Department of Bioengineering, University of Washington, 3720 15(th) Ave NE, Seattle, WA 98195, USA.
Department of Bioengineering, University of Washington, 3720 15(th) Ave NE, Seattle, WA 98195, USA.
J Control Release. 2024 Mar;367:649-660. doi: 10.1016/j.jconrel.2024.01.062. Epub 2024 Feb 8.
The oral mucosa is an attractive site for immunization due to its accessibility and ability to elicit local and systemic immune responses. However, evaluating oral mucosal immunogenicity has proven challenging due to the physical barriers and immunological complexity of the oral mucosa. Microneedles can overcome these physical barriers, but previous work has been limited in the scope of microneedle delivery site, geometry, and release kinetics, all of which are expected to affect physiological responses. Here, we develop integrated fiber microneedle devices, an oral dosage form with tunable geometries and material configurations capable of both burst and sustained release to controlled depths in the oral mucosa. Integrated fiber microneedles administered to either the buccal or sublingual mucosa result in seroconversion and antigen-specific interferon-γ secretion in splenocytes. The dynamics and magnitude of the resulting immune response can be modulated by tuning microneedle release kinetics. Optimal microneedle geometry is site-specific, with longer microneedles eliciting greater immunogenicity in the buccal mucosa, and shorter microneedles eliciting greater immunogenicity in the sublingual mucosa. The Th1/Th2 phenotype of the resulting immune response is also dependent on integrated fiber microneedle length. Together, these results establish integrated fiber microneedles as a multifunctional delivery system for the oral mucosa and motivate further exploration using tunable delivery systems to better understand oral mucosal immunity.
口腔黏膜因其易于接近和能够引发局部和全身免疫反应而成为免疫接种的一个有吸引力的部位。然而,由于口腔黏膜的物理屏障和免疫复杂性,评估口腔黏膜免疫原性被证明具有挑战性。微针可以克服这些物理障碍,但以前的工作在微针给药部位、几何形状和释放动力学的范围上受到限制,所有这些都可能影响生理反应。在这里,我们开发了集成纤维微针装置,这是一种具有可调几何形状和材料配置的口腔剂型,能够在口腔黏膜中以可控的深度进行爆发式和持续释放。将集成纤维微针施用于颊黏膜或舌下黏膜,均可导致血清转化和脾细胞中抗原特异性干扰素-γ的分泌。通过调整微针释放动力学,可以调节产生的免疫反应的动力学和幅度。最佳微针几何形状是特定于部位的,较长的微针在颊黏膜中引起更强的免疫原性,较短的微针在舌下黏膜中引起更强的免疫原性。产生的免疫反应的 Th1/Th2 表型也依赖于集成纤维微针的长度。总之,这些结果确立了集成纤维微针作为口腔黏膜的多功能给药系统,并通过使用可调给药系统进一步探索,以更好地了解口腔黏膜免疫。