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Harnessing the power of cell-penetrating peptides: Activatable carriers for targeting systemic delivery of cancer therapeutics and imaging agents

机译:利用细胞穿透肽的强大功能:可激活的载体,用于靶向靶向治疗和成像剂的系统递送

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Targeted delivery of cancer therapeutics and imaging agents aims to enhance the accumulation of these molecules in a solid tumor while avoiding uptake in healthy tissues. Tumor-specific accumulation has been pursued with passive targeting by the enhanced permeability and retention effect, as well as with active targeting strategies. Active targeting is achieved by functionalization of carriers to allow specific interactions between the carrier and the tumor environment. Functionalization of carriers with ligands that specifically interact with overexpressed receptors on cancer cells represents a classic approach to active tumor targeting. Cell-penetrating peptides (CPPs) provide a non-specific and receptor-independent mechanism to enhance cellular uptake that offers an exciting alternative to traditional active targeting approaches. While the non-specificity of CPP-mediated internalization has the intriguing potential to make this approach applicable to a wide range of tumor types, their promiscuity is, however, a significant barrier to their clinical utility for systemically administered applications. Many approaches have been investigated to selectively turn on the function of systemically delivered CPP-functionalized carriers specifically in tumors to achieve targeted delivery of cancer therapeutics and imaging agents.
机译:癌症治疗剂和成像剂的靶向递送旨在增强这些分子在实体瘤中的积累,同时避免被健康组织吸收。通过增强的通透性和保留效果以及主动靶向策略,可以通过被动靶向来追求肿瘤特异性蓄积。主动靶向通过载体的功能化来实现,以使载体与肿瘤环境之间发生特定的相互作用。用与癌细胞上过表达的受体特异性相互作用的配体对载体进行功能化代表了主动靶向肿瘤的经典方法。细胞穿透肽(CPP)提供了一种非特异性和受体独立的机制来增强细胞摄取,为传统的主动靶向方法提供了令人兴奋的替代方法。尽管CPP介导的内在化的非特异性具有使这种方法适用于多种肿瘤的诱人潜力,但它们的混杂性严重阻碍了其全身应用的临床应用。已经研究了许多方法来选择性地开启全身递送的CPP-功能化载体的功能,特别是在肿瘤中,以实现癌症治疗剂和显像剂的靶向递送。

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