大理学院学报
大理學院學報
대이학원학보
JOURNAL OF DALI COLLEGE
2013年
9期
17-20
,共4页
刘颖琳%李燕来%刘浩然%马丽雪
劉穎琳%李燕來%劉浩然%馬麗雪
류영림%리연래%류호연%마려설
阿魏酸%一氧化氮供体%高效液相色谱%药动学
阿魏痠%一氧化氮供體%高效液相色譜%藥動學
아위산%일양화담공체%고효액상색보%약동학
ferulic acid%nitric oxide donors%high performance liquid chromatograph%pharmacokinetics
目的:建立阿魏酸甲酯一氧化氮供体(FMND)的反相高效液相色谱分析方法,并对其在小鼠体内的药动学参数进行测定。方法:以乙酸乙酯提取后,漩涡,高速离心,氮气吹干,流动相复溶后进样。色谱条件:流动相为甲醇:水(70∶30),流速:1.0 mL/min。柱温:30℃。结果:小鼠灌胃给予50 mg/kg的FMND后吸收较快,迟滞时间为6.6 min,约1.5 h达到血药浓度高峰。体内分布符合有时滞的二室模型。分布半衰期为1.04 h,消除半衰期为9.44 h,吸收半衰期为0.94 h。结论:阿魏酸甲酯一氧化氮供体在小鼠体内吸收较快,分布平衡相对较快,消除半衰期较长。
目的:建立阿魏痠甲酯一氧化氮供體(FMND)的反相高效液相色譜分析方法,併對其在小鼠體內的藥動學參數進行測定。方法:以乙痠乙酯提取後,漩渦,高速離心,氮氣吹榦,流動相複溶後進樣。色譜條件:流動相為甲醇:水(70∶30),流速:1.0 mL/min。柱溫:30℃。結果:小鼠灌胃給予50 mg/kg的FMND後吸收較快,遲滯時間為6.6 min,約1.5 h達到血藥濃度高峰。體內分佈符閤有時滯的二室模型。分佈半衰期為1.04 h,消除半衰期為9.44 h,吸收半衰期為0.94 h。結論:阿魏痠甲酯一氧化氮供體在小鼠體內吸收較快,分佈平衡相對較快,消除半衰期較長。
목적:건립아위산갑지일양화담공체(FMND)적반상고효액상색보분석방법,병대기재소서체내적약동학삼수진행측정。방법:이을산을지제취후,선와,고속리심,담기취간,류동상복용후진양。색보조건:류동상위갑순:수(70∶30),류속:1.0 mL/min。주온:30℃。결과:소서관위급여50 mg/kg적FMND후흡수교쾌,지체시간위6.6 min,약1.5 h체도혈약농도고봉。체내분포부합유시체적이실모형。분포반쇠기위1.04 h,소제반쇠기위9.44 h,흡수반쇠기위0.94 h。결론:아위산갑지일양화담공체재소서체내흡수교쾌,분포평형상대교쾌,소제반쇠기교장。
Objective: To develop the assay method by RP-HPLC for ferulic acid methylester nitric oxide donor (FMND) and determine the pharmacokinetics parameters in mice after oral administration. Methods: The sample was extracted by acetoacetate, followed by vortex and high speed centrifugation, dried by nitrogen flow and dissolved by mobile phase before HPLC analysis. The HPLC condition was applied with mobile phase at methanol: water (70∶30), flow rate at 1.0 mL/min, column temperature at 30 ℃. Results: FMND was absorbed quickly with a lag time of 6.6 min after oral administration in mice at the dose of 50 mg/kg, and arrived to the peak concentration at about 1.5 h. The distribution in vivo matched two-compartment model with a lag time. The distribute half life time(t1/2α)was 1.04 h, the eliminate half life time(t1/2β)was 9.44 h, the absorb half life time(t1/2 Ka)was 0.94 h. Conclusion: FMND was absorbed quickly in mice after oral administration, and the distribute equilibrium arrived moderately with a long eliminate half life time.