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Heather Fahlenkamp
Assistant Professor

 

Major Areas of Interest

 

Dr. Fahlenkamp has been an instructor for the Chemical Engineering Unit Operations Laboratory class for senior chemical engineering students (CHE 4112).  In Spring 2007, she will teach Bioprocess Engineering for senior and graduate level students in chemical and biosystems and agricultural engineering (CHE/BAE 4283, CHE 5283, and BAE 5030).

 

RESEARCH INTERESTS:

 

Advancing the Development of Drug Delivery Devices by Utilizing Tissue-Engineered Constructs:

Particles have been used for many years in a wide variety of applications in the following industries: pharmaceutical, vaccine, cosmeceutical, chemical, materials, and medical device.  They continue to grow in popularity as candidates for drug delivery devices.  When preparing microparticles for drug delivery, the particles can be characterized by their loading efficiency, release rates, and interactions with their environment (i.e. with cells).  All of these are influenced by several factors including particle size, particle morphology (porous or smooth surface), chemistry of the bulk material and the surface material (charged, hydrophobicity, etc.), biocompatibility of the material, and the method and rate of degradation.  In turn, all of these factors are influenced by the methods and materials used to prepare the microparticles.   One area of my research includes characterizing and optimizing the methods and materials used to prepare microparticles to enhance their drug delivery properties.  My past research experience has included fabrication of particles using a wide variety of biomaterials (natural and synthetic) and fabrication methods.

Directly related to my research area of microparticles for use in drug delivery is the development of functional in vitro tissue models to investigate particle interactions with cells and/or the extracellular matrix.  Current models used to test particles include 1) two-dimensional models consisting of various aqueous media environments that may or may not contain cells and 2) animal models.  Two-dimensional culture models lack the complexity of three-dimensional tissue models to properly predict particle interactions with cells and the extracellular matrix components.  Even though animal models may provide a more complex system, data do not always correlate with human data due to obvious differences.  An alternative to currently used models is the development of three-dimensional in vitro cellular and tissue constructs, or their equivalents, to mimic the normal human tissues that may interact with particles.  My past research experience in this area has included the development of several tissue models for the diagnosis and prevention of disease.

 

The following engineering principles would be utilized in this research area:

 

  • Transport Phenomenon

  • Modeling

  • Optimization

 

This research would result in experience in the following areas:

 

  • Chemical Engineering

  • Biomaterials

  • Tissue Engineering

  • Cell Biology

  • Immunology

 

RECENT PAPERS:

 

Scientific Journals:

Gappa-Fahlenkamp, H. and Lewis, R. (2005) Improved haemocompatibility of poly(ethylene terephthalate) modified with various thiol-containing groups.  Biomaterials 26(17) 3479-85.

 

Gappa-Fahlenkamp, H., Duan, X., and Lewis, R. (2004) Analysis of immobilized L-cysteine on polymeric surfaces.  Journal of Biomedical Materials Research 71(3) 519-527.

 

Gappa, H., Baudys, M., Koh, J. J., Kim, S. W., and Bae, Y. H. (2001) The effect of zinc-crystallized glucagon-like peptide-1 on insulin secretion of macroencapsulated pancreatic islets. Tissue Engineering 7(1), 35-44.

 

Patents:

Artificial immune system: methods for making and use WO 2005 / 104755, also published as US 2005 / 0282148                                                                    Warren, Fahlenkamp, Higbee, Kachurin, Li, Nguyen, Parkhill, Sanchez-Schmitz, Irvine, Randolph, Hacohen, Torbett

 

Immunotherapy compositions, method of making and method of use thereof  WO 2005 / 072088, also published as US 2005 / 0244505   Higbee, Barber, Kachurin, Fahlenkamp, Warren, Balachandran, Thomas, Parkhill

 

Automatable artificial immune system (AIS) US Application number 11/375,033                     Parkhill, Nguyen, Sanchez-Schmitz, Fahlenkamp, Higbee, Drake, Kachurin, Moe, Warren

 

Mucosal tissue equivalent US Application number 11/375,126 Sanchez-Schmitz, Higbee, Fahlenkamp, Warren, Drake, Tew

 

In vitro germinal centers US provisional patent application, serial # 60/752,034 Sukumar, El Shikh, Tew, Sanchez-Schmitz, Drake, Mosquera, Li, Kachurin, Higbee, Fahlenkamp, Warren

A porous membrane device that promotes differentiation of monocytes into dendritic cells                                                                      US provisional patent application, serial # 60/752,033 Drake, Moe, Li, Fahlenkamp, Sanchez-Schmitz, Higbee, Parkhill, Warren

Disease Model Incorporation into an Artificial Immune System (AIS)                                                                  Filed (6/15/06) as a continuation-in-part of US 2005 / 0282148, above Advance serial #11/453,003       Higbee, Mishkin, Warren, Sanchez-Schmitz, Fahlenkamp, Rivard

Controlling Dendritic Cell Maturation State in the Lymphoid Tissue Equivalent of an Artificial Immune System                                                                            Filed (6/06) as a continuation-in-part of US 2005 / 0282148, above                                                     Sanchez-Schmitz, Higbee, Fahlenkamp, Irvine, Warren, Drake

 

B.S., 1997, Chemical Engineering, Oklahoma State University.

M.S., 2000, Bioengineering, University of Utah.

Ph.D., 2003, Chemical Engineering, Oklahoma State University.

Bioengineer, VaxDesign Corporation, 2003-2006, Orlando, FL.

E-mail: heather.fahlenkamp@okstate.edu

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