Kumar Lalit, Verma Shivani, Vaidya Bhuvaneshwar
Department of Pharmaceutics, Shivalik College of Pharmacy, Nangal, Punjab 140126, India.
I. K. Gujral Punjab Technical University, Jalandhar, Punjab 144601, India.
Ther Deliv. 2017 Oct;8(10):855-866. doi: 10.4155/tde-2017-0026.
Streptokinase is an efficient thrombolytic agent used to treat thromboembolic disorders. Conventional streptokinase formulations have limited thrombolytic activity and several shortcomings because of their immunogenicity and dose-related side effects including short half-life, lack of tissue targeting and peripheral bleeding. Different liposomal formulations have been explored by researchers in order to improve thrombolytic activity of streptokinase. Liposomal formulations could improve plasma stability, retain drug for longer periods of time in the circulation and promote selective delivery to the thrombus. Side effects of conventional streptokinase formulations, such as immunogenicity and hemorrhage, can also be reduced by using liposomal carriers. In vivo therapeutic efficacy of the liposomal streptokinase has been demonstrated well in animal models. In the present review, we will discuss the potential of different liposomal carriers to improve thrombolytic efficacy of streptokinase.
链激酶是一种用于治疗血栓栓塞性疾病的有效溶栓剂。传统的链激酶制剂由于其免疫原性和剂量相关的副作用,包括半衰期短、缺乏组织靶向性和外周出血等,溶栓活性有限且存在若干缺点。研究人员探索了不同的脂质体制剂,以提高链激酶的溶栓活性。脂质体制剂可以提高血浆稳定性,使药物在循环中保留更长时间,并促进向血栓的选择性递送。使用脂质体载体还可以降低传统链激酶制剂的副作用,如免疫原性和出血。脂质体链激酶在动物模型中的体内治疗效果已得到充分证明。在本综述中,我们将讨论不同脂质体载体提高链激酶溶栓疗效的潜力。