Mycology Reference and Research Laboratory (National Centre for Microbiology CNM-ISCIII), Instituto de Salud Carlos III Carretera Majadahonda-Pozuelo Km 2 28220 Madrid, Spain.
Center for Biomedical Research in Network in Infectious Diseases (CIBERINFEC-CB21/13/00105), Instituto de Salud Carlos III. Carretera Majadahonda-Pozuelo Km 2 Madrid, Spain.
Med Mycol. 2023 Aug 2;61(8). doi: 10.1093/mmy/myad086.
We aimed to assess patient exposure to isavuconazole (ISZ) from samples received in our laboratory for therapeutic antifungal monitoring. We used liquid chromatography coupled with ultraviolet (UV) absorbance detection adapted from a multiplex-validated method with photodiode array (PDA) detection to monitor the analytes. The latter device allows the characterization of the azoles UV spectra. The method was validated according to international guidelines for efficient ISZ monitoring. The assay exhibited linearity between 0.25 and 16 mg/l for ISZ. Accuracy and intra- and inter-day precision were within acceptable ranges, and the method was successfully applied to quantify azoles and major metabolites from clinical samples collected from treated patients. We focus on ISZ blood concentrations and compared them to those of voriconazole, posaconazole, and itraconazole for a period of 5 years (2017-2021). Median ISZ concentration was 2.92 mg/l (interquartile range 1.82-5.33 mg/l) with 89% of measurements classified as adequate exposure (> 1 mg/l). Additionally, 71% of samples reach concentration values > 2 mg/l. Different ISZ exposure between adults to children were found. In conclusion, ISZ achieves excellent blood concentrations compared to other azole drugs, they are almost identical to those previously described, they exceed the MICs of most fungi for which its use was recommended and they differ depending on the patient's age. The method we describe for antifungal monitoring is simple, robust, and efficient. It simultaneously analyzes azoles and metabolites, and can be used for tailored interventions, achieve exposures associated with therapeutic success, decrease treatment-related toxicity, and help prevent resistance emergence due to continuous azole sub-optimal concentrations.
我们旨在评估从实验室收到的用于治疗性抗真菌监测的样本中患者接触伊曲康唑(ISZ)的情况。我们使用液相色谱法与紫外线(UV)吸收检测相结合,该方法源自一种具有光电二极管阵列(PDA)检测的多重验证方法,用于监测分析物。后者的设备允许对唑类药物的 UV 光谱进行特征描述。该方法根据国际指南进行了有效的 ISZ 监测验证。该测定法在 0.25 至 16mg/l 范围内对 ISZ 表现出线性关系。准确度和日内及日间精密度均在可接受范围内,该方法成功应用于从接受治疗的患者采集的临床样本中定量测定唑类药物和主要代谢物。我们专注于 ISZ 的血液浓度,并将其与伏立康唑、泊沙康唑和伊曲康唑进行了 5 年(2017-2021 年)的比较。ISZ 的中位数浓度为 2.92mg/l(四分位距 1.82-5.33mg/l),89%的测量值被归类为充分暴露(>1mg/l)。此外,71%的样本达到了>2mg/l 的浓度值。我们发现成人和儿童之间的 ISZ 暴露量存在差异。总之,ISZ 与其他唑类药物相比,血液浓度优异,与之前描述的浓度几乎相同,超过了建议使用其治疗的大多数真菌的 MIC 值,并且根据患者的年龄而有所不同。我们描述的用于抗真菌监测的方法简单、稳健、高效。它可以同时分析唑类药物及其代谢物,并可用于针对性干预,实现与治疗成功相关的暴露,降低与治疗相关的毒性,并有助于防止由于连续唑类药物浓度不理想而导致的耐药性出现。