Pérez-Pacheco Yaride, Tylkowski Bartosz, García-Valls Ricard
Department of Chemical Engineering, Universitat Rovira i Virgili, Av. Països Catalans 26, Campus Sescelades, 43007 Tarragona, Spain.
Eurecat, Centre Tecnològic de Catalunya, Chemical Technologies Unit, Marcel_lí Domingo s/n, 43007 Tarragona, Spain.
Molecules. 2025 Jan 10;30(2):252. doi: 10.3390/molecules30020252.
pH sensitivity of chitosan allows for precise phase transitions in acidic environments, controlling swelling and shrinking, making chitosan suitable for drug delivery systems. pH transitions are modulated by the presence of cross-linkers by the functionalization of the chitosan chain. This review relays a summary of chitosan functionalization and tailoring to optimize drug release. The potential to customize chitosan for different environments and therapeutic uses introduces opportunities for drug encapsulation and release. The focus on improving drug encapsulation and sustained release in specific tissues is an advanced interpretation, reflecting the evolving role of chitosan in achieving targeted and more efficient therapeutic outcomes. This review describes strategies to improve solubility and stability and ensure the controlled release of encapsulated drugs. The discussion on optimizing factors like cross-linking density, particle size, and pH for controlled drug release introduces a deeper understanding of how to achieve specific therapeutic effects. These strategies represent a refined approach to designing chitosan-based systems, pushing the boundaries of sustained release technologies and offering new avenues for precise drug delivery profiles.
壳聚糖的pH敏感性使其在酸性环境中能够发生精确的相变,控制溶胀和收缩,这使得壳聚糖适用于药物递送系统。通过壳聚糖链的功能化,交联剂的存在可调节pH转变。本综述总结了壳聚糖功能化和定制以优化药物释放的情况。为不同环境和治疗用途定制壳聚糖的潜力为药物封装和释放带来了机遇。专注于改善特定组织中的药物封装和持续释放是一种先进的诠释,反映了壳聚糖在实现靶向和更高效治疗效果方面不断演变的作用。本综述描述了提高溶解度和稳定性以及确保封装药物控释的策略。关于优化交联密度、粒径和pH等因素以实现药物控释的讨论,加深了人们对如何实现特定治疗效果的理解。这些策略代表了一种设计基于壳聚糖系统的精细方法,拓展了持续释放技术的边界,并为精确的药物递送概况提供了新途径。