Evidence map›Paper›PMID 41149382›Full record

ArticleGels (Basel, Switzerland)2025

Antibody-Integrated Solid-to-Gel Microfilm for Protection Against Botulinum Neurotoxin Type A.

Ji-Hwan Ha, Sohee Jeon, Yun-Woo Lee, Soon Hyoung Hwang, Byung-Ho Kang, Young Jo Song, Ji-Su Lim, Hyunbeen Kim, Yoosik Yoon, Jun-Ho Jeong

Abstract read
In one paragraph

Article in Gels (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

10 authors.

Ji-Hwan HaNano Lithography and Manufacturing Research Center, Korea Institute of Machinery and Materials (KIMM), Daejeon 34103, Republic of Korea.
Sohee JeonNano Lithography and Manufacturing Research Center, Korea Institute of Machinery and Materials (KIMM), Daejeon 34103, Republic of Korea.
Yun-Woo LeeNano Lithography and Manufacturing Research Center, Korea Institute of Machinery and Materials (KIMM), Daejeon 34103, Republic of Korea.
Soon Hyoung HwangNano Lithography and Manufacturing Research Center, Korea Institute of Machinery and Materials (KIMM), Daejeon 34103, Republic of Korea.
Byung-Ho KangNano Lithography and Manufacturing Research Center, Korea Institute of Machinery and Materials (KIMM), Daejeon 34103, Republic of Korea.
Young Jo SongThe 3rd R&D Institute, Agency for Defense Development, Daejeon 34186, Republic of Korea.
Ji-Su LimCollege of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
Hyunbeen KimCollege of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.
Yoosik YoonCollege of Medicine, Chung-Ang University, Seoul 06974, Republic of Korea.ORCID 0000-0002-9823-4555
Jun-Ho JeongNano Lithography and Manufacturing Research Center, Korea Institute of Machinery and Materials (KIMM), Daejeon 34103, Republic of Korea.

Funding

Agency for Defense Development (ADD) Defense Acquisition Program Administration (DAPA) in 2025 (No. 915063201)
6 · The paper itself

Abstract

Antibodies are indispensable for protection against biological toxins and pathogens, yet their conventional liquid formulations impose severe constraints, including dosing inaccuracy caused by residual fluid remaining in the syringe and limited user convenience such as pain caused by fluid-induced tissue distension and nerve stimulation as well as instability in ambient temperature, and the requirement for low-temperature storage and logistics. These limitations critically impair rapid deployment during golden hour following acute exposure. Here, we report an antibody-integrated solid-to-gel microfilm-demonstrated with a 100 µg anti-BoNT/A dose-jet-printed and low-temperature dried directly onto metal needles for consistent, on-demand use. Upon intradermal insertion, the microfilm fully dissolves within 5 min, driven by hydration-induced swelling of a hyaluronic acid (HA) support layer and rapid release of the antibody. Time-resolved microscopy and UV-vis analysis showed a decrease in residual solid from 2.34 mm

Indexed as

antibody-integrated solid-to-gel microfilmantibody microfilm-coated needlesanti-BoNT/A antibodyBoNT/A protectiongel-integrated antibody

Identifiers

PMID41149382
PMCPMC12563112

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Registered trials

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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.