Study of forced decomposition behavior of lamivudine using LC, LC-MS/TOF and MSn

被引:37
作者
Bedse, Gaurav [1 ]
Kumar, Vijay [1 ]
Singh, Saranjit [1 ]
机构
[1] NIPER, Dept Pharmaceut Anal, SAS Nagar 160062, Punjab, India
关键词
Lamivudine; Stress Studies; Stability-indicating assay method; MSn; LC-MS/TOF; Degradation pathway; Mechanism; HUMAN PLASMA; (-)-2'-DEOXY-3'-THIACYTIDINE; DEGRADATION; ZIDOVUDINE; STABILITY; FLUID; ASSAY;
D O I
10.1016/j.jpba.2008.10.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Lamivudine was subjected to forced decomposition conditions of hydrolysis (neutral, acidic and alkaline), oxidation, photolysis and thermal stress, as suggested in the ICH guideline Q1A(R2). The drug showed instability in acid and alkali, while it remained stable in neutral conditions. It also degraded extensively under oxidative environment. It remained stable to light and thermal stress. In total, five degradation products were formed, which could be separated by LC on a C18 column using a gradient method. To characterize the products, first a complete fragmentation pathway of the drug was established by carrying out multi-stage (MSn) and MS/TOF accurate mass studies. The same was compared to fragment pattern of the degradation products resulting from LC-MS/TOF studies. The accurate mass values obtained from LC-MS/TOF were used to obtain elemental compositions, and the total information helped in identification of the degradation products. Subsequently, degradation pathway of the drug was laid down, along with mechanisms of formation of the degradation products. There is no previous information on these aspects on the drug in the literature. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:55 / 63
页数:9
相关论文
共 21 条
[1]   Determination of lamivudine in plasma, amniotic fluid, and rat tissues by liquid chromatography [J].
Alnouti, Y ;
White, CA ;
Bartlett, MG .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 803 (02) :279-284
[2]   Collisionally activated dissociation of protonated 2′-deoxycytidine, 2′-deoxyuridine, and their oxidatively damaged derivatives [J].
Cao, Huachuan ;
Wang, Yinsheng .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2006, 17 (10) :1335-1341
[3]   (-)-2'-DEOXY-3'-THIACYTIDINE IS A POTENT, HIGHLY SELECTIVE INHIBITOR OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 AND TYPE-2 REPLICATION INVITRO [J].
COATES, JAV ;
CAMMACK, N ;
JENKINSON, HJ ;
JOWETT, AJ ;
JOWETT, MI ;
PEARSON, BA ;
PENN, CR ;
ROUSE, PL ;
VINER, KC ;
CAMERON, JM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1992, 36 (04) :733-739
[4]   Mechanistic explanation to the variable degradation behaviour of stavudine and zidovudine under hydrolytic, oxidative and photolytic conditions [J].
Dunge, A ;
Chakraborti, AK ;
Singh, S .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2004, 35 (04) :965-970
[5]   Analysis of antiretroviral nucleosides by electrospray ionization mass spectrometry and collision induced dissociation [J].
Font, E ;
Lasanta, S ;
Rosario, O ;
Rodríguez, JF .
NUCLEOSIDES & NUCLEOTIDES, 1998, 17 (05) :845-853
[6]   Quantitative determination of (-)-2′-deoxy-3′-thiacytidine (lamivudine) in human plasma, saliva and cerebrospinal fluid by high-performance liquid chromatography with ultraviolet detection [J].
Hoetelmans, RMW ;
Profijt, M ;
Meenhorst, PL ;
Mulder, JW ;
Beijnen, JH .
JOURNAL OF CHROMATOGRAPHY B, 1998, 713 (02) :387-394
[7]  
*ICH Q1A R2, 2003, INT C HARM IFPMA GEN
[8]  
*ICH Q1B, 1996, INT C HARM IFPMA GEN
[9]  
*ICH Q2 R1, 2005, INT C HARM IFPMA GEN
[10]   The mechanisms of action of antivirals against hepatitis B virus infection [J].
Kamiya, N .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 51 (05) :1085-1089