首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Core/shell cellulose-based microspheres for oral administration of Ketoprofen Lysinate
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Core/shell cellulose-based microspheres for oral administration of Ketoprofen Lysinate

机译:基于核心/壳纤维素的酮类酮磷酸酯的磷酸溶纤维素

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Herein, we propose the fabrication of a new carrier with core/shell structureinner core of cellulose acetate (CA) coated by a micrometric layer of chitosan (CS)fabricated through an integrated process, which combines Electro Dynamic Atomization (EDA) and layer-by-layer (LbL) technique. We demonstrate that CA based microspheres possess a unique capability to relevantly retain the drugsthat is, Ketoprofen Lysinate (KL)along the gastric tract, while providing a massive release along the intestine. CS shell slightly influences the morphology and water retention under different pH conditions, improving drug encapsulation without compromising drug release kinetics. In vitro studies in simulated gastric and intestine fluids (SGF, SIF) with physiological enzymes, show a moderate release of LSK during the first 2 h (ca. 20% at pH 2), followed by a sustained release during the next 6 h (ca. 80% at pH 7). The obtained results demonstrate that CA-based microspheres hold strong potential to be used as carriers for a delayed oral administration of anti-inflammatory drugs. (c) 2018 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 106B: 2636-2644, 2018.
机译:在此,我们提出了通过通过综合过程制造的微米壳聚糖(CS)的微米乙酸醋酸纤维素(CA)的纤维素/壳结构芯的制造,其结合了电动雾化(EDA)和层-Layer(LBL)技术。我们证明了基于CA的微球具有与胃道沿胃泌素酮酮催化剂(KL)相关的独特能力,同时提供沿肠道的大规模释放。 CS壳略微影响不同pH条件下的形态和水保留,改善药物包封而不损害药物释放动力学。在模拟胃肠和肠道流体(SGF,SIF)的体外研究(SGF,SIF)与生理酶,在前2H(CA.在pH 2时20%)期间,LSK的中等释放,然后在接下来的6小时内进行持续释放( CA.PH 7时80%)。所得结果表明,基于CA的微球容量用作延迟口服抗炎药物的载体的强潜力。 (c)2018 Wiley期刊,Inc.J生物保解率A型B:苹果生物粉末,106B:2636-2644,2018。

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