Abstract
We have studied fluorescence cellular imaging with randomly distributed localized near-field induced by silver nanoislands. For the fabrication of nanoislands, a 10-nm silver thin film evaporated on a BK7 glass substrate with an adhesion layer of 2-nm thick chromium. Micrometer sized silver square pattern was defined using e-beam lithography and then the film was annealed at ∼ 200°C. Raw images were restored using electric field distribution produced on the surface of random nanoislands. Nanoislands were modeled from SEM images. 488-nm p-polarized light source was set to be incident at 60°. Simulation results show that localized electric fields were created among nanoislands and that their average size was found to be ∼135 nm. The feasibility was tested using conventional total internal reflection fluorescence microscopy while the angle of incidence was adjusted to maximize field enhancement. Mouse microphage cells were cultured on nanoislands, and actin filaments were selectively stained with FITC-conjugated phalloidin. Acquired images were deconvolved based on linear imaging theory, in which molecular distribution was sampled by randomly distributed localized near-field and blurred by point spread function of far-field optics. The optimum fluorophore distribution was probabilistically estimated by repetitively matching a raw image. The deconvolved images are estimated to have a resolution in the range of 100-150 nm largely determined by the size of localized near-fields. We also discuss and compare the results with images acquired with periodic nanoaperture arrays in various optical configurations to excite localized plasmonic fields and to produce superresolved molecular images.
| Original language | English |
|---|---|
| Title of host publication | Plasmonics in Biology and Medicine XIV |
| Publisher | SPIE |
| Volume | 10080 |
| ISBN (Electronic) | 9781510606012 |
| DOIs | |
| Publication status | Published - 2017 Jan 1 |
| Event | Plasmonics in Biology and Medicine XIV - San Francisco, United States Duration: 2017 Jan 30 → … |
Other
| Other | Plasmonics in Biology and Medicine XIV |
|---|---|
| Country | United States |
| City | San Francisco |
| Period | 17/1/30 → … |
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All Science Journal Classification (ASJC) codes
- Electronic, Optical and Magnetic Materials
- Biomaterials
- Atomic and Molecular Physics, and Optics
- Radiology Nuclear Medicine and imaging
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Localized surface plasmon enhanced cellular imaging using random metallic structures. / Son, Taehwang; Lee, Wonju; Kim, Donghyun.
Plasmonics in Biology and Medicine XIV. Vol. 10080 SPIE, 2017. 100800E.Research output: Chapter in Book/Report/Conference proceeding › Conference contribution
TY - GEN
T1 - Localized surface plasmon enhanced cellular imaging using random metallic structures
AU - Son, Taehwang
AU - Lee, Wonju
AU - Kim, Donghyun
PY - 2017/1/1
Y1 - 2017/1/1
N2 - We have studied fluorescence cellular imaging with randomly distributed localized near-field induced by silver nanoislands. For the fabrication of nanoislands, a 10-nm silver thin film evaporated on a BK7 glass substrate with an adhesion layer of 2-nm thick chromium. Micrometer sized silver square pattern was defined using e-beam lithography and then the film was annealed at ∼ 200°C. Raw images were restored using electric field distribution produced on the surface of random nanoislands. Nanoislands were modeled from SEM images. 488-nm p-polarized light source was set to be incident at 60°. Simulation results show that localized electric fields were created among nanoislands and that their average size was found to be ∼135 nm. The feasibility was tested using conventional total internal reflection fluorescence microscopy while the angle of incidence was adjusted to maximize field enhancement. Mouse microphage cells were cultured on nanoislands, and actin filaments were selectively stained with FITC-conjugated phalloidin. Acquired images were deconvolved based on linear imaging theory, in which molecular distribution was sampled by randomly distributed localized near-field and blurred by point spread function of far-field optics. The optimum fluorophore distribution was probabilistically estimated by repetitively matching a raw image. The deconvolved images are estimated to have a resolution in the range of 100-150 nm largely determined by the size of localized near-fields. We also discuss and compare the results with images acquired with periodic nanoaperture arrays in various optical configurations to excite localized plasmonic fields and to produce superresolved molecular images.
AB - We have studied fluorescence cellular imaging with randomly distributed localized near-field induced by silver nanoislands. For the fabrication of nanoislands, a 10-nm silver thin film evaporated on a BK7 glass substrate with an adhesion layer of 2-nm thick chromium. Micrometer sized silver square pattern was defined using e-beam lithography and then the film was annealed at ∼ 200°C. Raw images were restored using electric field distribution produced on the surface of random nanoislands. Nanoislands were modeled from SEM images. 488-nm p-polarized light source was set to be incident at 60°. Simulation results show that localized electric fields were created among nanoislands and that their average size was found to be ∼135 nm. The feasibility was tested using conventional total internal reflection fluorescence microscopy while the angle of incidence was adjusted to maximize field enhancement. Mouse microphage cells were cultured on nanoislands, and actin filaments were selectively stained with FITC-conjugated phalloidin. Acquired images were deconvolved based on linear imaging theory, in which molecular distribution was sampled by randomly distributed localized near-field and blurred by point spread function of far-field optics. The optimum fluorophore distribution was probabilistically estimated by repetitively matching a raw image. The deconvolved images are estimated to have a resolution in the range of 100-150 nm largely determined by the size of localized near-fields. We also discuss and compare the results with images acquired with periodic nanoaperture arrays in various optical configurations to excite localized plasmonic fields and to produce superresolved molecular images.
UR - http://www.scopus.com/inward/record.url?scp=85019226508&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85019226508&partnerID=8YFLogxK
U2 - 10.1117/12.2251763
DO - 10.1117/12.2251763
M3 - Conference contribution
AN - SCOPUS:85019226508
VL - 10080
BT - Plasmonics in Biology and Medicine XIV
PB - SPIE
ER -