College of Marine Life Science, Ocean University of China, 5# Yushan Road, Qingdao, 266003, PR China.
Colloids Surf B Biointerfaces. 2010 Jun 1;77(2):125-30. doi: 10.1016/j.colsurfb.2009.12.020. Epub 2010 Jan 11.
Self-assembled oleoyl-chitosan (OCH) nanoparticles based on chitosan with different molecular weights (5kDa, 38kDa and 300kDa) were prepared by oil/water (O/W) emulsification method. The nanoparticles have spherical shape and the mean diameters were 131.8nm, 255.3nm and 334.1nm, respectively. Doxorubicin hydrochloride (DOX) was efficiently loaded into OCH nanoparticles and shown to be sustained release in PBS. The loading efficiency and the DOX release rate increased as the molecular weight of chitosan decreased. The blank OCH nanoparticles showed no cytotoxicity to mouse embryo fibroblasts and human lung cancer cell line A549. The inhibitory rates of DOX-loaded OCH nanoparticle suspension to A549 cells significantly outperformed that of DOX solution, and decreased with the increase of molecular weight. These results revealed the promising potential of low molecular weight OCH nanoparticles as carriers for antitumor agents.
基于不同相对分子质量(5kDa、38kDa 和 300kDa)壳聚糖的油包水(O/W)乳化法制备了自组装油酰化壳聚糖(OCH)纳米粒。纳米粒呈球形,平均粒径分别为 131.8nm、255.3nm 和 334.1nm。盐酸阿霉素(DOX)能有效地被包载到 OCH 纳米粒中,并在 PBS 中呈现出持续释放。包载效率和 DOX 释放率随着壳聚糖相对分子质量的降低而增加。空白 OCH 纳米粒对小鼠胚胎成纤维细胞和人肺癌细胞系 A549 均无细胞毒性。载 DOX 的 OCH 纳米粒混悬液对 A549 细胞的抑制率明显优于 DOX 溶液,且随着相对分子质量的增加而降低。这些结果表明低相对分子质量 OCH 纳米粒作为抗肿瘤药物载体具有良好的应用前景。