Modified high shear homogenization and ultrasound techniques were employed to produce solid lipid nanoparticles (SLNs). Model drug mifepristone had been incorporated in SLNs. The mean particle size measured by laser diffractometry (LD) was found to be 106 nm with a narrow particle distribution of polydispersity index, 0.278. Differential scanning calorimetry and X-ray diffraction measurements suggested that the majority of the SLNs were less ordered arrangement of crystals, and this was favorable for increasing the drug loading capacity. The drug entrapment efficiency (EE%) of SLNs was more than 87 percent and showed relatively long-term physical stability as the leakage was very small after being stored for one month. Therefore, seemed this modified method could prepare high quality SLNs loading lipophilic drugs. It is a simple, available and effective method to produce SLNs.

译文

:采用改良的高剪切均质化和超声技术生产固体脂质纳米颗粒(SLN)。模型药物米非司酮已被纳入SLN中。发现通过激光衍射法(LD)测量的平均粒径为106nm,多分散指数为0.278,具有窄的粒径分布。差示扫描量热法和X射线衍射测量表明,大多数SLNs的晶体排列较不规则,这有利于增加载药量。 SLNs的药物包封率(EE%)超过87%,并且由于在储存一个月后泄漏非常小,因此显示出相对长期的物理稳定性。因此,似乎这种改进的方法可以制备出高质量的负载SLNs的亲脂性药物。这是一种生产SLN的简单,可用和有效的方法。

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