马霞, 李路遥, 张缅缅, 于海燕. pH敏感γ-聚谷氨酸/聚乙烯醇水凝胶的溶胀动力学[J]. 农业工程学报, 2016, 32(z1): 333-338. DOI: 10.11975/j.issn.1002-6819.2016.z1.046
    引用本文: 马霞, 李路遥, 张缅缅, 于海燕. pH敏感γ-聚谷氨酸/聚乙烯醇水凝胶的溶胀动力学[J]. 农业工程学报, 2016, 32(z1): 333-338. DOI: 10.11975/j.issn.1002-6819.2016.z1.046
    Ma Xia, Li Luyao, Zhang Mianmian, Yu Haiyan. Study on hydrogels of swelling kinetics of pH-sensitive γ-PGA/PVA[J]. Transactions of the Chinese Society of Agricultural Engineering (Transactions of the CSAE), 2016, 32(z1): 333-338. DOI: 10.11975/j.issn.1002-6819.2016.z1.046
    Citation: Ma Xia, Li Luyao, Zhang Mianmian, Yu Haiyan. Study on hydrogels of swelling kinetics of pH-sensitive γ-PGA/PVA[J]. Transactions of the Chinese Society of Agricultural Engineering (Transactions of the CSAE), 2016, 32(z1): 333-338. DOI: 10.11975/j.issn.1002-6819.2016.z1.046

    pH敏感γ-聚谷氨酸/聚乙烯醇水凝胶的溶胀动力学

    Study on hydrogels of swelling kinetics of pH-sensitive γ-PGA/PVA

    • 摘要: 为了获得具有较好的持水性、生物相容性且没有细胞毒性的水凝胶,该文在不经过任何化学处理的条件下,将γ-聚谷氨酸(γ-polyglutamic acid,γ-PGA)与聚乙烯醇(polyvinyl alcohol,PVA)以3∶7,4∶6,5∶5,6∶4,7∶3的质量配比进行反应,制得pH敏感型水凝胶。对制得的水凝胶进行性能和结构表征,研究不同单体配比的水凝胶在不同pH值溶液(pH值分别为4.0,7.4,9.0)中的溶胀动力学,同时对制备的水凝胶进行了药物缓释性能初步研究。结果表明,γ-聚谷氨酸/聚乙烯醇水凝胶具备pH敏感性,溶胀度随着γ-聚谷氨酸量的增加而减小,保水率及热稳定性均随着γ-聚谷氨酸量的增加而升高。溶胀性能研究表明不同pH值的溶液媒介对水凝胶的初始扩散行为没有影响,都属于non-Fickian扩散模式,而且不同水凝胶样品在不同pH值环境中的溶胀速率的变化趋势类似,说明了在γ-PGA/PVA水凝胶的溶胀初期,水分子的扩散速率与网络大分子的松弛速率相当。不同配比的水凝胶在相同pH值环境中,水的扩散系数随着水凝胶的溶胀速率的增大而增大,且溶胀速率值又会随着PVA含量的增加而增大。药物缓释研究显示Gel3/7、Gel4/6、Gel5/5、Gel6/4、Gel7/3的包埋率分别为79.87%、75.75%、74.00%、73.50%和70.25%,说明5组水凝胶样品包埋效果较为理想,pH值的变化对5组水凝胶样品的释放性能的影响是一致的,均在pH值为7.4的缓冲溶液中药物释放较快,在pH值为1.2的缓冲溶液中释放较为平缓,释放周期加长;随着γ-PGA含量的增加,PVA含量的减少,药物的释放速率也随之减小,最终的平衡释药百分数变小,释药周期加长。研究结果为γ-聚谷氨酸/聚乙烯醇水凝胶材料在生物技术、医学以及工业领域的应用提供参考。

       

      Abstract: Abstract: In order to obtain non-cytotoxic hydrogel of superior water holding capacity and biocompatibility, this paper reported about the production of pH-sensitive hydrogels at different gamma poly glutamic acid (γ-glutamic acid, γ-PGA)/polyvinyl alcohol (PVA) mass radios of 3:7, 4:6, 5:5, 6:4 and 7:3 with no use of any chemical reagents. Then the properties and structure of the prepared hydrogels were characterized and the swelling kinetics of the different feed composition in different pH value (pH values of 4.0, 7.4 and 9.0)solutions were studied. The preliminary research on the drug slow-release of the prepared hydrogels were also conducted. The results showed that the γ-PGA/PVA hydrogels have the pH sensitivity and swelling-deswelling properties. With the amount of γ-PGA increasing, the swelling degree would decrease and hydrogels would show higher endurance of heat. Meanwhile, since the hydrogen bonds between γ-PGA and PVA were enhanced, the structure of the hydrogel would become more compact which would hinder the diffusion of water in the hydrogel and lead to the enhancement of its water-retention rate. The kinetic studies showed that the different pH values of solution had no effect on the initial diffusion behavior of the hydrogel which all belong to the non-Fickian diffusion model. It was also proved that different hydrogel samples in different pH values shared the same change trend of swelling rate which indicated that in the initial swelling process of γ-PGA/PVA hydrogel, the diffusion rates of water molecules and the relaxation rate of macromolecules were almost the same which also indicated that hydrogel with different components shared the same swelling kinetics process. In the same pH value environment, the water diffusion coefficient would increase along with the increase of hydrogel swelling rate, the value of characteristic constant would increase with the increasing content of PVA. The drug release study showed that 5 groups of hydrogel samples of drug embedding effect was more ideal and the embedding rates were between 70%-80%. The changes of pH value had consistent effects on the release properties of 5 groups samples. The hydrogel released rapidly in the buffer solution of pH value 7.4 with release rate of about 80%, and the release period of the buffer solution in pH value 1.2 was lengthened with final release rate of about 40%. With the increase of PGA content and the decrease of PVA content, the release rate of the drug decreased along with a lower final equilibrium release percentage and a longer release period. In addition, it was found that the drug embedding rate of the 5 groups of hydrogel samples was higher, and the performance was satisfactory. This may be due to the structure of the hydrogel containing carboxyl group, which belongs to pH sensitive hydrogel and the hydrogel in an acidic medium swelling rate and swelling degree smaller than in alkaline medium. The results provide a reference in the application of biotechnology, medical and industrial.

       

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