<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">MSCE</journal-id><journal-title-group><journal-title>Journal of Materials Science and Chemical Engineering</journal-title></journal-title-group><issn pub-type="epub">2327-6045</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/msce.2015.37010</article-id><article-id pub-id-type="publisher-id">MSCE-57685</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Chemistry&amp;Materials Science</subject></subj-group></article-categories><title-group><article-title>
 
 
  The Application of Molecularly Imprinted Polymers
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ming</surname><given-names>Zhao</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Guijun</surname><given-names>Shen</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>College of Environmental and Chemical Engineering, Dalian University, Dalian, China</addr-line></aff><pub-date pub-type="epub"><day>19</day><month>06</month><year>2015</year></pub-date><volume>03</volume><issue>07</issue><fpage>87</fpage><lpage>89</lpage><history><date date-type="received"><day>16</day>	<month>April</month>	<year>2015</year></date><date date-type="rev-recd"><day>accepted</day>	<month>24</month>	<year>June</year>	</date><date date-type="accepted"><day>1</day>	<month>July</month>	<year>2015</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
   Molecularly imprinted technology (MIT) has the characteristics of specificity and high selectivity, which is one of the most promising methodologies. Besides, the polymers are made using MIT as the functional material of solid-phase extraction and chromatographic fractionating and sensor, because of the characteristics of the high selectivity, the better stability and easy preparation. This review introduces the progress in the application of MIT and summarizes its application in the chemistry. 
 
</p></abstract><kwd-group><kwd>Molecularly Imprinted Polymers</kwd><kwd> Solid Phase Extraction</kwd><kwd> Chromatographic Fractionating</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Molecular imprinting received a wide range of concerns since the publicly synthesis of molecularly imprinted polymers by Wulff in 1972 [<xref ref-type="bibr" rid="scirp.57685-ref1">1</xref>]. Molecular imprinting technology originated in antigen as template to synthesize antibodies that the template molecule, specific functional monomers and cross-linking agents are to obtain solid polymers. Molecularly imprinted polymers (MIPs), as man-made material of antibodies, possess recognition sites within the polymers that are adapted to the three-dimensional shape [<xref ref-type="bibr" rid="scirp.57685-ref2">2</xref>].</p></sec><sec id="s2"><title>2. Preparation of MIPs</title><p>Combin template and functional monomer in the specific dispersion system, adding cross-linking agent (or adding sorbent) and initiator, and then that will get the high alternate and robust polymer by non-covalent interaction or reversible covalent interaction [<xref ref-type="bibr" rid="scirp.57685-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.57685-ref4">4</xref>]. Consequentially, the template molecule was washed out from the polymer under harsh physics or chemistry conditions, which obtain a three-dimensional hole can identify the template molecule [<xref ref-type="bibr" rid="scirp.57685-ref5">5</xref>]. MIPs are gaining in importance as robust molecular recognition elements in analytical and separation sciences. What we can do is just to overcome the difficulty of choosing the appropriate conditions by chemical synthesis.</p><p>According to the property of the additive polymer made by template and functional monomers, there are covalent imprinting and non-covalent imprinting. Covalent imprinting, in which the process is explicit, distinct, steady and hard, is the less used technology for preparing MIPs than non-covalent imprinting, in which the complex of template and functional monomer is formed in situ by non-covalent interactions. Non-covalent interactions is the widely used, because the interaction is relative quick, and the template molecule was washed out from the polymer in the temperate condition. What is more, a planty of the functional monomers will have non-typical binding point, so that it deduces the ability of the selectivity of the synthetic substrate. There are several polymerization method such as suspension polymerization, situ polymerization, bulk polymerization, surface polymerization, dispersion polymerization, precipitation polymerization and swelling polymerization. Above all, bulk polymerization is the most common method in which template, functional monomer, cross- linking agent, adding sorbent and initiator dissolve in an inert solvent in appropriate proportions, which carry out in the light or thermal initiation under anaerobic conditions. We will get the particle what size we want through polymers obtained by crushing, grinding and sieving.