Evidence map›Paper›PMID 31123843›Full record

ArticleAnnals of biomedical engineering2020

X-ray CT in Phase Contrast Enhancement Geometry of Alginate Microbeads in a Whole-Animal Model.

Jacob Brown, Sami Somo, Frank Brooks, Sergey Komarov, Weimin Zhou, Mark Anastasio, Eric Brey

Abstract read
In one paragraph

Article in Annals of biomedical engineering, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

7 authors.

Jacob BrownUniversity of Texas at San Antonio, San Antonio, USA. she460@my.utsa.edu.ORCID http://orcid.org/0000-0002-0422-8163
Sami SomoIllinois Institute of Technology, Chicago, USA.
Frank BrooksWashington University in St. Louis, St. Louis, USA.
Sergey KomarovWashington University in St. Louis, St. Louis, USA.
Weimin ZhouWashington University in St. Louis, St. Louis, USA.
Mark AnastasioWashington University in St. Louis, St. Louis, USA.
Eric BreyUniversity of Texas at San Antonio, San Antonio, USA.

Funding

AN ENABLING TECHNOLOGY FOR PRECLINICAL X-RAY IMAGING OF BIOMATERIALS IN-VIVOR01EB020604 · NIBIB · WASHINGTON UNIVERSITY · PI ANASTASIO, MARK A, BREY, ERIC M · 2016 to 2019
$2.3M
DEVELOPMENT OF A RAPID METHOD FOR IMAGING REGIONAL VENTILATION IN SMALL ANIMALS W/O CONTRAST AGENTSR01EB023045 · NIBIB · WASHINGTON UNIVERSITY · PI ANASTASIO, MARK A · 2017 to 2020
$1.7M
Synthetic Matrices for Vascularization of Engineered TissuesI01BX000418 · VA · EDWARD HINES JR VA HOSPITAL · PI BREY, ERIC M · 2010 to 2017
–
BLRD VA I01 BX000418Foundation for the National Institutes of Health 5R01EB020604National Science Foundation CBET-1263994National Science Foundation IIS-1125412NIBIB NIH HHS R01 EB020604NIBIB NIH HHS R01 EB023045U.S. Department of Veterans Affairs 5 I01 BX000418-06
6 · The paper itself

Abstract

Imaging soft biomaterials in vivo is a significant challenge, as most conventional techniques are limited by biomaterial contrast, penetration depth, or spatial resolution. Exogeneous contrast agents used to increase contrast may also alter material properties or exhibit local toxicity. The capability to observe biomaterial constructs in vivo without introducing exogenous contrast would improve preclinical testing and evaluation. Conventional X-ray Computed Tomography allows fast, high-resolution imaging at high penetration depth, but biomaterial contrast is low. Previous studies employing X-ray phase contrast (XPC) and utilizing a synchrotron source provided support for the significant potential of XPC in imaging biomaterials without contrast agents. In this study, XPC tomography was used to image alginate hydrogel microspheres within a small animal omental pouch model using a commercially available X-ray source. Multilayer microbeads could be identified in the XPC images with volumetric and structural information not possible in histological analysis. The number of microbeads present and microbead volume and diameter could be quantified from the images. The results of this study show that XPC tomography can be a useful tool for monitoring of implanted soft biomaterials in small animal models.

Indexed as

AlginatesBiocompatible MaterialsMicrospheresAnimalsHydrogelsMaleOmentumRats, Sprague-DawleyTomography, X-Ray ComputedAlginatesBiocompatible MaterialsHydrogelsAlginateMicrobeadsTomographyXPC

Identifiers

PMID31123843
PMCPMC6874731

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Registered trials

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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.