Evidence map›Paper›PMID 29706682›Full record

ArticleProceedings of SPIE--the International Society for Optical Engineering2017

Fast axial scanning for 2-photon microscopy using liquid lens technology.

Kayvan Forouhesh Tehrani, Min Kyoung Sun, Lohitash Karumbaiah, Luke J Mortensen

Abstract read
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Article in Proceedings of SPIE--the International Society for Optical Engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Kayvan Forouhesh TehraniRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Min Kyoung SunRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Lohitash KarumbaiahRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.
Luke J MortensenRegenerative Bioscience Center, Rhodes Center for ADS, University of Georgia, Athens, GA 30602, USA.

Funding

Creating Endogenous Stem Cell Niches to Promote Functional Brain Repair Post-TBIR01NS099596 · NINDS · UNIVERSITY OF GEORGIA · PI KARUMBAIAH, LOHITASH · 2017 to 2021
$1.6M
NINDS NIH HHS R01 NS099596
6 · The paper itself

Abstract

Scanning microscopy methods require movement of the focus in Z coordinates to produce an image of a 3-dimensional volume. In a typical imaging system, the optical setup is kept fixed and either the sample or the objective is translated with a mechanical stage driven by a stepper motor or a piezoelectric element. Mechanical Z scanning is precise, but its slow response and vulnerability to mechanical vibrations and stress make it disadvantageous to image dynamic, time-varying samples such as live cell structures. An alternative method less susceptible to these problems is to change the focal plane using conjugate optics. Deformable mirrors, acoustooptics, and electrically tunable lenses have been experimented with to achieve this goal and have attained very fast and precise Z-scanning without physically moving the sample. Here, we present the use of a liquid lens for fast axial scanning. Liquid lenses have a long functional life, high degree of phase shift, and low sensitivity to mechanical stress. They work on the principle of refraction at a liquid-liquid interface. At the boundary of a polar and an apolar liquid a spherical surface is formed whose curvature can be controlled by adjusting its relative wettability using electrowetting. We characterize the effects of the lens on attainable Z displacement, beam spectral characteristics, and pulse duration as compared with mechanical scanning.

Indexed as

Active opticsLiquid lensMulti-photon microscopyRemote focusing

Identifiers

PMID29706682
PMCPMC5918272

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.