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Published byHomer Harris Modified over 8 years ago
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Group members:Benjun Liu Junjie Yang Runmin Zhang Yuxiang Qin
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Introduction Experimentation Outlook Contents
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Introduction Experimentation Outlook Contents
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Why ? How?
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Ag NPs CTAB “glues” MUA “switch” Ag Dimers
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CTAB and MUA’s roles in synthesizing Ag Dimers
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Introduction Experimentation Outlook Contents
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Preparation of Ag NPs Glass slide’s Modification with APS Self-Assembly of Ag Dimer Experiment Section
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PVP@EG 10g PVP(MW=10000)@75mL EG +Ag 400mg AgNO 3 added with continuous stirring Heat room temperature to 120℃ 1℃/min then 1h at 120℃
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Small peak at 600nm ——Overheated ?
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PVP@EG 10g PVP(MW=10000)@75mL EG +Ag 400mg AgNO 3 added with continuous stirring Heat 30min at 120℃
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Clean glass slides Immerse the slides into APS solutions for 12h Rinse with extensive water
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Ag NPs CTAB 0.1mM×0.2mL 15min MCA 0.2mM×1mL Self- assemble
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Ag NPs CTAB 0.1mM×0.2mL 15min MPA 0.2mM×1mL Self- assemble
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Absorption Spectrum
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UnannealedAnnealed
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UnannealedAnnealed
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Ag NPsAg Dimers
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Introduction Experimentation Outlook Contents
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Without bringing in any external label, fluorescence enhancements with Ag Dimers could detect DNA/RNA sensitively Direct and non-damage detection of DNA/RNA provide an important new tool for management of patients with other cancers Fast Detection of Circulating Tumor Cells
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Lakowicz J R, Shen B, Gryczysnki Z, et al. Biochem. Biophys. Res. Commun., 2001, 286 : 875 —879 DNA/RNA signals: weak, short life Ag Dimers: Enhancing fluorescence signals
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Traditional Methods : Cell Culturing Low Specificity Low Sensitivity Time Consuming Surface-Enhanced Raman Spectroscopy Specific Sensitive Convenient
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Could probably improve the intensity with Ag dimers Xu Wang, Ximei Qian, Jonathan J. Beitler, et al. , Cancer Res 2011;71:1526-1532
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