Leal Jasmim, Smyth Hugh D C, Ghosh Debadyuti
Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, 2409 University Ave., Austin, TX 78712, USA.
Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, 2409 University Ave., Austin, TX 78712, USA.
Int J Pharm. 2017 Oct 30;532(1):555-572. doi: 10.1016/j.ijpharm.2017.09.018. Epub 2017 Sep 14.
Mucus is a selective barrier to particles and molecules, preventing penetration to the epithelial surface of mucosal tissues. Significant advances in transmucosal drug delivery have recently been made and have emphasized that an understanding of the basic structure, viscoelastic properties, and interactions of mucus is of great value in the design of efficient drug delivery systems. Mucins, the primary non-aqueous component of mucus, are polymers carrying a complex and heterogeneous structure with domains that undergo a variety of molecular interactions, such as hydrophilic/hydrophobic, hydrogen bonds and electrostatic interactions. These properties are directly relevant to the numerous mucin-associated diseases, as well as delivering drugs across the mucus barrier. Therefore, in this review we discuss regional differences in mucus composition, mucus physicochemical properties, such as pore size, viscoelasticity, pH, and ionic strength. These factors are also discussed with respect to changes in mucus properties as a function of disease state. Collectively, the review seeks to provide a state of the art roadmap for researchers who must contend with this critical barrier to drug delivery.
黏液是对颗粒和分子的选择性屏障,可防止其穿透至黏膜组织的上皮表面。近来,经黏膜给药取得了重大进展,这强调了了解黏液的基本结构、粘弹性特性及其相互作用对于设计高效给药系统具有重要价值。黏蛋白是黏液的主要非水成分,是具有复杂且异质结构的聚合物,其结构域会发生多种分子相互作用,如亲水/疏水、氢键和静电相互作用。这些特性与众多与黏蛋白相关的疾病直接相关,也与药物透过黏液屏障的递送有关。因此,在本综述中,我们讨论了黏液组成的区域差异、黏液的物理化学性质,如孔径、粘弹性、pH值和离子强度。还讨论了这些因素与疾病状态导致的黏液性质变化的关系。总体而言,本综述旨在为必须应对这一关键给药屏障的研究人员提供一份最新路线图。