Affinity distributions of a molecularly imprinted polymer calculated numerically by the expectation-maximization method

被引:44
作者
Stanley, BJ
Szabelski, P
Chen, YB
Sellergren, B
Guiochon, G [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Oak Ridge Natl Lab, Div Chem & Analyt Sci, Oak Ridge, TN 37831 USA
[3] Calif State Univ San Bernardino, Dept Chem, San Bernardino, CA 92407 USA
[4] Marie Curie Sklodowska Univ, Dept Theoret Chem, PL-20031 Lublin, Poland
[5] Fox Chase Canc Ctr, Biotech Facil, Philadelphia, PA 19111 USA
[6] Univ Mainz, Dept Inorgan Chem & Analyt Chem, D-55099 Mainz, Germany
关键词
D O I
10.1021/la020747y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Affinity distributions are calculated from adsorption isotherm data obtained for the enantiomers of Land D-phenylalanine anilide (PA) on native and thermally annealed polymers molecularly imprinted with L-PA. The calculation is obtained with an iterative algorithm called expectation-maximization that does not require prior fit of the data to an isotherm model before inversion and thus yields a distribution indicative of the data only. The results show bimodal distributions, suggestive of a two-site model describing relatively selective and nonselective adsorption modes of the L-enantiomer and a corresponding unimodal/nonselective adsorption mode for the D-enantiomer. The nonselective adsorption region of the distributions exponentially decreases with increasing association constant, whereas the selective adsorption is Gaussian in appearance. The thermally annealed polymer exhibits altered affinity distributions that are somewhat less heterogeneous and more selective. Their selective sites have a lower saturation capacity than the native polymer. The capacity of the nonselective sites is inconclusive due to undersaturation of these lower energy sites, but it appears to be greater.
引用
收藏
页码:772 / 778
页数:7
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