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在大鼠皮下模型中,快速戊二醛稳定化处理与多步ADAPT(R)处理后,冷冻保存的人心包的生物稳定性、耐久性和钙化情况。

Biostability, durability and calcification of cryopreserved human pericardium after rapid glutaraldehyde-stabilization versus multistep ADAPT(R) treatment in a subcutaneous rat model.

作者信息

Neethling William, Brizard Christian, Firth Laura, Glancy Ross

机构信息

Department of Cardiothoracic Surgery, Fremantle Heart Institute, Fremantle Hospital and School of Surgery, University of Western Australia, Fremantle, WA, Australia.

出版信息

Eur J Cardiothorac Surg. 2014 Apr;45(4):e110-7. doi: 10.1093/ejcts/ezt623. Epub 2014 Jan 14.

Abstract

OBJECTIVES

Autologous pericardium rapidly fixed with glutaraldehyde (GA) in theatre is considered in many cardiac surgery centres the best material currently available for intracardiac, valvular or vascular repair. Implanted non-fixed autologous tissues suffer rapid degeneration, shrinkage and absorption whereas standard xenotypic fixed tissues cause local cytotoxicity and calcification. In the present study, using a subcutaneous rat model, we tested the biostability, durability and calcification potential of four different pericardium patches treated with GA and relevant to current clinical practice.

METHODS

Pericardium samples were divided into four groups according to the method of treatment. Group I consisted of bovine pericardium (BP) fixed with 0.6% GA (control), Group II cryopreserved human pericardium (CHP) rapidly fixed with 0.6% GA for 4 min and detoxified with MgCl2, Group III CHP treated with the multistep ADAPT(®) process (delipidized, decellularized with Tx-100, deoxycholate, IgePal CA-630 and denucleased, fixed in 0.05% monomeric GA and detoxified) and Group IV BP treated with the multistep ADAPT(®) process (CardioCel(®)). Biostability was determined by shrinkage temperature which measures the degree of cross-linking, and durability assessed by resistance to a mixture of proteinases (pronase digestion). Treated pericardium samples (n = 10 in each of Groups I-IV) were implanted in the subcutaneous rat model for 8 and 16 weeks, followed by histology and calcium analysis (atomic absorption spectrophotometry).

RESULTS

The biostability and the durability of both CHP and BP after the multistep ADAPT(®) treatment remained stable without any microscopic calcification. Extractable calcium levels of CHP were significantly (P < 0.01) reduced in Group II (1.89 ± 0.77 μg Ca/mg tissue) compared with Group I (64.37 ± 6.25 μg/mg) after 8 weeks. Calcification of CHP (Group III) and BP (Group IV) after the multistep ADAPT(®) treatment was significantly reduced (1.43 ± 0.48 µg/mg and 0.75 ± 0.10 μg/mg, respectively) compared with Group I (282.52 ± 18.26 μg/mg) and the rapidly treated CHP in Group II (11.32 ± 3.21 μg/mg) after 16 weeks.

CONCLUSIONS

Improved biostability and durability with reduced calcification of tissues after the multistep ADAPT(®) tissue treatment suggest improved alternative substitutes to autologous pericardium.

摘要

目的

在许多心脏外科中心,术中用戊二醛(GA)快速固定的自体心包被认为是目前用于心内、瓣膜或血管修复的最佳材料。植入的未固定自体组织会迅速退化、收缩和吸收,而标准的异种固定组织会导致局部细胞毒性和钙化。在本研究中,我们使用大鼠皮下模型,测试了四种经GA处理且与当前临床实践相关的不同心包补片的生物稳定性、耐久性和钙化潜能。

方法

根据处理方法将心包样本分为四组。第一组由用0.6% GA固定的牛心包(BP)组成(对照),第二组为用0.6% GA快速固定4分钟并用MgCl2解毒的冷冻保存人心包(CHP),第三组为用多步骤ADAPT(®)工艺处理的CHP(脱脂、用Tx - 100、脱氧胆酸盐、IgePal CA - 630脱细胞并去除核酸,用0.05%单体GA固定并解毒),第四组为用多步骤ADAPT(®)工艺处理的BP(CardioCel(®))。通过测量交联程度的收缩温度来确定生物稳定性,通过对蛋白酶混合物的抗性(链霉蛋白酶消化)来评估耐久性。将处理过的心包样本(每组I - IV各10个)植入大鼠皮下模型8周和16周,随后进行组织学和钙分析(原子吸收分光光度法)。

结果

经过多步骤ADAPT(®)处理后,CHP和BP的生物稳定性和耐久性均保持稳定,且无任何微观钙化。与第一组(64.37 ± 6.25 μg/mg)相比,第二组CHP在8周后的可提取钙水平显著降低(P < 0.01)(1.89 ± 0.77 μg Ca/mg组织)。与第一组(282.52 ± 18.26 μg/mg)和第二组快速处理的CHP(11.32 ± 3.21 μg/mg)相比,经过多步骤ADAPT(®)处理后,第三组CHP和第四组BP在16周后的钙化显著降低(分别为1.43 ± 0.48 µg/mg和0.75 ± 0.10 μg/mg)。

结论

多步骤ADAPT(®)组织处理后组织的生物稳定性和耐久性得到改善,钙化减少,这表明有更好的自体心包替代物。

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