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影响聚酯微球中药物释放的因素 被引量:1

Factors affecting the drug release of PLA and PLGA microspheres
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摘要 聚酯材料因其原料易得、容易加工、生物相容性好、具有可生物降解性等优点,已经成为当今药物载体材料中的一大研究热点。现综合国内外的有关报道对可生物降解聚酯材料作为药物载体制备微球制剂的研究进展进行了综述。针对目前限制聚酯材料微球制剂临床应用存在的问题,从聚合物、药物、制备工艺、附加剂、辐射灭菌5个方面对影响聚乳酸(PLA)和聚乳酸乙醇酸共聚物(PLGA)缓释微球中药物释放的因素进行了重点介绍,为研究聚酯微球中药物的释放提供思路。 The research of polyester materials has become a hot spot in modern pharmaceutics, because of their availability, easy to processing, fine biocompatibility and biodegradability. The researches of preparation and drug release characteristics of poly lactate acid (PLA) and poly lactate glycollic acid(PLGA) microspheres for the drug delivery system are summarized. It focuses on the recent developments in resolving the existent problems of clinic, such as controlled release and initial burst release. This review presents advances of factors influencing the microspheres drug release in polymer,drug, preparation, supplemental agent and radiation sterilization, which may have significant implications for the research on the microspheres drug release.
作者 杨阳 高永良
出处 《中国新药杂志》 CAS CSCD 北大核心 2007年第18期1458-1463,共6页 Chinese Journal of New Drugs
关键词 微球 突释 控释 聚乳酸 聚乳酸乙醇酸共聚物 microspheres initial burst release controlled release poly lactate acid (PLA) poly lactate glycollic acid(PLGA)
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参考文献37

  • 1LANGER R.Biomaterials in drug delivery and tissue engineering:one laboratory's experience[J].Acc Chem Res,2000,33 (2):94-101.
  • 2FREITAS S,MERKLE HP,GANDER B.Microencapsulation by solvent extraction/evaporation:reviewing the state of the art of microsphere preparation process technology[J].J Control Release,2005,102(2):313-332.
  • 3赵锋,高永良.聚乳酸微球生物降解机制和生物相容性研究进展[J].中国新药杂志,2002,11(1):67-71. 被引量:19
  • 4YANG YY,CHUNG TS,NG NP.Morphology,drug distribution,and in vitro release profiles of biodegradable polymeric microspheres containing protein fabricated by double-emulsion solvent extraction/evaporation method[J].Biomaterials,2001,22(3):231-241.
  • 5SHENDEROVA A,BURKE TG,SCHWENDEMAN SP.Stabilization of 10-hydroxycampthecin in poly (lactide-coglycolide) microsphere delivery vechicles[J].Pharm Res,1997,14 (10):1406-1418.
  • 6TAKENAGA M,YAMAGUCHI Y,KITAGAWA A,et al.A novel sustained-release formulation of insulin with dramatic reduction in initial rapid release[J].J Control Release,2002,79 (1/3):81-91.
  • 7HOMAYOUN P,MANDAL T,LANDR YD,et al.Control release of anti-cocaine catalytic antibody from biodegradable polymer microspheres[J].J Pharm Pharmacol,2003,55 (7):933-938.
  • 8RAHMAN NA,MATHIOWITZ E.Localization of bovine serum albumin in double-walled microspheres[J].J Control Release,2004,94 (1):163-175.
  • 9LEE TH,WANG JJ,WANG CH.Double-walled microspheres for the sustained release of a highly water-soluble drug:characterization and irradiation studies[J].J Control Release,2002,83(3):437-452.
  • 10FU YJ,SHY SS,FU HS,et al.Development of biodegradable copoly(-lactic/glycolic acid) microspheres for the controlled release of 5-FU by the spray drying method[J] Colloids Surf B Biointerfaces,2002,25 (4):269-279.

二级参考文献55

  • 1[1]Anderson JM.Perspectives on the in vivo responses of biodegradable polymers[A].In:Biomedical applications of synthetic biodegradable polymers[M].Boca Raton:CRC Press,FL,1995.223-233.
  • 2[2]Okada H,Toguchi H.Biodegradable microspheres in drug delivery[J].Crit Rev Therap,1995,12∶1-99.
  • 3[3]Li S,Vert M.Biodegradation of aliphatic polyesters[A],In:Scott G,Gilead D eds.Degradable Polymers[M].London:Chapman and Hall.1995.43-87.
  • 4[4]Schakenraad JM,Hardon MJ,Feijen J,et al.Enzymatic activity toward poly(L-Lactic acid)implants[J].J Biomed Mater Res,1990,24∶529-545.
  • 5[5]Bodmeier R,Chen H.Effect of the addition of low molecular weight poly(dl-lactide)on drug release from biodegradable poly(dl-lactide) drug delivery system[J].Int J Pharm,1989,51∶1-8.
  • 6[6]Vert M,Mauduit J,Li S.Biodegradation of PLA/GA polymers: increasing complexity[J].Biomaterials,1994,15∶1209-1213.
  • 7[7]Grizzi I,Garreau H,Li S,et al.Hydrolytic degradation of devices based on poly(DL-lactic acid) size-dependence[J].Biomaterials,1995,16∶305-311.
  • 8[8]Spenlehauer G,Vert M,Benoit JP,et al.In vitro and in vivo degradation of poly(DL-lactide/glycolide) type microspheres made by solvent evaporation method[J].Biomaterials,1989,10∶557-563.
  • 9[9]Beck LR,Cowsar DR,Lewis DH.Systemic and local delivery of contraceptive steroids using biodegradable microspheres[A].In:Hafez ESE, WAA Van Os eds.Biodegradables and delivery systems for contraception[M].MTP Press Limited,1980. 63-82.
  • 10[10]Tice TR,Lewis DH,Dunn RL,et al.Biodegradation of microspheres and biomedical devices prepared with resorbable polyesters[A].In:9th international symposium on controlled release of bioactive materials[C].The Controlled Release Society,Inc,1982.21-25.

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