The Experts below are selected from a list of 72 Experts worldwide ranked by ideXlab platform

Weilung Tseng - One of the best experts on this subject based on the ideXlab platform.

Jasjeet K. Sahni - One of the best experts on this subject based on the ideXlab platform.

  • Mechanistic approach for the development of ultrafine oil-water emulsions using monoglyceride and blends of medium and long chain triglycerides: enhancement of the solubility and bioavailability of Perphenazine.
    2020
    Co-Authors: Sanjula Baboota, Gulam Mustafa, Jasjeet K. Sahni
    Abstract:

    A kinetically stable ultra-fine oil-water (o/w) emulsion containing Perphenazine and blends of long and medium chain triglycerides was prepared. The purpose of the ultra-fine emulsion was to increase the oral bioavailability of Perphenazine. The formulations were prepared using a low energy emulsification phase titration method. The optimized formulations consisted of blends of linseed oil and Sefsol 218 (1:1) (oil phase), Polysorbate 40 (surfactant), polyethylene glycol 400 (cosurfactant) and distilled water (dispersion medium). Characterization of viscosity, refractive index, particle size distribution, spectral transmittance and surface morphology of the formulations was performed. The release rate of Perphenazine from the formulations was quantified using the everted gut sac of rat intestinal mucosa. The ex vivo release data demonstrated that the formulated nanoemulsions increased significantly the permeation rate of Perphenazine when compared with a suspension. Following oral administration of selected nanoemulsions in Wistar rats, the AUC and C max of Perphenazine increased by 2.9 and 2.54-fold respectively compared with the Perphenazine suspension. The observed increase in bioavailability may be due to the increase in the dissolution rate from the molecularly dissolved drug in the oil phase and an increased rate of dispersion of the drug in the gastrointestinal (GI) tract which leads to greater absorption into the blood.

  • Mechanistic approach for the development of ultrafine o/w emulsions using blends medium and long chain triglycerides: solubility and bioavailability enhancement of perphenazine
    Journal of Excipients and Food Chemicals, 2013
    Co-Authors: Sanjula Baboota, Abdullah Abdullah, Gulam Mustafa, Jasjeet K. Sahni
    Abstract:

    A thermodynamically stable ultrafine (o/w) emulsion containing perphenazine for solubility and oral bioavailability enhancement using blends of long and medium chain triglyceride was developed. Formulation was prepared using low energy emulsification phase titration method. The optimized formulations consisted of blend of linseed and sefsol 218 (1:1), Polysorbate 40, polyethylene glycol 400 and distilled water as an oil, surfactant, cosurfactant and dispersion phase respectively. The formulations were characterized on the basis of viscosity, refractive index, particle size distribution, spectral transmittance and surface morphology. Formulations were evaluated for release study by everted gut sac using intestinal mucosa. The ex vivo release data showed that nanoemulsions significantly increased the permeation rate of perphenazine over the simple suspension. Following oral administration of nanoemulsion in wistar rats, both AUC and C max of perphenazine increased by 2.9 fold and 2.54-fold respectively compared with the perphenazine suspension. The resultant bioavailability might be due to increased solubility, bypassing the first-pass metabolism through lymphatic absorption and enhanced permeation potential of perphenazine.

Sanjula Baboota - One of the best experts on this subject based on the ideXlab platform.

  • Mechanistic approach for the development of ultrafine oil-water emulsions using monoglyceride and blends of medium and long chain triglycerides: enhancement of the solubility and bioavailability of Perphenazine.
    2020
    Co-Authors: Sanjula Baboota, Gulam Mustafa, Jasjeet K. Sahni
    Abstract:

    A kinetically stable ultra-fine oil-water (o/w) emulsion containing Perphenazine and blends of long and medium chain triglycerides was prepared. The purpose of the ultra-fine emulsion was to increase the oral bioavailability of Perphenazine. The formulations were prepared using a low energy emulsification phase titration method. The optimized formulations consisted of blends of linseed oil and Sefsol 218 (1:1) (oil phase), Polysorbate 40 (surfactant), polyethylene glycol 400 (cosurfactant) and distilled water (dispersion medium). Characterization of viscosity, refractive index, particle size distribution, spectral transmittance and surface morphology of the formulations was performed. The release rate of Perphenazine from the formulations was quantified using the everted gut sac of rat intestinal mucosa. The ex vivo release data demonstrated that the formulated nanoemulsions increased significantly the permeation rate of Perphenazine when compared with a suspension. Following oral administration of selected nanoemulsions in Wistar rats, the AUC and C max of Perphenazine increased by 2.9 and 2.54-fold respectively compared with the Perphenazine suspension. The observed increase in bioavailability may be due to the increase in the dissolution rate from the molecularly dissolved drug in the oil phase and an increased rate of dispersion of the drug in the gastrointestinal (GI) tract which leads to greater absorption into the blood.

