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用于溃疡性结肠炎靶向药物递送的热响应性甲基纤维素/透明质酸-美沙拉嗪水凝胶

Thermo-responsive methylcellulose/hyaluronic acid-mesalamine hydrogel in targeted drug delivery for ulcerative colitis.

作者信息

Kuo Sheng-Nan, Wu Pei-Xhan, Huang Shu-Ling, Hsu Yu-Ci, Huang Jen-Huang

机构信息

Department of Chemical Engineering, National Tsing Hua University Hsinchu 30013 Taiwan

Department of Chemical Engineering, National United University Miaoli 36003 Taiwan

出版信息

RSC Adv. 2025 May 1;15(18):14126-14135. doi: 10.1039/d5ra00216h. eCollection 2025 Apr 28.

Abstract

Current treatments for ulcerative colitis (UC), including mesalamine (Me) enemas, face limitations such as poor colonic retention, systemic side effects, and suboptimal patient compliance. To address these challenges, this study developed a thermo-responsive hydrogel combining hyaluronic acid-mesalamine (HA-Me) conjugates with methylcellulose (MC), providing a targeted and sustained drug delivery platform for UC treatment. HA-Me conjugates were synthesized a nucleophilic addition-elimination reaction, with FT-IR and H-NMR confirming successful conjugation and a grafting ratio of 12.45%. Rheological analysis revealed a lower critical solution temperature (LCST) of 36.7-37.7 °C, ensuring gelation at body temperature when the MC concentration was 5-7 wt%. The optimized hydrogel exhibits intestinal retention properties, thereby improving drug bioavailability. The results confirmed that this hydrogel not only improved drug release time but also provided a protective barrier for inflamed wounds, facilitating wound healing, reducing the risk of reinfection, and improving medical compliance. Its mucoadhesive properties further supported effective drug delivery and localized therapeutic effects. This study highlights the potential of the MC/HA-Me hydrogel as a platform for overcoming the limitations of conventional UC treatments, offering opportunities for tailored therapeutic applications and future clinical development.

摘要

目前治疗溃疡性结肠炎(UC)的方法,包括美沙拉嗪(Me)灌肠剂,存在诸如结肠滞留性差、全身副作用以及患者依从性欠佳等局限性。为应对这些挑战,本研究开发了一种热响应水凝胶,它将透明质酸-美沙拉嗪(HA-Me)偶联物与甲基纤维素(MC)相结合,为UC治疗提供了一个靶向且持续的药物递送平台。通过亲核加成-消除反应合成了HA-Me偶联物,傅里叶变换红外光谱(FT-IR)和氢核磁共振(H-NMR)证实了偶联成功且接枝率为12.45%。流变学分析表明其低临界溶液温度(LCST)为36.7 - 37.7°C,当MC浓度为5 - 7 wt%时可确保在体温下凝胶化。优化后的水凝胶具有肠道滞留特性,从而提高了药物生物利用度。结果证实,这种水凝胶不仅延长了药物释放时间,还为炎症伤口提供了保护屏障,促进伤口愈合,降低再次感染的风险,并提高了医疗依从性。其粘膜粘附特性进一步支持了有效的药物递送和局部治疗效果。本研究突出了MC/HA-Me水凝胶作为克服传统UC治疗局限性的平台的潜力,为定制治疗应用和未来临床开发提供了机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4528/12044526/f305d2f1de0f/d5ra00216h-s1.jpg

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