Evidence map›Paper›PMID 29317375›Full record

ArticleDiagnostic and interventional radiology (Ankara, Turkey)

Does doxorubicin survive thermal ablation? Results of an ex vivo bench top study.

Joseph D Morrison, Collin K Schlager, Amanda E Lee, Richard B van Breemen, Ron C Gaba

Abstract read
In one paragraph

Article in Diagnostic and interventional radiology (Ankara, Turkey). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Joseph D MorrisonDepartment of Radiology, University of Illinois College of Medicine, Chicago, Illinois, USA.
Collin K SchlagerDivision of Interventional Radiology, University of Illinois College of Medicine, Chicago, Illinois, USA.
Amanda E LeeDepartment of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois Hospital and Health Sciences System, Chicago, IL, USA.
Richard B van BreemenDepartment of Medicinal Chemistry and Pharmacognosy, College of Pharmacy, University of Illinois Hospital and Health Sciences System, Chicago, IL, USA.
Ron C GabaDivision of Interventional Radiology, University of Illinois College of Medicine, Chicago, Illinois, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe aimed to test the hypothesis that doxorubicin (DOX) survives thermal ablative heating in an ex vivo model of combined transarterial chemoembolization (TACE) and thermal ablation.

methodsFresh porcine psoas major muscle (3 samples, 15×10×3 cm) was submerged in aqueous DOX solution (60 µg/mL, 0.1 M) for 24 hours to passively saturate tissue. DOX-infused tissue was then dried and treated with microwave ablation (MWA) using a 2.45 GHz antenna at 65 W for 2, 5, and 10 minutes. Ablations were repeated in triplicate (9 total). Tissue was then sampled at both ablated and unablated control sites, and DOX concentration was quantified via ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS), with samples analyzed in triplicate. Tissue DOX levels in ablation and control groups were compared using one-way ANOVA.

resultsHomogeneous DOX uptake into porcine tissue was evident in all three samples. Mean DOX concentration in unablated tissue was 8.0±2.2 µg/mL. MWA was technically successful in all 9 procedures (100%), with tissue heating to 95-100°C. Mean tissue DOX concentration showed progressive reduction with increasing ablation time, measuring 6.7±1.3, 4.9±0.9, and 4.8±1.3 µg/mL in MWA-treated tissue after 2, 5, and 10 minutes, respectively. Differences in tissue DOX levels between unablated tissue and MWA groups were statistically significant (P < 0.001).

conclusionContrary to the initial hypothesis, tissue DOX concentration progressively decreased after MWA of longer ablation times. These results suggest that TACE followed by ablation may result in lower intratumoral DOX than would otherwise be anticipated for TACE alone.

Indexed as

Catheter AblationChemoembolization, TherapeuticAnimalsAntibiotics, AntineoplasticChromatography, LiquidDoxorubicinMuscle, SkeletalSwineTandem Mass SpectrometryAntibiotics, AntineoplasticDoxorubicin

Identifiers

PMID29317375
PMCPMC5765925

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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.