Department of Mechanical Engineering, University College London, Torrington Place, London WC1E 7JE, UK.
J R Soc Interface. 2010 Aug 6;7 Suppl 4(Suppl 4):S393-402. doi: 10.1098/rsif.2010.0099.focus. Epub 2010 Jun 2.
In this investigation, biodegradable polycaprolactone polymeric particles (300-4500 nm in diameter) were prepared by jetting a solution in an electric field. An extensive study has been carried out to determine how the size and size distribution of the particles generated can be controlled by systematically varying the polymer concentration in solution (and thereby its viscosity and electrical conductivity), and also the selected flow rate (2-50 microl min(-1)) and applied voltage (0-15 kV) during particle generation. Change in these parameters affects the mode of jetting, and within the stable cone-jet mode window, an increase in the applied voltage (approx. 15 kV) resulted in a reduction in particle size and this was more pronounced at high flow rates (such as; 30, 40 and 50 microl min(-1)) in the same region. The carrier particles were more polydisperse at the peripheral regions of the stable cone-jet mode, as defined in the applied voltage-flow rate parametric map. The effect of loading a drug on the particle size, size distribution and encapsulation efficiency was also studied. Release from drug-loaded particles was investigated using UV spectrophotometry over 45 days. This work demonstrates a powerful method of generating drug-loaded polymeric particles, with the ability to control size and polydispersivity, which has great potential in several categories of biotechnology requiring carrier particles, such as drug delivery and gene therapy.
在这项研究中,通过在电场中喷射溶液来制备生物可降解的聚己内酯聚合物颗粒(直径为 300-4500nm)。已经进行了广泛的研究,以确定如何通过系统地改变溶液中的聚合物浓度(从而改变其粘度和电导率),以及选择的流速(2-50μl min(-1))和在颗粒生成过程中施加的电压(0-15kV)来控制生成的颗粒的大小和尺寸分布。这些参数的变化会影响喷射模式,在稳定的锥形射流模式窗口内,施加电压(约 15kV)的增加会导致颗粒尺寸减小,而在相同区域内的高流速(例如 30、40 和 50μl min(-1))下,这种减小更为明显。在施加电压-流速参数图中定义的稳定锥形射流模式的外围区域,载体颗粒的多分散性更高。还研究了载药对颗粒大小、粒径分布和包封效率的影响。使用紫外分光光度法在 45 天内研究了载药颗粒的释放情况。这项工作展示了一种生成载药聚合物颗粒的强大方法,具有控制大小和多分散性的能力,在需要载体颗粒的生物技术的几个领域具有巨大的潜力,例如药物输送和基因治疗。