Proceedings of the National Academy of Sciences · 2002 · 538 citations · 18 references
PharmacyChemical EngineeringPharmaceuticsDrug DeliveryNanomaterialsNanoparticle Drug DeliveryNanocarriers For TherapeuticsNanomaterials For Drug DeliveryNanoparticle CharacterizationNanoparticle Delivery SystemsNanoparticle FormulationsNanoparticle SynthesisDrug Delivery NanocarriersDrug Release MechanismsDryingParticle AerosolizationPeclet NumberPolymeric Nanoparticle Drug ReleasePéclet NumberThin-walled Structures
We have combined the drug release and delivery potential of nanoparticle (NP) systems with the ease of flow, processing, and aerosolization potential of large porous particle (LPP) systems by spray drying solutions of polymeric and nonpolymeric NPs into extremely thin-walled macroscale structures. These hybrid LPPs exhibit much better flow and aerosolization properties than the NPs; yet, unlike the LPPs, which dissolve in physiological conditions to produce molecular constituents, the hybrid LPPs dissolve to produce NPs, with the drug release and delivery advantages associated with NP delivery systems. Formation of the large porous NP (LPNP) aggregates occurs via a spray-drying process that ensures the drying time of the sprayed droplet is sufficiently shorter than the characteristic time for redistribution of NPs by diffusion within the drying droplet, implying a local Peclet number much greater than unity. Additional control over LPNPs physical characteristics is achieved by adding other components to the spray-dried solutions, including sugars, lipids, polymers, and proteins. The ability to produce LPNPs appears to be largely independent of molecular component type as well as the size or chemical nature of the NPs.
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Chaotic Mixer for Microchannels
Abraham D. Stroock, Stephan K. W. Dertinger, Armand Ajdari et al. · Science · 2002 · 3.4K citations
Two-Dimensional Interfacial Colloidal Crystals
P. Pierański · Physical Review Letters · 1980 · 1.4K citations
Natural Sciences, Chemistry, Physics +17
Large Porous Particles for Pulmonary Drug Delivery
David A. Edwards, Justin Hanes, Giovanni Caponetti et al. · Science · 1997 · 1.2K citations
Deposition of particles in the human respiratory tract in the size range 0.005–15 μm
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