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原位羧甲基纤维素改性细菌纤维素对其纳米/微观结构和甲氨蝶呤释放性能的影响。

Effect of in situ modification of bacterial cellulose with carboxymethylcellulose on its nano/microstructure and methotrexate release properties.

机构信息

University of Araraquara - UNIARA, 14801-320, Araraquara, SP, Brazil.

University of Araraquara - UNIARA, 14801-320, Araraquara, SP, Brazil; Interdisciplinary Laboratory of Advanced Materials, Centro de Ciências da Natureza- CNN, Federal University of Piaui - UFPI, 64049-550, Teresina, PI, Brazil.

出版信息

Carbohydr Polym. 2018 Jan 1;179:126-134. doi: 10.1016/j.carbpol.2017.09.061. Epub 2017 Sep 21.

Abstract

Bacterial cellulose/carboxymethylcelullose (BC/CMC) biocomposites with different DS-CMC (DS from 0.7 to 1.2) were developed in order to evaluate their impact as a drug delivery system. Biocomposites were loaded with methotrexate (MTX) as an alternative for the topical treatment of psoriasis. Scanning electron microscopy and atomic force microscopy showed that the CMC coated the cellulose nanofibers, leading to the decrease of the elastic modulus as the DS of CMC increased. BC/CMC0.9 exhibited the lower liquid uptake (up to 11 times lower), suggesting that the more linear structure of the intermediate substitute CMC grade (0.9) was able to interact more strongly with BC, resulting in a denser structure. All samples showed a typical burst release effect in the first 15min of test, however the BC/CMC0.9 biocomposite promoted a slight lowering of MTX release rates, suggesting that the DS of CMC can be considered the key factor to modulate the BC properties.

摘要

为了评估其作为药物传递系统的效果,制备了不同取代度羧甲基纤维素(取代度 0.7 至 1.2)的细菌纤维素/羧甲基纤维素(BC/CMC)生物复合材料。将甲氨蝶呤(MTX)负载于生物复合材料中,作为治疗银屑病的局部替代疗法。扫描电子显微镜和原子力显微镜显示,CMC 包覆在纤维素纳米纤维上,导致弹性模量随着 CMC 取代度的增加而降低。BC/CMC0.9 的吸液率最低(低至 11 倍),这表明中间替代 CMC 级(0.9)的更线性结构能够与 BC 更强地相互作用,从而形成更致密的结构。所有样品在前 15 分钟的测试中均表现出典型的突释效应,但 BC/CMC0.9 生物复合材料略微降低了 MTX 的释放速率,表明 CMC 的取代度可以被视为调节 BC 性能的关键因素。

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