Zhou Jiangtao, Tan Lihua, Xie Jianhui, Lai Zhengquan, Huang Yanfeng, Qu Chang, Luo Dandan, Lin Zhixiu, Huang Ping, Su Ziren, Xie Youliang
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.
Drug Deliv. 2017 Nov;24(1):1667-1679. doi: 10.1080/10717544.2017.1384521.
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.
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。