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阿昔洛韦外用制剂的溶出度试验 被引量:10

The dissolution test for dermal applied preparations of aciclovir in vitro
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摘要 目的:研究不同基质阿昔洛韦(ACV)外用制剂的药物溶出度,为开发新的ACV外用制剂提供依据。方法:用固体药物溶出试验仪测定3种基质、5个浓度的试样,比较各自的单位面积释药量(M)及累积释药百分率(Q)。结果:M值随主药浓度增加而增加,Q随主药浓度增加而降低;药物溶出速率:凝胶剂>霜剂>乳剂型软膏,凝胶剂的溶出速率是霜剂的2倍。结论:ACV凝胶的药物溶出优于霜剂和乳剂型软膏。 OBJECTIVES: To study the dissolution amounts of aciclovir (ACV) from differently based preparations and provide the evidence for the developement of new preparation of ACV. METHOD: The dissolution tester was applied for the quantitative determination of ACV released from 3 based formulations and 5 concentrations samples. The release amount per unit area (M) and the accumulative release percentage (Q) were compared respectively. RESULTS: The value for M was raised with the increase of the concentration of aciclovir in preparations, and for Q was reduced. The release rates of the aciclovir gel were at least two times faster than the creams and the ointment. CONCLUSION: The drug dissolution from ACV gel was better than the creams and the ointment. 10 g·kg-1 ACV in prearation was the suitable concentration.
作者 邵凤 张崇璞
出处 《中国药学杂志》 CAS CSCD 北大核心 1998年第4期237-239,共3页 Chinese Pharmaceutical Journal
关键词 阿昔洛韦 溶出度试验 凝胶 霜剂 乳剂型软膏 aciclovior, dissolution test, gel, cream, ointment
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参考文献3

  • 1梁文权,经皮给药制剂,1992年,55页
  • 2陆瑜,经皮给药制剂,1992年,250页
  • 3余敏,皮肤科外用制剂选编,1991年,52页

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