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Abstract] Objective To discuss the cooperation of dextran-40 and urokinase on anti-platelet agglutination.

目的 探讨低分子右旋糖酐与尿激酶在抗血小板聚集上的协同作用。

Methods The antianaphylaxis activities of myricetin was measured by passive cutaneous anaphylaxis, dextran-induced itch and DNCB-induced delayed type hypersensitivity in mice,respectively.

采用小鼠同种、异种被动皮肤过敏反应、右旋糖酐致小鼠全身瘙痒反应和2,4-二硝基氯苯所致小鼠耳廓皮肤迟发型超敏反应实验,探讨杨梅素的抗过敏作用。

Methods Clinical study was made in 13 cases with ARF by low Molecular Dextran.

回顾性 分析 13例低分子右旋糖酐致急性肾功能衰竭的临床资料。

And Catt in combination with poly-aerylamide gel preparative electrophoresis to isolate serum high density lipoprotein in a pure form was developed.

作者以多聚阴离子—硫酸右旋糖酐沉淀分离,再以聚丙烯酰胺凝胶制备电泳进一步纯化,可获得较纯净的血清高密度脂蛋白。

The first, selecting Mannitol of polyhydric and Dextran ofpolysaccharide as subsidiary material, In accordance with differentusing quantities, making up eight recipes, freeze-drying test is madewith eight recipes differently. By adjusting recipe, to select themethod of two factors three levels. The best recipe determined is thatof Mannitol(160mg/bottle) and Dextran(40mg/bottle), Solving theproblem of description、moisture(≤1.5%)、solution(≤6s)、stability(95.0~110.0%) etc., The quality of preparation has beenimproved.

首先,选择赋形剂多元醇类的甘露醇和多糖类的右旋糖酐作为辅料,按照不同的用量,组合成8种处方进行冷冻干燥试生产,采用二因素三水平的满因子分析法,通过处方调整,确定甘露醇160mg/瓶、右旋糖酐40mg/瓶为最佳处方,解决了冻干制剂在性状、水分(≤1.5%)、溶解性(≤6s)和含量稳定性(95.0~110.0%)等方面的不足,提高了产品质量。

Methods:148 cases with pseudobulbar palsy after cerebral infarction were randomly divided into two groups:76 cases were tretaed with UBIO plus medications known as UBIO group.

应用UBIO和低分子右旋糖酐、血塞通治疗急性脑梗塞合并假性球麻痹76例,对照组72例,单用低分子右旋糖酐、血塞通治疗。

Abstract] objective to compare with curative effect and adverse reaction on renal anemia of hemodialyses patients with fe3 dextran venously and ferromyn orally.methods 60 hd patients were divided into venous group and oral group randomly and there were 30 patients in each group,100 mg cosmofer were used one hour by vein point of dialyser before hd was completed in hemodialyses patients in venous group 200 mg amber acid subiron was taken by the patients in oral group three times a day and two months in total.recombinant human erythropoietine was used at a dose of 100~150 u/kg?

摘要] 目的比较静脉注射右旋糖酐氢氧化铁和口服琥珀酸亚铁治疗血液透析患者肾性贫血的疗效和不良反应。方法选择60例hd患者,分为静脉补铁组和口服补铁组,每组30例。静脉补铁组:每次透析结束前1 h注射100 mg右旋糖酐氢氧化铁,从透析器静脉端输入,时间维持1 h;口服补铁组:琥珀酸亚铁200 mg,每日3次,连续口服2个月。两组同时使用基因重组人红细胞生成素100~150 u/kg?

Methods 59type2diaˉbetes mellitus with blood hyperviscosity were invotved in a randmoized control clinical trial.30cases were treated with PGE 1 200μg solved in500ml inj dextran lowmolecular intravenously everyday for3weeks.29cases treated with the same basic hypolycemic therapy and blood-lipid lowering drugs as the PGE 1 group except500ml inj dextran lowmolecular inˉtravenously everyday for3weeks as controls.

59例糖尿病合并高粘血症患者随机分组对照观察,前列腺素E 1 治疗组30例给予前列腺素E 1 注射液200μg溶于低分子右旋糖酐注射液500ml中静滴,每日1次,共3周;对照组29例降血糖、降血脂等基本治疗与前列腺素E 1 组相同,另外只给予低分子右旋糖酐注射液500ml静滴,每日1次,共3周。

Objective To observe the effect of PGE 1 on diabetic blood hyperviscosity.Methods 59type2diaˉbetes mellitus with blood hyperviscosity were invotved in a randmoized control clinical trial.30cases were treated with PGE 1 200μg solved in500ml inj dextran lowmolecular intravenously everyday for3weeks.29cases treated with the same basic hypolycemic therapy and blood-lipid lowering drugs as the PGE 1 group except500ml inj dextran lowmolecular inˉtravenously everyday for3weeks as controls.

目的 观察列腺素E 1 治疗糖尿病高粘血症的临床效果方法 59例糖尿病合并高粘血症患者随机分组对照观察,前列腺素E 1 治疗组30例给予前列腺素E 1 注射液200μg溶于低分子右旋糖酐注射液500ml中静滴,每日1次,共3周;对照组29例降血糖、降血脂等基本治疗与前列腺素E 1 组相同,另外只给予低分子右旋糖酐注射液500ml静滴,每日1次,共3周。

Methods 59type2diaˉbetes mellitus with blood hyperviscosity were invotved in arandmoized control clinical trial.30cases were treated with PGE 1200μg solved in500ml inj dextran lowmolecular intravenously everyday for3weeks.29cases treated with the same basic hypolycemic therapy and blood-lipid lowering drugs as the PGE 1group except500ml inj dextran lowmolecular inˉtravenously everyday for3weeks as controls.

方法59例糖尿病合并高粘血症患者随机分组对照观察,前列腺素E 1治疗组30例给予前列腺素E 1注射液200μg溶于低分子右旋糖酐注射液500ml中静滴,每日1次,共3周;对照组29例降血糖、降血脂等基本治疗与前列腺素E 1组相同,另外只给予低分子右旋糖酐注射液500ml静滴,每日1次,共3周。

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