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乙酰化程度对聚(丙烯酸)和壳聚糖 LbL 多层组装的影响。

Influence of the percentage of acetylation on the assembly of LbL multilayers of poly(acrylic acid) and chitosan.

机构信息

Departamento de Química Física I, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n, 28040-Madrid, Spain.

出版信息

Phys Chem Chem Phys. 2011 Oct 28;13(40):18200-7. doi: 10.1039/c1cp21609k. Epub 2011 Sep 22.

Abstract

The Layer-by-Layer (LbL) self-assembly of polyelectrolyte multilayers (PEMs) formed by poly(acrylic acid) (PAA) and chitosan (CHI) of two different percentages of acetylation (AC) has been studied by dissipative quartz crystal microbalance (D-QCM) and ellipsometry. The results point out that the non-linear growth (exponential growth) of the films is not modified by the percentage of acetylation of the CHI (AC). The comparison of the thickness obtained by D-QCM and by ellipsometry has allowed us to calculate the water content of the films showing that the multilayers are highly hydrated. This agrees with the values of the complex shear modulus obtained from the analysis of D-QCM data that are in the MPa range, and show a transition from a viscous to mainly elastic behavior depending on the charge density of the CHI chains. The monomer surface density in each layer (obtained from the combination of ellipsometry and differential refractive index measurements) indicated that the mechanism of charge compensation depends on the percentage of acetylation of the CHI. It was found that the adsorption kinetics is a bimodal process with characteristic times that depend on the number and nature of each layer. The load capacity of the multilayers for a β-blocker, propranolol, was found to be higher for the lowest acetylation degree.

摘要

聚电解质多层(PEMs)的层层(LbL)自组装由两种不同乙酰化程度(AC)的聚丙烯酸(PAA)和壳聚糖(CHI)形成,已通过耗散石英晶体微天平(D-QCM)和椭圆光度法进行了研究。结果表明,薄膜的非线性生长(指数生长)不受 CHI(AC)乙酰化程度的影响。通过 D-QCM 和椭圆光度法获得的厚度的比较,使我们能够计算薄膜的含水量,表明多层高度水合。这与从 D-QCM 数据分析得出的复切变弹性模量值一致,该值在 MPa 范围内,并表现出根据 CHI 链电荷密度从粘性到主要弹性行为的转变。每层中的单体表面密度(通过椭圆光度法和微分折射率测量的组合获得)表明,电荷补偿的机制取决于 CHI 的乙酰化程度。发现吸附动力学是一个具有特征时间的双模态过程,该特征时间取决于每个层的数量和性质。对于最低乙酰化度,发现多层对β阻断剂普萘洛尔的负载能力更高。

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