助手标题  
全文文献 工具书 数字 学术定义 翻译助手 学术趋势 更多
查询帮助
意见反馈
   ibuprofen 在 药学 分类中 的翻译结果: 查询用时:0.214秒
图标索引 在分类学科中查询
所有学科
药学
有机化工
儿科学
化学
外科学
内分泌腺及全身性疾病
园艺
神经病学
肿瘤学
更多类别查询

图标索引 历史查询
 

ibuprofen
相关语句
  布洛芬
    STUDY ON PREPARATION AND DISSOLUTION OF IBUPROFEN SUSTAINED RELEASE GRANULES
    布洛芬缓释颗粒的制备及溶出度研究
短句来源
    Determination of Ibuprofen in Serum by RP-HPLC
    反相HPIC法测定血清布洛芬含量
短句来源
    STUDIES ON THE ANTIINFLAMMATORY DRUGS OF 2-ARYLPROPANOIC ACIDS 1.SYNTHESIS OF IBUPROFEN BY 1,2-ARYL REARRANGEMENT
    2-芳基丙酸类消炎镇痛药物的研究1 1,2─芳基重排法合成布洛芬
短句来源
    Studies on Bioequivalence of Domestic and Imported Tablets of Ibuprofen
    国产与进口布洛芬糖衣片生物等效性研究
短句来源
    Ibuprofen tablet dissolution improved by polysorbate 80
    聚山梨酯80改进布洛芬片溶出度的工艺探讨
短句来源
更多       
  “ibuprofen”译为未确定词的双语例句
    Effects of dexamethasone and ibuprofen on LPS induced gene expression of TNF α, IL 1β, and MIP 1α in rat lung
    Effects of dexamethasone and ibuprofen on LPS-induced gene expresion of TNF_ α,IL-1β,and MIP-1α in rat lung
短句来源
    Results Inter-day RSD of ibuprofen was 0.35% and intra-day less than 0.68%,respectively. The average recovery rate of ibuprofen was 100.4%.
    结果本法的日内RSD为0.35%,日间RSD为0.68%,平均回收率为100.4%。
短句来源
    Preparation and Quality Controll of Ibuprofen Lysine Sterilized powder for Injection
    注射用赖氨洛芬的研制及其质量控制
短句来源
    The absoluterecoveries were found to be 101. 22±1.96%for Ibuprofen, Precision studies for withinday at defferent concentrations providedCV values of less than 1.47%. The chro-matographic elution was 6.15 min. andibuprofen quantities as low as 0.1μg/ml.
    该法快速灵敏,重现性好,相关系数为0.9998,不同浓度水平测定结果的日内变异系数小于2%,检出限为0.1μg/ml,回收率为101.22±1.96%。
短句来源
    Pretreated with Azone propylene glycol and N-methyl-2-pyrrol idoncp, the percutaneous fluxrates of ibuprofen increased 8,3. 5 and 1 fold rcspcctivcly.
    采用月桂氮酮、丙二醇、N-甲基-2-毗咯烷酮预处理后药物的透皮速率分别增加8倍、3.5倍和1倍。
短句来源
更多       
查询“ibuprofen”译词为用户自定义的双语例句

    我想查看译文中含有:的双语例句
例句
为了更好的帮助您理解掌握查询词或其译词在地道英语中的实际用法,我们为您准备了出自英文原文的大量英语例句,供您参考。
  ibuprofen
These features were exploited to improve analytical performances in simultaneous determination of the minor ingredient of pseudoephedrine hydrochloride and the major ingredient of ibuprofen in a pharmaceutical preparation.
      
Relative standard deviations (RSDs) of 2.8% for the minor ingredient and 1.2% for the major ingredient were produced in 11 runs of a test solution containing 13.1 mg/l pseudoephedrine hydrochloride and 81.4 mg/l ibuprofen.
      
Analytical results for two batches of compound ibuprofen tablets by the SEKI-based FI-CE approach were in good agreement with that obtained by a conventional high performance liquid chromatographic method.
      
A simple, rapid, and precise high-performance liquid chromatographic method for the determination of nimesulide in pharmaceutical preparations was proposed using Ibuprofen as an internal standard.
      
It was shown that the enantiomeric composition and the concentration of the active component in Ibuprofen can be determined.
      
更多          


Serum concentrations of ibuprofen were determined by an improved method on high-performance liquid chromatograph (HPLC) . Comparative bioavailability studies for evaluation of the ibuprofen suppository, the commercially available tablet and powder were conducted on 9 adult male volunteers using the Latin-Square crossover design (3×3). Variance analyses of the pharmaookinetio parameters (including tmax, cmax and AUC ) following a single dose (300 mg) of any formulation showed no statistical difference...

Serum concentrations of ibuprofen were determined by an improved method on high-performance liquid chromatograph (HPLC) . Comparative bioavailability studies for evaluation of the ibuprofen suppository, the commercially available tablet and powder were conducted on 9 adult male volunteers using the Latin-Square crossover design (3×3). Variance analyses of the pharmaookinetio parameters (including tmax, cmax and AUC ) following a single dose (300 mg) of any formulation showed no statistical difference (p>0.05), indicating that the ibuprofen suppository, tablet or powder formulations were bioequivalent.

