Plasmonic silver nanoshells for drug and metabolite detection

In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance...

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Published inNature communications Vol. 8; no. 1; pp. 220 - 10
Main Authors Huang, Lin, Wan, Jingjing, Wei, Xiang, Liu, Yu, Huang, Jingyi, Sun, Xuming, Zhang, Ru, Gurav, Deepanjali D., Vedarethinam, Vadanasundari, Li, Yan, Chen, Ruoping, Qian, Kun
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LanguageEnglish
Published London Nature Publishing Group UK 09.08.2017
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Abstract In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance. A further challenge is to construct diagnostic tools. Herein, we developed a platform using silver nanoshells. We synthesized SiO 2 @Ag with tunable shell structures by multi-cycled silver mirror reactions. Optimized nanoshells achieved direct laser desorption/ionization mass spectrometry in 0.5 μL of bio-fluids. We applied these nanoshells for disease diagnosis and therapeutic evaluation. We identified patients with postoperative brain infection through daily monitoring and glucose quantitation in cerebrospinal fluid. We measured drug distribution in blood and cerebrospinal fluid systems and validated the function of blood-brain/cerebrospinal fluid-barriers for pharmacokinetics. Our work sheds light on the design of materials for advanced metabolic analysis and precision diagnostics. Preparation of samples for diagnosis can affect the detection of biomarkers and metabolites. Here, the authors use a silver nanoparticle plasmonics approach for the detection of biomarkers in patients as well as investigate the distribution of drugs in serum and cerebral spinal fluid.
AbstractList In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance. A further challenge is to construct diagnostic tools. Herein, we developed a platform using silver nanoshells. We synthesized SiO @Ag with tunable shell structures by multi-cycled silver mirror reactions. Optimized nanoshells achieved direct laser desorption/ionization mass spectrometry in 0.5 μL of bio-fluids. We applied these nanoshells for disease diagnosis and therapeutic evaluation. We identified patients with postoperative brain infection through daily monitoring and glucose quantitation in cerebrospinal fluid. We measured drug distribution in blood and cerebrospinal fluid systems and validated the function of blood-brain/cerebrospinal fluid-barriers for pharmacokinetics. Our work sheds light on the design of materials for advanced metabolic analysis and precision diagnostics.Preparation of samples for diagnosis can affect the detection of biomarkers and metabolites. Here, the authors use a silver nanoparticle plasmonics approach for the detection of biomarkers in patients as well as investigate the distribution of drugs in serum and cerebral spinal fluid.
In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance. A further challenge is to construct diagnostic tools. Herein, we developed a platform using silver nanoshells. We synthesized SiO 2 @Ag with tunable shell structures by multi-cycled silver mirror reactions. Optimized nanoshells achieved direct laser desorption/ionization mass spectrometry in 0.5 μL of bio-fluids. We applied these nanoshells for disease diagnosis and therapeutic evaluation. We identified patients with postoperative brain infection through daily monitoring and glucose quantitation in cerebrospinal fluid. We measured drug distribution in blood and cerebrospinal fluid systems and validated the function of blood-brain/cerebrospinal fluid-barriers for pharmacokinetics. Our work sheds light on the design of materials for advanced metabolic analysis and precision diagnostics. Preparation of samples for diagnosis can affect the detection of biomarkers and metabolites. Here, the authors use a silver nanoparticle plasmonics approach for the detection of biomarkers in patients as well as investigate the distribution of drugs in serum and cerebral spinal fluid.
In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance. A further challenge is to construct diagnostic tools. Herein, we developed a platform using silver nanoshells. We synthesized SiO2@Ag with tunable shell structures by multi-cycled silver mirror reactions. Optimized nanoshells achieved direct laser desorption/ionization mass spectrometry in 0.5 μL of bio-fluids. We applied these nanoshells for disease diagnosis and therapeutic evaluation. We identified patients with postoperative brain infection through daily monitoring and glucose quantitation in cerebrospinal fluid. We measured drug distribution in blood and cerebrospinal fluid systems and validated the function of blood-brain/cerebrospinal fluid-barriers for pharmacokinetics. Our work sheds light on the design of materials for advanced metabolic analysis and precision diagnostics.
