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易于制造均匀大小可控的微球及微/纳米颗粒串联药物输送系统的潜力。

Facile fabrication of uniform size-controlled microparticles and potentiality for tandem drug delivery system of micro/nanoparticles.

机构信息

Institute of Industrial Science, The University of Tokyo, Tokyo 153-8904, Japan.

出版信息

Colloids Surf B Biointerfaces. 2013 Sep 1;109:301-6. doi: 10.1016/j.colsurfb.2013.04.007. Epub 2013 Apr 19.

DOI:10.1016/j.colsurfb.2013.04.007
PMID:23668984
Abstract

This article describes a rapid and facile method for manufacturing various size-controlled gel particles with utilizing inkjet printing technology. Generally, the size of droplets could be controlled by changing nozzle heads of inkjet printer, from which ink solution is ejected. However, this method uses drying process before gelling microparticles, and with that, the size of microparticles was easily controlled by only altering the concentration of ejected solution. When sodium alginate solution with various concentrations was ejected from inkjet printer, we found that the concentration of alginate solution vs. the volume of dried alginate particle showed an almost linear relationship in the concentration range from 0.1 to 3.0%. After dried alginate particles were soaked into calcium chloride solution, the size of microgel beads were obtained almost without increasing their size. The microparticles including various sizes of nanoparticles were easily manufactured by ejecting nanoparticle-dispersed alginate solution. The release of 25-nm sized nanoparticles from alginate microgel beads was finished in a relatively-rapid manner, whereas 100-nm sized nanoparticles were partially released from those ones. Moreover, most of 250-nm sized nanoparticles were not released from alginate microgel beads even after 24-h soaking. This particle fabricating method would enable the tandem drug delivery system with a combination of the release from nano and microparticles, and be expected for the biological and tissue engineering application.

摘要

本文描述了一种利用喷墨打印技术快速简便地制造各种尺寸可控的凝胶颗粒的方法。通常,可以通过改变喷墨打印机的喷嘴头来控制液滴的大小,从而将油墨溶液喷出。然而,该方法在凝胶化微颗粒之前使用干燥过程,通过仅改变喷出溶液的浓度,很容易控制微颗粒的大小。当从喷墨打印机中喷出各种浓度的海藻酸钠溶液时,我们发现海藻酸钠溶液的浓度与干燥海藻酸钠颗粒的体积之间呈几乎线性关系,在 0.1 到 3.0%的浓度范围内。将干燥的海藻酸钠颗粒浸泡在氯化钙溶液中后,微凝胶珠的尺寸几乎没有增加。通过喷出分散有纳米颗粒的海藻酸钠溶液,很容易制造出各种尺寸的纳米颗粒微颗粒。25nm 大小的纳米颗粒从海藻酸钠微凝胶珠中的释放速度较快,而 100nm 大小的纳米颗粒则部分释放。此外,即使浸泡 24 小时后,大多数 250nm 大小的纳米颗粒也不会从海藻酸钠微凝胶珠中释放出来。这种颗粒制造方法将使具有纳米和微颗粒释放的串联药物输送系统成为可能,并有望应用于生物和组织工程。

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