Department of Drug Metabolism and Pharmacokinetics, Novartis Institutes for Biomedical Research, One Health Plaza, East Hanover, NJ 07936, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Aug 15;879(24):2376-82. doi: 10.1016/j.jchromb.2011.06.030. Epub 2011 Jun 26.
A high-performance liquid chromatography-tandem mass spectrometric (LC-MS/MS) method has been developed and validated for the quantitative analysis of NIM811, a cyclophilin inhibitor, in human dried blood spot (DBS) samples, which were produced by spotting 20 μl whole blood onto FTA cards. A 3mm disc was cut from the DBS samples and extracted using methanol, followed by liquid-liquid extraction with MTBE. The reconstituted extracts were chromatographed using a Halo C(18) column and gradient elution for MS/MS detection. The possible impact of hematocrit, blood sample volume and punching location on DBS sampling was investigated. The results showed that blood sample volume or punching location has no impact on assay performance, but the presence of a high hematocrit resulted in significantly increased analyte concentrations measured from the high QC samples. The current method was fully validated over the range of 10.0-5000 ng/ml with correlation coefficients (r(2)) for three validation batches equal to or better than 0.991. The accuracy and precision (CV) at the LLOQ were -0.7 to 6.0% bias of the nominal value (10.0 ng/ml) and 10.2-2.3%, respectively. For the balance of QC samples (20.0, 50.0, 750, 1500 and 3750 ng/ml), the precision (CV) ranged from 3.2 to 11.7% and from 5.6 to 10.2%, respectively, for the intra-day and inter-day evaluations. The accuracy ranged from -6.8 to 8.5% and -0.2% to 2.7% bias, respectively, for the intra-day and inter-day batches. NIM811 is stable in the DBS samples for at least 24h at room temperature and 4h at 60°C. Interestingly, the long term stability (LTS) assessment showed that the stability of the analyte is better when the DBS samples were stored at a lower storage temperature (e.g. ≤ -60°C) compared to storage at room temperature. This is probably due to the interaction of the additives and/or other materials (e.g. cellulose, etc) on the DBS card with NIM811, a cyclic peptide. The current methodology has been applied to determine the NIM811 levels in DBS samples prepared from a clinical study.
已开发并验证了一种高效液相色谱-串联质谱(LC-MS/MS)方法,用于定量分析人干血斑(DBS)样品中的环孢素抑制剂 NIM811,通过将 20μl 全血点样到 FTA 卡上可制备 DBS 样品。从 DBS 样品中切下 3mm 圆片,用甲醇提取,然后用 MTBE 进行液液萃取。提取的产物在 Halo C(18)柱上进行色谱分离,采用梯度洗脱进行 MS/MS 检测。研究了红细胞压积、血样体积和打孔位置对 DBS 取样的可能影响。结果表明,血样体积或打孔位置对检测无影响,但高红细胞压积会导致高 QC 样品中分析物浓度显著增加。目前的方法在 10.0-5000ng/ml 范围内进行了充分验证,三个验证批次的相关系数(r(2))等于或大于 0.991。LLOQ 时的准确度和精密度(CV)为名义值(10.0ng/ml)的-0.7 至 6.0%偏差和 10.2-2.3%,分别。对于 QC 样品的其余部分(20.0、50.0、750、1500 和 3750ng/ml),日内和日间评估的精密度(CV)分别为 3.2-11.7%和 5.6-10.2%,准确度分别为-6.8-8.5%和 0.2-2.7%偏差。NIM811 在室温下至少 24 小时和 60°C 下 4 小时在 DBS 样品中稳定。有趣的是,长期稳定性(LTS)评估表明,与室温储存相比,当 DBS 样品储存在较低温度(例如≤-60°C)下时,分析物的稳定性更好。这可能是由于添加剂和/或其他材料(例如纤维素等)与环肽 NIM811 在 DBS 卡上的相互作用所致。目前的方法已应用于从临床研究中确定 DBS 样品中的 NIM811 水平。