TY - JOUR
T1 - Modelling and simulation of the hydrodynamics and mixing profiles in the human proximal colon using Discrete Multiphysics
AU - Schütt, M.
AU - Stamatopoulos, K.
AU - Simmons, M. J.H.
AU - Batchelor, H. K.
AU - Alexiadis, A.
PY - 2020/6/30
Y1 - 2020/6/30
N2 - The proximal part of the colon offers opportunities to prolong the absorption window following oral administration of a drug. In this work, we used computer simulations to understand how the hydrodynamics in the proximal colon might affect the release from dosage forms designed to target the colon. For this purpose, we developed and compared three different models: a completely-filled colon, a partially-filled colon and a partially-filled colon with a gaseous phase present (gas-liquid model). The highest velocities of the liquid were found in the completely-filled model, which also shows the best mixing profile, defined by the distribution of tracking particles over time. No significant differences with regard to the mixing and velocity profiles were found between the partially-filled model and the gas-liquid model. The fastest transit time of an undissolved tablet was found in the completely-filled model. The velocities of the liquid in the gas-liquid model are slightly higher along the colon than in the partially-filled model. The filling level has an impact on the exsisting shear forces and shear rates, which are decisive factors in the development of new drugs and formulations.
AB - The proximal part of the colon offers opportunities to prolong the absorption window following oral administration of a drug. In this work, we used computer simulations to understand how the hydrodynamics in the proximal colon might affect the release from dosage forms designed to target the colon. For this purpose, we developed and compared three different models: a completely-filled colon, a partially-filled colon and a partially-filled colon with a gaseous phase present (gas-liquid model). The highest velocities of the liquid were found in the completely-filled model, which also shows the best mixing profile, defined by the distribution of tracking particles over time. No significant differences with regard to the mixing and velocity profiles were found between the partially-filled model and the gas-liquid model. The fastest transit time of an undissolved tablet was found in the completely-filled model. The velocities of the liquid in the gas-liquid model are slightly higher along the colon than in the partially-filled model. The filling level has an impact on the exsisting shear forces and shear rates, which are decisive factors in the development of new drugs and formulations.
KW - colon
KW - drug delivery
KW - fluid dynamics
KW - fluid-structure interactions
KW - large intestine
KW - mathematical modelling
KW - peristalsis
KW - proximal colon
KW - Smoothed Particle Hydrodynamics (SPH)
UR - https://www.sciencedirect.com/journal/computers-in-biology-and-medicine
U2 - 10.1016/j.compbiomed.2020.103819
DO - 10.1016/j.compbiomed.2020.103819
M3 - Article
C2 - 32568686
AN - SCOPUS:85084953420
SN - 0010-4825
VL - 121
JO - Computers in Biology and Medicine
JF - Computers in Biology and Medicine
M1 - 103819
ER -