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Self‐assembly of a bioelastomeric structure: Solution dynamics and the spinodal and coacervation lines
Author(s) -
Sciortino F.,
Urry D. W.,
Palma M. U.,
Prasad K. U.
Publication year - 1990
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.360291007
Subject(s) - coacervate , spinodal , metastability , chemistry , chemical physics , spinodal decomposition , polymer , aqueous solution , scattering , instability , light scattering , statistical physics , stability (learning theory) , dynamics (music) , impurity , phase (matter) , thermodynamics , physics , optics , quantum mechanics , chromatography , organic chemistry , machine learning , computer science , acoustics
The stability, metastability, and instability regions of aqueous solutions of a representative synthetic bioelastomeric polymer, poly (Val‐Pro‐Gly‐Val‐Gly), were determined by a combined used of elastic and quasi‐elastic light scattering experiments. The approach followed here offers the attractive advantage of singling out the relevant contributions to the total scattering even in the presence of traces of noninteracting larger sized impurities. Conclusions so reached were checked by means of independent experiments. The present results provide descriptions of the very early events in the physics of bioelastogenesis in terms of general polymer science and phase transitions, and in terms of an unexpected possible functional role of density fluctuations.

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