Evidence map›Paper›PMID 41034515›Full record

ArticleNature biomedical engineering2026

One-day rapid sterility test for human-derived biopharmaceuticals.

Junwon Kang, Hamin Kim, Haewook Jang, Hyelyn Joo, Soobin Lee, Gi Yoon Lee, Hyoung Jin Kang, Youngmin Kim, Tae Hyun Kim, Sunghoon Kwon and 1 more

Abstract read
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In one paragraph

Article in Nature biomedical engineering, 2026. 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
–field-weighted citation impact
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.

  1. Review
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

11 authors.

Junwon Kang *Interdisciplinary Program in Bioengineering, Seoul National University, Seoul, Korea.
Hamin Kim *Interdisciplinary Program in Bioengineering, Seoul National University, Seoul, Korea.
Haewook Jang *Interdisciplinary Program in Bioengineering, Seoul National University, Seoul, Korea.
Hyelyn JooInterdisciplinary Program in Bioengineering, Seoul National University, Seoul, Korea.
Soobin LeeDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, Korea.ORCID http://orcid.org/0009-0007-4972-2863
Gi Yoon LeeDepartment of Electrical and Computer Engineering, Seoul National University, Seoul, Korea.
Hyoung Jin KangDepartment of Pediatrics, Seoul National University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0003-1009-6002
Youngmin KimInterdisciplinary Program in Stem Cell Biology, Seoul National University College of Medicine, Seoul, Korea.
Tae Hyun KimKU-KIST Graduate School of Converging Science and Technology, Korea University, Seoul, Korea. taehyunkim@korea.ac.kr.ORCID http://orcid.org/0000-0003-3856-5325
Sunghoon KwonInterdisciplinary Program in Bioengineering, Seoul National University, Seoul, Korea. skwon@snu.ac.kr.ORCID http://orcid.org/0000-0003-3514-1738
Eun Ju LeeInterdisciplinary Program in Stem Cell Biology, Seoul National University College of Medicine, Seoul, Korea. leeunju@snu.ac.kr.ORCID http://orcid.org/0000-0001-8489-271X

Funding

Ministry of Health and Welfare (Ministry of Health, Welfare and Family Affairs) HI14C1277Ministry of Health and Welfare (Ministry of Health, Welfare and Family Affairs) RS-2024-00438476National Research Foundation of Korea (NRF) 2020R1A2C1007242National Research Foundation of Korea (NRF) RS-2024-00347997
6 · The paper itself

Abstract

Biopharmaceuticals are emerging as viable alternatives to chemically synthesized drugs for potential treatment to various diseases. However, many of these human-derived components cannot withstand terminal sterilization procedures, and the duration of conventional sterility testing methods often exceeds their limited shelf life. Consequently, biopharmaceuticals are now frequently administered to patients before sterility confirmation. Here we present a nanoparticle-based enrichment and rapid sterility test that can determine product sterility within a single day, mitigating clinical risks of biopharmaceuticals and maintaining therapeutic efficacies during delivery. The assay incorporates synthetic beta-2-glycoprotein I peptides for selective isolation and purification of a broad spectrum of microorganisms and a microfluidic chip designed to automatically monitor their metabolic activities via fluorescence imaging, which are inferred from the reduction of a non-toxic dye as they grow. Compared with conventional approaches, the turnaround time was substantially reduced by >58 h with 100% accuracy and a limit of detection down to a concentration of 1 colony forming unit per millilitre. We validate our approach using various forms of clinical-grade biopharmaceutical products.

Indexed as

Biological ProductsHumansNanoparticlesBiological Products

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

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 Socratic graph.