Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review,        editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code

QIAN Qingqing, JI Minchun, SUN Guangchun. Study on plasma concentration and pharmacoknetics of lamotrigine in cerebral ischemia model rats by LC-MS/MS[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 443-445,460. doi: 10.3969/j.issn.1006-0111.2018.05.013
Citation: QIAN Qingqing, JI Minchun, SUN Guangchun. Study on plasma concentration and pharmacoknetics of lamotrigine in cerebral ischemia model rats by LC-MS/MS[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 443-445,460. doi: 10.3969/j.issn.1006-0111.2018.05.013

Study on plasma concentration and pharmacoknetics of lamotrigine in cerebral ischemia model rats by LC-MS/MS

doi: 10.3969/j.issn.1006-0111.2018.05.013
  • Received Date: 2017-08-30
  • Rev Recd Date: 2018-09-03
  • Objective To establish a sensitive method for determination of concentration of lamotrigine (LTG) in rat plasma and to study the pharmacokinetics by LC-MS/MS. Methods 12 rats were divided evenly into model group and shame-operated group. LTG was given as single dose of 10 mg/kg via intragastrical administration. Blood samples were collected from orbital saphenous venous plexus at 5 min,0.25,0.5,1,2,4,6,8,12,24 and 36 h after dosing. The LTG concentrations in rat plasma were assayed by LC-MS/MS. The pharmacokinetic parameters were calculated by DAS software. Results In shame-operated group,cmax (1 382.87±61.17) μg/L,t1/2 (40.43±6.77) h; AUC0-∞(123.45±70.70) mg·h/L. In model group, cmax(1 713.50±65.11) μg/L, t1/2(73.72±17.46) h, AUC0-∞(188.15±76.37) mg·h/L. Conclusion The method is proved to be suitable for the determination of LTG in rat plasma. LTG concentration reached peak value at 2 h in both groups. However, model group had a longer t1/2 and higher concentration than that in shame-operated group, which is a valuable information for further pharmacodynamics study.
  • [1] CALABRESI P, CUPINI LM, CENTONZE D,et al.Antiepileptic drugs as a possible neuroprotective strategy in brain ischemia[J]. Ann Neurol, 2003,53(6):693-702.
    [2] YI YH, GUO WC, SUN WW, et al.Neuroprotection of lamotrigine on hypoxic-ischemic brain damage in neonatal rats:relations to administration time and doses[J]. Biologics, 2008, 2(2):339-344.
    [3] SHUAIB A, MAHMOOD RH, WISHART T, et al.Neuroprotective effects of lamotrigine in global ischemia in gerbils. A histological, in vivo microdialysis and behavioral study[J]. Brain Res,1995, 702(1-2):199-206.
    [4] WIARD RP, DICKERSON MC, BEEK O, et al.Neuroprotective properties of the novel antiepileptic lamotrigine in a gerbil model of global cerebral ischemia[J]. Stroke,1995,26(3):466-472.
    [5] CALABRESI P, SINISCALCHI A, PISANI A, et al.A field potential analysis on the effects of lamotrigine, GP 47779, and felbamate in neocortical slices[J]. Neurology, 1996,47(2):557-562.
    [6] AHMAD S, FOWLER LJ, WHITTON PS, et al.Effects of combined lamotrigine and valproate on basal and stimulated extracellular amino acids and monoamines in the hippocampus of freely moving rats[J]. Naunyn Schmiedebergs Arch Pharmacol, 2005,371(1):1-8.
    [7] WALKER MC, TONG X, PERRY H, et al.comparison of serum, cerebrospinal fluid and brain extracellular fluid pharmacokinetics of lamotrigine[J]. Brit J Pharmacol, 2000, 130(2):242-248.
    [8] LEE W, KIM JH, KIM HS, et al.Determination of lamotrigine in human serum by high-performance liquid chromatography-tandem mass spectrometry[J]. Neurol Sci,2010,31(6):717-720.
    [9] 叶广仁,宋志彬,郑国俊,等. 中国成年人拉莫三嗪药代动力学及丙戊酸对其影响[J].神经疾病与精神卫生,2007,7(3):191-193.
  • 加载中
通讯作者: 陈斌, [email protected]
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索

Article Metrics

Article views(2848) PDF downloads(310) Cited by()

Related
Proportional views

Study on plasma concentration and pharmacoknetics of lamotrigine in cerebral ischemia model rats by LC-MS/MS

doi: 10.3969/j.issn.1006-0111.2018.05.013

Abstract: Objective To establish a sensitive method for determination of concentration of lamotrigine (LTG) in rat plasma and to study the pharmacokinetics by LC-MS/MS. Methods 12 rats were divided evenly into model group and shame-operated group. LTG was given as single dose of 10 mg/kg via intragastrical administration. Blood samples were collected from orbital saphenous venous plexus at 5 min,0.25,0.5,1,2,4,6,8,12,24 and 36 h after dosing. The LTG concentrations in rat plasma were assayed by LC-MS/MS. The pharmacokinetic parameters were calculated by DAS software. Results In shame-operated group,cmax (1 382.87±61.17) μg/L,t1/2 (40.43±6.77) h; AUC0-∞(123.45±70.70) mg·h/L. In model group, cmax(1 713.50±65.11) μg/L, t1/2(73.72±17.46) h, AUC0-∞(188.15±76.37) mg·h/L. Conclusion The method is proved to be suitable for the determination of LTG in rat plasma. LTG concentration reached peak value at 2 h in both groups. However, model group had a longer t1/2 and higher concentration than that in shame-operated group, which is a valuable information for further pharmacodynamics study.

QIAN Qingqing, JI Minchun, SUN Guangchun. Study on plasma concentration and pharmacoknetics of lamotrigine in cerebral ischemia model rats by LC-MS/MS[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 443-445,460. doi: 10.3969/j.issn.1006-0111.2018.05.013
Citation: QIAN Qingqing, JI Minchun, SUN Guangchun. Study on plasma concentration and pharmacoknetics of lamotrigine in cerebral ischemia model rats by LC-MS/MS[J]. Journal of Pharmaceutical Practice and Service, 2018, 36(5): 443-445,460. doi: 10.3969/j.issn.1006-0111.2018.05.013
Reference (9)

Catalog

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return