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   diclofenac potassium 的翻译结果: 查询用时:0.231秒
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diclofenac potassium
相关语句
  双氯芬酸钾
     It can be used as the determination method of the quality standard of diclofenac potassium.
     结论 :该方法准确灵敏 ,精密度好 ,可以作为双氯芬酸钾质量标准的测定方法。
短句来源
     AIM To investigate the effectiveness and safety of 1% diclofenac potassium gel(DPG) for external application in the treatment of patients with osteoarthritis(OA).
     目的 探讨 1%的双氯芬酸钾凝胶 (diclofenacpotassium gel,DPG)局部外用治疗骨关节炎 (osteoarthritis,OA)的疗效和安全性。
短句来源
     Clinical trial of diclofenac potassium in treatment of osteoarthritis
     双氯芬酸钾(久宁)治疗骨关节炎临床试验
短句来源
     CONCLUSION:The2kinds of diclofenac potassium capsules are bioequivalent.
     结论:2种双氯芬酸钾胶囊具有生物等效性。
短句来源
     OBJECTIVE:To study the bioequiavailability of2kinds of diclofenac potassium capsules in human body.
     目的:研究2种双氯芬酸钾胶囊的人体生物等效性。
短句来源
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  双氯酚酸钾
     The diclofenac potassium yielded a catalytic hydrogen wave whose peak potential was-1.15 V(vs.SCE) in 0.25 mol·L~(-1) HAc-NaAc(pH 5.0±0.1) supporting electrolyte.
     在HAc-NaAc(pH 5.0±0.1)支持电解质中,双氯酚酸钾产生一催化氢波,峰电位Vp=-1.15 V(vs.SCE)。
短句来源
     Study on the Bioequivalence of Diclofenac Potassium Granule and Diclofenac Potassium Tablet in Man
     双氯酚酸钾颗粒与双氯酚酸钾片的人体生物等效性研究
短句来源
     Polarographic Determination of Diclofenac Potassium Using Its Parallel Catalytic Hydrogen Wave
     平行催化氢波法测定双氯酚酸钾
短句来源
     The statistical results showed the pharmacokinetic parameters of the two preparations had no significant differences( P >0 05). The relative bioavailabilities of diclofenac potassium capsules compared with tablets were 99 66±7 80%.
     经统计学处理 :两制剂的药动学参数无显著性差异(P >0 0 5 ) ,双氯酚酸钾胶囊剂相对于片剂的生物利用度F为 (99 6 6± 7 80 ) % .
短句来源
     The pharmacokinetic parameters showed no significant differences between two products(P>0.05). The relative bioavailablity of diclofenac potassium granule was(99.47±9.79)%.
     两药各药代动力学参数间均无统计学差异 ,双氯酚酸钾颗粒相对生物利用度 (F)为 (99 47±9 79) %。
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  “diclofenac potassium”译为未确定词的双语例句
     RESULTS:The average recovery rates of Nitroglycerin,papaverine hydrochloride and diclofenac potassium were100.65%、99.86%、100.55%respectively,and RSD equal to0.4945%、0.1719%、0.3205%respectively(n=3).
     结果 :硝酸甘油、盐酸罂粟碱、双氯芬酸钾的平均回收率分别为100 65 %、99 86 %、100 55 %,相对标准差分别为0 4945 %、0 1719 %、0 3205 %(n=3)。
短句来源
     Results:The standard curves for diclofenac potassium were linear in the range of 10-200 μg·mL -1 , Y =2.19×10 -3 +0.0158 X , r =0.999 9. Conclusion:The method is sensitive and accurate.
     结果 :线性范围 10~ 2 0 0 μg·mL 1 ,Y =2 .19× 10 3 + 0 .0 15 8X ,r =0 .9999。
短句来源
     The second derivative peak current of the parallel catalytic hydrogen wave was rectilinear to the diclofenac potassium concentration in the range of 1.0×10~(-7) mol·L~(-1) and 5.0×10~(-6) mol·L~(-1)(r=0.998 6,n=8).
     L-1范围内呈线性关系(r=0.998 6,n=8),检出限为5.0×10-8mol.
短句来源
     Three batches of (Ⅰ) contained not less than 95.0% and not more than 105.0% of the labeled amount of diclofenac potassium. Thier release percentage at 0.25 h, 6 h and 10 h was 20%~40%, 60%~80%and more than 80% of the label amount respectively.
     三批双层片在0.2h、5h、6h和10h的释放量均控制在标示量的20%~40%、60%~80%和80%以上。
短句来源
     Result: The standard curves for diclofenac potassium were linear in the range of with the correlation A = 30. 7424815 xAmt + 1. 299051 r-0.9999 Conclusion: The methed is sensitive and accurate .
     0.9999,回归方程A=30.7424815 xAmt+1.2990519。 3种浓度的平均回收率为101.3,日内和日间RSD均小于5%。
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  diclofenac potassium
Evaluation of the combination of amoxicillin trihydrate, diclofenac potassium and ornidazol for the management of endodontic pai
      


