Evidence map›Paper›PMID 30794612›Full record

ArticlePloS one2019

Development of novel biocompatible thermosensitive anti-adhesive agents using human-derived acellular dermal matrix.

Jong Ju Jeong, Dong Won Lee, Seung Yong Song, Yerin Park, Ji Hee Kim, Jang Il Kim, Hyung Goo Kim, Ki Taek Nam, Won Jai Lee, Kee-Hyun Nam and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Adhesion Reduction Agent Guardix-SGClinical Medicine Insights. Oncology · 2024
    Article
  5. Review
  6. Article
  7. Biomaterials to Prevent Post-Operative Adhesion.Materials (Basel, Switzerland) · 2020
    Review
  8. 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 at 2 institutions in 1 country.

Jong Ju JeongDepartment of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID 0000-0002-4155-6035
Dong Won LeeDepartment of Plastic and Reconstructive Surgery, Institute for Human Tissue Restoration, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seung Yong SongDepartment of Plastic and Reconstructive Surgery, Institute for Human Tissue Restoration, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yerin ParkR&D Center, L&C BIO Co., Ltd, Gyeonggi-do, Republic of Korea.
Ji Hee KimDepartment of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jang Il KimR&D Center, L&C BIO Co., Ltd, Gyeonggi-do, Republic of Korea.
Hyung Goo KimR&D Center, L&C BIO Co., Ltd, Gyeonggi-do, Republic of Korea.
Ki Taek NamSeverance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Won Jai LeeDepartment of Plastic and Reconstructive Surgery, Institute for Human Tissue Restoration, Yonsei University College of Medicine, Seoul, Republic of Korea.
Kee-Hyun NamDepartment of Surgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Ju Hee LeeDepartment of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yonsei University · KRBio-Medical Science (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Postoperative adhesion is a natural phenomenon that occurs in damaged tissue cells. Several anti-adhesion agents are currently used, but there is no leading-edge product with excellent adhesion-preventive effects. The purpose of this study was to develop ideal anti-adhesive agents using human-derived acellular dermal matrix (ADM). We developed 5 new biocompatible thermosensitive anti-adhesion barriers (AABs) using micronized human-derived ADM, hyaluronic acid, and temperature-sensitive and biocompatible synthesized polymers. The biocompatibility, anti-adhesion effect, and biodegradability of these AABs were compared with those of commercial thermosensitive anti-adhesion agents. No cytotoxic effects were observed in vitro and in vivo. Animal testing of adhesion resistance confirmed that the adhesion area, strength, and grade of AAB03 were statistically superior to those of the control group. Factors related to adhesion formation, such as lymphocytes, macrophages, microvessels, and collagen fiber density, were observed using specific staining methods; the results confirmed that AAB03 group exhibited significantly lower macrophage counts, microvessel density, and collagen fiber density than the control groups. Furthermore, AAB03 was completely absorbed by 6 weeks. Thus, AAB03 has the potential to be used as a high-performance anti-adhesion agent.

Indexed as

Biocompatible MaterialsMaterials TestingAnimalsCell LineDermisExtracellular MatrixHumansMaleMiceRatsRats, Sprague-DawleyTissue AdhesionsBiocompatible Materials

Identifiers

PMID30794612
PMCPMC6386309
OpenAlexW2915912287

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.