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In order to create a functionalized biodegradable polymer for vascular tissue engineering application,poly(DL- lactide-co-RS-β-malic acid)(PDLLMAc)was synthesized.PDLLMAc was obtained after hydrogenolysis of poly(DL- lactide-co-RS-β-benzyl malolactonate)(PDLLMA),which was from the ring-opening polymerization of DL-lactide(DLLA) and RS-β-benzyl malolactonate(MA)using stannous octoate as catalyst.The copolymers were characterized by ~1H-NMR, FTIR,GPC and DSC.The tensile strength and water uptake of the cop... 相似文献
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Several new monomers, β-(acetylsalicylyloxy)ethyl methacrylate, β-(acetylsalicylyloxy)propyl methacrylate, β-(acetylsalicylyloxy)ethyl acrylate, β-hydroxy-Υ-(acetylsalicylyloxy)propyl methacrylate, β-hydroxy-Υ-(acetylsalicylyloxy)propyl acrylate have been synthesized from aspirin with corresponding hydroxyalkyl or glycidyl acrylates, and then polymerized by free radical initiator. 相似文献
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胶束电动毛细管色谱法分离左旋十八甲基炔诺酮、睾酮和孕酮 总被引:4,自引:0,他引:4
胶束电动毛细管色谱法(MECC)被用于左施十八甲基炔诺酮(LNC)、睾酮(T)和孕酮(P)的分离。电泳缓冲液中含一定量的乙腈或甲醇等有机添加剂时,可以改善分离。当乙睛体积分数为0~15%时,样品的迁移时间tm随着乙腈体积分数的增加而增加,但当已腈体积分数大于15%时,样品的tm随乙腈体积分数的增加反而减少。如采用20mmol/L的2,6-二甲基-β-环糊精(DM-β-CD)作添加剂,不仅可提高分高度,而且能缩短分析时间,实现最佳分离。 相似文献
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以3-氯代丙二醇为起始原料,通过3-苄氧基甘油酸(3-O-BGA)为中间体,首次合成了作为一种新型聚羟基酸前体的,具有苄氧保护基的六元环状二交酯—3-苄氧次甲基-1,4-二氧六环-2,5-二酮(3-BMG)。该单体具有通常交酯的聚合特性,很容易以辛酸亚锡为催化剂,在140℃下开环聚合得到高分子量的聚合物。在双金属(Al/Zn)烷氧化合物引发体系下也能够进行开环聚合。所得聚合物在Pd/C催化下氢解,可以定量地去除苄基保护基,从而得到侧链带有羟基的新型功能性可生物降解聚酯。DSC实验结果显示脱保护的聚合物的玻璃化转化温度下降,并在120℃附近出现熔点。通过吸水率与动态接触角的测定,脱保护后聚合物的亲水性显著提高,明显高于传统的聚酯。 相似文献
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l-(Acetylsalicylyl)-benzotriazole, a new active amide of acetylsalicylic acid has been synthesized either from acetylsalicylic acid and benzotriazole using DCCI as condensation agent or via acetylsalicylyl chloride and benzotriazole in the presence of triethylamine. The obtained active amide reacted readily with the hydroxyl group of PVA to produce the acetylsalicylyl ester of PVA. 相似文献
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An anti-tumor drug doxorubicin was encapsulated in micelles of poly(ethylene glycol)-b-poly(2,2-dihydroxyl-methyl propylene carbonate)(PEG-b-PDHPC) diblock copolymers.The morphology of both blank micelles and drug loaded micelles was characterized by TEM.The in vitro drug release profiles of micelles were investigated.The cytotoxicity of the micelles was evaluated by incubating with Hela tumor cells and 3T3 fibroblasts.The drug loaded micelles were co-cultured with HepG2 cells to evaluate the in vitro anti-tumor efficacies.The results showed that the mean sizes of both micelles with different copolymer compositions increased after being loaded with drugs.The drug release rate of PEG45-b-PDHPC34 micelles was faster than that of mPEG114-b-PDHPC26,micelles.Both of the two block copolymers were non-toxic.The confocal laser scanning microscopy and flow cytometry results showed that both the drug loaded micelles could be internalized efficiently in HepG2 cells.The PEG45-b-PDHPC34 micelles exhibited higher anti-tumor activity comparing to mPEG114-b-PDHPC26 micelles. 相似文献
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