The pharmacokinetic and bioavailability of diclofenac potassium (DK) capsule was studied in 10 healthy male volunteers. A single oral dose of 50 mg DK of reference (tablet) or test drugs was given to each 10 volunteers in an open randomized crossover study. Drug concentration in plasma was determined by HPLC method. The pharmacokinetic parameters of DK were: Tmax 1.22±1.10 h and 0.63±0.57 h; Cmax 1931.1±911.6 μg·L-1 and 2028.9±1020.8 μg·L-1; T1/2 2.15 ±0.44 h and 2.26±0.58 h;AUC 3696.6±673.1 μg·h·L-1...

The pharmacokinetic and bioavailability of diclofenac potassium (DK) capsule was studied in 10 healthy male volunteers. A single oral dose of 50 mg DK of reference (tablet) or test drugs was given to each 10 volunteers in an open randomized crossover study. Drug concentration in plasma was determined by HPLC method. The pharmacokinetic parameters of DK were: Tmax 1.22±1.10 h and 0.63±0.57 h; Cmax 1931.1±911.6 μg·L-1 and 2028.9±1020.8 μg·L-1; T1/2 2.15 ±0.44 h and 2.26±0.58 h;AUC 3696.6±673.1 μg·h·L-1 and 3778.4±492.9 μg·h·L-1 for tablet and capsule, respectively.

10名志愿者自身交叉对照,口服单剂量双氯酚酸钾(DK)胶囊剂或片剂50mg,1周后自身交叉服用。用反相HPLC法测得血浆中双氯酚酸胶囊剂和片剂的药代动力学参数Tmax为0.63±0.57h和1.22±1.10h,Cmax为2028.9±1020.8μg·L-1和1931.1±911.6μg·L-1,T1/2为2.26±0.58h和2.15±0.44h,血药浓度曲线下的面积(AUC)分别为3778.4±492.9μg·h·L-1和3696.6±673.1μg·h·L-1,胶囊剂相对于片剂的生物利用度为103.12±8.55%。其药代动力学参数和AUC值经配对T检验P>0.05,均无显著性差异。AUC和ln(AUC)用NDST程序作等效性检验具有生物等效性。

Diclofenac potassium was studied by laser desorption ionization mass spectrometry.The spectra and mass data were determined for both positive and negative ions. The structure informations were obtained and the possible route of ion fragmentation was deduced by accurate mass measurement of quasi-molecular ions and some characteristic fragment ions.

应用激光解吸离子化/傅里叶变换质谱法进行双氯芬酸钾的正负离子质谱研究,由正负离子质谱中准分子离子及重要碎片离子的准确质量和元素组成,获取其结构信息并推测其可能的质谱裂解途径。

A HPLC method was developed for the determination of diclofenac potassium (I) permeation through excised mouse skin pretreated with various enhancers in different concentration.The result showed that the order of the effect of enhancers was as follows:isoPrOH>isoPrOH/PG(1:1)>PG>laurocapram>isoPrOH/PG(1:2)>isoPrOH/PG(2:1).For all cases the drug penetration process could be described by zeroorder kinetic mechanism.

采用预处理法研究了不同种类及不同配比的促进剂对双氯芬酸钾在离体小鼠皮肤经皮吸收的增强作用,并建立了双氯芬酸钾体外经皮释放的检测方法。结果表明,药物经皮吸收渗透符合零级动力学过程。几种促进剂的促进作用为:异丙醇>异丙醇/丙二醇(1∶1)>丙二醇>月桂氮酮>异丙醇/丙二醇(1∶2)>异丙醇/丙二醇(2∶1)。

 
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