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mPEG-PLGA多孔微球的制备及其对降钙素的吸附行为

Preparation of mPEG—PLGA Porous Microspheres and Their Adsorption to Salcatonin
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摘要 以聚乙二醇聚(乳酸乙醇酸)共聚物(mPEG-PLGA)为材料,采用溶剂挥发法与快速膜乳化法制备了尺寸均一的mPEG-PLGA多孔微球,用其吸附降钙素,考察了降钙素浓度、吸附时间、离子浓度、温度及pH值及微球性质对吸附的影响.结果表明,优化的吸附条件为:降钙素浓度1.0 mg/mL,pH 7.4,NaCl浓度0.2 mol/L,14℃下吸附8 h,该条件下,微球吸附量为48.9 mg/g;吸附量与微球比表面积正相关. Relatively uniform size porous methoxy poly(ethylene glycol-L-lactic-co-glycolic acid) (mPEG-PLGA) microspheres were successfully prepared by premix membrane emulsification with solvent evaporate method. The effects of salcatonin concentration, salt concentration, pH value, adsorption temperature and time, and properties of microspheres on the adsorption capacity of salcatonin were investigated. The results showed that the adsorption capacity of porous microspheres reached 48.9 mg/g under the conditions of 1.0 mg/mL salcatonin concentration, pH value 7.4 of phosphate buffer, 0.2 mol/L NaCl concentration, 14 ℃ adsorption temperature and 8 h adsorption time. In addition, the adsorption capacity increased with the increase of specific surface area.
出处 《过程工程学报》 CAS CSCD 北大核心 2013年第5期870-876,共7页 The Chinese Journal of Process Engineering
基金 国家自然科学基金资助项目(编号:51173187 20706053)
关键词 mPEG—PLGA 多孔微球 降钙素 吸附 比表面积 methoxy poly(ethylene glycol-L-lactic-co-glycolic acid) porous microspheres salcatonin adsorption specific surface area
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  • 1赵玉增,白锋,黄文强.聚二乙烯基苯微球的合成及其表征研究[J].高分子学报,2004,14(3):410-414. 被引量:8
  • 2Ehtezazi T, Washington C. Controlled Release of Macromolecules from PLA Microspheres: Using Porous Structure Topology [J]. J. Controlled Release, 2000, 68(3): 361-372.
  • 3Niu X F, Feng Q L, Wang M B. In vitro Degradation and Release Behavior of Porous Poly(lactic acid) Scaffolds Containing Chitosan Microspheres as a Carrier for BMP-2-derived Synthetic Peptide [J]. Polym. Degrad. Stab., 2009, 94(2): 176-182.
  • 4Dai C L, Wang Y J, Hou X. Preparation and Protein Adsorption of Porous Dextran Microspheres [J]. Carbohydr. Polym., 2012, 87(3): 2338-2343.
  • 5Patel B, Gupta V, Ahsan F. PEG-PLGA Based Large Porous Particles for Pulmonary Delivery of a Highly Soluble Drug, Low Molecular Weight Heparin [J]. J. Controlled Release, 2012, 162(2): 310-320.
  • 6李凤红,张宝砚,李颖祎,李华.生物医用功能材料前驱体壳寡糖接枝聚己内酯的制备与表征[J].功能材料,2008,39(9):1511-1514. 被引量:4
  • 7Hou X, Wang X K, Gao B. Preparation and Characterization of Porous Polysucrose Microspheres [J]. Carbohydr. Polym., 2008, 72(2): 248-254.
  • 8Zhang H, Ju X J, Xie R. A Microfluidic Approach Fabricate Monodisperse Hollow or Porous Poly(HEMA-MMA) Microspheres Using Single Emulsions as Templates [J]. J. Colloid Interface Sci., 2009, 336(1): 235-243.
  • 9Du J J, Chen W, Zhang C. Hydrothermal Synthesis of Porous TiO2 Microspheres and Their Photocatalytic Degradation of Gaseous Benzene [J]. Chem. Eng. J., 2011, 170(1): 53-58.
  • 10Wu Y M, Wang Y P, Yu Y Q. Dispersion Polymerization of Acrylamid with 2-Arcylamido-2-methyl-l-propane Sulfonated inAqueous Solution [J]. J. Polym. Sci. A: Polym. Chem., 2006, 102(2): 2379-2385.

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