Construction of a ternary component chip with enhanced desorption efficiency for laser desorption/ionization mass spectrometry based metabolic fingerprinting

被引:3
作者
Ding, Yajie [1 ]
Pei, Congcong [1 ]
Li, Kai [2 ]
Shu, Weikang [1 ]
Hu, Wenli [1 ]
Li, Rongxin [1 ]
Zeng, Yu [1 ]
Wan, Jingjing [1 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai, Peoples R China
[2] Nankai Univ, Dept Urol, Tianjin Cent Hosp 3, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
mass spectrometry; on-chip analysis; mesoporous silica membrane; metabolomics; kidney stone; SMALL MOLECULES; MATRIX; SERUM; SILICON; LIPIDS; STONE;
D O I
10.3389/fbioe.2023.1118911
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: In vitro metabolic fingerprinting encodes diverse diseases for clinical practice, while tedious sample pretreatment in bio-samples has largely hindered its universal application. Designed materials are highly demanded to construct diagnostic tools for high-throughput metabolic information extraction. Results: Herein, a ternary component chip composed of mesoporous silica substrate, plasmonic matrix, and perfluoroalkyl initiator is constructed for direct metabolic fingerprinting of biofluids by laser desorption/ionization mass spectrometry. Method: The performance of the designed chip is optimized in terms of silica pore size, gold sputtering time, and initiator loading parameter. The optimized chip can be coupled with microarrays to realize fast, high-throughput (similar to second/sample), and microscaled (similar to 1 mu L) sample analysis in human urine without any enrichment or purification. On-chip urine fingerprints further allow for differentiation between kidney stone patients and healthy controls. Discussion: Given the fast, high throughput, and easy operation, our approach brings a new dimension to designing nano-material-based chips for high-performance metabolic analysis and large-scale diagnostic use.
引用
收藏
页数:11
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