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采用高效液相色谱法测定药物制剂中依巴斯汀的含量。

Determination of ebastine in pharmaceutical formulations by HPLC.

作者信息

Prabu S L, Kumar C Dinesh, Shirwaikar A, Shirwaikar Annie

机构信息

Department of Pharmaceutical Quality Assurance, Manipal College of Pharmaceutical Sciences, Manipal-576 104, India.

出版信息

Indian J Pharm Sci. 2008 May-Jun;70(3):406-7. doi: 10.4103/0250-474X.43022.

DOI:10.4103/0250-474X.43022
PMID:20046762
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2792524/
Abstract

A simple, precise and rapid RP-HPLC method was developed for the determination of ebastine in pharmaceutical formulations. The method was carried out on a Phenomenex RP-C18 column using a mixture of methanol and water (90:10) and detection was done at 262 nm. The linearity range was 5-100 mug/ml. The intra-day and inter-day precision were in the range of 0.22% to 0.49% and 0.24% to 0.73%, respectively.

摘要

建立了一种简单、精确且快速的反相高效液相色谱法(RP-HPLC)用于测定药物制剂中的依巴斯汀。该方法采用菲罗门RP-C18柱,以甲醇和水(90:10)的混合物为流动相,在262 nm波长处进行检测。线性范围为5 - 100 μg/ml。日内精密度在0.22%至0.49%之间,日间精密度在0.24%至0.73%之间。

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本文引用的文献

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J Chromatogr B Analyt Technol Biomed Life Sci. 2004 Dec 25;813(1-2):75-80. doi: 10.1016/j.jchromb.2004.09.017.
2
Comparative antiallergic effects of second-generation H1-antihistamines ebastine, cetirizine and loratadine in preclinical models.第二代H1抗组胺药依巴斯汀、西替利嗪和氯雷他定在临床前模型中的抗组胺作用比较
Arzneimittelforschung. 2003;53(2):93-7. doi: 10.1055/s-0031-1297078.
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Effect of age and gender on the pharmacokinetics of ebastine after single and repeated dosing in healthy subjects.年龄和性别对健康受试者单次及重复给药后依巴斯汀药代动力学的影响。
Int J Clin Pharmacol Ther. 2001 Mar;39(3):126-34. doi: 10.5414/cpp39126.
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Clinical pharmacology of new histamine H1 receptor antagonists.新型组胺H1受体拮抗剂的临床药理学
Clin Pharmacokinet. 1999 May;36(5):329-52. doi: 10.2165/00003088-199936050-00003.
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Sedation and antihistaminics.
Arzneimittelforschung. 1982;32(9a):1193-5.