New Alcohol and Onyx Mixture for Embolization: Feasibility and Proof of Concept in Both In Vitro and In Vivo Models
Creators
- 1. Centre Hospitalier Universitaire (CHRU) de Lille, Hôpital cardiologique (France)
- 2. école de technologie supérieure (ETS) & CHUM Research center (CRCHUM), Department of Mechanical Engineering (Canada)
- 3. Centre Hospitalier de l'Université de Montréal, Department of Radiology (Canada)
- 4. University Hospital Timone, Department of Medical Imaging (France)
- 5. King Faisal Specialist Hospital and Research Center, Radiology Department (Saudi Arabia)
Description
IntroductionOnyx and ethanol are well-known embolic and sclerotic agents that are frequently used in embolization. These agents present advantages and disadvantages regarding visibility, injection control and penetration depth. Mixing both products might yield a new product with different characteristics. The aim of this study is to evaluate the injectability, radiopacity, and mechanical and occlusive properties of different mixtures of Onyx 18 and ethanol in vitro and in vivo (in a swine model).Materials and MethodsVarious Onyx 18 and ethanol formulations were prepared and tested in vitro for their injectability, solidification rate and shrinkage, cohesion and occlusive properties. In vivo tests were performed using 3 swine. Ease of injection, radiopacity, cohesiveness and penetration were analyzed using fluoroscopy and high-resolution CT.ResultsAll mixtures were easy to inject through a microcatheter with no resistance or blockage in vitro and in vivo. The 50%-ethanol mixture showed delayed copolymerization with fragmentation and proximal occlusion. The 75%-ethanol mixture showed poor radiopacity in vivo and was not tested in vitro. The 25%-ethanol mixture showed good occlusive properties and accepted penetration and radiopacity.ConclusionMixing Onyx and ethanol is feasible. The mixture of 25% of ethanol and 75% of Onyx 18 could be a new sclero-embolic agent. Further research is needed to study the chemical changes of the mixture, to confirm the significance of the added sclerotic effect and to find out the ideal mixture percentages.
Additional details
Identifiers
Publishing Information
- Journal Title
- Cardiovascular and Interventional Radiology
- Journal Volume
- 40
- Journal Issue
- 5
- Journal Page Range
- p. 735-743
- ISSN
- 0174-1551
- CODEN
- CAIRDG
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48093816
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- COMPUTERIZED TOMOGRAPHY; COPOLYMERIZATION; FLUOROSCOPY; IN VITRO; IN VIVO; INJECTION; PENETRATION DEPTH; SHRINKAGE; SOLIDIFICATION; SWINE; VASCULAR DISEASES; VISIBILITY
- Descriptors DEC
- ANIMALS; BIOMEDICAL RADIOGRAPHY; CARDIOVASCULAR DISEASES; CHEMICAL REACTIONS; DIAGNOSTIC TECHNIQUES; DISEASES; DOMESTIC ANIMALS; INTAKE; MAMMALS; MEDICINE; NUCLEAR MEDICINE; PHASE TRANSFORMATIONS; POLYMERIZATION; RADIOLOGY; TOMOGRAPHY; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2017 Springer Science+Business Media New York and the Cardiovascular and Interventional Radiological Society of Europe (CIRSE)
- Notes
- http://www.springer-ny.com