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Co-delivery of paclitaxel and doxorubicin using polypeptide-engineered nanogels for combination therapy of tumor
被引:8
|作者:
Yang, Jie
[1
]
Jin, Rui-Mei
[2
]
Wang, Shen-Yan
[3
,4
]
Xie, Xiao-Ting
[1
]
Hu, Wei
[3
,4
]
Tang, Hong-Feng
[3
,4
]
Liu, Bo
[1
]
机构:
[1] Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Britton Chance Ctr Biomed Photon,Hubei Bioinforma, Dept Biomed Engn,Wuhan Natl Lab Optoelect, Wuhan 430074, Hubei, Peoples R China
[2] Zhengzhou Univ, Sch Life Sci, 100 Sci Rd, Zhengzhou 450001, Peoples R China
[3] Wuhan Donghu Univ, Coll Nursing & Hlth Management, Innovat Inst Biomed Mat, Wuhan 430212, Hubei, Peoples R China
[4] Wuhan Donghu Univ, Coll Life Sci & Chem, Wuhan 430212, Peoples R China
基金:
中国国家自然科学基金;
关键词:
co-delivery;
engineered polypeptide;
nanogel;
chemotherapy;
synergistic therapy;
CANCER;
D O I:
10.1088/1361-6528/ac46b4
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Loading of chemotherapeutic agents into nanoparticles has been demonstrated to be an effective strategy for cancer therapy. However, simultaneous delivery of different functional drugs to tumor sites for chemotherapy still remains challenging. In this study, nanogels formed by an engineered coiled-coil polypeptide PC(10)A were designed and prepared as a carrier for co-delivery of paclitaxel (PTX) and doxorubicin (DOX) through ultrasonic treatment and electrostatic adsorption. The drug loading content and encapsulation efficiency of PTX and DOX in the PC(10)A/PTX/DOX nanogels were 5.98 wt%, 70 wt%, and 8.55 wt%, 83 wt%, respectively. Because the polypeptide PC(10)A was non-toxic and biodegradable, the PC(10)A/PTX/DOX nanogels exhibited good biocompatibility. The in vitro and in vivo antitumor experiments showed that the PC(10)A/PTX/DOX nanogels possessed obviously synergistic therapy effect of tumors and lower side effects compared with free PTX/DOX. Therefore, the PC(10)A/PTX/DOX nanogels are promising to provide a new strategy for combination therapy of different functional drugs.
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页数:10
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