open access

Vol 75, No 2 (2016)
Original article
Submitted: 2015-06-20
Accepted: 2015-09-16
Published online: 2015-11-06
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Porcine liver vascular bed in Biodur E20 corrosion casts

L. Eberlova, V. Liska, H. Mirka, T. Gregor, Z. Tonar, R. Palek, M. Skala, J. Bruha, O. Vycital, K. Kalusova, S. Haviar, M. Kralickova, A. Lametschwandtner
·
Pubmed: 26542961
·
Folia Morphol 2016;75(2):154-161.

open access

Vol 75, No 2 (2016)
ORIGINAL ARTICLES
Submitted: 2015-06-20
Accepted: 2015-09-16
Published online: 2015-11-06

Abstract

Background: Pigs are frequently used as animal models in experimental medicine. To identify processes of vascular development or regression, vascular elements must be recognised and quantified in a three-dimensional (3D) arrangement. Vascular corrosion casts enable the creation of 3D replicas of vascular trees. The aim of our study was to identify suitable casting media and optimise the protocol for porcine liver vascular corrosion casting.

Materials and methods: Mercox II® (Ladd Research, Williston, Vermont, USA) and Biodur E20® Plus (Biodur Products, Heidelberg, Germany) were tested in 4 porcine livers. The resins (volume approximately 700 mL) were injected via the portal vein. Corrosion casts were examined by macro-computed tomography, micro-computed tomography and scanning electron microscopy.

Results: For hepatectomies, the operating protocol was optimised to avoid gas or blood clot embolisation. We present a protocol for porcine liver vascular bed casting based on corrosion specimens prepared using Biodur E20® epoxy resin.

Conclusions: Only Biodur E20®Plus appeared to be suitable for high-volume vascular corrosion casting due to its optimal permeability, sufficient processing time and minimum fragility. Biodur E20® Plus is slightly elastic, radio-opaque and alcohol-resistant. These properties make this acrylic resin suitable for not only vascular research but also teaching purposes.  

Abstract

Background: Pigs are frequently used as animal models in experimental medicine. To identify processes of vascular development or regression, vascular elements must be recognised and quantified in a three-dimensional (3D) arrangement. Vascular corrosion casts enable the creation of 3D replicas of vascular trees. The aim of our study was to identify suitable casting media and optimise the protocol for porcine liver vascular corrosion casting.

Materials and methods: Mercox II® (Ladd Research, Williston, Vermont, USA) and Biodur E20® Plus (Biodur Products, Heidelberg, Germany) were tested in 4 porcine livers. The resins (volume approximately 700 mL) were injected via the portal vein. Corrosion casts were examined by macro-computed tomography, micro-computed tomography and scanning electron microscopy.

Results: For hepatectomies, the operating protocol was optimised to avoid gas or blood clot embolisation. We present a protocol for porcine liver vascular bed casting based on corrosion specimens prepared using Biodur E20® epoxy resin.

Conclusions: Only Biodur E20®Plus appeared to be suitable for high-volume vascular corrosion casting due to its optimal permeability, sufficient processing time and minimum fragility. Biodur E20® Plus is slightly elastic, radio-opaque and alcohol-resistant. These properties make this acrylic resin suitable for not only vascular research but also teaching purposes.  

Get Citation

Keywords

porcine liver, vascular corrosion cast, Biodur E20, micro-computed tomography, scanning electron microscopy

About this article
Title

Porcine liver vascular bed in Biodur E20 corrosion casts

Journal

Folia Morphologica

Issue

Vol 75, No 2 (2016)

Article type

Original article

Pages

154-161

Published online

2015-11-06

Page views

2156

Article views/downloads

1841

DOI

10.5603/FM.a2015.0094

Pubmed

26542961

Bibliographic record

Folia Morphol 2016;75(2):154-161.

Keywords

porcine liver
vascular corrosion cast
Biodur E20
micro-computed tomography
scanning electron microscopy

Authors

L. Eberlova
V. Liska
H. Mirka
T. Gregor
Z. Tonar
R. Palek
M. Skala
J. Bruha
O. Vycital
K. Kalusova
S. Haviar
M. Kralickova
A. Lametschwandtner

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