{"title":"人脑切片P40塑化:不同浸泡和浸渍条件的比较","authors":"M. Șora, P. Brugger, H. Traxler","doi":"10.56507/xlsj5724","DOIUrl":null,"url":null,"abstract":"One human brain was used for this study. The brain was fixed in 5% formalin for two months, rinced and cut in two halves on the sagital plane. Both brain halves were sagitally sliced at a tickness of 4 mm. From each brain half we selected 8 slices and plastinated them with P40 using different immersion and impregnation conditions. Two points were marked on each slice and subsequently an imprint of the slices was drawn on transparency film. After dehydration in -25°C acetone, the slices of the left brain half were immersed at -25°C, for two days in P40 and then impregnated for 24 hours. The slices of the right brain half were immersed at +5°C for two days and impregnated at room temperature at+15°C for 24 hours. All impregnated slices were cured with UV light. The imprints of the fixed brain slices were scanned into a computer, as well as the plastinated slices. By using a Kontron KSA 400 v. 2.0 (ZEISS) software we calculated the area of the plastinated brain slices as well as the area of the scanned imprints. By comparing the obtained data we were able to determine the shrinkage rate of the slices. The slices processed at -25°C showed a shrinkage rate of 4.41%. In comparison the slices immersed at +5°C and impregnated at +15°C showed a shrinkage rate of 6.96%.","PeriodicalId":343741,"journal":{"name":"Journal of the International Society for Plastination","volume":"83 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1999-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"15","resultStr":"{\"title\":\"P40 Plastination of Human Brain Slices: Comparison between Different Immersion and Impregnation Conditions\",\"authors\":\"M. Șora, P. Brugger, H. Traxler\",\"doi\":\"10.56507/xlsj5724\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"One human brain was used for this study. The brain was fixed in 5% formalin for two months, rinced and cut in two halves on the sagital plane. Both brain halves were sagitally sliced at a tickness of 4 mm. From each brain half we selected 8 slices and plastinated them with P40 using different immersion and impregnation conditions. Two points were marked on each slice and subsequently an imprint of the slices was drawn on transparency film. After dehydration in -25°C acetone, the slices of the left brain half were immersed at -25°C, for two days in P40 and then impregnated for 24 hours. The slices of the right brain half were immersed at +5°C for two days and impregnated at room temperature at+15°C for 24 hours. All impregnated slices were cured with UV light. The imprints of the fixed brain slices were scanned into a computer, as well as the plastinated slices. By using a Kontron KSA 400 v. 2.0 (ZEISS) software we calculated the area of the plastinated brain slices as well as the area of the scanned imprints. By comparing the obtained data we were able to determine the shrinkage rate of the slices. The slices processed at -25°C showed a shrinkage rate of 4.41%. In comparison the slices immersed at +5°C and impregnated at +15°C showed a shrinkage rate of 6.96%.\",\"PeriodicalId\":343741,\"journal\":{\"name\":\"Journal of the International Society for Plastination\",\"volume\":\"83 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1999-07-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"15\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of the International Society for Plastination\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.56507/xlsj5724\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the International Society for Plastination","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.56507/xlsj5724","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 15
摘要
这项研究使用了一个人的大脑。大脑在5%的福尔马林中固定两个月,在矢状平面上冲洗并切成两半。两半脑矢状切片,厚度为4mm。每半脑各取8片,用P40在不同浸泡和浸渍条件下塑化。在每个切片上标记两个点,然后在透明薄膜上绘制切片的印记。左脑切片-25℃丙酮脱水后,-25℃P40浸泡2天,浸渍24小时。右脑切片+5℃浸泡2天,+15℃室温浸渍24小时。所有浸渍片都用紫外光固化。固定脑切片的印记和塑化脑切片一样被扫描到电脑中。通过使用Kontron KSA 400 v. 2.0(蔡司)软件,我们计算了塑化脑切片的面积以及扫描印迹的面积。通过比较得到的数据,我们能够确定薄片的收缩率。在-25℃下加工的薄片收缩率为4.41%。+5℃浸渍和+15℃浸渍试样的收缩率为6.96%。
P40 Plastination of Human Brain Slices: Comparison between Different Immersion and Impregnation Conditions
One human brain was used for this study. The brain was fixed in 5% formalin for two months, rinced and cut in two halves on the sagital plane. Both brain halves were sagitally sliced at a tickness of 4 mm. From each brain half we selected 8 slices and plastinated them with P40 using different immersion and impregnation conditions. Two points were marked on each slice and subsequently an imprint of the slices was drawn on transparency film. After dehydration in -25°C acetone, the slices of the left brain half were immersed at -25°C, for two days in P40 and then impregnated for 24 hours. The slices of the right brain half were immersed at +5°C for two days and impregnated at room temperature at+15°C for 24 hours. All impregnated slices were cured with UV light. The imprints of the fixed brain slices were scanned into a computer, as well as the plastinated slices. By using a Kontron KSA 400 v. 2.0 (ZEISS) software we calculated the area of the plastinated brain slices as well as the area of the scanned imprints. By comparing the obtained data we were able to determine the shrinkage rate of the slices. The slices processed at -25°C showed a shrinkage rate of 4.41%. In comparison the slices immersed at +5°C and impregnated at +15°C showed a shrinkage rate of 6.96%.