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In vitro degradation of in situ crosslinkable poly(propylene fumarate-co-ethylene glycol)-based macroporous hydrogels

机译:原位可交联聚富马酸丙二醇酯-乙二醇共聚物的大孔水凝胶的体外降解

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The effect of crosslinking density and porosity on the degradation of macroporous hydrogels (MPHs) was evaluated in this study. MPHs were synthesized from aqueous solutions of poly(propylene fumarate-co-ethylene glycol) (P(PF-co-EG)) and poly(ethylene glycol)-diacrylate (PEG-DA) with concurrent free-radical initiation and pore formation reactions involving ammonium persulfate (APS), L-ascorbic acid (AH), and sodium bicarbonate (SB). The crosslinking density was controlled by the ratio of P(PF-co-EG):PEG-DA to obtain molecular weights between crosslinks (M/sub c/) of 1000/spl plusmn/100 and 1880/spl plusmn/320 g/mol. Porosity was controlled by sodium bicarbonate and ascorbic acid concentrations and ranged between 78/spl plusmn/2 and 89/spl plusmn/3%. In vitro degradation was carried out in phosphate buffer saline (PBS) at 37/spl deg/C and a pH of 7.4. MPHs degradation was assessed at 0, 2, 4, 8, and 12-weeks by evaluating the mass loss, volume change, elastic modulus under confined compression, and porosity via /spl mu/CT. Both Mc and porosity had a significant effect on the modulus at the initial time-point. The Mc had the greatest effect on the degradation of these MPHs with percent mass loss up to 62/spl plusmn/8% after 12 weeks.
机译:在这项研究中评估了交联密度和孔隙率对大孔水凝胶(MPHs)降解的影响。 MPH由聚富马酸丙二醇酯-共-乙二醇(P(PF-co-EG))和聚(乙二醇)-二丙烯酸酯(PEG-DA)的水溶液合成,同时发生自由基引发和孔形成反应涉及过硫酸铵(APS),L-抗坏血酸(AH)和碳酸氢钠(SB)。通过P(PF-co-EG):PEG-DA的比例控制交联密度,以得到交联之间的分子量(M / sub c /)为1000 / spl plusmn / 100和1880 / spl plusmn / 320 g /摩尔孔隙率由碳酸氢钠和抗坏血酸浓度控制,范围在78 / spl plusmn / 2和89 / spl plusmn / 3%之间。体外降解是在磷酸盐缓冲盐水(PBS)中以37 / spl deg / C和pH 7.4进行的。通过评估质量损失,体积变化,有限压缩下的弹性模量和通过/ spl mu / CT的孔隙率,在0、2、4、8和12周评估了MPHs的降解。在初始时间点,Mc和孔隙率都对模量有显着影响。 Mc对这些MPH的降解影响最大,12周后质量损失百分数高达62 / spl plusmn / 8%。

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