Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Winship Cancer Institute, Emory University, Atlanta, GA 30322, USA.
J Control Release. 2023 May;357:394-403. doi: 10.1016/j.jconrel.2023.04.005. Epub 2023 Apr 12.
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.
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。