journal article·2013-02

Novel comb-like ionenes with aliphatic side chains: synthesis and antimicrobial properties

Xiang Xu, Huining Xiao, Zainab Ziaee, Hao Wang, Yong Guan, Anna Zheng

Journal of Materials Science· Volume 48· Issue 3
Publisher page

Abstract

A series of comb-like ionenes (C-ionenes) with aliphatic side chains were prepared via the Menschutkin reaction from amine, epichlorohydrin, and N,N,N′,N′-tetramethyl-1,6-hexanediamine. The structures of the resulting ionenes were characterized by means of charge density, 1H-NMR, and 13C-NMR. The antimicrobial properties of the ionenes were also investigated by measuring the minimum inhibition concentration (MIC) against Escherichia coli (E. coli). The corresponding antimicrobial dynamics were studied by detecting the UV absorbance of the E. coli suspension. It was found that in comparison to the linear ionenes (L-ionenes), C-ionenes exhibited lower MIC values and faster antimicrobial effect influenced by the side chains. In particular, C-ionene with 4-carbon side chains showed MIC at 7.8 μg/mL and its aqueous solution (31.2 μg/mL) inhibited 99.9 % E. coli within 2 min. The morphologies of C-ionenes in aqueous solution were investigated by measuring their particle sizes and zeta potentials. In addition, the anti-mold tests against Aspergillus niger and Chaetomium globosum suggested that the comb-like ionenes were effective at inhibiting the growth of the fungi.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Antimicrobial agents and applications · Environmental Chemistry and Analysis · Luminescence and Fluorescent Materials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (35)

Show source-provided references
1. Patel MB, Patel SA, Ray A, Patel RM (2009) J Appl Polym Sci 89:895–90010.1002/app.11970 ↗
2. Kenawy ER, Worley SD, Broughton R (2007) Biomacromolecules 8(5):1359–138410.1021/bm061150q ↗
3. Tashiro T (2001) Macromol Mater Eng 286(2):63–8710.1002/1439-2054(20010201)286:2<63::AID-MAME63>3.0.CO;2-H ↗
4. Ikeda T, Hirayama H, Yamaguchi H, Tazuke S, Watanabe M (1986) Antimicrob Agents Chemother 30:132–13610.1128/AAC.30.1.132 ↗
5. Bromberg L, Hatton T (2007) Polymer 48(26):7490–749810.1016/j.polymer.2007.10.040 ↗
6. Gibbs CF, Littmann ER, Marvel CS (1933) J Am Chem Soc 55:753–75710.1021/ja01329a046 ↗
7. Abboud JLM, Notario R, Bertrán J, Solà M (1993) Prog Phys Org Chem 19:1–18210.1002/9780470171981.ch1 ↗
8. Williams SR, Barta Z, Ramirez SM, Long TE (2009) Macromol Chem Phys 210:555–56410.1002/macp.200800522 ↗
9. Rembaum A, Noguchi H (1972) Macromolecules 5:261–27210.1021/ma60027a007 ↗
10. Pirogov AV, Stepanov KV, Shpigun OA (2003) J Anal Chem 58:478–48410.1023/A:1024086316240 ↗
11. Zelikin AN, Litmanovich AA, Paraschuk VV, Sybatchin AV, Izumrudov VA (2003) Macromolecules 36:2066–207110.1021/ma021361x ↗
12. Zelikin AN, Izumrudov VA (2002) Macromol Biosci 2:78–8110.1002/1616-5195(20020201)2:2<78::AID-MABI78>3.0.CO;2-7 ↗
13. Ramirez SM, Layman JM, Long TE (2009) Macromol Biosci 9:1127–113410.1002/mabi.200900137 ↗
14. De S, Ramakrishnan S (2009) Macromolecules 42:8599–860310.1021/ma901954x ↗
15. Vanherk AM, Tullemans AHJ, Vanwelzen J, German AL (1988) J Mol Catal 44:269–27710.1016/0304-5102(88)80037-3 ↗
16. Welzen JV, Herk AMV, Kramer H, German AL (1999) J Mol Catal 59:29110.1016/0304-5102(90)85102-N ↗
17. Schipper ETWM, Roelofs AHC, Piet P, German AL (1995) Langmuir 11:1595–159910.1021/la00005a030 ↗
18. Chen L, Yu SY, Kagami Y, Gong JP, Osada Y (1998) Macromolecules 31:787–79410.1021/ma971228i ↗
19. Pirogov AV, Platonov MM, Shpigun OA (1999) J Chromatogr A 850:53–6310.1016/S0021-9673(99)00370-2 ↗
20. Pirogov AV, Krokhin OV, Platonov MM, Deryugina YI, Shpigun OA (2000) J Chromatogr A 884:31–3910.1016/S0021-9673(00)00273-9 ↗
21. Raskop MP, Grimm A, Seubert A (2007) Microchim Acta 158:85–9410.1007/s00604-006-0650-6 ↗
22. Yildiz UH, Koynov K, Grohn F (2009) Macromol Chem Phys 210:1678–169010.1002/macp.200900224 ↗
23. Burmistr MV, Sukhyy KM, Shilov VV (2005) Polymer 46:12226–1223210.1016/j.polymer.2005.10.094 ↗
24. Pirogov AV, Yur’ev AV, Shpigun OA (2003) J Anal Chem 58:781–78410.1023/A:1025047913692 ↗
25. Erdmenger T, Perevyazko I, Vitz J, Pavlov G, Schubert US (2010) J Mater Chem 20:3583–358510.1039/b921525e ↗
26. Grassl B, Meurer B, Scheer M, Galin JC (1997) Macromolecules 30:236–24510.1021/ma960643s ↗
27. Grassl B, Mathis A, Rawiso M, Galin JC (1997) Macromolecules 30:2075–208410.1021/ma960880v ↗
28. Ziaee Z, Qian L, Guan Y, Fatehi P, Xiao HN (2010) J Biomater Sci 21:1359–137010.1163/092050609X12517190417795 ↗
29. Ikeda T, Hirayama H, Suzuki K, Yamaguchi H, Tazuke S (1986) Makromol Chem 187:333–34010.1002/macp.1986.021870212 ↗
30. Ikeda T, Tazuke S, Suzuki Y (1984) Macromol Chem Phys 185:869–87610.1002/macp.1984.021850503 ↗
31. Ikeda T, Yamaguchi H, Tazuke S (1984) Antimicrob Agents Chemother 26:139–14410.1128/AAC.26.2.139 ↗
32. Qian LY, Xiao HN (2011) Appl Mater Interfaces 3:1895–190110.1021/am200094u ↗
33. Chen CZS, Cooper SL (2002) Biomaterials 23:3359–336810.1016/S0142-9612(02)00036-4 ↗
34. Broxton P, Woodcock PM (1984) J Appl Bacteriol 57:115–12410.1111/j.1365-2672.1984.tb02363.x ↗
35. Burke J (1984) Solubility parameters: theory and application. Oakland, pp 13–14