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全血氧解离曲线的连续测定。

Continuous determination of the oxygen dissociation curve for whole blood.

作者信息

Rossi-Bernardi L, Luzzana M, Samaja M, Davi M, DaRiva-Ricci D, Minoli J, Seaton B, Berger R L

出版信息

Clin Chem. 1975 Nov;21(12):1747-53.

PMID:241510
Abstract

We report here the development of a new method that allows continuous determination of the oxygen dissociation curve for microsamples (600 mul) of whole blood under conditions of pH, pCO2, methemoglobin concentration, and 2,3-diphosphoglycerate content closely approaching those found in the circulatory system. The method consists of gradually oxygenating a blood sample by adding H2O2 in the presence of catalase (EC 1.11.1.6), to produce the reaction H2O2 leads to H2O + 1/2 O2. Because the total oxygen content of blood can be derived from the known rate of H202 addition and the pO2 is determined in the liquid phase by an oxygen electrode, the two functions (total O2 content) and (% oxygen saturation) vs. pO2 are simple to calculate. pCO2 and pH are controlled by adding base simultaneously with the gradual oxygenation of blood. The method described thus avoids the direct measurement of oxygen saturation of whole blood.

摘要

我们在此报告一种新方法的开发情况,该方法能够在pH值、二氧化碳分压、高铁血红蛋白浓度以及2,3 - 二磷酸甘油酸含量与循环系统中相近的条件下,对全血微量样本(600微升)的氧解离曲线进行连续测定。该方法是在过氧化氢酶(EC 1.11.1.6)存在的情况下,通过添加过氧化氢逐步使血液样本氧合,以产生反应H₂O₂→H₂O + 1/2 O₂。由于血液中的总氧含量可从已知的过氧化氢添加速率得出,并且通过氧电极在液相中测定氧分压,所以(总氧含量)和(氧饱和度百分比)与氧分压的两个函数很容易计算。在血液逐步氧合的同时添加碱来控制二氧化碳分压和pH值。因此,所描述的方法避免了对全血氧饱和度的直接测量。

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