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首页> 外文期刊>Nanotechnology >Design Expert (R) supported optimization and predictive analysis of selegiline nanoemulsion via the olfactory region with enhanced behavioural performance in Parkinson's disease
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Design Expert (R) supported optimization and predictive analysis of selegiline nanoemulsion via the olfactory region with enhanced behavioural performance in Parkinson's disease

机译:Design Expert(R)通过嗅觉区域支持司来吉兰纳米乳剂的优化和预测分析,并增强了帕金森氏病的行为表现

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Selegiline is a monoamine oxidase B (MAO-B) inhibitor and is used in the treatment of Parkinson's disease. The main problem associated with its oral administration is its low oral bioavailability (10%) due to its poor aqueous solubility and extensive first pass metabolism. The aim of the present research work was to develop a nanoemulsion loaded with selegiline for direct nose-to-brain delivery for the better management of Parkinson's disease. A quality by design (QbD) approach was used in a statistical multivariate method for the preparation and optimization of nanoemulsion. In this study, four independent variables were chosen, in which two were compositions and two were process variables, while droplet size, transmittance, zeta potential and drug release were selected as response variables. The optimized formulation was assessed for efficacy in Parkinson's disease using behavioural studies, namely forced swimming, locomotor, catalepsy, muscle coordination, akinesia and bradykinesia or pole test in Wistar rats. The observed droplet size, polydispersity index (PDI), refractive index, transmittance, zeta potential and viscosity of selegiline nanoemulsion were found to be 61.43 +/- 4.10 nm, 0.203 +/- 0.005, 1.30 +/- 0.01, 99.80 +/- 0.04%, -34 mV and 31.85 +/- 0.24 mPas respectively. Surface characterization studies demonstrated a spherical shape of nanoemulsion which showed 3.7 times enhancement in drug permeation as compared to drug suspension. The results of behaviour studies showed that treatment of haloperidol induced Parkinson's disease in rats with selegiline nanoemulsion (administered intranasally) showed significant improvement in behavioural activities in comparison to orally administered drug. These findings demonstrate that nanoemulsion could be a promising new drug delivery carrier for intranasal delivery of selegiline in the treatment of Parkinson's disease.
机译:司来吉兰是一种单胺氧化酶B(MAO-B)抑制剂,用于治疗帕金森氏病。其口服给药的主要问题是由于其水溶性差和首过代谢广泛,其口服生物利用度低(10%)。本研究工作的目的是开发一种载有司来吉兰的纳米乳剂,以直接鼻鼻给药,以更好地治疗帕金森氏病。统计多变量方法中使用质量设计(QbD)方法来制备和优化纳米乳液。在这项研究中,选择了四个独立变量,其中两个是成分,两个是过程变量,同时选择液滴大小,透射率,ζ电势和药物释放作为响应变量。使用行为研究评估了优化的制剂在帕金森氏病中的功效,这些行为研究是在Wistar大鼠中进行强迫游泳,运动,僵直,肌肉协调,运动障碍和运动迟缓或极点试验。司来吉兰纳米乳液的观察到的液滴尺寸,多分散指数(PDI),折射率,透射率,ζ电势和粘度为61.43 +/- 4.10 nm,0.203 +/- 0.005、1.30 +/- 0.01、99.80 +/-分别为0.04%,-34 mV和31.85 +/- 0.24 mPas。表面表征研究表明,纳米乳液呈球形,与药物悬浮液相比,其药物渗透性提高了3.7倍。行为研究的结果表明,与口服药物相比,司来吉兰纳米乳剂(鼻内给药)对氟哌啶醇诱导的帕金森氏病的治疗显示出明显的行为活性改善。这些发现表明,纳米乳剂可能是司来吉兰经鼻内递送治疗帕金森氏病的一种有希望的新药物递送载体。

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