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透明质酸修饰的紫杉醇簇作为选择性肿瘤靶向的纳米载体。

Paclitaxel-clusters coated with hyaluronan as selective tumor-targeted nanovectors.

机构信息

Department of Biochemistry and Molecular Biology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.

出版信息

Biomaterials. 2010 Sep;31(27):7106-14. doi: 10.1016/j.biomaterials.2010.05.067. Epub 2010 Jun 17.

Abstract

Paclitaxel (PTX) is a widely used anti-tumor agent in the treatment of solid tumors. Lack of selective strategies to target PTX into tumor cells together with poor solubility necessitating detergent, are severe clinical limitations. To address these hurdles, we devised a strategy that utilized PTX insolubility, mixing it with lipids that self-assemble into nanoparticle-like clusters. These clusters were then coated with hyaluronan, a glycosaminoglycan (GAG), and termed PTX-GAGs. These particles, delivered PTX selectively into tumor cells in a CD44-dependent manner. Injected systemically to mice bearing solid tumors, the PTX-GAGs showed high safety profile and tumor accumulation. Tumor progression was exponential upon treatment with free PTX or PTX in albumin nanoparticles (the FDA-approved Taxol and Abraxane, respectively). Under the same conditions, PTX-GAGs induced tumor arrest and were as potent as a 4-fold higher Taxol dose. Our findings suggest GAGs merit further investigation as vehicles for taxanes, and may be applicable as carriers in other therapeutic settings.

摘要

紫杉醇(PTX)是一种广泛应用于治疗实体瘤的抗肿瘤药物。缺乏将 PTX 靶向递送至肿瘤细胞的选择性策略,加上较差的溶解性需要使用去污剂,这些都是严重的临床限制。为了解决这些难题,我们设计了一种策略,利用 PTX 的不溶性,将其与脂质混合,脂质会自组装成类似纳米颗粒的聚集体。这些聚集体然后用透明质酸(一种糖胺聚糖,GAG)进行涂层,称为 PTX-GAGs。这些颗粒以 CD44 依赖的方式将 PTX 选择性递送至肿瘤细胞。将其系统地注射到患有实体瘤的小鼠体内,PTX-GAGs 表现出高安全性和肿瘤积累。在用游离 PTX 或白蛋白纳米粒中的 PTX(分别为 FDA 批准的 Taxol 和 Abraxane)治疗时,肿瘤进展呈指数增长。在相同条件下,PTX-GAGs 诱导肿瘤停滞,与高 4 倍的 Taxol 剂量一样有效。我们的研究结果表明,GAGs 值得进一步研究作为紫杉烷的载体,并且可能适用于其他治疗环境中的载体。

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