Evidence map›Paper›PMID 37532922›Full record

ArticleEuropean radiology experimental2023

A microCT-based platform to quantify drug targeting.

Brandon J Ausk, Adam N Tucker, Philippe Huber, Reza Firoozabadi, Jeffrey M Gross, Ted S Gross, Steven D Bain

Open access · goldAbstract read
In one paragraph

Article in European radiology experimental, 2023. 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
0.2field-weighted citation impact, top 40% of its field
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 citations in OpenAlex.

  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 at 3 institutions in 2 countries.

Brandon J AuskIn Situ Therapeutic Solutions Inc, Seattle, USA. brandon.ausk@istherasol.com.ORCID 0000-0003-3533-8303
Adam N TuckerDepartment of Orthopaedics and Sports Medicine, University of Washington, Seattle, USA.
Philippe HuberDepartment of Orthopaedics and Sports Medicine, University of Washington, Seattle, USA.
Reza FiroozabadiDepartment of Orthopaedics and Sports Medicine, University of Washington, Seattle, USA.
Jeffrey M GrossIn Situ Therapeutic Solutions Inc, Seattle, USA.
Ted S GrossDepartment of Orthopaedics and Sports Medicine, University of Washington, Seattle, USA.
Steven D BainDepartment of Orthopaedics and Sports Medicine, University of Washington, Seattle, USA.
University of Washington · USBrandon University · CASeattle University · US

Funding

A Device to Inhibit Heterotopic OssificationR41AR074337 · NIAMS · IN SITU THERAPEUTIC SOLUTIONS, INC. · PI BAIN, STEVEN D, GROSS, JEFFREY · 2019 to 2019
$225k
NIAMS NIH HHS R41 AR074337
6 · The paper itself

Abstract

backgroundHeterotopic ossification (HO) is a frequent and debilitating complication of traumatic musculoskeletal injuries and orthopedic procedures. Prophylactic dosing of botulinum toxin type A (BTxA) holds potential as a novel treatment option if accurately distributed throughout soft-tissue volumes where protection is clinically desired. We developed a high-resolution, microcomputed tomography (microCT)-based imaging strategy to assess drug distribution and validated this platform by quantifying distribution achieved via a prototype delivery system versus a single-bolus injection.

methodsWe injected an iodine-containing contrast agent (iodixanol 320 mg I/mL) into dissected rabbit musculature followed by microCT imaging and analysis. To contrast the performance of distributed versus bolus injections, a three-dimensional (3D) 64-cm

resultsThe microCT-based approach enabled high-resolution quantification of injection distribution within soft tissue. The distributed dosing prototype provided significantly greater tissue coverage of the targeted VOI (72 ± 3%, mean ± standard deviation) when compared to an equal volume bolus dose (43 ± 5%, p = 0.031) while also enhancing the precision of injection targeting.

conclusionsA microCT-based imaging technique precisely quantifies drug distribution within a soft-tissue VOI, providing a path to overcome a barrier for clinical translation of prophylactic inhibition of HO by BTxA. RELEVANCE STATEMENT: This platform will facilitate rapid optimization of injection parameters for clinical devices used to effectively and safely inhibit the formation of heterotopic ossification. KEY POINTS: • MicroCT provides high-resolution quantification of soft-tissue drug distribution. • Distributed dosing is required to maximize soft-tissue drug coverage. • Imaging platform will enable rapid screening of 3D-printed drug distribution prototypes.

Indexed as

IodineOssification, HeterotopicAnimalsDrug Delivery SystemsRabbitsX-Ray MicrotomographyIodineDrug delivery systemsOrthopedicsOssification (heterotopic)RabbitsX-ray microtomography

Identifiers

PMID37532922
PMCPMC10397158
OpenAlexW4385480005

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.