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  button  High-throughput Method for Determining Young’s Modulus of Polymer Blends
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High-throughput Method for Determining Young’s Modulus of Polymer Blends

 

Introduction

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Manufacturing industries have a long history of using polymer blending as an inexpensive method to create new materials with desirable properties. Blending can be used to optimize modulus, strength, morphology and crystallinity and for these reasons blending is also receiving attention from the tissue engineering community. Since a one-sample-for-one-measurement approach can be slow, we have developed a high-throughput method for determining the modulus of polymer blends in order to accelerate development of new materials.
 

Experimental Approach

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A polymer blend gradient library of poly(L-lactic acid) (PLLA) and poly(D,L-lactic acid) (PDLLA) was created using a three-syringe pump system and a translation stage. The library was a strip-shaped film approximately 3 mm wide, 50 mm long and 4 micrometers thick which was formed on a glass substrate and its composition was measured by Fourier transform infrared (FTIR) microspectroscopy. A gradient in composition ran along the long axis of the film being PLLA-rich on one end and PDLLA-rich on the opposite end. Nanoindentation measurements were made across the gradient to obtain quantitative modulus data over a wide range of PLLA-PDLLA blend compositions using only a single polymer specimen.
 

Results

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Image of a polymer solution being deposited from the sampling syringe onto a glass substrate to form a strip-shaped film.
Image of a polymer solution being deposited from the sampling syringe onto a glass substrate to form a strip-shaped film.
FTIR microspectroscopy was used to determine composition of six PLLA-PDLLA gradients. Orange corresponds to PLLA and blue corresponds to PDLLA.
FTIR microspectroscopy was used to determine composition of six PLLA-PDLLA gradients. Orange corresponds to PLLA and blue corresponds to PDLLA.
The compositions of the six PLLA-PDLLA gradients determined with FTIR-RTM were averaged and plotted versus position along the gradient.
The compositions of the six PLLA-PDLLA gradients determined with FTIR-RTM were averaged and plotted versus position along the gradient.
Young’s modulus was measured on the gradients using nanoindentation and average values (solid circles) were plotted against composition (bottom y-axis) and position (top y-axis). Open triangles are the modulus from control discrete blend specimens (0, 25, 50, 75 & 100% PLLA) plotted against composition [use the bottom y-axis only; the top y-axis (“Position”) does not apply to these data].
Young’s modulus was measured on the gradients using nanoindentation and average values (solid circles) were plotted against composition (bottom y-axis) and position (top y-axis). Open triangles are the modulus from control discrete blend specimens (0, 25, 50, 75 & 100% PLLA) plotted against composition [use the bottom y-axis only; the top y-axis (“Position”) does not apply to these data].
 

Future Activities

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Examine cell adhesion, morphology, proliferation and differentiation after culture on composition gradients.
Make gradients of other polymer blends (tyrosine polycarbonates) to explore applicability of the method.
 

Publications

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  • PAPER: Simon Jr CG, Deng Y, Eidelman N, Washburn NR (2005) High-throughput method for determining Young’s modulus of polymer blends. Nature Materials, in preparation.
  • PAPER: Eidelman N, Simon Jr CG (2004) Characterization of combinatorial polymer blend composition gradients by FTIR microspectroscopy. Journal of Research of the National Institute of Standards and Technology, in press.
  • POSTER: Simon Jr CG, Kennedy SB, Amis EJ, Eidelman N, Washburn NR. “Gradient Libraries for Combinatorial and High-Throughput Investigations of Polymeric Biomaterials”, 7th World Biomaterials Congress, Australia, 2004.
  • POSTER: Simon Jr CG, Kennedy SB, Amis EJ, Eidelman N, Washburn NR. “High-throughput Methods for Biomaterials Development”, NIST Combinatorial Methods Center 4th Annual Meeting, Gaithersburg, MD, 2003.
  • POSTER: Simon Jr CG, Kennedy SB, Amis EJ, Eidelman N, Washburn NR. “High-throughput Methods for Biomaterials Development”, Symposium on Metrology and Standards for Cell Signaling, NIST, Gaithersburg, MD, 2003.
  • POSTER: Simon Jr CG, Kennedy SB, Amis EJ, Eidelman N, “Washburn NR. High-throughput Methods for Biomaterials Development”, RESBIO Kickoff Even, Rutgers University, NJ 2003.
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    NIST Contributors:

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    Carl G. Simon, Jr
    Newell R. Washburn
    Gale A. Holmes
    Yan Deng
    Naomi Eidelman
    Chetan A. Khatri
    Amit Sehgal
    Michael D. Weir
     

    Collaborators:

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    Joachim Kohn
    (Rutgers University)
     
     
     
     
     
     
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    Biomaterials Group
    Polymers Division
    Materials Science and Engineering Laboratory

     
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