Smalley James, Kadiyala Pathanjali, Xin Baomin, Balimane Praveen, Olah Timothy
Pharmaceutical Candidate Optimization, Pharmaceutical Research Institute, Bristol-Myers Squibb, P.O. Box 5400, Princeton, NJ 08543-5400, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Jan 18;830(2):270-7. doi: 10.1016/j.jchromb.2005.11.006. Epub 2005 Nov 22.
Caco-2 cells are frequently used for screening compounds for their permeability characteristics and P-glycoprotein (P-gp) interaction potential. Bi-directional permeability studies performed on Caco-2 cells followed by analysis by HPLC-UV or LC-MS method constitutes the "method of choice" for the functional assessment of efflux characteristics of a test compound. A high throughput LC-MS/MS method has been developed using on-line extraction turbulent flow chromatography coupled to tandem mass spectrometric detection to analyze multiple compounds present in Hanks balanced salt solution in a single analytical run. All standard curves (P-gp substrates: quinidine, etoposide, rhodamine 123, dexamethasone, and verapamil and non-substrates: metoprolol, sulfasalazine, propranolol, nadolol, and furosemide) were prepared in a cassette mode (ten-in-one) while Caco-2 cell incubations were performed both in discreet mode and in cassette mode. The standard curve range for most compounds was 10-2500 nM with regression coefficients (R(2)) greater than 0.99 for all compounds. The applicability and reliability of the analysis method was evaluated by successful demonstration of efflux ratio greater than 1 for the P-gp substrates studied in the Caco-2 cell model. The use of cassette mode analysis through selected reaction monitoring mass spectrometry presents an attractive option to increase the throughput, sensitivity, selectivity, and efficiency of the model over discreet mode UV detection.
Caco-2细胞常用于筛选具有通透性特征和P-糖蛋白(P-gp)相互作用潜力的化合物。在Caco-2细胞上进行双向通透性研究,随后通过HPLC-UV或LC-MS方法进行分析,构成了用于评估受试化合物外排特征功能的“首选方法”。已开发出一种高通量LC-MS/MS方法,该方法使用在线萃取湍流色谱与串联质谱检测相结合,可在一次分析运行中分析汉克斯平衡盐溶液中存在的多种化合物。所有标准曲线(P-gp底物:奎尼丁、依托泊苷、罗丹明123、地塞米松和维拉帕米,以及非底物:美托洛尔、柳氮磺胺吡啶、普萘洛尔、纳多洛尔和呋塞米)均采用盒式模式(十合一)制备,而Caco-2细胞培养则以离散模式和盒式模式进行。大多数化合物的标准曲线范围为10-2500 nM,所有化合物的回归系数(R(2))均大于0.99。通过在Caco-2细胞模型中成功证明受试P-gp底物的外排率大于1,评估了分析方法的适用性和可靠性。与离散模式UV检测相比,通过选择反应监测质谱进行盒式模式分析为提高该模型的通量、灵敏度、选择性和效率提供了一个有吸引力的选择。