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缓慢降解的透明质酸水凝胶,用阳离子化石墨烯纳米片增强。

Slow degrading hyaluronic acid hydrogel reinforced with cationized graphene nanosheets.

机构信息

Uka Tarsadia University, Maliba Pharmacy College, Gopal-Vidyanagar Campus, Surat 394350, India.

Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400085, Maharashtra, India.

出版信息

Int J Biol Macromol. 2019 Dec 1;141:232-239. doi: 10.1016/j.ijbiomac.2019.08.243. Epub 2019 Aug 30.

Abstract

Graphene possesses a large surface area and offers high loading capacity for aromatic compounds. However, the load is quickly released in the absence of rate limiting diffusion barrier. In this study, we have explored the electrostatic interaction between polyanionic hyaluronic acid (HA) and cationized reduced graphene oxide (rGO) as a means to develop a reinforced hydrogel matrix. We tested if; (i) degradation kinetics of HA matrix can be modulated in the presence of cationized nanosheets, and (ii) reinforced hydrogel can offer controlled release of paclitaxel (PLX) stacked over the sheets. Successful synthesis, cationization and drug loading on graphene sheets were demonstrated using Raman and FT-IR spectroscopy. Reinforcement was confirmed through electron microscopy, neutron scattering and texture profile analyses. While incorporation of sheets enhanced the resistance of HA hydrogel against enzymatic digestion, a significant improvement in the biocompatibility of cationized rGO was obtained through this association. Reinforced gel offered sustained release of PLX up to 104 h which can further be extended by tuning its architecture.

摘要

石墨烯具有较大的表面积,可为芳香族化合物提供高负载容量。然而,在不存在限速扩散障碍的情况下,负载会迅速释放。在这项研究中,我们探索了聚阴离子透明质酸(HA)与阳离子化还原氧化石墨烯(rGO)之间的静电相互作用,以开发增强的水凝胶基质。我们测试了:(i)在存在纳米片的情况下,HA 基质的降解动力学是否可以被调节,以及(ii)增强的水凝胶是否可以提供堆积在纳米片上的紫杉醇(PLX)的控制释放。使用拉曼和傅里叶变换红外光谱成功地证明了石墨烯片上的合成、阳离子化和药物负载。通过电子显微镜、中子散射和纹理轮廓分析证实了增强作用。虽然纳米片的掺入增强了 HA 水凝胶对酶消化的抵抗力,但通过这种结合,显著提高了阳离子化 rGO 的生物相容性。增强的凝胶可实现 PLX 的持续释放,长达 104 小时,通过调整其结构可以进一步延长。

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