Evidence map›Paper›PMID 37070702›Full record

ArticleIranian biomedical journal2023

Trastuzumab Charge Variants: a Study on Physicochemical and Pharmacokinetic Properties.

Fatemeh Torkashvand, Mahsa Mehranfar, Mahsa Rashidi Gero, Parisa Jafarian, Esmat Mirabzadeh, Bahareh Azarian, Soroush Sardari, Behrouz Vaziri

Abstract read
In one paragraph

Article in Iranian biomedical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Fatemeh TorkashvandBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Mahsa MehranfarBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Mahsa Rashidi GeroBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Parisa JafarianBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Esmat MirabzadehBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Bahareh AzarianBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Soroush SardariBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Behrouz VaziriBiotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Post-translational modifications in bioprocessing and storage of recombinant mAbs are the main sources of charge variants. While the profile of these kinds of variants is considered an important attribute for the therapeutic mAbs, there is controversy about their direct role in safety and efficacy. In this study, the physicochemical and pharmacokinetic (PK) properties of the separated charge variants belonging to a trastuzumab potential biosimilar, were examined. Methods: The acidic peaks, basic peaks, and main variants of trastuzumab were separated and enriched by semi-preparative weak cation exchange. A panel of analytical techniques was utilized to characterize the physicochemical properties of these variants. The binding affinity to HER2 and FcγRs and the PK parameters were evaluated for each variant. Results: Based on the results, the charge variants of the proposed biosimilar had no significant influence on the examined efficacy and PK parameters. Conclusion: During the development and production of biosimilar monoclonal antibodies, evaluating the effect of their charge variants on efficacy and PK parameters is needed.

Indexed as

Biosimilar PharmaceuticalsAntibodies, MonoclonalTrastuzumabAntibodies, MonoclonalBiosimilar PharmaceuticalsTrastuzumabMonoclonal antibodiesPharmacokineticsTrastuzumab

Identifiers

PMID37070702
PMCPMC10314757

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