Indocyanine Green and Curcumin Co-Loaded Nano-Fireball-Like Albumin Nanoparticles Based on Near-Infrared-Induced Hyperthermia for Tumor Ablation

被引:23
作者
Pham, Phuong Thi Thu [1 ]
Le, Xuan Thien [1 ]
Kim, Hanju [1 ]
Kim, Hwang Kyung [1 ]
Lee, Eun Seong [2 ]
Oh, Kyung Taek [3 ]
Choi, Han-Gon [4 ]
Youn, Yu Seok [1 ]
机构
[1] Sungkyunkwan Univ, Sch Pharm, Suwon 16419, Gyeonggi Do, South Korea
[2] Catholic Univ Korea, Div Biotechnol, Bucheon 14662, Gyeonggi Do, South Korea
[3] Chung Ang Univ, Coll Pharm, Seoul 06974, South Korea
[4] Hanyang Univ, Coll Pharm, Ansan 15588, Gyeonggi Do, South Korea
基金
新加坡国家研究基金会;
关键词
indocyanine green; curcumin; photothermal therapy; albumin nanoparticles; tumor targeting; PHOTOTHERMAL THERAPY; ANTITUMOR EFFICACY; ENDOTHELIAL-CELLS; CANCER-THERAPY; DRUG CARRIER; IRON-OXIDE; PROTEIN; SIZE; DOXORUBICIN; ACTIVATION;
D O I
10.2147/IJN.S262690
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Indocyanine green (ICG) has received considerable interest as a biocompatible organic photothermal agent, and curcumin (Cur) is considered an attractive natural chemopreventive and chemotherapeutic compound. However, the in vivo applicability of ICG and Cur is significantly restricted by their poor ability to target tumors and their extremely low solubility. Materials and Methods: To address these problems, ICG/Cur-loaded albumin nanoparticles (ICG-BSA-Cur-NPs) based on the nab (TM) (nanoparticle albumin-bound) technology were applied to neuroblastomas in vivo. Results: The fabricated ICG-BSA-Cur-NPs were found to be spherical, similar to 150 nm in size and highly dispersible and stable in aqueous solution. Approximately 80% of the incorporated ICG and Cur were gradually released from the NPs over 48 h. All formulations of ICG-BSA-Cur-NPs (5 similar to 20 mu g/mL) showed efficient hyperthermia profiles (up to 50-60 degrees C within 5 min) in response to 808-nm NIR laser irradiation in vitro and in vivo. Notably, ICG-BSA-Cur-NPs illuminated with 808-nm laser irradiation (1.5 W/cm(2)) showed excellent cytotoxicity toward N2a cells in vitro and undisputable antitumor efficacy in N2a-xenografted mice in vivo, compared to other tested sample groups (tumor volumes for PBS, BSA-Cur-NPs, free ICG, and ICG-BSA-Cur-NPs groups were 1408.6 +/- 551.9, 1190.6 +/- 343.6, 888.6 +/- 566.2, and 103.0 +/- 111.3 mm(3), respectively). Conclusion: We demonstrate that these hyperthermal chemotherapeutic ICG-BSA-Cur-NPs have potential as a future brain tumor treatment.
引用
收藏
页码:6469 / 6484
页数:16
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