Development of an In Vitro Potency Assay System for Quality Control of Anti-Human Epidermal Growth Factor Receptor 2 Antibody Admixtures
By: LV, P
.
Contributor(s): HU, LIDE.
Publisher: Mumbai Indian Journal of Pharmaceutical Science 2021Edition: Vol.83(2), March-April.Description: 293-305p.Subject(s): PHARMACEUTICSOnline resources: Click here
In:
Indian journal of pharmaceutical sciencesSummary: 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.
| Item type | Current location | Call number | Status | Date due | Barcode | Item holds |
|---|---|---|---|---|---|---|
Articles Abstract Database
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School of Pharmacy Archieval Section | Not for loan | 2021-2022601 |
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.
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