Ji Weihong, Zhang Yuanxing, Shao Weichen, Kankala Ranjith Kumar, Chen Aizheng
Institute of Biomaterials and Tissue Engineering, Huaqiao University, Xiamen, Fujian 361021, PR China.
Fujian Provincial Key Laboratory of Biochemical Technology, Huaqiao University, Xiamen, Fujian 361021, PR China.
Regen Biomater. 2024 Jun 17;11:rbae071. doi: 10.1093/rb/rbae071. eCollection 2024.
Atherosclerosis, a chronic and progressive condition characterized by the accumulation of inflammatory cells and lipids within artery walls, remains a leading cause of cardiovascular diseases globally. Despite considerable advancements in drug therapeutic strategies aimed at managing atherosclerosis, more effective treatment options for atherosclerosis are still warranted. In this pursuit, the emergence of β-cyclodextrin (β-CD) as a promising therapeutic agent offers a novel therapeutic approach to drug delivery targeting atherosclerosis. The hydrophobic cavity of β-CD facilitates its role as a carrier, enabling the encapsulation and delivery of various therapeutic compounds to affected sites within the vasculature. Notably, β-CD-based nanoassemblies possess the ability to reduce cholesterol levels, mitigate inflammation, solubilize hydrophobic drugs and deliver drugs to affected tissues, making these nanocomponents promising candidates for atherosclerosis management. This review focuses on three major classes of β-CD-based nanoassemblies, including β-CD derivatives-based, β-CD/polymer conjugates-based and polymer β-CD-based nanoassemblies, highlighting a variety of formulations and assembly methods to improve drug delivery and therapeutic efficacy. These β-CD-based nanoassemblies exhibit a variety of therapeutic mechanisms for atherosclerosis and offer systematic strategies for overcoming barriers to drug delivery. Finally, we discuss the present obstacles and potential opportunities in the development and application of β-CD-based nanoassemblies as novel therapeutics for managing atherosclerosis and addressing cardiovascular diseases.
动脉粥样硬化是一种慢性进行性疾病,其特征是动脉壁内炎症细胞和脂质的积累,仍然是全球心血管疾病的主要原因。尽管在旨在治疗动脉粥样硬化的药物治疗策略方面取得了相当大的进展,但仍需要更有效的动脉粥样硬化治疗选择。在这一探索过程中,β-环糊精(β-CD)作为一种有前景的治疗剂的出现,为靶向治疗动脉粥样硬化的药物递送提供了一种新的治疗方法。β-CD的疏水腔促进了其作为载体的作用,能够将各种治疗化合物包裹并递送至脉管系统内的受影响部位。值得注意的是,基于β-CD的纳米组装体具有降低胆固醇水平、减轻炎症、溶解疏水药物以及将药物递送至受影响组织的能力,使这些纳米组分成为治疗动脉粥样硬化的有前景的候选物。本综述重点关注三类主要的基于β-CD的纳米组装体,包括基于β-CD衍生物的、基于β-CD/聚合物共轭物的和基于聚合物-β-CD的纳米组装体,强调了各种提高药物递送和治疗效果的制剂和组装方法。这些基于β-CD的纳米组装体展现出多种治疗动脉粥样硬化的机制,并提供了克服药物递送障碍的系统策略。最后,我们讨论了基于β-CD的纳米组装体作为治疗动脉粥样硬化和解决心血管疾病的新型疗法在开发和应用中目前存在的障碍和潜在机遇。