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Zeolite Formulation And Use Thereof For The Prevention And Therapy Of Diseases Caused By Infections With Herpes Simplex Virus Type 1 And Type 2

机译:沸石制剂及其在预防和治疗1型和2型单纯疱疹病毒感染引起的疾病中的用途

摘要

Antiviral medicine (compound) presented here is comprised of an active substance, a carrier of active substance and additives, and it is used for the prophylaxis, therapy and/or pre-respectively post-treatment of diseases caused by the infection with Herpes simplex virus type 1 and/or 2.;The active substance is represented by the synthetic zeolites in pure form, with defined crystal structures and chemical compositions. The active substance (zeolite) has a crystal size of 0.1-10 μm and specific surface of 400-1200 m2/g. The sodium ions can be partially or completely exchanged with other cations, e.g. K+, Ag+, NH4+, Ca2+, Mg2+, Mn2+, Zn2+, Cu2+, Fe2+ and Fe3+ in active substance of this antiviral compound.;The carrier of active compound is the organic gel, water, oil, cream, liposome and liposome-based systems with regular and/or prolonged activity. The weight ratio between the active substance and the carrier is 5×10−9-10−3, i.e. 5 ng to 1 mg of active substance per one gram of the carrier. The additives used are vitamines: Vitamin C (0-20 wt. %), vitamin E (0-0.01 wt. %), vitamin A (0-1 wt. %) and vitamin D3 (0-1 wt. %).;The efficacy of this preparation was demonstrated in in vitro experiments of the inhibition of HSV-1 and HSV-2 plaques formation in keratinocyte monolayers that were preincubated, coincubated or postincubated with the virus at the different time points (by up to 92%).
机译:本文介绍的抗病毒药物(化合物)由活性物质,活性物质的载体和添加剂组成,用于预防,治疗和/或分别预先治疗由单纯疱疹病毒感染引起的疾病类型1和/或2;活性物质由纯净的合成沸石代表,具有确定的晶体结构和化学组成。活性物质(沸石)的晶体尺寸为0.1-10μm,比表面积为400-1200 m 2 / g。钠离子可以与其他阳离子例如部分阳离子或部分阳离子完全交换。 K + ,Ag + ,NH 4 + ,Ca 2 + ,镁 2 + ,Mn 2 + ,Zn 2 + ,Cu 2 + ,Fe 2+ <该抗病毒化合物的活性物质中的/ Sup>和Fe 3 + 。;活性化合物的载体是基于有机凝胶,水,油,乳脂,脂质体和脂质体的系统,具有常规和/或长时间的活动。活性物质与载体之间的重量比为5×10 -9 -10 -3 ,即每1克载体5 ng至1 mg活性物质。所使用的添加剂是维生素:维生素C(0-20 wt。%),维生素E(0-0.01 wt。%),维生素A(0-1 wt。%)和维生素D3(0-1 wt。%)。 ;该制剂的功效在体外实验中得到了抑制,该实验在不同时间点与病毒预孵育,共孵育或后孵育后抑制了角质形成细胞单层中HSV-1和HSV-2斑块的形成(最多92%) 。

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