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用于口服给药系统的化学修饰透明质酸衍生物的生物分布特征分析。

Biodistribution profiling of the chemical modified hyaluronic acid derivatives used for oral delivery system.

机构信息

Department of Health Development and Health Marketing, School of Healthcare Management, Kainan University, Taoyuan, Taiwan, ROC.

School of Pharmacy, College of Pharmacy, Taipei Medical University, 250 Wu-Hsing Street, Taipei 110, Taiwan, ROC.

出版信息

Int J Biol Macromol. 2014 Mar;64:45-52. doi: 10.1016/j.ijbiomac.2013.11.027. Epub 2013 Dec 4.

Abstract

A series of adipic acid dihydrazide (ADH)-modified hyaluronic acid (HA-ADH) compounds were synthesized and conjugated with QDots (QDots-HA conjugates) to assess the effects of the molecular weight (MW) and extent of chemical modification of HA on its biodistribution. Their physicochemical structures were confirmed by complementary application of GPC, (1)H NMR, FTIR, and UV-vis spectroscopic methods. In vivo imaging of QDots-HA conjugates after oral administration was analyzed to investigate their biodistribution in nude mice. Simultaneously, real-time bioimaging was confirmed by an anatomical analysis to investigate the organ-specific accumulation of conjugates. QDot-HA conjugates with a higher MW of HA or high modification presented relatively slow clearance leading to an extension of the retention time for up to 10 days, whereas those with lower MWs of HA or a low modification extent exhibited quick absorption and elimination after oral administration. Taken together, HA derivatives with suitable MWs and chemical modification extents can be used to design new, more-sophisticated, and intelligent HA-based vehicles for oral delivery with diverse characteristics.

摘要

一系列己二酸二酰肼(ADH)修饰的透明质酸(HA-ADH)化合物被合成,并与量子点(QDots-HA 缀合物)缀合,以评估透明质酸的分子量(MW)和化学修饰程度对其分布的影响。通过凝胶渗透色谱、(1)H NMR、傅里叶变换红外光谱和紫外可见光谱等互补应用方法,证实了它们的物理化学结构。通过分析口服给药后 QDots-HA 缀合物的体内成像,研究了它们在裸鼠体内的分布。同时,通过解剖分析证实了实时生物成像,以研究缀合物的器官特异性积累。具有较高 MW 的 HA 或高修饰的 QDot-HA 缀合物呈现出相对较慢的清除速度,导致保留时间延长至 10 天,而具有较低 MW 的 HA 或低修饰程度的缀合物在口服给药后表现出快速吸收和消除。总之,具有合适 MW 和化学修饰程度的透明质酸衍生物可用于设计新的、更复杂的、基于透明质酸的智能口服给药载体,具有多样化的特性。

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