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用于溃疡性结肠炎治疗的 pH 敏感和结肠靶向 P(LE-IA-MEG)水凝胶微球的体内外研究。

In vitro and in vivo study of pH-sensitive and colon-targeting P(LE-IA-MEG) hydrogel microspheres used for ulcerative colitis therapy.

机构信息

Department of Pharmacy, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.

School of Pharmacy, Xi'an Jiaotong University, Xi'an, Shaanxi, China.

出版信息

Eur J Pharm Biopharm. 2018 Jan;122:70-77. doi: 10.1016/j.ejpb.2017.10.003. Epub 2017 Oct 7.

Abstract

Hydrocortisone sodium succinate (HSS) is an anti-inflammatory drug, but its application on ulcerative colitis (UC) treatment is limited by its associated side-effects. To solve this problem, a kind of pH-sensitive P(LE-IA-MEG) hydrogel microspheres (HMSs) were prepared as the drug carrier of hydrocortisone sodium succinate (HSS) for the treatment of UC. The P(LE-IA-MEG) HMSs were spherical in shape with good dispersion and the mean particle size was 34.87±0.90μm. HSS was successfully loaded into the P(LE-IA-MEG) HMSs. The in vitro release study of HSS-loaded HMSs (HSS-HMSs) revealed that the HSS-HMSs possessed desirable pH-sensitivity, the cumulative release rate was 4.07% and 94.64% in the solution with pH 1.2 and pH 7.4 solution during 12h, respectively. Furthermore, the study on pharmacokinetic, gastrointestinal drug residue and side-effects were conducted to evaluate the in vivo colon-targeting property of the HSS-HMSs. All the results showed that the HSS-HMSs could deliver HSS to the colon as well as reduce its premature absorption in the upper gastrointestinal tract. Finally, the HSS-HMSs showed better ameliorative effects and therapeutic effects on mice with experimental colitis as compared to HSS. In conclusion, the HSS-HMSs had great potential in the treatment of UC.

摘要

琥酸氢可的松(HSS)是一种抗炎药物,但由于其相关副作用,其在溃疡性结肠炎(UC)治疗中的应用受到限制。为了解决这个问题,我们制备了一种 pH 敏感的 P(LE-IA-MEG)水凝胶微球(HMSs)作为琥酸氢可的松(HSS)的药物载体,用于治疗 UC。P(LE-IA-MEG)HMSs 呈球形,分散性好,平均粒径为 34.87±0.90μm。HSS 成功载入 P(LE-IA-MEG)HMSs 中。HSS 载药 HMSs(HSS-HMSs)的体外释放研究表明,HSS-HMSs 具有良好的 pH 敏感性,在 pH 1.2 和 pH 7.4 的溶液中 12h 时的累积释放率分别为 4.07%和 94.64%。此外,还进行了药代动力学、胃肠道药物残留和副作用研究,以评估 HSS-HMSs 的体内结肠靶向特性。所有结果均表明,HSS-HMSs 可以将 HSS 递送到结肠,并减少其在上胃肠道的过早吸收。最后,与 HSS 相比,HSS-HMSs 对实验性结肠炎小鼠具有更好的改善作用和治疗效果。总之,HSS-HMSs 在治疗 UC 方面具有巨大的潜力。

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