Das Subhraseema, Subuddhi Usharani
Department of Chemistry, National Institute of Technology Rourkela, Rourkela 769008, India.
Department of Chemistry, National Institute of Technology Rourkela, Rourkela 769008, India.
Int J Biol Macromol. 2015 Aug;79:856-63. doi: 10.1016/j.ijbiomac.2015.06.008. Epub 2015 Jun 7.
pH-Responsive hydrogel systems based on guar gum (GG), poly(acrylic acid) (PAA) and β-cyclodextrin (CD) using a non-toxic crosslinker, tetraethyl orthosilicate for intestinal delivery of dexamethasone (DX) has been reported. Hydrogels of different compositions were synthesized and evaluated for the controlled delivery of DX. The hydrogels exhibited pH-responsive swelling behavior with a maximum swelling around neutral pH. The CD-containing hydrogels deliver the drug at much slower rate in contrast to the ones without CD. Moreover, the drug release rate is found to show a strong dependence on the GG content and the effect of GG is more pronounced in case of the CD containing hydrogels. As the GG content increases, the rate of drug release decreases considerably and the drug release is prolonged. The release studies in the simulated conditions reveal that these hydrogels can be used as delivery vehicles for oral administration of DX targeting the intestine. Cell viability studies reveal the hydrogels to be biocompatible in nature thus validating them as good drug delivery systems.
据报道,基于瓜尔胶(GG)、聚丙烯酸(PAA)和β-环糊精(CD),使用无毒交联剂原硅酸四乙酯构建的pH响应水凝胶系统,用于地塞米松(DX)的肠道递送。合成了不同组成的水凝胶,并对DX的控释性能进行了评估。水凝胶表现出pH响应性溶胀行为,在接近中性pH时溶胀最大。与不含CD的水凝胶相比,含CD的水凝胶释放药物的速度要慢得多。此外,发现药物释放速率强烈依赖于GG含量,并且在含CD的水凝胶中GG的作用更为明显。随着GG含量的增加,药物释放速率显著降低,药物释放时间延长。模拟条件下的释放研究表明,这些水凝胶可用作靶向肠道口服给药DX的载体。细胞活力研究表明水凝胶在本质上具有生物相容性,从而验证它们是良好的药物递送系统。