Development and validation by reverse phase high performance liquid chromatography method for the estimation of piperine and coenzyme q10 in bulk and pharmaceutical dosage form (Record no. 17233)

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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20220730103350.0
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fixed length control field 220730b xxu||||| |||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 17407
Author Sarkar, M.
245 ## - TITLE STATEMENT
Title Development and validation by reverse phase high performance liquid chromatography method for the estimation of piperine and coenzyme q10 in bulk and pharmaceutical dosage form
250 ## - EDITION STATEMENT
Volume, Issue number Vol.83(6), Nov-Dec
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Mumbai
Name of publisher, distributor, etc. Indian Journal of Pharmaceutical Science
Year 2021
300 ## - PHYSICAL DESCRIPTION
Pagination 1208-1214p.
520 ## - SUMMARY, ETC.
Summary, etc. Today people are focused on their health, as good health is a key to the happiness of our life. Medicine takes
a big responsibility to take care of our health. Various supplements are available to meet the nutritional
requirement. One such supplement is a combination of piperine and coenzyme Q10. The medicines have
to be analyzed properly before introducing them to the market. As no analytical method is available for
simultaneous estimation of the combination, hence an attempt was made to develop a validated method
for the estimation of piperine and coenzyme Q10 simultaneously in bulk and its dosage form. A simple,
precise, accurate and validated reversed phase high performance liquid chromatography technique was
developed for the estimation of piperine and coenzyme Q10 in bulk and its tablet formulation. In this
developed method, Waters X Bridge C 18 column (250 mm×4.6 mm, 5 μm) was used as a stationary phase
and acetonitrile, tetrahydrofuran and water was used in 65:32:3 (v/v) ratio as mobile phase with 1 ml/min
flow rate. This isocratic separation was accomplished using Waters 2707 Autosampler high performance
liquid chromatography system, Waters 515 solvent delivery system, with photodiode array detector
detection at 275 nm. Chromatographic data was processed by Empower 2 software. The retention times
of coenzyme Q10 and piperine were 4.56 and 8.19 min respectively. The linearity ranges have lied between
4-6 μg/ml, 240-360 μg/ml for piperine and coenzyme Q10 respectively with 0.997 as correlation coefficient
for both.
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) 17408
Co-Author Bag, Puja
773 0# - HOST ITEM ENTRY
Place, publisher, and date of publication New Delhi
Title Indian journal of pharmaceutical sciences
856 ## - ELECTRONIC LOCATION AND ACCESS
URL https://www.ijpsonline.com/articles/development-and-validation-by-reverse-phase-high-performance-liquid-chromatography-method-for-the-estimation-of-piperine.pdf
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          School of Pharmacy School of Pharmacy Archieval Section 2022-07-30 2022-1235 2022-07-30 2022-07-30 Articles Abstract Database
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