Sarwa Khomendra K, Suresh Preeti K, Rudrapal Mithun, Verma Vinod K
University Institute of Pharmacy, Pt. Ravishankar Shukla University, Raipur, Chhattisgarh, India 492010.
Curr Drug Deliv. 2014;11(3):332-7. doi: 10.2174/1567201811666140115113127.
In the present study, ethosomal and liposomal formulations containing tamoxifen citrate were prepared and evaluated for their penetration properties in human cadaver skin using Franz diffusion cell and confocal laser scanning microscope (CLSM). The results clearly revealed that ethosomal vesicles showed a better drug permeation profile than that of liposomal vesicles. In addition, low fluorescence intensity in CLSM was recorded with liposomes as compared to ethosomes, indicating lower cumulative amount of drug permeation from liposomal vesicles. Furthermore, CLSM showed uniform fluorescence intensity across the entire depth of skin in ethosomal treatment, indicating high penetrability of ethosomal vesicles through human cadaver skin. In contrast, low penetrability of conventional liposomal vesicles was recorded as penetration was limited to the 7(th) section (i.e. upper epidermis layer) of skin as evident from visualization of intact liposomal vesicles in CLSM.
在本研究中,制备了含有柠檬酸他莫昔芬的乙醇脂质体和脂质体制剂,并使用Franz扩散池和共聚焦激光扫描显微镜(CLSM)评估它们在人尸体皮肤中的渗透特性。结果清楚地表明,乙醇脂质体囊泡比脂质体囊泡显示出更好的药物渗透曲线。此外,与乙醇脂质体相比,脂质体在CLSM中记录到较低的荧光强度,表明从脂质体囊泡渗透的药物累积量较低。此外,CLSM显示在乙醇脂质体处理中,整个皮肤深度的荧光强度均匀,表明乙醇脂质体囊泡通过人尸体皮肤的高渗透性。相比之下,记录到传统脂质体囊泡的渗透性较低,因为从CLSM中完整脂质体囊泡的可视化可以明显看出,渗透仅限于皮肤的第7节(即上表皮层)。