Targeted hot ion therapy of infected wound by glycol chitosan and polydopamine grafted Cu-SiO2 nanoparticles
Source abstract
Abstract
Abstract Quick and effective elimination of drug-resistant bacteria and simultaneous repairing the infectious tissue remain challenging in clinics. In this study, multifunctional glycol chitosan and polydopamine coated copper-doped mesoporous silica (MCS@PDA@GCS) nanoparticles with near-infrared (NIR) photothermal conversion ability and bacteria-targeting property are prepared. When infection occurred, the environment becomes acidic, and MCS@PDA@GCS nanoparticles with pH-sensitive could be accumulated on the surface of the bacteria. The NIR light-induced heating and Cu ions released from MCS@PDA@GCS nanoparticles created a distinct “hot ions effect”, showing high-efficiency, quick and long-term inhibition of bacteria (methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli)) as well as biofilm. In addition, the MCS@PDA@GCS nanoparticles with “mild hot ions effect” could induce macrophages polarization into a pro-inflammatory M1 phenotype, resulting in the clearance of infection through the immune-antibacterial effect. Moreover, the “mild hot ions effect” endows MCS@PDA@GCS nanoparticles with remarkable bioactivity, which stimulates the migration and angiogenesis of endothelial cells. The in vivo results confirmed that MCS@PDA@GCS nanoparticles with laser irradiation could efficiently remove bacteria and significantly promote wounds closure, epithelization and angiogenesis during infectious wound healing process.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Wound Healing and Treatments · Bone Tissue Engineering Materials · Nanoplatforms for cancer theranostics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (48)
Show source-provided references
1. Berrios-Torres · JAMA Surg. · 2017 · 152 · 78410.1001/jamasurg.2017.0904 ↗
2. Xin · Nat. Commun. · 2018 · 9 · 278410.1038/s41467-018-04998-9 ↗
3. Zimmerli · N. Engl. J. Med. · 2004 · 351 · 164510.1056/NEJMra040181 ↗
4. Levin-Reisman · Science · 2017 · 355 · 82610.1126/science.aaj2191 ↗
5. Jin · Chem. Eng. J. · 2019 · 362 · 54810.1016/j.cej.2019.01.028 ↗
6. Yuqing · ACS Nano · 2021 · 15 · 707810.1021/acsnano.1c00204 ↗
7. Bauer · Sci. Rep. · 2019 · 9 · 1121510.1038/s41598-019-47315-0 ↗
8. Pang · Adv. Mater. · 2019 · 31
9. Fischbach · Curr. Opin. Microbiol. · 2011 · 14 · 51910.1016/j.mib.2011.08.003 ↗
10. Xu · ACS Appl. Mater. Interfaces · 2020 · 12 · 3125510.1021/acsami.0c08890 ↗
11. Yang · ACS Appl. Mater. Interfaces · 2018 · 10 · 1429910.1021/acsami.7b15678 ↗
12. Anuforom · Med. Microbiol. Immunol. · 2015 · 204 · 15110.1007/s00430-014-0355-0 ↗
13. Yang · Nanoscale · 2019 · 11 · 1769910.1039/C9NR05730G ↗
14. Liu · Biomaterials · 2019 · 208 · 810.1016/j.biomaterials.2019.04.008 ↗
15. Huang · Acta Biomater. · 2019 · 100 · 41510.1016/j.actbio.2019.09.030 ↗
16. Guo · Appl. Mater. Today · 2021 · 22
17. Li · Adv. Sci. · 2018 · 5 · 170080510.1002/advs.201700805 ↗
18. Yang · Chem. Eng. J. · 2021 · 419
19. Sheng · Biomaterials · 2021 · 26410.1016/j.biomaterials.2020.120414 ↗
20. Lyu · Chem. Eng. J. · 2015 · 274 · 29810.1016/j.cej.2015.03.137 ↗
21. Schneider · Arch. Dermatol. Res. · 2007 · 298 · 41310.1007/s00403-006-0713-x ↗
22. Qin · J. Semicond. · 2019 · 4010.1088/1674-4926/40/11/111607 ↗
23. Guo · ACS Nano · 2020 · 14 · 1339110.1021/acsnano.0c05255 ↗
24. Wan Ngah · React. Funct. Polym. · 2002 · 50 · 18110.1016/S1381-5148(01)00113-4 ↗
25. Zhang · Nanoscale · 2019 · 11 · 631510.1039/C8NR09818B ↗
26. Xi · ACS Nano · 2018 · 12 · 1077210.1021/acsnano.8b01152 ↗
27. Xin · Adv. Funct. Mater. · 2020 · 30 · 191074810.1002/adfm.201910748 ↗
28. Rodriguez de Evgrafov · Mol. Biol. Evol. · 2015 · 32 · 117510.1093/molbev/msv006 ↗
29. Yuan · ACS Nano · 2020 · 14 · 354610.1021/acsnano.9b09871 ↗
30. Zeng · Bioact. Mater. · 2021 · 6 · 2647
31. Korupalli · Biomaterials · 2017 · 116 · 110.1016/j.biomaterials.2016.11.045 ↗
32. Qian · Acta Biomater. · 2018 · 69 · 25610.1016/j.actbio.2018.01.022 ↗
33. Rauf · Dalton Trans. · 2019 · 48 · 1781010.1039/C9DT03649K ↗
34. Ning · Chem. Res. Toxicol. · 2015 · 28 · 181510.1021/acs.chemrestox.5b00258 ↗
35. Hu · ACS Nano · 2017 · 11 · 933010.1021/acsnano.7b04731 ↗
36. Li · Adv. Mater. · 2021 · 33
37. Locke Davenport · Adv. Funct. Mater. · 2020 · 190933110.1002/adfm.201909331 ↗
38. Chen · Adv. Funct. Mater. · 2021 · 31 · 210137210.1002/adfm.202101372 ↗
39. Bischof · Biophys. J. · 1995 · 68 · 260810.1016/S0006-3495(95)80445-5 ↗
40. Yuna · Chem. Eng. J. · 2021 · 417
41. Yongping · Small · 2019 · 1900046
42. He · Chem. Eng. J. · 2020 · 394
43. Meng · Chem. Mater. · 2020 · 9937
44. Yu · ACS Nano · 2018 · 12
45. Tian · RSC Adv. · 2016 · 6 · 4584010.1039/C6RA08145B ↗
46. He · Appl. Mater. Today · 2018 · 12 · 41510.1016/j.apmt.2018.07.006 ↗
47. Yang · Small · 2020 · 16 · 200151810.1002/smll.202001518 ↗
48. Liu · Biomaterials · 2019 · 208 · 2110.1016/j.biomaterials.2019.04.007 ↗