Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, 21521, Egypt.
Department of Pharmaceutics, Faculty of Pharmacy, Damanhour University, Egypt P.O. Box 22511, Damanhour, Egypt.
Int J Pharm. 2024 Aug 15;661:124449. doi: 10.1016/j.ijpharm.2024.124449. Epub 2024 Jul 9.
Despite the fact that several rheumatoid arthritis treatments have been utilized, none of them achieved complete joint healing and has been accompanied by several side effects that compromise patient compliance. This study aims to provide an effective safe RA treatment with minimum side effects through the encapsulation of melatonin (MEL) in hyalurosomes and loading these hyalurosomes in collagen thermos-sensitive poloxamer 407 (PCO) hydrogels, followed by their intra-articular administration in AIA model rats. In vitro characterization of MEL-hyalurosomes and PCO hydrogel along with in vivo evaluation of the selected formulation were conducted. Particle size, PDI and EE % of the selected formulation were 71.5 nm, 0.09 and 90 %. TEM micrographs demonstrated that the particles had spherical shape with no aggregation signs. Loading PCO hydrogels with MEL-hyalurosomes did not cause significant changes in pH although it increased its viscosity and injection time. FTIR analysis showed that no interactions were noted among the delivery system components. In vivo results revealed the superior effect of MEL-hyalurosomes PCO hydrogel over MEL-PCO hydrogel and blank PCO hydrogels in improving joint healing, cartilage repair, pannus formation and cell infiltrations. Also, MEL-hyalurosomes PCO hydrogel group showed comparable levels of TNF-α, IL1, MDA, NRF2 and HO-1 with the negative control group. These findings highlight the MEL encapsulation role in augmenting its pharmacological effects along with the synergistic effect of hyaluronic acid in hyalurosomes and collagen in PCO hydrogel in promoting joint healing.
尽管已经使用了几种类风湿关节炎治疗方法,但没有一种方法能实现完全的关节愈合,而且还伴随着许多副作用,降低了患者的依从性。本研究旨在通过将褪黑素(MEL)封装在透明质酸囊泡中,并将这些透明质酸囊泡载入胶原热敏泊洛沙姆 407(PCO)水凝胶中,随后在 AIA 模型大鼠的关节内给药,提供一种有效且安全的 RA 治疗方法,副作用最小。对 MEL-透明质酸囊泡和 PCO 水凝胶进行了体外表征,并对选定的配方进行了体内评价。选定配方的粒径、PDI 和 EE%分别为 71.5nm、0.09 和 90%。TEM 显微照片表明,这些颗粒具有球形形状,没有聚集的迹象。将 MEL-透明质酸囊泡载入 PCO 水凝胶中虽然增加了其粘度和注射时间,但对 pH 值没有显著影响。FTIR 分析表明,递药系统成分之间没有观察到相互作用。体内结果表明,MEL-透明质酸囊泡 PCO 水凝胶在改善关节愈合、软骨修复、血管翳形成和细胞浸润方面优于 MEL-PCO 水凝胶和空白 PCO 水凝胶。此外,MEL-透明质酸囊泡 PCO 水凝胶组与阴性对照组的 TNF-α、IL1、MDA、NRF2 和 HO-1 水平相当。这些发现强调了 MEL 包封在增强其药理作用中的作用,以及透明质酸囊泡中的透明质酸和 PCO 水凝胶中的胶原在促进关节愈合方面的协同作用。