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应中央军委要求,2022年9月起,《药学实践杂志》将更名为《药学实践与服务》,双月刊,正文96页;2023年1月起,拟出版月刊,正文64页,数据库收录情况与原《药学实践杂志》相同。欢迎作者踊跃投稿!

药物杂质研究现状概述

李娜 娄子洋

李娜, 娄子洋. 药物杂质研究现状概述[J]. 药学实践与服务, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005
引用本文: 李娜, 娄子洋. 药物杂质研究现状概述[J]. 药学实践与服务, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005
LI Na, LOU Ziyang. Overview of the research on drug impurity[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005
Citation: LI Na, LOU Ziyang. Overview of the research on drug impurity[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005

药物杂质研究现状概述

doi: 10.3969/j.issn.1006-0111.2014.03.005

Overview of the research on drug impurity

  • 摘要: 药品是一种特殊商品,与人们的健康和生命安全息息相关,药物杂质是影响药物稳定性和疗效的物质,与药品质量、安全性及效能密切相关。随着杂质控制在药物开发研究中越来越受到重视,研究者开始将注意力转移到痕量杂质的分析上。笔者总结近10年来国内外杂质研究的相关进展,内容涉及药物杂质研究的相关指导原则、杂质定性研究的相关技术以及杂质定量研究等的一般方法。
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    [19] Modhave D.T, Handa T, Shah RP. Successful characterization of degradation products of drugs using LC-MS tools: application to piroxicam and meloxicam[J]. Anal Methods,2011,3(12): 2864-2872.
    [20] Modhave DT, Handa T, Shah RP. Stress degradation studies on lornoxicam using LC, LC-MS/TOF and LC-MSn[J]. J Pharm Biomed Anal,2011,56(3): 538-545.
    [21] Shah RP, Singh S. Identification and characterization of a photolytic degradation product of telmisartan using LC-MS/TOF, LC-MSn, LC-NMR and on-line H/D exchange mass studies[J]. J Pharm.Biomed Anal,2010,53(3): 755-761.
    [22] Wang MJ, Pendela M, Hu CQ. Impurity profiling of acetylspiramycin by liquid chromatography-ion trap mass spectrometry[J]. J Chromatogr A, 2010, 1217(42): 6531-6544.
    [23] Mehta S, Shah RP, Priyadarshi R. LC and LC-MS/TOF studies on stress degradation behaviour of candesartan cilexetil[J]. J Pharm Biomed Anal,2010,52(3): 345-354.
    [24] Liu DQ, Wu L, Sun M. On-line H/D exchange LC-MS strategy for structural elucidation of pharmaceutical impurities[J]. J Pharm Biomed.Anal,2007,44(2): 320-329.
    [25] Shah RP, Sahu A, Singh S. Identification and characterization of degradation products of irbesartan using LC-MS/TOF, MSn, on-line H/D exchange and LC-NMR[J]. J Pharm Biomed Anal,2010,51(5): 1037-1046.
    [26] Thurman EM, Ferrer I. The isotopic mass defect: a tool for limiting molecular formulas by accurate mass[J]. Anal Bioanal Chem, 2010,397(7): 2807-2816.
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    [31] Carvalho AZ, Attug EMN, Zayed SE. Micellar electrokinetic chromatography method development for determination of impurities in ritonavir[J]. J Pharm Biomed Anal,2010,53(5): 1210-1216.
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    [37] 徐宜宏,蒋 施,付海滨,等.气相色谱-三重四极杆质谱法同时测定五味子中117种农药残留量[J]. 福建分析测试,2012,21(5):1-10.
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  • 收稿日期:  2013-11-06
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药物杂质研究现状概述

doi: 10.3969/j.issn.1006-0111.2014.03.005

摘要: 药品是一种特殊商品,与人们的健康和生命安全息息相关,药物杂质是影响药物稳定性和疗效的物质,与药品质量、安全性及效能密切相关。随着杂质控制在药物开发研究中越来越受到重视,研究者开始将注意力转移到痕量杂质的分析上。笔者总结近10年来国内外杂质研究的相关进展,内容涉及药物杂质研究的相关指导原则、杂质定性研究的相关技术以及杂质定量研究等的一般方法。

English Abstract

李娜, 娄子洋. 药物杂质研究现状概述[J]. 药学实践与服务, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005
引用本文: 李娜, 娄子洋. 药物杂质研究现状概述[J]. 药学实践与服务, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005
LI Na, LOU Ziyang. Overview of the research on drug impurity[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005
Citation: LI Na, LOU Ziyang. Overview of the research on drug impurity[J]. Journal of Pharmaceutical Practice and Service, 2014, 32(3): 179-185. doi: 10.3969/j.issn.1006-0111.2014.03.005
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