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1.
The objectives of this study were to determine the pharmacokinetics of toltrazuril and its metabolites in pregnant and nonpregnant ewes following a single oral dose and to determine the plasma concentrations of these compounds in milk, allantoic fluid, and newborn plasma. Eighteen healthy ewes were randomly divided into three groups (n = 6 each): pregnant ewes at 12–13 weeks of gestation (group A), nonpregnant ewes (group B), and pregnant ewes at 1–2 weeks before expected lambing date (group C). Ewes in all groups received a single oral dose of toltrazuril at 20 mg/kg body weight. In groups A and B, blood samples were collected at 1, 3, 5, 7, 9, 12, 15, 18 hr, every 6 hr to day 3, every 12 hr to day 7 and thereafter every 24 hr to day 14 post-toltrazuril administration. In group C, parturition was induced 24–36 hr after toltrazuril administration then milk, allantoic fluid, and newborn plasma samples were collected immediately after birth. Drug metabolites were assayed using ultra high-performance liquid chromatography–ultraviolet detection method (UHPLC-UV). The maximum concentration (Cmax), area under the plasma concentration-time curve (AUC0–t), AUC to 24 and 48 hr (AUC0–24), and (AUC0–48) were significantly higher in pregnant ewes. Longer apparent half-life (T1/2), significantly higher apparent volume of distribution (Vd/F) and total clearance (Cl/F) were observed in nonpregnant ewes. The time to maximum plasma concentration (Tmax), mean residence time (MRT) and elimination rate constant (Kel) were similar in both groups. The AUC0–24 and AUC0–48 were significantly higher in nonpregnant ewes. The AUC0–t was significantly higher in pregnant ones. The ratio of plasma toltrazuril concentrations in ewes and toltrazuril concentrations in newborn lambs' plasma, allantoic fluid, and milk were 68%, 2.3%, and 5.3%, respectively. Results of this study showed that toltrazuril is well absorbed after a single oral dose in ewes with widespread distribution in different body tissues.  相似文献   
2.
为了确定妥曲珠利纳米乳的处方和制备工艺,选用液体石蜡、乙酸乙酯、大豆油、IPM、油酸为油相,RH-40、EL-40、OP-10、吐温-80、司盘-80为表面活性剂,乙醇、1,2-丙二醇、异丙醇、丙三醇、PEG-400为助表面活性剂,通过伪三元相图筛选制备妥曲珠利纳米乳的最佳处方.结果表明,油相为乙酸乙酯、表面活性剂为吐温-80,助表面活性剂为1,2-丙二醇可形成纳米乳.优化处方为表面活性剂∶助表面活性剂∶油相∶水相=2∶1∶2∶5,增溶剂添加量为10%,在该处方下制备的妥曲珠利纳米乳稳定性良好.  相似文献   
3.
采用反溶剂法制备妥曲珠利微晶体,利用显微镜观察妥曲珠利微晶体与妥曲珠利原药显微特征差异,并在25℃条件下测定两者体外溶出速率差异。将12只家兔随机分为2组,每组6只,分别按药物剂量10mg/kg灌胃,单剂量给药,采用HPLC检测血药浓度;用DAS2.0药代动力学程序计算药代动力学参数。结果显示,成功制备了妥曲珠利微晶体,微晶体与原药的显微特征差异明显,体外溶出速率明显加快;家兔单剂量灌胃妥曲珠利和微晶体后,主要药动学参数Cmax分别为(8.925±0.360)mg/L和(12.510±0.525)mg/L,tmax均为24h,AUC(0-∞)分别为(411.605±20.918)mg/(L·h)和(578.650±11.664)mg/(L·h),相对生物利用度为140.6%,药时数据符合一级吸收二室模型。结果表明,HPLC法适用于妥曲珠利血浆浓度的测定;妥曲珠利微晶体与妥曲珠利原药相比,体内吸收速率和吸收程度有较大的提高。  相似文献   
4.
为了观察阿德呋啉水溶剂治疗艾美耳球虫的效果,试验设5个药物试验组、阳性及阴性对照组。70只13日龄的雏鸡随机分为7组,其中药物试验组鸡只开始给药。给药24 h后,除阴性对照组外,其余组鸡只均接种混合的球虫孢子化卵囊(5万/羽),试验后根据抗球虫指数(ACI)判断抗球虫药的疗效。结果显示所有给药组中65 mg/kg阿德呋啉水溶剂组ACI为185.54,抗球虫效果最好,为高效抗球虫药;其余阿德呋啉试验组ACI均低于180,浓度过高抗球虫效果差;妥曲珠利试验组ACI低于120,为低效抗球虫药。试验得到了最佳的使用浓度,为球虫病的防治提供了方法。  相似文献   
5.
建立了一种高效液相色谱法同时测定鸡肌肉中地克珠利、妥曲珠利、妥曲珠利砜及妥曲珠利亚砜残留量的方法。试样经乙腈涡旋提取,正己烷脱脂,经碱性氧化铝小柱净化,浓缩,流动相定容,高效液相色谱分离,紫外检测器检测,以保留时间定性,以峰面积定量。结果表明:该方法在0.05~5μg/m L浓度范围内线性关系良好,相关系数r均大于0.999。在50~500μg/kg添加浓度范围内,方法回收率在70%~110%之间,批内和批间变异系数均小于15%。方法简便、灵敏度高、稳定性好。  相似文献   
6.
AIM: To assess the efficacy of toltrazuril against the Eimeria spp. affecting brown kiwi (Apteryx mantelli).

