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Brain targeted oral delivery of doxycycline hydrochloride encapsulated Tween 80 coated chitosan nanoparticles against ketamine induced psychosis: behavioral, biochemical, neurochemical and histological alterations in mice

机译:脑靶向口服盐酸多西环素包裹的吐温80包覆的壳聚糖纳米颗粒对氯胺酮诱发的精神病的作用:小鼠的行为,生化,神经化学和组织学改变

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Abstract To develop statistically optimized brain targeted Tween 80 coated chitosan nanoparticulate formulation for oral delivery of doxycycline hydrochloride for the treatment of psychosis and to evaluate its protective effect on ketamine induced behavioral, biochemical, neurochemical and histological alterations in mice. 32 full factorial design was used to optimize the nanoparticulate formulation to minimize particle size and maximize entrapment efficiency, while independent variables chosen were concentration of chitosan and Tween 80. The optimized formulation was characterized by particle size, drug entrapment efficiency, Fourier transform infrared, Transmission electron microscopy analysis and drug release behavior. Pure doxycycline hydrochloride (25 and 50?mg/kg, p.o.) and optimized doxycycline hydrochloride encapsulated Tween 80 coated chitosan nanoparticles (DCNPopt) (equivalent to 25?mg/kg doxycycline hydrochloride, p.o.) were explored against ketamine induced psychosis in mice. The experimental studies for DCNPopt, with mean particle size 237?nm and entrapment efficiency 78.16%, elucidated that the formulation successfully passed through blood brain barrier and exhibited significant antipsychotic activity. The underlying mechanism of action was further confirmed by behavioral, biochemical, neurochemical estimations and histopathological study. Significantly enhanced GABA and GSH level and diminished MDA, TNF-α and dopamine levels were observed after administration of DCNPopt at just half the dose of pure doxycycline hydrochloride, showing better penetration of doxycyline hydrochloride in the form of Tween 80 coated nanoparticles through blood brain barrier. This study demonstrates the hydrophilic drug doxycycline hydrochloride, loaded in Tween 80 coated chitosan nanoparticles, can be effectively brain targeted through oral delivery and therefore represents a suitable approach for the treatment of psychotic symptoms.
机译:摘要目的开发经统计学优化的脑靶向吐温80包被的壳聚糖纳米颗粒制剂,用于口服多西环素盐酸盐治疗精神病,并评估其对氯胺酮诱导的小鼠行为,生化,神经化学和组织学改变的保护作用。 3 2 全因子设计用于优化纳米颗粒制剂,以最小化粒径和最大包封率,而选择的独立变量是壳聚糖和吐温80的浓度。优化后的制剂的特征在于粒径,药物包封率,傅立叶变换红外光谱,透射电镜分析和药物释放行为。探索了纯盐酸多西环素(25和50?mg / kg,口服)和优化的盐酸多西环素包裹的吐温80包被的壳聚糖纳米颗粒(DCNP opt )(相当于25?mg / kg盐酸多西环素,口服)。对抗氯胺酮诱发的小鼠精神病。对DCNP opt 的实验研究,平均粒径为237?nm,包封率为78.16%,说明该制剂成功通过了血脑屏障,并表现出显着的抗精神病活性。行为,生化,神经化学估计和组织病理学研究进一步证实了潜在的作用机理。仅以纯盐酸多西环素的一半剂量施用DCNP opt 后,观察到GABA和GSH水平显着提高,MDA,TNF-α和多巴胺水平降低,这表明盐酸多西环素以吐温80涂层的纳米颗粒通过血脑屏障。这项研究表明,装载在吐温80包被的壳聚糖纳米颗粒中的亲水性药物强力霉素盐酸盐可以通过口服递送有效地靶向大脑,因此代表了一种治疗精神病症状的合适方法。

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