Özkan Burcu, Altuntaş Ebru, Ünlü Ümmühan, Doğan Hasan Hüseyin, Özsoy Yıldız, Çakır Koç Rabia
Graduate School of Natural and Applied Science, Yildiz Technical University, Istanbul 34220, Turkey.
Faculty of Pharmacy, Department of Pharmaceutical Technology, Istanbul University, Istanbul 34116, Turkey.
Pharmaceutics. 2023 Jul 31;15(8):2055. doi: 10.3390/pharmaceutics15082055.
The human respiratory syncytial virus (hRSV) is a major cause of serious lower respiratory infections and poses a considerable risk to public health globally. Only a few treatments are currently used to treat RSV infections, and there is no RSV vaccination. Therefore, the need for clinically applicable, affordable, and safe RSV prevention and treatment solutions is urgent. In this study, an ion-activated in situ gelling formulation containing the broad-spectrum antiviral 18β-glycyrrhetinic acid (GA) was developed for its antiviral effect on RSV. In this context, pH, mechanical characteristics, ex vivo mucoadhesive strength, in vitro drug release pattern, sprayability, drug content, and stability were all examined. Rheological characteristics were also tested using in vitro gelation capacity and rheological synergism tests. Finally, the cytotoxic and antiviral activities of the optimized in situ gelling formulation on RSV cultured in the human laryngeal epidermoid carcinoma (HEp-2) cell line were evaluated. In conclusion, the optimized formulation prepared with a combination of 0.5% / gellan gum and 0.5% / sodium carboxymethylcellulose demonstrated good gelation capacity and sprayability (weight deviation between the first day of the experiment (T0) and the last day of the experiment (T14) was 0.34%), desired rheological synergism (mucoadhesive force (Fb): 9.53 Pa), mechanical characteristics (adhesiveness: 0.300 ± 0.05 mJ), ex vivo bioadhesion force (19.67 ± 1.90 g), drug content uniformity (RSD%: 0.494), and sustained drug release over a period of 6 h (24.56% ± 0.49). The optimized formulation demonstrated strong anti-hRSV activity (simultaneous half maximal effective concentration (EC) = 0.05 µg/mL; selectivity index (SI) = 306; pre-infection EC = 0.154 µg/mL; SI = 100), which was significantly higher than that of ribavirin (EC = 4.189 µg/mL; SI = 28) used as a positive control against hRSV, according to the results of the antiviral activity test. In conclusion, this study showed that nasal in situ gelling spray can prevent viral infection and replication by directly inhibiting viral entry or modulating viral replication.
人呼吸道合胞病毒(hRSV)是严重下呼吸道感染的主要病因,对全球公共卫生构成相当大的风险。目前仅有少数几种治疗方法用于治疗RSV感染,且尚无RSV疫苗。因此,迫切需要临床适用、价格合理且安全的RSV预防和治疗解决方案。在本研究中,开发了一种含有广谱抗病毒药物18β-甘草次酸(GA)的离子激活原位凝胶制剂,以研究其对RSV的抗病毒作用。在此背景下,对pH值、机械特性、离体黏膜粘附强度、体外药物释放模式、喷雾性、药物含量和稳定性进行了全面考察。还通过体外凝胶化能力和流变学协同作用试验对流变学特性进行了测试。最后,评估了优化后的原位凝胶制剂对人喉表皮样癌(HEp-2)细胞系中培养的RSV的细胞毒性和抗病毒活性。综上所述,以0.5%结冷胶和0.5%羧甲基纤维素钠组合制备的优化制剂表现出良好的凝胶化能力和喷雾性(实验第一天(T0)与实验最后一天(T14)之间的重量偏差为0.34%)、理想的流变学协同作用(黏膜粘附力(Fb):9.53 Pa)、机械特性(粘附性:0.300±0.05 mJ)、离体生物粘附力(19.67±1.90 g)、药物含量均匀性(相对标准偏差(RSD%):0.494)以及6小时内药物的持续释放(24.56%±0.49)。抗病毒活性测试结果表明,优化后的制剂表现出强大的抗hRSV活性(同时半数最大有效浓度(EC)=0.05μg/mL;选择性指数(SI)=306;感染前EC=0.154μg/mL;SI=100),显著高于用作抗hRSV阳性对照的利巴韦林(EC=4.189μg/mL;SI=28)。综上所述,本研究表明鼻腔原位凝胶喷雾剂可通过直接抑制病毒进入或调节病毒复制来预防病毒感染和复制。