首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of the free and total concentrations of vancomycin by two-dimensional liquid chromatography and its application in elderly patients
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Determination of the free and total concentrations of vancomycin by two-dimensional liquid chromatography and its application in elderly patients

机译:二维液相色谱法测定万古霉素的游离和总浓度及其在老年患者中的应用

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A robust two-dimensional liquid chromatography (2D-LC) method for determining the free and total concentrations of vancomycin in plasma was developed and validated. The 2D-LC system, which exhibited a strong capacity for inhibiting interference, comprised a unique RP1-IEX-RP_2 column system and an "Assistant Flow" configuration. Ultrafiltration technology was employed to separate free vancomycin from the protein-bound fraction in human plasma. The influence of ultrafiltration conditions on the free vancomycin concentration was evaluated. The calibration curve was linear over the 0.195-49.92 μg/ml range for the free and total vancomycin concentrations. The within- and between-run precision ranges were 1.5-3.9% and 2.0-4.7% for the total concentration, 1.4-3.3% and 2.4-4.0% for the free concentration, respectively. Ultrafiltration was susceptible to variations in the experimental conditions, including the centrifugation time, the centrifugal force, and the nominal molecular weight limit of the ultrafiltration membrane. A total of 101 serum samples from 84 elderly patients were analyzed by this method. The free vancomycin concentration was 5.88±3.75 μg/ml (range: 0.240-16.79 μg/ml), the total concentration was 12.36±5.36 μg/ml (range: 2.16-27.14 μg/ml), and the unbound fraction was 45.6±18.8% (range: 11.1-96.9%). There was a poor correlation between the free and total vancomycin concentrations (R2 = 0.596, p < 0.05). This method appears to be sensitive, precise, selective, and suitable for use in protein-binding studies of vancomycin.
机译:建立并验证了用于测定血浆中万古霉素游离和总浓度的稳健二维液相色谱(2D-LC)方法。展示出强大的抑制干扰能力的2D-LC系统包括独特的RP1-IEX-RP_2色谱柱系统和“辅助流”配置。采用超滤技术从人血浆中的蛋白质结合级分中分离出游离万古霉素。评估了超滤条件对游离万古霉素浓度的影响。游离和总万古霉素浓度的校准曲线在0.195-49.92μg/ ml范围内呈线性。批内和批间精密度范围分别为总浓度的1.5-3.9%和2.0-4.7%,自由浓度的分别为1.4-3.3%和2.4-4.0%。超滤易受实验条件变化的影响,包括离心时间,离心力和超滤膜的标称分子量极限。通过这种方法对来自84位老年患者的101份血清样品进行了分析。游离万古霉素浓度为5.88±3.75μg/ ml(范围:0.240-16.79μg/ ml),总浓度为12.36±5.36μg/ ml(范围:2.16-27.14μg/ ml),未结合分数为45.6± 18.8%(范围:11.1-96.9%)。游离和总万古霉素浓度之间的相关性很差(R2 = 0.596,p <0.05)。该方法似乎灵敏,精确,选择性强,适合用于万古霉素的蛋白质结合研究。

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