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Two stage EDTA anti-calcification method for bioprosthetic heart valve materials.

机译:生物假体心脏瓣膜材料的两阶段EDTA抗钙化方法。

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Background: The aim of this study was to investigate the effect of two-stageEDTA treatment in diminishing calcific degeneration in bovine pericardial bioprosthetic heart valve material.Material/Methods: Conventionally preserved pericardium specimens were divided into two groups. GroupI (controls, n=18) pieces were first fixed in phosphate-buffered solution (PBS)+0.6% glutaraldehyde at+4 degrees C for 24 hours, then stored in PBS+0.2% glutaraldehyde at room temperature for 6 days. GroupII (study group, n=18) pieces were treated with PBS containing 100 microg/ml ethylenediaminetetraaceticacid (EDTA) at +4 degrees C for 24 hours, then fixed in PBS+0.6% glutaraldehyde as was group I at +4degrees C for 24 hours. After a second exposure to PBS containing 100 microg/ml EDTA at room temperaturefor 24 hours, they were stored in PBS+0.2% glutaraldehyde at room temperature for 4 days. Pericardialpatches were inserted into the dorsal pouches of 18 juvenile male Wistar rats. After 7 weeks of implantation,all the pericardium pieces were harvested from sacrificed rats. The calcium content and biomechanicalproperties of the explanted tissues were evaluated and also examined histopathologically. Results: Thedifference in the calcium content of the control and study groups was statistically significant. Biomechanicaland histopathologic assessment also supported these findings. Conclusions: Application of two-stage EDTAwas found to be useful in the attenuation of calcification in bioprosthetic heart valve materials withmildly increased durability. As calcification was reduced by approximately 50%, it can be consideredfor use with other agents as an adjuvant treatment.
机译:背景:本研究的目的是研究两阶段EDTA治疗对减少牛心包生物人工心脏瓣膜材料钙化变性的作用。材料/方法:常规保存的心包标本分为两组。首先将I类(对照,n = 18)片在+ 4℃的磷酸盐缓冲溶液(PBS)+ 0.6%的戊二醛中固定24小时,然后在室温下于PBS + 0.2%的戊二醛中保存6天。 II组(研究组,n = 18)在+4摄氏度下用含100μg/ ml乙二胺四乙酸(EDTA)的PBS在+4摄氏度下处理24小时,然后像在I + 4摄氏度下一样在PBS + 0.6%戊二醛中固定24小时。小时。在室温下第二次暴露于含100μg/ ml EDTA的PBS中24小时后,将其在室温下于PBS + 0.2%戊二醛中保存4天。将心包膜插入18只幼年Wistar大鼠的背袋中。植入7周后,从处死的大鼠中收获所有心包碎片。评估了移植组织的钙含量和生物力学特性,并进行了病理组织学检查。结果:对照组和研究组的钙含量差异具有统计学意义。生物力学和组织病理学评估也支持了这些发现。结论:发现采用两阶段EDTA可以有效减轻生物人工心脏瓣膜材料中的钙化,并具有适度增加的耐久性。由于钙化减少了约50%,因此可以考虑与其他药物一起用作辅助治疗。

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