利用相对摩尔灵敏度开发一种高效液相色谱法,用于测量血液中九种药物化合物的浓度。

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Takashi Ohtsuki, Yi Huang, Ayane Kamiya, Yuki Nakayama, Miyuki Matsushita, Satoru Morikawa, Hiroshi Matsufuji
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引用次数: 0

摘要

我们开发了一种可靠的高效液相色谱分析方法,该方法采用相对摩尔灵敏度(RMS)技术,无需真实、相同的参照分析物,即可定量检测血清中卡马西平、苯妥英、伏立康唑、拉莫三嗪、美罗培南、霉酚酸、利奈唑胺、万古霉素和咖啡因的水平,用于常规血药浓度测量。卡马西平和咖啡因也被用作非分析物参考材料,用于计算每种分析物的有效值。根据校准方程(分析物/非分析物参比材料)的斜率比值计算出有效值,然后用来定量添加了卡马西平、苯妥英、伏立康唑、美罗培南、霉酚酸、利奈唑胺或万古霉素的对照血清样本中的分析物。此外,用拟议的 RMS 方法测定的对照血清样本中这六种药物的浓度与用传统方法测定的结果非常吻合。鉴于该方法的准确性、精密度和定量效率,建议的 RMS 方法有望成为临床测定这九种药物的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of an HPLC method using relative molar sensitivity for the measurement of blood concentrations of nine pharmaceutical compounds.

We developed a reliable high-performance liquid chromatographic analysis method using a relative molar sensitivity (RMS) technique that does not require an authentic, identical reference analyte material to quantify blood serum carbamazepine, phenytoin, voriconazole, lamotrigine, meropenem, mycophenolic acid, linezolid, vancomycin, and caffeine levels for routine blood concentration measurements. Carbamazepine and caffeine were also used as non-analyte reference materials to calculate the RMS of each analyte. The RMS was calculated from the ratio of the slope of the calibration equation (analyte/non-analyte reference material), then used to quantify analytes in control serum samples spiked with carbamazepine, phenytoin, voriconazole, meropenem, mycophenolic acid, linezolid or vancomycin. In addition, the concentrations of these six drugs in control serum samples determined by the proposed RMS method agreed well with that obtained using a conventional method. The proposed RMS method is a promising tool for the clinical determination of nine drugs, given the accuracy, precision, and efficiency of quantifying these analytes.

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来源期刊
CiteScore
1.80
自引率
0.00%
发文量
29
审稿时长
8 weeks
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