Sardella Roccaldo, Scorzoni Stefania, Conte Carmela, Lisanti Antonella, Ianni Federica, Natalini Benedetto
Department of Pharmaceutical Sciences, University of Perugia, via Fabretti 48, 06123 Perugia, Italy.
Department of Pharmaceutical Sciences, University of Perugia, via Fabretti 48, 06123 Perugia, Italy.
J Pharm Biomed Anal. 2014 Sep;98:253-9. doi: 10.1016/j.jpba.2014.05.018. Epub 2014 May 23.
Parkinson's disease is a multifactorial neurodegenerative disorder, characterized by a reduction of dopamine (DA) levels. The molecular pathways involved in the pathogenesis of disease have not yet been fully disclosed. Therefore, developing new diagnostic methods and tools to evaluate the depletion of DA and of some of its metabolites (3,4-dihydroxyphenylacetic acid, homovanillic acid, and 3-methoxytyramine) is of outstanding importance for biochemical evaluations. Moreover, neurons responsible for DA release also produce the neurotransmitter gamma-aminobutyric acid (GABA), thus, quantitative measurements of GABA levels can have a relevant impact for a further understanding of the biochemical processes involved in the neurodegenerative event. In the present study, two HPLC methods based on the reversed-phase ion-pairing chromatography (RP-IPC) and the hydrophilic liquid interaction chromatography (HILIC) concepts were developed to allow the quantification of DA and its metabolites as well as GABA levels in mouse striatal and cortical tissue homogenates. The two fairly orthogonal HPLC methods were directly applied to the biological samples, without preliminary derivatization of the compounds of interest. A high level of selectivity was obtained for DA metabolites and GABA by running the gradient RP-IPC method with a volatile ion-pairing reagent, which makes it suitable for the quantitative assay of four out of five compounds. Matrix deriving interferences unabled the base-line separation of DA which was instead successfully achieved with the HILIC-based method. To avail of HPLC methods providing distinct selectivity profiles, makes possible the correct species quantification and allows to compensate the intrinsic limits characterizing all chromatographic methods.
帕金森病是一种多因素神经退行性疾病,其特征是多巴胺(DA)水平降低。该疾病发病机制中涉及的分子途径尚未完全揭示。因此,开发新的诊断方法和工具来评估DA及其一些代谢物(3,4-二羟基苯乙酸、高香草酸和3-甲氧基酪胺)的消耗,对于生化评估具有极其重要的意义。此外,负责释放DA的神经元也会产生神经递质γ-氨基丁酸(GABA),因此,GABA水平的定量测量对于进一步了解神经退行性事件中涉及的生化过程可能会产生相关影响。在本研究中,开发了两种基于反相离子对色谱(RP-IPC)和亲水液相相互作用色谱(HILIC)概念的高效液相色谱方法,用于定量测定小鼠纹状体和皮质组织匀浆中的DA及其代谢物以及GABA水平。这两种相当正交的高效液相色谱方法直接应用于生物样品,无需对目标化合物进行预衍生化。通过使用挥发性离子对试剂运行梯度RP-IPC方法,对DA代谢物和GABA获得了高度的选择性,这使其适用于五种化合物中四种的定量测定。基质衍生干扰无法实现DA的基线分离,而基于HILIC的方法成功实现了基线分离。利用提供不同选择性谱的高效液相色谱方法,使得正确的物种定量成为可能,并允许补偿所有色谱方法固有的局限性。