journal article·2012-11

Synthesis, characterization, and controlled release antibacterial behavior of antibiotic intercalated Mg–Al layered double hydroxides

Yi Wang, Dun Zhang

Materials Research Bulletin· Volume 47· Issue 11
Publisher page

Abstract

Antibiotic-inorganic clay composites including four antibiotic anions, namely, benzoate (BZ), succinate (SO), benzylpenicillin (BP), and ticarcillin (TC) anions, intercalated Mg-Al layered double hydroxides (LDHs) were synthesized via ion-exchange. Powder X-ray diffraction and Fourier transform infrared spectrum analyses showed the successful intercalation of antibiotic anion into the LDH interlayer. BZ and BP anions were accommodated in the interlayer region as a bilayer, whereas SU and TC anions were intercalated in a monolayer arrangement. Kinetic simulation of the release data indicated that ion-exchange was responsible for the release process, and the diffusion through the particles was the rate-limiting step. The antibacterial capabilities of LDHs loaded with antibiotic anion toward Micrococcus lysodeikticus growth were analyzed using a turbidimetric method. Significant high inhibition rate was observed when LDH nanohybrid was introduced in 3.5% NaCl solution. Therefore, this hybrid material may be applied as nanocontainer in active antifouling coating for marine equipment. (C) 2012 Elsevier Ltd. All rights reserved.
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Research context

OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Polymer Surface Interaction Studies · Advanced Photocatalysis Techniques

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

References (52)

