适体
纳米技术
输送系统
癌症治疗
癌症治疗
材料科学
生物医学工程
癌症
医学
生物
分子生物学
内科学
作者
Elham Sameiyan,Elnaz Bagheri,Shahrzad Dehghani,Mohammad Ramezani,Mona Alibolandi,Khalil Abnous,Seyed Mohammad Taghdisi
标识
DOI:10.1016/j.actbio.2020.12.057
摘要
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.
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