首页> 外文期刊>Acta biomaterialia >Polyion complex hydrogels from chemically modified cellulose nanofibrils: Structure-function relationship and potential for controlled and pH-responsive release of doxorubicin
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Polyion complex hydrogels from chemically modified cellulose nanofibrils: Structure-function relationship and potential for controlled and pH-responsive release of doxorubicin

机译:聚硫末络合物水凝胶来自化学改性纤维素纳米纤维:多柔比星的受控和pH响应释放的结构 - 功能关系和潜力

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Herein, we report the fabrication of a polyion complex hydrogel from two oppositely charged derivatives of cellulose nanofibrils (CNF). CNF was produced from dissolving pulp through subsequent periodate oxidation, chemical modification, and microfluidization. Three different durations for periodate oxidation (30 min, 120 min, and 180 min) resulted in three different aldehyde contents. Further, two types of chemical modifications were introduced to react with the resulting aldehydes: chlorite oxidation to yield anionic CNF with carboxylic acid groups (DCC) and imination with Girard's reagent T to yield cationic CNF containing quaternary ammonium groups (CDAC). Functional group contents were assessed using conductometric titration and elemental analysis, while nanofibril morphologies were assessed using atomic force microscopy (AFM). Longer durations of periodate oxidation did not yield different width profile but was found to decrease fibril length. The formation of self-standing hydrogel through mixing of DCC and CDAC dispersions was investigated. Oscillatory rheology was performed to assess the relative strengths of different gels. Self-standing hydrogels were obtained from mixture of DCC180 and CDAC180 dispersions in acetate buffer at pH 4 and 5 at a low concentration of 0.5% w/w that displayed approximately 10-fold increase in storage and loss moduli compared to those of the individual dispersions. Self-standing gels containing doxorubicin (an anticancer drug) displayed pH-responsive release profiles. At physiological pH 7.4, approximately 65% of doxorubicin was retained past a burst release regime, while complete release was observed within 5 days at pH 4. Biocompatibility of DCC180, CDAC180, and their mixture were investigated through quantification of the metabolic activity of NIH3T3 cells in vitro. No significant cytotoxicity was observed at concentrations up to 900 mu g/mL. In short, the nanocellulose-based polyion complex hydrogels obtained in this study are promising nature-derived materials for biomedical applications. (C) 2018 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
机译:在此,我们报告了来自纤维素纳米纤维(CNF)的两个相对电荷的衍生物的聚硫络合物络合物水凝胶的制备。通过随后的周期氧化,化学改性和微流体来制备CNF从溶解纸浆制备。周期氧化(30分钟,120分钟和180分钟)的三种不同的持续时间导致三种不同的醛含量。此外,引入两种类型的化学修饰以与所得的醛:亚氯酸盐氧化反应,得到与羧酸基团(DCC)的阴离子CNF,与Girard的试剂T产生,以产生含有季铵基团(CDAC)的阳离子CNF。使用电导滴定和元素分析评估官能团内容物,而使用原子力显微镜(AFM)评估纳米纤维形态。较长的周期氧化持续时间没有产生不同的宽度曲线,但发现是减少原纤维长度。研究了通过混合DCC和CDAC分散体的形成自我保持水凝胶。进行振荡流变学,以评估不同凝胶的相对强度。从DCC180和CDAC180分散体的乙酸盐缓冲液的混合物以低浓度为0.5%w / w,从乙酸盐缓冲液的混合物中获得自我保持水凝胶,其与各个分散体的储存和损失模量增加约10倍。含有多柔比星(抗癌药物)的自静凝胶显示PH响应释放型材。在生理pH 7.4中,预先保留大约65%的多柔比星,通过定量NIH3T3细胞的代谢活性来在5天内观察到爆破释放方案。体外。在高达900μg/ ml的浓度下观察到没有显着的细胞毒性。简而言之,本研究中获得的纳米纤维素基聚炔络合物水凝胶是对生物医学应用的自然衍生材料。 (c)2018 Acta Materialia Inc.出版的Althervier Ltd.保留所有权利。

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