{"title":"静脉和口服喹诺酮及其主要代谢物在猪体内的药代动力学","authors":"Jia-lin ZHONG, Gui-jun ZHANG, Xiang-guang SHEN, Lin WANG, Bing-hu FANG, Huan-zhong DING","doi":"10.1016/S1671-2927(11)60121-1","DOIUrl":null,"url":null,"abstract":"<div><p>The pharmacokinetics of quinocetone and its major metabolites in healthy swine was investigated in this paper. Quinocetone was administered to 8 healthy cross-bread swine intravenously and orally at a dosage of 4 and 40 mg kg<sup>−1</sup> body weight respectively in a randomized crossover design test with two-week washout period. A sensitive high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was developed for the determination of quinocetone and its metabolite 1-desoxyquinocetone in plasma. Plasma concentration versus time profiles of quinocetone and its metabolite 1-desoxy quinocetone were analyzed by non-compartmental analysis using Winnonlin 5.2 software. Mean maximum concentrations (C<sub>max</sub>) for quinocetone was found to be (0.56±0.13) μg mL<sup>−1</sup> at 2.92 h, after oral administration of quinocetone. Mean maximum concentrations (C<sub>max</sub>) for 1-desoxy quinocetone after intravenous or oral administration of quinocetone were (0.0095±0.0012) μg mL·<sup>1</sup> at 0.083 h and (0.0067±0.0053) μg mL<sup>−1</sup> at 3.08 h. The apparent elimination half-lives (T<sub>1/2</sub>) for quinocetone and its metabolite 1-desoxy quinocetone were (2.24±0.24) and (5.23±0.56) h after intravenous administration of quinocetone and (2.91±0.29) and (11.85±2.89) h after oral administration of quinocetone, respectively. Mean areas under the plasma concentration-time curve (AUC<sub>0-x</sub>) for quinocetone and 1-desoxyquinocetone were (2.02±0.15) and (0.2±0.002) μg h mL<sup>−1</sup> respectively after intravenous administration of quinocetone, and (3.5±0.79) and (0.053±0.03) μg h mL<sup>−1</sup> after oral administration of quinocetone, respectively. Quinocetone was rapidly absorbed and metabolized in swine after oral and intravenous administration. The plasma concentration-time curve (AUC<sub>0-x</sub>) of 1-desoxy quinocetone were much smaller than those of quinocetone, while the elimination half-lives (T<sub>1/2</sub>) were much longer than those of quinocetone after intravenously (i.v.) or oral administration.</p></div>","PeriodicalId":7475,"journal":{"name":"Agricultural Sciences in China","volume":"10 8","pages":"Pages 1292-1300"},"PeriodicalIF":0.0000,"publicationDate":"2011-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1671-2927(11)60121-1","citationCount":"17","resultStr":"{\"title\":\"Pharmacokinetics of Quinocetone and Its Major Metabolites in Swine After Intravenous and Oral Administration\",\"authors\":\"Jia-lin ZHONG, Gui-jun ZHANG, Xiang-guang SHEN, Lin WANG, Bing-hu FANG, Huan-zhong DING\",\"doi\":\"10.1016/S1671-2927(11)60121-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The pharmacokinetics of quinocetone and its major metabolites in healthy swine was investigated in this paper. Quinocetone was administered to 8 healthy cross-bread swine intravenously and orally at a dosage of 4 and 40 mg kg<sup>−1</sup> body weight respectively in a randomized crossover design test with two-week washout period. A sensitive high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was developed for the determination of quinocetone and its metabolite 1-desoxyquinocetone in plasma. Plasma concentration versus time profiles of quinocetone and its metabolite 1-desoxy quinocetone were analyzed by non-compartmental analysis using Winnonlin 5.2 software. Mean maximum concentrations (C<sub>max</sub>) for quinocetone was found to be (0.56±0.13) μg mL<sup>−1</sup> at 2.92 h, after oral administration of