Bioavailability enhancement of artemether and lumefantrine by improving solubility and dissolution rate using solid dispersion technique (Record no. 16941)

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003 - CONTROL NUMBER IDENTIFIER
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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220628120641.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 220628b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 16877
Author Charde, Yogita
245 ## - TITLE STATEMENT
Title Bioavailability enhancement of artemether and lumefantrine by improving solubility and dissolution rate using solid dispersion technique
250 ## - EDITION STATEMENT
Volume, Issue number Vol.83(4), July-Aug
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Journal of Pharmaceutical Science
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 808-822p.
520 ## - SUMMARY, ETC.
Summary, etc. Artemether-lumefantrine is World Health Organization approved fixed dose combination for malaria<br/>treatment. These drugs have poor bioavailability due to low solubility and dissolution. The objective of this<br/>work was to improve bioavailability by increasing solubility and dissolution of both drugs. In this work solid<br/>dispersion using hydrophilic carriers like polyvinylpyrrolidone K-30, Soluplus and Lutrol F68 by solvent<br/>evaporation technique was prepared and evaluated for solubility, flow property, differential scanning<br/>calorimetry, x-ray diffraction analysis, scanning electron microscopy, disintegration and dissolution<br/>study. The drugs were determined simultaneously by high performance liquid chromatography method<br/>using various surfactants in different dissolution media. Solubility of the drugs was increased in all solid<br/>dispersions compared to pure drugs. Flow properties of solid dispersions containing polyvinylpyrrolidone<br/>K-30 were better than other carriers and the disintegration time of immediate release tablet containing<br/>drug and polyvinylpyrrolidone K-30 (1:0.2) was less than other solid dispersions. X-ray diffraction analysis,<br/>differential scanning calorimetry and scanning electron microscopy results indicated decrease in crystalline<br/>nature of drugs and their dissolution rate was enhanced than plain drugs and marketed formulations<br/>in acidic buffer containing myrj 52 (1 %) as dissolution medium. The pharmacokinetic studies in mice<br/>revealed that artemether-lumefantrine solid dispersion immediate release tablet had higher area under<br/>the curve, maximum plasma concentration for artemether and lumefantrine than plain and marketed<br/>tablet. Thus this technique successfully improved solubility, dissolution rate and hence the bioavailability<br/>of artemether and lumefantrine which was determined by single dissolution method.
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) 16878
Co-Author Avari, Jasmine
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication New Delhi
Title Indian journal of pharmaceutical sciences
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijpsonline.com/articles/bioavailability-enhancement-of-artemether-and-lumefantrine-by-improving-solubility-and-dissolution-rate-using-solid-disp.pdf
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 28/06/2022   2022-0934 28/06/2022 28/06/2022 Articles Abstract Database
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