转铁蛋白
紫杉醇
生物相容性
纳米颗粒
药物输送
化学
体外
药品
部分
靶向给药
转铁蛋白受体
纳米技术
二硫键
生物物理学
组合化学
材料科学
药理学
生物化学
立体化学
医学
有机化学
癌症
内科学
生物
作者
Kaikai Wang,Ahu Yuan,Jiaqian Yu,Jinhui Wu,Yiqiao Hu
标识
DOI:10.1016/j.xphs.2015.12.007
摘要
Protein-based nanoparticles hold great promise in both preclinical and clinical practices due to their high biocompatibility and biodegradability. However, the complicated preparations often denature proteins, which subsequently diminish their bioactivity. To overcome these drawbacks, we developed a one-step self-assembling method for preparing protein-based nanoparticles. Transferrin (Tf), a targeting protein, was mixed with 2-mercaptoethanol to break disulfide bonds. Using this method, Tf-PTX-NPs (paclitaxel-loaded Tf nanoparticles) could be readily obtained. Tf-PTX-NPs were round and their diameter could be controlled in the range of 5-200 nm. The bioactivity of Tf to its receptor after forming nanoparticles was also confirmed in vitro. Tf-PTX-NPs also could inhibit the tumor growth to some extent in a mice tumor xenograft model. Therefore, using this self-assembling method, we fabricated this antitumor Tf-based nanoparticle, in which Tf acted as both the targeting moiety and drug carrier.
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