Dual drug delivery and sequential release by amphiphilic Janus nanoparticles for liver cancer theranostics

被引:112
作者
Zhang, Lingyu [1 ]
Zhang, Manjie [1 ]
Zhou, Li [2 ]
Han, Qinghe [3 ]
Chen, Xiangjun [1 ]
Li, Shengnan [1 ]
Li, Lu [1 ]
Su, Zhongmin [1 ]
Wang, Chungang [1 ]
机构
[1] Northeast Normal Univ, Dept Chem, 5268 Renmin St, Changchun 130024, Jilin, Peoples R China
[2] UPMC Univ Paris 06, PSL Res Univ, CNRS, Ecole Normale Super,Dept Chem, F-75005 Paris, France
[3] Jilin Univ, Hosp 2, Radiol, Changchun 130022, Jilin, Peoples R China
基金
中国博士后科学基金;
关键词
Amphiphilic Janus nanoparticles; Dual drug delivery; Optional sequential release; Bimodal imaging; Synergistic therapy; MESOPOROUS SILICA NANOPARTICLES; GOLD NANOCAGES; FACILE SYNTHESIS; CO-DELIVERY; DOXORUBICIN; PH; PACLITAXEL; THERAPY; SYSTEM; NANOCARRIERS;
D O I
10.1016/j.biomaterials.2018.07.060
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Co-delivery of two drugs with diverse physicochemical properties and specific administration order for cancer theranostics are vitally important for drug resistance conquering and side effects reducing. Consequently, we explored a unique amphiphilic PCL-AuNC/Fe(OH)(3)-PAA Janus nanoparticle (JNP) to simultaneously preserve the hydrophilic drug (doxorubicin) and hydrophobic drug (docetaxel) in their distinct domains. Owing to their extraordinary heterostructure and independent pH and NIR sensitive properties, the optional sequential drug release by a single inorganic JNP was realized for the first time, and the results presented the synchronous release of two drugs had 5% better therapeutic effect. In addition, the excellent computed X-ray tomography/magnetic resonance (CT/MR) imaging capabilities from AuNC and Fe(OH)(3) suggested our JNPs could effectively guide the cancer therapy. Furthermore, the mice treated with dual drug loaded PCL-AuNC/Fe(OH)(3)-PAA JNPs under near infrared (NIR) laser irradiation showed better tumor inhibition than solo drug, cocktail and dual drug treated groups, indicating the effectivity and significance of combined cancer therapy.
引用
收藏
页码:113 / 125
页数:13
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