Formulation and evaluation of fast dissolving film of fosinopril (Record no. 8335)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20190314135758.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 190221b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 7652
Author Pande, V. V.
245 ## - TITLE STATEMENT
Title Formulation and evaluation of fast dissolving film of fosinopril
250 ## - EDITION STATEMENT
Volume, Issue number Vol. 55(12), December
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Drug Manufacture's Association - IDMA
Year 2018
300 ## - PHYSICAL DESCRIPTION
Pagination 34-40
520 ## - SUMMARY, ETC.
Summary, etc. The mouth dissolving film overcomes the shortfalls of conventional quick dispersing/dissolving intraoral tablets. Fosinopril is an angiotensin converting enzyme (ACE) inhibitor used for the treatment of hypertension and some types of chronic heart failure.It undergoes extensive hepatic first pass metabolism, with bioavailability being only 36%. In the present investigation, an attempt was made to formulate fast dissolving film of fosinopril sodium by Solvent casting method using various film forming polymers such as HPMC 5cps, HPMC E-3, HPMC E-15 each being varied at three different concentration(6%,8%,10%). Drug-excipient compatibility studies were carried out by FTIR spectroscopy and DSC. in order to establish compatibility between drug and excipients The results revealed that the drug and excipients were satisfactorily compatible, without any significant changes in the chemical nature of the drug. Prepared films were subjected to different evaluation parameters such as folding endurance, physical appearance, %moisture absorption,drug content uniformity, in vitro disintegration time, in vitro dissolution studies and stability studies. All the formulations show name accurred compliance with pharmacopoeial standards. The stability study shows that no significant changes in films after one month study. Results revealed that the formulations F1 containing 6% HPMC 5cps showed better release property, low disintegration time, good folding endurance and good physical appearance compared to other formulations, so it was selected as the best formulation.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
9 (RLIN) 4639
Topical term or geographic name entry element PHARMACEUTICS
653 ## - Keywords
Keywords Hydroxypropyl methlcellulose
653 ## - Keywords
Keywords Solvent casting
653 ## - Keywords
Keywords Fosinopril
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 7653
Co-Author Patel, A. A.
700 ## - ADDED ENTRY--PERSONAL NAME
9 (RLIN) 7654
Co-Author Patel, V. P.
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Mumbai Indian Drug Manufactures Association
Title Indian drugs
856 ## - ELECTRONIC LOCATION AND ACCESS
Link text Click here
URL https://www.indiandrugsonline.org/issuesarticle-details?id=ODc1
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme
Koha item type Articles Abstract Database
Holdings
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 2019-03-30 2018381 2019-06-19 2019-03-30 Articles Abstract Database
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