Lai Joanne, Azad Abul Kalam, Sulaiman Wan Mohd Azizi Wan, Kumarasamy Vinoth, Subramaniyan Vetriselvan, Alshehade Salah Abdalrazak
Faculty of Pharmacy, MAHSA University, Jenjarom 42610, Selangor, Malaysia.
Faculty of Pharmacy, University College of MAIWP International, Kuala Lumpur 68100, Selangor, Malaysia.
Pharmaceutics. 2024 Mar 6;16(3):370. doi: 10.3390/pharmaceutics16030370.
Alginate is a natural biopolymer widely studied for pharmaceutical applications due to its biocompatibility, low toxicity, and mild gelation abilities. This review summarizes recent advances in alginate-based encapsulation systems for targeted drug delivery. Alginate formulations like microparticles, nanoparticles, microgels, and composites fabricated by methods including ionic gelation, emulsification, spray drying, and freeze drying enable tailored drug loading, enhanced stability, and sustained release kinetics. Alginate microspheres prepared by spray drying or ionic gelation provide gastric protection and colon-targeted release of orally delivered drugs. Alginate nanoparticles exhibit enhanced cellular uptake and tumor-targeting capabilities through the enhanced permeation and retention effect. Crosslinked alginate microgels allow high drug loading and controlled release profiles. Composite alginate gels with cellulose, chitosan, or inorganic nanomaterials display improved mechanical properties, mucoadhesion, and tunable release kinetics. Alginate-based wound dressings containing antimicrobial nanoparticles promote healing of burns and chronic wounds through sustained topical delivery. Although alginate is well-established as a pharmaceutical excipient, more extensive in vivo testing is needed to assess clinical safety and efficacy of emerging formulations prior to human trials. Future opportunities include engineered systems combining stimuli-responsiveness, active targeting, and diagnostic capabilities. In summary, this review discusses recent advances in alginate encapsulation techniques for oral, transdermal, and intravenous delivery, with an emphasis on approaches enabling targeted and sustained drug release for enhanced therapeutic outcomes.
藻酸盐是一种天然生物聚合物,因其生物相容性、低毒性和温和的凝胶化能力而被广泛研究用于药物应用。本综述总结了基于藻酸盐的靶向给药封装系统的最新进展。通过离子凝胶化、乳化、喷雾干燥和冷冻干燥等方法制备的藻酸盐制剂,如微粒、纳米颗粒、微凝胶和复合材料,能够实现定制的药物负载、增强的稳定性和缓释动力学。通过喷雾干燥或离子凝胶化制备的藻酸盐微球可为口服给药提供胃保护和结肠靶向释放。藻酸盐纳米颗粒通过增强渗透和滞留效应表现出增强的细胞摄取和肿瘤靶向能力。交联藻酸盐微凝胶允许高药物负载和可控的释放曲线。与纤维素、壳聚糖或无机纳米材料复合的藻酸盐凝胶显示出改善的机械性能、粘膜粘附性和可调的释放动力学。含有抗菌纳米颗粒的藻酸盐基伤口敷料通过持续的局部给药促进烧伤和慢性伤口的愈合。尽管藻酸盐作为药物辅料已被广泛应用,但在进行人体试验之前,需要进行更广泛的体内测试以评估新制剂的临床安全性和有效性。未来的机遇包括结合刺激响应性、主动靶向和诊断能力的工程系统。总之,本综述讨论了藻酸盐封装技术在口服、透皮和静脉给药方面的最新进展,重点是实现靶向和持续药物释放以提高治疗效果的方法。