Difference between revisions of "Micro!uidic fabrication of smart microgels from macromolecular precursors"

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==Experimental==
 
==Experimental==
The formation of microgels from precursor polymers is illustrated by the sequence of reactions in Figure 1, where pNIPAAm is prepared from N-isopropylacrylamide and dimethylmaleimide. The resulting pNIPAAm is then photocrosslinked. Molecular weight is controlled by running the pNIPAAm precursor is controlled by running the copolymerization step in the prescence of sodium formate. This synthesis route allows the weight average molecular weight to be controlled between 100,000-2,000,000 g/mol.
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The formation of microgels from precursor polymers is illustrated by the sequence of reactions in Figure 1, where pNIPAAm is prepared from N-isopropylacrylamide and dimethylmaleimide. The resulting pNIPAAm is then photocrosslinked. Molecular weight is controlled by running the pNIPAAm precursor is controlled by running the copolymerization step in the presence of sodium formate. This synthesis route allows the weight average molecular weight to be controlled between 100,000-2,000,000 g/mol.
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Once the precursor polymers are formed, microfluidic devices are used to create monodisperse drops (Figure 2). The polymer precursor drops are then gelled via photocrosslinking. By separating particle formation from the polymer synthesis step, highly tailored, functionalized polymers can effectively be manufactured in a variety of particle geometries with minimal loss of functionality.
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==Examples==
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To illustrate the monodispersity and functionality of such systems, four different smart microgels were made with different ratios of precursor tagged with red and green dye (Figure 3). The ratios of red to green die were as follows: 15/0, 10/5, 5/10, 0/15 g/L. The gelled particles were then imaged with fluorescence microscopy and the relative intensity of each die was measured. Figure 4 shows that these results exactly reflect the intial fractions of red and green die within experimental error.

Revision as of 00:08, 28 November 2012

Page Currently Being Edited by Joseph Muth

Authorship

Title of Original Work: Mirofluidic Fabrication of Smart Microgels from Macromolecular Precursors

Journal of Original Work: Polymer, Volume 51, Pages 5883-5889, October 16, 2010

Authors: Sebastian Seiffert, David A. Weitz

Author of Review: Joseph Muth - AP 225 - Fall 2012 - 11/27/2012

Overview

Stimuli-responsive (smart) microgels are micron sized polymer particles that change shape in response to enviornmental stimuli. This responsiveness makes them useful in the fields of drug delivery, catalysis, sensing, and photonics. The most commonly used smart microgel material is poly(N-isopropylacrylamide) (pNIPAAm) because it has a lower critical solution temperature (LCST) around 32°C. Both the LCST and Tg of (pNIPAAm) are readily tunable by changing its composition or its particle geometry. As such controlling each of these aspects independently is critical to optimizing the characteristics of the microgel.

One way to achieve independent optimization is by using microfluidic techniques to template pre-fabricated precursor polymers. In this way simultaneous solidifcation and polymerization are avoided because gelation occurs via a polymeric analogous route instead of by monomeric chain growth. Using prefabricated precursor polymers, allows the molecular structure to be tuned through polymer synthesis, while microfluidics allows the shape to be accurately and precisely controlled. In this work, the author explores various ways to exploit this smart microgel fabrication technique.

Experimental

The formation of microgels from precursor polymers is illustrated by the sequence of reactions in Figure 1, where pNIPAAm is prepared from N-isopropylacrylamide and dimethylmaleimide. The resulting pNIPAAm is then photocrosslinked. Molecular weight is controlled by running the pNIPAAm precursor is controlled by running the copolymerization step in the presence of sodium formate. This synthesis route allows the weight average molecular weight to be controlled between 100,000-2,000,000 g/mol.

Once the precursor polymers are formed, microfluidic devices are used to create monodisperse drops (Figure 2). The polymer precursor drops are then gelled via photocrosslinking. By separating particle formation from the polymer synthesis step, highly tailored, functionalized polymers can effectively be manufactured in a variety of particle geometries with minimal loss of functionality.

Examples

To illustrate the monodispersity and functionality of such systems, four different smart microgels were made with different ratios of precursor tagged with red and green dye (Figure 3). The ratios of red to green die were as follows: 15/0, 10/5, 5/10, 0/15 g/L. The gelled particles were then imaged with fluorescence microscopy and the relative intensity of each die was measured. Figure 4 shows that these results exactly reflect the intial fractions of red and green die within experimental error.