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Magnetic Drug Targeting James A. Ritter, Armin D. Ebner and Jan Mangual Department of Chemical Engineering Swearingen Engineering Center University of South Carolina Columbia, SC 29208 Scientific Retreat on Bioengineering and Regenerative Medicine Charleston, SC March 24, 2010
Schematic of an MDT System ,[object Object],[object Object],[object Object]
Proposed Implant-Assisted MDT System ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Ferromagnetic Implant
[object Object],[object Object],[object Object],[object Object],Implant Assisted - MDT
Magnetic Fields from IA-MDT ,[object Object],[object Object],[object Object],[object Object]
Magnetic Drug Carrier Particles for IA-MDT Size : 50 - 2000 nm Superparamagnetic Particles -  FeCo, ferrites, etc. -  largest magnetization -  80 wt% max (40-50 vol%) Polymer -  biocompatible -  non-immunogenic -  biodegradable - porous for drug transport Drug -  free or fixed (radioactive)
MDCP Surrogates Bangs Laboratories, Inc. ~20 wt% Magnetite
Magnetic Implants for IA-MDT ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],They must be biocompatible! 0 - 80 cm/s 0 - 80 cm/s 0.01 - 1.0 cm/s Blood Vessel Velocity Range
Comsol Simulations Simulation for 0.96   m MDCPs with 60 wt% magnetite at an applied field of  0.65 T and a velocity of 2.1 cm/s.   Magnetic Field Gradients MDCP Streamlines Last captured particle Trajectory
In Vitro  Particle Capture Images Effect of Fluid Velocity on Particle Capture A1) A2) B1) B2) Images at velocities of A) 2.1, and B) 21.2 cm/s 1) before and 2) after 10 ml of solution have passed through the collection area at an applied magnetic field of 0.17 T.
Experimental and Model Results   Effect of Fluid Velocity D p  = 0.87   m x fm  = 25 wt% D w  = 125   m Velocity negatively affects capture, but even at high velocities capture is still attainable. Capture seems to reach a steady value, where decrease in capture is greatly reduced. model
Particle Capture Video D p  = 0.87   m  D w  = 125   m  u B = 2.12 cm/s  H  = 0.15 T
Biodegradable Magnetic Stent Fabrication ,[object Object],[object Object],[object Object],[object Object],[object Object],Extruder Parameters: Melt temperature: 120ºC Extruder screw speed: 50 RPM  Extruder speed: ~1000mm/min Torque: 30 ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],Thermogravimetric Analysis Results Magnetite content (%w/w) Expected TGA 0 10 1.08 ±0.028 11.61 ±0.807 40 38.25 ± 0.711
MDCP Capture Effect of Fluid Velocity ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MDCP Capture Effect of Concentration ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
MDCP Capture Magnetic Field Effect ,[object Object],[object Object],[object Object],[object Object],[object Object]
Implant Assisted-MDT Projects ,[object Object],[object Object],[object Object],[object Object]
Part IV: Heart Tissue Perfusion Model to Study Implant Assisted – Magnetic Drug Targeting Using a Ferromagnetic Stent ,[object Object]
Right Coronary Artery Perfusion ,[object Object],[object Object],[object Object],[object Object],Right Coronary Artery was cannulated Flow was  kept  at 40  mL/min Step Injection 1 ~500 mL of lidocaine/heparin/Saline Solution (400 mg/L Lidocaine, 5000 IU/L Heparin and 0.9w/w% NaCl) 2 Flush with 300 mL of saline solution (0.9wt% NaCl) 3 Inject 0.5 mL of  100 nm magnetite particle  suspension ( ~  2.8 mg/mL) 4 Flushed with 900 mL of saline solution (0.9w/w% NaCl)  5 Repeat steps 2 to 4 with the magnet
Artery Perfusion Experimental Setup Heart’s Right Ventricle Saline Solution  (0.9% NaCl)  Reservoir Peristaltic  Pump ~ 40 mL/min Seed suspension  100 nm Fe 3 O 4   2.8 mg/mL 0.5 ml Injection Collection vessel Magnet
Right Coronary Artery Results Samples were analyzed using Atomic Absorption Spectroscopy for iron. The stent is a SS430 500   m coil, 3 mm in diameter and 3 cm long,
Particle Capture at Stent Area From visual inspection the particles could be seen accumulated in the area where the stent is located. While there are particles in other areas of the artery, it appears to be less compared to the stent area.
Summary ,[object Object],[object Object],[object Object]
Concluding Remarks ,[object Object],[object Object],[object Object]
Concluding Remarks ,[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],Implant Assisted - MDT

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Magnetic Drug Targeting, James Ritter, PhD

  • 1. Magnetic Drug Targeting James A. Ritter, Armin D. Ebner and Jan Mangual Department of Chemical Engineering Swearingen Engineering Center University of South Carolina Columbia, SC 29208 Scientific Retreat on Bioengineering and Regenerative Medicine Charleston, SC March 24, 2010
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  • 6. Magnetic Drug Carrier Particles for IA-MDT Size : 50 - 2000 nm Superparamagnetic Particles - FeCo, ferrites, etc. - largest magnetization - 80 wt% max (40-50 vol%) Polymer - biocompatible - non-immunogenic - biodegradable - porous for drug transport Drug - free or fixed (radioactive)
  • 7. MDCP Surrogates Bangs Laboratories, Inc. ~20 wt% Magnetite
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  • 9. Comsol Simulations Simulation for 0.96  m MDCPs with 60 wt% magnetite at an applied field of 0.65 T and a velocity of 2.1 cm/s. Magnetic Field Gradients MDCP Streamlines Last captured particle Trajectory
  • 10. In Vitro Particle Capture Images Effect of Fluid Velocity on Particle Capture A1) A2) B1) B2) Images at velocities of A) 2.1, and B) 21.2 cm/s 1) before and 2) after 10 ml of solution have passed through the collection area at an applied magnetic field of 0.17 T.
  • 11. Experimental and Model Results Effect of Fluid Velocity D p = 0.87  m x fm = 25 wt% D w = 125  m Velocity negatively affects capture, but even at high velocities capture is still attainable. Capture seems to reach a steady value, where decrease in capture is greatly reduced. model
  • 12. Particle Capture Video D p = 0.87  m D w = 125  m u B = 2.12 cm/s H = 0.15 T
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  • 20. Artery Perfusion Experimental Setup Heart’s Right Ventricle Saline Solution (0.9% NaCl) Reservoir Peristaltic Pump ~ 40 mL/min Seed suspension 100 nm Fe 3 O 4 2.8 mg/mL 0.5 ml Injection Collection vessel Magnet
  • 21. Right Coronary Artery Results Samples were analyzed using Atomic Absorption Spectroscopy for iron. The stent is a SS430 500  m coil, 3 mm in diameter and 3 cm long,
  • 22. Particle Capture at Stent Area From visual inspection the particles could be seen accumulated in the area where the stent is located. While there are particles in other areas of the artery, it appears to be less compared to the stent area.
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