| Literature DB >> 33742513 |
Haiyang Su1,2, Xinxing Li3,4, Lin Huang5, Jing Cao1,2, Mengji Zhang1,2, Vadanasundari Vedarethinam1,2, Wen Di1,2, Zhiqian Hu3,4, Kun Qian1,2.
Abstract
Gastric cancer (GC) is a multifactorial process, accompanied by alterations in metabolic pathways. Non-invasive metabolic profiling facilitates GC diagnosis at early stage leading to an improved prognostic outcome. Herein, mesoporous PdPtAu alloys are designed to characterize the metabolic profiles in human blood. The elemental composition is optimized with heterogeneous surface plasmonic resonance, offering preferred charge transfer for photoinduced desorption/ionization and enhanced photothermal conversion for thermally driven desorption. The surface structure of PdPtAu is further tuned with controlled mesopores, accommodating metabolites only, rather than large interfering compounds. Consequently, the optimized PdPtAu alloy yields direct metabolic fingerprints by laser desorption/ionization mass spectrometry in seconds, consuming 500 nL of native plasma. A distinct metabolic phenotype is revealed for early GC by sparse learning, resulting in precise GC diagnosis with an area under the curve of 0.942. It is envisioned that the plasmonic alloy will open up a new era of minimally invasive blood analysis to improve the surveillance of cancer patients in the clinical setting.Entities:
Keywords: diagnosis; gastric cancer; metabolites; porous alloys; surface plasmon resonance
Year: 2021 PMID: 33742513 DOI: 10.1002/adma.202007978
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849