Zeta电位
体内
纳米颗粒
控制释放
惊厥
药理学
阳离子聚合
粒径
材料科学
癫痫
化学
核化学
纳米技术
医学
有机化学
生物
生物技术
物理化学
精神科
作者
Gülsel Yurtdaş Kırımlıoğlu,Yusuf́ Z. Menceloǵlu,Kevser Erol,Yasemin Yazan
标识
DOI:10.1080/02652048.2016.1234515
摘要
Objectives of this study were the delivery of gamma aminobutyric acid (GABA) into the brain by means of developing brain targeted, nanosized, non-toxic and biocompatible polymeric nanoparticles, and investigating their effectiveness in epilepsy. For this purpose, GABA conjugated N,N-dimethylacrylamide-based pegylated nanoparticles were designed and characterised for particle size, zeta potential, pH, morphology, DSC, XRD, FTIR, GABA quantification and in vitro release. Formulations showed smaller particle size, cationic zeta potential characteristic, possible GABA polymeric matrix interaction and prolonged release pattern. Brain responses were examined using epileptic rats. Both formulations prepared were found to increase latency of seizure, decrease ending time of convulsion, duration of severe convulsion and mortality rate significantly compared with GABA solution. When GABA concentration was measured in Stratum corsatum, there was no statistical difference between GABA solution and formulations. All findings suggested enhancement in all phases of seizures indicating efficient delivery of GABA into the brain via formulations.
科研通智能强力驱动
Strongly Powered by AbleSci AI