Kim I S, Choi H G, Choi H S, Kim B K, Kim C K
College of Pharmacy, Seoul National University, Korea.
Arch Pharm Res. 1998 Jun;21(3):248-52. doi: 10.1007/BF02975283.
To prolong the biological half-life of streptokinase, a thrombolytic agent, streptokinase-bearing liposome with and distearolyphosphatidyl ethanolamine-N-poly (ethylene glycol) 2000 (DSPE-PEG 2000) was prepared and evaluated. Streptokinase-bearing liposomes composed of distearolyphosphatidylcholine (DSPC), cholesterol and cholesterol-3-sulfate with DSPE-PEG 2000 was prepared by the freeze-thawing method and administered via femoral vein to rats (15,000 IU/kg). The activity of streptokinase in plasma was determined by the method based on the amidolytic activity of streptokinase-plasminogen complex. Pharmacokinetic parameters of streptokinase incorporated in liposomes were compared with those of streptokinase alone. The T1/2 and AUCinfinity of streptokinase incorporated in DSPC-PEG liposome increased 16.3- and 6.1-fold, respectively, compared with those of streptokinase alone. Streptokinase-bearing long-circulating liposome could increase the circulation time of streptokinase in blood and expect longer thrombolytic activity compared with streptokinase alone.
为延长溶栓剂链激酶的生物半衰期,制备并评估了负载链激酶的脂质体以及二硬脂酰磷脂酰乙醇胺 -N-聚乙二醇2000(DSPE-PEG 2000)。通过冻融法制备了由二硬脂酰磷脂酰胆碱(DSPC)、胆固醇和胆固醇 -3-硫酸盐与DSPE-PEG 2000组成的负载链激酶的脂质体,并经股静脉给予大鼠(15,000 IU/kg)。基于链激酶 - 纤溶酶原复合物的酰胺水解活性,采用该方法测定血浆中链激酶的活性。将脂质体包裹的链激酶的药代动力学参数与单独的链激酶进行比较。与单独的链激酶相比,DSPC-PEG脂质体包裹的链激酶的T1/2和AUCinfinity分别增加了16.3倍和6.1倍。与单独的链激酶相比,负载链激酶的长循环脂质体可延长链激酶在血液中的循环时间,并预期具有更长的溶栓活性。