Show source-provided references
1. Donlan · Clin. Infect. Dis. · 2001 · 33 · 138710.1086/322972 ↗
2. Cole · Invest. Ophth. Vis. Sci. · 2010 · 51 · 39010.1167/iovs.09-4068 ↗
3. Willcox · J. Appl. Microbiol. · 2008 · 105 · 181710.1111/j.1365-2672.2008.03942.x ↗
4. Yeh · Colloids Surf. B · 2007 · 59 · 6710.1016/j.colsurfb.2007.04.007 ↗
5. Li · Int. J. Food Sci. Technol. · 2009 · 44 · 216110.1111/j.1365-2621.2009.02055.x ↗
6. Sothornvit · LWT-Food Sci. Technol. · 2010 · 43 · 27910.1016/j.lwt.2009.08.010 ↗
7. Gemili · J. Food Eng. · 2009 · 90 · 45310.1016/j.jfoodeng.2008.07.014 ↗
8. Whitehead · Biofouling · 2009 · 25 · 74910.1080/08927010903161299 ↗
9. Almeida · Prog. Org. Coat. · 2007 · 59 · 210.1016/j.porgcoat.2007.01.017 ↗
10. Callow · Nat. Commun. · 2011 · 210.1038/ncomms1251 ↗
11. Banerjee · Adv. Mater. · 2011 · 23 · 69010.1002/adma.201001215 ↗
12. Upadhyayula · Biotechnol. Adv. · 2010 · 28 · 80210.1016/j.biotechadv.2010.06.006 ↗
13. Bezemer · J. Control. Release · 2000 · 64 · 17910.1016/S0168-3659(99)00127-3 ↗
14. Del Nobile · J. Food Eng. · 2008 · 89 · 5710.1016/j.jfoodeng.2008.04.004 ↗
15. Shukla · Biomaterials · 2010 · 31 · 234810.1016/j.biomaterials.2009.11.082 ↗
16. Buonocore · J. Control. Release · 2003 · 90 · 9710.1016/S0168-3659(03)00154-8 ↗
17. Nordstierna · Prog. Org. Coat. · 2010 · 69 · 4510.1016/j.porgcoat.2010.05.002 ↗
18. Malheiros · Trends Food Sci. Technol. · 2010 · 21 · 28410.1016/j.tifs.2010.03.003 ↗
19. Sokolova · Angew. Chem. Int. Ed. · 2008 · 47 · 138210.1002/anie.200703039 ↗
20. Del Hoyo · Appl. Clay Sci. · 2007 · 36 · 10310.1016/j.clay.2006.06.010 ↗
21. Li · Struct. Bond. · 2006 · 119 · 19310.1007/430_007 ↗
22. Evans · Struct. Bond. · 2006 · 119 · 1
23. Choy · Angew. Chem. Int. Ed. · 2000 · 39 · 404110.1002/1521-3773(20001117)39:22<4041::AID-ANIE4041>3.0.CO;2-C ↗
24. Tyner · J. Control. Release · 2004 · 100 · 39910.1016/j.jconrel.2004.07.035 ↗
25. Gasser · Colloids Surf. B · 2009 · 73 · 10310.1016/j.colsurfb.2009.05.005 ↗
26. Aisawa · J. Solid State Chem. · 2003 · 174 · 34210.1016/S0022-4596(03)00234-2 ↗
27. Touloupakis · Pest Manag. Sci. · 2011 · 67 · 83710.1002/ps.2121 ↗
28. Park · Environ. Sci. Pollut. Res. · 2010 · 17 · 20310.1007/s11356-009-0235-0 ↗
29. Zhang · J. Solid State Chem. · 2006 · 179 · 179210.1016/j.jssc.2006.03.019 ↗
30. Ha · Int. J. Pharmaceut. · 2011 · 414 · 32110.1016/j.ijpharm.2011.05.028 ↗
31. Yasin · J. Biomed. Nanotechnol. · 2011 · 7 · 48610.1166/jbn.2011.1307 ↗
32. Khan · Ind. Eng. Chem. Res. · 2009 · 48 · 1019610.1021/ie9012612 ↗
33. Ghotbi · J. Phys. Chem. Solids · 2010 · 71 · 156510.1016/j.jpcs.2010.08.003 ↗
34. Costantino · ACS Appl. Mater. Interfaces · 2009 · 1 · 66810.1021/am8001988 ↗
35. Ryu · J. Phys. Chem. Solids · 2010 · 71 · 68510.1016/j.jpcs.2009.12.066 ↗
36. Stanojevic · Bulg. J. Agric. Sci. · 2009 · 15 · 308
37. Ceylan · J. Food Sci. · 2004 · 69 · M10210.1111/j.1365-2621.2004.tb06348.x ↗
38. Ostergaard · Acta Odontol. Scand. · 1994 · 52 · 33510.3109/00016359409029031 ↗
39. Feng · Food Sci. Biotechnol. · 2010 · 19 · 3510.1007/s10068-010-0005-2 ↗
40. Rehman · Br. Med. J. · 2009 · 339
41. Jewett · J. Pediatr. · 1985 · 106 · 66910.1016/S0022-3476(85)80100-1 ↗
42. Bontchev · Chem. Mater. · 2003 · 15 · 366910.1021/cm034231r ↗
43. Xu · J. Phys. Chem. B · 2001 · 105 · 174310.1021/jp0029257 ↗
44. Velu · J. Mater. Sci. · 1997 · 32 · 95710.1023/A:1018561918863 ↗
45. Kovář · J. Mol. Model. · 2007 · 13 · 93710.1007/s00894-007-0217-4 ↗
46. Prevot · Inorg. Chem. · 1998 · 37 · 429310.1021/ic9801239 ↗
47. Dziegielewski · J. Appl. Spectrosc. · 1973 · 19 · 103110.1007/BF00610751 ↗
48. Zou · Chem. Eng. Sci. · 2007 · 62 · 202210.1016/j.ces.2006.12.041 ↗
49. Chern · Ind. Eng. Chem. Res. · 2004 · 43 · 615010.1021/ie049616d ↗
50. Serra · Biomaterials · 2006 · 27 · 544010.1016/j.biomaterials.2006.06.011 ↗
51. Ambrogi · Int. J. Pharmaceut. · 2001 · 220 · 2310.1016/S0378-5173(01)00629-9 ↗
52. Bhaskar · Int. J. Pharmaceut. · 1986 · 28 · 5910.1016/0378-5173(86)90147-X ↗