Petitjean Grégoire, Aman-Pommier Fabrice, Coudoré François, El Helali Najoua, Le Monnier Alban
Groupe Hospitalier Paris Saint-Joseph, Service de Microbiologie Clinique, Paris, France.
Plateforme de Dosage des Anti-Infectieux, Groupe Hospitalier Paris Saint-Joseph, Paris, France.
Biomed Chromatogr. 2020 Feb;34(2):e4759. doi: 10.1002/bmc.4759. Epub 2019 Dec 29.
Temocillin is a β-lactamase-resistant penicillin used for the treatment of multiple drug-resistant Gram-negative bacteria. To maximize efficacy and avoid adverse effects, the dose regimen has to be quickly adjusted to the clinical situations. This necessitates the development of a rapid, reliable and accurate analytical method. Temocillin and the stable isotopically labeled internal standard ([ C ]-amoxicillin) were extracted from either serum or cerebrospinal fluid by a turbulent flow liquid chromatographic method and eluted onto an octadecyl-silica phase with polar endcapping. Mass spectrometry was conducted using an exact mass determination method by electrospray positive ionization high-resolution mass spectrometry. The LLOQ and ULOQ of the present method were determined to be 0.4 and 200 μg/ml for serum and cerebrospinal fluid samples, respectively. The total analysis time was <7 min. The recovery ranged from 87.7 to 120.8%. Intra- and inter-day precision and trueness were tested at four concentration levels: 0.4, 8, 40 and 160 μg/ml. Values were 6.33 ± 1.53, 8.8 ± 1.3, 8.8 ± 0.36 and 2.1 ± 0.76%, and 5.0 ± 0.54, 9.9 ± 1.0, 5.8 ± 1.6 and 0.1 ± 1.1%, for inter- and intra-day analysis, respectively. Temocillin was found to be stable under all relevant laboratory conditions. The method was cross-validated with a microbiological assay. This method is suitable for accurate measurement of temocillin concentration in small volumes of serum or cerebrospinal fluid. Thanks to the online extraction procedure, the overall analytical time is compatible with high-throughput analysis for clinical application.
替莫西林是一种耐β-内酰胺酶的青霉素,用于治疗多重耐药革兰氏阴性菌。为了使疗效最大化并避免不良反应,必须根据临床情况快速调整给药方案。这就需要开发一种快速、可靠且准确的分析方法。采用湍流液相色谱法从血清或脑脊液中提取替莫西林和稳定同位素标记的内标物([C] -阿莫西林),并洗脱到带有极性封端的十八烷基硅胶柱上。通过电喷雾正离子高分辨率质谱法采用精确质量测定法进行质谱分析。本方法血清和脑脊液样本的定量下限(LLOQ)和定量上限(ULOQ)分别确定为0.4和200μg/ml。总分析时间<7分钟。回收率在87.7%至120.8%之间。在四个浓度水平:0.4、8、40和160μg/ml下测试了日内和日间精密度及准确性。日间分析的值分别为6.33±1.53%、8.8±1.3%、8.8±0.36%和2.1±0.76%,日内分析的值分别为5.0±0.54%、9.9±1.0%、5.8±1.6%和0.1±1.1%。发现替莫西林在所有相关实验室条件下均稳定。该方法与微生物测定法进行了交叉验证。此方法适用于准确测量少量血清或脑脊液中的替莫西林浓度。由于采用了在线提取程序,总体分析时间与临床应用的高通量分析兼容。