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国家自然科学基金(31172366)

作品数:3 被引量:5H指数:2
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Pharmacokinetics and Residues of Cefquinome in Milk of Lactating Chinese Dairy Cows After Intramammary Administration
2014年
The purpose of the study was to investigate the pharmacokinetics of cefquinome in plasma and milk samples of lactating Chinese Holstein following a single intramammary administration into one quarter at the dose of 75 mg. Residue depletion of cefquinome in milk administrated at one quarter following three consecutive infusions at the same dose were also carried out. Cefquinome concentrations in plasma and milk were determined by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method. A non-compartmental analysis was used to obtain the pharmacokinetic parameters of cefquinome. Following the single treatment, cefquinome wasn’t detected in any of the plasma samples. The concentration of cefquinome in milk reached peaked values (Cmax) of (599.00±322.00) μg mL-1 at 2 h after administration (Tmax), elimination half-life (t1/2λz) was (4.63±0.26) h, area under the concentration-time curve (AUC0-∞) was (4 890.19±1 906.98) μg mL-1 h, and mean residence time (MRT) was (6.03±2.27) h. In residue depletion study, cefquinome concentrations in 5 out of 6 milk samples at 72 h were lower than the maximum residue limit ifxed by the European regulatory agency (20μg kg-1 for cefquinome) and cefquinome still could be detected in milk of treated quarters at 120 h post-treatment. The maximum concentration (Cmax) of cefquinome in milk from treated quarters was (486.50±262.92) μg mL-1 and arrived at 6 h after administration (Tmax), elimination half-life (t1/2λz) was (6.30±0.76) h, area under the concentration-time curve (AUC0-∞) was (44 747.79±11 434.43) μg mL-1 h, and mean residence time (MRT) was (10.09±1.40) h. This study showed that cefquinome has the feature of poor penetration into blood and was eliminated quickly from milk in lactating cows after intramammary administration.
LI Ya-feiWANG LinGU Xiao-yanZENG Zhen-lingHE Li-minYANG FanYUAN BoSHU Jian-huaDING Huan-zhong
关键词:CEFQUINOMEPHARMACOKINETICSRESIDUEHPLC-MS/MS
长效土霉素注射液在猪体内的药动学及相对生物利用度研究被引量:3
2012年
对7头健康猪随机交叉设计进行单剂量肌肉注射国产30%长效土霉素注射液和进口20%长效土霉素注射液药动学试验,给药剂量以土霉素计均为20 mg/kg体重。用高效液相色谱法测定血药浓度,血药浓度-时间数据用MCPKP计算机程序处理。30%长效土霉素注射液和20%长效土霉素注射液主要药动学参数分别为:吸收半衰期(t1/2Ka)为(0.088±0.016)、(0.140±0.076)h;消除半衰期(t1/2β)为(52.499±22.885)、(36.481±21.673)h;达峰时间(Tmax)为(0.609±0.100)、(0.832±0.373)h;峰浓度(Cmax)为(4.956±1.171)、(5.018±0.948)μg/mL;药时曲线下面积(AUC)为(112.483±18.135)、(109.877±19.949)mg/L.h;以20%长效土霉素注射液为对照物,30%长效土霉素注射液的相对生物利用度(F)为(105.368±26.027)%。结果表明,国产30%长效土霉素注射液与进口20%长效土霉素注射液相比,主要药动学参数无显著差异。此结论为临床合理使用该剂型提供了依据和指导。
廖雪玲张炳旭丁焕中
关键词:土霉素长效注射液药动学相对生物利用度
基于防突变浓度的新型药动学-药效学-突变选择窗同步模型在临床用药上的指导作用被引量:2
2013年
文章综述了抗菌药药动学/药效学(PK/PD)模型的发展,详细阐述新型药动物学/药效学模型在抑制细菌耐药突变上的作用,为合理用药及新药研发提供指导,并指出了临床应用所存在的问题。
廖雪玲张炳旭丁焕中
关键词:药动学药效学模型突变选择窗
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