Su Yilin, Liu Lisha, Lin Chongyang, Deng Dashi, Li Yunfei, Huang Mou, Wang Yu, Ling Kangqiu, Wang Haobing, Chen Qiyu, Huang Guixiao
Institute of Urology, The Third Affiliated Hospital of Shenzhen University, Shenzhen University, Shenzhen, China.
Institute of Pain, The Affiliated Hospital of Southwest Jiaotong University, The Chengdu Third People's Hospital, Chengdu, China.
Front Pharmacol. 2024 Dec 3;15:1476739. doi: 10.3389/fphar.2024.1476739. eCollection 2024.
Oridonin (ORI), an ent-kaurane diterpenoid derived from Rabdosia rubescens (Hemsl.) H.Hara, serves as the primary bioactive component of this plant. It demonstrates a broad spectrum of therapeutic activities, including moderate to potent anticancer properties, alongside anti-inflammatory, antibacterial, antifibrotic, immunomodulatory, and neuromodulatory effects, thus influencing diverse biological processes. However, its clinical potential is significantly constrained by poor aqueous solubility and limited bioavailability. In alignment with the approach of developing drug candidates from natural compounds, various strategies, such as structural modification and nanocarrier systems, have been employed to address these challenges. This review provides an overview of ORI-based nano-delivery systems, emphasizing their potential to improve the clinical applicability of oridonin in oncology. Although some progress has been made in advancing ORI nano-delivery research, it remains insufficient for clinical implementation, necessitating further investigation.
冬凌草甲素(ORI)是一种从碎米桠[Rabdosia rubescens (Hemsl.) H.Hara]中提取的对映-贝壳杉烷二萜类化合物,是该植物的主要生物活性成分。它具有广泛的治疗活性,包括中度到强效的抗癌特性,以及抗炎、抗菌、抗纤维化、免疫调节和神经调节作用,从而影响多种生物学过程。然而,其临床应用潜力受到水溶性差和生物利用度有限的显著限制。为了与从天然化合物开发候选药物的方法保持一致,人们采用了各种策略,如结构修饰和纳米载体系统,来应对这些挑战。本综述概述了基于冬凌草甲素的纳米递送系统,强调了它们在提高冬凌草甲素在肿瘤学中的临床适用性方面的潜力。尽管在推进冬凌草甲素纳米递送研究方面已经取得了一些进展,但距离临床应用仍显不足,需要进一步研究。