In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance. A further challenge is to construct diagnostic tools. Herein, we developed a platform using silver nanoshells. We synthesized SiO2@Ag with tunable shell structures by multi-cycled silver mirror reactions. Optimized nanoshells achieved direct laser desorption/ionization mass spectrometry in 0.5 μL of bio-fluids. We applied these nanoshells for disease diagnosis and therapeutic evaluation. We identified patients with postoperative brain infection through daily monitoring and glucose quantitation in cerebrospinal fluid. We measured drug distribution in blood and cerebrospinal fluid systems and validated the function of blood-brain/cerebrospinal fluid-barriers for pharmacokinetics. Our work sheds light on the design of materials for advanced metabolic analysis and precision diagnostics.Preparation of samples for diagnosis can affect the detection of biomarkers and metabolites. Here, the authors use a silver nanoparticle plasmonics approach for the detection of biomarkers in patients as well as investigate the distribution of drugs in serum and cerebral spinal fluid.In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance. A further challenge is to construct diagnostic tools. Herein, we developed a platform using silver nanoshells. We synthesized SiO2@Ag with tunable shell structures by multi-cycled silver mirror reactions. Optimized nanoshells achieved direct laser desorption/ionization mass spectrometry in 0.5 μL of bio-fluids. We applied these nanoshells for disease diagnosis and therapeutic evaluation. We identified patients with postoperative brain infection through daily monitoring and glucose quantitation in cerebrospinal fluid. We measured drug distribution in blood and cerebrospinal fluid systems and validated the function of blood-brain/cerebrospinal fluid-barriers for pharmacokinetics. Our work sheds light on the design of materials for advanced metabolic analysis and precision diagnostics.Preparation of samples for diagnosis can affect the detection of biomarkers and metabolites. Here, the authors use a silver nanoparticle plasmonics approach for the detection of biomarkers in patients as well as investigate the distribution of drugs in serum and cerebral spinal fluid.
In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical practice. However, metabolic analysis in bio-samples needs tedious sample preparation, due to the sample complexity and low molecular abundance. A further challenge is to construct diagnostic tools. Herein, we developed a platform using silver nanoshells. We synthesized SiO 2 @Ag with tunable shell structures by multi-cycled silver mirror reactions. Optimized nanoshells achieved direct laser desorption/ionization mass spectrometry in 0.5 μL of bio-fluids. We applied these nanoshells for disease diagnosis and therapeutic evaluation. We identified patients with postoperative brain infection through daily monitoring and glucose quantitation in cerebrospinal fluid. We measured drug distribution in blood and cerebrospinal fluid systems and validated the function of blood-brain/cerebrospinal fluid-barriers for pharmacokinetics. Our work sheds light on the design of materials for advanced metabolic analysis and precision diagnostics.
Preparation of samples for diagnosis can affect the detection of biomarkers and metabolites. Here, the authors use a silver nanoparticle plasmonics approach for the detection of biomarkers in patients as well as investigate the distribution of drugs in serum and cerebral spinal fluid.
ArticleNumber 220
Author Chen, Ruoping
Liu, Yu
Qian, Kun
Sun, Xuming
Li, Yan
Wan, Jingjing
Zhang, Ru
Vedarethinam, Vadanasundari
Huang, Lin
Gurav, Deepanjali D.
Wei, Xiang
Huang, Jingyi
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  surname: Huang
  fullname: Huang, Lin
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
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  fullname: Wan, Jingjing
  organization: Department of Chemistry, Shanghai University
– sequence: 3
  givenname: Xiang
  surname: Wei
  fullname: Wei, Xiang
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
– sequence: 4
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  surname: Liu
  fullname: Liu, Yu
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
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  surname: Huang
  fullname: Huang, Jingyi
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
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  surname: Sun
  fullname: Sun, Xuming
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
– sequence: 7
  givenname: Ru
  surname: Zhang
  fullname: Zhang, Ru
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
– sequence: 8
  givenname: Deepanjali D.
  surname: Gurav
  fullname: Gurav, Deepanjali D.
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
– sequence: 9
  givenname: Vadanasundari
  surname: Vedarethinam
  fullname: Vedarethinam, Vadanasundari
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
– sequence: 10
  givenname: Yan
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  organization: Institute of Biophysics Key Laboratory of Interdisciplinary Research, Chinese Academy of Sciences
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  email: rubinchen@126.com
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  givenname: Kun
  surname: Qian
  fullname: Qian, Kun
  email: k.qian@sjtu.edu.cn
  organization: School of Biomedical Engineering, Children’s Hospital of Shanghai, and Med-X Research Institute, Shanghai Jiao Tong University
BackLink https://www.ncbi.nlm.nih.gov/pubmed/28790311$$D View this record in MEDLINE/PubMed
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SSID ssj0000391844
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Snippet In-vitro metabolite and drug detection rely on designed materials-based analytical platforms, which are universally used in biomedical research and clinical...
Preparation of samples for diagnosis can affect the detection of biomarkers and metabolites. Here, the authors use a silver nanoparticle plasmonics approach...
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StartPage 220
SubjectTerms 631/61/320
639/301/357/354
639/638/11/296
692/53/2421
Biomarkers
Blood
Brain Diseases - cerebrospinal fluid
Brain Diseases - diagnosis
Cerebrospinal fluid
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Title Plasmonic silver nanoshells for drug and metabolite detection
URI https://link.springer.com/article/10.1038/s41467-017-00220-4
https://www.ncbi.nlm.nih.gov/pubmed/28790311
https://www.proquest.com/docview/1927177188
https://www.proquest.com/docview/1927594958
https://pubmed.ncbi.nlm.nih.gov/PMC5548796
https://doaj.org/article/a92e3a1d876640c5b00846f49fee7c3b
Volume 8
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