Jones D E, Norton D A, Davies D J
Br J Ophthalmol. 1979 Dec;63(12):813-6. doi: 10.1136/bjo.63.12.813.
The effect of formulations of guanethidine and adrenaline of different composition has been tested in rabbits and in patients with glaucoma. The concentrations of guanethidine and adrenaline used for the rabbits were 5.0% and 1.0%; 2.5% and 0.5%; 1.0% and 0.2%; 0.5% and 0.1%. All except the lowest combination were equally effective in the magnitude of the decrease in intraocular pressure brought about and in their duration of activity. Two formulations containing guanethidine and adrenaline at concentrations of 3.0% and 0.5% and 1.0% and 0.2% respectively (formulated as Ganda drops by Smith and Nephew Pharmaceuticals Ltd) were tested in a blind, cross-over, short-term clinical trial on 20 patients. The drops containing the lower concentration of drugs were as effective as those of higher concentration. These results lead us to believe that most patients who respond to this treatment could be put on a reduced dosage regimen, which should result in a decreased incidence and severity of side effects.
已在兔子和青光眼患者身上测试了不同成分的胍乙啶和肾上腺素制剂的效果。用于兔子的胍乙啶和肾上腺素浓度分别为5.0%和1.0%;2.5%和0.5%;1.0%和0.2%;0.5%和0.1%。除最低浓度组合外,所有组合在降低眼压的幅度及其作用持续时间方面效果相同。两种分别含有浓度为3.0%和0.5%以及1.0%和0.2%的胍乙啶和肾上腺素的制剂(由施乐辉制药有限公司配制成甘达滴眼液)在20名患者身上进行了一项盲法、交叉、短期临床试验。含有较低药物浓度的滴眼液与较高浓度的滴眼液效果相同。这些结果使我们相信,大多数对这种治疗有反应的患者可以采用减少剂量的治疗方案,这将导致副作用的发生率和严重程度降低。