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mPEG-PLGA-mPEG系列纳米粒的毒性与其结构的关系 被引量:5

Preliminary investigation on the cytotoxicity-composition relationship of serials of novel mPEG-PLGA-mPEG nanoparticles
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摘要 目的研究丙交酯/乙交酯/聚乙二醇(LA/GA/PEG)共聚物(mPEG-PLGA-mPEG)系列材料所制备的空白纳米粒的细胞毒性,并考察毒性与材料结构的关系。方法采用MTT法测定与空白纳米粒培养48 h后的正常人肝细胞Chang的细胞存活率,采用Origin软件分析mPEG-PLGA-mPEG材料中的PEG分子量,并考察PEG的含量和LA/GA比例对毒性的交互作用。结果PEG的分子量和含量对纳米粒的毒性影响较明显,LA/GA比例对其影响较小。结论控制合成mPEG-PLGA-mPEG的材料中所使用PEG的分子量和含量,可降低mPEG-PLGA-mPEG所制备纳米粒的毒性。 OBJECTIVE To investigate the cytotoxicity and compositon - cytotoxicity relationship of serials of novel monomethoxy ( polyethylene glycol) - poly ( d, 1 - lactic - co - glycolic acid ) - monomethoxy ( polyethylene glycol) ( mPEG - PLGA - mPEG) blank nanoparticles. METHODS MTT assay was adopted to measure the relative growth rate (RGR) of Chang liver cells after incubation with blank nanoparticles for 48 hours. And the Origin software was applied to analyze the relationships between cytotoxicity and PEG molecular weight as well as PEG content and LA/GA ratio. RESULTS The molecular weight and content of PEG had remarkable in- fluence on the cytotoxicity of nanoparticles, while the LA/GA ratio had little influence on it. CONCLUSION By controlling the PEG molecular weight and content in the synthesis of mPEG - PLGA - mPEG, the cytotoxicity of blank nanoparticles would be reduced. And by this means the innoxious and safe nanoparticle materials for injection would be developed.
出处 《华西药学杂志》 CAS CSCD 北大核心 2009年第3期211-214,共4页 West China Journal of Pharmaceutical Sciences
基金 国家自然基金重点项目(批准号:30430770)
关键词 纳米粒 丙交酯/乙交酯/聚乙二醇共聚物 细胞毒性 Nanoparticles mPEG - PLGA - mPEG Cytotoxicity
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参考文献8

  • 1Soppimath KS,Aminabhavi TM,Kulkami AR,et al.Biodegradable polymeric nanoparticles as drug delivery devices[J].J Control Rel,2001,70:1-20.
  • 2Yamaguchi K,Anderson JM.In vivo biocompatibility studies of medisorb(R) 65/35 D,L-Iactide/glycolide copolymer microspheres[J].J Control Rel,1993,24:81-93.
  • 3Duan Y,Nie Y,Gong T,et al.Evaluation of blood compatibility of MeO-PEG-poly(D,Llactic-co-glycolic acid)-PEG-OMe tribloek copolymer[J].J Appl Polym Sci,2006,100:1019-1023.
  • 4段友容,张志荣,唐永刚,林芸竹.mPEG-PLGA-mPEG纳米粒的体外降解规律的研究[J].生物医学工程学杂志,2004,21(6):921-925. 被引量:11
  • 5Xu X,Fu Y,Hu H,et al.Quantitative determination of insulin entrapment efficiency in triblockcopolymeric nanoparticles by high-performance liquid chromatography[J].J Pharm Biomed Anal,2006,41:266-273.
  • 6Manceur A,Chellat F,Merhi Y,et al.In vitro cytotoxicity evaluation of a 50.8% NiTi single crystal[J].J Biomed Mater Rea Part A,2003,67:641-646.
  • 7王衍堂,李宏霞,张建军,王金勇,王莉.乌头碱对乳鼠心肌细胞的毒性作用[J].华西药学杂志,2007,22(1):4-6. 被引量:20
  • 8Avgoustakis K,Beletsi A,Panagi Z,et al.PLGA-mPEG nanoparticles of cisplatin:in vitro nanoparticle degradation,in vitro drug release and in vivo drug residence in blood properties[J].J Control Bel,2002,79:123-135.

二级参考文献14

  • 1孟甄,丁怡,鲁静,赵玉男,张聿梅,陶佳林,程杰,杜力军.生、制乌头总生物碱对心脏功能及其毒性的比较[J].中国药理学通报,2004,20(7):801-804. 被引量:20
  • 2白向阳.川乌的毒性与抗肿瘤作用概述[J].实用中医药杂志,2005,21(2):125-126. 被引量:19
  • 3王朝虹,叶敏,邢俊波,何毅,果德安.高效液相色谱-质谱法测定乌头碱在急性中毒大鼠体内的分布[J].色谱,2005,23(3):316-316. 被引量:8
  • 4Feng B, Chen JY, Zhang XD. Characterization of surface oxide films on titanium and bioactivity. Journal of Materials Science: Materials in Medicine, 2002;13∶457
  • 5Duan YR, Zhang ZR, Huang Y,et al. Preparation of nano-HAP as Vectors for Targeting Delivery System. Key Engineering Materials, 2003(in press)
  • 6Avgoustakis K, Beletsi A, Panagi Z, Klepetsanis P, et al. PLGA-mPEG nanoparticles of cisplatin: in vitro nanoparticle degradation, in vitro drug release and in vivo drug residence in blood properties. J Controlled Release, 2002;79∶123
  • 7Burkersoda F, Gref R, Gopferich A. Erosion of biodegradable block copolymers made of poly(D,L-lactic acid) and poly(ethylene glycol), Biomaterials, 1997; 18∶1599
  • 8Byeongmoon Jeong, You Han Bae, Sung Wan Kim. Biodegrad-able thermosensitive micelles of PEG-PLGA-PEG triblock copolymers. Colloids and Surface B: Biointerfaces, 1999; 16∶185
  • 9Vert M, Mauduit J, Li S. Biodegradation of PLA/GA polymers: increasing complexity. Biomaterials, 1994; 15∶1209
  • 10Spenlehauer G, Vert M, Benoit JP, et al. In vitro and in vivo degradation of poly(D,L-lactide/glycolide) type micro- spheres made by solvent evaporation method. Biomaterials, 1989; 10∶557

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