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一种基于多功能黑磷纳米片的免疫磁生物界面,用于胃癌患者外周血循环肿瘤细胞的异质性捕获及同步自我识别

A multifunctional black phosphorus nanosheet-based immunomagnetic bio-interface for heterogeneous circulating tumor cell capture and simultaneous self-identification in gastric cancer patients.

作者信息

Zuo Yifan, Xia Yi, Lu Wenwen, Li Yue, Xiao Yang, Gao Shuai, Zhou Zhiyi, Xu Hao, Feng Xingqing, Li Chenglin, Yu Yanyan

机构信息

Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical University, 209 Tongshan Road, Xuzhou 221004, Jiangsu, China.

School of Anesthesiology, Xuzhou Medical University, 209 Tongshan Road, Xuzhou 221004, Jiangsu, China.

出版信息

Nanoscale. 2023 Feb 23;15(8):3872-3883. doi: 10.1039/d2nr04277k.

Abstract

A single epithelial cell adhesion molecule (EpCAM) for circulating tumor cell (CTCs) isolation has been proved to be low in efficiency as it fails to recognize EpCAM-negative CTCs. Meanwhile, the current immunocytochemical (ICC) identification strategy for the captured cells is tedious and time-consuming. To address these issues, we designed a dual-labeled fluorescent immunomagnetic nanoprobe (BP-FeO-AuNR/Apt), by loading magnetic FeO nanoparticles and gold nanorods (AuNRs) onto black phosphorus (BP) nanosheets and then linking them with Cy3-labeled EpCAM and Texas red-labeled tyrosine protein kinase 7 (PTK7) aptamers, which created a high-performance bio-interface for efficient, heterogeneous CTC capture and rapid self-identification with high accuracy. As few as 5 CTCs could be captured from 1.0 mL PBS, mixed cell solution and lysed blood. What's more, the presence of BP and AuNRs on this capturing interface also allowed us to preliminarily investigate the potential photothermal therapeutic effect of the probe toward CTC elimination. The applicability of the probe was further demonstrated in gastric cancer patients. By detecting the number of CTCs in the blood of gastric cancer patients, the correlations between the CTC number and the disease stage, as well as distant metastasis were systematically explored.

摘要

已证明,用于循环肿瘤细胞(CTC)分离的单一上皮细胞粘附分子(EpCAM)效率较低,因为它无法识别EpCAM阴性的CTC。同时,当前针对捕获细胞的免疫细胞化学(ICC)鉴定策略繁琐且耗时。为了解决这些问题,我们设计了一种双标记荧光免疫磁性纳米探针(BP-FeO-AuNR/Apt),通过将磁性FeO纳米颗粒和金纳米棒(AuNRs)负载到黑磷(BP)纳米片上,然后将它们与Cy3标记的EpCAM和德克萨斯红标记的酪氨酸蛋白激酶7(PTK7)适体连接,从而创建了一个高性能的生物界面,用于高效、异质的CTC捕获和高精度的快速自我鉴定。从1.0 mL PBS、混合细胞溶液和裂解血液中,该探针能够捕获低至5个CTC。此外,该捕获界面上BP和AuNRs的存在还使我们能够初步研究该探针消除CTC的潜在光热治疗效果。该探针的适用性在胃癌患者中得到了进一步验证。通过检测胃癌患者血液中的CTC数量,系统地探索了CTC数量与疾病分期以及远处转移之间的相关性。

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