首页> 外文OA文献 >Preparation of hydrocortisone nanosuspension through a bottom-up nanoprecipitation technique using microfluidic reactors
【2h】

Preparation of hydrocortisone nanosuspension through a bottom-up nanoprecipitation technique using microfluidic reactors

机译:使用微流控反应器通过自下而上的纳米沉淀技术制备氢化可的松纳米悬浮液

摘要

In this work, the possibility of bottom-up creation of a relatively stable aqueous hydrocortisone nanosuspension using microfluidic reactors was examined. The first part of the work involved a study of the parameters of the microfluidic precipitation process that affect the size of generated drug particles. These parameters included flow rates of drug solution and antisolvent, microfluidic channel diameters, microreactors inlet angles and drug concentrations. The experimental results revealed that hydrocortisone nano-sized dispersions in the range of 80-450 nm were obtained and the mean particle size could be changed by modifying the experimental parameters and design of microreactors. The second part of the work studied the possibility of preparing a hydrocortisone nanosuspension using microfluidic reactors. The nano-sized particles generated from a microreactor were rapidly introduced into an aqueous solution of stabilizers stirred at high speed with a propeller mixer. A tangential flow filtration system was then used to concentrate the prepared nanosuspension. The nanosuspension produced was then characterized using photon correlation spectroscopy (PCS), Zeta potential measurement, transmission electron microscopy (TEM), differential scanning calorimetry (DSC) and X-ray analysis. Results showed that a narrow sized nanosuspension composed of amorphous spherical particles with a mean particle size of 500 ± 64 nm, a polydispersity index of 0.21 ± 0.026 and a zeta potential of -18 ± 2.84 mV was obtained. Physical stability studies showed that the hydrocortisone nanosuspension remained homogeneous with slight increase in mean particle size and polydispersity index over a 3-month period. © 2009 Elsevier B.V. All rights reserved.
机译:在这项工作中,研究了使用微流体反应器自底向上创建相对稳定的氢化可的松纳米水悬浮液的可能性。工作的第一部分涉及对影响所产生药物颗粒尺寸的微流控沉淀过程参数的研究。这些参数包括药物溶液和抗溶剂的流速,微流体通道直径,微反应器入口角和药物浓度。实验结果表明,获得了氢化可的松纳米尺寸的分散体,其分散度为80-450 nm,并且可以通过修改实验参数和设计微反应器来改变平均粒径。工作的第二部分研究了使用微流控反应器制备氢化可的松纳米悬浮液的可能性。将由微反应器产生的纳米级颗粒快速引入到稳定剂的水溶液中,该稳定剂用螺旋桨混合器高速搅拌。然后使用切向流过滤系统浓缩制备的纳米悬浮液。然后使用光子相关光谱(PCS),Zeta电位测量,透射电子显微镜(TEM),差示扫描量热法(DSC)和X射线分析对产生的纳米悬浮液进行表征。结果表明,由平均粒径为500±64 nm,多分散指数为0.21±0.026和ζ电位为-18±2.84 mV的无定形球形颗粒组成的窄尺寸纳米悬浮液。物理稳定性研究表明,氢化可的松纳米悬浮液在3个月的时间内保持均匀,平均粒径和多分散指数略有增加。 ©2009 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号