Han Moohyun, Beon Jiyun, Lee Ju Young, Oh Seung Soo
Department of Materials Science and Engineering, Pohang University of Science Technology (POSTECH), Pohang, Gyeongbuk, 37673 Korea.
Research Center for Bio-based Chemistry, Korea Research Institute of Chemical Technology (KRICT), Ulsan, 44429 Korea.
Macromol Res. 2021;29(10):665-680. doi: 10.1007/s13233-021-9093-5. Epub 2021 Nov 5.
The potential of oligonucleotides is exceptional in therapeutics because of their high safety, potency, and specificity compared to conventional therapeutic agents. However, many obstacles, such as low stability and poor cellular uptake, have hampered their clinical success. Use of polymeric carriers can be an effective approach for overcoming the biological barriers and thereby maximizing the therapeutic efficacy of the oligonucleotides due to the availability of highly tunable synthesis and functional modification of various polymers. As loaded in the polymeric carriers, the therapeutic oligonucleotides, such as antisense oligonucleotides, small interfering RNAs, microRNAs, and even messenger RNAs, become nuclease-resistant by bypassing renal filtration and can be efficiently internalized into disease cells. In this review, we introduced a variety of systematic combinations between the therapeutic oligonucleotides and the synthetic polymers, including the uses of highly functionalized polymers responding to a wide range of endogenous and exogenous stimuli for spatiotemporal control of oligonucleotide release. We also presented intriguing characteristics of oligonucleotides suitable for targeted therapy and immunotherapy, which can be fully supported by versatile polymeric carriers.
与传统治疗药物相比,寡核苷酸在治疗方面具有卓越的潜力,因为它们具有高安全性、高效力和高特异性。然而,许多障碍,如稳定性低和细胞摄取差,阻碍了它们在临床上的成功应用。由于各种聚合物具有高度可调节的合成和功能修饰,使用聚合物载体可能是克服生物屏障从而最大化寡核苷酸治疗效果的有效方法。当治疗性寡核苷酸,如反义寡核苷酸、小干扰RNA、微小RNA甚至信使RNA,负载在聚合物载体中时,它们可以绕过肾脏过滤,变得对核酸酶具有抗性,并能有效地内化到疾病细胞中。在这篇综述中,我们介绍了治疗性寡核苷酸与合成聚合物之间的多种系统组合,包括使用对广泛的内源性和外源性刺激有响应的高功能化聚合物来时空控制寡核苷酸的释放。我们还展示了适用于靶向治疗和免疫治疗的寡核苷酸的有趣特性,这些特性可以得到多功能聚合物载体的充分支持。