Validation parameters of the analytical method by UPLC-MS/MS, to quantify ifosfamide in DBS at 30% HTC.

SD: Standard Deviation. CV: Coefficient of Variation. N/R: Not required according to the guidelines. Theoretical amounts for QC1, QC2 and QC3 were 300, 4000 and 8000 ng/mL, respectively.Validation parameters of the analytical method by UPLC-MS/MS, to quantify ifosfamide in DBS at 30% HTC.SD：标准差（Standard Deviation）；CV：变异系数（Coefficient of Variation）；N/R：根据指南规定无需提供。质控样本QC1、QC2及QC3的理论浓度分别为300、4000、8000 ng/mL。本数据集涵盖了在30% HTC条件下，采用超高效液相色谱-串联质谱（UPLC-MS/MS）分析方法定量干血斑（DBS）中异环磷酰胺（ifosfamide）的方法学验证参数。