论文部分内容阅读
目的研究喉咽清水蜜丸的制剂工艺及质量标准，并通过体外溶出度探讨自研样品处方和工艺的可行性。方法按照中药制剂方法研制水蜜丸，按照中国药典１９９５年版要求检测并测定溶出度，用二阶导数光谱法测橙皮甙含量来确定水蜜丸的溶出曲线。结果所制水蜜丸符合药典要求。结论喉咽清水蜜丸的处方和工艺是可行的。
Objective To study the preparation process and quality standards of the throat throat Qingshui honey pill, and to explore the feasibility of the self-research sample prescription and technology through in vitro dissolution. Methods According to the method of traditional Chinese medicine preparation Shui Mi Wan, according to the requirements of the Chinese Pharmacopoeia 1995 edition to detect and determine the dissolution rate, using the second derivative spectrum method to determine the content of Hesperidin to determine the dissolution profile of Shui Mi Wan. As a result, the produced honeydew pill meets the pharmacopoeia requirements. Conclusion The prescription and technology of the throat throat clear water honey pill is feasible.