Mikhel Iosif, Bakhrushina Elena, Stepanova Olga, Prilepskaya Sofiya, Kosenkov Dmitriy, Belyatskaya Anastasia, Evzikov Grigory, Demina Natalia, Krasnyuk Ivan, Krasnyuk Ivan
Department of Pharmaceutical Technology, A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow119048, Russia.
Department of Pharmacology, A.P. Nelyubin Institute of Pharmacy, I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow119048, Russia.
Curr Drug Deliv. 2024 Aug 26. doi: 10.2174/0115672018305548240614113451.
Ribavirin has been used as an antiviral agent to treat a variety of viral infections since the 1970s. Over the past few decades, studies have been conducted on the pharmacology of ribavirin, and the possibility of its use in new indications has been explored. According to the results of a number of studies, ribavirin efficacy in the therapy of malignant neoplasms of various genesis has been proven. Furthermore, due to the complexity of brain tumor therapy using surgical methods, targeted delivery of ribavirin to the brain becomes a promising alternative to existing treatment methods. Targeting of active pharmaceutical ingredient (API) to the brain tumor is achieved by intranasal drug delivery via a Nose-to-Brain mechanism. In addition, using this delivery mechanism, it is possible to reach the brain while bypassing the blood-brain barrier (BBB), thus avoiding the effects of the first passage through the liver. Despite the significant advantages of the method, there are limiting factors to its application - mucociliary clearance, which aims to remove foreign bodies from the surface of the nasal mucosa. In situ, systems are able to reduce the intensity of interfering factors on API and allow the achievement of maximum bioavailability during intranasal administration.
自20世纪70年代以来,利巴韦林一直被用作抗病毒药物来治疗各种病毒感染。在过去几十年里,人们对利巴韦林的药理学进行了研究,并探索了其在新适应症中的应用可能性。根据多项研究结果,利巴韦林在治疗各种起源的恶性肿瘤方面的疗效已得到证实。此外,由于使用手术方法治疗脑肿瘤的复杂性,将利巴韦林靶向递送至脑部成为现有治疗方法的一个有前景的替代方案。通过鼻脑机制经鼻给药可实现活性药物成分(API)向脑肿瘤的靶向递送。此外,利用这种给药机制,可以绕过血脑屏障(BBB)到达脑部,从而避免首过肝脏的影响。尽管该方法具有显著优势,但其应用存在限制因素——黏液纤毛清除,其目的是从鼻黏膜表面清除异物。原位系统能够降低干扰因素对API的影响强度,并在鼻腔给药期间实现最大生物利用度。