氯喹诺尔
PLGA公司
药理学
化学
MTT法
神经保护
活力测定
活性氧
细胞培养
氧化应激
体内
生物物理学
细胞
体外
生物化学
医学
生物
遗传学
生物技术
作者
Emilia Barcia,Alaa H. Salama,Ana Fernández-Carballido,Sofı́a Negro
标识
DOI:10.3109/1061186x.2010.523789
摘要
Background: Clioquinol (CQ), a metal chelator, has gained renewed attention due to its ability to modulate metal homeostasis in neurodegenerative disorders such as Alzheimer's disease.Purpose: To investigate the protective effects of a wide range of concentrations of CQ on two human neuroblastoma cell lines (IMR-32 and SKN-AS) and to develop and characterize a new controlled release system of CQ consisting of biodegradable microspheres.Results: H2O2 (400 μM) adequately induced death cell in IMR-32 and SKN-AS cell lines thereby resulting in a useful model for neuroprotective studies. CQ (20–50 μM) induced a potent and robust protective effect against peroxide-mediated oxidative stress in human neuronal-like cells (SKN-AS) determined by both MTT and flow cytometry (cell viability). These results were also confirmed by means of reactive oxygen species (ROS) production. Biodegradable poly(dl-lactic-co-glycolic acid) (PLGA) resomers assayed for microspheres preparation were PLGA-502 and PLGA-502H. Optimization by using an experimental design resulted in a formulation prepared with CQ (112 mg) and PLGA-502H (400 mg). With this formulation, mean encapsulation efficiency of 82.37% ± 6.67% and, zero-order release rate of 58 ± 3µg CQ/day/10 mg microspheres between Days 10 and 35 were obtained.Conclusion: We have developed a promising formulation for the treatment of Alzheimer's disease.
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