Medda S, Das N, Bachhawat B K, Mahato S B, Basu M K
Biomembrane Division, Indian Institute of Chemical Biology, Calcutta.
Biotechnol Appl Biochem. 1990 Oct;12(5):537-43.
The possibility of using liposomes as an effective drug delivery system has been studied by incorporation of two plant glycosides of varying terminal sugar residues onto the surface of liposomes and examination of their distribution in different tissues. The two glycosides, corchorusin D and asiaticoside having glucose and rhamnose respectively at the terminal ends wee selected for the purpose. The hepatic uptake of liposomes made from egg lecithin, cholesterol and dicetyl phosphate and either of the two glycosides was compared. The hepatic uptake of asiaticoside bearing liposomes was reduced, whereas that of corchorusin D bearing liposomes was enhanced and was specific for glucose. Liver perfusion followed by cell separation showed that the uptake is mostly into the non-parenchymal cells of liver. The distribution of corchorusin D bearing liposomes was maximal in the lysosomal fraction of the non-parenchymal cells. Ways of using corchorusin D bearing liposomes as delivery systems for drugs or enzymes to lysosomes have been sought.
通过将两种末端糖残基不同的植物糖苷掺入脂质体表面并检查它们在不同组织中的分布,研究了将脂质体用作有效药物递送系统的可能性。为此目的,选择了两种糖苷,分别是末端具有葡萄糖的黄麻苷D和具有鼠李糖的积雪草苷。比较了由卵磷脂、胆固醇和磷酸二鲸蜡酯以及两种糖苷之一制成的脂质体的肝脏摄取情况。含积雪草苷的脂质体的肝脏摄取减少,而含黄麻苷D的脂质体的肝脏摄取增强,且对葡萄糖具有特异性。肝脏灌注后进行细胞分离表明,摄取主要进入肝脏的非实质细胞。含黄麻苷D的脂质体在非实质细胞的溶酶体部分分布最多。人们一直在寻找将含黄麻苷D的脂质体用作药物或酶向溶酶体递送系统的方法。