Roth Jeffrey, Peer Cody J, Widemann Brigitte, Cole Diane E, Ershler Rachel, Helman Lee, Schrump David, Figg William D
Clinical Pharmacology Program, National Cancer Institute, Bethesda, MD, United States.
Pediatric Oncology Branch, National Cancer Institute, Bethesda, MD, United States.
J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Nov 1;970:95-101. doi: 10.1016/j.jchromb.2014.08.021. Epub 2014 Sep 6.
Mithramycin is a neoplastic antibiotic synthesized by various Streptomyces bacteria. It is under investigation as a chemotherapeutic treatment for a wide variety of cancers. Ongoing and forthcoming clinical trials will require pharmacokinetic analysis of mithramycin in humans, both to see if target concentrations are achieved and to optimize dosing and correlate outcomes (response/toxicity) with pharmacokinetics. Two published methods for mithramycin quantitation exist, but both are immunoassays that lack current bioanalytical standards of selectivity and sensitivity. To provide an upgraded and more widely applicable assay, a UPLC-MS/MS method for quantitation of mithramycin in human plasma was developed. Solid-phase extraction allowed for excellent recoveries (>90%) necessary for high throughput analyses on sensitive instrumentation. However, a ∼55% reduction in analyte signal was observed as a result of plasma matrix effects. Mithramycin and the internal standard chromomycin were separated on a Waters Acquity BEH C18 column (2.1×50 mm, 1.7 μm) and detected using electrospray ionization operated in the negative mode at mass transitions m/z 1083.5→268.9 and 1181.5→269.0, respectively, on an AB Sciex QTrap 5500. The assay range was 0.5-500 ng/mL and proved to be linear (r(2)>0.996), accurate (≤10% deviation), and precise (CV<15%). Mithramycin was stable in plasma at room temperature for 24 h, as well as through three freeze-thaw cycles. This method was subsequently used to quantitate mithramycin plasma concentrations from patients enrolled on two clinical trials at the NCI.
光辉霉素是由多种链霉菌属细菌合成的一种抗肿瘤抗生素。它正在作为多种癌症的化疗药物进行研究。正在进行和即将开展的临床试验将需要对人体中的光辉霉素进行药代动力学分析,以确定是否能达到目标浓度,并优化给药剂量,以及将结果(反应/毒性)与药代动力学相关联。目前存在两种已发表的光辉霉素定量方法,但都是免疫测定法,缺乏当前生物分析所需的选择性和灵敏度标准。为了提供一种升级且更广泛适用的测定方法,开发了一种用于定量人血浆中光辉霉素的超高效液相色谱-串联质谱(UPLC-MS/MS)方法。固相萃取实现了在灵敏仪器上进行高通量分析所需的出色回收率(>90%)。然而,由于血浆基质效应,观察到分析物信号降低了约55%。光辉霉素和内标嗜铬霉素在沃特世 Acquity BEH C18 柱(2.1×50 mm,1.7 μm)上分离,并在 AB Sciex QTrap 5500 上使用电喷雾电离以负离子模式进行检测,质量转移分别为 m/z 1083.5→268.9 和 1181.5→269.0。测定范围为 0.5 - 500 ng/mL,证明是线性的(r(2)>0.996)、准确的(偏差≤10%)和精密的(CV<15%)。光辉霉素在血浆中于室温下稳定24小时,并且经过三个冻融循环仍保持稳定。该方法随后用于定量美国国立癌症研究所(NCI)两项临床试验中患者的血浆光辉霉素浓度。