Peng Xiong, Yang Yuping, Guo Chenqi, He Qin, Li Yan, Gong Tao, Li Jia
Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu, China.
Sichuan Institute for Drug Control, NMPA Key Laboratory for Quality Control and Evaluation of Vaccines and Biological Products, Chengdu, China.
Front Pharmacol. 2023 Jul 20;14:1210129. doi: 10.3389/fphar.2023.1210129. eCollection 2023.
Berberine (BBR) has a long history of use in the treatment of Rheumatoid arthritis (RA) and is considered one of the most promising natural product for the treatment of RA. However, oral administration of berberine has low bioavailability and requires frequent administration, resulting in poor patient compliance. In this study, we developed a BBR-loaded phospholipid-based phase separation gel (BBR-PPSG) to achieve sustained drug release and long-term therapeutic effect. The stability of BBR-PPSG was verified and it was found that it can be stored for a long time. The pharmacokinetic study on rats and rabbits showed that BBR-PPSG not only achieved 1-month of sustained release, but also significantly increased the area under the curve (AUC) by nearly 9-fold and prolonged the half-life (t) by 10-fold. By constructing rat and rabbit models of RA, we also proved that BBR-PPSG administration once a month effectively alleviated joint swelling, and significantly reduce TNF-α levels in AIA rats and OIA rabbits. Histopathological analysis of rabbit joint sections revealed that after intra-articular injection of BBR-PPSG, the synovial cell layer remained intact, while in the model group, the synovial cells were significantly reduced and exhibited necrosis. MicroCT data analysis showed that the values of Tb.N and Tb. Sp in the BBR-PPSG group were significantly better than those in the model group ( < 0.05). This study addressed the limitations of frequent administration of BBR by developing a phospholipid-based phase separation gel system for berberine delivery, achieving long-term sustained release. The BBR-PPSG demonstrated good biocompatibility, simple preparation and excellent stability, thus holding potential as a novel pharmaceutical formulation for RA treatment.
黄连素(BBR)在治疗类风湿性关节炎(RA)方面有着悠久的应用历史,被认为是治疗RA最有前景的天然产物之一。然而,口服黄连素生物利用度低,需要频繁给药,导致患者依从性差。在本研究中,我们开发了一种载有BBR的磷脂基相分离凝胶(BBR-PPSG),以实现药物的持续释放和长期治疗效果。验证了BBR-PPSG的稳定性,发现其可长期储存。对大鼠和兔子的药代动力学研究表明,BBR-PPSG不仅实现了1个月的持续释放,还使曲线下面积(AUC)显著增加了近9倍,半衰期(t)延长了10倍。通过构建大鼠和兔子的RA模型,我们还证明每月一次给予BBR-PPSG可有效减轻关节肿胀,并显著降低佐剂性关节炎(AIA)大鼠和胶原诱导性关节炎(OIA)兔子的肿瘤坏死因子-α(TNF-α)水平。对兔子关节切片的组织病理学分析显示,关节腔内注射BBR-PPSG后,滑膜细胞层保持完整,而在模型组中,滑膜细胞显著减少并出现坏死。显微CT数据分析表明,BBR-PPSG组的骨小梁数量(Tb.N)和骨小梁间距(Tb.Sp)值显著优于模型组(P<0.05)。本研究通过开发一种用于黄连素递送的磷脂基相分离凝胶系统,解决了BBR频繁给药的局限性,实现了长期持续释放。BBR-PPSG表现出良好的生物相容性、制备简单和优异的稳定性,因此作为一种治疗RA的新型药物制剂具有潜力。