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

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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
treatment. These drugs have poor bioavailability due to low solubility and dissolution. The objective of this
work was to improve bioavailability by increasing solubility and dissolution of both drugs. In this work solid
dispersion using hydrophilic carriers like polyvinylpyrrolidone K-30, Soluplus and Lutrol F68 by solvent
evaporation technique was prepared and evaluated for solubility, flow property, differential scanning
calorimetry, x-ray diffraction analysis, scanning electron microscopy, disintegration and dissolution
study. The drugs were determined simultaneously by high performance liquid chromatography method
using various surfactants in different dissolution media. Solubility of the drugs was increased in all solid
dispersions compared to pure drugs. Flow properties of solid dispersions containing polyvinylpyrrolidone
K-30 were better than other carriers and the disintegration time of immediate release tablet containing
drug and polyvinylpyrrolidone K-30 (1:0.2) was less than other solid dispersions. X-ray diffraction analysis,
differential scanning calorimetry and scanning electron microscopy results indicated decrease in crystalline
nature of drugs and their dissolution rate was enhanced than plain drugs and marketed formulations
in acidic buffer containing myrj 52 (1 %) as dissolution medium. The pharmacokinetic studies in mice
revealed that artemether-lumefantrine solid dispersion immediate release tablet had higher area under
the curve, maximum plasma concentration for artemether and lumefantrine than plain and marketed
tablet. Thus this technique successfully improved solubility, dissolution rate and hence the bioavailability
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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          School of Pharmacy School of Pharmacy Archieval Section 2022-06-28 2022-0934 2022-06-28 2022-06-28 Articles Abstract Database
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