Prilling and supercritical drying: A successful duo to produce core-shell polysaccharide aerogel beads for wound healing

被引:79
作者
De Cicco, Felicetta [1 ]
Russo, Paola [1 ]
Reverchon, Ernesto [2 ]
Garcia-Gonzalez, Carlos A. [3 ]
Aquino, Rita Patrizia [1 ]
Del Gaudio, Pasquale [1 ]
机构
[1] Univ Salerno, Dept Pharm, Via Giovanni Paolo II, I-84084 Fisciano, SA, Italy
[2] Univ Salerno, Dept Ind Engn, Via Giovanni Paolo II, I-84084 Fisciano, SA, Italy
[3] Univ Santiago Compostela, Dept Pharm & Pharmaceut Technol, E-15782 Santiago De Compostela, Spain
关键词
Aerogel; Alginate; Pectin; Doxycycline; Prilling; Supercritical CO2; DRUG-DELIVERY SYSTEMS; TUMOR-NECROSIS-FACTOR; CONTROLLED-RELEASE; IN-VIVO; ANTIINFLAMMATORY DRUGS; ALGINATE BEADS; DOSAGE FORMS; DESIGN; DOXYCYCLINE; DRESSINGS;
D O I
10.1016/j.carbpol.2016.04.031
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Bacterial infections often affect the wound, delaying healing and causing areas of necrosis. In this work, an aerogel in form of core-shell particles, able to prolong drug activity on wounds and to be easily removed was developed. Aerogel microcapsules consisted of a core made by amidated pectin hosting doxycycline, an antibiotic drug with a broad spectrum of action, and a shell consisting of high mannuronic content alginate. Particles were obtained by prilling using a coaxial nozzle for drop production and an ethanolic solution of CaCl2 as gelling promoter. The alcogels where dried using supercritical CO2. The influence of polysaccharides and drug concentrations on aerogel properties was evaluated. Spherical particles with high drug encapsulation efficiency (87%) correlated to alginate concentration in the processed liquid feeds were obtained. The release of the drug, mainly concentrated into the pectin core, was prolonged till 48 h, and dependent on both drug/pectin ratio and alginate concentration. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:482 / 489
页数:8
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