Based on literature studies of the deposition patterns of Relenza in healthy human volunteers, it is known that 77% of the emitted drug from the commercial product is deposited in the oropharynx rather than the lung [22]. Thus, the in vitro results presented here suggest

that the PRINT-zanamivir aerosol would translate to significantly more efficient lung delivery compared to Relenza. Figure 4 Favorable properties of PRINT aerosols Inhibitors,research,lifescience,medical for dry powder pharmaceutical use. (a, b) Comparison of 1.5μm torus PRINT-zanamivir particles against the marketed product Relenza (active pharmaceutical ingredient zanamivir) using an NGI. (b) PS: … 3.4. PRINT Aerosols with Narrow Size Distributions Exhibit Distinct In Vivo Lung Deposition Patterns Finally, we demonstrated the ability of PRINT selleckchem particle aerosols to control in vivo pulmonary delivery using a canine deposition model. Inhibitors,research,lifescience,medical PRINT aerosols composed of lactose, albumin, and leucine (64/32/4 mass ratio) were prepared, radiolabeled with technetium-99, and aerosolized into the respiratory tract of beagle

dogs using an endotracheal dosing apparatus. As shown in the gamma scintigraphic images (Figure 4(c)), significantly more Inhibitors,research,lifescience,medical whole-lung deposition was achieved with 1.5μm versus 6μm torus particles (1.3μm and 4.6μm MMAD, resp.), as would be expected from the relative aerodynamic sizes of these particles. Image analysis and quantification of the radioactivity counts confirmed this observation. In addition, the torus 1.5μm particles showed a greater than twofold enhancement of whole-lung deposition counts normalized Inhibitors,research,lifescience,medical to trachea deposition. This ability to tailor particle lung deposition could have broad applicability for respiratory drug delivery, particularly in scenarios where peripheral lung deposition should be enhanced or avoided depending on clinical application. 4. Discussion The PRINT fabrication approach predictably controls particle geometric and aerodynamic features, a differentiating attribute as compared to traditional particle generation approaches. In particular, micromolding

Inhibitors,research,lifescience,medical strategies such as PRINT represent one of the only methods to precisely control particle shape and size. For PRINT, the particle geometry is directly derived from the semiconductor wafer, bringing inherent nanoscale precision to the particle geometry and offering the capability to generate unique, nonspherical shapes. It is possible to control geometric features such as length, many aspect ratio, and edge curvature, as well as adding unique features such as fenestrations and biomimetic designs, as shown in Figure 2. The capability of PRINT to prepare micro- and nanoparticles of a diverse set of materials is due to the ability to mold materials in a variety of physical forms. In addition to the detailed studies presented here, particles have been prepared by polymerization [11] or solvent evaporation [23].