Design of Experiments Approach to Discriminatory Dissolution Method Development of Poorly Soluble Drug in Immediate Release Dosage Form (Record no. 9761)

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control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20191018144132.0
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fixed length control field 191018b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 9942
Author Kolla, Sudheer Babu
245 ## - TITLE STATEMENT
Title Design of Experiments Approach to Discriminatory Dissolution Method Development of Poorly Soluble Drug in Immediate Release Dosage Form
250 ## - EDITION STATEMENT
Volume, Issue number Vol.53(3), Jul-Sep
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Karnataka
Name of publisher, distributor, etc. Indian journal of pharmaceutical education and research
Year 2019
300 ## - PHYSICAL DESCRIPTION
Pagination 435-445p.
520 ## - SUMMARY, ETC.
Summary, etc. Aim: The study involved design of experiment guided discriminatory dissolution method development for poorly soluble, ezetimibe tablets. Objective: In the current scope of study, ezetimibe tablets are selected as a suitable drug product candidate to evaluate the application of design of experiments in discriminatory dissolution method development for poorly soluble drug. Ezetimibe is practically insoluble in all the aqueous buffers. Methodology: 2-Level factorial design is selected as suitable model to build the experimental setup. Different factors like pH of dissolution media, sodium lauryl sulphate concentration, dissolution media volume and agitation speed (RPM) are selected for the study and dissolution % release at 5, 10, 15, 20, 45 min and % RSD of dissolution values at 20 min were selected as responses based on prior experience. The responses are evaluated for statistical significance and for adequacy of the built design with the help of different tools like ANOVA and diagnostic graphs. Results: It is observed that pH of dissolution media, surfactant concentration are having minimal positive effect on all of the responses. Whereas agitation speed and dissolution media volume were having significant positive effect on all responses, except for % RSD at 20 min and is inversely proportional to agitation speed. Conclusion: With the current scope of study design of experiments as an effective tool for discriminatory dissolution method development is employed to prove adequacy. Selected solutions from predictions were executed for experimental results and were compared against predictions to validate model.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
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9 (RLIN) 9943
Co-Author Vallabhaneni, Madhusudhan Rao
773 0# - HOST ITEM ENTRY
International Standard Serial Number 0019-5464
Place, publisher, and date of publication Bengluru Association of Pharmaceutical Teachers of India (APTI)
Title Indian journal of pharmaceutical education and research
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijper.org/sites/default/files/IndJPhaEdRes_53_3_435-445.pdf
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
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Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Permanent Location Current Location Shelving location Date acquired Barcode Date last seen Price effective from Koha item type
          School of Pharmacy School of Pharmacy Archieval Section 2019-10-18 2019914 2019-10-18 2019-10-18 Articles Abstract Database
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