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Age of first drug taking: men and women who first took drug mainly at the age from 21 to 25 years old, while women took drug earlier than men did, which ranges from 15 to 25 years old; Academic background: 86.3 percent of respondents receive education below primary and middle school; Marriage: the unmarried take 48.6 percent and the divorced, 12.0 percent; Profession: the inoccupation, such as housewives, are the majority of drug addicts with 53.0 percent; Total rate of relapse: the rate of relapse within 6 months after detoxification climbs to 67.9 percent.

1首次吸毒年龄看:男、女性吸毒者的首次吸毒年龄分布集中在21-25岁,但女性吸毒者的首次吸毒年龄较之男性早,主要分布为15岁-25岁间;学历:初小以下占86.3%;婚姻:未婚者占48.6%,离婚占12.0%;职业:无职业为主占53.0%;总复吸率:脱毒后复吸的时间6月内高达67.9%。

All enhancers did not significantly change the transcorneal lag time of ENX. The irritancy of poloxamer and Azone was observed.? The results of in vitro release studies showed that the ENX gel based 3% HPMC K4M and 3%HPMC F4M povided sustained release of the drug over an 8-h period in vitro.Diffusion area has significantly effect on drug release, and pH value of medium and rotation rate have effcet on drug release.However, the diffusion shield has no effect on drug release. The P_ value of the preparation based on 3% HPMC F4M was 1.34-fold of conventional eye drops of ENX.

体外溶出度试验结果表明,以3%的HPMC K4M和F4M为基质制备的ENX凝胶剂的体外释放行为符合眼用缓释制剂的要求;体外释放度影响因素试验结果表明,释放面积对释放度有显著性影响,pH值和转速略有影响,而扩散屏障没有影响;离体角膜透过实验结果表明,以F4M为基质制备的凝胶剂中ENX的表观渗透系数P_(app是对照组的1.34倍,说明F4M与眼角膜的相容性较好,是一种理想的眼用制剂增稠剂,可以在眼用制剂中广泛采用。

Based on a survey findings to 168 new-type drug abusers in Yunnan,the author figured out that there are two major pernicious aspects on new-type drug abuse,such as on one hand,the perniciousness towards drug abusers physical condition and work abilities;on the other hand,the perniciousness towards drug abusers psychological states.

通过对168份新型毒品滥用问卷的实证分析,认为新型毒品滥用的主要危害主要表现在两个方面:一是对滥用者身体能力、生产能力的危害;二是对滥用者心理能力的危害。

By introducing anti-drug publicity, major education institutions and infrastructure construction of Hong Kong, it analyzes the characteristics of the anti-drug publicity and education aiming at young people so as to change and improve the anti-drug education for the young people in Chinese Mainland. It advances such quaternity working model as concerning about the mental health, strengthening the organizations, constructing professional squads and improving the form of anti-drug education.

通过介绍香港禁毒宣传和毒品教育的主要机构和设施建设的情况,分析其针对青少年禁毒宣传和毒品教育的工作特点,从而调整和改进我国大陆的青少年禁毒教育工作的思路,提出了构建关注心理健康、健全组织机构、打造专业队伍和改进教育形式的四位一体的禁毒教育工作模式。

At present, the central police station of the two security have been taken to Qujing City CDC detection; Wang Qiaotao drug addicts were sent to compulsory drug treatment in Luliang County, forced isolation by the drug two years, after the expiry of drug transferred to the Detention Unit in administrative detention on the 15th.

