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二胺扩链的戊二醛和碳二亚胺交联在减轻生物人工主动脉壁钙化方面具有协同作用。

Diamine-extended glutaraldehyde- and carbodiimide crosslinks act synergistically in mitigating bioprosthetic aortic wall calcification.

作者信息

Zilla Peter, Bezuidenhout Deon, Torrianni Mark, Hendriks Marc, Human Paul

机构信息

Department of Cardiothoracic Surgery, Cape Heart Centre, University of Cape Town, South Africa.

出版信息

J Heart Valve Dis. 2005 Jul;14(4):538-45.

Abstract

BACKGROUND AND AIM OF THE STUDY

The extension of glutaraldehyde (GA) crosslinks with diamine bridges was shown previously to reduce bioprosthetic heart valve calcification to a significant degree. The aim of the present study was to investigate whether the additional crosslinking of functional carboxyl groups could augment this anticalcific effect at the low glutaraldehyde concentrations typically used in commercial heart valve production.

METHODS

Entire aortic roots of medium-sized pigs were fixed after 48 h of cold storage. Crosslinking of amino-functional groups was achieved either by GA fixation alone (0.2% or 0.7%) or with an interim treatment with the diamine L-lysine (25, 50 or 100 mM; 37 degrees C; 2 days). Carboxyl groups were activated with carbodiimide (N'-{3-dimethylaminopropyl}-N-ethyl carbodiimide hydrochloride (EDC), 240 mM) and crosslinked with an oligomeric diamine (polypropylene glycol-bis-aminopropyl ether (Jeffamine), 60 mM, 230D). By permutation of treatments and combinations thereof, a total of 17 groups was compared. Aortic wall discs (12 mm diameter) were implanted subcutaneously into seven-week-old Long-Evans rats for 60 days. Tissue calcification was determined by histology and atomic absorption spectrophotometry.

RESULTS

There was no significant difference in tissue calcification if either GA or carbodiimide fixation was used alone. Equally, the combined crosslinking with GA and EDC/Jeffamine did not achieve a mitigation of tissue calcification below levels seen in at least one of the two treatments alone. When commercial GA fixation was mildly diamine-enhanced with L-lysine (25 mM), additional EDC/Jeffamine crosslinking of carboxyl groups resulted in a distinct additive effect in both 0.2% (-31%; p < 0.0002) and 0.7% (-36%; p = 0.0073) GA-fixed tissue. Relative to conventional GA fixation, this combination mitigated aortic wall calcification by 43% (p < 0.0001) and 34% (p = 0.0014) in 0.2% and 0.7% GA-fixed tissue, respectively. An increase in L-lysine concentration to 100 mM further reduced calcification of 0.7% GA-fixed tissue (18.5%; p = 0.016), but had no additional effect on 0.2% GA-fixed tissue (0.6%; p = 0.463).

CONCLUSION

A distinct reduction in bioprosthetic aortic wall calcification can be achieved by combining diamine-extended conventional GA fixation with a diamine-extended carbodiimide based crosslinking step.

摘要

研究背景与目的

先前研究表明,通过二胺桥扩展戊二醛(GA)交联可显著降低生物人工心脏瓣膜钙化。本研究旨在探讨在商业心脏瓣膜生产中常用的低戊二醛浓度下,对功能性羧基进行额外交联是否能增强这种抗钙化效果。

方法

中型猪的整个主动脉根部在冷藏48小时后进行固定。氨基官能团的交联可通过单独的GA固定(0.2%或0.7%)或先用二胺L-赖氨酸(25、50或100 mM;37℃;2天)进行中间处理来实现。羧基用碳二亚胺(N'-{3-二甲基氨基丙基}-N-乙基碳二亚胺盐酸盐(EDC),240 mM)活化,并用低聚二胺(聚丙二醇-双-氨丙基醚(Jeffamine),60 mM,230D)交联。通过排列处理及其组合,共比较了17组。将直径12毫米的主动脉壁圆盘皮下植入7周龄的Long-Evans大鼠体内60天。通过组织学和原子吸收分光光度法测定组织钙化情况。

结果

单独使用GA或碳二亚胺固定时,组织钙化无显著差异。同样,GA与EDC/Jeffamine的联合交联也未使组织钙化减轻至单独两种处理中至少一种所见水平以下。当商业GA固定用L-赖氨酸(25 mM)轻度增强二胺时,羧基的额外EDC/Jeffamine交联在0.2%(-31%;p < 0.0002)和0.7%(-36%;p = 0.0073)GA固定组织中均产生明显的累加效应。相对于传统GA固定,该组合在0.2%和0.7%GA固定组织中分别使主动脉壁钙化减轻43%(p < 0.0001)和34%(p = 0.0014)。将L-赖氨酸浓度提高到100 mM进一步降低了0.7%GA固定组织的钙化(18.5%;p = 0.016),但对0.2%GA固定组织无额外影响(0.6%;p = 0.463)。

结论

将基于二胺扩展的传统GA固定与基于二胺扩展的碳二亚胺交联步骤相结合,可显著降低生物人工主动脉壁钙化。

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