Tadros Andrew R, Guo Xin Dong, Prausnitz Mark R
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive, Atlanta, Georgia, 30332-0100, U.S.A.
School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, 311 Ferst Drive, Atlanta, Georgia, 30332-0100, U.S.A..
AAPS PharmSciTech. 2025 Jan 3;26(1):19. doi: 10.1208/s12249-024-03016-0.
Delivery of therapies into skin is attractive for medical indications including vaccination and treatment of dermatoses but is highly constrained by the stratum corneum barrier. Microneedle (MN) patches have emerged as a promising technology to enable non-invasive, intuitive, and low-cost skin delivery. When combined with biodegradable polymer formulations, MN patches can further enable controlled-release drug delivery without injection. Herein, we sought to expand on the capability of MN patches to deliver therapies into skin by providing improved spatiotemporal control. Polylactic-co-glycolic acid (PLGA) microspheres were used to encapsulate model dye and then loaded into MN patches through a layer-by-layer fabrication method that created multiple layers of different composition within each MN. MN patches were loaded with up to 5 μg/MN of PLGA microspheres. Mechanical testing demonstrated that mechanical strength of MNs decreased with increasing number of microsphere layers. Microsphere-loaded MN patches inserted into porcine skin ex vivo and murine skin in vivo fully dissolved within 15 min, administering drug-loaded microspheres for controlled release lasting over 45 days. These data support the feasibility of multi-layered, microsphere-loaded MN patches designed for spatially targeted and sustained delivery of therapies into skin.
将治疗药物递送至皮肤对于包括疫苗接种和皮肤病治疗在内的医学适应症具有吸引力,但受到角质层屏障的高度限制。微针(MN)贴片已成为一种有前景的技术,可实现非侵入性、直观且低成本的皮肤给药。当与可生物降解的聚合物制剂结合时,MN贴片可以进一步实现无需注射的控释药物递送。在此,我们试图通过提供改进的时空控制来扩展MN贴片将治疗药物递送至皮肤的能力。聚乳酸-乙醇酸共聚物(PLGA)微球用于包裹模型染料,然后通过逐层制造方法加载到MN贴片中,该方法在每个MN内创建了多层不同组成的层。MN贴片加载的PLGA微球量高达5μg/MN。力学测试表明,MN的机械强度随着微球层数的增加而降低。体外插入猪皮肤和体内插入小鼠皮肤的载微球MN贴片在15分钟内完全溶解,给药载药微球以实现持续超过45天的控释。这些数据支持了多层载微球MN贴片用于将治疗药物空间靶向和持续递送至皮肤的可行性。