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   a good linearity 的翻译结果: 查询用时:0.015秒
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a good linearity
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  良好的线性关系
     RESULTS A good linearity was obtained in the range of 0.02 - 0.20 g ·L -1 (r= 0.999 8), and the average recovery was 100.9% with RSD of 2.4% (n=6).
     结果:芍药苷进样量与色谱峰面积在0.02~0.20g·L-1范围内呈良好的线性关系(r=0.999 8),平均加样回收率为100.9%,RSD为2.4%(n=6)。
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     The hesperidin show a good linearity at the range of 1.25μg~10.0μg,r=0.9993,the average recovery was 98.22%,RSD=2.19%.
     橙皮苷在1.25μg~10.0μg范围内呈良好的线性关系,r=0.9993,平均回收率为98.22%,RSD为2.79%。
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     Result:The three components had a good linearity relationship between1.08~6.48μg、0.678~4.068μg、1.024~6.144μg.
     结果:人参皂苷Rg1、Re、Rb1分别在1.08~6.48μg、0.678~4.068μg、1.024~6.144μg呈良好的线性关系
     Results Cefixime had the highest absorption peak at 288 nm and a good linearity within the range of 1.5~37.5 μg/ml(A=0.0457C-0.0037,r=0.9999).
     结果头孢克肟在288 nm处有最大吸收,在1.5~37.5μg/mL范围内与吸收度呈良好的线性关系:A=0.0457ρ-0.0037,r=0.9999。
短句来源
     The results showed that the regression equation, within the range of the standard sampleconcentration in 5-50μg/ml, was A=3.166×10-3X-9.0×10-3, with a good linearity(r=0.9999)between the absorbance andconcentration.
     实验结果表明:标液浓度在5~50μg/ml范围内,吸光度与浓度呈良好的线性关系,回归方程为A=3.166×10-3X-9.0×10-3,r=0.9999(n=5)。
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  “a good linearity”译为未确定词的双语例句
     RESULTS Imperialine had a good linearity from 0.1086 mg·ml~-1 to 0.5430 mg·ml~-1 and the regression equation was lnC=0.7586lnA-~10.183 (r=0.9999,n=5).
     结果西贝碱在0.1086~0.5430mg·ml-1之间线性关系良好,回归方程为lnC=0.7586lnA-10.183(r=0.9999,n=5);
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     Results A good linearity of puerarin, hesperidin, eugenol, honokiol and magnolol was in the range of 0.125~2.000 μg, 0.031~1.020 μg, 0.117~2.340 μg, 0.142~2.280 μg and 0.117~1.880μg respectively;
     结果葛根素、橙皮苷、丁香酚、和厚朴酚、厚朴酚的线性范围分别为0.125~2.000μg、0.031~1.020μg、0.117~2.340μg、0.142~2.280μg、0.117~1.880μg;
短句来源
     A good linearity was shown in the concentration range of 1.896~18.96 μg/mL(r=0.9999),RSD was 1.12%(n=6),and the recovery was 99.74%~102.05%.
     虾青素在1.896~18.96μg/mL范围内线性关系良好,r=0.9999,RSD=1.12%(n=6),回收率为99.69%~102.6%。
短句来源
     There was a good linearity within the ranger of 41 μg/mL ~ 328 μg/mL(r = 0.9998), The mean recovery was 100.5 %, relative standaral deviation(RSD) 0.5 %(n=9).
     氟伐他汀钠在41μg/mL~328μg/mL浓度范围内线性关系良好(r=0.9998),平均回收率为100.5%,相对标准偏差(relative standaral deviation,RSD)0.5%(n=9)。
短句来源
     Result: The salviolⅡA showed a good linearity at the range of 0.0845~0.2535μg,r=0.9983,the average recovery was 98.15%,RSD was 1.05%(n=6).
     结果:丹参酮ⅡA在0.0845~0.2535μg间呈良好线性关系,r=0.9983,平均回收率为98.15%,RSD为1.05%(n=6)。
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  相似匹配句对
     The linearity is good.
     其相关系数为 0 .9989,线性关系良好 ,检出限为 0 .0 2 1mg/ L。
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     Be a good man
     寻觅真正好男人
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     and A.
     和展毛大渡乌头A .
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     G. A.
     作者采用美国燃气协会(A.G.A.)
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     The linearity is good.
     其相关系数为 0 .9989,线性关系良好 ,检出限为 0 .0 2 1mg/ L。
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  a good linearity
H2 concentration from 0.5% to 4% showed a good linearity against voltage.
      
The proposed method is simple, rapid, sensitive, and has a good linearity.
      
Diagrams of W+Mo, and Pb+Zn deposits show a good linearity between ore value and logarithms of cumulative ore tonnage.
      
And when the concentration of the NFA is 1.95×10-5 mol L-1, they possess a good linearity in the concentration of DNA ranged from 4.7×10-6 to 2.8×10-5 mol L-1.It is a good method due to the high sensitivity and selectivity.
      
An equation proposed by us for the relation between the integral irradiance and the depth of cure indicated a good linearity (r=0.997) in the wavelength range between 460 and 480 nm when different VL curing units were used.
      
