Suppr超能文献

胃肠外铁制剂中的不稳定铁:一项定量与比较研究。

Labile iron in parenteral iron formulations: a quantitative and comparative study.

作者信息

Van Wyck David, Anderson Jaime, Johnson Kevin

机构信息

University of Arizona College of Medicine, Tucson, USA.

出版信息

Nephrol Dial Transplant. 2004 Mar;19(3):561-5. doi: 10.1093/ndt/gfg579.

Abstract

BACKGROUND

Evidence of iron-mediated oxidative stress, neutrophil dysfunction and enhanced bacterial growth after intravenous (IV) iron administration has been ascribed to a labile or bioactive iron fraction present in all IV iron agents.

METHODS

To quantify and compare the size of the labile fraction in several classes of IV iron agents, we examined iron donation to transferrin (Tf) in vitro. We added dilutions of ferric gluconate, iron sucrose and each of two iron dextran preparations to serum in vitro, passed the resulting samples through alumina columns to remove iron agent and free organic iron, and measured Tf-bound iron in the resulting eluates. Comparing results to serum samples without added iron, we calculated delta Tf-bound iron for each agent at each concentration. Finally, we compared delta Tf-bound iron to the concentration of added agent and calculated the percent iron donation to Tf.

RESULTS

We found that Tf-bound iron increased with added iron concentration for each agent: delta Tf-bound iron was directly related to the concentration and type of iron agent (P<0.001). Mean percent iron donation to Tf ranged from 2.5 to 5.8% with the following progression: iron dextran-Dexferrum<iron dextran-INFeD<iron sucrose<ferric gluconate. Pairwise differences between agents for percent iron donation were statistically significant (P<0.05) only between ferric gluconate and both iron dextran agents, and between iron sucrose and iron dextran-Dexferrum.

CONCLUSIONS

Approximately 2-6% of total iron in commonly used IV iron compounds is available for in vitro iron donation to Tf. This fraction may contribute to evidence of bioactive iron in patients after IV iron administration.

摘要

背景

静脉注射铁剂后,铁介导的氧化应激、中性粒细胞功能障碍及细菌生长增强的证据被归因于所有静脉铁剂中存在的不稳定或生物活性铁部分。

方法

为了量化和比较几类静脉铁剂中不稳定部分的大小,我们在体外检测了铁向转铁蛋白(Tf)的转移情况。我们在体外将葡萄糖酸铁、蔗糖铁的稀释液以及两种葡聚糖铁制剂分别加入血清中,使所得样品通过氧化铝柱以去除铁剂和游离有机铁,然后测量所得洗脱液中转铁蛋白结合铁的含量。将结果与未添加铁的血清样品进行比较,我们计算了每种试剂在每个浓度下转铁蛋白结合铁的变化量(ΔTf-结合铁)。最后,我们将ΔTf-结合铁与添加试剂的浓度进行比较,并计算铁向转铁蛋白的转移百分比。

结果

我们发现,每种试剂的转铁蛋白结合铁均随添加铁浓度的增加而增加:ΔTf-结合铁与铁剂的浓度和类型直接相关(P<0.001)。铁向转铁蛋白的平均转移百分比范围为2.5%至5.8%,顺序如下:葡聚糖铁-右旋糖酐铁<葡聚糖铁-中分子右旋糖酐铁<蔗糖铁<葡萄糖酸铁。仅葡萄糖酸铁与两种葡聚糖铁试剂之间以及蔗糖铁与葡聚糖铁-右旋糖酐铁之间,试剂在铁转移百分比上的两两差异具有统计学意义(P<0.05)。

结论

常用静脉铁化合物中约2%-6%的总铁可用于体外向转铁蛋白的铁转移。这一部分可能是静脉注射铁剂后患者体内生物活性铁证据的原因之一。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验