Zhou Da-Wei, Wang Ke, Zhang Ying-Ao, Ma Ke, Yang Xiao-Chun, Li Zhen-Yi, Yu Shou-Shan, Chen Ke-Zheng, Qiao Sheng-Lin
Lab of Functional and Biomedical Nanomaterials, College of Materials Science and Engineering, Qingdao University of Science and Technology (QUST), Qingdao, 266042, P. R. China.
J Mater Chem B. 2023 Apr 26;11(16):3484-3510. doi: 10.1039/d2tb02782h.
Messenger RNA (mRNA) has become a key focus in the development of therapeutic agents, showing significant potential in preventing and treating a wide range of diseases. The COVID-19 pandemic in 2020 has accelerated the development of mRNA nucleic therapeutics and attracted significant investment from global biopharmaceutical companies. These therapeutics deliver genetic information into cells without altering the host genome, making them a promising treatment option. However, their clinical applications have been limited by issues such as instability, inefficient delivery, and low translational efficiency. Recent advances in molecular design and nanotechnology have helped overcome these challenges, and several mRNA formulations have demonstrated promising results in both animal and human testing against infectious diseases and cancer. This review provides an overview of the latest research progress in structural optimization strategies and delivery systems, and discusses key considerations for their future clinical use.
信使核糖核酸(mRNA)已成为治疗药物开发的关键焦点,在预防和治疗多种疾病方面显示出巨大潜力。2020年的新冠疫情加速了mRNA核酸疗法的发展,并吸引了全球生物制药公司的大量投资。这些疗法可将遗传信息传递到细胞中而不改变宿主基因组,使其成为一种有前景的治疗选择。然而,它们的临床应用受到稳定性、递送效率低和翻译效率低等问题的限制。分子设计和纳米技术的最新进展有助于克服这些挑战,几种mRNA制剂在针对传染病和癌症的动物和人体试验中均已显示出有前景的结果。本综述概述了结构优化策略和递送系统的最新研究进展,并讨论了它们未来临床应用的关键注意事项。