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紫外分光光度法测定塞曲司特片的溶出度

Dissolution determination of Seratrodast Tablets by UV spectrophotography
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摘要 目的 建立紫外分光光度法测定塞曲司特片的溶出度。方法 于400~200nm波长处扫描,确定塞曲司特在266nm处有最大吸收。结果 塞曲司特浓度与吸光度值A呈良好的线性关系,线性范围4-20μg·mL^-1(r=0.9994),平均回收率为100.2%,RSD为0.45%(n=3)。结论 该方法测定塞曲司特片溶出度,结果准确,重现性好。 OBJECTIVE To establish an UV spectrophotography method for dissolution determination of Seratrodast tablets. METHODS To scan in the wavelength range of 400-200nm,and make sure Seratrodast had the largest absorption at wave length of 266nm. RESULTS The absorption was linear in the concentration range of 4-20μg·mL^-1 ( r =0. 9994). The average recovery was 99. 9%, RSD = 0. 45% ( n = 3). CONCLUSION The method was good,accurate and reproducible.
出处 《齐鲁药事》 2008年第1期25-26,共2页 qilu pharmaceutical affairs
关键词 塞曲司特片 溶出度 紫外分光光度法 Seratrodast Tablets dissolution UV spectrophotography
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参考文献4

  • 1《中国药典》2005年版(二部).北京:化学工业出版社,2005:附录23.
  • 2胡雪莲,黄华,李英博.口腔崩解片的研究进展[J].中国医院药学杂志,2005,25(2):167-169. 被引量:27
  • 3ANON K.AA-2414.Drugs Future,1990,15(8):783-785.
  • 4Shiraishi M,Kato K,Temo s,et al.Quinones.4 novel eicosanoid antagonists:synthesis and pharmacyological evaluation.J Med Chem,1989,32(9):2214-2221.

二级参考文献10

  • 1Loder E, Brandes JL, Siberstein S, et al. Preference comparison of rizatriptan ODT 10-mg and suma tr-iptan 50-mg tablet in migraine[J]. Headache, 2001,41 (8):745.
  • 2Sumiya K, Baba Y, lnomata S,et al. Preparation and clinical evaluation orally disintegrating clonidine hydrochloride tablets for preanesthetic medication[J]. Yakugaku Zasshi Journal of the Pharmaceutical Society of Japan,2000,1211(7): 652 .
  • 3Chue P,Jones B,Taylor CC,et al. Dissolution profile, tolerability,and acceptability of the orally disintegrating olanzapine tablet in patients with schizophrenia[J]. Can J Psychiatry, 2002, 47 (8) :771.
  • 4Dilip JG,Ann Arbor,Mich. Fast dissolving solid dosage form comprising a porous network of matrixmaterial[P]. US5,558,8801996.
  • 5Allen L,Wang BN,Davies JD. Rapidly dissolving oral dosage form[P]. World Intellectual Property Organization:9520377,1995,08-03.
  • 6Ishikawa T, Mukai B,Shiraishi S,et al. Preparation of rapidly disintegrating tablet using new types of microcrys-talline cellulose(pH-M Series) and low substituted-hydrixyproxypropylcellulose or spherical sugar granules by direct compression method[J].Chem Pharm Bull, 2001,49(2) : 134.
  • 7Ishikawa T,Watanabe Y. Preparation and evaluation of tablets rapidly disintegrating in saliva containing bitter-taste-masked granules by the compressionmethod[J]. Chem Pharm Bull, 1999, 47 (10):1451.
  • 8金一,大熊英树,汪成发,夏目秀视,杉林坚次,森本雍宪.尼可地尔口腔速溶片的研究(英文)[J].药学学报,2001,36(7):535-538. 被引量:19
  • 9施震,尹银嘉,张先洲.小剂量阿司匹林口腔崩解片的制备[J].中国医药工业杂志,2003,34(7):336-337. 被引量:13
  • 10叶兵,刘忠荣,及元乔,鲍锐.银杏叶口腔崩解片的研制及质量评价[J].天然产物研究与开发,2003,15(4):326-329. 被引量:37

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