Ertan G, Karasulu E, Abou-Nada M, Tosun M, Ozer A
University of Ege, Faculty of Pharmacy, Pharmaceutical Technology Department, Bornova, Izmir, Turkey.
J Microencapsul. 1994 Mar-Apr;11(2):137-40. doi: 10.3109/02652049409040444.
The in vivo absorption of crystalline nitrofurantoin and the dosage forms of nitrofurantoin prepared with microcapsules were carried out in man by determination of urinary excretion of unchanged nitrofurantoin. The cumulative amount of drug excreted and the duration of the therapeutic urine levels were compared. The microcapsule administration showed that the peak reached during the excretion of nitrofurantoin in urine, decreased significantly when compared to the pure drug. This could be an explanation for the decrease in side-effects of nitrofurantoin such as nausea and vomiting. Experiments in male albino rats showed that the microcapsules did not produce gastric haemorrhage seen with the same doses of the pure drug.
通过测定尿中未变化的呋喃妥因的排泄情况,对结晶型呋喃妥因以及用微囊体制备的呋喃妥因剂型在人体进行了体内吸收研究。比较了药物排泄的累积量和治疗性尿药浓度持续时间。微囊给药显示,尿中呋喃妥因排泄过程中达到的峰值,与纯药物相比显著降低。这可能是呋喃妥因副作用如恶心和呕吐减少的一个原因。雄性白化病大鼠实验表明,微囊不会产生相同剂量纯药物所导致的胃出血。