本文首次研究自制的氨基胍基螫合树脂吸附贵金属的行为。
SNG resin contains aminoguanidine as function group. We are the first who studied its adsorption behavior in detail for noble metals.
目的：探讨诱导型一氧化氮合酶抑制剂氨基胍对大鼠移植胰腺的保护作用。
Objective: to investigate the effect of inducible nitric oxide synthase inhibitor aminoguanidine on transplanted pancreas in rats.
目的：探讨d -半乳糖致大鼠眼晶体损伤及氨基胍的干预作用及其机制。
AIM: to investigate the effects of aminoguanidine intervention on lens cell damage induced by D-galactose in rat eyes and its mechanism of action.
目的：观察糖尿病大鼠视网膜组织学变化、神经细胞凋亡现象以及氨基胍的治疗作用。
AIM: to observe the histological change of retina and apoptosis of neurocyte and the therapeutical efficacy of aminoguanidine in diabetic rats.
用大肠杆菌内毒素（LPS）复制大鼠内毒素性休克模型，氨基胍治疗组采用氨基胍治疗。
Rats were challenged by E. coli LPS to set up the model of endotoxic shock, AG group were treated by aminoguanidine.
对二甲氨基苯甲醛同时亦与氨基胍重碳酸盐反应，生成更为稳定的化合物，而使该橙色产物分解而褪色。
However, 2 could also react with 1 simultaneously in the same reaction system, the product was more stable, and that made the orange compound decomposed and faded.
结果氨基胍和同种异体松质骨复合物在骨缺损愈合过程中成骨量、成骨速度、时间均优于单纯同种异体松质骨。
Result:The compound of cancellous allograft bone and AG were superior in term of the amount and speed of new bone formation on region of bone defect to the simple cancellous allograft bone.
结果：与阳性药氨基胍相比，灌服糖肾安的大鼠血清对体外糖基化反应有明显的抑制作用，相对抑制率为1 0 2 . 2 %。
Results: as compared with positive drug aminoguanidine, the sera of rats treated with TSA showed significantly inhibitory effect on glycation in vitro, and the relative inhibitory rate was 102 2%.
L-1剂量范围内均可有效抑制蛋白糖化终末产物的生成，当药物浓度达2.0g·L-1时其抑制作用相当于同剂量的氨基胍。
The inhibitory effects of EGB and EGS (2.0 g·L-1) on the generation of AGEs were almost the same as that of aminoguanidine at the same concentration.
L-1剂量范围内均可有效抑制蛋白糖化终末产物的生成，当药物浓度达2.0g·L-1时其抑制作用相当于同剂量的氨基胍。
The inhibitory effects of EGB and EGS (2.0 g·L-1) on the generation of AGEs were almost the same as that of aminoguanidine at the same concentration.
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