Tian Jiafeng, Xu Rong, Wang Haozheng, Guan Ying, Zhang Yongjun
Key Laboratory of Functional Polymer Materials and State Key Laboratory of Medicinal Chemical Biology, Institute of Polymer Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Key Laboratory of Functional Polymer Materials and State Key Laboratory of Medicinal Chemical Biology, Institute of Polymer Chemistry, College of Chemistry, Nankai University, Tianjin 300071, China.
Mater Sci Eng C Mater Biol Appl. 2020 Nov;116:111244. doi: 10.1016/j.msec.2020.111244. Epub 2020 Jun 29.
Unlike conventional drug carriers, time-controlled release systems do not release drug immediately, but start to release drug after a predetermined lag time. Coating a drug-loaded core with an erodible barrier is a valid way to defer drug release, however, the complicated erosion behavior of the erodible coatings makes it difficult to predict and tune the lag time. Herein we proposed that dynamic layer-by-layer films, using hydrogen-bonded poly(ethylene glycol)/tannic acid (PEG/TA) film as an example, are ideal erodible coatings, because their erosion mechanism is clear and simple, and they disintegrate at constant rate. As a proof, we demonstrated that the release of bovine serum albumin (BSA) from BMS spheres can be deferred by PEG/TA coating. More importantly, the lag time can be simply tuned by the thickness of the coating. By mixing bimodal mesoporous silica (BMS) spheres coated with different thickness PEG/TA films, multiple pulse release was achieved. Similar release patterns were also successfully achieved in vivo.
与传统药物载体不同,时间控制释放系统不会立即释放药物,而是在预定的滞后时间后开始释放药物。用可蚀屏障包裹载药核心是延迟药物释放的有效方法,然而,可蚀涂层复杂的侵蚀行为使得难以预测和调整滞后时间。在此,我们提出以氢键结合的聚乙二醇/单宁酸(PEG/TA)薄膜为例的动态层层薄膜是理想的可蚀涂层,因为它们的侵蚀机制清晰简单,且以恒定速率分解。作为例证,我们证明了PEG/TA涂层可延迟牛血清白蛋白(BSA)从BMS微球中的释放。更重要的是,滞后时间可通过涂层厚度简单调整。通过混合涂覆有不同厚度PEG/TA薄膜的双峰介孔二氧化硅(BMS)微球,实现了多次脉冲释放。在体内也成功实现了类似的释放模式。