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一种通过与1-氟-2,4-二硝基苯衍生化来测定剂型中盐酸美金刚的稳定性指示高效液相色谱法。

A Stability-Indicating HPLC Method for the Determination of Memantine Hydrochloride in Dosage Forms through Derivatization with 1-Fluoro-2,4-dinitrobenzene.

作者信息

Jalalizadeh Hassan, Raei Mahdi, Tafti Razieh Fallah, Farsam Hassan, Kebriaeezadeh Abbas, Souri Effat

机构信息

Department of Research & Development, Osvah Pharmaceutical Co. Tehran, Iran.

Department of Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Sci Pharm. 2013 Dec 9;82(2):265-79. doi: 10.3797/scipharm.1310-09. Print 2014 Apr-Jun.

DOI:10.3797/scipharm.1310-09
PMID:24959398
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4065122/
Abstract

Memantine is chemically a tricyclic amine and is used for Parkinson's disease and movement disorders. Although several HPLC methods with different derivatization reagents have been developed for the determination of memantine in biological fluids, there are some complications which limit the use of these methods in routine analysis of memantine in in vitro tests. We established a simple, sensitive, precise, and accurate HPLC method for the quantification of memantine in dosage forms. Pre-column derivatization of memantine was performed with 1-fluoro-2,4-dinitrobenzene and the reaction product was separated on a Nova-Pak C18 column. A mixture of acetonitrile and sodium dihydrogenphosphate (pH 2.5; 0.05 M) (70: 30, v/v) was used as the mobile phase. UV detection was performed at 360 nm. Forced degradation studies were performed on a powdered tablet sample of memantine hydro-chloride using acidic (0.1 M hydrochloric acid), basic (0.1 M sodium hydroxide), oxidative (10% hydrogen peroxide), thermal (105°C), photolytic, and humidity conditions. Good linearity (r(2)=0.999) was obtained over the range of 1-12 μg mL(-1) of memantine hydrochloride with acceptable within-day and between-day precision values in the range of 0.05-0.95%. The proposed method was used for the assay determination and dissolution rate study of memantine dosage forms with excellent specificity.

摘要

美金刚在化学上是一种三环胺,用于治疗帕金森病和运动障碍。尽管已经开发了几种使用不同衍生化试剂的高效液相色谱(HPLC)方法来测定生物流体中的美金刚,但仍存在一些问题,限制了这些方法在体外试验中美金刚常规分析中的应用。我们建立了一种简单、灵敏、精确且准确的HPLC方法,用于定量剂型中的美金刚。美金刚的柱前衍生化使用1-氟-2,4-二硝基苯进行,反应产物在Nova-Pak C18柱上分离。乙腈和磷酸二氢钠(pH 2.5;0.05 M)(70:30,v/v)的混合物用作流动相。在360 nm处进行紫外检测。使用酸性(0.1 M盐酸)、碱性(0.1 M氢氧化钠)、氧化(10%过氧化氢)、热(105°C)、光解和湿度条件对盐酸美金刚的粉末状片剂样品进行强制降解研究。在1-12 μg mL(-1)盐酸美金刚范围内获得了良好的线性关系(r(2)=0.999),日内和日间精密度值在0.05-0.95%范围内可接受。所提出的方法用于美金刚剂型的含量测定和溶出度研究,具有出色的特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/dc644f94b1e0/scipharm.2014.82.265f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/6186ab3c7fe6/scipharm.2014.82.265f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/4891aca8354e/scipharm.2014.82.265f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/32073862b7cf/scipharm.2014.82.265f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/866cfa90602e/scipharm.2014.82.265f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/86fefaf359ec/scipharm.2014.82.265f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/524558dfa858/scipharm.2014.82.265f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/dc644f94b1e0/scipharm.2014.82.265f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/6186ab3c7fe6/scipharm.2014.82.265f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/4891aca8354e/scipharm.2014.82.265f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/32073862b7cf/scipharm.2014.82.265f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/866cfa90602e/scipharm.2014.82.265f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/86fefaf359ec/scipharm.2014.82.265f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/524558dfa858/scipharm.2014.82.265f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2627/4065122/dc644f94b1e0/scipharm.2014.82.265f7.jpg

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