  • Mechanistic approach for the development of ultrafine o/w emulsions using blends medium and long chain triglycerides: solubility and bioavailability enhancement of perphenazine
    Journal of Excipients and Food Chemicals, 2013
    Co-Authors: Sanjula Baboota, Abdullah Abdullah, Gulam Mustafa, Jasjeet K. Sahni
    Abstract:

    A thermodynamically stable ultrafine (o/w) emulsion containing perphenazine for solubility and oral bioavailability enhancement using blends of long and medium chain triglyceride was developed. Formulation was prepared using low energy emulsification phase titration method. The optimized formulations consisted of blend of linseed and sefsol 218 (1:1), Polysorbate 40, polyethylene glycol 400 and distilled water as an oil, surfactant, cosurfactant and dispersion phase respectively. The formulations were characterized on the basis of viscosity, refractive index, particle size distribution, spectral transmittance and surface morphology. Formulations were evaluated for release study by everted gut sac using intestinal mucosa. The ex vivo release data showed that nanoemulsions significantly increased the permeation rate of perphenazine over the simple suspension. Following oral administration of nanoemulsion in wistar rats, both AUC and C max of perphenazine increased by 2.9 fold and 2.54-fold respectively compared with the perphenazine suspension. The resultant bioavailability might be due to increased solubility, bypassing the first-pass metabolism through lymphatic absorption and enhanced permeation potential of perphenazine.

Navideh Anarjan - One of the best experts on this subject based on the ideXlab platform.

  • effects of selected Polysorbate and sucrose ester emulsifiers on the physicochemical properties of astaxanthin nanodispersions
    Molecules, 2013
    Co-Authors: Navideh Anarjan
    Abstract:

    The effects of selected nonionic emulsifiers on the physicochemical characteristics of astaxanthin nanodispersions produced by an emulsification/evaporation technique were studied. The emulsifiers used were Polysorbates (Polysorbate 20, Polysorbate 40, Polysorbate 60 and Polysorbate 80) and sucrose esters of fatty acids (sucrose laurate, palmitate, stearate and oleate). The mean particle diameters of the nanodispersions ranged from 70 nm to 150 nm, depending on the emulsifier used. In the prepared nanodispersions, the astaxanthin particle diameter decreased with increasing emulsifier hydrophilicity and decreasing carbon number of the fatty acid in the emulsifier structure. Astaxanthin nanodispersions with the smallest particle diameters were produced with Polysorbate 20 and sucrose laurate among the Polysorbates and the sucrose esters, respectively. We also found that the Polysorbate 80- and sucrose oleate-stabilized nanodispersions had the highest astaxanthin losses (i.e., the lowest astaxanthin contents in the final products) among the nanodispersions. This work demonstrated the importance of emulsifier type in determining the physicochemical characteristics of astaxanthin nano-dispersions.

Gulam Mustafa - One of the best experts on this subject based on the ideXlab platform.

  • Mechanistic approach for the development of ultrafine oil-water emulsions using monoglyceride and blends of medium and long chain triglycerides: enhancement of the solubility and bioavailability of Perphenazine.
    2020
    Co-Authors: Sanjula Baboota, Gulam Mustafa, Jasjeet K. Sahni
    Abstract:

    A kinetically stable ultra-fine oil-water (o/w) emulsion containing Perphenazine and blends of long and medium chain triglycerides was prepared. The purpose of the ultra-fine emulsion was to increase the oral bioavailability of Perphenazine. The formulations were prepared using a low energy emulsification phase titration method. The optimized formulations consisted of blends of linseed oil and Sefsol 218 (1:1) (oil phase), Polysorbate 40 (surfactant), polyethylene glycol 400 (cosurfactant) and distilled water (dispersion medium). Characterization of viscosity, refractive index, particle size distribution, spectral transmittance and surface morphology of the formulations was performed. The release rate of Perphenazine from the formulations was quantified using the everted gut sac of rat intestinal mucosa. The ex vivo release data demonstrated that the formulated nanoemulsions increased significantly the permeation rate of Perphenazine when compared with a suspension. Following oral administration of selected nanoemulsions in Wistar rats, the AUC and C max of Perphenazine increased by 2.9 and 2.54-fold respectively compared with the Perphenazine suspension. The observed increase in bioavailability may be due to the increase in the dissolution rate from the molecularly dissolved drug in the oil phase and an increased rate of dispersion of the drug in the gastrointestinal (GI) tract which leads to greater absorption into the blood.

  • Mechanistic approach for the development of ultrafine o/w emulsions using blends medium and long chain triglycerides: solubility and bioavailability enhancement of perphenazine
    Journal of Excipients and Food Chemicals, 2013
    Co-Authors: Sanjula Baboota, Abdullah Abdullah, Gulam Mustafa, Jasjeet K. Sahni
    Abstract:

    A thermodynamically stable ultrafine (o/w) emulsion containing perphenazine for solubility and oral bioavailability enhancement using blends of long and medium chain triglyceride was developed. Formulation was prepared using low energy emulsification phase titration method. The optimized formulations consisted of blend of linseed and sefsol 218 (1:1), Polysorbate 40, polyethylene glycol 400 and distilled water as an oil, surfactant, cosurfactant and dispersion phase respectively. The formulations were characterized on the basis of viscosity, refractive index, particle size distribution, spectral transmittance and surface morphology. Formulations were evaluated for release study by everted gut sac using intestinal mucosa. The ex vivo release data showed that nanoemulsions significantly increased the permeation rate of perphenazine over the simple suspension. Following oral administration of nanoemulsion in wistar rats, both AUC and C max of perphenazine increased by 2.9 fold and 2.54-fold respectively compared with the perphenazine suspension. The resultant bioavailability might be due to increased solubility, bypassing the first-pass metabolism through lymphatic absorption and enhanced permeation potential of perphenazine.