Gelatin-Coated ZnO Array Nanoplatform for Capture, Drug Resistance Identification, and Recovery of Circulating Tumor Cells

被引:2
作者
Dai, Jiahao [1 ,2 ]
Cai, Bo [1 ]
Zhang, Yan [1 ,3 ]
Zhao, Shukun [4 ]
Zhao, Xingzhong [4 ]
Wang, Guobin [2 ]
Wang, Lin [1 ,3 ]
Wang, Zheng [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Res Ctr Tissue Engn & Regenerat Med, Wuhan 430022, Peoples R China
[2] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Gastrointestinal Surg, Wuhan 430022, Peoples R China
[3] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Clin Lab, Wuhan 430022, Peoples R China
[4] Wuhan Univ, Sch Phys & Technol, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
cell capture; cell release; circulating tumor cells; drug resistance; electrochemical detection; EFFICIENT CAPTURE; NANOROD ARRAYS; NANOPARTICLES; CYTOTOXICITY; MUTATIONS; BIOMARKER; GROWTH;
D O I
10.1002/admt.202201584
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Drug resistance causes failure of cancer treatment. Identifying drug sensitivity of tumors can guide therapeutic administration for cancer patients, however this approach lacks a facile, fast, and noninvasive evaluation platform. Herein, a gelatin-coated ZnO array nanoplatform to isolate circulating tumor cells (CTCs) is developed, and their drug resistance for inspecting tumor sensitivity is assessed. The nanoplatform is comprised of a nanosubstrate of ZnO submicropillars (ZnO SMPs) for efficiently isolating cancer cells, and Au nanoparticles (AuNPs) based electrochemical probes for evaluating drug resistance of the captured cells. Gelatin, an extracellular matrix-like and enzyme-degradable material, is used to coat ZnO SMPs and AuNPs, endowing the nanoplatform with the ability to maintain cancer cell viability and realize enzyme-responsive cell recovery for downstream bioanalysis. This nanoplatform is expected to noninvasively evaluate drug sensitivity of cancer patients through simple liquid biopsy of CTCs in peripheral blood and benefit the treatment.
引用
收藏
页数:9
相关论文
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