Stem Cell-Based Delivery of Gold/Chlorin e6 Nanocomplexes for Combined Photothermal and Photodynamic Therapy

被引:37
作者
Chuang, Chun-Chiao [1 ]
Chen, Yi-Ning [1 ]
Wang, Yi-Ya [1 ]
Huang, Yu-Chen [1 ]
Lin, Ssu-Yu [1 ]
Huang, Rih-Yang [1 ]
Jang, Yu-Yun [1 ]
Yang, Chun-Chi [1 ]
Huang, Yu-Fen [2 ]
Chang, Chien-Wen [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Biomed Engn & Environm Sci, Hsinchu 30013, Taiwan
[2] Natl Tsing Hua Univ, Inst Analyt & Environm Sci, Hsinchu 30013, Taiwan
关键词
stem cells; drug delivery; photothermal therapy; photodynamic therapy; tumor penetration; SEED-MEDIATED SYNTHESIS; GOLD NANORODS; GROWTH-FACTOR; NANOPARTICLES; MIGRATION; RELEASE;
D O I
10.1021/acsami.0c03446
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Combining photothermal and photodynamic modalities has shown encouraging therapeutic efficacy against various malignant cancers. Developing a delivery method for targeting and penetrating tumors is still a major focus for advancing this therapeutic approach. Herein, we report a novel strategy involving the utilization of stem cells as a live carrier to codeliver photothermal and photodynamic agents for cancer therapy. To this end, a novel gold nanorod (AuNR)-PEG-PEI (APP)/chlorin e6 (Ce6)-loaded adipose-derived stem cell (ADSC) system is proposed in which AuNRs and Ce6 act as the photothermal and photodynamic agents, respectively. To integrate with stem cells, the APP/Ce6 nanocomplexes exhibit advantages of low drug leakage, low cytotoxicity, efficient cellular uptake, and redox- responsive release. After loading of APP/Ce6 nanocomplexes, the ADSCs still maintained good tumor tropism and were capable of penetrating into the tumor spheroids. The photothermal effect induced by exposure to near-infrared light irradiation at 808 nm promoted the release of Ce6 from the stem cells into the surroundings and hence increased its availability to treat cancer cells. APP/Ce6-loaded ADSCs exerted effective dose-dependent in vitro anticancer activities via anticipated photothermal and photodynamic effects. In a murine CT26 colon cancer model, APP/Ce6 delivered by ADSCs resulted in superior tumor suppression compared to other delivery strategies. It was also noted that in vivo applications of APP/Ce6-loaded ADSCs did not induce noticeable detrimental effects on normal tissues/organs.
引用
收藏
页码:30021 / 30030
页数:10
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