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

机译:布鲁他酚自微乳化给药系统的表征及其对葡聚糖硫酸钠诱发的小鼠溃疡性结肠炎的治疗作用

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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.
机译:摘要Brusatol(BR)是源自Brucea javanica的主要生物活性成分之一,Brucea javanica是一种历史上用于治疗痢疾性疾病(也称为溃疡性结肠炎(UC))的草药。由于其水溶性差,开发了一种新的布鲁萨特酚自微乳化药物递送系统(BR-SMEDDS)纳米制剂,具有较小的尺寸,较高的负ζ电势和较高的药物含量,并具有出色的稳定性。 BR-SMEDDS的外观保持透明且透明,并且透射电子显微镜显示微乳液液滴为球形且具有均匀分布。药代动力学参数表明,与水性悬浮液相比,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,纳米结构显着减少了体重减轻,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,减少了氧化应激,并抑制了骨髓分化因子88(MyD88)的结肠表达, Toll样受体4(TLR4)和核因子κB p65(NF-κBp65)蛋白。我们的发现首次证明BR可以通过抗氧化和抗炎状态的良好调节以及TLR4连接的NF-κB信号通路的抑制,至少部分地有效减轻小鼠的结肠炎症。在治疗实验性UC中,BR纳米制剂优于BR悬浮液和柳氮磺吡啶,并以硫唑嘌呤表现出相似的作用,且剂量小得多。 BR增强的抗UC效应可能与SMEDDS改善的药代动力学特性密切相关。因此,发达的纳米递送系统可能是结肠炎治疗的有希望的候选者。

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