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Adsorption and encapsulation of flexible polyelectrolytes in charged spherical vesicles

机译:带电球形囊泡中柔性聚电解质的吸附和封装

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We present a theory of adsorption of flexible polyelectrolytes on the interior and exterior surfaces of a charged vesicle in an electrolyte solution. The criteria for adsorption and the density profiles of the adsorbed polymer chain are derived in terms of various characteristics of the polymer, vesicle, and medium, such as the charge density and length of the polymer, charge density and size of the vesicle, electrolyte concentration and dielectric constant of the medium. For adsorption inside the vesicle, the competition between the loss of conformational entropy and gain in adsorption energy results in two kinds of encapsulated states, depending on the strength of the polymer-vesicle interaction. By considering also the adsorption from outside the vesicle, we derive the entropic and energy contributions to the free energy change to transfer an adsorbed chain in the interior to an adsorbed chain on the exterior. In this paper, we have used the Wentzel-Kramers-Brillouin (WKB) method to solve the equation for the probability distribution function of the chain. The present WKB results are compared with the previous results based on variational methods. The WKB and variational results are in good agreement for both the interior and exterior states of adsorption, except in the zero-salt limit for adsorption in the exterior region. The adsorption criteria and density profiles for both the interior and exterior states are presented in terms of various experimentally controllable variables. Calculation of the dependencies of free energy change to transfer an adsorbed chain from the interior to the exterior surface on salt concentration and vesicle radius shows that the free energy penalty to expel a chain from a vesicle is only of the order of thermal energy. Published by AIP Publishing.
机译:我们在电解质溶液中介绍了在带电囊泡的内部和外表面上的柔性聚电解质的吸附理论。吸附和吸附性聚合物链的密度分布的标准是根据聚合物,囊泡和培养基的各种特性来推导的,例如聚合物的电荷密度和长度,囊泡的电荷密度和尺寸,电解质浓度和介质的介电常数。对于囊泡内的吸附,构象熵丧失与吸附能量之间的竞争导致两种包封状态,这取决于聚合物 - 囊泡相互作用的强度。通过考虑来自囊泡外部的吸附,我们将熵和能量贡献导出到自由能量变化,以将内部的吸附链转移到外部的吸附链。在本文中,我们使用了WEDZEL-KRamers-Brillouin(WKB)方法来解决链条概率分布函数的方程。将本WKB结果与基于变分方法的先前结果进行比较。除了在外部区域中吸附的零盐极限之外,WKB和变分效果对吸附的内部和外部状态非常一致。在各种实验可控变量方面,呈现了内部和外部状态的吸附标准和密度曲线。从盐浓度和囊泡半径的内部到外表面向外表面的自由能量变化的依赖性的计算表明,从囊泡排出链的自由能损失是热能的阶。通过AIP发布发布。

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