Complex Coacervates as a Promising Vehicle for mRNA Delivery: A Comprehensive Review of Recent Advances and Challenges

IF 4.5 2区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Chloe Forenzo,  and , Jessica Larsen*, 
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引用次数: 0

Abstract

Messenger RNA (mRNA)-based therapies have gained significant attention, following the successful deployment of mRNA-based COVID-19 vaccines. Compared with traditional methods of genetic modification, mRNA-based therapies offer several advantages, including a lower risk of genetic mutations, temporary and controlled therapeutic gene expression, and a shorter production time, which facilitates rapid responses to emerging health challenges. Moreover, mRNA-based therapies have shown immense potential in treating a wide range of diseases including cancers, immune diseases, and neurological disorders. However, the current limitations of non-viral vectors for efficient and safe delivery of mRNA therapies, such as low encapsulation efficiency, potential toxicity, and limited stability, necessitate the exploration of novel strategies to overcome these challenges and fully realize the potential of mRNA-based therapeutics. Coacervate-based delivery systems have recently emerged as promising strategies for enhancing mRNA delivery. Coacervates, which are formed by the aggregation of two or more macromolecules, have shown great potential in delivering a wide range of therapeutics due to their ability to form a separated macromolecular-rich fluid phase in an aqueous environment. This phase separation enables the entrapment and protection of therapeutic agents from degradation as well as efficient cellular uptake and controlled release. Additionally, the natural affinity of coacervates for mRNA molecules presents an excellent opportunity for enhancing mRNA delivery to targeted cells and tissues, making coacervate-based delivery systems an attractive option for mRNA-based therapies. This review highlights the limitations of current strategies for mRNA delivery and the advantages of coacervate-based delivery systems to enable mRNA therapeutics. Coacervates protect mRNA from enzymatic degradation and enhance cellular uptake, leading to sustained and controlled gene expression. Despite their promising properties, the specific use of coacervates as mRNA delivery vehicles remains underexplored. This review aims to provide a comprehensive overview of coacervate-mediated delivery of mRNA, exploring the properties and applications of different coacervating agents as well as the challenges and optimization strategies involved in mRNA encapsulation, release, stability, and translation via coacervate-mediated delivery. Through a comprehensive analysis of recent advancements and recommended future directions, our review sheds light on the promising role of coacervate-mediated delivery for RNA therapeutics, highlighting its potential to enable groundbreaking applications in drug delivery and gene therapy.

Abstract Image

复杂凝聚体作为mRNA传递的有前途的载体:近期进展和挑战的综合综述
在基于信使RNA的COVID-19疫苗成功部署之后,基于信使RNA (mRNA)的疗法获得了极大的关注。与传统的基因修饰方法相比,基于mrna的疗法具有若干优势,包括较低的基因突变风险、暂时和受控的治疗性基因表达以及较短的生产时间,这有助于对新出现的健康挑战作出快速反应。此外,基于mrna的疗法在治疗包括癌症、免疫疾病和神经系统疾病在内的广泛疾病方面显示出巨大的潜力。然而,目前非病毒载体有效和安全递送mRNA治疗的局限性,如低封装效率、潜在毒性和有限的稳定性,需要探索新的策略来克服这些挑战,充分发挥基于mRNA治疗的潜力。基于凝聚体的递送系统最近成为增强mRNA递送的有前途的策略。凝聚体是由两个或多个大分子聚集形成的,由于它们能够在水环境中形成分离的富含大分子的流体相,因此在提供广泛的治疗方面显示出巨大的潜力。这种相分离使治疗剂的包裹和保护免受降解,以及有效的细胞摄取和控制释放。此外,凝聚体对mRNA分子的天然亲和力为增强mRNA向靶细胞和组织的递送提供了极好的机会,使基于凝聚体的递送系统成为基于mRNA的治疗的一个有吸引力的选择。这篇综述强调了目前mRNA递送策略的局限性,以及基于凝聚体的递送系统在mRNA治疗方面的优势。凝聚体保护mRNA免受酶降解并增强细胞摄取,从而导致持续和受控的基因表达。尽管凝聚体具有很好的特性,但其作为mRNA递送载体的具体用途仍未得到充分探索。本文旨在全面概述凝聚体介导的mRNA传递,探讨不同凝聚剂的特性和应用,以及通过凝聚体介导的mRNA包封、释放、稳定性和翻译所涉及的挑战和优化策略。通过对最近进展的综合分析和建议的未来方向,我们的综述揭示了凝聚体介导的RNA治疗的有希望的作用,强调了它在药物传递和基因治疗方面的突破性应用潜力。
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来源期刊
Molecular Pharmaceutics
Molecular Pharmaceutics 医学-药学
CiteScore
8.00
自引率
6.10%
发文量
391
审稿时长
2 months
期刊介绍: Molecular Pharmaceutics publishes the results of original research that contributes significantly to the molecular mechanistic understanding of drug delivery and drug delivery systems. The journal encourages contributions describing research at the interface of drug discovery and drug development. Scientific areas within the scope of the journal include physical and pharmaceutical chemistry, biochemistry and biophysics, molecular and cellular biology, and polymer and materials science as they relate to drug and drug delivery system efficacy. Mechanistic Drug Delivery and Drug Targeting research on modulating activity and efficacy of a drug or drug product is within the scope of Molecular Pharmaceutics. Theoretical and experimental peer-reviewed research articles, communications, reviews, and perspectives are welcomed.
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