Department of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, Beijing 100850, China; School of Medicine, Shandong University of Traditional Chinese Medicine, Jinan 250355, China.
Department of Pharmaceutical Sciences, Beijing Institute of Radiation Medicine, Beijing 100850, China; Anhui Medical University, Hefei 230032, China.
Int J Pharm. 2020 Jun 15;583:119384. doi: 10.1016/j.ijpharm.2020.119384. Epub 2020 May 1.
The brain is the most sensitive organ to microwave radiation. However, few effective drugs are available for the treatment of microwave-induced brain injury due to the poor drug permeation into the brain. Here, intranasal tetrandrine (TET) temperature-sensitive in situ hydrogels (ISGs) were prepared with poloxamers 407 and 188. Its characteristics were evaluated, including rheological properties, drug release in vitro, and mucosal irritation. The pharmacodynamics and brain-targeting effects were also studied. The highly viscous ISGs remained in the nasal cavity for a long time with the sustained release of TET and no obvious ciliary toxicity. Intranasal temperature-sensitive TET ISGs markedly improved the spatial memory and spontaneous exploratory behavior induced by microwave with the Morris water maze (MWM) and the open field test (OFT) compared to the model. The ISGs alleviated the microwave-induced brain damage and inhibited the certain mRNA expressions of calcium channels in the brain. Intranasal temperature-sensitive TET ISGs was rapidly absorbed with a shorter T (4.8 h) compared to that of oral TET (8.4 h). The brain targeting index of intranasal temperature-sensitive TET ISGs was as 2.26 times as that of the oral TET. Intranasal temperature-sensitive TET ISGs are a promising brain-targeted medication for the treatment of microwave-induced brain injury.
大脑是对微波辐射最敏感的器官。然而,由于药物难以渗透到大脑中,因此治疗微波诱导的脑损伤的有效药物很少。本文制备了聚氧乙烯醚 407 和 188 鼻内四氢巴马汀(TET)温敏原位凝胶(ISG)。对其流变性能、体外药物释放和黏膜刺激性进行了评价。还研究了其药效学和脑靶向作用。高粘性 ISG 可在鼻腔中长时间停留,TET 持续释放,且无明显纤毛毒性。与模型组相比,鼻内温敏 TET-ISG 通过 Morris 水迷宫(MWM)和旷场试验(OFT)显著改善了微波诱导的空间记忆和自发探索行为。ISG 减轻了微波诱导的脑损伤,并抑制了脑内钙通道的某些 mRNA 表达。与口服 TET(8.4 h)相比,鼻内温敏 TET-ISG 的吸收更快,T(4.8 h)更短。鼻内温敏 TET-ISG 的脑靶向指数是口服 TET 的 2.26 倍。鼻内温敏 TET-ISG 是一种有前途的治疗微波诱导脑损伤的脑靶向药物。