Manosroi A, Kongkaneramit L, Manosroi J
Pharmaceutical-Cosmetics Raw Materials and Natural Products Research and Development Center, Institute for Science and Technology Research and Development, Faculty of Pharmacy, Chiang Mai University, Chiang Mai, Thailand.
Drug Dev Ind Pharm. 2004 May;30(5):535-43. doi: 10.1081/ddc-120037484.
Liposomes composed of hydrogenated soya phosphatidylcholine (Emulmetik 950)/cholesterol/charged lipids [dicetyl phosphate (-) or stearylamine (+)] were developed. The hydrogenated soya phosphatidylcholine/cholesterol/charged lipid liposomes at molar ratios of 1:1:0, 7:2:0, 7:2:1 (-), and 7:2:1 (+), with and without the entrapped amphotericin B (0.05 mg AmB/mg lipid), were prepared by a chloroform-film method with sonication. The charges of liposomes were characterized by a Zeta-Meter. The negative liposomes with and without the entrapped AmB showed higher surface charge density than other formulations. The size distribution of liposomes determined by standard error of the mean (SEM) was in the range of 0.115 to 0.364 microm. The smallest size was observed in the negative liposomes with the entrapped drug [7:2:1 (-) AmB]. The lamellarity of more than 15 layers was observed by transmission electron microscope (TEM) in the neutral liposomes with the entrapped drug [7:2 AmB]. The transition temperature and enthalpy of transition (deltaH) were determined by differential scanning calorimetry (DSC). Positive liposomes with the entrapped and unentrapped AmB demonstrated higher deltaH of the first peak than other formulations, indicating higher rigidity of liposomal membrane. The AmB contents in liposomes were determined by high-performance liquid chromatography (HPLC) with ultraviolet (UV) detection at 382 nm. The percentages of entrapment of AmB in all formulations were above 85%. The positive liposome [7:2:1 (+) AmB] formulation, which gave the highest thermal stability, was selected for further skin absorption evaluation.
制备了由氢化大豆磷脂酰胆碱(Emulmetik 950)/胆固醇/带电脂质[磷酸二鲸蜡酯(-)或硬脂胺(+)]组成的脂质体。采用氯仿薄膜法并超声处理,制备了摩尔比为1:1:0、7:2:0、7:2:1(-)和7:2:1(+)的氢化大豆磷脂酰胆碱/胆固醇/带电脂质脂质体,其中部分脂质体包封了两性霉素B(0.05 mg两性霉素B/ mg脂质),部分未包封。通过Zeta仪对脂质体的电荷进行表征。包封和未包封两性霉素B的负电荷脂质体比其他制剂表现出更高的表面电荷密度。通过平均标准误差(SEM)测定的脂质体大小分布在0.115至0.364微米范围内。在包封药物的负电荷脂质体[7:2:1(-)两性霉素B]中观察到最小尺寸。通过透射电子显微镜(TEM)在包封药物的中性脂质体[7:2两性霉素B]中观察到超过15层的片层结构。通过差示扫描量热法(DSC)测定转变温度和转变焓(ΔH)。包封和未包封两性霉素B的正电荷脂质体的第一个峰的ΔH高于其他制剂,表明脂质体膜的刚性更高。通过在382 nm处进行紫外(UV)检测的高效液相色谱(HPLC)测定脂质体中的两性霉素B含量。所有制剂中两性霉素B的包封率均高于85%。选择具有最高热稳定性的正电荷脂质体[7:2:1(+)两性霉素B]制剂进行进一步的皮肤吸收评估。