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毛果算盘子素自微乳化给药系统的表征及其对葡聚糖硫酸钠诱导的小鼠溃疡性结肠炎的治疗作用

Characterization of brusatol self-microemulsifying drug delivery system and its therapeutic effect against dextran sodium sulfate-induced ulcerative colitis in mice.

作者信息

Zhou Jiangtao, Tan Lihua, Xie Jianhui, Lai Zhengquan, Huang Yanfeng, Qu Chang, Luo Dandan, Lin Zhixiu, Huang Ping, Su Ziren, Xie Youliang

机构信息

a School of Pharmaceutical Sciences , Guangzhou University of Chinese Medicine , Guangzhou , PR China.

b Mathematical Engineering Academy of Chinese Medicine , Guangzhou University of Chinese Medicine , Guangzhou , PR China.

出版信息

Drug Deliv. 2017 Nov;24(1):1667-1679. doi: 10.1080/10717544.2017.1384521.

Abstract

Brusatol (BR) is one of the main bioactive components derived from Brucea javanica, a medicinal herb historically used in the treatment of dysenteric disorders (also known as ulcerative colitis(UC)). Due to its poor aqueous solubility, a novel brusatol self-microemulsifying drug delivery system (BR-SMEDDS) nanoformulation with smaller size, higher negative zeta potential and drug content, and excellent stability was developed. The appearance of BR-SMEDDS remained clear and transparent, and transmission electron microscopy showed microemulsion droplets to be spherical with homogeneous distribution. Pharmacokinetic parameters indicated that oral bioavailability was greatly improved by BR-SMEDDS as compared with aqueous suspension. Meanwhile, the anti-colitis activity of BR-SMEDDS was evaluated on dextran sodium sulfate (DSS)-induced colitis mice model. The result illustrated that the nano-formation significantly reduced the body weight loss, recovered colon length, decreased disease activity index and microscopic score, regulated immune-inflammatory cytokines, diminished oxidative stress and repressed the colonic expression of myeloid differentiation factor 88 (MyD88), toll-like receptor 4 (TLR4) and nuclear factor kappa B p65 (NF-κB p65) proteins. Our findings demonstrated for the first time that BR could effectively attenuate colonic inflammation in mice, at least partially, via favorable regulation of anti-oxidative and anti-inflammatory status and inhibition of the TLR4-linked NF-κB signaling pathway. The BR nano-formulation was superior to BR suspension and sulphasalazine, in treating experimental UC, and exhibited similar effect with azathioprine, with much smaller dosage. The enhanced anti-UC effect of BR might be intimately associated with the improved pharmacokinetic property by SMEDDS. The developed nano-delivery system might thus be a promising candidate for colitis treatment.

摘要

鸦胆子苦醇(BR)是鸦胆子的主要生物活性成分之一,鸦胆子是一种历史上用于治疗痢疾(也称为溃疡性结肠炎(UC))的草药。由于其水溶性差,开发了一种新型的鸦胆子苦醇自微乳化药物递送系统(BR-SMEDDS)纳米制剂,该制剂具有更小的尺寸、更高的负zeta电位和药物含量,以及出色的稳定性。BR-SMEDDS的外观保持清澈透明,透射电子显微镜显示微乳液滴呈球形且分布均匀。药代动力学参数表明,与水悬浮液相比,BR-SMEDDS大大提高了口服生物利用度。同时,在葡聚糖硫酸钠(DSS)诱导的结肠炎小鼠模型上评估了BR-SMEDDS的抗结肠炎活性。结果表明,该纳米制剂显著减轻了体重减轻,恢复了结肠长度,降低了疾病活动指数和显微镜评分,调节了免疫炎症细胞因子,减轻了氧化应激,并抑制了髓样分化因子88(MyD88)、Toll样受体4(TLR4)和核因子κB p65(NF-κB p65)蛋白在结肠中的表达。我们的研究首次证明,BR可以至少部分地通过有利地调节抗氧化和抗炎状态以及抑制TLR4相关的NF-κB信号通路,有效减轻小鼠的结肠炎症。在治疗实验性UC方面,BR纳米制剂优于BR悬浮液和柳氮磺胺吡啶,并且在剂量小得多的情况下表现出与硫唑嘌呤相似的效果。BR抗UC作用增强可能与SMEDDS改善药代动力学性质密切相关。因此,开发的纳米递送系统可能是治疗结肠炎的有前途的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d0d/8253134/fcb9f92f9616/IDRD_A_1384521_F0001_C.jpg

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