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水中阳离子纤维素与卡波姆974P相互作用的流变学评估

Rheological evaluation of the interactions between cationic celluloses and Carbopol 974P in water.

作者信息

Rodríguez R, Alvarez-Lorenzo C, Concheiro A

机构信息

Departamento de Farmacia y Tecnología Farmacéutica, Facultad de Farmacia, Universidad de Santiago de Compostela, 15706 Santiago de Compostela, Spain.

出版信息

Biomacromolecules. 2001 Fall;2(3):886-93. doi: 10.1021/bm010049c.

Abstract

This paper reports on the influence of the structural properties of two cationic hydroxyethylecelluloses, polyquaternium-4 (PQ-4; 1.13-1.27% N) and polyquaternium-10 (PQ-10; 1.88-1.95% N), on the rheological behavior of their dispersions and of the dispersions of their blends with Carbopol 974P (60.9% COOH) in water. Dynamic shear oscillation measurements showed that the rheological behavior of 1 and 2% (w/w) cellulose polymers was mainly viscous. Flow curves of PQ-10 dispersions presented a higher consistency and pseudoplasticity than PQ-4 dispersions, in which the thixotropy was higher. Structural features, such as type and distribution of substituents and molecular weight, explain why they behave different. The presence of 0.00125-0.02% Carbopol in diluted cationic cellulose (0.01-0.08%) dispersions produced an important decrease in viscosity, due to a strong associative process via an electrostatic interaction phenomenon. Similar results were obtained when sodium acetate was added instead of Carbopol. In contrast, in the concentrated range (1% cellulose polymer), the viscous (G") and especially the elastic (G') moduli of the dispersions increased monotonically with Carbopol concentration (0.010-0.125%) and became physical gels, except in the proximity of the neutralization of the ammonium groups (0.07% Carbopol for PQ-4, and 0.1% Carbopol for PQ-10) in which G" and G' decreased. The concentrated dispersions showed pH-sensitivity when the Carbopol added was around or above the neutralization point. In dispersions with this composition, consistency increased dramatically when pH changed from 4.5 to 7.4. This property can open a wide range of applications, especially in the pharmaceutical field to prepare gelling in situ systems.

摘要

本文报道了两种阳离子羟乙基纤维素——聚季铵盐-4(PQ-4;含氮量1.13 - 1.27%)和聚季铵盐-10(PQ-10;含氮量1.88 - 1.95%)的结构性质对其在水中分散体以及与卡波姆974P(60.9%的羧基)共混物分散体流变行为的影响。动态剪切振荡测量表明,1%和2%(w/w)纤维素聚合物的流变行为主要表现为粘性。PQ-10分散体的流动曲线比PQ-4分散体具有更高的稠度和假塑性,其中PQ-4分散体的触变性更高。结构特征,如取代基的类型和分布以及分子量,解释了它们为何表现不同。在稀释的阳离子纤维素(0.01 - 0.08%)分散体中加入0.00125 - 0.02%的卡波姆,由于通过静电相互作用现象发生的强烈缔合过程,导致粘度显著降低。当加入醋酸钠代替卡波姆时,也得到了类似的结果。相反,在高浓度范围(1%纤维素聚合物),分散体的粘性模量(G"),尤其是弹性模量(G')随着卡波姆浓度(0.010 - 0.125%)单调增加,并形成物理凝胶,但在铵基中和点附近(PQ-4为0.07%卡波姆,PQ-10为0.1%卡波姆),G"和G'会降低。当加入的卡波姆接近或高于中和点时,高浓度分散体表现出pH敏感性。在具有这种组成的分散体中,当pH从4.5变为7.4时,稠度会急剧增加。这一特性可开拓广泛的应用领域,尤其是在制药领域用于制备原位凝胶系统。

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