Formulation and in vitro evaluation of fast dissolving tablet of verapamil hydrochiloride (Record no. 8454)

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control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20190315092828.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 190307b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 7891
Author Shinkar, Dattatraya M.
245 ## - TITLE STATEMENT
Title Formulation and in vitro evaluation of fast dissolving tablet of verapamil hydrochiloride
250 ## - EDITION STATEMENT
Volume, Issue number Vol. 10(10), July-August
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M. P.
Name of publisher, distributor, etc. Innovare Academic Sciences Pvt Ltd
Year 2018
300 ## - PHYSICAL DESCRIPTION
Pagination 93-99
520 ## - SUMMARY, ETC.
Summary, etc. Objective:The main objective of this research work was to formulate and evaluate fast dissolving tablet of verapamil hydrochloride for the treatment of hypertension.Methods: In this study, fast dissolving tablet were prepared by wet granulation method by using croscarmellose sodium and sodium starch glycolate as superdisintegrants in the concentration of 2%, 4%, and 6%. Polyvinyl pyrollidone K30 is used as a binder. The designed tablets were subjected to various assessment parameters like friability test, hardness test, disintegration test, wetting time, in vitro drug release and drug content. Results: All the prepared formulations were subjected to various assessment parameters, and the findings obtain within the prescribed limit. The calibration curve of pure drug using various solvents like distilled water, phosphate buffer pH 6.8 was plotted. F1-F9 containing croscarmellose sodium and sodium starch glycolate in various concentration demonstrate the minimum disintegration time. Among all these formulations F8 shows disintegration time upto 19±0.06 seconds due to the high concentration of superdisintegrants.In vitro drug release was tested in phosphate buffer pH 6.8 at a time interval of 0, 1, 3,6,9,12,15 min. The F8 shows drug release 98.5±0.567%. Accelerated stability study of optimized formulation (F8) up to 2 mo showed there was no change in disintegration time and percentage drug release. Conclusion:The results obtained in the research work clearly showed a promising potential of fast dissolving tablets containing a specific ratio of crosscarmellose sodium and sodium starch glycolate as superdisintegrants for the effective treatment of hypertension.
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) 7892
Co-Author Aher, Pooja S.
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 7893
Co-Author Parag, D.
773 0# - HOST ITEM ENTRY
Title International journal of pharmacy and pharmaceutical science
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
International Standard Serial Number 0975 – 1491
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/28714/15896
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 30/03/2019   2018424 19/06/2019 30/03/2019 Articles Abstract Database
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