Canzani Daniele, Hsieh Kevin, Standland Matthew, Hammack Walter, Aldeek Fadi
Florida Department of Agriculture and Consumer Services, Division of Food Safety, 3125 Conner Boulevard, Tallahassee, FL, 32399-1650, United States.
Florida Department of Agriculture and Consumer Services, Division of Food Safety, 3125 Conner Boulevard, Tallahassee, FL, 32399-1650, United States.
J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Feb 15;1044-1045:87-94. doi: 10.1016/j.jchromb.2017.01.012. Epub 2017 Jan 10.
Penicillin G has been applied to citrus trees as a potential treatment in the fight against Huanglongbing (HLB). Here, we have developed and validated a method to identify and quantitate penicillin G and two of its metabolites, penillic acid and penilloic acid, in citrus fruit using ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). This method improves upon a previous method by incorporating isotopically labeled internal standards, namely, penillic acid-D, and penilloic acid-D. These standards greatly enhanced the accuracy and precision of our measurements by compensating for recovery losses, degradation, and matrix effects. When 2g of citrus fruit sample is extracted, the limits of detection (LOD) were determined to be 0.1ng/g for penicillin G and penilloic acid, and 0.25ng/g for penillic acid. At fortification levels of 0.1, 0.25, 1, and 10ng/g, absolute recoveries for penillic and penilloic acids were generally between 50-70%. Recoveries corrected with the isotopically labeled standards were approximately 90-110%. This method will be useful for the identification and quantitation of drug residues and their degradation products using isotopically labeled standards and UHPLC-MS/MS.
青霉素G已被应用于柑橘树,作为对抗黄龙病(HLB)的一种潜在治疗方法。在此,我们开发并验证了一种使用超高效液相色谱-串联质谱法(UHPLC-MS/MS)来鉴定和定量柑橘类水果中青霉素G及其两种代谢产物青霉酸和青霉醛酸的方法。该方法通过加入同位素标记的内标物,即青霉酸-D和青霉醛酸-D,对先前的方法进行了改进。这些标准品通过补偿回收率损失、降解和基质效应,极大地提高了我们测量的准确性和精密度。当提取2g柑橘类水果样品时,青霉素G和青霉醛酸的检测限(LOD)确定为0.1ng/g,青霉酸的检测限为0.2ng/g。在0.1、0.25、1和10ng/g的加标水平下,青霉酸和青霉醛酸的绝对回收率一般在50%-70%之间。用同位素标记标准品校正后的回收率约为90%-110%。该方法将有助于使用同位素标记标准品和UHPLC-MS/MS鉴定和定量药物残留及其降解产物。