Key Laboratory of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry and Materials Science, Northwest University, Xi'an, 710069, Shaanxi, People's Republic of China.
Colloids Surf B Biointerfaces. 2018 Dec 1;172:464-470. doi: 10.1016/j.colsurfb.2018.09.001. Epub 2018 Sep 3.
Drug delivery systems with high drug encapsulation efficiency and controlled release are of great importance in biomedical fields. Herein, we report an ingenious approach inspired from the lotus leaf possessing the ability of strong repellency to water, which enables the rapid fabrication of drug-loaded calcium alginate (Ca-Alg) particles with high drug encapsulation efficiency and controlled drug delivery. The design is achieved by introducing aqueous droplets containing the mixture of dilute sodium alginate solution, dilute calcium chloride solution, and drug onto the superhydrophobic substrate. Due to water evaporation both the concentration of sodium alginate and calcium chloride within the droplets will gradually increase, and the ionic crosslinking reaction of sodium alginate with Ca is further occurred to form the drug-embedded Ca-Alg hydrogel particles. The results indicate that the controllable fabrication of Ca-Alg particles can be easily achieved on the superhydrophobic surface, and the swelling behavior can be tuned by the pH of the buffer solution. Importantly, the drug encapsulation efficiencies are measured to be over 88% and the drug exhibits obvious pH responsive release. Findings from this study are expected to contribute to the rational design of drug delivery systems with high drug encapsulation efficiency and controlled release for pharmaceutic science and tissue engineering.
具有高药物包封效率和控制释放的药物传递系统在生物医学领域具有重要意义。本文受荷叶具有强斥水性的启发,报道了一种巧妙的方法,能够快速制备载药海藻酸钠(Ca-Alg)颗粒,具有高药物包封效率和控制药物释放。该设计是通过将含有海藻酸钠稀溶液、氯化钙稀溶液和药物的水相液滴引入超疏水基底上实现的。由于水的蒸发,液滴内的海藻酸钠和氯化钙的浓度将逐渐增加,并且海藻酸钠与 Ca 的离子交联反应进一步发生,形成包埋药物的 Ca-Alg 水凝胶颗粒。结果表明,可在超疏水表面上轻松实现 Ca-Alg 颗粒的可控制备,并且通过缓冲溶液的 pH 值可以调节溶胀行为。重要的是,药物包封效率超过 88%,并且药物表现出明显的 pH 响应释放。本研究的结果有望为药物传递系统的合理设计提供参考,这些系统具有高药物包封效率和控制释放,可用于药剂学和组织工程。