Ibeas Moreno Elena, Alonso María José, Abbadessa Anna
Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), University of Santiago de Compostela, Campus Vida, 15782, Santiago de Compostela, Spain.
Department of Pharmacology, Pharmacy and Pharmaceutical Technology, School of Pharmacy, University of Santiago de Compostela, Campus Vida, 15782, Santiago de Compostela, Spain.
Mater Today Bio. 2025 Apr 12;32:101767. doi: 10.1016/j.mtbio.2025.101767. eCollection 2025 Jun.
The rising global life expectancy has led to a growing prevalence of ophthalmic diseases, while current treatments face important limitations in terms of efficacy, costs, and patient compliance. The use of injectable hydrogels as drug and cell carriers is a promising approach, compared to the injection of drug solutions or cell suspensions. This is because the hydrogel matrix may offer protection against clearance or degradation, may modulate drug/cell release, and provide a biomimetic substrate for differentiating cells while being minimally invasive. On one hand, injectable hydrogels for ocular drug delivery have been traditionally designed to host and release small drugs or proteins. However, limitations such as high burst release and difficulty of entrapping hydrophobic molecules led to the emergence of nanocomposite hydrogels, where the drug is entrapped in nanoparticles prior hydrogel incorporation. Composite systems offer great advantages over the injection of particle suspensions, improving particle fate and drug release kinetics. On the other hand, injectable hydrogels offer a cell-friendly environment to seek tissue regeneration, providing biomechanical and biochemical cues for cellular cross-talk, differentiation, and formation of new extracellular matrix. This review critically discusses recent advancements in the development of novel injectable hydrogels as delivery vehicles for drug-loaded nanoparticles and cells, with a major focus on the formulation components, administration routes, and other factors affecting performance, highlighting promising aspects and challenges to address in the future.
全球预期寿命的不断提高导致眼科疾病的患病率日益上升,而目前的治疗方法在疗效、成本和患者依从性方面面临着重大限制。与注射药物溶液或细胞悬液相比,使用可注射水凝胶作为药物和细胞载体是一种很有前景的方法。这是因为水凝胶基质可以提供保护,防止其被清除或降解,可以调节药物/细胞的释放,并为分化细胞提供仿生基质,同时具有微创性。一方面,传统上用于眼部药物递送的可注射水凝胶被设计用于容纳和释放小分子药物或蛋白质。然而,诸如高突释和难以包封疏水分子等限制导致了纳米复合水凝胶的出现,即在水凝胶掺入之前将药物包封在纳米颗粒中。复合系统比注射颗粒悬液具有更大的优势,可改善颗粒命运和药物释放动力学。另一方面,可注射水凝胶为组织再生提供了一个细胞友好的环境,为细胞间的相互作用、分化和新细胞外基质的形成提供生物力学和生化线索。本综述批判性地讨论了新型可注射水凝胶作为载药纳米颗粒和细胞递送载体开发的最新进展,主要关注制剂成分、给药途径和其他影响性能的因素,突出了未来有前景的方面和需要解决的挑战。