Kaewpradit Sirikanya, Yusakul Gorawit, Rojsitthisak Pornchai, Jantarat Chutima
School of Pharmacy, Walailak University, Thasala, Nakhon Si Thammarat, 80160, Thailand.
Drug and Cosmetics Excellence Center, Walailak University, Thasala, Nakhon Si Thammarat, 80160, Thailand.
Heliyon. 2024 Mar 13;10(6):e27875. doi: 10.1016/j.heliyon.2024.e27875. eCollection 2024 Mar 30.
This study presents an efficient high-performance liquid chromatography with ultraviolet detection (HPLC-UV) method for monitoring valproic acid (VPA) level in human plasma. This method is distinguished by its simplicity, cost-effectiveness, and rapid execution, addressing the limitations associated with other advanced analytical techniques like liquid chromatography-mass spectrometry (LC-MS), gas chromatography-mass spectrometry (GC-MS), and immunoassays, which are generally complex and costly for routine application. A challenge in analyzing VPA is its non-linear protein binding profile and the absence of a chromophore in its structure, making direct detection difficult. To overcome this, the study developed an efficient HPLC-UV for VPA determination in human plasma, utilizing a simplified and rapid microwave-assisted derivatization process. Due to the lack of a chromophore in VPA structure, this work developed a microwave-assisted derivatization of VPA using phenylhydrazine hydrochloride (PH HCl). The process optimization was achieved at 450 W for 50 s, facilitating effective HPLC-UV detection. The derivatized product was characterized using H nuclear magnetic resonance (NMR) and Fourier transform infrared spectrometer (FT-IR). The derivative, identified as -phenyl-2-propylpentanehydrazonic acid, demonstrated specificity in plasma analysis with no detectable interference. The method exhibited a linear response for VPA concentrations ranging from 30 to 150 μg/mL, with a correlation coefficient exceeding 0.99. Recovery varied between 86.7% and 107%, with a maximum coefficient of variation (CV) of 10.0%. The findings suggest that the microwave-assisted derivatization technique substantially improves the feasibility and cost-effectiveness of HPLC-UV for the analysis of VPA in plasma. This method provides a viable alternative to conventional HPLC methodologies, offering a balance of efficiency and economic practicality for VPA quantification.
本研究提出了一种高效的带有紫外检测的高效液相色谱法(HPLC-UV),用于监测人血浆中的丙戊酸(VPA)水平。该方法具有操作简便、成本效益高和执行快速的特点,克服了与其他先进分析技术(如液相色谱-质谱联用(LC-MS)、气相色谱-质谱联用(GC-MS)和免疫测定)相关的局限性,这些技术通常复杂且成本高昂,不适合常规应用。分析VPA的一个挑战是其非线性蛋白质结合特性以及结构中缺乏发色团,这使得直接检测变得困难。为克服这一问题,该研究开发了一种用于测定人血浆中VPA的高效HPLC-UV方法,采用了简化且快速的微波辅助衍生化过程。由于VPA结构中缺乏发色团,本研究使用盐酸苯肼(PH HCl)对VPA进行微波辅助衍生化。在450W功率下进行50s可实现过程优化,便于进行有效的HPLC-UV检测。使用氢核磁共振(NMR)和傅里叶变换红外光谱仪(FT-IR)对衍生化产物进行了表征。该衍生物被鉴定为-苯基-2-丙基戊烷腙酸,在血浆分析中表现出特异性,无明显干扰。该方法对VPA浓度在30至150μg/mL范围内呈线性响应,相关系数超过0.99。回收率在86.7%至107%之间,最大变异系数(CV)为10.0%。研究结果表明,微波辅助衍生化技术显著提高了HPLC-UV分析血浆中VPA的可行性和成本效益。该方法为传统HPLC方法提供了一种可行的替代方案,在VPA定量分析中实现了效率与经济实用性的平衡。