Carbon dot incorporated mesoporous silica nanoparticles for targeted cancer therapy and fluorescence imaging

被引:13
作者
Kajani, Abolghasem Abbasi [1 ]
Rafiee, Laleh [2 ]
Javanmard, Shaghayegh Haghjooy [2 ]
Dana, Nasim [2 ]
Jandaghian, Setareh [2 ]
机构
[1] Univ Isfahan, Fac Biol Sci & Technol, Dept Biotechnol, Esfahan 8174673441, Iran
[2] Isfahan Univ Med Sci, Cardiovasc Res Inst, Appl Physiol Res Ctr, Esfahan 8174673461, Iran
关键词
DRUG-DELIVERY; PH; CHITOSAN; APTAMER; CARRIERS;
D O I
10.1039/d3ra00768e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new and efficient theranostic nanoplatform was developed via a green approach for targeted cancer therapy and fluorescence imaging, without the use of any anticancer chemotherapeutic drugs. Toward this aim, monodisperse and spherical mesoporous silica nanoparticles (MSNs) of approximately 50 nm diameter were first synthesized using the sol-gel method and loaded with hydrothermally synthesized anticancer carbon dots (CDs). The resulting MSNs-CDs were then functionalized with chitosan and targeted by an anti-MUC1 aptamer, using the glutaraldehyde cross-linker, and fully characterized by TEM, FE-SEM, EDS, FTIR, TGA, XRD, and BET analysis. Potent and selective anticancer activity was obtained against MCF-7 and MDA-MB-231 cancer cells with the maximum cell mortalities of 66.2 +/- 1.97 and 71.8 +/- 3%, respectively, after 48 h exposure with 100 mu g mL(-1) of the functionalized MSNs-CDs. The maximum mortality of 40.66 +/- 1.3% of normal HUVEC cells was obtained under the same conditions. Based on the results of flowcytometry analysis, the apoptotic mediated cell death was recognized as the main anticancer mechanism of the MSNs-CDs. The fluorescence imaging of MCF-7 cancer cells was also studied after exposure with MSNs-CDs. The overall results indicated the high potential of the developed nanoplatform for targeted cancer theranostics.
引用
收藏
页码:9491 / 9500
页数:10
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