Tanori Mirella, Pitaro Michele, Fratini Emiliano, Colantoni Eleonora, Amoresano Angela, Celentano Simona, Chiaramonte Barbara, Mancuso Mariateresa
Laboratory of Biomedical Technologies, Italian National Agency for New Technologies, Energy and Sustainable Economic Development (ENEA), Via Anguillarese 301, 00123 Rome, Italy.
INBB-Biostructures and Biosystems National Institute, Viale delle Medaglie d'Oro 305, 00136 Rome, Italy.
Pharmaceutics. 2023 Feb 9;15(2):591. doi: 10.3390/pharmaceutics15020591.
Hexedra+ is a nasal spray containing hydroxypropyl methylcellulose, beta-cyclodextrin, and usnic acid. It has been developed with the aim of reducing the risk of transmission of airborne viral infections, with particular reference to influenza and COVID-19. As part of the preclinical development of the product, we carried out a study on thirty male Wistar rats divided into three study groups and treated with Hexedra+, an alternative formulation containing a double concentration of usnic acid (0.015% instead of 0.0075%) or saline solution. Products were administered at the dose of 30 μL into each nostril, three times a day for seven consecutive days by means of a micropipette. By the end of the treatment period, no significant changes were observed in body weight. Histological examination of nasal mucosa and soft organs did not show any significant difference in the three study groups. Serum transaminase level remained in the normal limit in all the animals treated. The serum level of usnic acid was measured in order to assess the absorption of the molecule through the nasal mucosa. By the end of the study period, the usnic acid serum level was negligible in all the animals treated. In conclusion, the safety profile of Hexedra+ appears favorable in the animal model studied.
Hexedra+是一种含有羟丙基甲基纤维素、β-环糊精和松萝酸的鼻喷雾剂。其研发目的是降低空气传播病毒感染的传播风险,尤其针对流感和新冠病毒。作为该产品临床前开发的一部分,我们对30只雄性Wistar大鼠进行了一项研究,将它们分为三个研究组,分别用Hexedra+、一种含有双倍松萝酸浓度(0.015%而非0.0075%)的替代制剂或生理盐水进行治疗。通过微量移液器,以每侧鼻孔30μL的剂量,连续7天每天给药3次。到治疗期结束时,未观察到体重有显著变化。鼻黏膜和软组织器官的组织学检查显示,三个研究组之间没有任何显著差异。所有接受治疗的动物血清转氨酶水平均保持在正常范围内。为了评估该分子通过鼻黏膜的吸收情况,检测了松萝酸的血清水平。到研究期结束时,所有接受治疗的动物血清中的松萝酸水平均可忽略不计。总之,在我们所研究的动物模型中,Hexedra+的安全性表现良好。