Marzoli Francesca, Marianecci Carlotta, Rinaldi Federica, Passeri Daniele, Rossi Marco, Minosi Paola, Carafa Maria, Pieretti Stefano
Istituto Superiore di Sanità, National Center for Drug Research and Evaluation, 00161 Rome, Italy.
Department of Drug Chemistry and Technology, Sapienza University of Rome, 00185 Rome, Italy.
Pharmaceutics. 2019 Feb 1;11(2):62. doi: 10.3390/pharmaceutics11020062.
Ibuprofen is one of the non-steroidal anti-inflammatory drugs (NSAIDs) widely used to treat pain conditions. NSAIDs encounter several obstacles to passing across biological membranes. To overcome these constraints, we decided to study the effects of a new pH-sensitive formulation of niosomes containing Polysorbate 20 derivatized by Glycine and loaded with ibuprofen (NioIbu) in several animal models of pain in mice. We performed two tests commonly used to study acute antinociceptive activity, namely the writhing test and the capsaicin test. Our results demonstrated that NioIbu, administered 2 h before testing, reduced nociception, whereas the free form of ibuprofen was ineffective. In a model of inflammatory pain, hyperalgesia induced by zymosan, NioIbu induced a long-lasting reduction in hyperalgesia in treated mice. In a model of neuropathic pain induced by sciatic nerve chronic constriction, NioIbu reduced both neuropathy-induced allodynia and hyperalgesia. The results obtained in our experiments suggest that pH-sensitive niosomes containing Polysorbate 20 derivatized by Glycine is an effective model for NSAIDs delivery, providing durable antinociceptive effects and reducing the incidence of side effects.
布洛芬是广泛用于治疗疼痛病症的非甾体抗炎药(NSAIDs)之一。NSAIDs在穿过生物膜时会遇到几个障碍。为了克服这些限制,我们决定在几种小鼠疼痛动物模型中研究一种新的pH敏感型脂质体的效果,该脂质体含有经甘氨酸衍生化的聚山梨酯20并负载有布洛芬(NioIbu)。我们进行了两项常用于研究急性抗伤害感受活性的试验,即扭体试验和辣椒素试验。我们的结果表明,在测试前2小时给药的NioIbu可减轻伤害感受,而布洛芬的游离形式则无效。在酵母聚糖诱导的炎性疼痛模型中,NioIbu可使治疗小鼠的痛觉过敏得到持久减轻。在坐骨神经慢性压迫诱导的神经性疼痛模型中,NioIbu可减轻神经病变诱导的异常性疼痛和痛觉过敏。我们实验中获得的结果表明,含有经甘氨酸衍生化的聚山梨酯20的pH敏感型脂质体是一种有效的NSAIDs递送模型,可提供持久的抗伤害感受作用并降低副作用的发生率。