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壳聚糖包覆葛根素脂质体的制备及理化性质考察 被引量:10

Preparation and Characterization of Chitosan Coated Puerarin Liposomes
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摘要 目的:制备壳聚糖包覆葛根素脂质体并对其理化性质进行考察。方法:采用逆相蒸发法制备葛根素脂质体,并用壳聚糖包覆。通过正交设计对制备工艺中影响脂质体包封率的主要因素进行优化;分别对未包覆脂质体和包覆脂质体的粒径分布、微观形态、Zeta电位、包封率进行考察。结果:未包覆和壳聚糖包覆葛根素脂质体均为圆形,包覆前后平均粒径分别为220.7 nm和632.6 nm,Zeta电位分别为-14.44 mV和+35.61 mV,包封率分别为50.6%和51.1%。结论:逆相蒸发法可以制备包封率较高且图整、平滑的葛根素脂质体。葛根素脂质体用壳聚糖包覆后粒径增加,表面电荷由负电荷变为正电荷。 Objective: To prepare chitosan coated puerarin liposomes and investigate their physicochemical properties. Methods: Puerarin liposomes were prepared by reverse phase evaperation technique and then coated with chitosan. Using encapsulation efficiency as index of examination and designing an orthogonal experiment, the optimal formulation of liposomes was determined. The physicochemical properties of uncoatd and chitosan coated puerarin liposomes were investigated, respectively. Results: Uncoatd and chitosan coated puerarin liposomes were spherelike and smooth. The mean particles size of uncoated and coated liposomes were 217.3nm and 632. 6nm, respectively. The Zeta potential were -14. 44mV and + 35. 61mV, respectively. The encapsulating efficency was 50. 6% and 51.1%, respectively. Conclusion: Puerarin liposomes can be prepared by reverse phase evaporation technique successfully. The chitosan coated purarin liposomes ware spherelike and smooth.
机构地区 山东大学药学院
出处 《中药材》 CAS CSCD 北大核心 2007年第1期89-92,共4页 Journal of Chinese Medicinal Materials
关键词 葛根素 脂质体 壳聚糖 Puerarin Liposome Chitosan
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参考文献8

  • 1吴燕红,苏子仁,赖小平,林吉.愈风宁心片中葛根素在Beagle犬体内药动学研究[J].中成药,2006,28(2):215-218. 被引量:12
  • 2Galovic RR,Barisic K,Pavelic Z,et al.High efficiency entrapment of superoxide dismutase into mucoadhesive chitosan-coated liposomes.Eur J Pharm Sci JT,2002,15(5):441-448.
  • 3Schipper NG,Olsson S,Hoogstraate JA,et al.Chitosans as absorption enhancrs for poorly absorbable durgs 2:mechanism of absorption enhancement.Pharm Res JT,1997,14(7):923-929.
  • 4Szoka F,Olason F,Heath T,et al.Preparation of unilamellar liposomes of intermediate size (0.1-0.2 mumol) by a combination of reverse phase evaporation and extrusion through polycarbonate membranes.Biochim BIophys Acta JT,1980,601(3):559-571.
  • 5Janes KA,Calvo P,Alonso MJ.Polysaccharide colloidal particles as delivery systems for macromolecules.Adv Drug Deliv Rev JT,2001,47(1):83-97.
  • 6赵荣生,侯新朴,严宝霞.两性霉素B脂质体的制备及稳定性研究[J].中国医药工业杂志,2001,32(4):160-162. 被引量:22
  • 7Deamer D,Bangham AD.Large volume liposomes by an ether vaporization method.Biochim Biophys Acta JT,1976,443(3):629-634.
  • 8Janes KA,Caivo P.Polysaccharide colloidal particles as delivery systems for macromolecules.Adv Drug Deliv,2001,47:83-87.

二级参考文献14

  • 1吴燕红,苏子仁,赖小平,姚红,林吉.愈风宁心片中葛根素在小鼠体内的药动学和生物利用度研究[J].中药新药与临床药理,2004,15(4):259-261. 被引量:19
  • 2吴燕红,苏子仁,陈建南,林吉,赖小平.从小鼠体内血药浓度时间曲线与组织分布特征评价葛根素的给药途径[J].中药新药与临床药理,2005,16(2):112-115. 被引量:18
  • 3朱秀媛.葛根有效成分的代谢研究Ⅲ:葛根素的代谢及其药代动力学分析[J].药学学报,1979,14:339-341.
  • 4.中国药典一部[S].,1995.630.
  • 5苏成业 朱秀媛 李振华.葛根有效成分的代谢研究Ⅱ—14C—黄豆苷元在大鼠体内的吸收、分布和消除[J].药学学报,1979,14(3):129-133.
  • 6Keung W M,Lazo O,Kunze L,et al.Potentiation of the bioavailability of daidzin by an extract of Radix puerariae[J].Proceedings of the National Academy of Sciences of the United States of America,1996,93(9),4284-4288.
  • 7陆彬,药物新剂型与新技术,1998年,123页
  • 8魏树礼,生物药剂学与药物动力学,1997年,200页
  • 9Lee J W,Antimicrob Agents Chemother,1994年,38卷,4期,713页
  • 10Wang L H,J Chromatogr,1992年,579卷,259页

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