docusate-sodium and acryloyl-chloride

docusate-sodium has been researched along with acryloyl-chloride* in 1 studies

Other Studies

1 other study(ies) available for docusate-sodium and acryloyl-chloride

Article	Year
Preparation, characterization and in vitro drug release studies of novel polymeric nanoparticles. International journal of pharmaceutics, 2006, Oct-12, Volume: 323, Issue:1-2 Polymeric nanoparticles of AADG cross-linked with MBA encapsulating water soluble macromolecules such as FITC-Dextran have been prepared in the reverse micellar system. The particles obtained were of >85nm in diameter which were highly monodisperse. An optically clear solution was obtained on redispersing these nanoparticles in aqueous buffer. Size and morphology of the particles remains the same on re-dispersing the lyophilized powder of these nanoparticles in aqueous buffer. The size dependency of the particles on the monomer and surfactant concentration was observed. The average size of the nanoparticles as obtained from DLS studies ranges from 74 to 114nm in case 0.06M AOT and 62-104nm in case of 0.1M AOT concentration. FITC-Dextran was entrapped into nanoparticles with high efficiency (>70%). The pH dependent release of the entrapped molecules from these nanoparticles was also studied. At pH 5.0 solution, approximately 43% of FITC-Dx was released and at pH 7.4 it was about 70%. Topics: Acrylamides; Acrylates; Acrylic Resins; Delayed-Action Preparations; Dextrans; Drug Carriers; Drug Compounding; Drug Delivery Systems; Fluorescein-5-isothiocyanate; Glucosamine; Light; Microscopy, Electron, Transmission; Nanoparticles; Particle Size; Polymers; Scattering, Radiation; Spectroscopy, Fourier Transform Infrared; Succinates	2006

Article

Year

Preparation, characterization and in vitro drug release studies of novel polymeric nanoparticles.

International journal of pharmaceutics, 2006, Oct-12, Volume: 323, Issue:1-2

Polymeric nanoparticles of AADG cross-linked with MBA encapsulating water soluble macromolecules such as FITC-Dextran have been prepared in the reverse micellar system. The particles obtained were of >85nm in diameter which were highly monodisperse. An optically clear solution was obtained on redispersing these nanoparticles in aqueous buffer. Size and morphology of the particles remains the same on re-dispersing the lyophilized powder of these nanoparticles in aqueous buffer. The size dependency of the particles on the monomer and surfactant concentration was observed. The average size of the nanoparticles as obtained from DLS studies ranges from 74 to 114nm in case 0.06M AOT and 62-104nm in case of 0.1M AOT concentration. FITC-Dextran was entrapped into nanoparticles with high efficiency (>70%). The pH dependent release of the entrapped molecules from these nanoparticles was also studied. At pH 5.0 solution, approximately 43% of FITC-Dx was released and at pH 7.4 it was about 70%.

Topics: Acrylamides; Acrylates; Acrylic Resins; Delayed-Action Preparations; Dextrans; Drug Carriers; Drug Compounding; Drug Delivery Systems; Fluorescein-5-isothiocyanate; Glucosamine; Light; Microscopy, Electron, Transmission; Nanoparticles; Particle Size; Polymers; Scattering, Radiation; Spectroscopy, Fourier Transform Infrared; Succinates

2006