formulation design and development of self-nanoemulsifying drug delivery systems containing a hydrophobic selective β1-adrenoreceptor blocker
نویسندگان
چکیده
the present work was aimed to design and develop self-nanoemulsifying drug delivery systems (snedds) with the objective to overcome the problems associated with the delivery of talinolol, a hydrophobic and poorly bioavailable drugs having ph dependant solubility. the solubility of talinolol in various oils, surfactants, cosurfactants and aqueous phases were determined to identify and select the best combination with proper dose incorporation. various surfactants and co-surfactants were screened for their ability to emulsify the selected oil. the area of nanoemulsification formation for the selected systems was identified by constructing the pseudoternary phase diagrams. the resulted nanoemulsions were found to be transparent without any phase separation and precipitation of drug. the influence of drug incorporation and ph of the dilution medium was also assessed on the phase behavior and droplet size of the selected systems. the developed formulations needed less than 45% of surfactant and yielded nanoemulsion of droplet size in the range of 20-150 nm, which was not affected by the ph of the dilution medium. whereas, the corresponding monophasic region in the respective phase diagram decreased under the influence of drug incorporation and ph of the dilution medium. furthermore, the droplet sizes measured by transmission electron microscopy analysis were in agreement with the analysis using photon correlation spectroscopy. the release rate of designed snedds formulation was investigated using an in vitro dissolution test showed a complete drug release within 15 minutes irrespective of the ph of dissolution medium as compared with the plain drug, which showed a limited dissolution rate.
منابع مشابه
Formulation Design and Development of Self-Nanoemulsifying Drug Delivery Systems Containing a Hydrophobic Selective β1-Adrenoreceptor Blocker
The present work was aimed to design and develop self-nanoemulsifying drug delivery systems (SNEDDS) with the objective to overcome the problems associated with the delivery of talinolol, a hydrophobic and poorly bioavailable drugs having pH dependant solubility. The solubility of talinolol in various oils, surfactants, cosurfactants and aqueous phases were determined to identify and select the...
متن کاملdevelopment and optimization of sirolimus self nanoemulsifying drug delivery systems containing bioavailability enhancers
متن کامل
Formulation Development and Bioavailability Evaluation of a Self-nanoemulsifying Drug Delivery System (SNEDDS) of Atorvastatin Calcium
The main purpose of the present investigation is to enhance the solubility and bioavailability of poorly watersoluble atorvastatin calcium (ATR) through the self nanoemulsifying drug delivery system (SNEDDS).The components for self-nanoemulsion were identified by solubility studies and tendency for self-emulsification in various excipients. Sefsol 218, Cremophor RH 40 and Propylene glycol were ...
متن کاملFormulation Design and In vitro Evaluation of Berberine- Loaded Self-Nanoemulsifying Drug Delivery System
Purpose: To improve the oral bioavailability of berberine using a new self-nanoemulsifying drug delivery system (SNEDDS). Methods: Berberine SNEDDS was designed using solubility studies and phase diagram construction. A series of tests were carried out to study the effect of oil content, dilution, and drug loading on particle size. The morphology of the nanoemulsion was examined with a transmis...
متن کاملSelf-Nanoemulsifying Drug Delivery Systems Containing Plantago lanceolata-An Assessment of Their Antioxidant and Antiinflammatory Effects.
The most important components of Plantago lanceolata L. leaves are catalpol, aucubin, and acteoside (=verbascoside). These bioactive compounds possess different pharmacological effects: anti-inflammatory, antioxidant, antineoplastic, and hepatoprotective. The aim of this study was to protect Plantago lanceolata extract from hydrolysis and to improve its antioxidant effect using self-nano-emulsi...
متن کاملDesign and optimization of self-nanoemulsifying drug delivery systems for improved bioavailability of cyclovirobuxine D
BACKGROUND The main purpose of this research was to design a self-nanoemulsifying drug delivery system (SNEDDS) for improving the bioavailability of cyclovirobuxine D as a poorly water-soluble drug. MATERIALS AND METHODS Solubility trials, emulsifying studies, and pseudo-ternary phase diagrams were used to screen the SNEDDS formulations. The optimized drug-loaded SNEDDS was prepared at a mass...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
international journal of nanoscience and nanotechnologyناشر: iranian nano society
ISSN 1735-7004
دوره 6
شماره 3 2010
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023