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   invitro release 的翻译结果: 查询用时:0.171秒
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invitro release     
相关语句
  体外释放
     The in vitro release profiles could be expressed by Ritger-Peppas equation with t_(1/2)=242.05 h.
     体外释放符合Ritger-Peppas方程,t1/2=242.05 h。
短句来源
     The in vitro release percents of A,B,C types of TAA/SGS at 14 days were 18.18%,19.38%and 22.38%respectively.
     14d时的体外释放度分别达到18.18%,19.38%,22.38%。
短句来源
     Results In vitro release study revealed that the accumulative release rate of ADM was(30.53±0.56)% 2h after incubation and it rose to(42.16±0.86)% 24h later. The release process went to a balance condition 120h later.
     结果体外释放实验显示,2h后ADM的累积释放率为(30.53±0.56)%,24h后为(42.16±0.86)%,120h后释放趋于平衡。
短句来源
     Preparation and in vitro release of famotidine pulsed-release capsule
     法莫替丁脉冲控释微丸胶囊的制备及其体外释放
短句来源
     RESULTS The activity of enzymes in rat ceca and colon content and β-mannase were 80%~90% maximal activity of enzymes in in vitro release condition of 37 ℃ and pH(6.8);
     结果酶的活性研究表明,在体外释放37℃,pH 6.8介质条件下,内容物降解酶和β-甘露聚糖酶可保持较高活性(为最大酶活性的80%~90%);
短句来源
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  体外释药
     The in vitro release properties could be expressed by such equation as: 1 Q=0.7654(1 t/t ∞) 3 +0.1868 ( r =0.9983).
     微球的体外释药行为的拟合方程为 :1 -Q=0 .76 5 4 ( 1 -t/t∞ ) 3 + 0 .1 86 8( r=0 .9983)。
短句来源
     The in vitro release properties could be expressed by the following equation:1-Q=(0.7610)(1-t/too) 3 +0.1901 (r=0.9983).
     微球的体外释药行为的拟合方程为 :1-Q =0 .76 10 (1-t/too) 3 +0 .190 1(r =0 .9983)。
短句来源
     Results The accumulated release rate of total sal- vianolic acid in R7 was the best,and the in vitro release behavior was consistent with Higuchi equation:M_1/M_∞= 0.363 4t~(1/2)-0.1656,r= 0.996 2.Conclusion R7 is the first choice dosage form for the preparation of the sus- tained-released Danshen extraction preparations.
     结果R7总丹酚酸的累积释放度最好,体外释药符合Higuchi方程:M_1/M_∞=0.363 4t~(1/2)- 0.165 6,r=0.996 2。 结论R7是丹参提取物缓释剂的首选剂型结构。
短句来源
     The reappearance of pharmaceutical technology was good. The in vitro release properties could be expressed by the Higuchi's equation:Q=2.193 7+22.009t~(0.5),r=0.990 4;
     体外释药符合Higuchi方程Q=-2.193 7+22.009t0.5,r=0.990 4;
短句来源
     RESULTS The mean diameter of ACV BSA MS prepared under optimum conditions was (0.94±0.15) μm. The drug loading was (16.07±1.04)%. The in vitro release equation was 1-Q=0.8151e -0.66402t +0.1625e -0.01657t ,t 1/2α =1.044 h,t 1/2β =41.82 h.
     结果 微球平均粒径为 (0 .94± 0 .15 ) μm ,载药量为 (16 .0 7± 1.0 4) % ,体外释药方程 1-Q=0 .815e-0 .664 0 2t+0 .16 2 5e-0 .0 1657tt1/ 2α=1.0 44h ,t1/ 2 β=41.82h。
短句来源
更多       
  体外释放度
     The in vitro release percents of A,B,C types of TAA/SGS at 14 days were 18.18%,19.38%and 22.38%respectively.
     14d时的体外释放度分别达到18.18%,19.38%,22.38%。
短句来源
     Study on preparation and in vitro release of Amoxicilin Floating Sustained Release Tablets
     阿莫西林漂浮缓释片的制备及体外释放度研究
短句来源
     Objective To evaluate in vitro release and in vivo absorption of two strengths of isosorbide-5-mononitrate sustained-release capsules(5-ISMN-SRC).
     目的评价两种规格5-单硝酸异山梨酯缓释胶囊(5-ISMN-SRC)体外释放度与体内吸收的相关性,为5ISMNSRC的质量控制提供依据。
短句来源
     In vitro release of theophylline in 3 mediums of different pH was tested and the accumulated release percentage was calculated.
     在3种不同pH的介质中进行体外释放度试验 ,计算相应时间内的累积释放百分率。
短句来源
     The accumulative percentage of release(10 h)from the sustained release tablets in the in vitro release test was above 70%. The drug release pattern was in accord with the zero equation .
     体外释放度实验证明 ,10h累积释放量 >70 % ,其释放行为基本符合零级方程 .
短句来源
更多       
  体外释
     The in vitro release properties could be expressed by such equation as: 1 Q=0.7654(1 t/t ∞) 3 +0.1868 ( r =0.9983).
     微球的体外释药行为的拟合方程为 :1 -Q=0 .76 5 4 ( 1 -t/t∞ ) 3 + 0 .1 86 8( r=0 .9983)。
短句来源
     The in vitro release properties could be expressed by the following equation:1-Q=(0.7610)(1-t/too) 3 +0.1901 (r=0.9983).
     微球的体外释药行为的拟合方程为 :1-Q =0 .76 10 (1-t/too) 3 +0 .190 1(r =0 .9983)。
短句来源
     Results The accumulated release rate of total sal- vianolic acid in R7 was the best,and the in vitro release behavior was consistent with Higuchi equation:M_1/M_∞= 0.363 4t~(1/2)-0.1656,r= 0.996 2.Conclusion R7 is the first choice dosage form for the preparation of the sus- tained-released Danshen extraction preparations.
     结果R7总丹酚酸的累积释放度最好,体外释药符合Higuchi方程:M_1/M_∞=0.363 4t~(1/2)- 0.165 6,r=0.996 2。 结论R7是丹参提取物缓释剂的首选剂型结构。
短句来源
     The reappearance of pharmaceutical technology was good. The in vitro release properties could be expressed by the Higuchi's equation:Q=2.193 7+22.009t~(0.5),r=0.990 4;
     体外释药符合Higuchi方程Q=-2.193 7+22.009t0.5,r=0.990 4;
短句来源
     RESULTS The mean diameter of ACV BSA MS prepared under optimum conditions was (0.94±0.15) μm. The drug loading was (16.07±1.04)%. The in vitro release equation was 1-Q=0.8151e -0.66402t +0.1625e -0.01657t ,t 1/2α =1.044 h,t 1/2β =41.82 h.
     结果 微球平均粒径为 (0 .94± 0 .15 ) μm ,载药量为 (16 .0 7± 1.0 4) % ,体外释药方程 1-Q=0 .815e-0 .664 0 2t+0 .16 2 5e-0 .0 1657tt1/ 2α=1.0 44h ,t1/ 2 β=41.82h。
短句来源
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  invitro release
Study of the Influence of Several Stabilizing Agents on the Entrapment and InVitro Release of pBC 264 from Poly(Lactide-Co-Glyco
      
The in vivoand in vitrorelease rates were almost identical and subjectindependent.
      
Drug loading, type of active agent, and additional coating of the implant surface all have significant contributions to the in vitrorelease profile.
      
The in vitrorelease of lysozyme from SG microspheres occurred up to 122 h, compared to 96 h for gelatin microspheres, for the release of most of the lysozyme incorporated.
      


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