Arya Neha, Chakraborty Syandan, Dube Nikhil, Katti Dhirendra S
Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur - 208016, India.
J Biomed Mater Res B Appl Biomater. 2009 Jan;88(1):17-31. doi: 10.1002/jbm.b.31085.
Electrospraying is a novel technique for the generation of micro/nanospheres for biomedical applications. Apart from being a high yield technique; electrospraying has an added advantage of not making use of an external dispersion/emulsion phase which often involves ingredients that are undesirable for biomedical applications. In this study, we report the use of electrospraying for the synthesis of chitosan micro/nanospheres. The focus was to optimize the fabrication parameters involved in electrospraying for reproducible synthesis of chitosan based micro/nanospheres and to study their potential as delivery vehicles for bioactive agents. The influence of the following was studied (i) electrospraying voltage, (ii) needle gauge, (iii) concentration of chitosan solution, (iv) concentration of acetic acid solution, and (v) electrospraying distance. SEM analysis demonstrated that microspheres of less than 1 mum were obtained when chitosan concentration was 2% dissolved in 90% acetic acid. The working distance and needle gauge that yielded favorable results were 7 cm and 26 g, respectively. Average particle size of ampicillin loaded chitosan micro/nanospheres was 520 nm with zeta potential of +28.2 mV and encapsulation efficiency of 80.4%. The particles were characterized for drug release kinetics and results demonstrated an initial burst release followed by a sustained release over a period of 120 h. Further, antibacterial activity of drug loaded micro/nanospheres demonstrated that the encapsulated drug was in its active form postexposure to high voltage during electrospraying. This study indicates that electrospraying is a facile technique for the synthesis of chitosan micro/nanospheres for drug delivery applications.
电喷雾是一种用于生物医学应用中制备微/纳米球的新技术。除了是一种高产技术外,电喷雾还有一个额外的优点,即不使用外部分散/乳液相,而这种相通常包含对生物医学应用不利的成分。在本研究中,我们报告了用电喷雾法合成壳聚糖微/纳米球。重点是优化电喷雾过程中涉及的制备参数,以可重复地合成基于壳聚糖的微/纳米球,并研究它们作为生物活性剂载体的潜力。研究了以下因素的影响:(i)电喷雾电压,(ii)针规,(iii)壳聚糖溶液浓度,(iv)乙酸溶液浓度,以及(v)电喷雾距离。扫描电子显微镜分析表明,当壳聚糖溶解于90%乙酸中的浓度为2%时,可获得直径小于1μm的微球。产生良好结果的工作距离和针规分别为7 cm和26 G。载有氨苄青霉素的壳聚糖微/纳米球的平均粒径为520 nm,ζ电位为+28.2 mV,包封率为80.4%。对这些颗粒进行了药物释放动力学表征,结果表明,最初有一个突释阶段,随后在120小时内持续释放。此外,载药微/纳米球的抗菌活性表明,在电喷雾过程中暴露于高压后,包封的药物仍保持其活性形式。本研究表明,电喷雾是一种用于药物递送应用的壳聚糖微/纳米球合成的简便技术。