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柱切换高效液相色谱法测定血清中的万古霉素。

Column-switching high-performance liquid chromatographic determination of vancomycin in serum.

作者信息

Demotes-Mainard F, Labat L, Vinçon G, Bannwarth B

机构信息

Department of Clinical Pharmacology and Toxicology, Hôpital Pellegrin, Bordeaux, France.

出版信息

Ther Drug Monit. 1994 Jun;16(3):293-7. doi: 10.1097/00007691-199406000-00011.

Abstract

Concentrations of vancomycin in serum were measured by an automatic high-performance liquid chromatographic (HPLC) micromethod. Vancomycin is a glycopeptide antibiotic with broad application in the therapy of gram-positive infections. As this drug is potentially nephro- and ototoxic, a method to maximize its therapeutic benefit while minimizing the risk of toxicity is desirable. This fully automated HPLC method did not involve a sample pretreatment step. The configuration of the apparatus permitted a solid phase extraction of the serum sample on two precolumns filled with a reversed-phase material, followed by a chromatographic separation of the sample constituents on an analytical column. The reversed phase analytical column (muBondapak C18) was flushed with a mobile phase of water-acetonitrile-triethylamine, 870: 130: 4 (vol/vol/vol); the pH was adjusted to 3.0 with orthophosphoric acid. Precision was expressed as the coefficient of variation (CV), which was always < or = 4.13% for intra- and inter-assays (n = 10) in the range 2-50 micrograms/ml. We compared this specific HPLC determination to an enzyme-multiplied immunoassay (EMIT). Fifty clinical samples obtained from patients under vancomycin therapy were assayed by each method and results compared using a linear regression analysis. There was a significant correlation between results from HPLC and EMIT: EMIT = 0.51 + 1 x HPLC (r = 0.963; p < 0.0001). The rapidity and specificity of this HPLC micromethod make it suitable for use in the monitoring of serum levels of vancomycin and for use in pharmacokinetic studies of this antibiotic.

摘要

采用自动高效液相色谱微方法测定血清中万古霉素的浓度。万古霉素是一种糖肽类抗生素,在革兰氏阳性菌感染治疗中应用广泛。由于该药物具有潜在的肾毒性和耳毒性,因此需要一种方法来在将毒性风险降至最低的同时,最大程度地发挥其治疗效果。这种全自动高效液相色谱方法无需样品预处理步骤。该仪器的配置允许在两根填充反相材料的预柱上对血清样品进行固相萃取,随后在分析柱上对样品成分进行色谱分离。反相分析柱(μBondapak C18)用体积比为870:130:4(体积/体积/体积)的水-乙腈-三乙胺流动相冲洗;用正磷酸将pH值调至3.0。精密度用变异系数(CV)表示,在2 - 50微克/毫升范围内,批内和批间分析(n = 10)的CV始终≤4.13%。我们将这种特定的高效液相色谱测定法与酶放大免疫分析(EMIT)进行了比较。用这两种方法对50份接受万古霉素治疗患者的临床样本进行检测,并使用线性回归分析比较结果。高效液相色谱法和酶放大免疫分析法的结果之间存在显著相关性:酶放大免疫分析法结果 = 0.51 + 1×高效液相色谱法结果(r = 0.963;p < 0.0001)。这种高效液相色谱微方法的快速性和特异性使其适用于监测血清中万古霉素水平以及该抗生素的药代动力学研究。

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