Yildiz Hasan M, Speciner Lauren, Ozdemir Cafer, Cohen David E, Carrier Rebecca L
Department of Chemical Engineering, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, USA.
Department of Bioengineering, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, USA.
Biomaterials. 2015 Jun;54:1-8. doi: 10.1016/j.biomaterials.2015.02.118. Epub 2015 Mar 27.
Orally delivered drugs and nutrients must diffuse through mucus to enter the circulatory system, but the barrier properties of mucus and their modulation by physiological factors are generally poorly characterized. The main objective of this study was to examine the impact of physicochemical changes occurring upon food ingestion on gastrointestinal (GI) mucus barrier properties. Lipids representative of postprandial intestinal contents enhanced mucus barriers, as indicated by a 10-142-fold reduction in the transport rate of 200 nm microspheres through mucus, depending on surface chemistry. Physiologically relevant increases in [Ca(2+)] resulted in a 2-4-fold reduction of transport rates, likely due to enhanced cross-linking of the mucus gel network. Reduction of pH from 6.5 to 3.5 also affected mucus viscoelasticity, reducing particle transport rates approximately 5-10-fold. Macroscopic visual observation and micro-scale lectin staining revealed mucus gel structural changes, including clumping into regions into which particles did not penetrate. Histological examination indicated food ingestion can prevent microsphere contact with and endocytosis by intestinal epithelium. Taken together, these results demonstrate that GI mucus barriers are significantly altered by stimuli associated with eating and potentially dosing of lipid-based delivery systems; these stimuli represent broadly relevant variables to consider upon designing oral therapies.
口服给药的药物和营养物质必须通过黏液扩散才能进入循环系统,但黏液的屏障特性及其受生理因素的调节作用通常尚未得到充分表征。本研究的主要目的是研究进食后发生的物理化学变化对胃肠道(GI)黏液屏障特性的影响。餐后肠内容物中的代表性脂质增强了黏液屏障,这表现为200纳米微球通过黏液的转运速率降低了10至142倍,具体取决于表面化学性质。生理相关的[Ca(2+)]增加导致转运速率降低2至4倍,这可能是由于黏液凝胶网络的交联增强所致。pH从6.5降至3.5也影响了黏液的粘弹性,使颗粒转运速率降低了约5至10倍。宏观视觉观察和微观凝集素染色显示黏液凝胶结构发生了变化,包括聚集成颗粒无法穿透的区域。组织学检查表明,进食可防止微球与肠上皮细胞接触并被其内化。综上所述,这些结果表明,胃肠道黏液屏障会因与进食及可能的基于脂质的给药系统给药相关的刺激而发生显著改变;这些刺激是设计口服疗法时需要考虑的广泛相关变量。