Doxorubicin-loaded PLGA microparticles with internal pores for long-acting release in pulmonary tumor inhalation treatment

被引:15
作者
Feng, Tian-shi [1 ,2 ,3 ,4 ]
Tian, Hua-yu [2 ]
Xu, Cai-na [2 ]
Lin, Lin [2 ]
Lam, Michael Hon-Wah [3 ,4 ]
Liang, Hao-jun [1 ,4 ]
Chen, Xue-si [2 ]
机构
[1] Univ Sci & Technol China, Dept Polymer Sci & Engn, CAS Key Lab Soft Matter Chem, Hefei 230026, Peoples R China
[2] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[3] City Univ Hong Kong, Dept Biol & Chem, Kowloon, Hong Kong, Peoples R China
[4] USTC City U, Adv Lab Environm Res & Technol ALERT, Joint Adv Res Ctr, Suzhou 215124, Peoples R China
基金
中国国家自然科学基金;
关键词
Doxorubicin; Poly(lactic-co-glycolic acid); Internal pores; Long-acting release; Pulmonary inhalation; DRY POWDER INHALATION; POROUS MICROSPHERES; IN-VITRO; DELIVERY; NANOPARTICLES; FORMULATION; PARTICLES; INHALERS; CARRIERS; GENE;
D O I
10.1007/s10118-015-1642-y
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Doxorubicin (DOX) loaded poly(lactic-co-glycolic acid) (PLGA) microparticles with internal pores (MP-D) were developed for long-acting release in pulmonary inhalation treatment. The PLGA microparticles exhibited favorable aerodynamic properties for pulmonary delivery. In vitro drug release profile suggested that MP-D have the advantage of long-term maintenance of drug concentrations. MTT assay demonstrated the in vitro anti-tumor efficiency of the DOX loaded PLGA microparticles. Furthermore, melanoma lung metastasis model was established to determine the in vivo antitumor efficiency. The mice treated with MP-D showed significantly fewer lesions than the untreated ones. The survival analysis indicated that MP-D prolonged the survival time of tumor-bearing mice. These results suggested that DOX loaded PLGA microparticles with internal pores have the potential to be used as long-acting release carriers in clinical lung cancer treatment.
引用
收藏
页码:947 / 954
页数:8
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