File Download
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1117/12.2038766
- Scopus: eid_2-s2.0-84901779012
- WOS: WOS:000336037200050
- Find via
Supplementary
- Citations:
- Appears in Collections:
Conference Paper: Revisit laser scanning fluorescence microscopy performance under fluorescence-lifetime-limited regime
Title | Revisit laser scanning fluorescence microscopy performance under fluorescence-lifetime-limited regime |
---|---|
Authors | |
Keywords | Image resolution Laser scanning fluorescence microscopy Signal-to-noise ratio Speed limit |
Issue Date | 2014 |
Publisher | SPIE - International Society for Optical Engineering. |
Citation | Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XII, San Francisco, CA, 3-6 February 2014. In Proceedings of SPIE, 2014, v. 8947, article no. 894726 How to Cite? |
Abstract | Continuing desire for higher-speed laser scanning fluorescence microscopy (LSFM) and progressive advancement in ultrafast and sensitive photodetectors might imply that our conventional understanding of LSFM is not adequate when approaching to the intrinsic speed limit - fluorescence lifetime. In this regard, we here revisit the theoretical framework of LSFM and evaluate its general performance in lifetime-limited and noise-limited regimes. Our model suggests that there still exists an order-of-magnitude gap between the current LSFM speed and the intrinsic limit. An imaging frame rate of > 100 kHz could be viable with the emerging laser-scanning techniques using ultrafast wavelength-swept sources, or optical time-stretch. © 2014 SPIE. |
Persistent Identifier | http://hdl.handle.net/10722/201229 |
ISBN | |
ISSN | 2023 SCImago Journal Rankings: 0.226 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chan, ACS | en_US |
dc.contributor.author | Wong, TTW | en_US |
dc.contributor.author | Wong, KKY | en_US |
dc.contributor.author | Lam, EYM | en_US |
dc.contributor.author | Tsia, KKM | en_US |
dc.date.accessioned | 2014-08-21T07:18:17Z | - |
dc.date.available | 2014-08-21T07:18:17Z | - |
dc.date.issued | 2014 | en_US |
dc.identifier.citation | Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XII, San Francisco, CA, 3-6 February 2014. In Proceedings of SPIE, 2014, v. 8947, article no. 894726 | en_US |
dc.identifier.isbn | 978-081949860-1 | - |
dc.identifier.issn | 1605-7422 | - |
dc.identifier.uri | http://hdl.handle.net/10722/201229 | - |
dc.description.abstract | Continuing desire for higher-speed laser scanning fluorescence microscopy (LSFM) and progressive advancement in ultrafast and sensitive photodetectors might imply that our conventional understanding of LSFM is not adequate when approaching to the intrinsic speed limit - fluorescence lifetime. In this regard, we here revisit the theoretical framework of LSFM and evaluate its general performance in lifetime-limited and noise-limited regimes. Our model suggests that there still exists an order-of-magnitude gap between the current LSFM speed and the intrinsic limit. An imaging frame rate of > 100 kHz could be viable with the emerging laser-scanning techniques using ultrafast wavelength-swept sources, or optical time-stretch. © 2014 SPIE. | - |
dc.language | eng | en_US |
dc.publisher | SPIE - International Society for Optical Engineering. | - |
dc.relation.ispartof | Progress in Biomedical Optics and Imaging: Proceedings of the SPIE | en_US |
dc.rights | Copyright 2014 Society of Photo‑Optical Instrumentation Engineers (SPIE). One print or electronic copy may be made for personal use only. Systematic reproduction and distribution, duplication of any material in this publication for a fee or for commercial purposes, and modification of the contents of the publication are prohibited. This article is available online at https://doi.org/10.1117/12.2038766 | - |
dc.subject | Image resolution | - |
dc.subject | Laser scanning fluorescence microscopy | - |
dc.subject | Signal-to-noise ratio | - |
dc.subject | Speed limit | - |
dc.title | Revisit laser scanning fluorescence microscopy performance under fluorescence-lifetime-limited regime | en_US |
dc.type | Conference_Paper | en_US |
dc.identifier.email | Wong, KKY: kywong04@hkucc.hku.hk | en_US |
dc.identifier.email | Lam, EYM: elam@eee.hku.hk | en_US |
dc.identifier.email | Tsia, KKM: tsia@hku.hk | en_US |
dc.identifier.authority | Wong, KKY=rp00189 | en_US |
dc.identifier.authority | Lam, EYM=rp00131 | en_US |
dc.identifier.authority | Tsia, KKM=rp01389 | en_US |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1117/12.2038766 | - |
dc.identifier.scopus | eid_2-s2.0-84901779012 | - |
dc.identifier.hkuros | 233699 | en_US |
dc.identifier.volume | 8947 | - |
dc.identifier.spage | article no. 894726 | - |
dc.identifier.epage | article no. 894726 | - |
dc.identifier.isi | WOS:000336037200050 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1605-7422 | - |