• DocumentCode
    2373746
  • Title

    Respiration triggered magnetic drug targeting in the lungs

  • Author

    Dahmani, C. ; Götz, S. ; Weyh, Thomas ; Renner, R. ; Rosenecker, M. ; Rudolph, C.

  • Author_Institution
    Heinz Nixdorf-Lehrstuhl fur Medizinische Elektron., Tech. Univ. Munchen, Munich, Germany
  • fYear
    2009
  • fDate
    3-6 Sept. 2009
  • Firstpage
    5440
  • Lastpage
    5443
  • Abstract
    Lung cancer kills per year 1.3 million people worldwide. It is the most fatal cancer type as far as men are concerned and the second deadliest for women. One of the recent technologies to treat carcinomas in the lungs consists in delivering drugs through the pulmonary pathways directly to the tumor cells over actively loaded superparamagnetic nanoparticles that are encapsulated in aerosols and guided by external magnetic fields. However, first implementations of this technique assumed a continuous application of the magnetic field all through the inspiration and expiration phases of the artificial respiratory act that supplies the patient. We observed that applying the field this way forced the magnetic aerosols to sediment at regions far from the target, mainly in the trachea and main bronchioles, because of the force inducing magnetic field gradients that are present over the whole field application area. We developed an approach to avoid this effect by punctually generating the aerosol cloud exactly at the beginning of the inspiration phase, which would propel the particles to the deepest parts of the lung and therefore to the targeted cells as well, and by synchronizing the magnetic field activation with the breathing process. Our developed system analyzes the relevant respiration parameters such as pressure and flow and detects the end of the inspiration phase to trigger the magnet exactly at that point in time, when particles have reached the deepest alveoli, including the targeted zones, and do not experience forces due to the streaming any more. The magnetic field is then held on during the expiration phase to assure the retention of the aerosols at the targeted sites, which increases the efficiency and focality of the treatment. This way, only target cells are subjected to the deposition of the drug carrying aerosols, while the other healthy regions of the lungs remain unaltered by side effects.
  • Keywords
    aerosols; drug delivery systems; lung; nanobiotechnology; nanoparticles; pneumodynamics; superparamagnetism; aerosols; breathing flow; breathing pressure; lung cancer; magnetic drug targeting; respiration; superparamagnetic nanoparticles; aerosols; breath triggering; deposition; magnetic drug targeting; superparamagnetic nanoparticles; Drug Delivery Systems; Humans; Lung; Magnetics; Organ Specificity; Respiration; Time Factors;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Engineering in Medicine and Biology Society, 2009. EMBC 2009. Annual International Conference of the IEEE
  • Conference_Location
    Minneapolis, MN
  • ISSN
    1557-170X
  • Print_ISBN
    978-1-4244-3296-7
  • Electronic_ISBN
    1557-170X
  • Type

    conf

  • DOI
    10.1109/IEMBS.2009.5332476
  • Filename
    5332476