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脂质体结合的人α干扰素的药理学特性改变。II.

Altered pharmacologic properties of liposome-associated human interferon-alpha. II.

作者信息

Eppstein D A

出版信息

J Interferon Res. 1982;2(1):117-25. doi: 10.1089/jir.1982.2.117.

Abstract

Association of human interferon-alpha with multilamellar vesicles and reverse-phase evaporation vesicles resulted in altered retention and distribution of the interferon after injection into mice. Intramuscular injection of liposomal-interferon, after extrusion through 0.2 mu filters, resulted in significantly increased localized retention of interferon. Liposomal-interferon was retained locally from one to three days, depending on liposome composition, whereas an equivalent injection of free interferon was undetectable after 24 hrs. Intravenous injection of the liposomal-interferon preparations resulted in increased interferon levels in lung, spleen, and liver as compared to injection of free interferon. Preparation of small unilamellar vesicles in the presence of interferon revealed differences in modes of association of different species with the liposomes, based on differential titers on human vs. bovine cells.

摘要

人α干扰素与多层囊泡和反相蒸发囊泡结合后,注射到小鼠体内会导致干扰素的保留和分布发生改变。经0.2微米滤器挤出后的脂质体干扰素肌内注射,会使干扰素的局部保留显著增加。脂质体干扰素在局部保留1至3天,具体取决于脂质体组成,而等量的游离干扰素注射24小时后就检测不到了。与注射游离干扰素相比,脂质体干扰素制剂静脉注射会使肺、脾和肝脏中的干扰素水平升高。在干扰素存在的情况下制备小单层囊泡,基于人源细胞与牛源细胞上的不同滴度,揭示了不同种类与脂质体结合方式的差异。

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