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ORIGINAL ARTICLE

Molecularly imprinted cryogels for chondroitin sulfate recognition

Pages 610-617 | Received 10 Sep 2014, Accepted 07 Oct 2014, Published online: 29 Oct 2014

Figures & data

Figure 1. SEM images of A) CsMIP, B) NIP cryogel.

Figure 1. SEM images of A) CsMIP, B) NIP cryogel.

Figure 2. FTIR spectrum of Cs, VIM and VIM-Cu(II)-Cs precomplex.

Figure 2. FTIR spectrum of Cs, VIM and VIM-Cu(II)-Cs precomplex.

Figure 3. FTIR spectrum of CsMIP and NIP columns.

Figure 3. FTIR spectrum of CsMIP and NIP columns.

Figure 4. Effect of equilibrium concentration of Cs on the Cs adsorption amount, and the Langmuir and Freundlich adsorption isotherms. V: 5 mL, Mdry: 0.263 g.

Figure 4. Effect of equilibrium concentration of Cs on the Cs adsorption amount, and the Langmuir and Freundlich adsorption isotherms. V: 5 mL, Mdry: 0.263 g.

Table I. Langmuir and Freundlich adsorption isotherm constants and correlation coefficients for Cs.

Figure 5. Reusability of the CsMIP cryogel column. Cycle number 10, V: 5 mL, Cs: 0.2 mg/mL, Mdry: 0.263 g.

Figure 5. Reusability of the CsMIP cryogel column. Cycle number 10, V: 5 mL, Cs: 0.2 mg/mL, Mdry: 0.263 g.

Figure 6. Amount of compounds adsorbed onto the CsMIP and NIP columns. Ceq: 2 mg/mL, V: 5 mL, t: 120 min, Mdry: 0.63 g.

Figure 6. Amount of compounds adsorbed onto the CsMIP and NIP columns. Ceq: 2 mg/mL, V: 5 mL, t: 120 min, Mdry: 0.63 g.

Table II. Selectivity constant values (k, Kd, k’) of Cs.

Figure 7. Fast protein liquid chromatography (FPLC) system separation of Cs from aqueous Cs-Hp solution.

Figure 7. Fast protein liquid chromatography (FPLC) system separation of Cs from aqueous Cs-Hp solution.

Table III. Chromatographic separation data of the FPLC study.

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