Comparative Study of the Outcome of Forced Impregnation of Whole Brains at Cold Temperature, and an Alternative Diffusion/Impregnation Process

Q4 Medicine Journal of Plastination Pub Date : 2019-07-31 DOI:10.56507/rtig2240
O. Joshua, A. Olawale, F. Oluseyi, O. Sunday, O. John, Obaoye Afoluwajuwonlo
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Abstract

3 Internal Medicine, Yale University, USA ABSTRACT: Plastination is a modern method of preservation of biological specimens, including human cadavers. This study elucidated how temperature might affect plastination, noting that there is sparse scientific literature on this technique, especially from Africa. It is also relevant to the feasibility of adapting and adopting the technique as a feasible and useful laboratory technique in developing countries, where technological advancement, finance, and socio-cultural factors are suspected to be strong determinants to this effect. The S10 plastination technique is usually done at cold temperature (-25° C), but this study investigated and compared the effects of plastinating at room temperature (~25° C). The four main stages of plastination were carried for the control group while the ‘diffusion’ principle was employed for Group B. The forced impregnation process is typically carried out under vacuum at cold temperature (-25° C) with the use of an additional, relatively costly, refrigerated impregation chamber. Ten adult (n=10) human brains were randomly assigned to two groups (A and B), comprising 5 brains each. Forced impregnation of the Group A brains was performed at -25° C (cold temperature), and the ‘diffusion’ impregnation procedure was carried out for the Group B brains at 25° C (room temperature). The Group B brains required less time for draining compared to Group A. Both methods yielded brain plastinates with the basic features of plastination outcomes. The weights of the brains (g) were recorded at each stage of the process using the digital Sartorius ENTRIS 4202-1S balance. The volumes were also measured at each stage using Archimedes’ principles of fluid displacement in a calibrated glass jar (cm3). The room temperature specimens yielded better specimens in terms of relative weight loss, relative colour preservation, physical properties, and texture and preservation of surface features and brain surface topographies.
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低温下全脑强制浸渍与另一种扩散/浸渍方法的比较研究
3美国耶鲁大学内科摘要:塑化是一种现代的生物标本保存方法,包括人体尸体。这项研究阐明了温度如何影响塑化,并指出关于这项技术的科学文献很少,尤其是来自非洲的文献。这也与在发展中国家将该技术作为一种可行和有用的实验室技术进行调整和采用的可行性有关,在发展中国家,技术进步、金融和社会文化因素被怀疑是这一影响的有力决定因素。S10塑化技术通常在低温(-25°C)下进行,但本研究调查并比较了室温(~25°C)塑化的效果。对照组采用塑化的四个主要阶段,而B组采用“扩散”原理。强制浸渍过程通常在低温(-25°C)的真空下进行,并使用额外的、相对昂贵的冷藏浸渍室。10个成人(n=10)大脑被随机分配到两组(A和B),每组包括5个大脑。A组大脑的强制浸渍在-25°C(低温)下进行,B组大脑的“扩散”浸渍程序在25°C(室温)下进行。与A组相比,B组的大脑需要更少的引流时间。这两种方法都产生了具有塑化结果基本特征的大脑塑化物。使用数字Sartorius ENTRIS 4202-1S天平在该过程的每个阶段记录大脑的重量(g)。还使用阿基米德流体位移原理在校准的玻璃罐(cm3)中测量每个阶段的体积。室温标本在相对重量减轻、相对颜色保持、物理特性和纹理以及表面特征和脑表面地形的保持方面产生了更好的标本。
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来源期刊
Journal of Plastination
Journal of Plastination Health Professions-Medical Laboratory Technology
CiteScore
0.40
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0.00%
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0
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