胰腺癌
基质
药物输送
癌症研究
微气泡
整合素
紫杉醇
纤维连接蛋白
体内
间质细胞
癌细胞
医学
化疗
癌症
药理学
细胞
材料科学
化学
病理
生物
超声波
内科学
生物化学
纳米技术
免疫组织化学
生物技术
放射科
作者
Lulu Zhang,Lihong Sun,Qingshuang Tang,Suhui Sun,Lan Zeng,Jiuyi Ma,Xiaoda Li,Huiyu Ge,Xiaolong Liang
出处
期刊:ACS Biomaterials Science & Engineering
[American Chemical Society]
日期:2022-03-09
卷期号:8 (4): 1583-1595
被引量:9
标识
DOI:10.1021/acsbiomaterials.2c00069
摘要
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 via 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 (α5β1) on the cell surface. Finally, another targeting cRGD peptide modified on PTX-RCNPs would further promote PTX uptake via targeting the integrin (αvβ3) on the cell surface. This strategy significantly increased the delivery of PTX into tumor tissues. Moreover, the in vivo 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.
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