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Dive into the research topics where Samuel Shefer is active.

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Featured researches published by Samuel Shefer.


Journal of Controlled Release | 1999

Thermodynamic prediction of active ingredient loading in polymeric microparticles.

Ginger Tse; Daniel Blankschtein; Adi Shefer; Samuel Shefer

The growing use of microparticles as a controlled-delivery system for pharmaceutical and non-pharmaceutical active ingredients (AIs) has prompted a costly trial-and-error development of new and effective microparticle systems. In order to facilitate a more rational design and optimization of AI loadings in microparticles, we have developed a molecular-thermodynamic theory to predict the loading of liquid AIs in polymeric microparticles that are manufactured by a solvent evaporation process. This process involves the emulsification of a liquid polymer solution (consisting of polymer and AI dissolved in a volatile solvent) in an aqueous surfactant solution. The theory describes the equilibrium distribution of the AI between the aqueous phase and the dispersed polymeric droplets. The universal functional activity coefficient (UNIFAC) and UNIFAC-Free Volume (FV) group-contribution methods are utilized to model the nonidealities in the water and polymeric droplet phases, respectively. The inputs to the theory are: (i) the chemical structures, densities and total masses of the manufacturing ingredients, (ii) the manufacturing temperature and (iii) the glass transition temperature of the polymer. Since surfactant concentrations exceeding the critical micellar concentration (CMC) are often required in order to stabilize the dispersed polymeric droplets during the emulsion manufacturing process, the theory also accounts for AI solubilization in surfactant micelles present in the manufacturing solution. To test the AI loading predictions, we compare theoretical predictions of AI loadings in poly(lactic acid), poly(methyl methacrylate) and polystyrene microparticles to experimentally measured ones for five model AIs with varying degrees of hydrophobicity (benzyl alcohol, n-octanol, geraniol, farnesol and galaxolide). We also demonstrate how the developed theory can be utilized to screen polymers with respect to their abilities to load a given AI, as well as to provide guidelines for manufacturing microparticles having the desired AI loading.


Archive | 2003

Multi component controlled release system for oral care, food products, nutraceutical, and beverages

Adi Shefer; Samuel Shefer


Archive | 2002

Multi component controlled delivery system for fabric care products

Adi Shefer; Samuel Shefer


Archive | 2004

Multi component controlled delivery system for soap bars

Adi Shefer; Samuel Shefer


Archive | 2002

Stabilized retinol for cosmetic dermatological, and pharmaceutical compositions, and use thereof

Adi Shefer; Samuel Shefer


Archive | 2002

PH triggered targeted controlled release systems for the delivery of pharmaceutical active ingredients

Adi Shefer; Samuel Shefer


Archive | 2002

Surface dissolution and/or bulk erosion controlled release compositions and devices

Adi Shefer; Samuel Shefer


Archive | 2002

Compositions and method for targeted controlled delivery of active ingredients and sensory markers onto hair, skin, and fabric

Adi Shefer; Samuel Shefer


Archive | 2003

Moisture triggered sealed release system

Adi Shefer; Samuel Shefer


Archive | 2004

pH triggered site specific targeted controlled drug delivery system for the treatment of cancer

Adi Shefer; Samuel Shefer

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Daniel Blankschtein

Massachusetts Institute of Technology

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Ginger Tse

Massachusetts Institute of Technology

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