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首页> 外文期刊>Journal of Microencapsulation: Microcapsules Liposomes Nanoparticles Microcells Microspheres >Immune responses to orally administered PLGA microparticles: influence of oil vehicles and surfactive agents
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Immune responses to orally administered PLGA microparticles: influence of oil vehicles and surfactive agents

机译:对口服PLGA微粒的免疫反应:石油载体和表面活性剂的影响

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摘要

Lipid vehicles and surfactive agents have been successfully used to increases oral absorption and availability of free and encapsulated proteins. In order to investigate if these vehicles could also enhance the serum IgG responses elicited after the oral administration of protein antigens, free bovine serum albumin (BSA) was orally administered to Balb/c mice in different vehicles: a 0.3% sodium bicarbonate aqueous solution, an ethyl oleate/0.3% sodium bicarbonate o/w emulsion (1:9 v/v containing 0.01M sodium deoxycholate and 1% poloxamer 188) or ethyl oleate containing the previously described surfactive agents. The immune response elicited by the free antigen was enhanced by the use of these substances, especially when the free protein was administered as an oil suspension containing the surfactive agents. However, when protein loaded 1 mum PLGA particles were orally administered, the use of these enhancers did not result in an improvement of the serum IgG responses, and the bile salt elicited a similar immune response to that achieved with their suspension into an aqueous solution without any enhancer, which suggests that these enhancers are not capable of increasing the absorption of particulated antigens.
机译:脂质载体和表面活性剂已成功用于增加口服吸收以及游离和包封蛋白的利用率。为了研究这些媒介物是否也能增强口服蛋白质抗原后引起的血清IgG反应,在不同媒介物中分别向Balb / c小鼠口服了游离牛血清白蛋白(BSA):0.3%碳酸氢钠水溶液,油酸乙酯/0.3%碳酸氢钠o / w乳液(含有0.01M脱氧胆酸钠和1%泊洛沙姆188的1:9 v / v)或含有前述表面活性剂的油酸乙酯。通过使用这些物质增强了由游离抗原引起的免疫应答,特别是当游离蛋白以含有表面活性剂的油悬浮液形式给药时。然而,当口服施用载有蛋白质的1微米PLGA颗粒时,使用这些增强剂并不能改善血清IgG反应,并且胆汁盐引起的免疫反应与其悬浮于水溶液中所获得的免疫反应相似。任何增强剂,表明这些增强剂不能增加颗粒状抗原的吸收。

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