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级联递药通过胰腺癌细胞的肿瘤屏障 超声联合功能微泡。

Cascade Drug Delivery through Tumor Barriers of Pancreatic Cancer Ultrasound in Combination with Functional Microbubbles.

机构信息

Department of Ultrasound, Peking University Third Hospital, 49 North Garden Rd, Haidian District, Beijing 100191, China.

School of Basic Medical Sciences, Peking University Health Science Center, 38 College Rd, Haidian District, Beijing 100190, China.

出版信息

ACS Biomater Sci Eng. 2022 Apr 11;8(4):1583-1595. doi: 10.1021/acsbiomaterials.2c00069. Epub 2022 Mar 9.

Abstract

The abundant desmoplastic stroma and the lack of sufficient targets on pancreatic cancer cells render poor drug penetration and cellular uptake, which significantly compromise the chemotherapy efficacy. Herein, we reported a three-step cascade delivery strategy for selective delivery of paclitaxel (PTX) to achieve a targeted therapy for pancreatic cancer. cRGD and cCLT1 peptides, which could target the integrin and fibronectin, respectively, overexpressed in pancreatic cancer cells and stroma, were decorated on PTX-loaded microbubbles, resulting in the formation of dual-targeting PTX-RCMBs. In this strategy, ultrasound in combination with PTX-RCMBs first enhanced the permeability of tumor vessels cavitation effects and simultaneously helped the generated PTX-RCNPs penetrate into the stroma. Then, the cCLT1 peptide modified on PTX-RCNPs selectively bound the fibronectin highly expressed in the stroma and later targeted the integrin (αβ) on the cell surface. Finally, another targeting cRGD peptide modified on PTX-RCNPs would further promote PTX uptake targeting the integrin (αβ) on the cell surface. This strategy significantly increased the delivery of PTX into tumor tissues. Moreover, the effective accumulation of PTX was monitored by ultrasound and fluorescence bimodal imaging. The tumor growth inhibition was investigated on subcutaneous tumor mouse models with 89.8% growth inhibition rate during 21 days of treatment, showing great potential for improving pancreatic cancer therapy.

摘要

丰富的促结缔组织反应性基质和胰腺癌细胞上缺乏足够的靶点,导致药物渗透和细胞摄取不良,从而显著降低化疗效果。在此,我们报道了一种三步级联递药策略,用于选择性递紫杉醇(PTX),以实现针对胰腺癌的靶向治疗。能够分别靶向胰腺癌细胞和基质中过度表达的整合素和纤连蛋白的 cRGD 和 cCLT1 肽被修饰在载紫杉醇的微泡上,形成双靶向 PTX-RCMBs。在该策略中,超声联合 PTX-RCMBs 首先通过空化效应增强肿瘤血管的通透性,同时帮助生成的 PTX-RCNPs 渗透到基质中。然后,修饰在 PTX-RCNPs 上的 cCLT1 肽选择性结合基质中高度表达的纤连蛋白,随后靶向细胞表面的整合素(αβ)。最后,修饰在 PTX-RCNPs 上的另一个靶向 cRGD 肽将进一步促进 PTX 的摄取,靶向细胞表面的整合素(αβ)。该策略显著增加了 PTX 递送到肿瘤组织中的量。此外,通过超声和荧光双模式成像监测 PTX 的有效积累。在皮下肿瘤小鼠模型中进行了肿瘤生长抑制研究,在 21 天的治疗期间,肿瘤生长抑制率达到 89.8%,显示出改善胰腺癌治疗的巨大潜力。

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