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新型载钆硅纳米杂化材料:一种潜在的表皮生长因子受体表达癌细胞靶向磁共振成像对比剂。

Novel Gd-Loaded Silicon Nanohybrid: A Potential Epidermal Growth Factor Receptor Expressing Cancer Cell Targeting Magnetic Resonance Imaging Contrast Agent.

机构信息

ARC Centre of Excellence in Convergent Bio-Nano Science and Technology, Future Industries Institute, University of South Australia , Mawson Lakes, South Australia 5095, Australia.

Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University , 381 Royal Parade, Parkville, Victoria 3052, Australia.

出版信息

ACS Appl Mater Interfaces. 2017 Dec 13;9(49):42601-42611. doi: 10.1021/acsami.7b14538. Epub 2017 Dec 1.

Abstract

Continuing our research efforts in developing mesoporous silicon nanoparticle-based biomaterials for cancer therapy, we employed here porous silicon nanoparticles as a nanocarrier to deliver contrast agents to diseased cells. Nanoconfinement of small molecule Gd-chelates (L1-Gd) enhanced the T contrast dramatically compared to distinct Gd-chelate (L1-Gd) by virtue of its slow tumbling rate, increased number of bound water molecules, and their occupancy time. The newly synthesized Gd-chelate (L1-Gd) was covalently grafted on silicon nanostructures and conjugated to an antibody specific for epidermal growth factor receptor (EGFR) via a hydrazone linkage. The salient feature of this nanosized contrast agent is the capability of EGFR targeted delivery to cancer cells. Mesoporous silicon nanoparticles were chosen as the nanocarrier because of their high porosity, high surface area, and excellent biodegradability. This type of nanosized contrast agent also performs well in high magnetic fields.

摘要

在开发基于介孔硅纳米粒子的癌症治疗生物材料的研究工作中,我们使用多孔硅纳米粒子作为纳米载体,将造影剂递送到病变细胞。小分子 Gd-螯合物 (L1-Gd) 的纳米限域作用由于其缓慢的翻滚速率、结合水分子的数量增加及其占据时间,显著增强了 T1 对比。新合成的 Gd-螯合物 (L1-Gd) 通过腙键与针对表皮生长因子受体 (EGFR) 的抗体共价接枝到硅纳米结构上。这种纳米级造影剂的突出特点是能够将 EGFR 靶向递送到癌细胞。选择介孔硅纳米粒子作为纳米载体是因为它们具有高孔隙率、高比表面积和优异的生物降解性。这种纳米级造影剂在强磁场中也表现良好。

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