Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran; Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
Acta Biomater. 2021 Mar 15;123:110-122. doi: 10.1016/j.actbio.2020.12.057. Epub 2021 Jan 13.
In recent years, many stimuli-triggered drug delivery platforms have been designed to deliver drugs accurately to specific sites and reduce their side effects, improving "on-demand" therapeutic efficacy. Adenosine-5'-triphosphate (ATP)-responsive drug delivery methods are examples of these systems that use ATP molecules as a trigger for delivery of therapeutic agents. Since intra- and extra-cellular ATP concentrations are significantly different from each other (1-10 mM and <0.4 mM, respectively), the use of ATP can be a practical method for regulating drug release. Aptamers possess unique properties including, ligand-specific response, short sequence (~ 20-80 bases) and easy functionalization. Thus, their combination with ATP-responsive systems results in more accurate drug delivery systems and greater control of drug release. A wide range of nanoparticles, such as polymeric nanogels, liposomes, metallic nanoparticles, protein, or DNA nano-assemblies, have been employed in the fabrication of nanocarriers. In this review, we describe several ATP-responsive drug delivery systems based on the various carriers and discuss the challenges and strengths of each method.
近年来,许多刺激触发的药物输送平台被设计用于将药物精确递送到特定部位,并减少其副作用,从而提高“按需”治疗效果。三磷酸腺苷 (ATP) 响应性药物输送方法就是此类系统的示例,它们使用 ATP 分子作为输送治疗剂的触发物。由于细胞内和细胞外 ATP 浓度差异很大(分别为 1-10mM 和 <0.4mM),因此使用 ATP 可以是调节药物释放的一种实用方法。适体具有独特的性质,包括配体特异性响应、短序列(约 20-80 个碱基)和易于功能化。因此,它们与 ATP 响应系统的结合导致更精确的药物输送系统和对药物释放的更好控制。各种纳米载体,如聚合物纳米凝胶、脂质体、金属纳米粒子、蛋白质或 DNA 纳米组装体,已被用于制造纳米载体。在本文综述中,我们描述了几种基于各种载体的 ATP 响应性药物输送系统,并讨论了每种方法的挑战和优势。