vitro antimalarial screening (Record no. 17606)

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003 - CONTROL NUMBER IDENTIFIER
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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220922151121.0
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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) 18043
Author Kanojiya, Pranita Sunil
245 ## - TITLE STATEMENT
Title Solid dispersion of lumefantrine using soluplus® by solvent evaporation method: formulation, characterization and in-vitro antimalarial screening
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 121-132p.
520 ## - SUMMARY, ETC.
Summary, etc. Objectives: Lumefantrine (LUM) is an antimalarial drug having poor aqueous solubility.<br/>The objective was to formulate the solid dispersion of LUM and improve the solubility<br/>and dissolution rate. Materials and Methods: Solvent evaporation technique was used<br/>to prepare solid dispersions (SDs) with Soluplus® (SOL) using a rotary evaporator. The<br/>feasibility of the formation of SD for LUM and SOL was assessed by the Hansen solubility<br/>parameter. The drug solubility was analyzed by the HPLC method and the ratio of LUM:<br/>SOL was optimized to 1:2. The SD was characterized by DSC, FTIR, XRD and SEM.<br/>Results: The results showed that the LUM and SOL had groups that lead to the interaction<br/>between them and this led to conversion from crystalline to amorphous form and thus<br/>improved the dissolution rate. The solubility of L2 was found to be 135 ± 3.3 μg/mL<br/>using the selected dissolution media (0.1 N HCl+1% Myrj 52). The<br/>in-vitro antimalarial<br/>screening was performed using the<br/>P. falciparum 3D7 strain and the<br/>in-vitro cytotoxicity<br/>test was performed using the Vero cell line. The higher antimalarial efficacy of L2 SD<br/>was observed as compared to plain LUM. The selectivity index value of LUM SD depicted<br/>its non-toxicity. Stability study was carried out for three months and the SDs were<br/>evaluated for the drug content, change in weight and<br/>in-vitro drug release. No significant<br/>changes were observed after three months in the drug content, SD weight and<br/>in-vitro<br/>drug release. Thus the L2 SD was found to be stable. Conclusion: The prepared SD<br/>improved the solubility as well as the dissolution rate of the drug.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4774
Topical term or geographic name entry element PHARMACOLOGY
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 16877
Co-Author Charde, Yogita
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
International Standard Serial Number 0019-5464
Title Indian journal of pharmaceutical education and research
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-1-121.pdf
Link text Click here
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 22/09/2022   2022-1707 22/09/2022 22/09/2022 Articles Abstract Database
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