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J Control Release ; 125(3): 263-72, 2008 Feb 11.
Article in English | MEDLINE | ID: mdl-18053607

ABSTRACT

Our ability to precisely manipulate size, shape and composition of nanoscale carriers is essential for controlling their in-vivo transport, bio-distribution and drug release mechanism. Shape-specific, "smart" nanoparticles that deliver drugs or imaging agents to target tissues primarily in response to disease-specific or physiological signals could significantly improve therapeutic care of complex diseases. Current methods in nanoparticle synthesis do not allow such simultaneous control over particle size, shape and environmentally-triggered drug release, especially at the sub 100 nm range. We report here a high-throughput nanofabrication technique using synthetic and biological macromers (peptides) to produce highly monodisperse, enzymatically-triggered nanoparticles of precise sizes and shapes. Particles as small as 50 nm were fabricated on silicon wafers and harvested directly into aqueous buffers using a biocompatible, one-step release technique. We further demonstrate successful encapsulation and precisely controlled enzyme-triggered release of antibodies and nucleic acids from these nanoparticles, thus providing a potential means for disease-controlled delivery of biomolecules.


Subject(s)
Enzymes/pharmacology , Nanoparticles/chemistry , Nanotechnology/methods , Antibodies/metabolism , Biocompatible Materials/chemistry , Buffers , Cathepsin B/analysis , Cathepsin B/pharmacology , DNA/metabolism , Drug Carriers/chemistry , Fluorescent Antibody Technique, Indirect , Fluorescent Dyes/metabolism , Hydrogels/metabolism , Kinetics , Lysine/analogs & derivatives , Lysine/metabolism , Nanoparticles/ultrastructure , Nanotechnology/instrumentation , Organic Chemicals/metabolism , Particle Size , Plasmids , Polyethylene Glycols/chemistry , Silicon/chemistry , Streptavidin/metabolism , Surface Properties , Time Factors , Water/chemistry
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