Long circulating 10-hydroxycamptothecin-loaded nanoparticles fabricated from poly(ethylene glycol)/poly(L-lactic acid) multiblock copolymers

被引:0
|
作者
Wang, Yuexia [1 ,2 ]
Tan, Yebang [1 ]
机构
[1] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Peoples R China
[2] Qilu Univ Technol, Sch Chem & Pharmaceut Engn, Jinan, Peoples R China
来源
JOURNAL OF MACROMOLECULAR SCIENCE PART A-PURE AND APPLIED CHEMISTRY | 2016年 / 53卷 / 12期
关键词
Nanoparticles; 10-Hydroxycamptothecin; multiblock copolymer; cytotoxicity; circulation time; DRUG-RELEASE; LOADED NANOPARTICLES; TRIBLOCK COPOLYMER; MIXED MICELLES; BIODISTRIBUTION; PHARMACOKINETICS; CAMPTOTHECIN; DELIVERY; FORM;
D O I
10.1080/10601325.2016.1237816
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of poly(ethylene glycol) (PEG)/poly(L-lactic acid) (PLLA) multiblock copolymers were facilely synthesized using triphosgene as coupling agent. With the resulting multiblock copolymers, 10-hydroxycamptothecin (HCPT)-loaded nanoparticles were successfully prepared by dialysis method. The results obtained from dynamic light scattering (DLS) measurements confirmed that HCPT-loaded nanoparticles had the size of less than 200nm and the average diameter decreased with increasing PLLA content. TEM images demonstrated that most of the drug-loaded nanoparticles had a distinct spherical shape and smooth surface without any aggregation. Atomic force microscopy (AFM) images further indicated that the nanoparticles were in spherical shape with smooth surface, no drug crystal was visualized on their surface. To investigate the drug state in HCPT-loaded nanoparticles, differential scanning calorimetry (DSC) and X-ray powder diffraction (XRD) measurements were carried out. The results from these tests suggested that HCPT was molecularly dispersed in the amorphous polymer matrix. Drug loading content and in vitro drug release behavior of HCPT-loaded nanoparticles showed dependence on polymer composition. Cytotoxicity test indicated that HCPT-loaded nanoparticles exhibited greatly superior cytotoxicity compared to free HCPT due to its molecular dispersion in the polymer matrix. Furthermore, the nanoparticles significantly increased the duration of the drug in circulation. All these results demonstrated that PEG/PLLA nanoparticles have great potential as promising delivery system for poorly soluble antitumor drugs.
引用
收藏
页码:773 / 780
页数:8
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