TY - GEN
T1 - Microfluidic synthesis of multi-layer nanoparticles for drug & gene delivery
AU - Chan, Peggy
AU - Qi, Aisha
AU - Rajapaksa, Anushi
AU - Friend, James
AU - Yeo, Leslie
PY - 2012
Y1 - 2012
N2 - Multiple layer nanoparticles offers a likelihood of success in drug delivery, as it provides a solution for a more controllable drug release, as with such structures, control over the capsule wall thickness, permeability, stability, and degradation characteristics can be achieved. Using PDMS microfluidic devices to synthesize polymeric multilayer micro/nanoparticles has become popular recently. The generation of complex emulsions, such as double and triple emulsions, is also achievable with such devices [1]. However, limitations with these devices are: (1) the microchannel surface property is crucial to maintain the desired flow within the microdevice; (2) droplets which form within the microchannels require a cross-linking agent to be solidified into particles; (3) the size of the droplets is limited to the size of microchannels, usually around 50-100 mm, which is too large to be used for drug delivery; and (4) the amount of droplets or particles produced is limited as the droplets/particles are formed one by one. Therefore, in this study, we present a novel technique on fast multilayer polymeric nanoparticles synthesis via surface acoustic wave (SAW) atomization using a microfluidic device. We are able to show (1) successful synthesis of nanostructure including multilayer nanoparticles, and (2) fast generation of monodispersed particles in nanosize.
AB - Multiple layer nanoparticles offers a likelihood of success in drug delivery, as it provides a solution for a more controllable drug release, as with such structures, control over the capsule wall thickness, permeability, stability, and degradation characteristics can be achieved. Using PDMS microfluidic devices to synthesize polymeric multilayer micro/nanoparticles has become popular recently. The generation of complex emulsions, such as double and triple emulsions, is also achievable with such devices [1]. However, limitations with these devices are: (1) the microchannel surface property is crucial to maintain the desired flow within the microdevice; (2) droplets which form within the microchannels require a cross-linking agent to be solidified into particles; (3) the size of the droplets is limited to the size of microchannels, usually around 50-100 mm, which is too large to be used for drug delivery; and (4) the amount of droplets or particles produced is limited as the droplets/particles are formed one by one. Therefore, in this study, we present a novel technique on fast multilayer polymeric nanoparticles synthesis via surface acoustic wave (SAW) atomization using a microfluidic device. We are able to show (1) successful synthesis of nanostructure including multilayer nanoparticles, and (2) fast generation of monodispersed particles in nanosize.
KW - Gene delivery
KW - Microfluidic synthesis
KW - Multi-layer nanoparticles
KW - Surface acoustic wave
UR - https://www.scopus.com/pages/publications/84901745859
M3 - Conference contribution
AN - SCOPUS:84901745859
SN - 9780979806452
T3 - Proceedings of the 16th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2012
SP - 728
EP - 730
BT - Proceedings of the 16th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2012
PB - Chemical and Biological Microsystems Society
T2 - 16th International Conference on Miniaturized Systems for Chemistry and Life Sciences, MicroTAS 2012
Y2 - 28 October 2012 through 1 November 2012
ER -