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test tablets
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     METHODS: Plasma samples of 20 healthy male volunteers, who were administrated with a single oral dose of lisinopril test tablets (10 mg) and reference tablets (10 mg) according to a random 2-way crossover design, were prepared by a simple protein precipitation and then were determined by LC-MS/MS method.
     方法:20名志愿者随机单剂量双交叉口服赖诺普利试验片和参比片10 mg,采用沉淀蛋白法预处理血浆样品后,进行LC-MS-MS法测定。
短句来源
     Calculating by AUC0-36, the relative bioavailability of lisinopril test tablets was (102±8) %.
     按AUC0~36计算,赖诺普利试验片的相对生物利用度为(102±8)%。
短句来源
     Results The pharmacokinetic parameters obtained after single oral administration of the two formulations to the subjects in cross_over design showed that there was not significant difference between the two formulations in maximum concentration(Cmax) and the area under the time_concentration curve (AUC) (P>0.05), whereas the time to reach the Cmax of the test tablets (TT) was shorter than that of the reference tablets (RT),with a significant difference between them.
     结果两种片剂的Cmax 和AUC无显著差异(P>0.05),但试验片给药后的达峰时间(Tpeak)显著小于对照片 ,与对照片相比有非常显著差异(P<0.01)。
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     Conclusion The related bioavailability of the test tablets versus the reference tablets is 93.9%. The two formulations of ubiquinone 10 are bioequivalent.
     结论辅酶Q10 试验片与对照片剂的相对生物利用度为93.9 % ,经等效性分析表明这两种制剂具有生物等效性
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  “test tablets”译为未确定词的双语例句
     AUC_(0~24)(17.18±2.46)μg/(mL·h)、(17.19±2.55)μg/(mL·h); The relative bioavailability of the test tablets was(100.3±9.4)%.
     AUC0~24分别为(17.18±2.46)μg/(mL.h)(、17.19±2.55)μg/(mL.h),乳酸左氧氟沙星片供试制剂的相对生物利用度为(100.3±9.4)%。
短句来源
     The relative bioavailability of telmisartan test tablets and capsules were (98.21±22.34)% and (102.95±32.14)%, respectively.
     受试片剂与胶囊剂的相对生物利用度分别为(98.21±22.34)%和(102.95±32.14)%。
短句来源
     The relative bioavailability of test tablets was(102.2±11.7) %.
     试验制剂的相对生物利用度为(102.2±11.7)%。
短句来源
     AUC_~0-∞ was 63.23±16.80 and 65.10±14.15mg·h·L~-1 , respectively. And the relative bioavailability of the test tablets was 103.5%±13.3%.
     AUC0-∞分别为63.23±16.80、65.10±14.15mg·h·L-1,受试制剂对参比制剂的相对生物利用度为97.13%。
短句来源
     The relative bioavailability of test tablets and test capsules were((106.8)±(29.5))% and((108.3)±(34.6))%,respectively.
     受试雷贝拉唑钠肠溶片、肠溶胶囊与市售雷贝拉唑钠肠溶片比较的人体相对生物利用度为(106.8±29.5)%和(108.3±34.6)%。
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  test tablets
The test tablets were made with this Perilla extract, lactose, and cellulose powder.
      
The placebo tablets were made in the same manner as the test tablets but without Perilla extract.
      
The lag time of DS release from the test tablets was significantly longer than that of reference enteric tablets.
      
Flavor and pigment were added to the placebo tablets in order to match those added to the test tablets.
      
All test tablets were prepared by Meiji Seika Kaisha, Ltd.
      


(1) Whole saliva, concentrated ten fold, was subject to polyacrylamide gel electrophoresis.(2) At least 13 protein bands were found. Among them five were strongly, others moderately dyed. Still others showed only faint color.(3) To facilitate characterization, the 13 bands were arbitrarily divided, starting from the cathode side to the anode side, into five zones, i. e. zones A, B, C, D and E.(4) 11S IgA was found in zone A. IgG, however, cannot be detected.(5) Amylase is the main protein of saliva. Its activity...

(1) Whole saliva, concentrated ten fold, was subject to polyacrylamide gel electrophoresis.(2) At least 13 protein bands were found. Among them five were strongly, others moderately dyed. Still others showed only faint color.(3) To facilitate characterization, the 13 bands were arbitrarily divided, starting from the cathode side to the anode side, into five zones, i. e. zones A, B, C, D and E.(4) 11S IgA was found in zone A. IgG, however, cannot be detected.(5) Amylase is the main protein of saliva. Its activity is very high. By means of "Phadebas" amylase test tablet, amylase was found to be located mainly in zone B.(6) Most of the lysozyme activity was present in zone C, though a smaller activity was also detected in zone A.

