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Macrophages as an active tumour-targeting carrier of SN38-nanoparticles for cancer therapy

机译:巨噬细胞作为癌症治疗的SN38-纳米粒子的活性肿瘤靶向载体

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Taking advantage of their enhanced permeability and retention (EPR) effect, nanomedicines have been extensively studied for targeted drug delivery to tumour tissues. However, tumour heterogeneity restricts the EPR effect and drug penetration into tumours, and nanoformulations only generate a limited therapeutic improvement in clinical settings. Macrophages have the inherent ability of tumour homing, stealth in blood circulation, and phagocytosis of particles. In this study, we used peritoneal macrophages as carriers for the delivery of SN38 nanoparticles (SN38-NPs) for cancer treatment. SN38-NPs were internalised by macrophages without any obvious effect on viability and migration, and not only induced apoptosis of tumour cells in vitro, but also accumulated in tumour tissues in vivo. In addition, the macrophage-based delivery system for SN38-NPs showed improved therapeutic effect than an equivalent dose of CPT-11 in an A549 subcutaneous tumour model. ? 2017 Informa UK Limited, trading as Taylor & Francis Group.
机译:利用其增强的渗透性和保留(EPR)效应,纳米海内西森林已经广泛研究了针对肿瘤组织的靶向药物递送。然而,肿瘤异质性限制了EPR效应和药物渗透到肿瘤中,并且纳米族种类仅在临床环境中产生有限的治疗性。巨噬细胞具有肿瘤归巢,隐身在血液循环的固有能力,以及颗粒的吞噬作用。在本研究中,我们使用腹膜巨噬细胞作为携带SN38纳米颗粒(SN38-NPS)的载体进行癌症治疗。 SN38-NPS被巨噬细胞内化,对活力和迁移没有任何明显影响,并且不仅在体外诱导肿瘤细胞的凋亡,而且在体内肿瘤组织中积累。此外,SN38-NPS的基于巨噬细胞的递送系统显示出改善的治疗效果,而不是A549皮下肿瘤模型中的等效剂量的CPT-11。还2017年Informa UK Limited,贸易为泰勒&弗朗西斯集团。

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