Development of an In Vitro Potency Assay System for Quality Control of Anti-Human Epidermal Growth Factor Receptor 2 Antibody Admixtures (Record no. 15782)

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005 - DATE AND TIME OF LATEST TRANSACTION
control field 20211228115310.0
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040 ## - CATALOGING SOURCE
Original cataloging agency AIKTC-KRRC
Transcribing agency AIKTC-KRRC
100 ## - MAIN ENTRY--PERSONAL NAME
9 (RLIN) 15138
Author LV, P.
245 ## - TITLE STATEMENT
Title Development of an In Vitro Potency Assay System for Quality Control of Anti-Human Epidermal Growth Factor Receptor 2 Antibody Admixtures
250 ## - EDITION STATEMENT
Volume, Issue number Vol.83(2), March-April
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 293-305p.
520 ## - SUMMARY, ETC.
Summary, etc. Although the physical/chemical stability and potential interactions of trastuzumab and pertuzumab in
a single infusion bag before co-administration have been evaluated preliminarily, it is not easy to clarify
which monoclonal antibodies changes when the admixtures were analyzed as a whole, especially forin vitro
potency evaluation. In this study, take admixtures of pertuzumab and trastuzumab biosimilar products
as samples, an in vitro potency assay system was developed that can monitor the changes of potency of
each monoclonal antibodies as well as their admixtures. Development of the assay system included 3 steps,
the first step is to develop protein quantification assay for each monoclonal antibodies by specific antigen
based enzyme-linked immunosorbent assay, then a specified cell based potency assay that could be used
to measure the biological potency of each monoclonal antibodies and their admixtures was developed.
After that, the enzyme-linked immunosorbent assay based protein quantification assay and the specified
cell based potency assay were qualified for accuracy and precision. Meanwhile, admixtures containing
different amount ratios of pertuzumab and trastuzumab biosimilar products were prepared and measured
by the well qualified assays. Finally, the potency test data generated from admixtures of different amount
ratio were summarized as an analysis table. The analysis table plus protein quantification results were
then used as the basic tool for further in vitro potency evaluation of unknown admixtures. Using this
system, the change of potency of each monoclonal antibodies in admixtures could be monitored. The
in vitro potency assay system was then qualified in evaluating forced degraded samples. This study represents
a good example on thorough biological potency evaluation for monoclonal antibodies admixtures.
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) 15139
Co-Author HU, LIDE
773 0# - HOST ITEM ENTRY
Title Indian journal of pharmaceutical sciences
Place, publisher, and date of publication New Delhi
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URL https://www.ijpsonline.com/articles/development-of-an-emin-vitroem-potency-assay-system-for-quality-control-of-anti-human-epidermal-growth-factor-receptor-2.pdf
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          School of Pharmacy School of Pharmacy Archieval Section 2021-12-28 2021-2022601 2021-12-28 2021-12-28 Articles Abstract Database
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