Division of Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, 2464 Charlotte Street, Kansas City, MO 64108, USA.
Adv Drug Deliv Rev. 2011 Jul 18;63(8):659-70. doi: 10.1016/j.addr.2011.02.002. Epub 2011 Feb 17.
As the mainstay in the treatment of various cancers for several decades, chemotherapy is successful but still faces challenges including non-selectivity and high toxicity. Improving the selectivity is therefore a critical step to improve the therapeutic efficacy of chemotherapy. Prodrug is one of the most promising approaches to increase the selectivity and efficacy of a chemotherapy drug. The classical prodrug approach is to improve the pharmaceutical properties (solubility, stability, permeability, irritation, distribution, etc.) via a simple chemical modification. This review will focus on various targeted prodrug designs that have been developed to increase the selectivity of chemotherapy drugs. Various tumor-targeting ligands, transporter-associated ligands, and polymers can be incorporated in a prodrug to enhance the tumor uptake. Prodrugs can also be activated by enzymes that are specifically expressed at a higher level in tumors, leading to a selective anti-tumor effect. This can be achieved by conjugating the enzyme to a tumor-specific antibody, or delivering a vector expressing the enzyme into tumor cells.
作为几十年来治疗各种癌症的主要手段,化疗虽然取得了成功,但仍面临非选择性和高毒性等挑战。因此,提高选择性是提高化疗疗效的关键步骤。前药是提高化疗药物选择性和疗效的最有前途的方法之一。经典的前药方法是通过简单的化学修饰来改善药物的理化性质(溶解度、稳定性、通透性、刺激性、分布等)。本文综述了各种靶向前药设计,旨在提高化疗药物的选择性。各种肿瘤靶向配体、转运体相关配体和聚合物可以被整合到前药中,以增强肿瘤摄取。前药也可以通过在肿瘤中高表达的酶来激活,从而产生选择性的抗肿瘤作用。这可以通过将酶与肿瘤特异性抗体偶联,或向肿瘤细胞中递送表达酶的载体来实现。