Abd Elbary A, Fadel H M, Nour S A
Pharmazie. 1984 Feb;39(2):110-2.
The dissolution rate of chloramphenicol from its hard gelatin capsules containing different formulations either in the form of fine powdered blend or granules was investigated. The granules were prepared by the wet method using ethanol 60%, gelatin, carboyme thyl cellulose (CMC) sodium or polyvinylpyrrolidone (PVP) as binders or by slugging at different mechanical strengths. Results showed that the more hydrophilic the formula, the more the dissolution rate of chloramphenicol. Capsules filled with fine powdered blend gave a higher dissolution of the drug than those filled with granules prepared by the wet method or granules prepared from slugs of high mechanical strengths. Of the binding agents tested in the wet method, alcohol excelled gelatin, and the latter excelled CMC sodium and PVP. Capsules filled with granules prepared from slugs of 1 kg hardness gave a dissolution rate which was either higher than or nearly approaching that of capsules filled with the corresponding fine powdered blend.
研究了氯霉素从其含有不同制剂(呈细粉混合物或颗粒形式)的硬明胶胶囊中的溶出速率。颗粒通过湿法制备,使用60%乙醇、明胶、羧甲基纤维素钠(CMC)或聚乙烯吡咯烷酮(PVP)作为粘合剂,或者通过在不同机械强度下压片制备。结果表明,配方越亲水,氯霉素的溶出速率越高。填充细粉混合物的胶囊比填充湿法制备的颗粒或高机械强度压片制备的颗粒的胶囊具有更高的药物溶出度。在湿法测试的粘合剂中,乙醇优于明胶,而明胶又优于CMC钠和PVP。填充硬度为1 kg压片制备的颗粒的胶囊的溶出速率高于或几乎接近填充相应细粉混合物的胶囊的溶出速率。