INNOVATIVE METHOD DEVELOPMENT AND FORCED DEGRADATION STUDIES FOR SIMULTANEOUS ESTIMATION OF SOFOSBUVIR AND LEDIPASVIR BY RP HPLC (Record no. 11146)

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fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200210151942.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200210b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12064
Author Reddy, B. Anjaneyulu
245 ## - TITLE STATEMENT
Title INNOVATIVE METHOD DEVELOPMENT AND FORCED DEGRADATION STUDIES FOR SIMULTANEOUS ESTIMATION OF SOFOSBUVIR AND LEDIPASVIR BY RP HPLC
250 ## - EDITION STATEMENT
Volume, Issue number Vol.11(2)
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. M P
Name of publisher, distributor, etc. Innovare Academic Sciences Pvt Ltd
Year 2019
300 ## - PHYSICAL DESCRIPTION
Pagination 34-41p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective: <br/>To develop an innovative, rapid, simple, cost<br/>-effective<br/>, stability indicating reverse phase<br/>-high performance liquid chromatography (RP<br/>-<br/>HPLC) method for simultaneous estimation of ledipasvir (LP) and sofosbuvir (SB) in combination pill dosage form.<br/>Method<br/>s: <br/>The method was developed using C8 column, 250<br/> mm<br/> x 4.6 mm, 5<br/> mm <br/>using mobile section comprising of 0.1%<br/> (v/v)<br/> orthophosphoric <br/>acid buffer<br/> at <br/>pH 2.2<br/> and acetonitrile in the ratio of 45:55 that was pumped through the column at a flow rate of 0.8 ml/min. Temperature <br/>was <br/>maintained at 30<br/> °C, the effluents w<br/>ere monitored at 260 nm with the help of usage of PDA detector.<br/>Result<br/>s: <br/>The retention time of LP and SB were found to be 2.246 min and 3.502 min.<br/> The approach was found to be linear with the variety of 9<br/>-36<br/>μg<br/>/ml<br/> and 40<br/>-<br/>240 μg<br/>/ml<br/> for LP and SB respectively, the assay of estimated compounds were found to be 99.65% and 99.73% w/v for LP and SB <br/>respectively.<br/>Conclusio<br/>n: <br/>The pressured samples changed into analyzed and this proposed a technique turned into determined to be particular and stability <br/>indicating as no interfering peaks of decay compound and excipients were observed. Hence, the approach was easy and economica<br/>l that may be <br/>efficiently applied for simultaneous estimation of both LP and SB in bulk and combination tablet system
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) 12065
Co-Author Md. Irshad Alam
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 2656-0097
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/29347/19150
Link text Click here
942 ## - ADDED ENTRY ELEMENTS (KOHA)
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    Dewey Decimal Classification     School of Pharmacy School of Pharmacy Archieval Section 10/02/2020   2020885 10/02/2020 10/02/2020 Articles Abstract Database
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