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机构地区:[1]浙江省食品药品检验所,杭州310004 [2]杭州市药品检验所,杭州310017
出 处:《西北药学杂志》2012年第6期569-571,共3页Northwest Pharmaceutical Journal
摘 要:目的建立炔诺酮片溶出度检查方法。方法采用桨法进行溶出度实验,高效液相色谱法测定介质中药物含量。结果溶出度检查方法为桨法,以5g.L-1十二烷基硫酸钠溶液500mL为溶出介质,转速为75r.min-1,取样时间为45min(薄膜衣片)或60min(糖衣片)。含量测定方法的线性方程为Y=64 743 X-208(r=1.000 0),在0.12~1.84μg.mL-1质量浓度范围内线性关系良好(r=1.000);A企业样品平均回收率为100.1%,RSD为1.3%,B企业样品平均回收率为100.8%,RSD为0.7%。结论该方法准确可靠,适用于该制剂的质量控制。Objective To establish a method for the determination of the dissolution rate of Norethisterone Tablets.Methods The method Ⅱ described in the appendix ⅩC of Chinese Pharmacopoeia(2010) was carried out and the HPLC method was adopted for detection of the dissolution rate.Results 500 mL of 5 g·L-1 SDS was used as a solvent with rotating speed of a paddle at 75 r·min-1.The sampling time was 45 min(film coated tablets) or 60 min(sugar-coat tablets) and was quantitatively analyzed by HPLC.The regression equation of norethisterone was Y=64 743X-208(r=1.000 0).The average recovery of norethisterone was 100.1%,with RSD of 1.3%(samples of factory A) and 100.8%,with RSD of 0.7%(samples of factory B).Conclusion The method is accurate and suitable for the dissolution determination for Norethisterone Tablets.
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