期刊文献+

交联聚维酮对对乙酰氨基酚片溶出度的影响 被引量:2

Crospovidone effects on the dissolution rate of paracetamol tablets
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摘要 目的:研究崩解剂交联聚维酮对对乙酰氨酚片溶出度的影响。方法:采用交联聚维酮不同用量,不同加入方法,放置时间和再次加工。结果:交联聚维酮不同用量、不同加入方法对溶出度有显著影响,放置时间、和再次加工对溶出度无影响。结论:应用交联维酮应考虑其用量和加入方法。 OBJECTIVE:To study crospovidone effect on the dissolution rate of paracetamol tablets.METHODS:It is adopted the different content of crospovidone,the different manufactured way,the stored time,and made tablets again.RESULTS:It is effects significantly on the dissolution of paracetamol tablets by the different content of crospovidone and the different manufactured way,but is not significantly by the stored time and made tablets again.CONCLUSIONS:The content and manufactured way are considered when crospovidone is applied.
出处 《中国医院药学杂志》 CAS CSCD 北大核心 1999年第11期670-672,共3页 Chinese Journal of Hospital Pharmacy
关键词 交联聚维酮 对乙酰氨基酚 溶出度 片剂 crospovidone,paracetamol,dissolution rate
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参考文献4

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  • 2上海医药工业研究院药物制剂研究室,药用辅料应用技术,1991年,119页
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同被引文献16

  • 1袁易,秦宗玲.石杉碱甲口腔崩解片的制备及溶出度考察[J].药学服务与研究,2006,6(4):274-276. 被引量:3
  • 2WILLIAMS H D, TREVASKIS N L, CHARMAN S, et al. Strategies to address low drug solubility in discovery and development [J]. Pharml Rev, 2013, 65(1): 319-320.
  • 3VASANTHAKUMAR S, VIJAYA R C. Immediate release tablets of telmisartan using superdisintegrant-formulation, evaluation and stability studies [J]. Chem Pharm Bull, 2008, 56(4): 575-577.
  • 4YELCHURIV R, JAGDISH B, KODURI B, et al. Impact of superdisintegrants on efavirenz release from tablet formulations [J]. Acta Pharm, 2010, 60(2): 185-195.
  • 5MORONI A. A novel copovidone binder for dry granulation and direct compression tabletting [J]. Pharm Technol, 2001, 24(9): 8-12.
  • 6CHEN S, ZHU J, MA F, et al. Preparation and characterization of solid dispersions of dipyridamole with a carrier "copolyvidonum pasdoneS-630'' [J]. Drug Dev Ind Pharm, 2007, 33(8): 888-889.
  • 7CHOKSHI R, SANDHU H, IYER R, et al. Characterization of physico-mechanical properties of indomethacin and polymers to assess their suitability for hot-melt extrusion process as a means to manufacture solid dispersion/solution [J]. Pharm Sci, 2005, 94(11): 2463-2470.
  • 8XU S, DAI W G. Drug precipitation inhibitors in supersaturable formulations [J]. Int J Pharm, 2013, 453(1): 36-43.
  • 9ILEVBARE G A, LIU H, EDGAR K J, et al. Maintaining supersaturation inaqueous drug solutions: impact of different polymers on induction times [J]. Cryst Growth Des, 2013, 13(2): 740-751.
  • 10孙志明,李小娜,陈苹苹,徐海燕,周洁.山茱萸总苷分散片的处方工艺研究[J].中国药房,2011,22(3):219-221. 被引量:5

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