摘要
目的:研制脑康口服液,并对其进行质量控制。方法:水提醇沉法制备该制剂并进行临床疗效考察。结果:本制剂工艺简单,薄层图谱斑点清晰,分离度好,临床有效率与对照组比较有显著性差异。结论:本制剂质量可控,临床有较好的疗效。
Objective: To develop the preparation procedure and quality control of Naokang oral fluid. Methods: The preparation procedure and quality control standard of Naokang oral fluid was established. Results: The preparation method was simple, and the studies showed that spots on TLC could be well separated. There was remarkable difference compared with routine treatment in the efficient rate. Conclusions: The quality control was reliable and the product has good clinical effect.
出处
《儿科药学杂志》
CAS
2005年第6期23-24,共2页
Journal of Pediatric Pharmacy
关键词
脑康口服液
制备
质量控制
临床应用
Naokang oral fluid
Preparation
Quality control
Clinical effect