Evidence map›Paper›PMID 36207535›Full record

ArticleAnalytical and bioanalytical chemistry2022

Identification and determination of structurally related peptide impurities in thymalfasin by liquid chromatography-high-resolution mass spectrometry.

Yuya Cheng, Peize Wu, Ying Kan, Ming Li, Hongmei Li

Abstract read
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In one paragraph

Article in Analytical and bioanalytical chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

5 authors at 1 institution in 1 country.

Yuya ChengDivision of Chemical Metrology & Analytical Science, National Institute of Metrology, Beijing, 100029, China.
Peize WuDivision of Chemical Metrology & Analytical Science, National Institute of Metrology, Beijing, 100029, China. wupz@nim.ac.cn.
Ying KanDivision of Chemical Metrology & Analytical Science, National Institute of Metrology, Beijing, 100029, China.
Ming LiDivision of Chemical Metrology & Analytical Science, National Institute of Metrology, Beijing, 100029, China. liming@nim.ac.cn.ORCID http://orcid.org/0000-0002-6762-2491
Hongmei LiDivision of Chemical Metrology & Analytical Science, National Institute of Metrology, Beijing, 100029, China.
National Institute of Metrology · CN

Funding

Ministry of Science and Technology of the People's Republic of China 2021YFF0600701Ministry of Science and Technology of the People's Republic of China No. 2017YFF0205403
6 · The paper itself

Abstract

Thymalfasin is an important peptide drug widely used for the single or combination treatment of hepatitis, sepsis, cancer, and immunodeficiency. Accurate purity assessment of thymalfasin material is essential for thymalfasin certified reference materials (CRMs) production and analytical method validation, in which comprehensive determination of thymalfasin-related impurities is required to avoid quantitative bias. In this study, liquid chromatography-high-resolution mass spectrometry (LC-hrMS) methods have been established to comprehensively characterize and quantify thymalfasin-related impurities using a thymalfasin China Pharmacopoeia (ChP) standard and then successfully applied to three commercial thymalfasin materials. A total of twenty-three thymalfasin-related impurities (> 0.1 mg/g) were separated, identified, and quantified in the ChP standard analyzed. The major impurities existing in thymalfasin ChP standard and commercial materials include deamination, amination, succinimide, amino acid insertion/deletion, dimers, and isomers at different mass fraction levels. In particular, over half of the thymalfasin-related impurities were found directly or indirectly arising from the labile C-terminal asparagine (Asn) residue. Given the 28th Asn residue at the C-terminus is not necessary for the biological activity of thymalfasin as reported previously, thus deletion, replacement, or modification of thymalfasin C-terminal Asn residue is proposed for new drug research and development. In summary, these results provide a further complement to the thymalfasin-related impurity profile and issue a warning for protection or processing of the thymalfasin C-terminal Asn residue.

Indexed as

Amino AcidsPeptidesAsparagineChromatography, High Pressure LiquidChromatography, LiquidDrug ContaminationMass SpectrometryThymalfasinAmino AcidsAsparaginePeptidesThymalfasinHigh-resolution mass spectrometryImpurityLiquid chromatographyPeptideThymalfasin

Identifiers

PMID36207535
OpenAlexW4303492143

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.