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PREPARATION AND CHARACTERIZATIONS OF A NOVEL COPOLYMER BASED ON AN EMULSION SOLVENT EVAPORATION METHOD

机译:基于乳液溶剂挥发法的新型共聚物的制备与表征

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A novel copolymer was synthesized by modifying starch-g-polylactic acid (MSt-g-PLA). The results indicated that the starch was efficiently esterified by maleic anhydride (MAH) (mass fractions, w = 2 %) with polyethylene glycol-400 (PEG-400, w = 1 %) as the dispersant. Then MSt-g-PLA was synthesized by employing the modified starch to react with D, L-lactic acid. The copolymer was amphiphilic and its molecular mass and molecular-mass distribution were 4.789 x 10~4 (M_n), 6.921 x 10~4 (M_w) and 1.445, respectively. Subsequently, CTX/MSt-g-PLA microspheres containing the model drug and cefotaxime sodium (CTX) were achieved. The appearance of the microspheres was smooth and regular. Some 90 % of the particle size was under 150.3 μm, and the mean diameter was 99.3 μm. The degradation rates of the microspheres increased with the increase of the pH value of the buffer. With the amphiphilic copolymer MSt-g-PLA as a drug carrier, the microspheres had no burst during the drug release, and had a similar sustainable release to the PLA carrier.
机译:通过改性淀粉-g-聚乳酸(MSt-g-PLA)合成了一种新型共聚物。结果表明,用聚乙二醇-400(PEG-400,w = 1%)作为分散剂,通过马来酸酐(MAH)(质量分数,w = 2%)有效地酯化了淀粉。然后通过使用改性淀粉与D,L-乳酸反应合成MSt-g-PLA。该共聚物是两亲性的,其分子量和分子质量分布分别为4.789×10〜4(M_n),6.921×10〜4(M_w)和1.445。随后,获得了包含模型药物和头孢噻肟钠(CTX)的CTX / MSt-g-PLA微球。微球的外观光滑且规则。 90%的粒径小于150.3μm,平均直径为99.3μm。微球的降解率随着缓冲液pH值的增加而增加。使用两亲共聚物MSt-g-PLA作为药物载体,微球在药物释放过程中不会破裂,并且具有与PLA载体相似的可持续释放。

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