Central Lab, Faculty of Pharmacy, Damanhour University, Damanhour, Egypt.
Department of Pharmaceutics, Faculty of Pharmacy, Alexandria University, Alexandria, Egypt.
Drug Deliv. 2022 Dec;29(1):652-663. doi: 10.1080/10717544.2022.2041130.
Novel intra-articular nanoreservoirs were implemented employing different cartilage targeting approaches to improve cartilage bioavailability of a chondroprotective drug, cassic acid (CA), for effective amelioration of cartilage deterioration off-targeting CA gastrointestinal disorders. Herein, we compared active cartilage-targeting approach via chondroitin sulfate (CHS) functionalization versus passive targeting using positively charged nanoparticles to target negatively charged cartilage matrix. Firstly, CA integrated nanoreservoirs (CA-NRs) were fabricated based on ionic conjugation between CA and cationic hydrophobic surface modifier octadecylamine (ODA) and were further functionalized with CHS to develop CHS-CA-NRs. Confocal laser microscope was used to visualize the accumulation of nanoparticles into the cartilage tissue. Both targeting approaches promoted CA local cartilage availability and prolonged its residence time. Compared to passive targeted CA-NRs, active targeted CHS-CA-NRs showed higher fluorescence signals in proximity to and inside chondrocytes which lasted for up to 21 days. In MIA-osteoarthritic rats, CHS-CA-NRs showed superior antiosteoarthritic activity, exhibiting highest cartilage repair compared to CA-NRs. Additionally, CHS-CA-NRs significantly inhibited OA inflammatory cytokine, degradation enzyme and oxidative stress and improved cartilage matrix biosynthesis. Conclusively, CHS-CA-NRs improved OA repair showing a superior efficacy for articular cartilage targeting with CHS which could be a potential advance for OA therapy.
新型关节内纳米储库采用了不同的软骨靶向方法,以提高软骨保护药物硫酸软骨素(chondroitin sulfate,CHS)的软骨生物利用度,有效改善软骨靶向 CA 胃肠道疾病的恶化。在此,我们比较了通过硫酸软骨素(chondroitin sulfate,CHS)功能化的主动软骨靶向方法与通过带正电荷的纳米颗粒被动靶向带负电荷的软骨基质的方法。首先,通过 CA 与疏水性阳离子表面改性剂十八胺(octadecylamine,ODA)之间的离子键合,制备了 CA 纳米储库(CA-NRs),并进一步用 CHS 进行功能化,以开发 CHS-CA-NRs。共聚焦激光显微镜用于观察纳米颗粒在软骨组织中的积累。这两种靶向方法都促进了 CA 在局部软骨中的可用性,并延长了其驻留时间。与被动靶向 CA-NRs 相比,主动靶向 CHS-CA-NRs 在软骨细胞附近和内部显示出更高的荧光信号,持续时间长达 21 天。在 MIA 骨关节炎大鼠中,CHS-CA-NRs 表现出更好的抗骨关节炎活性,与 CA-NRs 相比,表现出最高的软骨修复。此外,CHS-CA-NRs 显著抑制 OA 炎症细胞因子、降解酶和氧化应激,提高软骨基质生物合成。总之,CHS-CA-NRs 改善了 OA 修复,通过 CHS 对关节软骨靶向具有更好的疗效,这可能是 OA 治疗的一个潜在进展。