Self-nanoemulsfiying drug delivery system of bruceine D: a new approach for anti-ulcerative colitis

生物利用度 药代动力学 药理学 药物输送 肺表面活性物质 溃疡性结肠炎 Zeta电位 药品 化学 医学 材料科学 纳米颗粒 纳米技术 生物化学 病理 有机化学 疾病
作者
Yaoxing Dou,Jiangtao Zhou,Tongtong Wang,Yanfeng Huang,Vicky Ping Chen,Yinfeng Xie,Zhi‐Xiu Lin,Gao Jiansheng,Zi‐Ren Su,Hui Zeng
出处
期刊:International Journal of Nanomedicine [Dove Medical Press]
卷期号:Volume 13: 5887-5907 被引量:43
标识
DOI:10.2147/ijn.s174146
摘要

Bruceine D (BD) is a major bioactive component isolated from the traditional Chinese medicinal plant Brucea javanica which has been widely utilized to treat dysentery (also known as ulcerative colitis [UC]).To improve the water solubility and absolute bioavailability of BD, we developed a self-nanoemulsifying drug delivery system (SNEDDS) composing of MCT (oil), Solutol HS-15 (surfactant), propylene glycol (co-surfactant) and BD. The physicochemical properties and pharmacokinetics of BD-SNEDDS were characterized, and its anti-UC activity and potential mechanism were evaluated in TNBS-induced UC rat model.The prepared nanoemulsion has multiple beneficial aspects including small mean droplet size, low polydispersity index (PDI), high zeta potential (ZP) and excellent stability. Transmission electron microscopy showed that nanoemulsion droplets contained uniform shape and size of globules. Pharmacokinetic studies demonstrated that BD-SNEDDS exhibited enhanced pharmacokinetic parameters as compared with BD-suspension. Moreover, BD-SNEDDS significantly restored the colon length and body weight, reduced disease activity index (DAI) and colon pathology, decreased histological scores, diminished oxidative stress, and suppressed TLR4, MyD88, TRAF6, NF-κB p65 protein expressions in TNBS-induced UC rat model.These results demonstrated that BD-SNEDDS exhibited highly improved oral bioavailability and advanced anti-UC efficacy. In conclusion, our current results provided a foundation for further research of BD-SNEDDS as a potential complementary therapeutic agent for UC treatment.
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