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Surface-Enhanced Raman Spectroscopy on Liquid Interfacial Nanoparticle Arrays for Multiplex Detecting Drugs in Urine
Ma, Yongmei1,2; Liu, Honglin1,3,4; Mao, Mei1,5; Meng, Juan1; Yang, Liangbao1; Liu, Jinhuai1
2016-08-16
Source PublicationANALYTICAL CHEMISTRY
AbstractThe design and application of liquid interfacial plasmonic platform is still in its infancy but is an exciting topic in tunable optical devices, sensors, and catalysis. Here, we developed an interfacial surface-enhanced Raman scattering (SERS) platform through the large-scale self-assembly of gOld nanoparticle (GNP) arrays at the cyclohexane (CYH)/water interface for detecting trace drug molecules in the urine of humans. The molecules extracted by the CYH phase from a urine sample were directly localized into the self-organized plasmonic hotspots, yielded excellent Raman enhancerrient, and realized the substrate-free. interfacial SERS detection. Synchrotron radiation small-angle X-ray scattering' (SRSAXS) experiments reveals a good uniformity of approximately 2-3 nm interparticle distance in the GNP' arrays. SERS colocalization experiments demonstrated that amphetamine molecules of different concentration levels could be loaded into the interfacial GNP arrays and realized the coassembly together with hanoparticles at the liquid/liquid interface. Interfacial GNP arrays with dynamic nanogaps in liquid interfacial structure can make surrounding molecules easily diffuse into the nanogaps. In contrast, the fixed GNP arrays on Si wafer were more irregular, such as multilayer stack, random aggregates,, and voids, during the drying process. When the drugs directly participate in the Self assembly process, it becomes easier for analytes diffusing into the nanogaps of GNP arrays, produces a concentration effect,, and amplified the SERS sensitivity. This feature also enables molecules to be adsorbed evenly in the arrays and makes a more uniform distribution of both the analytes and. GNPs in the liquid interface and realizes the significant increase in signal reproducibility. Interfacial SERS produced a standard deviation of 12.5% at 1001 cm-' peak of methampheta,mine (MAMP) molecules under the concentration of 1 ppin, implying a good reproducibility. Moreover, dual-analyte detection at organic and aqueous phases was also realized and confirmed a good capability for analytes detection by liquid' interfacial SERS platform, which promises nonengineering detection of analytes dissolved in often-inaccessible environments.
SubtypeArticle
WOS HeadingsScience & Technology ; Physical Sciences
DOI10.1021/acs.analchem.6b01884
WOS KeywordTRINITROTOLUENE EXPLOSIVE LIGHTS ; SCATTERING DETECTION ; SILVER ; COLLOIDOSOMES ; AMPHETAMINE ; SOLS ; METHAMPHETAMINE ; NANOSTRUCTURES ; IDENTIFICATION ; CHROMATOGRAPHY
Indexed BySCI
Language英语
Funding OrganizationNational Natural Science Foundation of China(21305142 ; National Natural Science Foundation of China(21305142 ; National Natural Science Foundation of China(21305142 ; National Natural Science Foundation of China(21305142 ; China Postdoctoral Science Foundation(2015M582322 ; China Postdoctoral Science Foundation(2015M582322 ; China Postdoctoral Science Foundation(2015M582322 ; China Postdoctoral Science Foundation(2015M582322 ; Open Project of State Key Laboratory of Physical Chemistry at Xiamen University ; Open Project of State Key Laboratory of Physical Chemistry at Xiamen University ; Open Project of State Key Laboratory of Physical Chemistry at Xiamen University ; Open Project of State Key Laboratory of Physical Chemistry at Xiamen University ; Open Project of State Key Laboratory of Chemo/Biosensing and Chemometrics at Hunan University ; Open Project of State Key Laboratory of Chemo/Biosensing and Chemometrics at Hunan University ; Open Project of State Key Laboratory of Chemo/Biosensing and Chemometrics at Hunan University ; Open Project of State Key Laboratory of Chemo/Biosensing and Chemometrics at Hunan University ; (Z14sr0017) ; (Z14sr0017) ; (Z14sr0017) ; (Z14sr0017) ; 21271136) ; 21271136) ; 21271136) ; 21271136) ; 2016T90748) ; 2016T90748) ; 2016T90748) ; 2016T90748)
WOS Research AreaChemistry
WOS SubjectChemistry, Analytical
WOS IDWOS:000381654800037
Citation statistics
Cited Times:64[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.hfcas.ac.cn:8080/handle/334002/24395
Collection中科院合肥智能机械研究所
Affiliation1.Chinese Acad Sci, Hefei Inst Phys Sci, Inst Intelligent Machines, Hefei 230031, Peoples R China
2.Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Chongqing 400714, Peoples R China
3.Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Mol Sci & Biomed Lab, Changsha 410082, Hunan, Peoples R China
4.Hunan Univ, Coll Biol, Collaborat Innovat Ctr Mol Engn & Theranost, Changsha 410082, Hunan, Peoples R China
5.Univ Sci & Technol China, Dept Chem, Hefei 230026, Peoples R China
Recommended Citation
GB/T 7714
Ma, Yongmei,Liu, Honglin,Mao, Mei,et al. Surface-Enhanced Raman Spectroscopy on Liquid Interfacial Nanoparticle Arrays for Multiplex Detecting Drugs in Urine[J]. ANALYTICAL CHEMISTRY,2016,88(16):8145-8151.
APA Ma, Yongmei,Liu, Honglin,Mao, Mei,Meng, Juan,Yang, Liangbao,&Liu, Jinhuai.(2016).Surface-Enhanced Raman Spectroscopy on Liquid Interfacial Nanoparticle Arrays for Multiplex Detecting Drugs in Urine.ANALYTICAL CHEMISTRY,88(16),8145-8151.
MLA Ma, Yongmei,et al."Surface-Enhanced Raman Spectroscopy on Liquid Interfacial Nanoparticle Arrays for Multiplex Detecting Drugs in Urine".ANALYTICAL CHEMISTRY 88.16(2016):8145-8151.
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