Targeted Indocyanine-Green-Loaded Calcium Phosphosilicate Nanoparticles for In Vivo Photodynamic Therapy of Leukemia

被引:161
作者
Barth, Brian M. [1 ]
Altinoglu, Erhan I. [2 ]
Shanmugavelandy, Sriram S. [1 ]
Kaiser, James M. [1 ]
Crespo-Gonzalez, Daniza [3 ]
DiVittore, Nicole A. [1 ,4 ]
McGovern, Christopher [5 ]
Goff, Trevor M. [2 ]
Keasey, Nicole R. [4 ,5 ]
Adair, James H. [2 ]
Loughran, Thomas P., Jr. [4 ,5 ]
Claxton, David F. [4 ,5 ]
Kester, Mark [1 ,4 ]
机构
[1] Penn State Univ, Dept Pharmacol, Coll Med, Hershey, PA 17033 USA
[2] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
[3] Univ Puerto Rico, Dept Chem, Mayaguez, PR 00681 USA
[4] Penn State Univ, Coll Med, Penn State Hershey Canc Inst, Hershey, PA 17033 USA
[5] Penn State Univ, Coll Med, Dept Med, Hershey, PA 17033 USA
关键词
calcium phosphosilicate nanoparticles; photodynamic therapy; leukemia; leukemia stem cells; bioconjugation; PHOSPHATE NANOCOMPOSITE PARTICLES; BCR-ABL KINASE; STEM-CELLS; CANCER-CELLS; INTERNALIZATION; PROGENITORS; MECHANISMS; EXPRESSION; INDUCTION; PATHWAYS;
D O I
10.1021/nn2005766
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Leukemia is one of the most common and aggressive adult cancers, as well as the most prevalent childhood cancer. Leukemia is a cancer of the hematological system and can be divided into a diversity of unique malignancies based on the onset of the disease as well as the specific cell lineages involved. Cancer stem cells, including recently identified leukemia stem cells (LSCs), are hypothesized to be responsible for cancer development, relapse, and resistance to treatment, and new therapeutics targeting these cellular populations are urgently needed. Nontoxic and nonaggregating: calcium phosphosilicate nanoparticles (CPSNPs) encapsulating the near-infrared fluoroprobe indocyanine green (ICG) were recently developed for diagnostic imaging and drug delivery as well as for photodynamic therapy (PDT) of solid tumors. Prior studies revealed that specific targeting of CPSNPs allowed for enhanced accumulation within breast cancer tumors, via CD71 targeting, or pancreatic cancer tumors, via gastrin receptor targeting. In the present study, ICG-loaded CPSNPs were evaluated as photosensitizers for PDT of leukemia. Using a novel bioconjugation approach to specifically target CD117 or CD96, surface features enhanced on leukemia stem cells, in vitro ICG-CPSNP PDT of a marine leukemia cell line and human leukemia samples were dramatically improved. Furthermore, the in vivo efficacy of PDT was dramatically enhanced in a murine leukemia model by utilizing CD117-targeted ICG-CPSNPs, resulting in 29% disease-free survival. Altogether, this study demonstrates that leukemia-targeted ICG-loaded CPSNPs offer the promise to effectively treat relapsing and multidrug-resistant leukemia and to Improve the life of leukemia patients.
引用
收藏
页码:5325 / 5337
页数:13
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