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Real time detection of bio-nanoparticle using 
localised surface plasmon 
Presented by: 
Amit Kumar Tagore 
M.Tech. 1st year(1411NT02) Nanoscience & Technology 
IIT Patna
Outline 
Why single molecule detection needed. 
 Detection with labels and its disadvantages. 
 Label free detection. 
 Localized Surface Plasmon Resonance of Gold Nanoparticles. 
 Different illumination techniques. 
 Conclusion.
Why single molecule detection needed? 
• Virus detection is dead easy. 
• Early stage detection of cancer. 
• All dangerous disease can be detected at very early stage.
Detection with labels 
Single molecule is 
fluroscence labeled
Contd…
Drawback of detection with labels 
• Fluorescent labels are necessary (destructive technique) 
• Not a real time detection (not useful in doctor’s office) 
• Extraction of virus information is impossible 
• Selective virus detection is difficult 
• Multi-virus detection is difficult
Label free detection technique 
• This technique monitor inherent properties of the molecules such as 
mass, optical and dielectric properties. 
• Unlike label-based detection methods, these techniques avoid any tagging of the 
query molecules thereby preventing changes in structure and function. 
• They do not involve laborious procedures but have their own pitfalls such as 
sensitivity and specificity issues.
• Fibre-optic biosensors 
• Fabry-Perot interferometers 
• Interferometric biosensors 
• Optical resonance of a microresonator 
• Localized surface plasmonic biosensors 
• Surface Plasmon biosensors 
Optical 
Plasmonic
Localized Surface Plasmon Resonance 
• Surface Plasmon resonance (SPR) is the resonant oscillation of conduction 
electrons at the interface between a negative and positive permittivity material 
stimulated by incident light. 
• The resonance condition is established when the frequency of incident 
photons matches the natural frequency of surface electrons oscillating against 
the restoring force of positive nuclei. 
• A Localized Surface Plasmon (LSP) is the result of the confinement of a 
surface Plasmon in a nanoparticle of size comparable to or smaller than the 
wavelength of light used to excite the Plasmon. 
• The Plasmon resonant frequency is highly sensitive to the refractive index of 
the environment; a change in refractive index results in a shift in the resonant 
frequency.
Nanosphere
Contd…
Nanoellipsoidal
Localized Surface Plasmon Resonance of Gold Nanorod
Wavelength shift
Single Unlabeled Protein Detection on Individual Plasmonic 
Nanoparticles 
Irene Ament,† Janak Prasad,†,‡ Andreas Henkel,† Sebastian Schmachtel,† 
and Carsten Sönnichsen*,† 
†Institute for Physical Chemistry, University of Mainz, D-55128 Mainz, 
Germany 
‡Graduate School Materials Science in Mainz, Staudingerweg 9, D-55128 
Mainz, Germany 
Label free detection of single 
protein molecules using a single 
plasmonic particle
Conclusion 
• we can detect single molecule using label free biosensors. 
• Nanoparticle based sensors provide a useful biophysical 
tool for the interrogation of single binding events.
detection of single molecules

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detection of single molecules

  • 1. Real time detection of bio-nanoparticle using localised surface plasmon Presented by: Amit Kumar Tagore M.Tech. 1st year(1411NT02) Nanoscience & Technology IIT Patna
  • 2. Outline Why single molecule detection needed.  Detection with labels and its disadvantages.  Label free detection.  Localized Surface Plasmon Resonance of Gold Nanoparticles.  Different illumination techniques.  Conclusion.
  • 3. Why single molecule detection needed? • Virus detection is dead easy. • Early stage detection of cancer. • All dangerous disease can be detected at very early stage.
  • 4. Detection with labels Single molecule is fluroscence labeled
  • 6. Drawback of detection with labels • Fluorescent labels are necessary (destructive technique) • Not a real time detection (not useful in doctor’s office) • Extraction of virus information is impossible • Selective virus detection is difficult • Multi-virus detection is difficult
  • 7. Label free detection technique • This technique monitor inherent properties of the molecules such as mass, optical and dielectric properties. • Unlike label-based detection methods, these techniques avoid any tagging of the query molecules thereby preventing changes in structure and function. • They do not involve laborious procedures but have their own pitfalls such as sensitivity and specificity issues.
  • 8. • Fibre-optic biosensors • Fabry-Perot interferometers • Interferometric biosensors • Optical resonance of a microresonator • Localized surface plasmonic biosensors • Surface Plasmon biosensors Optical Plasmonic
  • 9. Localized Surface Plasmon Resonance • Surface Plasmon resonance (SPR) is the resonant oscillation of conduction electrons at the interface between a negative and positive permittivity material stimulated by incident light. • The resonance condition is established when the frequency of incident photons matches the natural frequency of surface electrons oscillating against the restoring force of positive nuclei. • A Localized Surface Plasmon (LSP) is the result of the confinement of a surface Plasmon in a nanoparticle of size comparable to or smaller than the wavelength of light used to excite the Plasmon. • The Plasmon resonant frequency is highly sensitive to the refractive index of the environment; a change in refractive index results in a shift in the resonant frequency.
  • 13. Localized Surface Plasmon Resonance of Gold Nanorod
  • 15.
  • 16. Single Unlabeled Protein Detection on Individual Plasmonic Nanoparticles Irene Ament,† Janak Prasad,†,‡ Andreas Henkel,† Sebastian Schmachtel,† and Carsten Sönnichsen*,† †Institute for Physical Chemistry, University of Mainz, D-55128 Mainz, Germany ‡Graduate School Materials Science in Mainz, Staudingerweg 9, D-55128 Mainz, Germany Label free detection of single protein molecules using a single plasmonic particle
  • 17. Conclusion • we can detect single molecule using label free biosensors. • Nanoparticle based sensors provide a useful biophysical tool for the interrogation of single binding events.