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首页> 外文期刊>Journal of Colloid and Interface Science >Intercellular adhesion molecule 1 antibody-mediated mesoporous drug delivery system for targeted treatment of triple-negative breast cancer
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Intercellular adhesion molecule 1 antibody-mediated mesoporous drug delivery system for targeted treatment of triple-negative breast cancer

机译:细胞间粘附分子1抗体介导的介孔药物递送系统,用于针对三重阴性乳腺癌的靶向治疗

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摘要

The development of effective targeted therapies for triple negative breast cancer (TNBC) remains a challenge. This targeted drug delivery system used a near-infrared fluorescence dye cyanine 5.5 (Cy5.5) and an ICAM-1 antibody on thioether-bridged periodic mesoporous organosilica nanoparticles (PMOs). The ICAM-1 antibody and cyanine 5.5-engineered PMOs (PMO-Cy5.5-ICAM) offer excellent in vivo and in vitro biocompatibility. The PMO-Cy5.5-ICAM shows a loading capacity up to 400 mg/g of doxorubicin (DOX). The drug release profile of the DOX-loaded targeted delivery system (DOX@PMO-Cy5.5-ICAM) is pH-sensitive. Confocal microscopy showed that the PMO-Cy5.5-ICAM efficiently targets and enters TNBC cells. In in vivo experiments, the DOX@PMO-Cy5.5-ICAM accumulates more in TNBCs than in the control groups and exhibits better therapeutic effects on TNBC; thus, it is a promising treatment strategy for TNBC. (C) 2018 Elsevier Inc. All rights reserved.
机译:有效靶向三重乳腺癌(TNBC)的有效疗法的发展仍然是一个挑战。 该靶向药物递送系统使用近红外荧光染料花青5.5(Cy5.5)和硫醚桥接的周期性介孔有机碱纳米颗粒(PMOS)上的ICAM-1抗体。 ICAM-1抗体和青色5.5工程的PMOS(PMO-CY5.5-ICAM)提供优异的体内和体外生物相容性。 PMO-CY5.5-ICAM显示出高达400mg / g多柔比星(DOX)的装载能力。 DOX装载的目标输送系统(DOX@pmo-cy5.5-ICAM)的药物释放曲线是pH敏感的。 共聚焦显微镜显示PMO-CY5.5-ICAM有效靶向并进入TNBC细胞。 在体内实验中,DOX@pmo-cy5.5-iCam在TNBC中积累了比对照组更多,对TNBC表现出更好的治疗效果; 因此,它是TNBC的有希望的治疗策略。 (c)2018 Elsevier Inc.保留所有权利。

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