Sapra Bharti, Jain Subheet, Tiwary Ashok K
Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala, India.
AAPS PharmSciTech. 2009;10(1):199-210. doi: 10.1208/s12249-009-9198-1. Epub 2009 Feb 24.
This study was designed for investigating the effect of Asparagus racemosus (AR) extract and chitosan (CTN) in facilitating the permeation of carvedilol (CDL) across rat epidermis. Transdermal flux of carvedilol through heat-separated rat epidermis was investigated in vitro using vertical Keshary-Chien diffusion cells. Biophysical and microscopic manifestations of epidermis treated with AR extract, CTN, and AR extract-CTN mixture were investigated by using differential scanning calorimetry, transepidermal water loss, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Biochemical estimations of cholesterol, sphingosine, and triglycerides were carried out for treated excised as well as viable rat epidermis. The antihypertensive activity of the patches in comparison with that of oral carvedilol was studied in deoxycorticosterone acetate-induced hypertensive rats. The permeation of carvedilol across excised rat epidermis was significantly higher (p < 0.05) when AR extract, CTN, or AR extract-CTN mixture was used as donor vehicle as compared to propylene glycol/ethanol (7:3) mixture. Epidermis obtained after 12 h treatment of viable rat skin with AR extract-CTN mixture showed significantly higher (p < 0.05) permeability to CDL as compared to that after treatment with AR extract or CTN alone. Further, the application of patches containing AR extract-CTN mixture resulted in sustained release of CDL which was able to control the hypertension in deoxycorticosterone acetate-induced hypertensive rats through 36 h. Estimation of micro constituents in rat epidermis revealed maximum extraction of cholesterol, sphingosine, and triglycerides after treatment with AR extract-CTN mixture. This was manifested in altered lipid and protein-specific thermotropic transitions. Further, increase in intercellular space, disordered lipid structure, and corneocyte detachment as observed in SEM and TEM suggested great potential of AR extract for use as percutaneous permeation enhancer. The developed transdermal patches of CDL containing AR extract-CTN mixture exhibited better performance as compared to oral administration in controlling hypertension in rats.
本研究旨在探讨印度人参(AR)提取物和壳聚糖(CTN)对卡维地洛(CDL)透过大鼠表皮渗透的促进作用。采用垂直式Keshary-Chien扩散池体外研究卡维地洛透过热分离大鼠表皮的透皮通量。通过差示扫描量热法、经皮水分流失、扫描电子显微镜(SEM)和透射电子显微镜(TEM)研究AR提取物、CTN以及AR提取物-CTN混合物处理后表皮的生物物理和微观表现。对处理后的离体及存活大鼠表皮进行胆固醇、鞘氨醇和甘油三酯的生化测定。在醋酸脱氧皮质酮诱导的高血压大鼠中研究贴剂与口服卡维地洛相比的降压活性。与丙二醇/乙醇(7:3)混合物相比,当使用AR提取物、CTN或AR提取物-CTN混合物作为供体载体时,卡维地洛透过离体大鼠表皮的渗透率显著更高(p < 0.05)。与单独用AR提取物或CTN处理相比,用AR提取物-CTN混合物处理存活大鼠皮肤12小时后获得的表皮对CDL的渗透率显著更高(p < 0.05)。此外,含有AR提取物-CTN混合物的贴剂的应用导致CDL的持续释放,其能够在36小时内控制醋酸脱氧皮质酮诱导的高血压大鼠的高血压。大鼠表皮中微量成分的测定显示,用AR提取物-CTN混合物处理后胆固醇、鞘氨醇和甘油三酯的提取量最大。这表现为脂质和蛋白质特异性热致转变的改变。此外,在SEM和TEM中观察到的细胞间空间增加、脂质结构紊乱和角质形成细胞脱离表明AR提取物作为经皮渗透促进剂具有巨大潜力。与口服给药相比,所开发的含有AR提取物-CTN混合物的CDL透皮贴剂在控制大鼠高血压方面表现出更好的性能。