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两亲嵌段共聚物靶向脂质纳米颗粒:受限撞击射流混合器制备的新一代核酸给药系统。

Diblock Copolymer Targeted Lipid Nanoparticles: Next-Generation Nucleic Acid Delivery System Produced by Confined Impinging Jet Mixers.

机构信息

Department of Chemical and Biological Engineering, Princeton University, Princeton, New Jersey 08544, United States.

Department of Biomedical Engineering, Columbia University, New York, New York 10027, United States.

出版信息

ACS Appl Bio Mater. 2024 Nov 18;7(11):7595-7607. doi: 10.1021/acsabm.4c01176. Epub 2024 Oct 31.

Abstract

Despite the recent advances and clinical demonstration of lipid nanoparticles (LNPs) for therapeutic and prophylactic applications, the extrahepatic delivery of nucleic acids remains a significant challenge in the field. This limitation arises from the rapid desorption of lipid-PEG in the bloodstream and clearance to the liver, which hinders extrahepatic delivery. In response, we explore the substitution of lipid-PEG with biodegradable block copolymers (BCPs), specifically poly(ε-caprolactone)--poly(ethylene glycol) (PCL--PEG). BCPs offer strong anchoring for large macromolecules, potentially enhancing cell-specific targeting. To develop and optimize BCP-stabilized LNPs (BCP-LNPs), we employed a Design of Experiment (DOE) approach. Through a systematic exploration, we identified optimal formulations for BCP-LNPs, achieving desirable physicochemical properties and encapsulation efficiency. Notably, BCP-LNPs exhibit surprising trends in transfection efficiency, with certain formulations showing up to a 40-fold increase in transfection in Hela cells, while maintaining minimal cytotoxicity. The lipid compositions that optimized PCL--PEG LNP transfection were different from the compositions that optimized PEG-lipid LNP transfection. Furthermore, our study confirms the versatility of BCP-LNPs in encapsulating and delivering both mRNA and pDNA, demonstrating their cargo-agnostic nature. Lastly, we showcased the targeted BCP-LNPs using a Cetuximab-conjugated formulation. These targeted LNPs show significant promise in delivering cargo specific to EGFR-overexpressing cells (A549 cells), with up to 2.4 times higher transfection compared to nontargeted LNPs. This finding underscores the potential of BCP-LNPs in targeted gene therapy, especially in challenging scenarios such as tumor targeting. Overall, our study establishes the viability of BCP-LNPs as a versatile, efficient, and targeted delivery platform for nucleic acids, opening avenues for advanced therapeutic applications.

摘要

尽管脂质纳米粒(LNPs)在治疗和预防应用方面取得了近期进展和临床验证,但核酸的肝外递送仍然是该领域的一个重大挑战。这种限制源于脂质-PEG 在血液中的快速解吸和向肝脏的清除,这阻碍了肝外递送。有鉴于此,我们探索用可生物降解的嵌段共聚物(BCPs)替代脂质-PEG,特别是聚(ε-己内酯)-聚(乙二醇)(PCL-PEG)。BCPs 为大分子提供了强大的锚定,可能增强细胞特异性靶向。为了开发和优化 BCP 稳定的 LNPs(BCP-LNPs),我们采用了实验设计(DoE)方法。通过系统探索,我们确定了 BCP-LNPs 的最佳配方,实现了理想的物理化学性质和封装效率。值得注意的是,BCP-LNPs 在转染效率方面表现出惊人的趋势,某些配方在 Hela 细胞中的转染效率提高了 40 倍,同时保持最小的细胞毒性。优化 PCL-PEG LNP 转染的脂质组成与优化 PEG-脂质 LNP 转染的脂质组成不同。此外,我们的研究证实了 BCP-LNPs 在封装和递送 mRNA 和 pDNA 方面的多功能性,证明了它们对货物的无差别性质。最后,我们使用 Cetuximab 缀合配方展示了靶向 BCP-LNPs。这些靶向 LNPs 在递送到 EGFR 过表达细胞(A549 细胞)的特定货物方面显示出巨大的潜力,与非靶向 LNPs 相比,转染效率提高了 2.4 倍。这一发现突显了 BCP-LNPs 在靶向基因治疗中的潜力,特别是在肿瘤靶向等具有挑战性的情况下。总的来说,我们的研究确立了 BCP-LNPs 作为一种多功能、高效和靶向的核酸递药平台的可行性,为高级治疗应用开辟了途径。

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