Pöttgen Simon, Wischke Christian
Martin-Luther-University Halle-Wittenberg, Institute of Pharmacy, Kurt-Mothes-Str. 3, 06120, Halle, Germany.
Pharm Res. 2025 Sep 11. doi: 10.1007/s11095-025-03923-2.
Microparticles have been established as injectable drug carriers designed to enable a long-term release of the encapsulated active pharmaceutical ingredients (API). To regulate this release, the diffusion barrier provided by the matrix material - typically hydrolytically degradable polyesters - must be controlled through precise levels of matrix porosity. This mini-review presents processing methods that are alternatives to the most common batch emulsification techniques for the manufacturing of porous polymer particles. A focus is placed on mechanistically describing the particle and pore formation in droplet-based microfluidics, electrospraying, and by supercritical fluids, critically discussing their opportunities and challenges. Ultimately, this review assesses the potential of these techniques in advancing the engineering of porous polymeric carrier systems in the light of scale-up and continuous production.
微粒已被确立为可注射药物载体,旨在实现包封的活性药物成分(API)的长期释放。为了调节这种释放,由基质材料(通常是可水解降解的聚酯)提供的扩散屏障必须通过精确的基质孔隙率水平来控制。本综述介绍了一些加工方法,这些方法是制造多孔聚合物颗粒时最常见的批量乳化技术的替代方法。重点是从机理上描述基于液滴的微流控、电喷雾和超临界流体中颗粒和孔隙的形成,并批判性地讨论它们的机遇和挑战。最终,本综述根据放大和连续生产评估了这些技术在推进多孔聚合物载体系统工程方面的潜力。