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Organelle Targeted Drug Delivery: Key Challenges, Recent Advancements and Therapeutic Implications
Endocrine, Metabolic & Immune Disorders - Drug Targets ( IF 1.9 ) Pub Date : 2024-02-02 , DOI: 10.2174/0118715303282573240112104035
Dilpreet Singh 1
Affiliation  

: Organelle-specific targeted drug delivery has emerged as a promising approach in the field of drug delivery and therapeutics. This innovative strategy involves the precise delivery of therapeutic agents to specific organelles within cells, such as the nucleus, mitochondria, endoplasmic reticulum, or lysosomes, with the aim of enhancing drug efficacy while minimizing offtarget effects. Despite its tremendous potential, organelle-specific drug delivery faces several key challenges. One major challenge is the development of delivery systems that can accurately navigate the complex intracellular environment and deliver drugs exclusively to the desired organelles. Achieving this level of precision demands advanced nanotechnology and biomaterials engineering. Furthermore, ensuring the safety and biocompatibility of these delivery systems is paramount. Recent advancements in this field include the development of nanocarriers, such as liposomes, nanoparticles, and dendrimers, designed to target specific organelles through ligandreceptor interactions or pH-responsive mechanisms. Additionally, advancements in molecular biology and genetic engineering have enabled the design of genetically encoded organellespecific drug delivery systems. The therapeutic implications of organelle-specific drug delivery are vast. This approach has the potential to revolutionize the treatment of diseases with organelle- specific pathologies, such as neurodegenerative disorders, cancer, and mitochondrial diseases. By precisely targeting the organelles involved in disease progression, the efficacy of therapies can be significantly improved while minimizing collateral damage to healthy tissues.

中文翻译:

细胞器靶向给药:主要挑战、最新进展和治疗意义

:细胞器特异性靶向药物递送已成为药物递送和治疗领域的一种有前途的方法。这一创新策略涉及将治疗药物精确递送至细胞内的特定细胞器,如细胞核、线粒体、内质网或溶酶体,目的是增强药物疗效,同时最大限度地减少脱靶效应。尽管具有巨大的潜力,细胞器特异性药物输送仍面临几个关键挑战。一项主要挑战是开发能够准确导航复杂的细胞内环境并将药物专门输送到所需细胞器的输送系统。达到这种精度水平需要先进的纳米技术和生物材料工程。此外,确保这些输送系统的安全性和生物相容性至关重要。该领域的最新进展包括纳米载体的开发,例如脂质体、纳米颗粒和树枝状聚合物,旨在通过配体受体相互作用或 pH 响应机制靶向特定细胞器。此外,分子生物学和基因工程的进步使得基因编码的细胞器特异性药物输送系统的设计成为可能。细胞器特异性药物输送的治疗意义是巨大的。这种方法有可能彻底改变细胞器特异性病理疾病的治疗,例如神经退行性疾病、癌症和线粒体疾病。通过精确靶向参与疾病进展的细胞器,可以显着提高治疗效果,同时最大限度地减少对健康组织的附带损害。
更新日期:2024-02-02
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