Kosmotrope-like hydration behavior of polyethylene glycol from microcalorimetry and binding isotherm measurements

Polyethylene glycol (PEG) at various molecular weights (MWs) has been regarded as a wonder molecule in biomedical applications. For instance, PEG serves as a unique moiety for pegylation of "biobetter" drug development, PEG provides controlled-release and preserved activity of biologics, a...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 29(2013), 13 vom: 02. Apr., Seite 4259-65
1. Verfasser: Chen, Wen-Yih (VerfasserIn)
Weitere Verfasser: Hsu, Min-Yen, Tsai, Ching-Wei, Chang, Yung, Ruaan, Rouh-Chyu, Kao, Wei-Hung, Huang, E-Wen, Chuan, Hsiao-Yeh-Tzu Chung
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Water 059QF0KO0R Polyethylene Glycols 3WJQ0SDW1A Muramidase EC 3.2.1.17
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245 1 0 |a Kosmotrope-like hydration behavior of polyethylene glycol from microcalorimetry and binding isotherm measurements 
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520 |a Polyethylene glycol (PEG) at various molecular weights (MWs) has been regarded as a wonder molecule in biomedical applications. For instance, PEG serves as a unique moiety for pegylation of "biobetter" drug development, PEG provides controlled-release and preserved activity of biologics, and PEG modified surface works as an antibiofouling surface. The primary characteristics of PEG molecules used in relevant applications have been attributed mainly to the hydration behavior in aqueous solutions. However, the effects on the solvation of solutes in solution caused by presenting PEG molecules as a cosolvent, as well as the thermodynamics aspect of the hydration behavior of PEG in solution, have not been well documented. The solvation behavior of solutes, such as protein, with PEG as a cosolvent, indicates the success of PEG applications, such as biofouling and controlled release. In this investigation, we examined the effects of a buffer solution containing PEG molecules on the solution behavior of solute and the interactions between solid surfaces with solutes. We adapted the study by selecting a lysozyme as a solute in a buffer solution with either ammonium sulfate (kosmotrope) or sodium chloride (chaotrope) and anionic resin (SP-Sepharose) as solid surfaces. The experiments primarily involved binding equilibrium measurements and thermodynamics analysis. The results revealed that, in both saline buffers, adding PEG increases the binding affinity between the lysozyme and the resin, similar to kosmotropic salt in the examined salt concentrations. The thermodynamics analyses involving microcalorimetric measurements show that the bindings are mainly driven by enthalpy, indicating that electrostatic interaction was the primary binding force under these experimental conditions. The variations of the enthalpy and entropy of the binding thermodynamics when adding PEG to different salt types in the buffer solution showed opposite behavior, and the results support the concept of kosmotrope-like behavior of PEG. The equilibrium and thermodynamics data demonstrate that PEG has a kosmotrope-like hydration behavior, and the extent of kosmotrope-like behavior depends on the molecular weight of PEG with the outcomes of various molecular weights of PEG being added to the binding solution. The results of this study provide essential knowledge for PEG as an additive (or cosolvent) in various research applications 
650 4 |a Journal Article 
650 4 |a Research Support, Non-U.S. Gov't 
650 7 |a Water  |2 NLM 
650 7 |a 059QF0KO0R  |2 NLM 
650 7 |a Polyethylene Glycols  |2 NLM 
650 7 |a 3WJQ0SDW1A  |2 NLM 
650 7 |a Muramidase  |2 NLM 
650 7 |a EC 3.2.1.17  |2 NLM 
700 1 |a Hsu, Min-Yen  |e verfasserin  |4 aut 
700 1 |a Tsai, Ching-Wei  |e verfasserin  |4 aut 
700 1 |a Chang, Yung  |e verfasserin  |4 aut 
700 1 |a Ruaan, Rouh-Chyu  |e verfasserin  |4 aut 
700 1 |a Kao, Wei-Hung  |e verfasserin  |4 aut 
700 1 |a Huang, E-Wen  |e verfasserin  |4 aut 
700 1 |a Chuan, Hsiao-Yeh-Tzu Chung  |e verfasserin  |4 aut 
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773 1 8 |g volume:29  |g year:2013  |g number:13  |g day:02  |g month:04  |g pages:4259-65 
856 4 0 |u http://dx.doi.org/10.1021/la304500w  |3 Volltext 
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