1.应用聚丙烯酰胺凝胶电泳可将浓缩10倍的正常人全唾液分成至少13种以上蛋白质成分。2.为了便于鉴定,将电泳后的蛋白质各区带自阴极向阳极分为A,B,C,D,E五个区带组。3.经免疫双扩散法证实,最靠近阴极的A区带组为11S IgA,IgG在本实验中未能检出。4.淀粉酶是唾液中的主要蛋白质,活力很高,经Phadebas淀粉酶试验片定位鉴定,发现它主要存在于B区带。5.唾液中含有溶菌酶,对M.lysodeikticus有明显溶菌效应,其电泳泳动位置与C区带相当,A区带组也有溶菌作用,但活性较C区带组为低。

(1) Whole saliva, concentrated ten fold, was subject to polyacrylamide gel elec trophoresis.(2) At least 13 protein bands were found. Among them five were strongly, others moderately dyed. Still others showed only faint color.(3) To facilitate characterization, the 13 bands were arbitrarily divided, starting from the cathode side to the anode side, into five zones, i. e. zones A, B, C, D and E.(4) llS IgA was found in zone A. IgG, however, cannot be deteoted.(5) Amylase is the main protein of saliva. Its activity...

(1) Whole saliva, concentrated ten fold, was subject to polyacrylamide gel elec trophoresis.(2) At least 13 protein bands were found. Among them five were strongly, others moderately dyed. Still others showed only faint color.(3) To facilitate characterization, the 13 bands were arbitrarily divided, starting from the cathode side to the anode side, into five zones, i. e. zones A, B, C, D and E.(4) llS IgA was found in zone A. IgG, however, cannot be deteoted.(5) Amylase is the main protein of saliva. Its activity is very high. By means of "Phadebas" amylase test tablet, amylase was found to be located mainly in zone B.(6) Most of the lysozyme activity was present in zone C, though a smaller activity was also detected in zone A.

1.应用聚丙烯酰胺凝胶电泳可将浓缩10倍的正常人全唾液分成至少13种以上蛋白质成分。2.为了便于鉴定,将电泳后的蛋白质各区带自阴极向阳极分为A,B,C,D,E五个区带组。3.经免疫双扩散法证实,最靠近阴极的A区带组为11S IgA,IgG在本实验中未能检出。4.淀粉酶是唾液中的主要蛋白质,活力很高,经Phadebas淀粉酶试验片定位鉴定,发现它主要存在于B区带。5.唾液中含有溶菌酶,对M.lysodeikticus有明显溶菌效应,其电泳冰动位置与C区带相当,A区带组也有溶菌作用,但活性较C区带组为低。

A rapid determination method of vitamin C(vitamin C rapid test tablet) was developed. Two steps (standardizing of vitamin C and 2,6-Dichloro-phenol-ind-ophenol) were omitted by the use of the method. The relative errors of tablet, weight and 2,6-DICP content were 0.91% and 0.98% respectively .The accuracy precision and recovery of determination were 2.57%, 1.2-1.7% and 97.07-99.10% respectively. Effects of light, temperature and moisture on the stability of vitamin C rapid tablet were studied....

A rapid determination method of vitamin C(vitamin C rapid test tablet) was developed. Two steps (standardizing of vitamin C and 2,6-Dichloro-phenol-ind-ophenol) were omitted by the use of the method. The relative errors of tablet, weight and 2,6-DICP content were 0.91% and 0.98% respectively .The accuracy precision and recovery of determination were 2.57%, 1.2-1.7% and 97.07-99.10% respectively. Effects of light, temperature and moisture on the stability of vitamin C rapid tablet were studied. The content of 2, 6-DICP was stable at room temperature for more than two years when the tablets had been packed in sealed aluminum foil.

本文利用2,6—二氯靛酚,并选择合适辅料,制成定量测定Vc的速测片,每片相当于1.000毫克的Vc。试验对Vc速测片的片剂性能进行了测定:测得片重的相对误差为0.91%,片中主药即2,6—二氯靛酚含量的相对误差为0.98%,测定的准确度、精密度高,回收率为97.07~99.10%。片剂对光不敏感,由于采用铝箔包装,故不易受温度等的影响,稳定性好。常温贮存两年以上,其中2,6—二氯靛酚含量不变。使用时将其溶解可滴定样品。方法快速简便,准确可靠。

 
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