引用本文:
林友文, 黄尊行, 罗红斌. N-(4-羟基-3-甲氧基苯甲基)壳聚糖的制备及其水凝胶的pH敏感性[J]. 应用化学,
2006, 23(7): 770-775.
Citation: LIN You-Wen, HUANG Zun-Xin, LUO Hong-Bing. Synthesis and Characterization of N-(4-Hydroxy-3mehtoxybenzyl) chitosan and pH Sensitivity of Its Hydrogel[J]. Chinese Journal of Applied Chemistry, 2006, 23(7): 770-775.

Citation: LIN You-Wen, HUANG Zun-Xin, LUO Hong-Bing. Synthesis and Characterization of N-(4-Hydroxy-3mehtoxybenzyl) chitosan and pH Sensitivity of Its Hydrogel[J]. Chinese Journal of Applied Chemistry, 2006, 23(7): 770-775.

N-(4-羟基-3-甲氧基苯甲基)壳聚糖的制备及其水凝胶的pH敏感性
摘要:
通过香草醛与壳聚糖反应合成席夫碱,用NaBH4还原后得到水溶性的N-(4-羟基-3-甲氧基苯甲基)壳聚糖(VCS),经IR、1H NMR和UV对产物进行结构表征。胶体滴定法测定N上4-羟基-3-甲氧基苯甲基的取代度为2.37 mmol/g。利用戊二醛交联制备N-(4-羟基-3-甲氧基苯甲基)壳聚糖水凝胶(VCSG),考察在不同pH缓冲溶液中的凝胶溶胀行为以及载药凝胶的体外释药行为。实验结果表明,不同交联度的VCSG在pH值在1.2~7.4之间随着pH值增大凝胶溶胀度逐渐减小,而在碱性介质中(pH值为9.0~11.0)随着pH值增大时溶胀度又有逐渐增大的趋势。低交联度的VCSG在pH=1.2缓冲液中的溶胀度显著大于在其它pH缓冲液中的溶胀度;交联度大的VCSG溶胀度小,且在不同pH缓冲液中溶胀度差异不大。以法莫替丁为模型药物,载药凝胶在pH为5.0~7.4缓冲溶液中的释药速度明显比在pH为1.0~3.0中的慢,具有更明显的缓释作用,显示VCSG具有pH敏感性。
English
Synthesis and Characterization of N-(4-Hydroxy-3mehtoxybenzyl) chitosan and pH Sensitivity of Its Hydrogel
Abstract:
By the reaction of chitosan with vanillin,Schiff's base was firstly obtained,followed by the eaction of NaBH4 with Schiff's base to yield water-soluble N-(4-hydroxy-3-mehtoxybenzyl) chitosan (VCS).The chemical structure of the modified chitosan VCS was characterized by FTIR,1H NMR and UV spectroscopies.Degree of substitution of N-4-hydroxy-3-mehtoxybenzyl determined with colloid titration was 2.37 mmol/g.The swelling characteristics of hydrogels(VCSG) prepared by cross-linking of glutaraldehyde with VCS were studied.The results showed that the swelling ratio(SR) of VCSG was decreased with the increasing of the dosage of glutaraldehyde.The swelling ratios of VCSG with different cross-linking degrees were decreased with the increasing of the pH value of the buffer solution between 1.2 to 7.4.The swelling ratios of VCSG were increased with the increasing of the pH value of the buffer solution between 9.0 to 11.0.The VCSG with a lower cross-linking degree swelled more significantly in a pH=1.2 buffer solution than in other medium,the VCSG with a high cross-linking degree swelled similarly and lower SR in buffer solution with different pH values.VCSG showed pH-sensitive in buffer solutions.The release behavior of famotidine entrapped in the hydrogel showed different speeds with the change of the pH value of medium in vitro.The release speeds of famotidine in VCSG in the media of pH=1.2 and 3.0 were much faster than those in the media of pH=5.0 and 7.4,both showed slow release effect.VCSG is pH sensitive and the swelling behavior of VCSG can be regulated by changing the dosage of the cross-linking agent,and has the potential as being the carrier for controlling drug release.
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Key words:
- chitosan
- / modification
- / pH-sensitivity
- / hydrogel
- / swelling ratio
- / drug release
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