Surface molecularly imprinted organic-inorganic polymers having affinity sites for cholesterol

Reactive and Functional Polymers

Volumn 109, Issue , 2016, Pages 88-98

  Polyakova, Irina ^a   Borovikova, Ludmila ^a   Osipenko, Aleksandra ^b   Vlasova, Elena ^a   Volchek, Boris ^a   Pisarev, Oleg ^a,b  

^a INSTITUTE OF MACROMOLECULAR COMPOUNDS   (Russian Federation)

^b PETER THE GREAT ST PETERSBURG POLYTECHNIC UNIVERSITY   (Russian Federation)

Author keywords

Specific cholesterol sorption; Surface molecular imprinting

Indexed keywords

ADSORPTION ISOTHERMS; BINDING SITES; BINS; CHOLESTEROL; ETHYLENE; ETHYLENE GLYCOL; HYDROGEN BONDS; INORGANIC POLYMERS; ISOTHERMS; MICROEMULSIONS; MOLECULES; ORGANIC POLYMERS; SCANNING ELECTRON MICROSCOPY; SORPTION;

2-HYDROXYETHYL METHACRYLATE; ETHYLENE GLYCOL DIMETHACRYLATE; MOLECULARLY IMPRINTED; MOLECULARLY IMPRINTED POLYMER; NON-IMPRINTED POLYMERS; ORGANIC INORGANIC POLYMERS; POLYVINYL PYRROLIDONE; SURFACE MOLECULAR IMPRINTING;

FOURIER TRANSFORM INFRARED SPECTROSCOPY;

EID: 84995483132     PISSN: 13815148     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.reactfunctpolym.2016.10.010     Document Type: Article

References (58)

