安徽医科大学学报
安徽醫科大學學報
안휘의과대학학보
ACTA UNIVERSITY MEDICINALIS ANHUI
2014年
7期
941-945,946
,共6页
郑海伦%胡咏梅%鲍峻峻%许建明
鄭海倫%鬍詠梅%鮑峻峻%許建明
정해륜%호영매%포준준%허건명
雷贝拉唑%阿莫西林%左氧氟沙星%幽门螺杆菌
雷貝拉唑%阿莫西林%左氧氟沙星%幽門螺桿菌
뢰패랍서%아막서림%좌양불사성%유문라간균
rabeprazole%amoxicillin%levofloxacin%Helicobacter pylori
目的:研究以雷贝拉唑、阿莫西林、左氧氟沙星组成的抗幽门螺杆菌( H. pylori)感染三联疗法中抗生素在大鼠胃内转运、分布特点及雷贝拉唑对其药动学和胃内转运的影响。方法建立大鼠胃内抗生素转运模型,给予相应药物后按时间点分别收集血浆、胃液、胃黏膜组织样本,采用高效液相色谱法检测各样本中抗生素的浓度,计算药物分布转运的药代动力学参数。结果大鼠血浆中阿莫西林半衰期( T1/2)约为1 h,雷贝拉唑对阿莫西林的药代动力学参数没有显著影响,但延长了左氧氟沙星的T1/2。阿莫西林在胃中的浓度显著低于血浆中的浓度,而左氧氟沙星在胃液中浓度比血浆中高。前胃黏膜中两种抗生素浓度低于腺胃黏膜中浓度,而抗生素在腺胃黏膜中不同区域浓度差异无统计学意义。结论抗H. pylori抗生素阿莫西林和左氧氟沙星能够从血中跨胃黏膜转运到胃中,但胃内不同区域胃黏膜中的浓度存在差异;胃内可能具有左氧氟沙星主动转运机制。左氧氟沙星药动力学参数受到了雷贝拉唑的影响。
目的:研究以雷貝拉唑、阿莫西林、左氧氟沙星組成的抗幽門螺桿菌( H. pylori)感染三聯療法中抗生素在大鼠胃內轉運、分佈特點及雷貝拉唑對其藥動學和胃內轉運的影響。方法建立大鼠胃內抗生素轉運模型,給予相應藥物後按時間點分彆收集血漿、胃液、胃黏膜組織樣本,採用高效液相色譜法檢測各樣本中抗生素的濃度,計算藥物分佈轉運的藥代動力學參數。結果大鼠血漿中阿莫西林半衰期( T1/2)約為1 h,雷貝拉唑對阿莫西林的藥代動力學參數沒有顯著影響,但延長瞭左氧氟沙星的T1/2。阿莫西林在胃中的濃度顯著低于血漿中的濃度,而左氧氟沙星在胃液中濃度比血漿中高。前胃黏膜中兩種抗生素濃度低于腺胃黏膜中濃度,而抗生素在腺胃黏膜中不同區域濃度差異無統計學意義。結論抗H. pylori抗生素阿莫西林和左氧氟沙星能夠從血中跨胃黏膜轉運到胃中,但胃內不同區域胃黏膜中的濃度存在差異;胃內可能具有左氧氟沙星主動轉運機製。左氧氟沙星藥動力學參數受到瞭雷貝拉唑的影響。
목적:연구이뢰패랍서、아막서림、좌양불사성조성적항유문라간균( H. pylori)감염삼련요법중항생소재대서위내전운、분포특점급뢰패랍서대기약동학화위내전운적영향。방법건립대서위내항생소전운모형,급여상응약물후안시간점분별수집혈장、위액、위점막조직양본,채용고효액상색보법검측각양본중항생소적농도,계산약물분포전운적약대동역학삼수。결과대서혈장중아막서림반쇠기( T1/2)약위1 h,뢰패랍서대아막서림적약대동역학삼수몰유현저영향,단연장료좌양불사성적T1/2。아막서림재위중적농도현저저우혈장중적농도,이좌양불사성재위액중농도비혈장중고。전위점막중량충항생소농도저우선위점막중농도,이항생소재선위점막중불동구역농도차이무통계학의의。결론항H. pylori항생소아막서림화좌양불사성능구종혈중과위점막전운도위중,단위내불동구역위점막중적농도존재차이;위내가능구유좌양불사성주동전운궤제。좌양불사성약동역학삼수수도료뢰패랍서적영향。
Objective To explore the characteristic of amoxicillin and levofloxacin in the transport and distribution in rat stomach in the triple therapy including rabeprazole used against Helicobacter pylori ( H. pylori) and the effect of rabeprazole on their pharmacokinetics. Methods The model for exploring the antibiotics transport and distribu-tion in rat stomach was prepared. The different sample in rat including blood, the different region gastric mucosa, and the total gastric juice were obtained in the different time point after administration. The antibiotic concentra-tions in the different sample were surveyed by high performance liquid chromatography ( H. PYLORILC) . The sta-tistical analysis of the pharmacokinetics parameters of the drugs transport and distribution were carried out. Results The amoxicillin T1/2 in rat blood was 1 h or so. Rabeprazole did not significantly change the pharmacokinetic pa-rameters of amoxicillin in the plasma, and lengthened the levofloxacin T1/2 in the plasma. Amoxicillin concentration in rat stomach was lower significantly than that in the plasma. Levofloxacin concentration in rat gastric juice was higher than that in the plasma. The two antibiotics concentration in the forestomach mucosa was lower than that in the glandular stomach mucosa. The deviation of two antibiotics concentration in the different region of the glandular stomach mucosa was not statistical significance. Conclusion The antibiotic amoxicillin and levofloxacin used a-gainst H. pylori could penetrate the gastric mucosa into the stomach. The antibiotic concentration in gastric mucosa in the different regions is different. The active transport mechanism of the transporting levofloxacin could exist in the stomach. Rabeprazole could affect levofloxacin kinetic parameter in blood or gastric mucosa.