中国基层医药
中國基層醫藥
중국기층의약
CHINESE JOURNAL OF PRIMARY MEDICINE AND PHARMACY
2008年
12期
1995-1997
,共3页
头孢克洛%质量标准%稳定性
頭孢剋洛%質量標準%穩定性
두포극락%질량표준%은정성
Cefaclor%Quality standard%Stability
目的 研究复方头孢克洛片的处方和制备工艺.方法 配制复方头孢克洛片,并制定质量标准,采用高效液相色谱法测定含量及进行稳定性考察.结果 以该处方工艺制成的片剂,质量可控,稳定性较好.结论 本品处方工艺成熟,质量可控,稳定性较好.
目的 研究複方頭孢剋洛片的處方和製備工藝.方法 配製複方頭孢剋洛片,併製定質量標準,採用高效液相色譜法測定含量及進行穩定性攷察.結果 以該處方工藝製成的片劑,質量可控,穩定性較好.結論 本品處方工藝成熟,質量可控,穩定性較好.
목적 연구복방두포극락편적처방화제비공예.방법 배제복방두포극락편,병제정질량표준,채용고효액상색보법측정함량급진행은정성고찰.결과 이해처방공예제성적편제,질량가공,은정성교호.결론 본품처방공예성숙,질량가공,은정성교호.
Objective To investigate the preparation and stability of compound cefaclor tablets.Methods The compound cefaclor tablets were prepared.The quality standard Were established.A HPLC method WaS established to determine the content and stability of samples.Results The prepared tablets was stable and the quality could be controlled.Conclusion The tablets were of reasonable formulation,good sample technology and good stability.The established method is accurate and reliable for the dissolution test for compound cefaclor tablets.The method can be used for quality control of compound cefaclor tablets.