1. [1] Schell, W.D., Myers, J.N., Prog. Cardiovasc. Dis. 39 (1997), 483–496.
2. [2] Feig, J.E., Ann. Glob. Health 80 (2014), 13–23.
3. [3] Sprecher, D.L., Schaefer, E.J., Kent, K.M., Gregg, R.E., Zech, L.A., Hoeg, J.M., McManus, B., Roberts, W.C., Brewer, H.B. Jr., Am. J. Cardiol. 54 (1984), 20–30.
4. [4] Kraft, H.G., Lingenhel, A., Raal, F.J., Hohenegger, M., Utermann, G., Arterioscler. Thromb. Vasc. Biol. 20 (2000), 522–528.
5. [5] Seidel, D., Armstrong, V.W., Schuff-Werner, P., HELP Study Group. Eur. J. Clin. Investig. 21 (1991), 375–383.
6. [6] Gordon, B.R., Kelsey, S.F., Bilheimer, D.W., Brown, D.C., Dau, P.C., Gotto, A.M. Jr., Illingworth, D.R., Jones, P.H., Leitman, S.F., Prihoda, J.S., Stein, E.A., Stern, T.N., Zavoral, J.H., Zwiener, R.J., Am. J. Cardiol. 70 (1992), 1010–1016.
7. [7] Agishi, T., Wood, W., Gordon, B., Curr. Ther. Res. 55 (1994), 879–904.
8. [8] Frishman, W.H., Beravo, P., Carosella, C., Dis. Mon. 55 (2009), 121–192.
9. [9] McGowan, M.P., J. Clin. Lipidol. 7 (2013), S21–S26.
10. [10] Alexander, C., Andersson, H.S., Andersson, L.I., Ansell, R.J., Kirsch, N., Nicholls, I.A., O'Mahony, J., M.J, J. Mol. Recognit. 19 (2006), 106–180.
11. [11] Whitcombe, M.J., Rodriguez, M.E., Villar, P., Vulfson, E.N., J. Am. Chem. Soc. 117 (1995), 7105–7111.
12. [12] Zhong, N., Byun, H., Bittman, R., Tetrahedron Lett. 42 (2001), 1839–1841.
13. [13] Puoci, F., Curcio, M., Cirillo, G., Iemma, F., Spizzirri, U.G., Picci, N., Food Chem. 106 (2008), 836–842.
14. [14] Shi, Y., Zhang, J.-H., Shi, D., Jiang, M., Zhu, Y.-X., Mei, S.-R., Zhou, Y.-K., Dai, K., Lu, B., J. Pharm. Biomed. Anal. 42 (2006), 549–555.
15. [15] Puoci, F., Iemma, F., Cirillo, G., Curcio, M., Parisi, O.I., Spizzirri, U.G., Picci, N., Eur. Polym. J. 45 (2009), 1634–1640.
16. [16] Zhang, H., Polymer 55 (2014), 699–714.
17. [17] Yavuz, H., Karakoc, V., Türkmen, D., Say, R., Denizli, A., J. Biol. Macromol. 41 (2007), 8–15.
18. [18] Benito-Peña, E., González-Vallejo, V., Rico-Yuste, A., Barbosa-Pereira, L., Cruz, J.M., Bilbao, A., Alvarez-Lorenzo, C., Cruz Moreno-Bondi, M., J. Food Chem. 190 (2016), 487–494.
19. [19] Polyakova, I.V., Ezhova, N.M., Osipenko, A.A., Pisarev, O.A., Russ. Zh. Fiz. Khim. 89 (2015), 312–315.
20. [20] Poma, A., Turner, A.P.F., Piletsky, S.A., Trends Biotechnol. 28 (2010), 629–637.
21. [21] Flores, A., Cunliff, D., Whitcombe, M.J., E.N, J. Appl. Polym. Sci. 77 (2000), 1841–1850.
22. [22] Lee, W.-C., Hung, C.-Y., Hwang, C.-C., Chem. Biochem. Eng. Q. 22 (2008), 151–156.
23. [23] Perez, N., Whitcombe, M.J., Vulfson, E.N., Macromolecules 34 (2001), 830–836.
24. [24] Kitahara, K., Yoshihama, I., Hanada, T., Kokuba, H., Arai, S., J. Chromatogr. A 1217 (2010), 7149–7254.
25. [25] Clausen, D.N., Ruiz Pires, I.M., Teixeira Tarley, C.R., Mater. Sci. Eng. C 44 (2014), 99–108.
26. [26] Zengin, A., Yildirim, E., Tamer, U., Caykara, T., Analyst 138 (2013), 7238–7245.
27. [27] Pérez, N., Whitcombe, M.J., Vulfson, E.N., J. Appl. Polym. Sci. 77 (2000), 1851–1859.
28. [28] Moczko, E., Poma, A., Guerreiro, A., de Vargas Sansalvador, I.P., Caygill, S., Canfarotta, F., Whitcombe, M.J., Piletsky, S., Nanoscale 5 (2013), 3733–3741.
29. [29] Ramsden, W., Proc. R. Soc. 72 (1903), 156–164.
30. [30] Pickering, S.U., J. Chem. Soc. 91 (1907), 2001–2021.
31. [31] Torres, L.G., Iturbe, R., Snowden, M.J., Chowdhry, B.Z., Leharne, S.A., Colloids Surf. A Physicochem. Eng. Asp. 302 (2007), 439–448.
32. [32] Kawano, S., Kida, T., Akashi, M., Sato, H., Shizuma, M., Ono, D., J. Org. Chem. 11 (2015), 2355–2364.
33. [33] Kok, F.J., Hofman, A., Witteman, J.C.M., de Bruijn, A.M., Kruyssen, D.H., de Bruin, M., Valkenburg, H.A., JAMA 261 (1989), 1161–1164.
34. [34] Frishman, W.H., Beravol, P., Carosella, C., Dis. Mon. 55 (2009), 121–192.
35. [35] He, H.-Y., Cao, X., Lee, L.-J., J. Control. Release 95 (2004), 391–402.
36. [36] Moukwa, M., J. Met. 49 (1997), 46–50.
37. [37] Dunn, S.E., Brindley, A., Davis, S.S., Davies, M.C., Illum, L., Pharm. Res. 11 (1994), 1016–1022.
38. [38] Adali, T., Yilmaz, E., Carbohydr. Polym. 77 (2009), 136–141.
39. [39] Polyakova, I.V., Osipenko, A.A., Borovikova, L.N., Ezhova, N.M., Pisarev, O.A., Vlasova, E.N., Volchek, B.Z., J. Appl. Chem. 88 (2015), 1617–1626.
40. [40] Shaker, A.M., J. Colloid Interface Sci. 180 (1996), 225–231.
41. [41] Kopeikin, V.V., Valueva, S.V., Kipper, A.I., Borovikova, L.N., Fillipov, A.P., J. Polym. Sci. A 45 (2003), 374–379.
42. [42] Pisarev, O.A., Polyakova, I.V., Trends. Chromatogr. 7 (2013), 85–106.
43. [43] Gomez, C.G., Pastrana, G., Serrano, D., Zuzek, E., Villar, M.A., Strumia, M.C., Macroporous poly(EGDMA-co-HEMA) Networks: Morphological Characterization From Their Behaviour in the Swelling Process Polymer. 53, 2012, 2949–2955.
44. [44] Bonner, O.D., Argersinger, W.J., Davidson, A.W., J. Am. Chem. Soc. 74 (1952), 1044–1047.
45. [45] Hammett, L., Physical Organic Chemistry. second ed., 1970, McGraw-Hill, New York.
46. [46] Belami, L., IR Spectra of Complex Molecules [Russian Translation]. 1963, Izd. Inostr. Lit, Moscow.
47. [47] Freundlich, H.M.F., J. Phys. Chem. A 57 (1906), 385–470.
48. [48] Langmuir, I., J. Am. Chem. Soc. 38 (1916), 2221–2295.
49. [49] Temkin, M., Pyzhev, V., Acta Phys. Chim. USSR 12 (1940), 327–356.
50. [50] Brunauer, S., Emmett, P.H., Teller, E., J. Am. Chem. Soc. 60 (1938), 309–319.
51. [51] Umpleby, R.J. II, Baxter, S.C., Chen, Y., Shah, R.N., Shimizu, K.D., Anal. Chem. 73 (2001), 4584–4591.
52. [52] Ho, Y.-S., Wang, C.-C., J. Hazard. Mater. 156 (2008), 398–404.
53. [53] Foo, K.Y., Hameed, B.H., Chem. Eng. J. 156 (2010), 2–10.
54. [54] Tseng, R.-L., Wu, F.-C., J. Hazard. Mater. 155 (2008), 277–287.
55. [55] Voudrias, E., Fytianos, F., Bozani, E., Global Nest. Int. J. 4 (2002), 75–83.
56. [56] Mohan, S., J. Karthikeyan. Environ. Pollut. 97 (1997), 183–187.
57. [57] Bae, Y.S., Snurr, R.Q., Yazaydin, O., Langmuir 26 (2010), 5475–5483.
58. [58] Günay, A., Arslankaya, E., Tosun, I., J. Hazard. Mater. 146 (2007), 362–371.