Abstract
Intranasal administration is a non-invasive and effective way for the delivery of drugs to brain that circumvents the blood– brain barrier (BBB). Taking this into account it was planned to formulate a thermodynamically stable and infinite dilutable nanoemulsion (o/w) encapsulating Ropinirole (rop), an anti-Parkinson drug, using a surfactant in a minimum concentration that could improve its solubility, stability and intransnasal flux. Various surfactants, co-surfactants and their mixtures were screened for their ability to emulsify the selected oil. Ternary phase diagrams were constructed to locate the area of nanoemulsion for. The optimized formulation contained 2 mg of Ropinirole along with Sefsol 218 (10% v/v), tween 80 (18% v/v), Transcutol (18% v/v) and water (54% v/v) as matrix, surfactant, cosurfactant and aqueous phase respectively. The optimized formulation showed adequate drug release (72.23±9.56%), globule size (58.61±5.18), polydispersity (0.201), viscosity (31.42±6.97 mpas), and infinite dispersion capability. The ex vivo study showed significant high (p<0.005) drug translocation in different parts of Wister rat brain. From in vitro, ex vivo and in vivo results conclude the promising approach of intranasal Ropinirole nanoemulsion as a better management option for Parkinson’s disease.
Keywords: Ropinirole, Nanoemulsion, Thermodynamic stability, Phase diagram, Intratracheal intubation model, transmission electron microscopy, matrix
Current Nanoscience
Title:Formulation Development of Chitosan Coated Intra Nasal Ropinirole Nanoemulsion for Better Management Option of Parkinson: An In Vitro Ex Vivo Evaluation
Volume: 8 Issue: 3
Author(s): Gulam Mustafa, Sanjula Baboota, Alka Ahuja and Javed Ali
Affiliation:
Keywords: Ropinirole, Nanoemulsion, Thermodynamic stability, Phase diagram, Intratracheal intubation model, transmission electron microscopy, matrix
Abstract: Intranasal administration is a non-invasive and effective way for the delivery of drugs to brain that circumvents the blood– brain barrier (BBB). Taking this into account it was planned to formulate a thermodynamically stable and infinite dilutable nanoemulsion (o/w) encapsulating Ropinirole (rop), an anti-Parkinson drug, using a surfactant in a minimum concentration that could improve its solubility, stability and intransnasal flux. Various surfactants, co-surfactants and their mixtures were screened for their ability to emulsify the selected oil. Ternary phase diagrams were constructed to locate the area of nanoemulsion for. The optimized formulation contained 2 mg of Ropinirole along with Sefsol 218 (10% v/v), tween 80 (18% v/v), Transcutol (18% v/v) and water (54% v/v) as matrix, surfactant, cosurfactant and aqueous phase respectively. The optimized formulation showed adequate drug release (72.23±9.56%), globule size (58.61±5.18), polydispersity (0.201), viscosity (31.42±6.97 mpas), and infinite dispersion capability. The ex vivo study showed significant high (p<0.005) drug translocation in different parts of Wister rat brain. From in vitro, ex vivo and in vivo results conclude the promising approach of intranasal Ropinirole nanoemulsion as a better management option for Parkinson’s disease.
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Cite this article as:
Mustafa Gulam, Baboota Sanjula, Ahuja Alka and Ali Javed, Formulation Development of Chitosan Coated Intra Nasal Ropinirole Nanoemulsion for Better Management Option of Parkinson: An In Vitro Ex Vivo Evaluation, Current Nanoscience 2012; 8 (3) . https://dx.doi.org/10.2174/157341312800620331
DOI https://dx.doi.org/10.2174/157341312800620331 |
Print ISSN 1573-4137 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6786 |
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