给药
- Administration;dose
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CPA单次给药造成骨髓细胞G2/M期细胞的比例稍有升高,出现明显的尿蛋白和尿潜血。
Single dose of CPA resulted in a slight increase of G_2 / M myelocytes together with higher incidence of urine protein and occult blood .
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方法:采用1次、1d及2周给药方法,观察其药物不良反应。
Methods : The drug was given in a once daily dose for 2 weeks to observe its ADRs .
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结论:阿替洛尔凝胶可用于鼻腔给药。
Conclusions atenolol gel can be used for intranasal administration .
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静脉输液也可作为一种给药方法
Intravenous infusions are also used to administer medications .
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结论经鼓室给药的DSP原位凝胶对耳蜗具有明显的定位释药作用和缓释效果。
Conclusion DSP thermosensitive in situ gel following IT has significant cochlea-oriented and sustained-release effect .
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一种新型给药系统&聚烯烃非PVC软包装输液
A Novel Type of Administration System & Non - PVC Polyolefin Soft - packing Transfusion
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本组均给予维生素K1治疗,大部分给药3~5天,血障碍迅速改善。
All the patients were given vitamin K1 for 3 to 5 days . Coagulation disturbance was quickly corrected .
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C组为对照组即NEC模型后未给药组:D组为正常组。
No dose was administered in Group C ; Group D was control group .
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血卟啉衍生物不同途径给药并光照小鼠移植瘤的形态观察及DNA定量测定
Morphological Obervation and DNA Quantitative Analysis of Murine H_ ( 22 ) Hepatoma after Being Injected with HPD in Different Pathway and Lighted
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基于MonteCarlo模型的微型PLGA给药系统建模及仿真
Modeling and Simulation of the Drug Release from PLGA Drug Delivery Micro-system Based on Monte Carlo model
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经腹膜外盆腔淋巴间隙给药对妇科肿瘤患者外周血T细胞亚群及NK细胞的影响
Effect of Thrapy via Pelvic Retroperitoneal Space on the T Subpopulation and NK Cell in Gynecological Cancer
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结果:PICC置管途径给药无静脉炎及药液外渗;
Results Patients with PICC had no phlebitis and physic liquor exosmosis .
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1亦能恢复环磷酰胺iv给药或ip接种Ehrlich腹水瘤细胞后引发的DTH反应。
Also restored DTH response impaired by injection of cyclophosphamide or inoculation with Ehrlich ascites tumour intraperitoneally .
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结论TNF能成倍提高化学药物的细胞毒作用,且应在先使用化学药物的基础上给药。
Conclusion TNF can remarkably increase the cytotoxicity of antitumor drugs . In clinical therapy , we should give TNF after antitumor drugs administration .
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各组小鼠分别于末次给药后24h,进行血常规检测。
Routine blood examination was conducted 24 hours after the last administration in mice of each group .
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结果rhG-CSF给药后可明显减轻中毒症状和改善造血机能。
Results rhG-CSF could relieve poisoning symptoms and improve hematopoietic functions .
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结果复心片高、中剂量组可以延长大鼠颈总动脉OT,复心片体外给药使血小板聚集率明显降低。
Results High-dose and middle-dose groups of Fuxin tablet could prolong OT and decrease the aggregation of platelet .
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给药后取血及脑组织,高效液相色谱法(HPLC)测定药物浓度。
The animals received CZP intraperitoneally and the concentrations of CZP in the serum and brain were determined by high performance liquid chromatography ( HPLC ) .
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方法HPLC测定三七总皂苷混悬液大鼠鼻腔给药后血样中人参皂苷Rg1的浓度,考察药物在体内的动力学过程,并计算其绝对生物利用度;
Methods After administration , Rg1 concentration in the serum was analyzed by HPLC and the absolute bioavailability was calculated .
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结果不同浓度美洛昔康体内、外给药,对脾淋巴细胞增殖、腹腔MΦ产生IL-1和对足爪肿胀的抑制作用,均随药物剂量增大而增强,且呈剂量依赖性。
Results Dose dependent inhibitory activities of meloxicam on lymphocyte proliferation , IL 1 production and swollen feet and paws were shown .
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连续给药3d后,尾静脉注射绵羊红细胞悬液0.1mL进行致敏。
0.1 mL of sheep erythrocyte suspension was injected via the vena caudalis after 3-day administration to allergize .
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方法(1)CCI手术前2h单次给药;
Methods ( 1 ) A single intraperitoneal administration of drugs was given 2h before nerve injury ;
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方法采用自身注射前后对照方法,对符合纳入标准的研究对象分别经静脉注入稀释的全氟丙烷人血白蛋白微球注射剂0.01ml/kg,由A和B研究者分别独立进行给药前、后造影效果评判比较。
Methods Diluted perfluoropropane-albumin microsphere injection was given intravenously to permitted objects at a dose of 0.01 ml / kg . Observers A and observers B evaluated the contrast effect respectively by self-comparison between pre-injection and post-injection .
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末次给药后,取肝称重,计算肝指数,酶法测定肝脏TC、TG。
The livers were harvested to obtain the TI and the levels of hepatic TC , TG were detected by enzyme methods after the last treatment .
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LHRH固体脂质纳米粒口服给药系统的研究
Study on LHRH-loaded solid lipid nanoparticles for oral administration
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GCs灌胃给药15天,一次性训练被动回避跳台实验和Y型电迷宫空间分辨能力测试测定小鼠学习记忆能力;
The learning and memory of mice were observed by one time training passive avoidance step-down and Y-maze spatial location task ;
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rhIL-11不同时间给药对急性放射病猕猴造血系统的影响
Therapeutic effect of rhIL-11 administered at different times on acute radiation sickness in rhesus monkeys
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方法模型大鼠随机分组,灌胃法给药,给药结束后采血作血糖、CHO、TG、HDLc、LDLc和血液流变学测定以及耳廓微循环检测,进行组间比较。
METHOD Rat models were randomly divided into groups and given the extract . Blood sugar , CHO , TG , HDL-C , LDL-C and blood rheology were determined and auricle microcirculation examined .
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方法:Wistar大鼠随机分为假手术组、缺血再灌注组(I/R)、缺血前给药组和再灌时给药组。
Wistar rats were divided randomly into sham operated group , ischemia-reperfusion ( I / R ) group , pretreatment with liposomes group and treatment with liposomes at reperfusion group .
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运动对照组(TC)和给药运动组(TT)进行递增负荷强度的跑台运动,训练时间共为7周,最后一次训练至力竭。
TC and TT groups were trained with increasing load of treadmill running for 7 weeks till exhausted in the last training . TT groups received intrapearitioneal ( i. p. )