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基于黄原胶和壳聚糖在液体中再凝胶化的新型原位形成水凝胶,用于局部药物递送。

Novel in situ forming hydrogel based on xanthan and chitosan re-gelifying in liquids for local drug delivery.

机构信息

Department of Surgery, Jinling Hospital, Nanjing, China; Medical School of Southeast University, Nanjing, China.

Department of Surgery, Jinling Hospital, Nanjing, China; Medical School of Nanjing University, Nanjing, China.

出版信息

Carbohydr Polym. 2018 Apr 15;186:54-63. doi: 10.1016/j.carbpol.2018.01.025. Epub 2018 Jan 10.

Abstract

Injectable hydrogels have been an attractive topic in biomaterials. However, during gelation in vivo, they are easy to disperse due to tissue exudates, thus leading to failure of controlled drug release. To solve this problem, we present a novel polysaccharide-based injectable hydrogel via self-crosslinking of aldehyde-modified xanthan (Xan-CHO) and carboxymethyl-modified chitosan (NOCC). The physical properties were optimized by adjusting the mass ratio of Xan-CHO and NOCC. Experiments revealed that this material exhibited the characteristics of self-healing, anti-enzymatic hydrolysis, biocompatibility and biodegradability. The releasing curve demonstrated stable release of BSA-FITC within 10 h after injection in liquids. After incorporation with a vascular endothelial growth factor, there was an interaction between this biomaterial and the host, which accelerated the reconstruction of the abdominal wall in rats. Therefore, this injectable hydrogel, as a drug delivery system, can prevent drug outburst in a variety of settings and function as a tissue scaffold.

摘要

可注射水凝胶一直是生物材料领域的一个热门话题。然而,在体内凝胶化过程中,由于组织渗出物的存在,它们很容易分散,从而导致药物控制释放失败。为了解决这个问题,我们通过醛基修饰的黄原胶(Xan-CHO)和羧甲基修饰的壳聚糖(NOCC)的自交联,提出了一种新型的基于多糖的可注射水凝胶。通过调整 Xan-CHO 和 NOCC 的质量比来优化其物理性能。实验表明,该材料具有自修复、抗酶解、生物相容性和可生物降解性等特点。在液体中注射后 10 小时内,BSA-FITC 呈现出稳定的释放曲线。加入血管内皮生长因子后,这种生物材料与宿主之间发生相互作用,加速了大鼠腹壁的重建。因此,这种可注射水凝胶作为药物传递系统,可以防止药物在多种情况下爆发,并作为组织支架发挥作用。

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