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实际应用中游离吡仑帕奈浓度的治疗药物监测:一种基于离心超滤样品分离的实用分析技术。

Therapeutic drug monitoring of free perampanel concentrations in practice: A practical analytical technique based on centrifugal ultrafiltration sample separation.

作者信息

Ma Ying-Hua, Dong Lei, Wu Jia-Xuan, Hu Shi-Yuan, Meng Xiang-Fei, Zhao Yi-Le, Liu Kang, Yan Dan-Ni, Sun Su-Zhen

机构信息

Department of Pharmacy, Children's Hospital of Hebei Province, Shijiazhuang, 050031, PR China.

College of Pharmacy, Hebei Medical University, Shijiazhuang, Hebei, 050017, PR China.

出版信息

Heliyon. 2024 Aug 3;10(15):e35734. doi: 10.1016/j.heliyon.2024.e35734. eCollection 2024 Aug 15.

Abstract

OBJECTIVES

The centrifugal ultrafiltration-high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was established to determine the free perampanel (PER) concentration in children with epilepsy.

METHODS

Free PER concentration was obtained using centrifugal ultrafiltration devices. The internal standard was PER-D5. The method was investigated for selectivity, carryover, lower limit of quantification, calibration curve, accuracy, precision, matrix effects, recovery, and stability. The Spearman's correlation coefficient was used to evaluate the correlation between the free and total PER concentrations. A nonparametric test was used to estimate the effects of PER along with other antiepileptic drugs on the total and free PER concentrations.

RESULTS

The free PER concentration was positively correlated with the total PER concentration in the 57 plasma samples ( = 0.793 > 0,  < 0.001). Additionally, the free PER concentrations were significantly ( < 0.05) increased in valproic acid (VPA) co-therapy (9.87 ± 5.83) compared with non-VPA co-therapy (5.03 ± 4.57).

CONCLUSIONS

The proposed method is efficient, sensitive, and suitable for detecting free PER concentrations in children with epilepsy. Simultaneously, the free PER concentration response to clinical outcomes in children with epilepsy was more clinically significant, particularly when combined with VPA.

摘要

目的

建立离心超滤-高效液相色谱-串联质谱(HPLC-MS/MS)法测定癫痫患儿中游离吡仑帕奈(PER)的浓度。

方法

使用离心超滤装置获得游离PER浓度。内标为PER-D5。对该方法进行选择性、残留、定量下限、校准曲线、准确度、精密度、基质效应、回收率和稳定性研究。采用Spearman相关系数评估游离和总PER浓度之间的相关性。使用非参数检验评估PER与其他抗癫痫药物对总PER和游离PER浓度的影响。

结果

在57份血浆样本中,游离PER浓度与总PER浓度呈正相关(r = 0.793 > 0,P < 0.001)。此外,与非丙戊酸(VPA)联合治疗(5.03 ± 4.57)相比,VPA联合治疗时游离PER浓度显著升高(P < 0.05)(9.87 ± 5.83)。

结论

所提出的方法高效、灵敏,适用于检测癫痫患儿中游离PER的浓度。同时,游离PER浓度对癫痫患儿临床结局的反应在临床上更具意义,尤其是与VPA联合使用时。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b15e/11336813/0617bfc8b526/ga1.jpg

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