journal article·2018-10-24

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, Chuanbin Mao, Li Ren, Yingjun Wang

ACS Applied Materials & Interfaces· Volume 10· Issue 42
Publisher page

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.
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Research context

OpenAlex topics: Antimicrobial Peptides and Activities · Antimicrobial agents and applications · Polydiacetylene-based materials and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China

National Engineering Research Center for Tissue Restoration and Reconstruction, Guangzhou 510006, China

Department of Chemistry and Biochemistry, Stephenson Life Sciences Research Center, Institute for Biomedical Engineering, Science and Technology, University of Oklahoma, Norman, Oklahoma 73019, United States

Funding

National Cancer Institute · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Guangzhou Municipality · Pearl River S and T Nova Program of Guangzhou

References (34)

Show source-provided references
1. 10.1021/acsami.5b0226210.1021/acsami.5b02262 ↗
2. 10.1056/nejmra03541510.1056/nejmra035415 ↗
3. 10.1021/es102538210.1021/es1025382 ↗
4. 10.1038/nm114510.1038/nm1145 ↗
5. 10.1039/c3cc47922f10.1039/c3cc47922f ↗
6. 10.1002/adfm.20150324810.1002/adfm.201503248 ↗
7. 10.1002/ange.20150714010.1002/ange.201507140 ↗
8. 10.1002/anie.20170607110.1002/anie.201706071 ↗
9. 10.1016/j.actbio.2013.08.04310.1016/j.actbio.2013.08.043 ↗
10. 10.1039/c5cc04010h10.1039/c5cc04010h ↗
11. 10.1039/c3cc47922f10.1039/c3cc47922f ↗
12. 10.1016/j.actbio.2016.01.03510.1016/j.actbio.2016.01.035 ↗
13. 10.1039/c4tb01318b10.1039/c4tb01318b ↗
14. 10.1016/j.biomaterials.2010.07.06210.1016/j.biomaterials.2010.07.062 ↗
15. 10.1016/j.biomaterials.2014.04.05410.1016/j.biomaterials.2014.04.054 ↗
16. 10.1016/j.biomaterials.2013.08.08010.1016/j.biomaterials.2013.08.080 ↗
17. 10.1038/nmat410610.1038/nmat4106 ↗
18. 10.1038/nmat410610.1038/nmat4106 ↗
19. 10.1002/adma.20150157810.1002/adma.201501578 ↗
20. 10.1002/adma.20150157810.1002/adma.201501578 ↗
21. 10.1039/c5nr05844a10.1039/c5nr05844a ↗
22. 10.1039/c7tb02557b10.1039/c7tb02557b ↗
23. 10.1016/j.biomaterials.2013.04.03610.1016/j.biomaterials.2013.04.036 ↗
24. 10.1002/anie.20160563010.1002/anie.201605630 ↗
25. 10.1002/adma.20150213310.1002/adma.201502133 ↗
26. 10.1021/ma100726z10.1021/ma100726z ↗
27. 10.1016/j.biotechadv.2010.08.01210.1016/j.biotechadv.2010.08.012 ↗
28. 10.1038/nrd359110.1038/nrd3591 ↗
29. 10.1002/adfm.20100073010.1002/adfm.201000730 ↗
30. 10.1016/j.biomaterials.2015.06.04010.1016/j.biomaterials.2015.06.040 ↗
31. 10.1016/j.biomaterials.2014.07.04010.1016/j.biomaterials.2014.07.040 ↗
32. 10.1021/am502591c10.1021/am502591c ↗
33. 10.1021/acsami.5b0226210.1021/acsami.5b02262 ↗
34. 10.1021/acsnano.6b0386210.1021/acsnano.6b03862 ↗