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Modeling the depletion effect caused by an addition of polymer to monoclonal antibody solutions

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F44555601%3A13440%2F18%3A43894213" target="_blank" >RIV/44555601:13440/18:43894213 - isvavai.cz</a>

  • Result on the web

    <a href="http://iopscience.iop.org/article/10.1088/1361-648X/aae914/pdf" target="_blank" >http://iopscience.iop.org/article/10.1088/1361-648X/aae914/pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1088/1361-648X/aae914" target="_blank" >10.1088/1361-648X/aae914</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Modeling the depletion effect caused by an addition of polymer to monoclonal antibody solutions

  • Original language description

    We present a theoretical study of colloidal stability of the model mixtures of monoclonal antibody molecules and non-adsorbing (no polymer-protein attraction) polymers. The antibodies are pictured as an assembly of seven hard spheres assuming a Y-like shape. Polymers present in the mixture are modeled as chain-like molecules having from 32 up to 128 monomers represented as hard spheres. We use Wertheim&apos;s thermodynamic perturbation theory to construct the two molecular species and to calculate measurable properties. The calculations are performed in the osmotic ensemble. In view that no direct attractive interaction is present in the model Hamiltonian, we only account for the entropic contribution to the phase equilibrium. We calculate chemical potentials and the equation of state for the model mixture to determine the liquid-liquid part of the phase diagram. We investigate how the critical antibody number density depends on the degree of polymerization and the bead size ratio of the polymer and protein components. The model mixture qualitatively correctly predicts some basic features of real systems. The effects of the model &apos;protein&apos; geometry, that is the difference in results for the flexible Y-shaped protein versus the rigid spherical one, are also examined.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Result continuities

  • Project

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Physics-Condensed Matter

  • ISSN

    0953-8984

  • e-ISSN

  • Volume of the periodical

    30

  • Issue of the periodical within the volume

    48

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    "nestrankovano"

  • UT code for WoS article

    000450249200001

  • EID of the result in the Scopus database

    2-s2.0-85056518306