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首页> 外文期刊>Archives of dermatological research. >Measurement of 5-methoxypsoralen and 8-methoxypsoralen in saliva of PUVA patients as a noninvasive, clinically relevant alternative to monitoring in blood.
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Measurement of 5-methoxypsoralen and 8-methoxypsoralen in saliva of PUVA patients as a noninvasive, clinically relevant alternative to monitoring in blood.

机译:测量PUVA患者唾液中的5-甲氧基补骨脂素和8-甲氧基补骨脂素是一种无创,临床相关的监测血液的替代方法。

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BACKGROUND: Monitoring of psoralen concentration and time-course in PUVA patients is vital for efficient PUVA therapy. Blood sampling is invasive and labour-intensive and thus unsuited for routine use and repeat measurements over the course of therapy. OBJECTIVE: Psoralen pharmacokinetics in saliva were investigated and validated as a noninvasive, simple and biologically relevant alternative to measurements in blood. METHODS: The time-course of psoralen concentration was measured in saliva and serum of volunteers and patients receiving PUVA or extracorporeal photopheresis therapy. The samples were analysed by high-performance liquid chromatography. Three commonly used oral psoralen preparations were tested: Psoraderm5 (5-methoxypsoralen; 5-MOP), Meladinine and Oxsoralen (both 8-methoxypsoralen; 8-MOP). RESULTS: The pharmacokinetic parameter Cmax in saliva averaged 10% (range 6-20%) of the serum values for 8-MOP, and < or = 4% for 5-MOP. These concentrations correspond to the therapeutically relevant, non-albumin-bound fraction of psoralen in serum that is available to diffuse into the tissues. The parameter tmax in saliva and serum coincided, indicating that psoralens diffuse rapidly between the two compartments. CONCLUSION: Monitoring of psoralens in saliva is a valuable, noninvasive alternative to measurements in serum, suitable for routine use. A series of five or six saliva samples is sufficient to determine tmax in a patient beginning photochemotherapy. To determine Cmax, three independent saliva measurements at t = tmax are recommended.
机译:背景:监测PUVA患者的补骨脂素浓度和时程对于有效的PUVA治疗至关重要。血液采样是侵入性的和劳动密集型的,因此不适合常规使用并在治疗过程中重复测量。目的:对唾液中补骨脂素的药代动力学进行了研究,并被确认为一种无创,简单且生物学相关的替代品,可用于血液测量。方法:测定志愿者和接受PUVA或体外光采疗法的患者的唾液和血清中补骨脂素浓度的时程。通过高效液相色谱分析样品。测试了三种常用的口服补骨脂素制剂:Psoraderm5(5-甲氧基补骨脂素; 5-MOP),美拉敏宁和Oxsoralen(8-甲氧基补骨脂素; 8-MOP)。结果:唾液中的药代动力学参数Cmax平均为8-MOP的血清值的10%(范围6-20%),而对于5-MOP的平均值为<或= 4%。这些浓度对应于血清中补骨脂素的治疗相关的,非白蛋白结合的级分,其可扩散到组织中。唾液和血清中的参数tmax重合,表明补骨脂素在两个腔室之间迅速扩散。结论:唾液中补骨脂素的监测是一种有价值的,无创的替代血清测量方法的方法,适合常规使用。一系列五个或六个唾液样本足以确定开始光化学疗法的患者的tmax。为了确定Cmax,建议在t = tmax时进行三个独立的唾液测量。

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