On-demand preparation of calcium alginate microspheres via piezoelectric microfluidics

海藻酸钙 微球 微流控 按需 纳米技术 材料科学 压电 化学 化学工程 计算机科学 复合材料 工程类 冶金 多媒体
作者
Kai Li,Jianhua Sun,Shaopeng He,Xianxin Zhou,Hengyu Li,Yingxiang Liu
出处
期刊:Sensors and Actuators A-physical [Elsevier BV]
卷期号:347: 113925-113925 被引量:12
标识
DOI:10.1016/j.sna.2022.113925
摘要

Calcium alginate microspheres (CAMs) have attracted extensive attention as a novel drug carrier due to their cheapness, biodegradability, biocompatibility and nontoxicity. The existing preparation technologies of CAMs require complex process steps and involve multiple types of equipment, which are difficult to achieve the real-time and on-demand supply of microspheres in micro-reaction experiments. In this work, CAMs for prolonged drug release are prepared by the designed piezoelectric microfluidic devices using sodium alginate (NaAlg) and calcium chloride (CaCl 2 ). Specifically, the on-demand CAMs are synthesized timely by piezoelectric micro-jet followed by the transportation of piezoelectric micro-pump. Furthermore, various solution concentrations, main parameters of excitation signal and different nozzle diameters are evaluated in terms of size, morphology and drug release rate. The control method of CAMs’ size is obtained based on the multi-physics coupling analysis. Experimental results show that the doxorubicin hydrochloride loaded CAMs (DOX-CAMs) which can be prepared on demand, have excellent uniformity and dispersion, and the minimum average particle size is about 81.9 µm. The controlled drug release rate of DOX-CAMs reaches 83.2 % after 24 h. Moreover, the piezoelectric microfluidic devices and corresponding control methods may have potentials to be adapted for synthesizing other inorganic composite microspheres. • Piezoelectric microfluidics realize the timely supply of microspheres on demand. • The control strategy of microspheres was obtained by simulation analysis. • Preparation of high-quality microspheres with uniformity and dispersion. • Microspheres have excellent drug release performance.
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