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An Improved Immunosuppressant Drug Research Method Based on a Novel SPLC-MS/MS System

机译:基于新型SPLC-MS / MS系统的改进的免疫抑制药物研究方法

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Improved reliability and economy was achieved for ISD analysis for research purposes by using a novel SPLC-MS/MS system and method. 1. Ion suppression of ISDs by co-eluting phospholipids was largely avoided by using the short Accucore C8 HPLC column. 2. Using 1/x weighting, correlation coefficients (r2) > 0.995 were typical for: (1) Cyclosporin A, from 25 to 1250 ng/mL, (2) Everolimus, Sirolimus & Tacrolimus, from 2.5 to 50 ng/mL. 3. Carryover, measured by peak areas corresponding to the ISDs from blank injections following the highest calibrators, was typically less than 0.1%. 4. Reproducible ISD QC results were obtained from three research test sites evaluating this method with the Prelude SPLC-TSQ Vantage system. 5. A reduction in solvent waste of about 40% was achieved, comparable to legacy TurboFlow methods for ISDs.
机译:通过使用新的SPLC-MS / MS系统和方法,实现了研究目的的ISD分析的改进的可靠性和经济。通过使用短Accocorce C8 HPLC柱,通过共洗脱磷脂进行ISDS的离子抑制。 2.使用1 / x加权,相关系数(R2)> 0.995典型为:(1)环孢菌素A,25至1250ng / ml,(2)everolimus,西罗莫司和Tacrolimus,来自2.5-50ng / ml。 3.通过与最高校准仪之后的空白注射相对应的峰面积测量的携带,通常小于0.1%。 4.可重复的ISD QC结果是从第三种研究试验站点获得了评估了这种方法的研究方法,采用前奏SPLC-TSQ Vantage系统。 5.达到约40%的溶剂废物的降低,可与ISDS的遗留涡轮机方法相媲美。

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