期刊文献+

依托泊苷长循环亚微乳的制备和理化性质研究 被引量:6

Preparation and physico-chemical properties of etoposide long circulating submicroemulsion
原文传递
导出
摘要 目的制备依托泊苷长循环亚微乳,并对其进行理化性质研究。方法在依托泊苷亚微乳处方的基础上,通过考察乳粒表面固有水化层厚度与聚乙二醇2000-二硬脂酰磷脂酰乙醇胺(PEG2000-DSPE)用量的关系,确定PEG2000-DSPE用量,从而确定了依托泊苷长循环亚微乳的处方和制备工艺,并进行了理化性质研究。结果依托泊苷长循环亚微乳的浓度为0.8mg/mL,平均粒径为(185.4±5.7)nm,Zeta电位为(?51.6±0.8)mV,药物包封率为97.52%。结论得到了包封率在95%以上的依托泊苷浓度为0.8mg/mL的依托泊苷长循环亚微乳的处方和制备工艺。 Objective To prepare etoposide long circulating submicroemulsion(ELCSE) and to study its physico-chemical properties.Methods Based on the formulation of etoposide submicroemulsion,the quantity of PEG 2000-DSPE was decided by studying the relationship between the fixed aqueous layer thickness(FALT) of emulsion drop surface and the quantity of PEG 2000-DSPE.Then the ELCSE formulation and the preparing technique were decided,and the physico-chemical properties were studied.Results The concentration of etoposide was 0.8 mg/mL.The mean particle size,Zeta potential,and encapsulation efficiency of ELCSE were(185.4 ± 5.7) nm,(?51.6 ± 0.8) mV,and 97.52%,respectively.Conclusion The ELCSE formulation and preparing technique with etoposide concentration of 0.8 mg/mL and encapsulation efficiency over 95% are obtained.
出处 《现代药物与临床》 CAS 2013年第2期164-169,共6页 Drugs & Clinic
基金 国家重点基础研究发展计划(973计划)资助项目(2010CB735602 2012CB724002)
关键词 依托泊苷长循环亚微乳 依托泊苷 长循环亚微乳 聚乙二醇2000-二硬脂酰磷脂酰乙醇胺(PEG2000-DSPE) etoposide long circulating submicroemulsion etoposide long circulating submicroemulsion PEG 2000-DSPE
  • 相关文献

参考文献4

  • 1Sinkule J A. Etoposide: a semisynthetic epipodophyllotoxin. chemistry, pharmacology, pharmacokinetics, adverse effects and use as an antineoplastic agent [J]. Pharmacotherapy, 1984, 4(2): 61-73.
  • 2Lundberg B B, Mortimer B C, Redgrave T (2 Submicron lipid emulsion containing amphipathic polyethylene.glycol for as drug-carriers with prolonged circulation time [J]. lnt J Pharm, 1996, 134(1/2): 119-127.
  • 3Shimada K, Miyagishima A, Sadzuka Y, et al. Determination of the thickness of the fixed aqueous layer around polyethyleneglycol-coated liposomes [J]. J Drug Target, 1995, 3(4): 283-289.
  • 4Venkateswarlu V, Manjunath K. Preparation, characterization and in vitro release kinetics of clozapine solid lipid nanoparticles [J]. J Control Release, 2004, 95(3): 627-638.

同被引文献54

  • 1路虹,王建东,孔为民.多西他赛作为一线用药治疗卵巢癌研究进展[J].肿瘤防治杂志,2005,12(15):1194-1196. 被引量:21
  • 2夏修龙.灯盏花的研究与临床应用[J].九江学院学报(自然科学版),2006,21(3):86-89. 被引量:4
  • 3尹东东,王杏林,赵广荣,李萌.依托泊苷微乳的HPLC测定[J].中国医药工业杂志,2007,38(2):121-122. 被引量:16
  • 4van de Waterbeemd H,Lennernas H, Artursson P.药物生物利用度[M].何仲贵,钟大放主译.北京:化学工业出版社,2007:81.
  • 5Kogan A, Aserin A, Garti N. Improved solubilization of carbamazepine and structural Transitions in nonionic microemulsions upon aqueous phase dilution [J]. Colloid Interface Sci, 2007, 315(2): 637-647.
  • 6Beijnen J H, Holthuis J J M, Kerkdijk H G, et al. Degradation kinetics of etoposide in aqueous solution[J].Int J Pharm Sci, 1988, 41(1/2): 169-178.
  • 7Smit E F, Camey D N, Harford P, et al. Phase II study of oral etoposide in ederly patients with small cell lung cancer[J].Thorax, 1989, 44(8): 257-263.
  • 8Hande K R. Etoposide: four decades of development of a topoisomerase II inhibitor[J].Eur J Cancer, 1998, 34(10): 1514-1521.
  • 9Sinkule J A. Etoposide: a semisynthetic epipodophyllotoxin. Chemistry, pharmacology, pharmacokinetics, adverse effects and use as an antineoplastic agent[J].Pharmacotherapy, 1984, 4(2): 61-73.
  • 10Shah J C, Chen J R, Chow D. Preformulation study of etoposide: identification of physicochemical characteristics responsible for the low and erratic oral bioavailability of etoposide[J].Pharm Res, 1989, 6(5): 408-412.

引证文献6

二级引证文献26

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部