Biodegradable Alginate-Chitosan Hollow Nanospheres for Codelivery of Doxorubicin and Paclitaxel for the Effect of Human Lung Cancer A549 Cells

被引:30
|
作者
Tao, Liu [1 ]
Jiang, Jie [2 ]
Gao, Yu [3 ]
Wu, Chao [2 ]
Liu, Ying [2 ]
机构
[1] Jinzhou Med Univ, Nursing Coll, 40 Songpo Rd, Jinzhou 121000, Liaoning, Peoples R China
[2] Jinzhou Med Univ, Pharmacy Sch, 40 Songpo Rd, Jinzhou 121000, Liaoning, Peoples R China
[3] Jinzhou Med Univ, Affiliated Hosp 1, Dept Med Oncol, 40 Songpo Rd, Jinzhou 121001, Liaoning, Peoples R China
基金
中国国家自然科学基金;
关键词
SYNERGISTIC CO-DELIVERY; SILICA NANOSPHERES; TARGETED DELIVERY; NANOPARTICLES; DRUG; APOPTOSIS; RELEASE; MICROCAPSULES; MICROSPHERES; COPOLYMER;
D O I
10.1155/2018/4607945
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A biodegradable alginate coated chitosan hollow nanosphere (ACHN) was prepared by a hard template method and used for codelivery of doxorubicin (DOX) and paclitaxel (PTX) to investigate the effect on human lung cancer A549 cells. PTX was loaded into the nanometer hollow structure of ACHN through adsorption method. DOX was coated on surface of ACHN through electrostatic interaction. Drug release studies exhibited a sustained-release effect. According to X-ray diffraction patterns (XRD), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FT-IR) analysis, DOX structure in the loading samples (DOX-PTX-ACHN) was of amorphous state while PTX was microcrystalline. Cytotoxicity experiments showed ACHN was nontoxic as carrier material and the combination of DOX and PTX in DOX-PTX-ACHN exhibited a good inhibiting effect on cell proliferation. Cell uptake experiments demonstrated that DOX-PTX-ACHN accumulated in the cytoplasm. Degradation experiments illustrated that ACHN was a biodegradable material. In summary, these results clearly indicate that ACHN can be utilized as a potential biomaterial to transport multiple drugs to be used in combination therapy.
引用
收藏
页数:11
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