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   累积渗透量 的翻译结果: 查询用时:0.319秒
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累积渗透量
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  amount iontophoretic flux
     RESULTS When the continuous time of iontophoresis was 15,30,45,60,90 and 120minute,the amount iontophoretic flux of tetracaine hydrochloride jel was 5.74,11.25,15.37, 20.97 ,28.82 and 36.96mg/cm 2 respectively.
     结果 离子导入持续时间为 15 ,30 ,4 5 ,6 0 ,90 ,12 0min时 ,稳态累积渗透量分别为 5 .74 ,11.2 5 ,15 .37,2 0 .97,2 8.82和 36 .96 μg/cm2 。
短句来源
     CONCLUSION The amount iontophoretic flux of jel is proportional to the applied continuous time.
     结论 在一定的电流强度和漏槽条件下 ,盐酸丁卡因离子导入凝胶累积渗透量与持续时间有较好的线性关系。
短句来源
  cumulative permeation quantity
     The permeability coefficient and cumulative permeation quantity(8 h) of DET sustained release cream were 0.0157 mg·cm-2·h-1 and 0.13 mg·cm-2,respectively.
     cm-. 2h-1,8 h累积渗透量为0.13 mg.
短句来源
     The penetration of ketoprofen in the cataplasm through the BLAB/c mouse skin followed zero-order dynamics in 24 h. Its release equation in vitro was Q= 10. 196 t-7. 954 7 (r=0. 998 8). The cumulative permeation quantity in 24 h was 244. 70μg/cm2 through BLAB/c mouse skin in vitro.
     巴布剂中的酮洛芬24 h内以零级动力学经皮渗透,体外经皮释药方程为Q=10.196 t-7.954 7(r=0.998 8),24 h累积渗透量为244.70μg/cm2。
短句来源
     METHODS Using improved Franz-type diffusion cell and mouse skin in vitro as transdermal barrier,the concentration of methyltestosterone in different kind and concentration enhancers was determined by HPLC,then cumulative permeation quantity (Q) of methyltestosterone was calculated.
     方法:用改良的Franz透皮扩散池,以离体鼠皮为屏障,制备包含不同种类和浓度的促渗剂的甲睾酮乙醇溶液,高效液相色谱法测定甲睾酮累积渗透量及渗透速率。
短句来源
     METHOD: Using improved Franz-type diffusion cel l and excised rabbit skin in vitro as transdermal barrier, the kinetics parame ters such as cumulative permeation quantity, permeation rate,permea tion lagged time and permeation coefficient were determ ined by RP-HPL C.
     方法 :采用改良的Franz扩散池 ,以离体新西兰家兔皮肤为透皮屏障 ,用高效液相色谱法测定不同透皮吸收促进剂对格列美脲累积渗透量、透皮吸收速率、透皮时滞和渗透系数等体外透皮吸收动力学参数的影响。
短句来源
     Methods: Sinomenine gel was prepared with carbopol 980 as base material. Using improved Franz-type diffusion cell and isolated rat skin as transdermal barrier,the cumulative permeation quantity of sinomenine was determined by HPLC method.
     方法:以卡波姆980为辅料制备青藤碱凝胶剂,采用改良Franz扩散池,以离体大鼠皮肤为透皮屏障,用HPLC法测定青藤碱的累积渗透量
短句来源
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  cumulation penetration
     The results showed that 1%~5% menthnol and 1%~5% azone markedly enhanced the cumulation penetration (Q) and the penetration rate ( k ) of 2% ketoprofen Gel ( P <0 01);
     比较其结果,1% ~5% 薄荷脑、1% ~5% 氮酮对2% 酮洛芬凝胶的累积渗透量Q 及渗透速率k 均显著地提高(P< 0.01);
短句来源
  “累积渗透量”译为未确定词的双语例句
     Results: The penetration equation of sinomenine gel was Q=65.852 t-55.677(r=0.991 9).
     结果:实验结果表明,青藤碱凝胶剂体外透皮释药方程为Q=65.852t-55.677(r=0.991 9),10 h累积渗透量为638μg/cm2。
短句来源
     The optimum permeation enhancer was azone, the penetration rate was (73.52±2.30)mgcm-2h-1 and the 24h cumulative amount reached 1700mg/cm2 when the microemulsion containing 5% azone.
     月桂氮酮是吲哚美辛微乳的最佳透皮促进剂,用量为5%时渗透速率为(73.52±2.30)mgcm-2h-1,24h累积渗透量可达1700mg/cm2。
短句来源
     The penetration of accumulation within 24 h and steady velocity of β-asarone in 20% ethanol were (352.624±87.049) μg/cm2, (18.902±4.840) μg/(cm2·h), respectively.
     β-细辛醚在 2 0 %乙醇中 ,2 4 h累积渗透量和稳态渗透速率分别为 (35 2 .6 2 4± 87.0 4 9) μg/ cm2、(18.90 2± 4 .84 0 ) μg/ (cm2· h)。
短句来源
     Results:1%~5% menthol and 1%~5% azone markedly enhanced Q and k of 2% amlodipine gel(P<0.01),but 10%~30% propylene glycol decreased Q and k value of 2% amlodipine gel(P<0.01).
     结果 :1%~ 5 %薄荷脑、1%~ 5 %氮酮对 2 %氨氯地平凝胶的累积渗透量Q及渗透速率k均显著地提高 (P <0 0 1) ;
短句来源
     RESUTLS:The cumulative permeation amount of calcium carbonate in micro pearl powder in 24 h was (2.13±s 0.23) mg·cm~(-2) ,while that of nano pearl powder were (3.01±0.14) mg·cm~(-2) with the significant difference between the two (P<0.01 ).
     结果:微米级珍珠粉24 h碳酸钙的累积渗透量为 (2.13±s 0.23)mg·cm~(-2),纳米级珍珠粉为(3.01±0.14)mg·cm~(-2),差异有非常显著意义(P<0.01)。
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An Aminophylline film was developed and its transdermal release rate on mice skin was determinated.The permeation of aminophylline in the film through the mice skin followed zero-order kinetics.The permeation rate was 77.68μg/h·cm2.This film showed a remarkable therapeutic effect on asthma.

