Nanohybrids for controlled antibiotic release in topical applications

被引:73
作者
Tammaro, L.
Costantino, U.
Bolognese, A.
Sammartino, G.
Marenzi, G.
Calignano, A.
Tete, S.
Mastrangelo, F.
Califano, L.
Vittoria, V.
机构
[1] Univ G DAnnunzio, Dept Oral Sci, I-66100 Chieti, Italy
[2] Univ Salerno, Dept Chem & Food Engn, I-84084 Fisciano, Sa, Italy
[3] Univ Perugia, Dept Chem, CEMIN, I-06123 Perugia, Italy
[4] Univ Naples Federico II, Dept Organ Chem & Biochem, I-80126 Naples, Italy
[5] Univ Naples Federico II, Dept Oral & Maxillofacial Sci, I-80131 Naples, Italy
[6] Univ Naples Federico II, Dept Expt Pharmacol, I-80131 Naples, Italy
关键词
nanohybrid; polycaprolactone; drug release; antibiotic molecules; hydrotalcites;
D O I
10.1016/j.ijantimicag.2006.11.019
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
New polymeric composite materials containing a nanohybrid to be used for the controlled release of an antibiotic molecule, chloramphenicol succinate, have been formulated, prepared and characterised. The nanohybrid consists of a layered double hydroxide of Mg-Al hydrotalcitetype, in which the nitrate anions present in the host galleries were replaced with chloramphenicol succinate anions (CFS-) by a simple ion-exchange reaction. Different amounts of the hybrid material were incorporated in polycaprolactone and processed as films of 0.15 mm thickness. The composite materials were analysed by X-ray diffractometry and thermogravimetry and their mechanical properties were determined. They showed properties even better than those of the pristine polymer. The release process of the antibiotic molecules was found to be very interesting and promising for tuneable drug delivery. It consists of two stages: an initial stage of a very rapid burst, in which a small fraction of drug is released; and a second stage that is much slower, extending for a longer and longer time. This behaviour is profoundly different and much slower than that of a sample in which the antibiotic molecule is directly incorporated into the polymeric matrix. The parameters influencing drug release have been individuated and discussed. (c) 2007 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
引用
收藏
页码:417 / 423
页数:7
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