Iwamoto Satoshi, Nakagawa Kei, Sugiura Shinji, Nakajima Mitsutoshi
Reaction & Separation Engineering Laboratory, National Food Research Institute, 2-1-12, Kannondai, Tsukuba, Ibaraki, 305-8642, Japan.
AAPS PharmSciTech. 2002;3(3):E25. doi: 10.1208/pt030325.
The purpose of this study was to prepare monodisperse gelatin microcapsules containing an active agent using microchannel (MC) emulsification, a novel technique for preparing water-in-oil (W/O) and oil-in-water (O/W) emulsions. As the first step in applying MC emulsification to the preparation of monodisperse gelatin microcapsules, simple gelatin microbeads were prepared using this technique. A W/O emulsion with a narrow size distribution containing gelatin in the aqueous phase was created as follows. First, the aqueous disperse phase was fed into the continuous phase through the MCs at 40 degrees C (operating pressure: 3.9 kPa). The emulsion droplets had an average particle diameter of 40.7 microm and a relative standard deviation of 5.1%. The temperature of the collected emulsion was reduced and maintained at 25 degrees C overnight. The gelatin microbeads had a smooth surface after overnight gelation; the average particle diameter was calculated to be 31.6 microm, and the relative standard deviation, 7.3%. The temperature was then lowered to 5 degrees C by rapid air cooling and finally dried. The gelatin beads were dried and could be resuspended well in iso-octane. They had an average particle diameter of 15.6 microm, and a relative standard deviation of 5.9%. Using MC emulsification, we were able to prepare gelatin microbeads with a narrow size distribution. Since this emulsification technique requires only a low-energy input, it may create desirable experimental conditions for microencapsulation of unstable substances such as peptides and proteins. This method is promising for making monodisperse microbeads.
本研究的目的是使用微通道(MC)乳化技术制备含有活性剂的单分散明胶微胶囊,MC乳化是一种制备油包水(W/O)和水包油(O/W)乳液的新技术。作为将MC乳化应用于制备单分散明胶微胶囊的第一步,使用该技术制备了简单的明胶微珠。通过以下方式制备了水相中含有明胶且尺寸分布狭窄的W/O乳液。首先,在40℃(操作压力:3.9kPa)下,将水性分散相通过微通道进料到连续相中。乳液滴的平均粒径为40.7微米,相对标准偏差为5.1%。收集的乳液温度降低并在25℃下保持过夜。过夜凝胶化后,明胶微珠表面光滑;计算得出平均粒径为31.6微米,相对标准偏差为7.3%。然后通过快速空气冷却将温度降至5℃,最后干燥。明胶珠干燥后可在异辛烷中良好重悬。它们的平均粒径为15.6微米,相对标准偏差为5.9%。使用MC乳化,我们能够制备尺寸分布狭窄的明胶微珠。由于这种乳化技术仅需要低能量输入,因此它可能为肽和蛋白质等不稳定物质的微囊化创造理想的实验条件。这种方法在制备单分散微珠方面很有前景。