Abstract :
The pharmaceutical and biotechnology industries are currently developing numerous peptides, proteins, biopolymer and macromolecular drugs for the treatment of a variety of diseases. However, many of these biological drug forms have poor bioavailability when administered orally due to degradation by proteolytic enzymes and loss of drug into the intestinal lumen. In order to overcome these disadvantages, increasing interest has been placed on advanced carrier systems for more efficient delivery. In response, the aim of this work was to fabricate microparticulate patch-like systems containing cytoadhesive properties using novel off-wafer approaches to traditional MEMS-based techniques. The use of micro fabrication techniques allowed for precise control over size and shape. The size of the microdevices was designed small enough to have adequate contact with the intestinal wall while large enough to prevent endocytosis of the entire particle. It was shown that these modified microdevices have improved cytoadhesive properties toward Caco-2 cell monolayers. Additionally, the modified microdevices remained anchored to the cells in comparison to the unstable attachment of microspheres. By examining trans epithelial electrical resistance and diffusion of phenol red through the monolayer, the microdevices were found to be biocompatible and perhaps even beneficial for paracellular transport
Keywords :
bioMEMS; cellular biophysics; drug delivery systems; monolayers; Caco-2 cell monolayer; MEMS; biocompatibility; biological drug; cytoadhesive micropatch system; disease; endocytosis; gastrointestinal tract; intestinal lumen; microfabrication technique; microparticulate patch-like system; micropost; mucus layer; off-wafer fabrication; polymeric microdevice; proteolytic enzyme; shed mucosa; targeted oral drug delivery; transepithelial electrical resistance; Biotechnology; Degradation; Diseases; Drug delivery; Fabrication; Intestines; Peptides; Pharmaceuticals; Protein engineering; Shape control;