quinocetone. Mean maximum concentrations (C<sub>max</sub>) for 1-desoxy quinocetone after intravenous or oral administration of quinocetone were (0.0095±0.0012) μg mL·<sup>1</sup> at 0.083 h and (0.0067±0.0053) μg mL<sup>−1</sup> at 3.08 h. The apparent elimination half-lives (T<sub>1/2</sub>) for quinocetone and its metabolite 1-desoxy quinocetone were (2.24±0.24) and (5.23±0.56) h after intravenous administration of quinocetone and (2.91±0.29) and (11.85±2.89) h after oral administration of quinocetone, respectively. Mean areas under the plasma concentration-time curve (AUC<sub>0-x</sub>) for quinocetone and 1-desoxyquinocetone were (2.02±0.15) and (0.2±0.002) μg h mL<sup>−1</sup> respectively after intravenous administration of quinocetone, and (3.5±0.79) and (0.053±0.03) μg h mL<sup>−1</sup> after oral administration of quinocetone, respectively. Quinocetone was rapidly absorbed and metabolized in swine after oral and intravenous administration. 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引用次数: 17
摘要
本文研究了喹诺酮及其主要代谢物在健康猪体内的药动学。采用随机交叉设计试验,8头健康十字面包猪分别以4和40 mg kg - 1体重静脉滴注喹诺酮和口服喹诺酮,洗脱期为2周。建立了高效液相色谱-串联质谱(HPLC-MS/MS)测定血浆中喹诺酮及其代谢产物1-去氧喹诺酮的方法。采用Winnonlin 5.2软件对喹诺酮及其代谢物1-去氧喹诺酮的血药浓度随时间变化曲线进行非区隔分析。口服喹诺酮后2.92 h,喹诺酮的平均最大浓度(Cmax)为(0.56±0.13)μ mL−1。静脉或口服喹诺酮后1-去氧基喹诺酮的平均最大浓度(Cmax)分别为(0.0095±0.0012)μ mL·1 (0.083 h)和(0.0067±0.0053)μ mL·1 (3.08 h)。喹诺酮及其代谢物1-去氧基喹诺酮的表观消除半衰期(T1/2)分别为(2.24±0.24)和(5.23±0.56)h,口服喹诺酮后分别为(2.91±0.29)和(11.85±2.89)h。静脉给药喹诺酮和1-去氧喹诺酮的血药浓度-时间曲线下平均面积(AUC0-x)分别为(2.02±0.15)和(0.2±0.002)μg h mL - 1,口服喹诺酮后分别为(3.5±0.79)和(0.053±0.03)μg h mL - 1。喹诺酮经口服和静脉给药后在猪体内被迅速吸收和代谢。1-去氧喹诺酮的血药浓度-时间曲线(AUC0-x)比喹诺酮小得多,其消除半衰期(T1/2)比喹诺酮静脉(i.v)或口服给药要长得多。
Pharmacokinetics of Quinocetone and Its Major Metabolites in Swine After Intravenous and Oral Administration
The pharmacokinetics of quinocetone and its major metabolites in healthy swine was investigated in this paper. Quinocetone was administered to 8 healthy cross-bread swine intravenously and orally at a dosage of 4 and 40 mg kg−1 body weight respectively in a randomized crossover design test with two-week washout period. A sensitive high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was developed for the determination of quinocetone and its metabolite 1-desoxyquinocetone in plasma. Plasma concentration versus time profiles of quinocetone and its metabolite 1-desoxy quinocetone were analyzed by non-compartmental analysis using Winnonlin 5.2 software. Mean maximum concentrations (Cmax) for quinocetone was found to be (0.56±0.13) μg mL−1 at 2.92 h, after oral administration of quinocetone. Mean maximum concentrations (Cmax) for 1-desoxy quinocetone after intravenous or oral administration of quinocetone were (0.0095±0.0012) μg mL·1 at 0.083 h and (0.0067±0.0053) μg mL−1 at 3.08 h. The apparent elimination half-lives (T1/2) for quinocetone and its metabolite 1-desoxy quinocetone were (2.24±0.24) and (5.23±0.56) h after intravenous administration of quinocetone and (2.91±0.29) and (11.85±2.89) h after oral administration of quinocetone, respectively. Mean areas under the plasma concentration-time curve (AUC0-x) for quinocetone and 1-desoxyquinocetone were (2.02±0.15) and (0.2±0.002) μg h mL−1 respectively after intravenous administration of quinocetone, and (3.5±0.79) and (0.053±0.03) μg h mL−1 after oral administration of quinocetone, respectively. Quinocetone was rapidly absorbed and metabolized in swine after oral and intravenous administration. The plasma concentration-time curve (AUC0-x) of 1-desoxy quinocetone were much smaller than those of quinocetone, while the elimination half-lives (T1/2) were much longer than those of quinocetone after intravenously (i.v.) or oral administration.