Niosome Encapsulated Bromelain Reduced IL-6 and TNF-α in LPS Induced Human Skin Fibroblast Cell Line

Siavash Hosseinpour Chermahini, F. A. Abdul Majid, A. Aziz, Roya Anvari
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Abstract

The topical delivery of bromelain as an anti-inflammatory solution for skin inflammation has attracted the attention of researchers. Due to the skin barrier issue, a new method was designed for the effective delivery of specific doses of bromelain to the desired action sites. A niosome was selected as a novel and practical transdermal vehicle for the delivery of bromelain to inflamed sites. In this regard, a lipopolysaccharide (LPS)-induced human skin fibroblast (HSF1184) cell line was assembled in-vitro as a simulated model. The levels of interleukin-6 (IL-6) and tumour necrosis factor alpha (TNF-α), the two immune-modulatory regulators of cell responses to inflammation, were measured to determine the response towards the niosome-encapsulated bromelain treatment. The results showed that the niosome-encapsulated bromelain significantly reduced the levels of IL-6 and TNF-α compared to the non-encapsulated bromelain, the vehicle (niosome) and the control.
膜小体包封菠萝蛋白酶降低LPS诱导的人皮肤成纤维细胞系IL-6和TNF-α
菠萝蛋白酶作为皮肤炎症的抗炎溶液的局部递送引起了研究人员的注意。由于皮肤屏障问题,设计了一种新的方法来有效地将特定剂量的菠萝蛋白酶输送到所需的作用部位。一个niosome被选择作为一种新颖和实用的透皮载体,用于将菠萝蛋白酶输送到炎症部位。为此,体外组装脂多糖(LPS)诱导的人皮肤成纤维细胞(HSF1184)细胞系作为模拟模型。白细胞介素-6 (IL-6)和肿瘤坏死因子α (TNF-α)的水平,这两种细胞对炎症反应的免疫调节因子,被测量以确定对nioome包封菠萝蛋白酶治疗的反应。结果表明,与未包封菠萝蛋白酶、载体(niosome)和对照组相比,niosome包封菠萝蛋白酶显著降低了IL-6和TNF-α水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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