journal article·2015-11-02Open access

Synthesis, characterisation and sustained release properties of layered zinc hydroxide intercalated with amoxicillin trihydrate

Hafezeh Nabipour, Moayad Hosaini Sadr, Nygil Thomas

Abstract

The intercalation of amoxicillin trihydrate (AMOX) into layered zinc hydroxide (LZH) has been achieved via ion-exchange method. The resulted nanocomposite (AMOX-LZH) has been thoroughly characterised by a number of techniques including powder X-ray diffraction (PXRD), FT-IR spectroscopy, TGA/DTG analysis and scanning electron microscopy (SEM). The PXRD results showed that the gallery height of LZH was expanded from 9.57 to 11.97 Å, indicating that the AMOX anions were successfully intercalated into the interlayer space of LZHs. The increased thermal stability of nanocomposite was confirmed by TGA/DTG analyses. Improved antibacterial activity and minimum inhibitory concentration of AMOX-LZH nanocomposite was evaluated against Gram-positive bacteria Staphylococcus aureus, Klebsiella pneumonia and Gram- negative Escherichia coli using the disk diffusion technique. The sustained release of amoxicillin drug from the AMOX-LZH nanocomposite was also verified.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Magnesium Oxide Properties and Applications · Advanced Photocatalysis Techniques

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

References (36)

Show source-provided references
1. 10.1016/j.tim.2006.02.00610.1016/j.tim.2006.02.006 ↗
2. 10.1016/j.jconrel.2011.07.00210.1016/j.jconrel.2011.07.002 ↗
3. 10.1016/j.ssi.2007.04.01610.1016/j.ssi.2007.04.016 ↗
4. 10.1016/S0169-1317(98)00058-110.1016/S0169-1317(98)00058-1 ↗
5. 10.1016/S1466-6049(00)00020-910.1016/S1466-6049(00)00020-9 ↗
6. 10.1016/j.jcis.2007.12.02510.1016/j.jcis.2007.12.025 ↗
7. 10.1021/nn900002m10.1021/nn900002m ↗
8. 10.1007/978-1-4614-0881-9_1510.1007/978-1-4614-0881-9_15 ↗
9. 10.1007/978-1-4614-0881-9_510.1007/978-1-4614-0881-9_5 ↗
10. 10.1021/ic00059a03010.1021/ic00059a030 ↗
11. 10.1590/S0100-4042200500010000510.1590/S0100-40422005000100005 ↗
12. 10.1016/0167-2738(90)90397-A10.1016/0167-2738(90)90397-A ↗
13. 10.1021/ic950965x10.1021/ic950965x ↗
14. 10.1016/S0040-4020(03)00554-410.1016/S0040-4020(03)00554-4 ↗
15. 10.1016/j.jssc.2008.06.00910.1016/j.jssc.2008.06.009 ↗
16. Faiz U · J Ayub Med Coll Abbottabad · 2011 · 23 · 18
17. 10.1007/s13204-012-0141-510.1007/s13204-012-0141-5 ↗
18. 10.1016/S0142-9612(02)00512-410.1016/S0142-9612(02)00512-4 ↗
19. 10.2174/156720181131002000410.2174/1567201811310020004 ↗
20. 10.1016/j.ijbiomac.2012.04.01810.1016/j.ijbiomac.2012.04.018 ↗
21. Boles MO · ActaCrystallogr. · 1976 · 34 · 461
22. 10.1111/j.1572-0241.1999.01065.x10.1111/j.1572-0241.1999.01065.x ↗
23. Buzas GM · Orv Hetil. · 1999 · 140 · 121
24. 10.1016/j.jiec.2014.04.02810.1016/j.jiec.2014.04.028 ↗
25. 10.1046/j.1365-2885.1998.00107.x10.1046/j.1365-2885.1998.00107.x ↗
26. Buchbinder M · Antimicrob Agents Chemother. · 1962 · 2 · 308
27. Al-Hıari YM · Asian J Chem. · 2006 · 18 · 2285
28. Golebiewski WM · Polish J Chem. · 2000 · 74 · 759
29. 10.1016/j.saa.2007.08.01210.1016/j.saa.2007.08.012 ↗
30. 10.1016/j.jcis.2008.10.08110.1016/j.jcis.2008.10.081 ↗
31. 10.1016/j.jssc.2005.09.04010.1016/j.jssc.2005.09.040 ↗
32. 10.1016/j.electacta.2005.04.07110.1016/j.electacta.2005.04.071 ↗
33. 10.1166/jnn.2005.03410.1166/jnn.2005.034 ↗
34. 10.1007/s11051-008-9428-610.1007/s11051-008-9428-6 ↗
35. 10.1016/j.colsurfa.2006.10.02410.1016/j.colsurfa.2006.10.024 ↗
36. 10.1021/nl052326h10.1021/nl052326h ↗