» Articles » PMID: 20574721

Improved Detection of Fluorescently Labeled Microspheres and Vessel Architecture with an Imaging Cryomicrotome

Overview
Publisher Springer
Date 2010 Jun 25
PMID 20574721
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Due to spectral overlap, the number of fluorescent labels for imaging cryomicrotome detection was limited to 4. The aim of this study was to increase the separation of fluorescent labels. In the new imaging cryomicrotome, the sample is cut in slices of 40 microm. Six images are taken for each cutting plane. Correction for spectral overlap is based on linear combinations of fluorescent images. Locations of microspheres are determined by using the system point spread function. Five differently colored microspheres were injected in vivo distributed over two major coronaries, the left anterior descending and left circumflex artery. Under absence of collateral flow, microspheres outside of target perfusion territories were not found and the procedure did not generate false positive detection when spectral overlap was relevant. In silico-generated microspheres were used to test the effect of background image, transparency correction, and color separation. The percentage of microspheres undetected was 2.3 +/- 0.8% in the presence and 1.5 +/- 0.4% in the absence of background structures with a density of 900 microspheres per color per cm(3). The image analysis method presented here, allows for an increased number of experimental conditions that can be investigated in studies of regional myocardial perfusion.

Citing Articles

Virtual Fluorescence Translation for Biological Tissue by Conditional Generative Adversarial Network.

Liu X, Li B, Liu C, Ta D Phenomics. 2023; 3(4):408-420.

PMID: 37589024 PMC: 10425324. DOI: 10.1007/s43657-023-00094-1.


Optimal slice thickness for improved accuracy of quantitative analysis of fluorescent cell and microsphere distribution in cryo-images.

Wuttisarnwattana P, Eck B, Gargesha M, Wilson D Sci Rep. 2023; 13(1):10907.

PMID: 37407807 PMC: 10322852. DOI: 10.1038/s41598-023-37927-y.


Spleen Tissue Segmentation Algorithm for Cryo-Imaging Data.

Wuttisarnwattana P, Auephanwiriyakul S J Digit Imaging. 2022; 36(2):588-602.

PMID: 36441277 PMC: 10039202. DOI: 10.1007/s10278-022-00736-2.


Developing a novel hyperspectral imaging cryomacrotome for whole body fluorescence imaging.

Meng B, Byrd B, Wirth D, Strawbridge R, Davis S Proc SPIE Int Soc Opt Eng. 2021; 11219.

PMID: 34446979 PMC: 8386500. DOI: 10.1117/12.2544497.


Hyperspectral imaging and spectral unmixing for improving whole-body fluorescence cryo-imaging.

Wirth D, Byrd B, Meng B, Strawbridge R, Samkoe K, Davis S Biomed Opt Express. 2021; 12(1):395-408.

PMID: 33520389 PMC: 7818953. DOI: 10.1364/BOE.410810.


References
1.
van den Wijngaard J, Horssen P, ter Wee R, Coronel R, de Bakker J, de Jonge N . Organization and collateralization of a subendocardial plexus in end-stage human heart failure. Am J Physiol Heart Circ Physiol. 2009; 298(1):H158-62. DOI: 10.1152/ajpheart.00654.2009. View

2.
Hales J, CLIFF W . Direct observations of the behaviour of microspheres in microvasculature. Bibl Anat. 1977; (15 Pt 1):87-91. View

3.
Bernard S, Ewen J, BARLOW C, Kelly J, McKinney S, Frazer D . High spatial resolution measurements of organ blood flow in small laboratory animals. Am J Physiol Heart Circ Physiol. 2000; 279(5):H2043-52. DOI: 10.1152/ajpheart.2000.279.5.H2043. View

4.
van Oosterhout M, Willigers H, Reneman R, Prinzen F . Fluorescent microspheres to measure organ perfusion: validation of a simplified sample processing technique. Am J Physiol. 1995; 269(2 Pt 2):H725-33. DOI: 10.1152/ajpheart.1995.269.2.H725. View

5.
McDevitt D, Nies A . Simultaneous measurement of cardiac output and its distribution with microspheres in the rat. Cardiovasc Res. 1976; 10(4):494-8. DOI: 10.1093/cvr/10.4.494. View