Calcium-silicate mesoporous nanoparticles loaded with chlorhexidine for both anti- Enterococcus faecalis and mineralization properties.
Calcium-silicate mesoporous nanoparticles loaded with chlorhexidine for both anti- Enterococcus faecalis and mineralization properties.
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负载洗必太的硅酸钙介孔纳米粒子,具有抗粪肠球菌和矿化特性
DOI:
10.1186/s12951-016-0224-7
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发表时间:
2016-10-21
影响因子:
10.2
通讯作者:
Fan B
中科院分区:
文献类型:
--
作者:
Fan W;Li Y;Sun Q;Ma T;Fan B
In infected periapical tissues, Enterococcus faecalis is one of the most common dominant bacteria. Chlorhexidine has been proved to show strong antibacterial ability against E. faecalis but is ineffective in promoting mineralization for tissues around root apex. Mesoporous calcium-silicate nanoparticles are newly synthesized biomaterials with excellent ability to promote mineralization and carry-release bioactive molecules in a controlled manner. In this study, mesoporous calcium-silicate nanoparticles were functionalized with chlorhexidine and their releasing profile, antibacterial ability, effect on cell proliferation and in vitro mineralization property were evaluated. The chlorhexidine was successfully incorporated into mesoporous calcium-silicate nanoparticles by a mixing-coupling method. The new material could release chlorhexidine as well as Ca2+ and SiO3 2− in a sustained manner with an alkaline pH value under different conditions. The antimicrobial ability against planktonic E. faecalis was dramatically improved after chlorhexidine incorporation. The nanoparticles with chlorhexidine showed no negative effect on cell proliferation with low concentrations. On dentin slices, the new synthesized material demonstrated a similar inhibitory effect on E. faecalis as the chlorhexidine. After being immersed in SBF for 9 days, numerous apatite crystals could be observed on surfaces of the material tablets. Mesoporous calcium-silicate nanoparticles loaded with chlorhexidine exhibited release of ions and chlorhexidine, low cytotoxicity, excellent antibacterial ability and in vitro mineralization. This material could be developed into a new effective intra-canal medication in dentistry or a new bone defect filling material for infected bone defects.
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影响因子:
5
作者:
Carrilho, Marcela R.;Carvalho, Ricardo M.;Sousa, Ethan N.;Nicolau, Jose;Breschi, Lorenzo;Mazzoni, Annalisa;Tjaderhane, Leo;Tay, Franklin R.;Agee, Kelli;Pashley, David H.
通讯作者:
Pashley, David H.
影响因子:
3.2
作者:
Giannelli, M.;Chellini, F.;Tani, A.
通讯作者:
Tani, A.
影响因子:
4.2
作者:
Distel, JW;Hatton, JF;Gillespie, MJ
通讯作者:
Gillespie, MJ
影响因子:
14.9
作者:
Maria Ferrer-Luque, Carmen;Teresa Arias-Moliz, Maria;Ruiz-Linares, Matilde;Martinez Garcia, Maria Elena;Baca, Pilar
通讯作者:
Baca, Pilar
影响因子:
1.9
作者:
Ceci, Monica;Delpech, Gaston;Baldaccini, Beatriz
通讯作者:
Baldaccini, Beatriz