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Thermoreversible mucoadhesive in situ nasal gel for treatment of Parkinson's disease

机译:用于治疗帕金森病的热处理粘膜粘附性

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Parkinson's disease is a degenerative disorder of the central nervous system (CNS). The most obvious symptoms are movement-related such as shaking, rigidity, slowness of movement and difficulty with walking, rigid muscular movements and difficulty in chewing and swallowing especially solid dosage forms. Ropinirole is an anti-Parkinson drug that has low oral bioavailability which is primarily due to first-pass metabolism. The objective of proposed work was to increase bioavailability of ropinirole and avoid patient discomfort by formulating thermoreversible in situ nasal gel. Thermoreversible nasal gels were prepared by cold method using Pluronic F-127 and hydroxy methyl propyl cellulose (HPMC K4M) as gelling agents. Formulations were evaluated for various parameters such as drug content, pH, gelling time, gelling temperature, gel strength, mucoadhesive force, ex vivo diffusion, histological studies and in vivo bioavailability. Formulations displayed gelation at nasal temperature and the gelation time was found to be less than mucociliary clearance time. The nasal residence time was seen to be increased due to mucoadhesion and increased gel strength. The nasal gel formulations showed ex vivo drug release between 56-100% in 5 h. Histological study of sheep nasal mucosa revealed that the gel had a protective effect on the mucosa unlike plain ropinirole which showed evidence of moderate cellular damage. A fivefold increase in bioavailability in brain was observed on nasal administration as compared to IV route. Thermoreversible in situ nasal gel was found to a promising drug delivery for Parkinsonian patients.
机译:帕金森病是中枢神经系统(CNS)的退行性疾病。最明显的症状是与运动相关的运动,例如摇晃,刚性,慢慢缓慢,难以携带,刚性肌肉运动和呼吸困难,咀嚼尤其是固体剂型。罗比里尔是一种抗帕金森药物,其具有低口服生物利用度,主要是由于首述的代谢。拟议工作的目的是增加罗比里尔的生物利用度,并避免在原位鼻凝胶中配制热可视性的患者不适。通过使用Pluronic F-127和羟基甲基丙基纤维素(HPMC K4M)作为胶凝剂,通过冷法制备热可逆的鼻凝胶。评估配方,例如药物含量,pH,胶凝时间,胶凝温度,凝胶强度,粘液粘附力,离体扩散,组织学研究和体内生物利用度等各种参数。制剂在鼻温下显示出凝胶化,发现凝胶化时间小于粘蛋白清除时间。由于粘膜粘附和增加的凝胶强度,鼻立停留时间被视为增加。鼻凝胶配方显示出56小时的56-100%之间的离体药物释放。绵羊鼻腔的组织学研究表明,凝胶对粘膜的保护作用不同,与普通的罗比里尔有显示出中度细胞损伤的证据。与IV途径相比,在鼻给药中观察到脑中生物利用度的五倍增加。对帕金森患者的有希望的药物递送,发现了原位鼻凝胶的热处理。

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