Study on solubility enhancement of etravirine by crystal engineering method (Record no. 18964)

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003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20230316105526.0
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fixed length control field 230316b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 14759
Author Bhattacharyya, Sayani
245 ## - TITLE STATEMENT
Title Study on solubility enhancement of etravirine by crystal engineering method
250 ## - EDITION STATEMENT
Volume, Issue number Vol.84(3), May-Jun
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Journal of Pharmaceutical Science
Year 2022
300 ## - PHYSICAL DESCRIPTION
Pagination 575-585p.
520 ## - SUMMARY, ETC.
Summary, etc. Etravirine, an antiretroviral agent, used in the treatment of human immunodeficiency virus belongs to<br/>biopharmaceutical classification system classification IV. The reported solubility of the drug is 0.0169 mg/<br/>ml. In the present study, an attempt was made to enhance the solubility of etravirine by crystal engineering<br/>technique. The cocrystallization method was carried out using 12 different coformers and each coformer<br/>was studied in two different stoichiometric ratios. A preliminary screening of all the cocrystals was done<br/>by determination of melting point and solubility. A statistical evaluation of all the cocrystals on solubility<br/>was carried out at a significance level of p<0.05. The best cocrystals were subjected to drug content, in vitro<br/>drug release, solid-state study (fourier transform infrared spectroscopy, differential scanning calorimetry,<br/>powder x-ray diffraction) and stability study for 3 mo. Coformer benzoic acid showed a significant<br/>improvement in etravirine solubility in the drug:coformer ratio of 1:1 and 1:2. The drug:benzoic acid<br/>ratio of 1:2 was found to have more solubility and showed enhanced dissolution compared to pure drug.<br/>The in vitro dissolution rate of the drug:benzoic acid ratio of 1:2 was found to be more than 90 % in 60<br/>min. Therefore, it can be concluded that the cocrystallization method with benzoic acid as coformer can be<br/>a promising approach for solubility improvement of etravirine.
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) 20152
Co-Author Adhikari, H.
773 0# - HOST ITEM ENTRY
International Standard Serial Number 0250-474X
Title Indian journal of pharmaceutical sciences
Place, publisher, and date of publication New Delhi Indian Pharmaceutical Association
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijpsonline.com/articles/a-study-on-solubility-enhancement-of-etravirine-by-crystal-engineering-method.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 16/03/2023   2023-0419 16/03/2023 16/03/2023 Articles Abstract Database
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