苦参怀化汤治疗溃疡性结肠炎的纳米分散体系研究。

Jingrui Liu, Haixia Tang, Liansheng Yang, Haibo Wang, Xiuyan Li, Zhixin Yang
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引用次数: 0

摘要

目的:中药汤剂在高温和复杂的化学环境下形成复杂的多相体系。然而,苦参怀化汤(DKH)治疗溃疡性结肠炎(UC)的有效分散体系尚未阐明。方法:采用超离心透析法将DKH按粒径分为沉淀相(DKH- p)、纳米相(DKH- n)和固相(DKH- s),采用透射电镜(TEM)和高效液相色谱(HPLC)分析各相组的粒径、形态、化学组成、含量等理化性质。采用酶联免疫吸附法(ELISA)和HE染色法评价不同相的抗uc作用。采用紫外分光光度法和高效液相色谱法对有效分散体系的组成和释放特性进行了研究。结果:DKH指纹图谱识别出Ru、Qu、Ka、Fo、Iso、Kur、SFG、OMT、OSC、MT、SC等11种关键成分,这些成分在DKH- n中的含量分别为DKH中相应含量的69.51%、88.30%、84.60%、82.92%、73.35%、77.03%、74.02%、89.95%、85.99%、79.53%、85.24%。药效学结果显示,DKH- n具有与DKH相同的抗UC作用,降低DAI、CMDI评分,提高IL-4、IL-10活性,降低IL-6、TNF-α、MPO表达,与模型组差异有统计学意义(** p)。结论:DKH- n可能是DKH治疗UC的有效分散系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanophase: An Effective Dispersion System for the Decoction of Kushen Huaihua for the Treatment of Ulcerative Colitis.

Objective: In traditional Chinese medicine, the decoction turns into a complex multiphase system following exposure to high temperatures and a complex chemical environment. However, the effective dispersion system of the decoction of Kushen Huaihua (DKH) for the treatment of ulcerative colitis (UC) has yet to be elucidated.

Methods: DKH was separated into precipitated phase (DKH-P), nanophase (DKH-N), and solution phase (DKH-S) according to the particle size by ultracentrifugation dialysis, and the physicochemical properties of each phase group, such as particle size, morphology, chemical composition, and content, were analysed by TEM and HPLC. The anti-UC effects of the different phases were evaluated by ELISA and HE staining. Furthermore, the composition of the effective dispersion system and release characteristics were investigated by UV and HPLC.

Results: The fingerprint analysis of DKH recognized 11 key components, namely Ru, Qu, Ka, Fo, Iso, Kur, SFG, OMT, OSC, MT, and SC. The content of these components in DKH-N was found to be 69.51%, 88.30%, 84.60%, 82.92%, 73.35%, 77.03%, 74.02%, 89.95%, 85.99%, 79.53%, and 85.24% of the corresponding levels in DKH, respectively. Pharmacodynamic results demonstrated that DKH-N exerted the same anti-UC effect as DKH, decreased DAI and CMDI scores, increased IL-4 and IL-10 activities, and reduced expression of IL-6, TNF-α, and MPO, which were significantly different from those of the model group (**P<0.01). Additionally, DKH-N was found to comprise 30.30% polysaccharides and 24.93% protein components. Furthermore, 11 components in DKH-N demonstrated more than 80% release in enzyme-containing simulated colonic fluid in 24 h.

Conclusion: DKH-N may be an effective dispersion system for DKH treatment of UC.

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