School of Materials Science and Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Shanghai Flowridge Material Technology Co., LTD, Shanghai, 201318, China.
Carbohydr Res. 2024 Sep;543:109206. doi: 10.1016/j.carres.2024.109206. Epub 2024 Jul 9.
The objective of this study is to develop a drug carrier to overcome the inherent drawbacks of 5-Fluorouracil (5-Fu), including low bioavailability, short half-life, and systemic toxicity. In the present work, mesoporous silica nanoparticles (MSNs) capped by chitosan (CS) to encapsulate 5-Fu (5-Fu MSNs/CS) were fabricated by the sol-gel process, ultrasonic impregnation, and emulsion cross-linking. The 5-Fu MSNs/CS microspheres exhibit pH-responsive drug release and remarkable drug encapsulation capacity, as well as perfect sphericity, high specific surface area (680.62 cm/g), and uniform particle size (2.64 ± 0.05 μm). The drug-loading content and encapsulation efficiency are 14.12 ± 0.53 % and 82.21 ± 2.13 %, respectively. The cumulative release of 5-Fu from MSNs/CS microspheres is fast and sustained at pH 5.0 (89.56 ± 0.97 %) compared to that at pH 7.4 (57.88 ± 0.91 %) in 96 h, and it is Fickian diffusion controlled. In conclusion, the MSNs/CS microspheres prepared in this study could be potential carriers for 5-Fu delivery.
本研究旨在开发一种药物载体,以克服 5-氟尿嘧啶(5-Fu)的固有缺陷,包括生物利用度低、半衰期短和全身毒性。在本工作中,通过溶胶-凝胶法、超声浸渍和乳液交联制备了壳聚糖(CS)封端的介孔硅纳米粒子(MSNs)包裹 5-Fu(5-Fu MSNs/CS)。5-Fu MSNs/CS 微球具有 pH 响应性药物释放和显著的药物包封能力,以及完美的球形、高比表面积(680.62 cm/g)和均匀的粒径(2.64 ± 0.05 μm)。载药量和包封效率分别为 14.12 ± 0.53%和 82.21 ± 2.13%。与 pH 7.4(57.88 ± 0.91%)相比,在 96 小时内,MSNs/CS 微球在 pH 5.0 时的 5-Fu 累积释放速度更快且持续(89.56 ± 0.97%),且为菲克扩散控制。总之,本研究制备的 MSNs/CS 微球可能是 5-Fu 传递的潜在载体。