Characterization and HPLC Method Validation for Determination of Dopamine Hydrochloride in Prepared Nano Particles and Pharmacokinetic Application

S. Neha, A. Mishra, Laxmi Rani, Suraj P. Verma, P. K. Sahoo
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Abstract

Abstract The emotional control monoamines neurotransmitter catecholamine group of chemicals is dopamine. It has been described and recognized that a lack of dopamine containing neurons contributes to neurological issues, such as Parkinsonism. Due to the incapability of dopamine HCl to cross the blood brain barrier, the advanced novel drug delivery of dopamine HCl is performed in the form of nano structure lipid carrier system (NLC-DOPA) to bypass the blood brain barrier using intranasal route of administration with improved compliance bioavailability and less side effect. The NLC-DOPA was prepared by the high pressure homogenizer ultra-probe sonicator and characterized by the particle size analyzer, zeta potential, transmission electron microscopy (TEM) and X-Ray diffraction (XRD). The determination of dopamine hydrochloride in formulation was evaluated by drug entrapment efficiency further it is validated by analytical method development using high performance liquid chromatography (HPLC) with C18 ODS column and 0.05 M KH2PO4 buffer pH 2.5 and Methanol (90:10) along with retention time 4.872 min at 280 nm wavelength. The method was validated for dopamine HCl in formulation with linearity, precision and recovery analysis. The study was shown that method was easy, rapid, accurate, specific and precise for quality analysis of dopamine HCl in NLC-DOPA formulation. The validated method of HPLC was further used for the biological application in term of the pharmacokinetic study to find out the concentration of drug in blood as well as brain. The pharmacokinetic parameters were calculated with help of the software PK solver 2.0 to determine the maximum concentration (Cmax), Maximum time (Tmax), Elimination half life (t1/2), Area under the curve (AUC0-t), volume of distribution (Vz/F_obs) and Clearance (Cl/F_obs) of all groups of animals (n=3). The study showed that the NLC-DOPA was producing a sustained and controlled release in appropriate amount of drug through intranasal bypass delivery into brain. GRAPHICAL ABSTRACT
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制备纳米颗粒中盐酸多巴胺含量的表征、HPLC法验证及药动学应用
控制情绪的单胺类神经递质儿茶酚胺类化学物质是多巴胺。人们已经描述并认识到,缺乏含有多巴胺的神经元会导致神经系统问题,如帕金森病。由于多巴胺HCl不能穿过血脑屏障,先进的新型给药多巴胺HCl以纳米结构脂质载体系统(NLC-DOPA)的形式通过鼻内给药途径绕过血脑屏障,具有更高的顺应性、生物利用度和更小的副作用。采用高压均质机超探针超声制备了NLC-DOPA,并用粒度分析仪、zeta电位、透射电子显微镜(TEM)和x射线衍射仪(XRD)对其进行了表征。采用高效液相色谱法(HPLC),色谱柱为C18 ODS,缓冲液为0.05 M KH2PO4, pH为2.5,甲醇(90:10),保留时间为4.872 min,波长为280 nm。该方法对盐酸多巴胺的线性、精密度和回收率进行了验证。结果表明,该方法简便、快速、准确、特异、精密度高,可用于NLC-DOPA制剂中多巴胺盐酸的质量分析。将验证后的高效液相色谱法进一步应用于生物药代动力学研究,了解药物在血药浓度和脑药浓度。利用PK求解器2.0软件计算药代动力学参数,确定各组动物(n=3)的最大浓度(Cmax)、最大时间(Tmax)、消除半衰期(t1/2)、曲线下面积(AUC0-t)、分布体积(Vz/F_obs)和清除率(Cl/F_obs)。研究表明,NLC-DOPA在适当剂量的情况下,通过鼻内旁路给药进入大脑,产生持续的、可控的释放。图形抽象
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