METHODS: Droppings were collected from three brown kiwi, aged <6 months old, at a captive rearing facility in the North Island of New Zealand, between 22 February and 20 April 2017, on 14 sampling dates. Only droppings (n=30) that were excreted between 03:00 and 07:00, as determined using video surveillance, were included for analysis, reflecting the peak time for shedding of coccidial oocysts for brown kiwi. Oocysts were quantified in each sample and Eimeria species identified on the basis of oocyst morphology. All samples were collected between 2 and 10 days after the birds had been treated with 25?mg/kg toltrazuril.

RESULTS: Eimeria spp. oocysts were identified in 28/30 individual samples and on 14/14 sampling dates. Oocyst counts varied from 0 to 328,080 oocysts per gram (opg), and at least one oocyst count >10,000 opg was measured on 12/14 sampling dates. Three species of Eimeria were observed, with Eimeria apteryxii and E. kiwii most commonly encountered, whereas only one sample contained E. paraurii.

CONCLUSIONS AND CLINICAL RELEVANCE: In the three birds monitored at this research site, there was a high abundance of E. apteryxii and E. kiwii oocysts in droppings despite recent administration of toltrazuril. These results suggest that the populations of Eimeria spp. affecting brown kiwi at this location appear to possess an ability to survive exposure to toltrazuril. Toltrazuril is widely used at captive rearing facilities to limit the effects of coccidiosis in juvenile kiwi. If a lack of efficacy is confirmed, it will be necessary to investigate alternative treatment regimens alongside broader environmental management strategies.  相似文献   

7.
妥曲珠利在健康和球虫感染肉鸡体内的药动学研究   总被引:3,自引:0,他引:3  
以高压液相色谱(HPLC)法为定量手段研究了妥曲珠利在健康和柔嫩艾美尔球虫感染肉鸡体内的药动学特征.30日龄艾维茵肉鸡30只,随机分为健康组和柔嫩艾美耳球虫感染组和感染对照组.健康组和柔嫩艾美耳球虫感染组灌服2.5%妥曲珠利溶液(8 mg·kg-1)后,血浆药物浓度-时间数据符合一级吸收二室开放模型,健康组和感染组主要动力学参数分别为:t1/2α为(4.31±0.85)和(4.29±1.03) h,t1/2β为(23.81±2.81)和(23.76±3.31) h,Vd为(0.39±0.09)和(0.40±0.07) L·kg-1,CL(s)为(0.05±0.01)和(0.05±0.01) L·h-1,AUC为(174.15±34.09)和(165.14±23.71) μg·h·mL-1.该结果表明球虫感染肉鸡单次灌服2.5%妥曲珠利溶液后药动学特征与健康鸡比较无显著差异,说明柔嫩艾美耳球虫感染对妥曲珠利在肉鸡体内的药动学过程无明显影响.  相似文献   
8.
液质联用方法测定鸡血浆中妥曲珠利及其代谢产物   总被引:2,自引:0,他引:2  
初步建立肉鸡血浆中抗球虫药物妥曲珠利及其代谢产物妥曲珠利砜的液质联用(LC/MS)定性定量的测定方法。血浆样品加乙腈混匀后离心,取上清液进行液质联用(LC/MS)分析。色谱分析采用C18反相柱,流动相为乙腈水溶液(体积比为55∶45),质谱分析采用ESI离子源、二级串联质谱、负离子检测方式进行检测,妥曲珠利定量分析采用分子离子峰。该方法可以准确测定妥曲珠利的变化并判断代谢物的产生,在1次进样中实现同时检测妥曲珠利及其代谢物,妥曲珠利检测的线性范围为1~500 ng.mL-1,定量检测下限为0.5 ng.mL-1。此方法与液相色谱法相比灵敏度高、可靠、快速,该方法的建立为今后同类药物的定性定量分析提供基础。  相似文献   
9.
国产妥曲珠利对小鼠的急性毒性和亚慢性毒性试验   总被引:3,自引:0,他引:3  
为了探讨妥曲珠利对小鼠的毒性作用,评价其临床用药的安全性,进行了妥曲珠利对小鼠的急性毒性和亚慢性毒性试验.结果表明,妥曲珠利对小鼠无毒性作用,经口LD50为5 011 mg/kg.妥曲珠利以500、100、20 mg/kg给小鼠连续灌胃30 d,500mg/kg表现出生长缓慢、肝脏损伤,100mg/kg和20 mg/kg剂量组鼠的体重、脏器系数、血液指标均与空白对照组无差异(P>0.05).表明妥曲珠利毒性小,临床推荐剂量是安全的.  相似文献   
10.
高效毛细管电泳法同时检测地克珠利和妥曲珠利的含量   总被引:1,自引:2,他引:1  
采用毛细管电泳-二极管阵列检测法建立了地克珠利和妥曲珠利两种结构相近的均三嗪类抗球虫药物的分离检测方法.同时还探讨了缓冲溶液的种类、浓度、pH值等诸多因素对分离检测结果的影响.上述两种药物在8 min内实现了基线分离.线性检测范围为0.5~100 μg/mL,检出限为0.1 μg/mL (S/N=3).  相似文献   
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