用改进的高效液相色谱法测定布洛芬血清浓度。在9名男性健康受试者中,按3×3拉丁方设计,对布洛芬栓剂、片剂和粉剂作了生物利用度比较。结果表明,9名受试者应用三种制剂各300mg后的达峰时间(t_(max))、血药峰浓度(c_(max))和药-时曲线下面积(AUC_(0→∞)),经方差分析无显著差异(p>0.05),提示布洛芬栓剂与片剂、粉剂具有生物等效性。

New formulations were developed to increase the relative bioavailability of ibuprofen tablets produced by Shan Dong Xin Hua Pharmaceutical Factory in China. The dissolution rates of the tablets available in the Chinese market(A), the tablets of the new formulations (B and C) and the reference tablets made by British Boots Company (D) were determined. Human bioavailability studies were conducted to assess the in vivo performances of A, B and C relative to D by GC. The particle sizes of ibuprofen raw...

New formulations were developed to increase the relative bioavailability of ibuprofen tablets produced by Shan Dong Xin Hua Pharmaceutical Factory in China. The dissolution rates of the tablets available in the Chinese market(A), the tablets of the new formulations (B and C) and the reference tablets made by British Boots Company (D) were determined. Human bioavailability studies were conducted to assess the in vivo performances of A, B and C relative to D by GC. The particle sizes of ibuprofen raw materials (A′, B′, D′) used for producing tablets (A, B and C, D) were ascertained and the differences of crystal forms between A′ and D′ were compared.

本文试制出新处方布洛芬片剂,选择山东新华制药厂三种片剂:市售处方A、新处方片剂B和C,以及英国Boots公司的片剂D,进行体外溶出速率和人体生物利用度试验,并测定了生产A,B(和C),D片剂的布洛芬原料A′,B′,D′的粒度,比较了A′,D′的晶型。实验表明,国内外原料晶型相同,A′,B′,D′平均粒径分别为130.0,36.6,56.6μm。A与D生物不等效,B和C与D生物等效。提高国产片剂生物利用度的因素主要与原料粒度、处方组成和制备工艺有关。

Mice pretreated with PG cyclo-oxygen-ase inhibitor aspirin, at 300 mg/kg/d×5,and ibuprofen, at 100 mg/kg/d×5 orallyand 20 mg/kg/d×3 intraperitoneally reveal-ed moderate chemoprophylactic effects andthe reduction of the penetration of worms by23% when compared to controls. Daily oraladministration of aspirin, at 300 mg/kg for15 days the worms reduction increased to41.7%.In estimation of PGE_1 in cercariae ofS.japonicum by radioimmunoassay, the PGE_1was 49 pg/100 cercariae. In normal mouseskin PGE_1 has...

Mice pretreated with PG cyclo-oxygen-ase inhibitor aspirin, at 300 mg/kg/d×5,and ibuprofen, at 100 mg/kg/d×5 orallyand 20 mg/kg/d×3 intraperitoneally reveal-ed moderate chemoprophylactic effects andthe reduction of the penetration of worms by23% when compared to controls. Daily oraladministration of aspirin, at 300 mg/kg for15 days the worms reduction increased to41.7%.In estimation of PGE_1 in cercariae ofS.japonicum by radioimmunoassay, the PGE_1was 49 pg/100 cercariae. In normal mouseskin PGE_1 has been measured to amount to3105±691.7 pg/10 mg on average. In cercarial penetrated mouse skin, 1.5hours after exposure the PGE_1 assesed in 100and 250 cercariae in the infected skin were5506±1127.1 and 12085±2622.9 pg/10 mgrespectively, which were significantlyhigher than that of the non-penetrated skin.These studies in conjunction with our pre-vious work indicate that: 1.PGs, similar toS. mansoni, were probably necessary forcercarial penetration. 2.PG inhibitors couldreduce cercarial penetration. Receptors antagonist etc. e.g. diphen-hydramine, chlorpheniramine, atropine,practolol could not reduce cerearial penetra-tion, but praziquantal in the pretreatedmice could reduce cercarial penetration sig-nificantly, e. g. 400 mg/kg orally 2 hoursprior to affection of cercariae about 100%reduction of the penetration, but if pre-treated with praziquantal, 4, 8, 24, 36hours prior to the affection the reductionpenetration decreased to 51.7, 46.1, 9.4,8.9% respectively.

作者用放射免疫法,测定感染日本血吸虫尾蚴的小鼠皮肤中前列腺素E_1(PGE_1)的含量。结果感染组的PGE_1显著高于正常对照组(P<0.01),且随感染尾蚴的数量增加而增加。使用7种PG抑制剂,其中阿斯匹林、布洛芬及消炎痛有一定预防尾蚴穿透作用,4种受体阻断剂无明显预防作用。抗血吸虫药吡喹酮400mg/kg,感染前2h减虫率最佳,用药至感染时间愈长,其预防作用愈弱。作者对以上结果进行了讨论,认为日本血吸虫尾蚴穿透皮肤的过程中,有PGE_1参与。前列腺素抑制剂具有一定的预防尾蚴穿透皮肤的作用。

 
<< 更多相关文摘    
图标索引 相关查询

 


 
CNKI小工具
在英文学术搜索中查有关ibuprofen的内容
在知识搜索中查有关ibuprofen的内容
在数字搜索中查有关ibuprofen的内容
在概念知识元中查有关ibuprofen的内容
在学术趋势中查有关ibuprofen的内容
 
 

CNKI主页设CNKI翻译助手为主页 | 收藏CNKI翻译助手 | 广告服务 | 英文学术搜索
版权图标  2008 CNKI-中国知网
京ICP证040431号 互联网出版许可证 新出网证(京)字008号
北京市公安局海淀分局 备案号:110 1081725
版权图标 2008中国知网(cnki) 中国学术期刊(光盘版)电子杂志社