Solid dispersion of artemether in fast disintegrating tablet to enhance dissolution rate and oral bioavailability (Record no. 17615)

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003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220922161819.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
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 artemether in fast disintegrating tablet to enhance dissolution rate and oral bioavailability
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 153-165p.
520 ## - SUMMARY, ETC.
Summary, etc. Objectives: Artemether (ART), an antimalarial drug, have poor solubility and low<br/>bioavailability. Therefore, solid dispersion of the drug was formulated using Soluplus<br/>(SOL) and was incorporated in the fast disintegrating tablet. Materials and Methods:<br/>The solid dispersion (SD) was prepared using the solvent evaporation method using a<br/>rotary evaporator. The optimized SD was evaluated and then incorporated into the tablet.<br/>Results: Solubility studies revealed that ART SD A3 of ratio 1:3 (ART: SOP) showed a<br/>significantly higher solubility and dissolution rate than plain ART. FTIR results indicated<br/>that there was no incompatibility between the drug and hydrophilic carrier. The DSC<br/>as well as XRD studies indicated the transformation from crystalline state of drug into<br/>the amorphous form. SEM studies revealed the deposition of ART on the surface of the<br/>hydrophilic carrier.<br/>In-vitro antimalarial activity was improved of the ART due to the SD<br/>formulation. Fast disintegrating tablet of ART SD A3 was produced by using directly<br/>compressible excipients such as Ludiflash and Ludipress. Ludiflash containing tablet<br/>showed fast disintegration with higher drug release. The pharmacokinetic study in mice<br/>showed increased Cmax and AUC0–24 by 1.88- and 3.19-fold as compared to those of plain<br/>drug. Conclusion: The prepared SDs using SOP provided a platform for increased solubility<br/>and also improved the bioavailability of ART with feasibility for tablet formulation.
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) 18055
Co-Author Charde, Yogita Manohar
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
Title Indian journal of pharmaceutical education and research
International Standard Serial Number 0019-5464
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes-56-1-153.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 22/09/2022   2022-1711 22/09/2022 22/09/2022 Articles Abstract Database
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