生物利用度
药代动力学
维生素
药理学
化学
蛋白质沉淀
伊马替尼
色谱法
血浆浓度
医学
内科学
生物化学
髓系白血病
作者
Hadir M. Maher,Nourah Z. Alzoman,Shereen M. Shehata
出处
期刊:Bioanalysis
[Future Science Ltd]
日期:2018-07-01
卷期号:10 (14): 1099-1113
被引量:6
标识
DOI:10.4155/bio-2018-0043
摘要
The growing interest of cancerous patients in using vitamins, while on imatinib (IMA) therapy, increased the risk of their pharmacokinetic interactions.Ultra-performance LC-MS/MS method was developed and validated for the determination of IMA following oral administration of selected vitamin preparations (vitamin A, E, D3 and C) in rat plasma using a hybrid sample preparation technique of protein precipitation followed by SPE.The method showed good linear response for IMA over the concentration range 1-500 ng/ml. Co-administered vitamin preparations could affect IMA pharmacokinetic profiling through either an increase (vitamin A and E) or a decrease (vitamin C) in IMA bioavailability. Vitamin D3 produced no significant effect on IMA bioavailability.Particular concern should be paid when vitamin preparations are administered with IMA.
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