Transepithelial Transport of Poly Amidoamine Dendrimers

University Of Maryland Baltimore, Baltimore MD

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Abstract

DESCRIPTION (provided by applicant): The broad long-term goal of this research is to develop an efficient oral drug delivery system using poly amidoamine (PAMAM) dendrimers as drug carriers. Generally, a polymeric component serves as a drug carrier in controlled drug delivery systems. These systems are usually administered parenterally (eg: intravenous) because polymeric carriers exhibit low permeability across the intestinal epithelial barrier. However, oral drug delivery is the most desired route of drug administration due to high patient compliance. PAMAM has been shown to have relatively high permeability across the intestinal epithelial barrier. This research proposal will investigate the factors that influence the permeability of PAMAM. First, Confocal Scanning Laser Microscopy (CSLM) techniques will be used to investigate the transport mechanisms of amine-terminated poly amidoamine (PAMAM-NH2) dendrimers across Caco-2 cell monolayers. The testable hypothesis is that the visualization of the transport pathways of fluorescently labeled PAMAM-NH2 dendrimers will elucidate possible contribution of the paracellular and/or transcellular routes in the permeability of PAMAM-NH2 dendrimers. Elucidation of the transport pathways utilized by PAMAM dendrimers will be determined by the visualization of Caco-2 cell monolayers upon incubation with fluorescently labeled PAMAM dendrimers using CSLM techniques. Furthermore, the effect of drug loading on the permeability of PAMAM-NH2 dendrimers across Caco-2 cells will be studied. The hypothesis to be tested is that an increase in hydrophobic drug loading is expected to increase the transcellular transport of PAMAM dendrimers. The effect of hydrophobic drug loading on PAMAM permeability will be assessed by examining PAMAM permeability upon increasing the extent of FlTC labeling per PAMAM generation (G0-G4). Finally, the influence of surface charge of PAMAM dendrimers on their transepithelial transport will be investigated. The hypothesis to be tested is that both negatively charged and positively charged dendrimers will have higher permeability values than the neutral dendrimers. The permeability of neutral, hydroxyl-terminated (PAMAM-OH, G2-G4) and anionic, carboxylate-terminated dendrimers (PAMAM-COOH, G0.5-G4.5) in comparison to the permeability of cationic, amine-terminated dendrimers (PAMAM-NH2, G0-G4) will be used to assess the effect of surface charge on PAMAM permeability.