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载多西紫杉醇的超小型纳米结构脂质载体用于癌症治疗:体外和体内评价。

Docetaxel-loaded ultrasmall nanostructured lipid carriers for cancer therapy: in vitro and in vivo evaluation.

机构信息

Department of Pharmacy, The First Affiliated Hospital of Zhengzhou University, No.1 Jianshe East Road, Erqi District, Zhengzhou, 450052, Henan, People's Republic of China.

Department of Emergency Surgery, The First Affiliated Hospital of Zhengzhou University, No.1 Jianshe East Road, Erqi District, Zhengzhou, 450052, Henan, People's Republic of China.

出版信息

Cancer Chemother Pharmacol. 2020 Apr;85(4):731-739. doi: 10.1007/s00280-020-04048-6. Epub 2020 Mar 7.

Abstract

Lack of cancer-targeted delivery of chemotherapeutics is one of the major obstacles for successful cancer therapy. Nanostructured lipid carriers (NLC) have shown great promise in drug-delivery applications since they are highly scalable, biodegradable nanocarriers with high-drug-loading capacity. However, traditional method prepared NLC, the diameter of which range from 80 to 200 nm, is easily blocked and trapped in perivascular regions without further penetration. As a result, ultrasmall NLC with size under 100 nm or lower range are reported to be ideally tumor targeting carrier as it allows for superior tumor accumulation and permeation. Moreover, surface modification of NLC with folic acid (FA) could significantly increase the drug-delivery efficiency through active targeting effect. In our study, an ultrasmall NLC with FA modification (FA-NLC) was prepared to load docetaxel (DTX) for cancer therapy. Our results showed that DTX-loaded FA-NLC comprised of homogeneous particles with size around 30 nm. In addition, it exhibited great colloidal stability, satisfactory drug-loading efficiency, and high biocompatibility in vitro. Meanwhile, in vivo studies indicated that ultrasmall FA-NLC exhibited greater tumor retention and enhanced antitumor effect compared with control.

摘要

化疗药物缺乏靶向递药是癌症治疗成功的主要障碍之一。由于具有高载药能力且高度可扩展、可生物降解的纳米载体,纳米结构脂质载体 (NLC) 在药物递送应用中显示出巨大的应用前景。然而,传统方法制备的 NLC 的直径范围为 80 至 200nm,很容易在血管周围区域被堵塞和捕获,而无法进一步渗透。因此,报道称尺寸小于 100nm 或更小范围的超小 NLC 是理想的肿瘤靶向载体,因为它允许更好的肿瘤积累和渗透。此外,用叶酸 (FA) 对 NLC 进行表面修饰可以通过主动靶向作用显著提高药物递送效率。在我们的研究中,制备了载有紫杉醇 (DTX) 的 FA 修饰的超小 NLC(FA-NLC)用于癌症治疗。结果表明,载有 DTX 的 FA-NLC 由粒径约为 30nm 的均匀颗粒组成。此外,它表现出良好的胶体稳定性、令人满意的载药效率和体外高生物相容性。同时,体内研究表明,与对照相比,超小 FA-NLC 具有更大的肿瘤保留和增强的抗肿瘤作用。

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