Tumor accumulation of neutron-activatable holmium-containing mesoporous silica nanoparticles in an orthotopic non-small cell lung cancer mouse model

被引:18
|
作者
Di Pasqua, Anthony J. [1 ]
Miller, Michael L. [2 ]
Lu, Xiuling [3 ]
Peng, Lei [1 ]
Jay, Michael [1 ]
机构
[1] Univ N Carolina, Eshelman Sch Pharm, Ctr Nanotechnol Drug Delivery, Div Mol Pharmaceut, Chapel Hill, NC 27599 USA
[2] Creighton Univ, Dept Chem, Omaha, NE 68178 USA
[3] Univ Connecticut, Sch Pharm, Dept Pharmaceut Sci, Storrs, CT 06269 USA
关键词
Holmium; Mesoporous silica MCM-41; Non-small cell lung cancer; Radiotherapeutic; Drug delivery; DRUG-DELIVERY; IMPROVE SURVIVAL; MICROSPHERES; CHEMOTHERAPY; THERAPY; GROWTH;
D O I
10.1016/j.ica.2012.06.016
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Mesoporous silica MCM-41 nanoparticles containing the stable isotope holmium-165 (Ho-165) were prepared by exposing the approximately 400 nm particles to an aqueous solution of Ho-165 acetylacetonate for 24 h at room temperature; the obtained solid was subsequently irradiated in a PULSTAR nuclear reactor (reactor power = 1 MW; thermal neutron flux of approximately 5.5 or 7.7 x 10(12) n/cm(2)s) to produce holmium-166-containing mesoporous silica (Ho-166-MCM-41) nanoparticles (20.8 +/- 1.9% w/w Ho-166). The Ho-166-MCM-41 nanoparticles were administered intravenously (i.v.) to orthotopic non-small cell lung cancer A549-luciferase tumor-bearing mice. After 24 h, 4.5 +/- 3.9% initial dose per gram (ID/g) of tissue was detected in tumors and after 1 week, this value increased to 58.8 +/- 34.7% ID/g. These results demonstrate that mesoporous silica MCM-41 nanoparticles can deliver significant amounts of a therapeutic radionuclide to tumors after i.v. injection. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:334 / 336
页数:3
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