</p></sec><sec id="s3"><title>3. The Application of MIPs</title><p>Based on the relevant characteristics of MIPs compared to other adsorbents such as selectivity, stability, sensitivity, high lifetime, etc. we perceive, it deserve arousing widely concern. The technique have already brought forward, successfully applying to solid phase extraction, chromatographic fractionating and bionic sensor.</p><sec id="s3_1"><title>3.1. Applications to Solid Phase Extraction (SPE)</title><p>Compared to the traditional extradition sorbent, MIPs are much better matched to the template molecule, so that they can identify the extract specifically. Particularly, MIPs, as the solid phase extraction, can reduce the question about complicated environmental sample system factor and heavy pretreatment factor, and then MIPs is widely used as solid phase material to separate and enrich (<xref ref-type="table" rid="table1">Table 1</xref>).</p></sec><sec id="s3_2"><title>3.2. Applications to Chromatographic Fractionating</title><p>Chromatographic methods, including HPLC, HPLC-MS and GC-MS [<xref ref-type="bibr" rid="scirp.57685-ref10">10</xref>], are able to provide molecular structure identification of the captured molecules. In order to reduce the limits of detecting instrument, we attach more importance to the effective enrichment approach. Obviously, MIPs is suited to be the analytical column and to separate sample (<xref ref-type="table" rid="table2">Table 2</xref>).</p></sec><sec id="s3_3"><title>3.3. Applications to Sensor</title><p>Recently, molecularly imprinted polymers (MIPs), as a recognition element for sensors, have made a great progress. Chemical (or biological) sensor consists of a recognition material and a response signal component. In</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Application of MIPs to SPE</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Template</th><th align="center" valign="middle" >Function monomer</th><th align="center" valign="middle" >Polymerization</th><th align="center" valign="middle" >Sample</th><th align="center" valign="middle" >Reference</th></tr></thead><tr><td align="center" valign="middle" >Iphenylguanidine</td><td align="center" valign="middle" >Iphenylguanidine</td><td align="center" valign="middle" >Bulk polymerization</td><td align="center" valign="middle" >Water</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.57685-ref6">6</xref>]</td></tr><tr><td align="center" valign="middle" >Lidocaine</td><td align="center" valign="middle" >Itaconic acid</td><td align="center" valign="middle" >Bulk polymerization</td><td align="center" valign="middle" >Serum</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.57685-ref7">7</xref>]</td></tr><tr><td align="center" valign="middle" >Methyltestosterone</td><td align="center" valign="middle" >Methacrylic acid</td><td align="center" valign="middle" >Bulk polymerization</td><td align="center" valign="middle" >Hormone</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.57685-ref8">8</xref>]</td></tr><tr><td align="center" valign="middle" >Dimethomorph</td><td align="center" valign="middle" >Methacrylate</td><td align="center" valign="middle" >Bulk polymerization and suspension polymerization</td><td align="center" valign="middle" >Antiseptic</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.57685-ref9">9</xref>]</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Application of MIPs to chromatographic fractionating</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Template</th><th align="center" valign="middle" >Function monomer</th><th align="center" valign="middle" >Sample</th><th align="center" valign="middle" >Analytical system</th><th align="center" valign="middle" >Reference</th></tr></thead><tr><td align="center" valign="middle" >Ractopamine</td><td align="center" valign="middle" >Acrylamide</td><td align="center" valign="middle" >Feed</td><td align="center" valign="middle" >MISPE-HPLC-FLD</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.57685-ref11">11</xref>]</td></tr><tr><td align="center" valign="middle" >Triadimenol</td><td align="center" valign="middle" >Methacrylate acid</td><td align="center" valign="middle" >Food</td><td align="center" valign="middle" >MISPE-HPLC</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.57685-ref12">12</xref>]</td></tr><tr><td align="center" valign="middle" >Nicotinamide</td><td align="center" valign="middle" >MAA</td><td align="center" valign="middle" >Drug</td><td align="center" valign="middle" >MISPE-HPLC-UV</td><td align="center" valign="middle" >[<xref ref-type="bibr" rid="scirp.57685-ref13">13</xref>]</td></tr></tbody></table></table-wrap><p>general, MIP film acts as the signal transducer that converts the binding signals from the molecular recognition to detectable electrical signals, and has an advantage of sensitivity of the sensing system [<xref ref-type="bibr" rid="scirp.57685-ref14">14</xref>].</p></sec></sec><sec id="s4"><title>Cite this paper</title><p>Ming Zhao,Guijun Shen, (2015) The Application of Molecularly Imprinted Polymers. 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