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Rutgers scientists have developed a novel platform of pharmaceutical product development by utilizing fluid bed impregnation (FBI) of API solutions onto porous carriers.
About
Rutgers scientists have developed a novel platform of pharmaceutical product development by utilizing fluid bed impregnation (FBI) of API solutions onto porous carriers. Impreg-nation of solutions into porous carriers allows extremely uniform distribution of small amounts of material, which can be used for drug dosage regulation. Currently, the method can be adjusted for drug content as low as 0.1% and as high as 10%, thus spanning the entire range of interest for poorly soluble, highly potent compounds in oral delivery applications. The drug release profile can also be controlled through the manufacturing process. Since the impregnated material can be filled directly into capsules, many inactive substances that were previously required for formula stability throughout encapsulation (i.e. compression aids, glidants, surfactants, disintegrants, or lubricants) can be eliminated as well. Also, the FBI method is uniquely suited for drug formulation development and clinical supply manufacturing, as it is safer than processes that require drugs to be handled in dry, powder form.
Key Benefits
Approach eliminates all API operations after synthesis and purification (i.e., crystallization, drying, milling,) making issues related to API crystallinity, physical stability, flow, cohesion, electrostatics, and particle size distribution no longer relevant; Extremely uniform material content in finished dosages; Enhances deliverability of poorly soluble drugs; Significant simplification of product manufacturing sequence; Safety and environmental improvements; Simplified scale-up procedure; Reduced number of critical raw material attributes and control parameters.
Applications
Therapeutics; Clinical Supply Manufacturing; Product Formulation and Development; Drug Loading; Drug Delivery; Controlled Release; Porous Carrier Technology.