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高通量筛选鉴定出一种脂质纳米颗粒,该颗粒在体内优先将 mRNA 递送至人类肿瘤。

High-throughput screens identify a lipid nanoparticle that preferentially delivers mRNA to human tumors in vivo.

机构信息

Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.

Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.

出版信息

J Control Release. 2023 May;357:394-403. doi: 10.1016/j.jconrel.2023.04.005. Epub 2023 Apr 12.

Abstract

Lipid nanoparticles (LNPs) are a clinically relevant way to deliver therapeutic mRNA to hepatocytes in patients. However, LNP-mRNA delivery to end-stage solid tumors such as head and neck squamous cell carcinoma (HNSCC) remains more challenging. While scientists have used in vitro assays to evaluate potential nanoparticles for HNSCC delivery, high-throughput delivery assays performed directly in vivo have not been reported. Here we use a high-throughput LNP assay to evaluate how 94 chemically distinct nanoparticles delivered nucleic acids to HNSCC solid tumors in vivo. DNA barcodes were used to identify LNP, a novel LNP for systemic delivery to HNSCC solid tumors. Importantly, LNP retains tropism to HNSCC solid tumors while minimizing off-target delivery to the liver.

摘要

脂质纳米颗粒(LNPs)是一种将治疗性 mRNA 递送至患者肝细胞的临床相关方法。然而,LNPs-mRNA 递送至头颈部鳞状细胞癌(HNSCC)等终末期实体瘤仍然更具挑战性。尽管科学家已经使用体外分析来评估用于 HNSCC 递药的潜在纳米颗粒,但尚未报道在体内直接进行的高通量递药分析。在这里,我们使用高通量 LNP 分析来评估 94 种不同化学组成的纳米颗粒在体内向 HNSCC 实体瘤递送核酸的情况。使用 DNA 条码来鉴定 LNP,这是一种新型的用于 HNSCC 实体瘤系统递药的 LNP。重要的是,LNP 保留了对 HNSCC 实体瘤的亲嗜性,同时最大限度地减少了对肝脏的非靶向递药。

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