Suppr超能文献

长期阴道抗体递送:递送系统与生物分布

Long-term vaginal antibody delivery: delivery systems and biodistribution.

作者信息

Saltzman W M, Sherwood J K, Adams D R, Castle P, Haller P

机构信息

School of Chemical Engineering, Cornell University, Ithaca, New York 14853, USA.

出版信息

Biotechnol Bioeng. 2000 Feb 5;67(3):253-64.

Abstract

Topical delivery systems can provide prolonged delivery of antibodies to the vaginal mucosal surface for long-term protection against infectious diseases. We examined the biodistribution of antibodies during 30 days of vaginal antibody delivery in mice. Different antibody preparations (including monoclonal IgG and IgM, as well as several different (125)I-labeled IgGs) were administered by polymer vaginal rings, which were designed to provide continuous antibody delivery. Antibody concentrations remained high in the vaginal secretions for up to 30 days after disk insertion; radiolabeled antibody was also found, at approximately 100 times lower concentration, in the blood and other tissues. The measured concentrations agreed reasonably well with a simple pharmacokinetic model, which was used to calculate mucosal and systemic concentrations as a function of antibody delivery and elimination rates. Results from the model were consistent with previously reported antibody pharmacokinetic measurements: the half-life for antibody elimination for the vagina was approximately 3 h; the half-life for IgG(1) clearance from the blood was >1 day; and the overall permeability constant for vaginal uptake of IgG was approximately 0.01 to 0.03 h(-1). These results provide important information for the design of controlled antibody delivery devices for vaginal use, and suggest that high-dose, long-term vaginal administration of antibodies may be a reasonable approach for achieving sustained mucosal and systemic antibody levels.

摘要

局部给药系统可以将抗体长时间递送至阴道黏膜表面,以提供针对传染病的长期保护。我们研究了小鼠阴道抗体给药30天期间抗体的生物分布情况。通过聚合物阴道环给予不同的抗体制剂(包括单克隆IgG和IgM,以及几种不同的(125)I标记的IgG),这些阴道环设计用于持续输送抗体。在插入圆盘后长达30天的时间里,阴道分泌物中的抗体浓度一直很高;在血液和其他组织中也发现了放射性标记的抗体,其浓度约低100倍。测得的浓度与一个简单的药代动力学模型相当吻合,该模型用于根据抗体输送和消除速率计算黏膜和全身浓度。模型结果与先前报道的抗体药代动力学测量结果一致:阴道中抗体消除的半衰期约为3小时;IgG(1)从血液中清除的半衰期>1天;IgG阴道摄取的总体渗透常数约为0.01至0.03 h(-1)。这些结果为设计用于阴道的可控抗体输送装置提供了重要信息,并表明高剂量、长期阴道给药抗体可能是实现黏膜和全身抗体水平持续稳定的合理方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验