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一种快速高效液相色谱法测定人血浆中利奈唑胺和达托霉素浓度的方法。

A rapid high-performance liquid chromatography method to measure linezolid and daptomycin concentrations in human plasma.

机构信息

Division of Pharmacology and Chemotherapy, Department of Internal Medicine, University of Pisa, Pisa, Italy.

出版信息

Ther Drug Monit. 2010 Apr;32(2):200-5. doi: 10.1097/FTD.0b013e3181d3f5cb.

Abstract

Daptomycin and linezolid, recently introduced to treat severe Gram-positive infections, are effective against multidrug-resistant Gram-positive microorganisms such as methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis, and vancomycin-resistant Enterococci bacteria that are less sensitive or frankly resistant, including methicillin-resistant S. aureus. However, alteration of their plasma profile has been described in some patients and this may be associated with toxicities or selection of resistant strains. The measurement of plasma concentrations of both drugs may allow the identification of those subjects at major risk of adverse events. Therefore, a rapid and sensitive high-performance liquid chromatography method for the analysis of daptomycin and linezolid was developed and applied in clinical settings. Drugs were extracted from plasma by adding methanol and, after centrifugation, clear supernatants were injected into the high-performance liquid chromatography system. Isocratic elution (1.5 mL/min) was performed using a mobile phase consisting of ammonium phosphate buffer 40 mM, pH 4.0, acetonitrile (70:30, vol/vol) through a BDS C8 Hypersil stationary phase (250 x 4.6 mm, 5 mum); ultraviolet detection was used at 214 nm. Linezolid and daptomycin eluted within 20 minutes from the injection, and mean recoveries ranged between 95.4% and 112.1%, respectively. The method was linear (coefficient of linearity, 0.998-0.999) over the full range of concentrations assayed, from 0.78125 mg/L (limit of quantitation) to 100 mg/L for both drugs. The Sy.x values were equal to 0.25 +/- 0.10 and 0.29 +/- 0.18 mg/L for daptomycin and linezolid, respectively. Precision values were lower than 20% over the entire range of calibration standard, and accuracy was within the range of 80% to 120% for all concentrations. The present method proved to be sensitive and specific to measure daptomycin and linezolid plasma concentrations in patients affected by severe Gram-positive infections, allowing therapeutic drug monitoring in those patients at major risk of severe adverse events.

摘要

达托霉素和利奈唑胺是最近被引入用于治疗严重革兰氏阳性感染的药物,它们对多种耐药革兰氏阳性微生物有效,如耐甲氧西林金黄色葡萄球菌、耐甲氧西林表皮葡萄球菌和万古霉素耐药肠球菌,这些微生物对这些药物的敏感性较低或完全耐药,包括耐甲氧西林金黄色葡萄球菌。然而,已经描述了一些患者中这些药物的血浆谱发生了改变,这可能与毒性或耐药株的选择有关。测量这两种药物的血浆浓度可以识别那些发生严重不良事件风险较高的患者。因此,开发了一种快速灵敏的高效液相色谱法来分析达托霉素和利奈唑胺,并将其应用于临床环境中。药物通过加入甲醇从血浆中提取,离心后,将澄清的上清液注入高效液相色谱系统。使用由 40 mM 磷酸铵缓冲液 pH 4.0、乙腈(70:30,体积/体积)组成的等度洗脱液(1.5 mL/min)通过 BDS C8 Hypersil 固定相(250 x 4.6 毫米,5 微米)进行洗脱;使用紫外检测在 214nm 处进行检测。利奈唑胺和达托霉素在注射后 20 分钟内洗脱,平均回收率分别在 95.4%至 112.1%之间。该方法在测定的全浓度范围内具有线性(线性度,0.998-0.999),对于两种药物,从 0.78125mg/L(定量下限)到 100mg/L。达托霉素和利奈唑胺的 Sy.x 值分别为 0.25 +/- 0.10 和 0.29 +/- 0.18mg/L。在整个校准标准范围内,精密度值低于 20%,准确度在所有浓度的 80%至 120%范围内。该方法对测量患有严重革兰氏阳性感染的患者的达托霉素和利奈唑胺血浆浓度敏感且特异性高,允许对发生严重不良事件风险较高的患者进行治疗药物监测。

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