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Design, synthesis and biological evaluation of brain targeting L-ascorbic acid prodrugs of ibuprofen with 'lock-in' function

机译:具有“锁定”功能的布洛芬靶向脑的L-抗坏血酸前药的设计,合成和生物学评估

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摘要

A novel brain targeting L-ascorbic acid derivatives with "lock-in" function were designed and synthesized as prodrugs to achieve the effective delivery of ibuprofen to brain by glucose transporter 1 (GLUT(1)) and the Na+-dependent vitamin C transporter SVCT2. Ibuprofen-loaded four prodrugs were tested in the animals. Results from the in vivo distribution study after i.v. administration of these four prodrugs and naked ibuprofen indicated that four prodrugs exhibited excellent transport ability across the BBB and significantly increased the level of ibuprofen in brain. Among them, prodrugs 4 showed higher brain concentration. Both biodistribution data and pharmacokinetic parameters suggested that L-ascorbic acid thiamine disulfide delivery system was a promising carrier to enhance CNS drug's delivery ability into brain. (C) 2014 Elsevier Masson SAS. All rights reserved.
机译:设计并合成了具有“锁定”功能的靶向L-抗坏血酸衍生物的新型大脑作为前药,以通过葡萄糖转运蛋白1(GLUT(1))和Na +依赖性维生素C转运蛋白SVCT2实现布洛芬向大脑的有效递送。 。在动物中测试了布洛芬负载的四种前药。静脉注射后体内分布研究的结果施用这四种前药和裸露的布洛芬表明,四种前药在BBB上表现出出色的转运能力,并显着提高了脑中布洛芬的水平。其中,前药4显示出较高的大脑集中度。生物分布数据和药代动力学参数均表明,L-抗坏血酸硫胺素二硫化物输送系统是增强中枢神经系统药物向大脑输送能力的有前途的载体。 (C)2014 Elsevier Masson SAS。版权所有。

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