目前,中枢派出所的两名保安已被送到曲靖市疾控中心检测;吸毒人员王乔涛被送陆良县强制戒毒所强制隔离戒毒两年,戒毒期满后移送拘留所行政拘留十五日。

The stable clones are further identified by RT-PCR and Western blot; 6 MTT assay is used to investigate the effect of ZNRD1 on the cell growth of cells (AGS, SGC7901, MKN28, NIH3T3, GES-1); 7 Soft agar assay is used to investigate the effect of ZNRD1 on the clonality of cells (AGS, MKN28); 8 Nude mice assay is used to investigate the effect of ZNRD1 on the cell growth of gastric cancer cells (AGS, MKN28); 9 Flow cytometry is used to investigate the effect of ZNRD1 on the cell cycle distribution of cells (AGS, MKN28, NIH3T3, GES-1); 10 Flow cytometry is used to investigate the effect of ZNRD1 on the cell apoptosis of cells (AGS, MKN28, NIH3T3); 11 MTT assay is used to investigate the effect of ZNRD1 on the drug sensitivity of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR) in vitro; 12 SRCA is used to investigate the effect of ZNRD1 on the drug sensitivity of gastric cancer cells (SGC7901, SGC7901/VCR) in vivo; 13 Flow cytometry is used to investigate the effect of ZNRD1 on adriamycin accumulation of cancer cells (SGC7901, SGC7901/VCR, HL-60, HL-60/VCR); 14 Transmission electron microscope is used to investigate the effect of ZNRD1 on the sensitivity of SGC7901 cells towards drug-induced apoptosis; 15 Flow cytometry and DNA ladder assay are used to investigate the effect of ZNRD1 on the sensitivity of cells (SGC7901, SGC7901/VCR, HL-60/VCR) towards drug-induced apoptosis; 16 Microarray is used to investigate the profiling of ZNRD1-responsive genes in gastric cancer cells (AGS, MKN28, SGC7901, SGC7901/VCR); 17 RT-PCR and Western blot are used to identify the results of microarray; 18 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of cyclin D1; 19 Reporter gene assay is used to investigate the effect of ZNRD1 on the transcriptional activity of MDR1; 20 Kinase assay is used to investigate the effect of ZNRD1 on the activity of cyclin E-CDK2 kinase; 21 The antisensenucleic acids of p21 is used to inhibit the expression of p21, and flow cytometry is used to investigate the effect of p21 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 22 The antisensenucleic acids of p27 is used to inhibit the expression of p27, and flow cytometry is used to investigate the effect of p27 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 23 Liposome is used to up-regulate the expression of Skp2, and flow cytometry is used to investigate the effect of Skp2 on ZNRD1-induced cell cycle arrest in gastric cancer cells; 24 Western blot is used to investigate the effect of ZNRD1 on the stability of Skp2 and p27 in gastric cancer cells; 25 MVD assay is used to investigate the effect of ZNRD1 on the angiopoietic activity of gastric cancer cells; 26 ELISA is used to investigate the effect of ZNRD1 on the expression of VEGF165 in gastric cancer cells; 27 The roles of DARPP-32 in MDR of gastric cancer cells are investigated using gene transfection, MTT assay, SRCA, flow cytometry and DNA ladder assay.

应用杂交瘤技术制备ZNRD1的首个单克隆抗体;2)利用RT-PCR、Western blot和免疫组化检测ZNRD1在胃癌组织、胃炎组织、正常胃上皮组织、胃癌细胞和正常胃组织上皮细胞中的表达;3)构建ZNRD1的小干扰RNA载体,并测序鉴定;4)利用脂质体将ZNRD1的真核表达载体及其空载体转染胃癌细胞(AGS、SGC7901、MKN28)和小鼠成纤维细胞(NIH3T3),G418筛选后进行鉴定;5)利用脂质体将ZNRD1的小干扰RNA载体及其空载体转染药敏胃癌细胞(SGC7901)、正常胃组织上皮细胞(GES-1)、对长春新碱耐药的胃癌细胞(SGC7901/VCR)、药敏白血病细胞(HL-60)、对长春新碱耐药的白血病细胞(HL-60/VCR),G418筛选后进行鉴定;6)利用MTT实验检测ZNRD1高/低表达对细胞(AGS、SGC7901、MKN28、NIH3T3、GES-1)生长的影响;7)通过软琼脂克隆形成实验检测上调ZNRD1对AGS、MKN28细胞克隆形成能力的影响;8)通过裸鼠成瘤实验检测上调ZNRD1对AGS、MKN28细胞体内成瘤性的影响;9)通过流式细胞仪分析ZNRD1高/低表达对细胞(AGS、MKN28、NIH3T3、GES-1)的细胞周期的影响;10)通过流式细胞仪分析上调ZNRD1对细胞(AGS、MKN28、NIH3T3)的凋亡的影响;11)通过MTT实验检测ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR、HL-60、HL-60/VCR)体外药物敏感性的影响;12)通过肾包膜下移植法检测ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR)体内药物敏感性的影响;13)通过流式细胞仪分析ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR、HL-60、HL-60/VCR)内阿霉素蓄积和泵出的影响;14)通过透射电镜检测上调ZNRD1对SGC7901细胞凋亡敏感性的影响;15)通过流式细胞仪和DNA梯度试验检测ZNRD1高/低表达对细胞(SGC7901、SGC7901/VCR、HL-60)凋亡敏感性的影响;16)通过基因芯片检测ZNRD1高/低表达对胃癌细胞内基因表达谱的影响;17)利用RT-PCR、Western blot对基因芯片的结果进行鉴定;18)利用报告基因实验检测ZNRD1对cyclin D1的启动子活性的调节作用;19)利用报告基因实验检测ZNRD1高/低表达对MDR1的启动子活性的调节作用;20)利用激酶试验检测ZNRD1对cyclin E-CDK2 激酶活力的影响;21)利用反义核酸技术抑制p21的表达;通过流式细胞仪检测抑制p21对ZNRD1介导的细胞周期阻滞的影响;22)利用反义核酸技术抑制p27的表达;通过流式细胞仪检测抑制p27对ZNRD1介导的细胞周期阻滞的影响;23)利用脂质体转染法上调Skp2的表达;通过流式细胞仪检测上调Skp2对ZNRD1介导的细胞周期阻滞的影响;24)利用Western blot检测ZNRD1对p27和Skp2的蛋白稳定性的影响;25)利用微血管密度实验检测ZNRD1对AGS、MKN28细胞裸鼠移植瘤微血管形成的影响;26)利用ELISA检测ZNRD1对AGS、MKN28细胞培养上清和移植瘤匀浆中VEGF165含量的影响;27)利用脂质体转染法、MTT实验、肾包膜下移植法、流式细胞仪和DNA梯度试验检测新耐药相关分子DARPP-32对细胞(SGC7901、SGC7901/VCR、对阿霉素耐药的胃癌细胞SGC7901/ADR)多药耐药表型的影响;利用脂质体转染法和MTT实验检测下调ZNRD1对DARPP-32介导的胃癌多药耐药的调控作用。

