Evidence map›Paper›PMID 42175758›Full record

ArticleTissue engineering. Part A2026

Functional Imaging for Regenerative Medicine: Tracking Vascularization of Intestinal Scaffolds.

Jared A Weis, Mani Ratnam Kothamasu, Nildris Cruz-Diaz, Marshall Z Schwartz, Anthony Atala, Mitchell R Ladd

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2026. 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

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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

5 · Who and what money

Authors and funding

6 authors.

Jared A WeisDepartment of Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Mani Ratnam KothamasuWake Forest Institute for Regenerative Medicine, Winston-Salem, North Carolina, USA.
Nildris Cruz-DiazDepartment of Surgery/Hypertension and Vascular Research Center, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Marshall Z SchwartzWake Forest Institute for Regenerative Medicine, Winston-Salem, North Carolina, USA.
Anthony AtalaDepartment of Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.
Mitchell R LaddDepartment of Biomedical Engineering, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.ORCID 0000-0001-5312-8452

Funding

Wake Forest Clinical and Translational Science AwardUL1TR001420 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ARD, JAMY D, FOLEY, KRISTIE L · 2015 to 2023
$32.3M
CTSA K12 Program at Wake ForestK12TR004931 · NCATS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Nicholette D. Allred · 2024 to 2026
$2.3M
Photoacoustic Imaging for Biophysical Physiological Indicators of Neonatal Intestinal Health and Necrotizing EnterocolitisR01DK135955 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Jared Anthony Weis · 2024 to 2026
$1.2M
NCATS NIH HHS K12 TR004931NCATS NIH HHS UL1 TR001420NIDDK NIH HHS R01 DK135955
6 · The paper itself

Abstract

Traditional approaches to tissue-engineered small intestine (TESI) require implanting a construct in the omentum of the abdominal cavity to allow for vascularization of the construct and tissue maturation. A second operation is then needed to implant the construct in continuity with the intestine. The timing of the second operation has historically been chosen based on predetermined biological endpoints. Currently, no well-validated method has been used to noninvasively monitor for vascular maturity which would better inform when the second operation should be performed. We hypothesized that photoacoustic imaging (PAI) could serve as a tool to noninvasively monitor regional and temporal changes in vascular maturity in scaffolds implanted in the omentum. For this pilot study, tubular scaffolds used for TESI were fabricated with electrospinning and implanted in the omentum of Sprague-Dawley rats for 1 and 2 months. Scaffolds were imaged with PAI and tissue oxygenation and hemoglobin concentration were quantified. PAI was then correlated with gross observations of vascularization at each time point. PAI was able to determine regional and temporal changes in tissue oxygenation and hemoglobin concentration. Specifically, the oxygenation and hemoglobin concentration of the top wall of the construct showed better vascular maturity compared with the bottom wall. In addition, vascular maturity seemed to improve in the top wall from 1 to 2 months. The bottom wall was not well covered by the omentum and thus did not vascularize as well as the top wall. The PAI findings were confirmed on gross examination of the scaffolds and upon quantification of the histological analysis of endothelial cell density. Thus, PAI may serve as a critical tool for monitoring vascular maturity in TE, specifically within the abdomen. This will be a critical tool in the preclinical development and clinical translation of TESI.Impact StatementImaging methods to track functional changes in tissue-engineered constructs are need. These critical tools will be essential for tissue-engineered small intestine (TESI) development and clinical translation. In particular, understanding when a TESI construct has achieved vascular maturity is required prior to placing the TESI in connection with native intestine. In this proof-of-concept study, we have shown that photoacoustic imaging can be used to noninvasively track construct vascular maturity and that the imaging correlates with end-point histology. In addition to TESI, this tool is broadly applicable to all tissue-engineered constructs.

Indexed as

functional imagingphotoacoustic imagingsmall intestinetissue engineering

Identifiers

PMID42175758
PMCPMC13659823

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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.