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超滤条件对苯妥英和丙戊酸游离分数的影响。

Influence of ultrafiltration conditions on the unbound fraction of phenytoin and valproic acid.

作者信息

Temme Pjotr P, van Luin Matthijs, Deenen Maarten J, Meijer Ron, Jager Nynke G L, Malingré Mirte M

机构信息

Department of Hospital Pharmacy, Meander Medical Centre, Amersfoort, the Netherlands.

Department of Clinical Pharmacy, Catharina Hospital, Eindhoven, the Netherlands.

出版信息

Eur J Clin Pharmacol. 2025 Sep 9. doi: 10.1007/s00228-025-03918-3.

Abstract

PURPOSE

This study was designed to analyse the influence of temperature, pH and storage time on unbound fractions of PHT and VPA.

METHODS

The influence of ultrafiltration (UF) temperature on measured unbound fractions of PHT and VPA in spiked samples was evaluated in a single laboratory experiment and in data from a national external quality control (EQC) database. The influence of pH adjustment with phosphate buffered saline (PBS) on measured unbound fractions of PHT and VPA was investigated in patient samples. The influence of storage time on unbound fractions of PHT and VPA was examined in patient samples by performing UF at various time points.

RESULTS

Performing UF at a temperature of 37 °C compared to 20 °C significantly increased (p < 0.05) the measured unbound fractions for both PHT (range 14.8-26.3%) and VPA (range 5.7-16.0%) in the single laboratory experiment. Consistent with these findings, reported unbound fractions in the ECQ database of PHT were significantly higher with UF at 37 °C compared to room temperature. For VPA, this was not the case. However, for both drugs, the number of laboratories performing UF at 37 °C was limited (n = 2-4). Adjustment of pH with PBS was unfeasible. After 4 days of storage at 5 °C, the unbound fraction of PHT seemed to remain stable whereas the unbound fraction of VPA appeared to increase (27.4%) (n = 3).

CONCLUSION

Higher UF temperatures led to an increase in measured unbound fractions of both PHT and to a lesser extent VPA. Storage time of plasma samples might influence the unbound fraction of VPA.

摘要

目的

本研究旨在分析温度、pH值和储存时间对苯妥英(PHT)和丙戊酸(VPA)游离分数的影响。

方法

在一项单一实验室实验以及来自国家外部质量控制(EQC)数据库的数据中,评估超滤(UF)温度对加标样品中PHT和VPA测定游离分数的影响。在患者样本中研究用磷酸盐缓冲盐水(PBS)调节pH值对PHT和VPA测定游离分数的影响。通过在不同时间点进行超滤,在患者样本中检测储存时间对PHT和VPA游离分数的影响。

结果

在单一实验室实验中,与20℃相比,在37℃进行超滤显著增加了(p<0.05)PHT(范围14.8 - 26.3%)和VPA(范围5.7 - 16.0%)的测定游离分数。与这些发现一致,在EQC数据库中,与室温相比,37℃超滤时PHT报告的游离分数显著更高。对于VPA,情况并非如此。然而,对于这两种药物,在37℃进行超滤的实验室数量有限(n = 2 - 4)。用PBS调节pH值不可行。在5℃储存4天后,PHT的游离分数似乎保持稳定,而VPA的游离分数似乎增加了(27.4%)(n = 3)。

结论

较高的超滤温度导致PHT的测定游离分数增加,VPA的增加幅度较小。血浆样本的储存时间可能会影响VPA的游离分数。

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