VALIDATED RP -HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF PYRANTEL PAMOATE AND PRAZIQUANTEL IN BULK AND PHARMACEUTICAL DOSAGE FORM (Record no. 11196)

000 -LEADER
fixed length control field a
003 - CONTROL NUMBER IDENTIFIER
control field OSt
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20200212135250.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200212b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 12152
Author Rajesh, R.
245 ## - TITLE STATEMENT
Title VALIDATED RP -HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF PYRANTEL PAMOATE AND PRAZIQUANTEL IN BULK AND PHARMACEUTICAL DOSAGE FORM
250 ## - EDITION STATEMENT
Volume, Issue number Vol.1(5)
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 62-67p.
520 ## - SUMMARY, ETC.
Summary, etc. Objective:
To develop a simple, accurate and precise
reverse-
phase high
-performance liquid chromatography (
RP
-HPLC
) metho
d and subsequently
validate
for the simultaneous estimation of praziquantel (PZ
Q) and pyrantel pamoate (PP) in the
pharmaceutical dosage form.
Method
s:
The chromatographic separation was achieved on Phenomenex Luna C
18
Result
s:
The retention time of PZQ and PP was found to be 3.897 min and 1.697 min re
spectively. The method was validated in terms of specificity,
accuracy, precision, linearity and robustness as per ICH guidelines. Linearity was obtained in the concentration range of
20

60 μg
/ml
for both PZQ
and PP with correlation coefficients of 0.987 and 0.998 respectively. The accuracy of the method was determined using a recov
ery test and found as
98.44 % to 100.35 %. All parameters are found to be within the acceptable limit.
column (250 mm × 4.6 mm, 5
μm) as st
ationary phase
maintained at an ambient temperature with a mobile phase comprising of wate
r:
acetonitrile (20
: 80) at a flow rate of 1.0 ml/min and UV detection
at 220 nm.
Conclu
sio
n:
The developed RP
-HPLC method was simple, rapid, accurate, precise for the simultaneous estimation of PZQ and PP in bulk and tablet
dosage form
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) 12153
Co-Author James,Jithu Jerin
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication Bhopal Innovare Academic Sciences Pvt Ltd
Title International journal of pharmacy and pharmaceutical science
International Standard Serial Number 2656-0097
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://innovareacademics.in/journals/index.php/ijpps/article/view/30488/19866
Link text Click here
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 2020-02-12 2020929 2020-02-12 2020-02-12 Articles Abstract Database
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