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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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    [14] 任丽萍, 田 芹, 潘灿平. 丁草胺原药中主要杂质的GC-MS定性分析[J]. 农药(Chinese Journal of Pesticides). 2005: 44(4): 74-78.
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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.
    [27] Bertinatto JA, Rodr'ıguez, Desimone MF. Validation of a capillary electrophoresis method for the analysis of ibandronate related impurities[J]. J Pharm Biomed Anal,2007,44(1): 305-308.
    [28] Wijk AMv, Muijselaar PG, Stegman K. Capillary electrophoresis-mass spectrometry for impurity profiling of basic pharmaceuticals using non-volatile background electrolytes[J]. J Chromatogr A,2007,1159(1-2): 175-184.
    [29] Mol R, Kragt E, Jimidar I. Micellar electrokinetic chromate graphy-electrospray ionization mass spectrometry for the identification of drug impurities[J]. J Chromatogr B,2006,843(2): 283-288.
    [30] Hernández SL,Ruiz GC, Crego AL. Sensitive determination of D-carnitine as enantiomeric impurity of levo-carnitine in pharmaceutical formulations by capillary electrophoresis-tandem mass spectrometry[J]. J Pharm Biomed Anal,2010,53(5): 1217-1223.
    [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.
    [32] Görög S. Identification and Determination of Impurities in Drugs[M].Amsterdam:Elsevier Science, 2000:67-82.
    [33] Murakami T, Konno H, Fukutsu N. Identification of a degradation product in stressed tablets of olmesartan medoxomil by the complementary use of HPLC hyphenated techniques[J]. J Pharm Biomed Anal, 2008,47(3):553-559.
    [34] Wolters AM, Jayawickrama DA, Larive CK. Capillary isotachophoresis/NMR: extension to trace impurity analysis and improved instrumental coupling[J]. Anal Chem, 2002,74(10): 2306-2313.
    [35] Prabha Srinivasu, Devarakonda V, SubbaRao A. validated stabilityúindicating LC method for acetazolamide in the presence of degradation products and its process-related impurities[J]. J Pharm Biomed Anal., 2011, 52(1):142-148.
    [36] Székely Gy, Henriques B, Gil M. Design of experiments as a tool for LC-MS/MS method development for the trace analysis of the potentially genotoxic 4-dimethy laminopyridine impurity in glucocorticoids[J]. J Pharm Biomed Anal, 2012,70:251-258.
    [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
  • 修回日期:  2014-01-16

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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