Evidence map›Paper›PMID 30360126›Full record

ArticleACS applied materials & interfaces2018

Temperature-Controlled Reversible Exposure and Hiding of Antimicrobial Peptides on an Implant for Killing Bacteria at Room Temperature and Improving Biocompatibility in Vivo.

Jiezhao Zhan, Lin Wang, Yuchen Zhu, Huichang Gao, Yunhua Chen, Junjian Chen, Yongguang Jia, Jingcai He, Zhou Fang, Ye Zhu and 3 more

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Article
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  9. Article
  10. Harnessing biomolecules for bioinspired dental biomaterials.Journal of materials chemistry. B · 2020
    Review
  11. 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

13 authors at 3 institutions in 2 countries.

Jiezhao ZhanSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
Lin WangSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
Yuchen ZhuSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
Huichang GaoNational Engineering Research Center for Tissue Restoration and Reconstruction , Guangzhou 510006 , China.
Yunhua ChenSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
Junjian ChenSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
Yongguang JiaNational Engineering Research Center for Tissue Restoration and Reconstruction , Guangzhou 510006 , China.
Jingcai HeSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
Zhou FangSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
Ye ZhuDepartment of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, Institute for Biomedical Engineering, Science and Technology , University of Oklahoma , Norman , Oklahoma 73019 , United States.
Chuanbin MaoDepartment of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, Institute for Biomedical Engineering, Science and Technology , University of Oklahoma , Norman , Oklahoma 73019 , United States.ORCID http://orcid.org/0000-0002-8142-3659
Li RenNational Engineering Research Center for Tissue Restoration and Reconstruction , Guangzhou 510006 , China.ORCID http://orcid.org/0000-0003-0604-9166
Yingjun WangSchool of Materials Science and Engineering , South China University of Technology , Guangzhou 510641 , China.
South China University of Technology · CNNational Research Center for Rehabilitation Technical Aids · CNUniversity of Oklahoma · US

Funding

Hiring Non-toxic Virus Nanoparticles to Count Cancer Biomarker MoleculesR21CA195607 · NCI · UNIVERSITY OF OKLAHOMA · PI MAO, CHUANBIN · 2015 to 2016
$359k
NCI NIH HHS R21 CA195607
6 · The paper itself

Abstract

Modification of implants by antimicrobial peptides (AMPs) can improve the antimicrobial activity of the implants. However, AMPs have some cytotoxicity in vivo when they are exposed at body temperature. To tackle this challenge, we propose to develop a new approach to generating a smart antimicrobial surface through exposure of AMPs on the surface. A polydopamine film was first formed on the substrates, followed by the conjugation of a temperature-sensitive polymer, poly( N-isopropylacrylamide) (pNIPAM), to the film through atom transfer radical polymerization (ATRP). Then, AMPs were conjugated to the NIPAM on the resultant pNIPAM-modified surface through a click chemistry reaction. Because of the temperature-sensitive property of pNIPAM, the AMPs motif was more exposed to the external environment at room temperature (25 °C) than at body temperature (37 °C), making the surface present a higher antimicrobial activity at room temperature than at body temperature. More importantly, such a smart behavior is accompanied with the increased biocompatibility of the surface at body temperature when compared to the substrates unmodified or modified by AMPs or pNIPAM alone. Our in vivo study further verified that pNIPAM-AMP dual modified bone implants showed increased biocompatibility even when they were challenged with the bacteria at room temperature before implantation. These results indicate that the implants are antibacterial at room temperature and can be safely employed during surgery, resulting in no infection after implantations. Our work represents a new promising strategy to fully explore the antimicrobial property of AMPs, while improving their biocompatibility in vivo. The higher exposure of AMPs at room temperature (the temperature for storing the implants before surgery) will help decrease the risk of bacterial infection, and the lower exposure of AMPs at body temperature (the temperature after the implants are placed into the body by surgery) will improve the biocompatibility of AMPs.

Indexed as

Anti-Bacterial AgentsAntimicrobial Cationic PeptidesTemperatureAcrylic ResinsAnimalsBone-Implant InterfaceCell LineEscherichia coliMaterials TestingRabbitsRatsStaphylococcus aureusSurface PropertiesAcrylic ResinsAnti-Bacterial AgentsAntimicrobial Cationic Peptidespoly-N-isopropylacrylamideantimicrobial peptidesbiocompatibilityclick chemistryimplantstemperature responsive

Identifiers

PMID30360126
PMCPMC6453715
OpenAlexW2897364181

What OpenQuestion holds

Textmetadata
LicenceTDM
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.