组织特异性药物输送的向策略
Zongmin Zhao1, Anvay Ukidve1, Jayoung Kim1
1John A. Paulson School of Engineering and Applied Sciences, Harvard University, MA 02138, USA; Wyss Institute of Biologically Inspired Engineering at Harvard University, Boston, MA 02115, USA.
Cell
|April 4, 2020
概括
向策略通过实现特定部位的输送,克服生物障碍,减少非向效应来提高药物的有效性. 这篇评论讨论了小分子,核酸,,抗体和基于细胞的组织特异性药物输送方法的进展.
科学领域:
- 药理学
- 提供药物
- 生物医学工程
背景情况:
- 系统性药物管理面临非目标效应的挑战,影响治疗效果和毒性.
- 生物障碍阻碍了组织特异性的药物输送,需要先进的策略.
- 克服这些障碍对于开发更安全,更有效的疗法至关重要.
研究的目的:
- 审查组织特异性药物输送的关键进展和新兴概念.
- 讨论克服药物供应的生物障碍的策略.
- 探索各种药物向方法的临床转化.
主要方法:
- 对药物向策略的临床前和临床研究的文献综述.
- 基于小分子,核酸,,抗体和细胞的输送系统的分析.
- 讨论生物障碍和克服它们的方法.
主要成果:
- 在过去的30年里,
- 这些策略包括小分子,核酸,,抗体和基于细胞的方法.
- 在调节特定组织的药物输送方面取得了显著进展.
结论:
- 组织特异性药物输送具有显著的前景,可以减少非目标效应和毒性.
- 继续研究克服生物障碍对于治疗进步至关重要.
- 将这些向策略转化为临床实践是未来药物开发的重点.
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