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首页> 外文期刊>Scientific reports. >Investigation of the adsorption capacity of the enterosorbent Enterosgel for a range of bacterial toxins, bile acids and pharmaceutical drugs
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Investigation of the adsorption capacity of the enterosorbent Enterosgel for a range of bacterial toxins, bile acids and pharmaceutical drugs

机译:对一系列细菌毒素,胆酸和药物药物进行肠球肠道吸附能力的研究

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摘要

Oral intestinal adsorbents (enterosorbents) are orally administered materials which pass through the gut where they bind (adsorb) various substances. The enterosorbent Enterosgel?(Polymethylsiloxane polyhdrate) is recommended as a symptomatic treatment for acute diarrhoea and chronic diarrhoea associated with irritable bowel syndrome (IBS). Since 1980’s there have been many Enterosgel clinical trials, however, the detailed mechanism of Enterosgel action towards specific toxins and interaction with concomitantly administered medications has not been fully investigated. Our in vitro study assessed the adsorption capacity of Enterosgel for bacterial enterotoxins and endotoxin, bile acids and interaction with the pharmaceutical drugs; Cetirizine and Amitriptyline hydrochloride. Our data demonstrate the good adsorption capacity of Enterosgel for bacterial toxins associated with gastrointestinal infection, with a lower than the comparator charcoal Charcodote capacity for bile acids whose levels can be raised in IBS patients. Adsorption capacity for the two drugs varied but was significantly lower than Charcodote. These findings suggest that the mechanism of Enterosgel action in the treatment of gastrointestinal infection or IBS is adsorption of target molecules followed by removal from the body. This therapy offers a drug free approach to prevention and treatment of infectious and chronic non-infectious diseases, where intestinal flora and endotoxemia play a role.
机译:口服肠道吸附剂(肠溶剂)是口服给药的材料,其通过肠道,其中它们结合(吸附)各种物质。肠伞肠道肠溶肠(聚甲基硅氧烷多水合物)被推荐为急性腹泻和慢性腹泻的对症治疗与肠易激综合征(IBS)相关的急性腹泻和慢性腹泻。自1980年以来,已经存在许多肠杆菌临床试验,但尚未完全研究肠杆菌对特异性毒素和与伴随药物的相互作用的详细机制。我们的体外研究评估了细菌肠毒素和内毒素,胆汁酸和与药物的相互作用的肠杆菌的吸附能力;盐酸香嗪和氨基丙啶素。我们的数据证明了与胃肠感染相关的细菌毒素的肠溶菌的良好吸附能力,低于比较器木炭致癌能力的胆汁酸,其水平可以在IBS患者中提高。两种药物的吸附能力变化但显着低于Charcodote。这些发现表明,在治疗胃肠感染或IBS治疗肠杆菌作用的机制是吸附靶分子,然后从体内移除。该疗法提供了一种可吸毒的方法来预防和治疗传染性和慢性非传染病,其中肠道菌群和内毒血症发挥作用。

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