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2种方法制备银杏内酯长循环固体脂质纳米粒的比较
引用本文:刘旻,陈建海,董芙蓉,刘园. 2种方法制备银杏内酯长循环固体脂质纳米粒的比较[J]. 中国药房, 2008, 19(12): 905-907
作者姓名:刘旻  陈建海  董芙蓉  刘园
作者单位:南方医科大学南方医院药学部,广州市,510515
摘    要:目的:研究银杏内酯AB长循环固体脂质纳米粒(GAB-LSLN)的制备方法,并探讨GAB-LSLN的主要理化性质。方法:分别采用超声法和高压乳匀法制备GAB-LSLN。在电镜下观察其形态,测定其粒径、Zeta电位和包封率,并在室温下放置4周,观察GAB-LSLN的稳定性。结果:超声法制备的GAB-LSLN在透射电镜下呈片状存在,形态不规则;高压乳匀法制备的GAB-LSLN呈球状,形态规则。超声法和高压乳匀法制备的GAB-LSLN粒径分别为(219.6±14.3)nm和(173.9±10.4)nm(P<0.001);Zeta电位分别为(—21.12±1.03)mv和(—27.43±2.14)mV(P<0.001),包封率分别为(85.05±0.67)%和(92.49±0.88)%(P<0.001)。高压乳匀法制备的GAB-LSLN室温放置4周后,粒径无显著增加(P>0.05)。结论:高压乳匀法制备GAB-LSLN具有粒径小、稳定性和包封率高的特点,优于超声法。

关 键 词:银杏内酯A、B  超声法  高压乳匀法  固体脂质纳米粒  长循环
文章编号:1001-0408(2008)12-0905-03
修稿时间:2007-05-12

Ultrasonication Versus High Pressure Homogenization in the Preparation of Ginkgolides A and B Long circulating Solid Lipid Nanoparticles
LIU Min,CHEN Jian-hai,DONG Fu-rong,LIU Yuan. Ultrasonication Versus High Pressure Homogenization in the Preparation of Ginkgolides A and B Long circulating Solid Lipid Nanoparticles[J]. China Pharmacy, 2008, 19(12): 905-907
Authors:LIU Min  CHEN Jian-hai  DONG Fu-rong  LIU Yuan
Affiliation:(Dept. of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China)
Abstract:OBJECTIVE: To study the preparative methods of the long-circulating solid lipid nanoparticles (LSLN) carrying ginkgolides A and B (GAB) and to study the physicochemical characteristics of the GAB-LSLN. METHODS: GAB-LSLN was prepared by ultrasonication or high pressure homogenization. Transmission electron microscopy was employed to study its shape. Particle size, zeta potential, and entrapment efficiency of GAB-LSLN were determined, and its stability after storage under room temperature for 4 weeks was determined as well. RESULTS: The GAB-LSLN prepared by uhrasonication was platelet-shaped and irregular, and that prepared by high pressure homogenization was spherical and regular in shape. The particle diameters of GAB - L SLN prepared by uhrasonication and high pressure homogenization were (219.6±14.3) nm and (173.9± 10.4) nm respectively (P〈0.001) ; the Zeta potentials were (-21.12±1.03) mv and(-27.43± 2.14) mv respectively(P〈0.001) ; the entrapment efficiencies were(85.05±0.67) % and(92.49 ±0.88) % (P〈0.001) respectively. GAB-LSLN prepared by high pressure homogenization showed no obvious increase in particle size after storage at room temperature for 4 weeks (P 〉 0.05) .CONCLUSION: High pressure homogenization is superior to uhrasonication in that the pre- pared GAB-LSLN has small particle size, high stability and high entrapment efficiency.
Keywords:Ginkgolides A and B  Ultrasonieation  High pressure homogenization  Solid lipid nanopartieles  Long-eirculating
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