羟基磷灰石结合肽脂纳米颗粒用于骨仿生mRNA递送

IF 3.7 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Joshua A. Choe, Jena E. Moseman, Jamie M. Jones, Jacobus C. Burger, Ashley M. Weichmann, Douglas G. McNeel, William L. Murphy
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引用次数: 0

摘要

针对骨的非病毒基因递送策略的发展可用于骨病理。应用包括风湿病、骨转移性疾病、造血功能缺陷的病理、骨髓炎和再生医学。然而,向骨骼等组织的特定递送是具有挑战性的。本文描述了用仿生羟基磷灰石结合肽(HABP-LNP)修饰的mRNA LNPs(脂质纳米颗粒),与假肽结合的mRNA LNPs (sham - lnp)相比,它与骨矿物质的结合更好。当与骨矿物质相关时,HABP-LNPs也增加转染。此外,HABP mRNA LNPs改善骨内转染,减少体内肝脏摄取。这些mRNA LNPs的持续发展可以导致骨病理的非病毒治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hydroxyapatite Binding Peptide Lipid Nanoparticles for Biomimetic mRNA Delivery to Bone

Development of strategies for non-viral gene delivery targeted to bone can be used for bone pathologies. Applications include rheumatologic disease, metastatic disease to the bone, pathologies with deficits in hematopoiesis, osteomyelitis, and regenerative medicine. However, specific delivery to tissues like bone is challenging. Here mRNA LNPs (lipid nanoparticles) decorated with a biomimetic hydroxyapatite-binding peptide (HABP-LNP) are described, which show improved binding to bone minerals compared to sham peptide conjugated mRNA LNPs (Sham-LNP). The HABP-LNPs also increase transfection when associated with bone mineral. Furthermore, HABP mRNA LNPs improve intraosseous transfection and reduce hepatic uptake in vivo. The continued development of these mRNA LNPs can result in non-viral therapies for bone pathologies.

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来源期刊
Advanced Therapeutics
Advanced Therapeutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.10
自引率
2.20%
发文量
130
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