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The processing technology of a high inductive intensity magnetic analyser is described. Good results of performance have been obtained by means of choosing material, forging press, annealing and machine processing strictly. The result has shown that magnetic intensity more than 13.5 Kilogauss in the magnetic gap has been obtained. A good linearity of the magnetic inductive intensity vs magnetizing current has been observed up to ll kilogauss.

本文主要介绍一台高磁感应强度的磁分析器的加工工艺。由于在选材、锻压、退火及加工过程中进行了严格的控制,取得了良好的效果,使磁极间的磁感应强度达到13.5仟高斯以上,I——B关系曲线中直线部分的磁感应强度最高达到了11仟高斯。

The molecular weight distribution and average molecular weights of the heparins were studied by gel chromatography, in which "mean eluted volumes" would becalculated on for the peaks of non-Gauss distribution; A polt Kavvs. M. W. with double log. for the heparin species has a good linearity. The average M. W. of heparins determined by gel chromatography is 10, 500, and is 10,700 by viscosity Method. The mean deviation of average M. W. between two methods is lower than+2%. We have found that M. W. of the...

The molecular weight distribution and average molecular weights of the heparins were studied by gel chromatography, in which "mean eluted volumes" would becalculated on for the peaks of non-Gauss distribution; A polt Kavvs. M. W. with double log. for the heparin species has a good linearity. The average M. W. of heparins determined by gel chromatography is 10, 500, and is 10,700 by viscosity Method. The mean deviation of average M. W. between two methods is lower than+2%. We have found that M. W. of the "macromalecular" heparin-species is 46, 000 and "small-molecular" heparen-species is 2, 400 in intestinal mucosa of pig.

用凝胶层析法研究了肝素的分子量分布及平均分子量.非高斯分布峰的平均洗脱体积可以按V_c=sum from i=1 to n(W_j/W)/V_(ci)来计算.肝素种类的K_(αV)对分子量的双对数图有很好的线性关系,用凝胶层析法测定的肝素平均分子量是10,500,用粘度法测定的是10,700.二种方法测定的平均分子量间的平均偏差小于±2%.并发现猪肠粘膜内有分子量为46,000的“大分子”肝素及分子量为2,400的“小分子”肝素.

A HPLC method for the determination of lidocaine, bupivacaine and tetracaine in human plasma with verapamil as internal standard has been established. This method was carried out on an ODS column using modified methanol (0.51 ml of n-butylamine and 0.3 ml of glacial acetic acid added to 300 ml of MeOH)-water (75:25) as mobile phase operated in recycling mode. The procedure is as follows: transfer 1.0 ml of plasma into a 12 ml glass centrifuge tube, add one drop of 2 N NaOH solution (if tetracaine is present,...

A HPLC method for the determination of lidocaine, bupivacaine and tetracaine in human plasma with verapamil as internal standard has been established. This method was carried out on an ODS column using modified methanol (0.51 ml of n-butylamine and 0.3 ml of glacial acetic acid added to 300 ml of MeOH)-water (75:25) as mobile phase operated in recycling mode. The procedure is as follows: transfer 1.0 ml of plasma into a 12 ml glass centrifuge tube, add one drop of 2 N NaOH solution (if tetracaine is present, one drop of 10% sodium metabisulfite solution and 0.1 ml of 2 N NaOH solution must be added to the specimen tube before collecting the sample in order to prevent hydrolysis), add 40μ1 of the internal standard (0.16μg/μ1)and 8 ml of ethyl ether-dichloromethane (10/8,V/V). shake for 10 minutes and centrifuge for 5 minutes at 3000g. Transfer the organic phase into another tube and evaporate to dryness at 50℃. Reconstitute the residuew ith 50μl of mobile phase and inject 20μl into the chromatograph using the following conditions: column, 15×0.46 cm packed with ODS (YWG-C_(18)H_(37), 10μm); flow rate, 1.5 ml/min; UV detector, 220 nm; range 5 mV; Chart speed, 5 mm/min.This method is simple, rapid, sensitive and has a good linearity. The absolute recoveries were found to be 101±3.6% for lidocaine, 89.3±4.1% for bupivacaine and 80±10.1% for tetracaine. Precisioin studies for both within day and day-to-day at different concentrations provided CV values of less than 10% except tetracaine which produced a CV of 10.5% for within day precision at high concentration.

应用改性甲醇—水为流动相,在YWG—C_(18)H_(37)反相柱上,以异搏定(verapamil)为内标,建立了适合于临床生化研究和药物代谢动力学研究的同时或分别测定人血浆中利多卡因(lidocaine),布比卡因(bupivacaine)和丁卡因(tetracaine)的高效液相色谱法。本法简便、快速、灵敏、重现性好,流动相可循环使用。利多卡因、布比卡因和丁卡因的平均回收率分别为101±3.6%,89.3±4.1%和80±10.1%,不同浓度水平测定结果的日内和日间变异系数一般小于10%,其检定限度(信噪比>3)分别为0.03,0.05和0.1μg/ml。

 
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