Department of Pharmaceutical Informatics, Graduate School of Biomedical Sciences, Nagasaki University, 1-7-1 Sakamoto, Nagasaki-shi, Nagasaki, Japan.
Department of Neurosurgery, Graduate School of Biomedical Sciences, Nagasaki University, 1-7-1 Sakamoto, Nagasaki-shi, Nagasaki, Japan.
Eur J Pharm Biopharm. 2024 Oct;203:114468. doi: 10.1016/j.ejpb.2024.114468. Epub 2024 Aug 22.
Lipid nanoparticles (LNPs) are promising delivery systems with the ability to deliver small interfering RNA (siRNA) and messenger RNA (mRNA) in diseased tissues and intracellular sites of action. However, delivery to non-hepatic tissues via systemic administration remains challenging. Antibody modification of LNPs is a hopeful approach for improving their selectivity to target tissues. The conventional method of antibody modification via thiol-maleimide linkage is concerned with reduced recognition efficiency of the disease-related target molecules owing to variations in antibody orientation on the surface of the LNPs. In this study, we developed a novel adapter lipopeptide for antibody modification of LNPs via the Fc-region. Here, we selected RI7-217, an anti-transferrin receptor antibody, as the ligand. Through optimization of spacer peptides, we found a FcBP-EKGG-lipid exhibits high water-dispersibility for post-insertion method to LNPs. We prepared RI7-217-modified LNPs by modifying LNPs with FcBP-EKGG-lipids and mixing the antibodies. We found that the luciferase protein expression of RI7-217-modified LNPs was significantly enhanced in an antibody-specific manner against transferrin receptor-expressing U-87 MG cells. This information would be valuable in the development of antibody-modified LNPs for cell-selective targeting.
脂质纳米粒(LNPs)是一种很有前途的递送系统,能够将小干扰 RNA(siRNA)和信使 RNA(mRNA)递送到病变组织和细胞内作用部位。然而,通过全身给药将其递送到非肝脏组织仍然具有挑战性。通过抗体修饰 LNPs 是提高其对靶组织选择性的有希望的方法。通过巯基-马来酰亚胺键进行抗体修饰的传统方法由于 LNPs 表面上抗体取向的变化而导致对疾病相关靶分子的识别效率降低。在这项研究中,我们开发了一种通过 Fc 区修饰 LNPs 的新型接头脂肽。在这里,我们选择了 RI7-217,一种抗转铁蛋白受体抗体作为配体。通过优化间隔肽,我们发现 FcBP-EKGG-脂质对于后插入方法具有高的水分散性。我们通过用 FcBP-EKGG-脂质修饰 LNPs 并混合抗体来制备 RI7-217 修饰的 LNPs。我们发现 RI7-217 修饰的 LNPs 在针对转铁蛋白受体表达的 U-87 MG 细胞的抗体特异性方式下,显著增强了荧光素酶蛋白的表达。这些信息对于开发用于细胞选择性靶向的抗体修饰 LNPs 具有重要意义。