Uniform, Shape-Specific Carriers for Vaccines, Biologics and Small Molecule Drugs

Joseph DeSimone, Director
Institutes of Nanomedicine and Advanced Materials, Nanoscience, and Technology
University of North Carolina (Chapel Hill)

Friday, Jan. 8, 2010
10:30 a.m., Green Auditorium
VTC to Boulder will be Room 1107

colloquim image
Graphics were provided by the speaker.

To translate promising molecular discoveries into benefits for patients, we are taking a pharmaco-engineering systems approach to develop the next generation of delivery systems with programmable multi-functional capability.  Our laboratory has pioneered the development of a technique called PRINT (Particle Replication in Non-wetting Templates).  PRINT is a top-down particle synthesis method that extends the nano-fabrication techniques from the semiconductor industry to a high throughput, continuous roll-to-roll process.  PRINT enables the fabrication of precisely defined micro- and nano-particles with control over particle size (20 nm to >20 micron), shape, chemical composition, cargo (proteins, adjuvants, therapeutics, oligonucleotides, siRNA, imaging agents), modulus (stiff, deformable - RBC mimics) and surface chemistries (antibodies, PEG chains, metal chelators), including the spatial distribution of proteins on the particle.  In the history of delivery, particles have never had the uniformity, precision and chemical and shape control afforded by PRINT.

Anyone outside NIST wishing to attend must be sponsored by a NIST employee and receive a visitor badge. For more information, call Kum J. Ham at 301-975-4203.

Colloquia are videotaped and available in the NIST Research Library.

Created January 14, 2010, Updated September 21, 2016