纳米体-寡核苷酸缀合物(核体):寡核苷酸治疗的下一个前沿。

IF 3.5 3区 医学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Pharmaceutical Research Pub Date : 2025-02-01 Epub Date: 2025-02-15 DOI:10.1007/s11095-025-03829-z
Rajan K Tripathy, Abhay H Pande
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引用次数: 0

摘要

截至目前,超过15种寡核苷酸药物,主要是小干扰rna和反义寡核苷酸类,已被美国FDA批准用于治疗用途,还有更多的药物正在临床试验中。然而,将基于寡核苷酸的药物安全有效地递送到靶组织仍然是一个主要的挑战。为了提高血浆半衰期,有效的内体释放和其他多种功能,多年来使用了各种载体分子。抗体-药物偶联物的成功治疗应用使抗体成为将寡核苷酸有效载荷递送到靶组织的流行选择。单链可变结构域重链抗体(纳米体)由于其体积小、对靶点亲和力高、细胞穿透能力强、制备简单等优点,近年来被证明是一种很有前途的抗体替代品。本文综述了寡核苷酸药物类型及其与纳米体(核体)的结合,以实现有效的靶向递送、检测和诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanobody-Oligonucleotide Conjugates (NucleoBodies): The Next Frontier in Oligonucleotide Therapy.

As of now, more than 15 oligonucleotide drugs, primarily small interfering RNAs and antisense oligonucleotide classes, have been approved by the US FDA for therapeutic use, and many more are under clinical trials. However, safe and effective delivery of the oligonucleotide-based drugs to the target tissue still remains a major challenge. For enhanced plasma half-life, effective endosomal release, and other multiple functionalities, various carrier molecules have been used over the years. The successful therapeutic application of antibody-drug conjugates has made antibodies a popular choice for the delivery of oligonucleotide payloads into the target tissues. Single-chain variable domains of heavy chain antibodies (nanobodies) have proven a promising alternative to antibodies in recent years due to their small size, high affinity for the target, cell-penetrating potency, simple and easy production. The present review highlights the oligonucleotide drug types and their conjugation with nanobodies called NucleoBodies for effective targeted delivery, detection and diagnostics.

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来源期刊
Pharmaceutical Research
Pharmaceutical Research 医学-化学综合
CiteScore
6.60
自引率
5.40%
发文量
276
审稿时长
3.4 months
期刊介绍: Pharmaceutical Research, an official journal of the American Association of Pharmaceutical Scientists, is committed to publishing novel research that is mechanism-based, hypothesis-driven and addresses significant issues in drug discovery, development and regulation. Current areas of interest include, but are not limited to: -(pre)formulation engineering and processing- computational biopharmaceutics- drug delivery and targeting- molecular biopharmaceutics and drug disposition (including cellular and molecular pharmacology)- pharmacokinetics, pharmacodynamics and pharmacogenetics. Research may involve nonclinical and clinical studies, and utilize both in vitro and in vivo approaches. Studies on small drug molecules, pharmaceutical solid materials (including biomaterials, polymers and nanoparticles) biotechnology products (including genes, peptides, proteins and vaccines), and genetically engineered cells are welcome.
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