氨茶碱涂膜剂为一种新颖的骨架型经皮给药系统。采用离体鼠皮进行该涂膜剂的体外渗透试验,并用组胺-乙酰胆碱引喘试验考察其平喘作用。结果表明,涂膜剂中氨茶碱以零级动力学经皮吸收;0~12h累积渗透量为40.4%,渗透速率77.68μg/cm2·h,本品有显著平喘作用,其作用优于氨茶碱溶液剂。

n this article the percutaneous

本文对吡罗昔康经由离体裸鼠皮肤的渗透性进行了测定,结果表明吡罗昔康的累积渗透量与时间存在线性关系(Q=2.211t-1.29,r=0.998),吡罗昔康在磷酸盐缓冲液(pH7.4)中经由离体裸鼠皮肤的渗透系数为719×10-cm/s,扩散系数为4.16×10-7cm2/s,滞后时间为0.72h;本文另以小白鼠皮肤为渗透屏障研究了吡罗昔康贴剂的体外经皮渗透性,考察了具体外的释放行为,结果表明该贴剂体外经皮渗透为零级过程,体外释放为t1/2级过程,该贴剂为皮控型局部用经皮吸收制剂。

OBJECTIVE: To prepare a ketoprofen film and study its transdermal delivery and anti inflammatory effect. METHODS: Ketoprofen permeation tests in vitro through rat skin in two compartment diffusion cells were performed and its anti inflammatory effect was studied on rats. RESULTS: The penetration equation of ketoprofen film was Q=0.438 5 t-0.103 0 (r=0.999 8). The cumulative release level in 8 h was 3.507 mg·cm -2 through rat skin in vitro. Ketoprofen film reduced the swelling of hind paw in rats caused...

OBJECTIVE: To prepare a ketoprofen film and study its transdermal delivery and anti inflammatory effect. METHODS: Ketoprofen permeation tests in vitro through rat skin in two compartment diffusion cells were performed and its anti inflammatory effect was studied on rats. RESULTS: The penetration equation of ketoprofen film was Q=0.438 5 t-0.103 0 (r=0.999 8). The cumulative release level in 8 h was 3.507 mg·cm -2 through rat skin in vitro. Ketoprofen film reduced the swelling of hind paw in rats caused by injection of carrageenin. It also inhibited the proliferation of granuloma induced by cotton pellet and reduced primary and recurrent inflammatory swelling of adjuvant arthritis in rat. CONCLUSION: The permeation of ketoprofen in film through the rat skin followed zero order kinetics. Ketoprofen film showed a remarkable anti inflammatory effect.

目的:制备酮基布洛芬(KTP)经皮吸收涂膜剂,研究其经皮吸收性能及抗炎作用。方法:采用双室渗透扩散装置,进行体外渗透试验;用大鼠为炎症模型,考察KTP涂膜剂的抗炎作用。结果:KTP涂膜剂体外透皮释药方程为:Q=0.4385t-0.1030(r=0.9998),8h累积渗透量为3.507mg·cm-2;本品对大鼠角叉莱胶性足趾肿胀,棉球性肉芽组织增生及大鼠佐剂性关节炎的原发病变和继发病变均有显著抑制作用。结论:涂膜剂使KTP以零级动力学透过皮肤,可以提供比口服制剂稳定的血药浓度;KTP具有显著抗炎作用。

 
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