4.7 Article

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

Journal

DRUG DELIVERY
Volume 24, Issue 1, Pages 1667-1679

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/10717544.2017.1384521

Keywords

Brusatol; self-microemulsifying drug delivery system; in vitro and in vivo evaluation; anti-colitis activity; anti-inflammation

Funding

  1. National Natural Science Foundation of China [81503202]
  2. Science and Technology Planning Project of Guangdong Province, China [2012B09060007, 2013B090600007, 2013B090800052, 2013B090600010, 2014A020221042, 2017A050506044]
  3. Hongkong, Macao and Taiwan Science & Technology Cooperation Program of China [2014DFH30010]
  4. Guangdong International Cooperation ProjecT [2013508102016]
  5. Science and Technology Major Project of Guangdong Province [2013A022100001]
  6. Natural Science Foundation of Guangdong Province [2015A030310217]
  7. Science and Technology Planning Project of Guangzhou, Guangdong, China [201704030028]

Ask authors/readers for more resources

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-kappa B 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-kappa B 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.

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