VALIDATED RP -HPLC METHOD FOR SIMULTANEOUS ESTIMATION OF PYRANTEL PAMOATE AND PRAZIQUANTEL IN BULK AND PHARMACEUTICAL DOSAGE FORM (Record no. 11196)
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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 | 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 |
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 |
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School of Pharmacy | School of Pharmacy | Archieval Section | 2020-02-12 | 2020929 | 2020-02-12 | 2020-02-12 | Articles Abstract Database |