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Combining particle tracking microrheology and viscometry for the study of DNA aqueous solutions
Author(s) -
Stefanopoulou Evdokia,
Papagiannopoulos Aristeidis
Publication year - 2020
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.23353
Subject(s) - microrheology , viscoelasticity , viscometer , chemistry , viscosity , shear thinning , power law , exponent , thermodynamics , rheology , particle (ecology) , molar mass , polymer , physics , organic chemistry , mathematics , statistics , linguistics , philosophy , oceanography , geology
We use video particle tracking microrheology (VPTMR) in order to investigate the viscoelasticity of salmon DNA and correlate it to its steady‐flow shear‐thinning viscosity. Aqueous solutions of DNA are tested in a wide concentration range from the dilute to the semidilute unentangled concentration regime. The observed mean squared displacement shows power‐law scaling with lag‐time which is equivalent to power‐law behavior of the complex modulus as a function of frequency that is, | G * ( ω )| = S ∙ ω α . The relaxation exponent α changes abruptly with concentration in the semidilute regime from about 1 to about 0.5 which is the exponent predicted by the Rouse model. The quasi‐property S follows the scaling of viscosity for uncharged polymers near θ ‐conditions in the semidilute regime that is, η ∼ c 1 / 3 ν eff − 1with ν eff = 0.50 − 0.51 . The shear‐thinning exponent observed by viscometry increases gradually towards the value of 0.5 which has been predicted for Rouse chains under flow. Our findings are in agreement with recent studies of DNA solutions where DNA is treated as a model polymer and addresses the low‐molar mass regime of DNA viscoelasticity. This work demonstrates that the combination of passive particle tracking with viscometry can provide a complete picture on the viscoelasticity of DNA‐based biopolymer materials.