No entire nitrendipine crystals were observed visually in SEM photos. The results of X-ray diffraction and differential scanning calorimetry analysis indicated that the crystalline form of nitrendipine was highly dispersed in microspheres, so as amorphous state. The drug release rate of microspheres could be controlled with adjusting the ratio of solid dispersion carriers and retarding agents formulated. The agitation speed and temperature of the preparation process have distinct effect on micromeritic properties of microspheres. The release profiles of the microspheres were mainly affected by the stirring rate of paddle, the concentration of SDS and pH of dissolution medium. Cooling speed and time, however, have no evident influence on the drug release rate of the microspheres. The dissolution data showed that the mechanism of drug release from microsphers was mainly diffusion-controlled. The incorporation efficiencies of 3 batches sample were exceed 96. 8%, which implied that the current method was suitable for design sustained-release dosage form for poorly water-soluble drug.

在扫描电子显微镜下观察,在微球内外未发现尼群地平的完整结晶,X-射线粉末衍射和差示扫描量热试验结果也显示,尼群地平已经被高度分散在微球中;微球的释药速度可通过调整处方中固体分散体载体和阻滞剂的比例控制;制备温度和搅拌速度对微球的质量影响较大;溶出仪的搅拌速度,释放介质的浓度和pH对微球的释放有较大的影响;制备过程中的冷却速度和冷却时间对微球的释放行为影响不很明显;方程拟合的结果表明缓释微球的释药行为符合扩散机制;测定三批微球样品的包封率均在96.8%以上,表明该法适合于制备难溶性药物的缓释微球。

Results: Cultures for Mycobacterium were positive in a total of 2657 people, among them 1848 strains (69.55%) were Mycobacterium tuberculosis, and 809 strains (30.45%) were Nontuberculous Mycobacterium. Among the 1848 strains of Mycobacterium tuberculosis, 337 strains (18.24%) were drug resistant, and 75 strains (4.06%) of them were resistant to both Isoniazid and Rifampin which made them multi-drug resistant. Among the 548 strains of Nontuberculous Mycobacterium, 453 strains (82.66%) were drug resistant. There were a total of 261 rapidly growing mycobacteria, and 242 (92.72%) of them were drug resistant.

结果:分枝杆菌培养阳性共2657菌株/人,其中1848株(69.55%)为结核分枝杆菌,809株(30.45%)为非典型结核分枝杆菌感染。1848株结核分枝杆菌中,337株(18.24%)有抗药性问题,其中75株(4.06%)同时对Isoniazid和Rifampin有抗药性为多重性抗药菌。548株非典型结核分枝杆菌中453株(82.66%)有抗药性问题;快速生长菌群共261株,其中242株(92.72%)有抗药性问题。

Objective To survey the infectious status and relevant risk behavior characteristics of HIV positives Methods Sero epidemiological survey was carried out in 986 drug users by means of questionnaire survey Results Three drug users were found to be infected with HIV with a positive rate of 0 3% Most of the drug users were young or in their prime of life, jobless or received little education The drug used was heroin and 63 3% was used through injection, 53 98% of them shared needles and syring...

目的 了解戒毒者的HIV感染情况以及艾滋病相关危险行为特征。方法采用血清学检测和问卷方法,对 986名戒毒者进行调查。结果检出HIV感染者 3例,阳性率为 0 3 0 %;以男性青壮年为主,无业者居多,文化程度低;海洛因为主要吸食毒品,静脉吸毒率为 63 69%,其中 5 3 98%的人有过共用注射器行为;性乱在男性与女性吸毒者中同样存在;有 81 0 7%在婚外或婚前性行为时从未使用过安全套。结论在吸毒人群中,特别是静脉吸毒人群中开展有效的健康教育和干预活动势在必行

Suitable implants, composite drug membranes, implanting under scleral flap for glaucoma or into suprachoroid space for perforating ocular injury were developed in this paper. The model drug in film could maintain sustained release. Thus it was advantageous to alleviate side effect to ocular tissue with an acute change in drug concentration and enhance utilization of drug.

本文旨在研究适于手术治疗青光眼和眼穿通伤的植入剂-复合药膜,植入脉络膜上腔或巩膜瓣下,维持模型药物的持续释放,有效避免药物的峰谷现象对眼组织的毒害作用,提高药物利用率。

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