Evidence map›Paper›PMID 36080616›Full record

ArticlePolymers2022

Optimization of Oligomer Chitosan/Polyvinylpyrrolidone Coating for Enhancing Antibacterial, Hemostatic Effects and Biocompatibility of Nanofibrous Wound Dressing.

Vinh Khanh Doan, Chien Minh Tran, Trinh Thi-Phuong Ho, Linh Kim-Khanh Nguyen, Yen Ngoc Nguyen, Ngan Tuan Tang, Tin Dai Luong, Nhi Ngoc-Thao Dang, Nam Minh-Phuong Tran, Binh Thanh Vu and 10 more

Abstract read
In one paragraph

Article in Polymers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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

20 authors.

Vinh Khanh DoanTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Chien Minh TranTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Trinh Thi-Phuong HoTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Linh Kim-Khanh NguyenTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Yen Ngoc NguyenTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Ngan Tuan TangTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0001-8762-880X
Tin Dai LuongTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Nhi Ngoc-Thao DangTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Nam Minh-Phuong TranTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Binh Thanh VuTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.
Hoai Thi-Thu NguyenVietnam National University, Ho Chi Minh City 700000, Vietnam.
Quyen Thuc HuynhVietnam National University, Ho Chi Minh City 700000, Vietnam.
Hien Quoc NguyenVietnam Atomic Energy Institute, 59 Ly Thuong Kiet, Hanoi 100000, Vietnam.
Chien Mau DangVietnam National University, Ho Chi Minh City 700000, Vietnam.
Thang Bach PhanVietnam National University, Ho Chi Minh City 700000, Vietnam.
Hanh Thi-Kieu TaVietnam National University, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0002-4975-4124
Viet Hung PhamKey Laboratory of Analytical Technology for Environmental Quality and Food Safety Control, University of Science, Vietnam National University, Hanoi 100000, Vietnam.
Thanh Dinh LeThong Nhat Hospital, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0001-5803-5714
Toi Van VoTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.ORCID 0000-0002-9551-6522
Hiep Thi NguyenTissue Engineering and Regenerative Medicine Laboratory, Department of Tissue Engineering and Regenerative Medicine, School of Biomedical Engineering, International University, Ho Chi Minh City 700000, Vietnam.

Funding

Department of Science and Technology of Ho Chi Minh City 01/2020/HĐ-QPTKHCN.
6 · The paper itself

Abstract

A synergistic multilayer membrane design is necessary to satisfy a multitude of requirements of an ideal wound dressing. In this study, trilayer dressings with asymmetric wettability, composed of electrospun polycaprolactone (PCL) base membranes coated with oligomer chitosan (COS) in various concentrations of polyvinylpyrrolidone (PVP), are fabricated for wound dressing application. The membranes are expected to synergize the hygroscopic, antibacterial, hemostatic, and biocompatible properties of PCL and COS. The wound dressing was coated by spraying the solution of 3% COS and 6% PVP on the PCL base membrane (PVP6-3) three times, which shows good interaction with biological subjects, including bacterial strains and blood components. PVP6-3 samples confirm the diameter of inhibition zones of 20.0 ± 2.5 and 17.9 ± 2.5 mm against

Indexed as

antibacterial wound dressinghemostatic effectoligomer chitosan (COS)polycaprolactone (PCL)polyvinylpyrrolidone (PVP)

Identifiers

PMID36080616
PMCPMC9460443

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.