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Dual role of layered double hydroxide nanocomposites on antibacterial activity and degradation of tetracycline and oxytetracyline
被引:28
作者:
Bouaziz, Zaineb
[1
,2
]
Soussan, Laurence
[1
]
Janot, Jean-Marc
[1
]
Jaber, Maguy
[3
]
Amara, Abdesslem Ben Haj
[2
]
Balme, Sebastien
[1
]
机构:
[1] UM, ENSM, CNRS, Inst Europeen Membranes,UMR5635, Pl Eugene Bataillon, F-34095 Montpellier 5, France
[2] Univ Carthage, Fac Sci Bizerte, Lab Phys Mat Lamellaires & Nanomat Hybrides, Tunis, Tunisia
[3] Sorbonne Univ, Lab Archeol Mol & Struct, CNRS, UMR 8220, Tour 23,3eme Etage,Couloir 23-33,BP 225, Paris, France
来源:
关键词:
Layered Double Hydroxide;
Oxytetracyline;
Tetracycline;
CONTROLLED-RELEASE;
CLAY-MINERALS;
ADSORPTION;
INTERCALATION;
MONTMORILLONITE;
ANTIBIOTICS;
NANOHYBRIDS;
ENVIRONMENT;
PH;
D O I:
10.1016/j.chemosphere.2018.05.003
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
The antibiotic intercalation inside the layered double hydroxide (LDH) layers was usually considered for water decontamination but rarely for drug delivery. Here, tetracycline (TCH) and oxytetracycline (OXY) were immobilized in Zn2Al-Cl LDH following two methods: co-precipitation and anionic exchange. The interfacial concentration of antibiotic varies from 0.04 to 0.5 depending the method of immobilization. The antibiotics are not intercalated in the interlayer space allowing their release in 10 Hours. The antibacterial activity against both E. coli and S. epidermidis revealed that the loaded antibiotics are still active but less efficient compared to the free ones. After exposition to UV light or to high temperature storage (30, 60 and 120 degrees C), their antibacterial activity significantly decreases due to their degradation especially when antibiotic is loaded on material by co-precipitation. These results are promise to reduce antibiotic contamination in waters. (C) 2018 Elsevier Ltd. All rights reserved.
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页码:175 / 183
页数:9
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