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Modular Nanotransporters for Targeted Intracellular Delivery of Drugs: Folate Receptors as Potential Targets

机译:模块化的纳米转运药物靶向细胞内递送:叶酸受体作为潜在靶标。

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摘要

The review is devoted to a subcellular drug delivery system, modular nanotransporters (MNT) that can penetrate into target cells and deliver a therapeutic into their subcellular compartments, particularly into the nucleus. The therapeutics which need such type of delivery belong to two groups: (i) those that exert their effect only when delivered into a certain cell compartment (like DNA delivered into the nucleus); and (ii) those drugs that are capable of exerting their effect in different parts of the cells, however there can be found a cell compartment that is the most sensitive to their effect. A particular interest attract such cytotoxic agents as Auger electron emitters which are known to be ineffective outside the cell nucleus, whereas they possess high cytotoxicity in the vicinity of nuclear DNA through the induction of non-reparable double-strand DNA breaks. The review discusses main approaches permitting to choose internalizable receptors permitting both recognition of target cells and penetration into them. Special interest attract folate receptors which become accessible to blood circulating therapeutics after malignant transformation or on activated macrophages which makes them an attractive target for both several oncological and inflammatory diseases, like atherosclerosis. In vitro and in vivo experiments demonstrated that MNT is a promising platform for targeted delivery of different therapeutics into the nuclei of target cells.
机译:该综述专门针对亚细胞药物递送系统,即模块化纳米转运蛋白(MNT),它可以穿透靶细胞并将治疗剂递送至其亚细胞区室,尤其是进入细胞核。需要这种递送方式的治疗剂分为两类:(i)仅在递送到某个细胞区室时才发挥作用的药物(如递送到细胞核中的DNA); (ii)能够在细胞的不同部位发挥作用的那些药物,但是可以发现对它们的作用最敏感的细胞室。引起人们特别关注的是诸如Auger电子发射器之类的细胞毒性剂,已知它们在细胞核外部无效,而它们通过诱导不可修复的双链DNA断裂而在核DNA附近具有很高的细胞毒性。该综述讨论了允许选择可内在受体的主要方法,这些受体既可以识别靶细胞又可以穿透靶细胞。叶酸受体引起了人们的特别兴趣,叶酸受体在恶性转化后或在活化的巨噬细胞上可用于血液循环治疗,这使其成为多种肿瘤和炎性疾病(如动脉粥样硬化)的有吸引力的靶标。体外和体内实验表明,MNT是将不同治疗药物靶向递送至靶细胞核的有前途的平台。

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