河南农业科学
河南農業科學
하남농업과학
JOURNAL OF HENAN AGRICULTURAL SCIENCES
2015年
5期
146-150
,共5页
梁俊平%段亚飞%葛倩倩%李健%聂国兴%孔祥会%常志强
樑俊平%段亞飛%葛倩倩%李健%聶國興%孔祥會%常誌彊
량준평%단아비%갈천천%리건%섭국흥%공상회%상지강
大菱鲆%氟甲喹%药代动力学%给药方案
大蔆鲆%氟甲喹%藥代動力學%給藥方案
대릉평%불갑규%약대동역학%급약방안
Scophthalmus maximus%flumequine%pharmacokinetics%dosage regimen
为探讨氟甲喹在大菱鲆体内的药代动力学特征,在水温14~17℃条件下,以20 mg/kg的剂量静脉注射和口服氟甲喹,分别于给药后15、30 min和1、2、4、6、8、12、16、24、36、48、72、96 h采血及各组织,利用高效液相色谱法测定血浆和各组织中的氟甲喹含量,采用DAS 2.0药动学软件中统计矩方法分析药代动力学参数。结果显示,静注给药后,血浆中氟甲喹的表观分布容积为5.46 L/kg,消除半衰期为56.93 h,曲线下面积、生物利用度分别为220.32 h·mg/L、100%;口服给药后,血浆中氟甲喹的曲线下面积、生物利用度分别为95.85 h·mg/L和43.51%,达峰时间为16 h,表观分布容积为4.21 L/kg,消除半衰期为14.12 h。结果表明,静注和口服氟甲喹在大菱鲆体内组织分布均较广,但静注消除慢,口服吸收差、消除快。口服给药后,血浆中氟甲喹浓度在24 h内高于对常见病菌的抑菌浓度,因此,每天以20 mg/kg的剂量给药1次,可对常见细菌疾病起到较好防治效果。
為探討氟甲喹在大蔆鲆體內的藥代動力學特徵,在水溫14~17℃條件下,以20 mg/kg的劑量靜脈註射和口服氟甲喹,分彆于給藥後15、30 min和1、2、4、6、8、12、16、24、36、48、72、96 h採血及各組織,利用高效液相色譜法測定血漿和各組織中的氟甲喹含量,採用DAS 2.0藥動學軟件中統計矩方法分析藥代動力學參數。結果顯示,靜註給藥後,血漿中氟甲喹的錶觀分佈容積為5.46 L/kg,消除半衰期為56.93 h,麯線下麵積、生物利用度分彆為220.32 h·mg/L、100%;口服給藥後,血漿中氟甲喹的麯線下麵積、生物利用度分彆為95.85 h·mg/L和43.51%,達峰時間為16 h,錶觀分佈容積為4.21 L/kg,消除半衰期為14.12 h。結果錶明,靜註和口服氟甲喹在大蔆鲆體內組織分佈均較廣,但靜註消除慢,口服吸收差、消除快。口服給藥後,血漿中氟甲喹濃度在24 h內高于對常見病菌的抑菌濃度,因此,每天以20 mg/kg的劑量給藥1次,可對常見細菌疾病起到較好防治效果。
위탐토불갑규재대릉평체내적약대동역학특정,재수온14~17℃조건하,이20 mg/kg적제량정맥주사화구복불갑규,분별우급약후15、30 min화1、2、4、6、8、12、16、24、36、48、72、96 h채혈급각조직,이용고효액상색보법측정혈장화각조직중적불갑규함량,채용DAS 2.0약동학연건중통계구방법분석약대동역학삼수。결과현시,정주급약후,혈장중불갑규적표관분포용적위5.46 L/kg,소제반쇠기위56.93 h,곡선하면적、생물이용도분별위220.32 h·mg/L、100%;구복급약후,혈장중불갑규적곡선하면적、생물이용도분별위95.85 h·mg/L화43.51%,체봉시간위16 h,표관분포용적위4.21 L/kg,소제반쇠기위14.12 h。결과표명,정주화구복불갑규재대릉평체내조직분포균교엄,단정주소제만,구복흡수차、소제쾌。구복급약후,혈장중불갑규농도재24 h내고우대상견병균적억균농도,인차,매천이20 mg/kg적제량급약1차,가대상견세균질병기도교호방치효과。
The purpose of this study was to investigate the pharmacokinetics behavior of flumequine,and calculate the dosage regimen of flumequine in Scophthalmus maximus. Six fish were randomly selected from the tank and sampled at 15,30 min and 1,2,4,6,8,12,16,24,36,48,72,96 h after intravenous and oral administration at 20 mg/kg flumequine,respectively,at 14—17 ℃ water temperature. The con-centrations of flumequine were determined by the high performance liquid chromatography. The data were analyzed with the pharmacokinetic program DAS 2 . 0 . The results showed that the apparent distribution volume,the elimination half-life, the area under concentration-time curve and the bioavailability were 5. 46 L/kg,56. 93 h,220. 32 h·mg/L and 100%,respectively,after intravenous administration. After oral administration, the area under concentration-time curve was 95. 85 h·mg/L,the bioavailability was 43. 51%,the time to peak concentration was 16 h,the apparent distribution volume was 4. 21 L/kg,and the elimination half-life was 14. 12 h. The results indicated that an adequate distribution from turbot plas-ma to various tissues after intravenous and oral administration,however,elimination rate was faster by oral administration than by intramuscular administration. According to the flumequine pharmacokinetics and the minimal inhibitory concentration of most fish bacterial pathogens,this study indicates that it is possible to obtain therapeutic flumequine blood concentrations via oral administration in turbot with the dose of 20 mg/kg at the interval of one day.