Novel T7-Modified pH-Responsive Targeted Nanosystem for Co-Delivery of Docetaxel and Curcumin in the Treatment of Esophageal Cancer

被引:17
作者
Deng, Lian [1 ]
Zhu, Xiongjie [1 ]
Yu, Zhongjian [1 ]
Li, Ying [1 ]
Qin, Lingyu [1 ]
Liu, Zhile [1 ]
Feng, Longbao [2 ]
Guo, Rui [2 ]
Zheng, Yanfang [1 ]
机构
[1] Southern Med Univ, Dept Oncol, Zhujiang Hosp, Guangzhou 510282, Peoples R China
[2] Jinan Univ, Guangdong Prov Engn & Technol Res Ctr Drug Carrie, Key Lab Biomat Guangdong Higher Educ Inst, Dept Biomed Engn, Guangzhou 510632, Peoples R China
基金
中国国家自然科学基金;
关键词
nanocarrier; T7; peptide; pH-responsive; docetaxel; esophageal cancer; CELL LUNG-CANCER; DRUG-DELIVERY; BREAST-CANCER; PHASE-II; THERAPY; NANOPARTICLES; METASTASIS; CARCINOMA; CISPLATIN; MICELLES;
D O I
10.2147/IJN.S257312
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: Although single-drug chemotherapy is still an effective treatment for esophageal cancer, its long-term application is limited by severe side-effects, poor bioavailability, and drug-resistance. Increasing attention has been paid to nanomedicines because of their good biological safety, targeting capabilities, and high-efficiency loading of multiple drugs. Herein, we have developed a novel T7 peptide-modified pH-responsive targeting nano-system co-loaded with docetaxel and curcumin for the treatment of esophageal cancer. Methods: Firstly, CM-beta-CD-PEI-PEG-T7/DTX/CUR (T7-NP-DC) was synthesized by the double emulsion (W/O/W) method. The targeting capacity of the nanocarrier was then investigated by in vitro and in vivo assays using targeted (T7-NP) and non-targeted nanoparticles (NP). Furthermore, the anti-tumor efficacy of T7-NP-DC was studied using esophageal cancer cells (KYSE150 and KYSE510) and a KYSE150 xenograft tumor model. Results: T7-NP-DC was synthesized successfully and its diameter was determined to be about 100 nm by transmission electron microscopy and dynamic light scattering. T7-NP-DC with docetaxel and curcumin loading of 10% and 6.1%, respectively, had good colloidal stability and exhibited pH-responsive drug release. Good biosafety was observed, even when the concentration was as high as 800 mu g/mL. Significant enhancement of T7-NP uptake was observed 6 hours after intravenous injection compared with NP. In addition, the therapeutic efficacy of T7-NP-DC was better than NP-DC and docetaxel in terms of growth suppression in the KYSE150 esophageal cancer model. Conclusion: The findings demonstrated that T7-NP-DC is a promising, non-toxic, and controllable nanoparticle that is capable of simultaneous delivery of the chemotherapy drug, docetaxel, and the Chinese Medicine, curcumin, for treatment of esophageal cancer. This novel T7-modified targeting nanosystem releases loaded drugs when exposed to the acidic microenvironment of the tumor and exerts a synergistic anti-tumor effect. The data indicate that the nanomaterials can safely exert synergistic anti-tumor effects and provide an excellent therapeutic platform for combination therapy of esophageal cancer.
引用
收藏
页码:7745 / 7762
页数:18
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