Label-free CARS microscopy through a multimode fiber endoscope
Optics Express, ISSN: 1094-4087, Vol: 27, Issue: 21, Page: 30055-30066
2019
- 72Citations
- 73Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations72
- Citation Indexes72
- 72
- CrossRef62
- Captures73
- Readers73
- 73
Article Description
Multimode fibres have recently been employed as high-resolution ultra-thin endoscopes, capable of imaging biological structures deep inside tissue in vivo. Here, we extend this technique to label-free non-linear microscopy with chemical contrast using coherent anti-Stokes Raman scattering (CARS) through a multimode fibre endoscope, which opens up new avenues for instant and in-situ diagnosis of potentially malignant tissue. We use a commercial 125 µm diameter, 0.29 NA GRIN fibre, and wavefront shaping on an SLM is used to create foci that are scanned behind the fibre facet across the sample. The chemical selectivity is demonstrated by imaging 2 µm polystyrene and 2.5 µm PMMA beads with per pixel integration time as low as 1 ms for epi-detection.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85073542251&origin=inward; http://dx.doi.org/10.1364/oe.27.030055; http://www.ncbi.nlm.nih.gov/pubmed/31684259; https://opg.optica.org/abstract.cfm?URI=oe-27-21-30055; https://oa.tib.eu/renate/handle/123456789/4800; https://dx.doi.org/10.1364/oe.27.030055; https://opg.optica.org/oe/abstract.cfm?uri=oe-27-21-30055; http://dx.doi.org/10.34657/71; https://dx.doi.org/10.34657/71; https://opg.optica.org/abstract.cfm?uri=oe-27-21-30055; https://opg.optica.org/viewmedia.cfm?uri=oe-27-21-30055&seq=0&html=true; https://opg.optica.org/viewmedia.cfm?uri=oe-27-21-30055&seq=0; https://oa.tib.eu/renate/bitstream/123456789/4800/1/Label-free%20CARS%20microscopy%20through%20a%20multimode%20fiber%20endoscope.pdf; https://www.osapublishing.org/abstract.cfm?URI=oe-27-21-30055; https://www.osapublishing.org/oe/abstract.cfm?uri=oe-27-21-30055; https://oar.tib.eu/jspui/handle/123456789/4800; https://www.osapublishing.org/oe/fulltext.cfm?uri=oe-27-21-30055&id=421966
Optica Publishing Group
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