TY - JOUR
T1 - Hydraulic permeability and compressive properties of porcine and human synovium
AU - Rohanifar, Milad
AU - Johnston, Benjamin B.
AU - Davis, Alexandra L.
AU - Guang, Young
AU - Nommensen, Kayla
AU - Fitzpatrick, James A.J.
AU - Pham, Christine N.
AU - Setton, Lori A.
N1 - Funding Information:
This work was supported with funds from the National Institutes of Health (R01 AR070975, R01 AR078776), the Washington University Center for Cellular Imaging which is funded by Washington University School of Medicine, the Children's Discovery Institute of Washington University and St. Louis Children's Hospital (CDI-CORE-2015-505 and CDI-CORE-2019-813), The Foundation for Barnes-Jewish Hospital (3770 and 4642), the Washington University Rheumatic Diseases Resource-based Research Center (RDRRC) (NIH P30AR073752), and the Washington University Musculoskeletal Research Center (NIH P30AR074992). The authors acknowledge the support of Dr. Michael Talcott, DVM, in the Division of Comparative Medicine, Washington University School of Medicine in St. Louis, for providing porcine samples, and the Mid-America Transplant Center for providing human samples. The FEBio software suite was developed with partial support from the NIH.
Funding Information:
This work was supported with funds from the National Institutes of Health ( R01 AR070975 , R01 AR078776 ), the Washington University Center for Cellular Imaging which is funded by Washington University School of Medicine, the Children’s Discovery Institute of Washington University and St. Louis Children’s Hospital ( CDI-CORE-2015-505 and CDI-CORE-2019-813 ), The Foundation for Barnes-Jewish Hospital ( 3770 and 4642 ), the Washington University Rheumatic Diseases Resource-based Research Center (RDRRC) ( NIH P30AR073752 ), and the Washington University Musculoskeletal Research Center ( NIH P30AR074992 ). The authors acknowledge the support of Dr. Michael Talcott, DVM, in the Division of Comparative Medicine, Washington University School of Medicine in St. Louis, for providing porcine samples, and the Mid-America Transplant Center for providing human samples. The FEBio software suite was developed with partial support from the NIH.
Publisher Copyright:
© 2022 Biophysical Society
PY - 2022/2/15
Y1 - 2022/2/15
N2 - The synovium is a multilayer connective tissue separating the intra-articular spaces of the diarthrodial joint from the extra-synovial vascular and lymphatic supply. Synovium regulates drug transport into and out of the joint, yet its material properties remain poorly characterized. Here, we measured the compressive properties (aggregate modulus, Young's modulus, and Poisson's ratio) and hydraulic permeability of synovium with a combined experimental-computational approach. A compressive aggregate modulus and Young's modulus for the solid phase of synovium were quantified from linear regression of the equilibrium confined and unconfined compressive stress upon strain, respectively (HA = 4.3 ± 2.0 kPa, Es = 2.1 ± 0.75, porcine; HA = 3.1 ± 2.0 kPa, Es = 2.8 ± 1.7, human). Poisson's ratio was estimated to be 0.39 and 0.40 for porcine and human tissue, respectively, from moduli values in a Monte Carlo simulation. To calculate hydraulic permeability, a biphasic finite element model's predictions were numerically matched to experimental data for the time-varying ramp and hold phase of a single increment of applied strain (k = 7.4 ± 4.1 × 10−15 m4/N.s, porcine; k = 7.4 ± 4.3 × 10−15 m4/N.s, human). We can use these newly measured properties to predict fluid flow gradients across the tissue in response to previously reported intra-articular pressures. These values for material constants are to our knowledge the first available measurements in synovium that are necessary to better understand drug transport in both healthy and pathological joints.
AB - The synovium is a multilayer connective tissue separating the intra-articular spaces of the diarthrodial joint from the extra-synovial vascular and lymphatic supply. Synovium regulates drug transport into and out of the joint, yet its material properties remain poorly characterized. Here, we measured the compressive properties (aggregate modulus, Young's modulus, and Poisson's ratio) and hydraulic permeability of synovium with a combined experimental-computational approach. A compressive aggregate modulus and Young's modulus for the solid phase of synovium were quantified from linear regression of the equilibrium confined and unconfined compressive stress upon strain, respectively (HA = 4.3 ± 2.0 kPa, Es = 2.1 ± 0.75, porcine; HA = 3.1 ± 2.0 kPa, Es = 2.8 ± 1.7, human). Poisson's ratio was estimated to be 0.39 and 0.40 for porcine and human tissue, respectively, from moduli values in a Monte Carlo simulation. To calculate hydraulic permeability, a biphasic finite element model's predictions were numerically matched to experimental data for the time-varying ramp and hold phase of a single increment of applied strain (k = 7.4 ± 4.1 × 10−15 m4/N.s, porcine; k = 7.4 ± 4.3 × 10−15 m4/N.s, human). We can use these newly measured properties to predict fluid flow gradients across the tissue in response to previously reported intra-articular pressures. These values for material constants are to our knowledge the first available measurements in synovium that are necessary to better understand drug transport in both healthy and pathological joints.
UR - http://www.scopus.com/inward/record.url?scp=85123678569&partnerID=8YFLogxK
U2 - 10.1016/j.bpj.2022.01.008
DO - 10.1016/j.bpj.2022.01.008
M3 - Article
C2 - 35032457
AN - SCOPUS:85123678569
SN - 0006-3495
VL - 121
SP - 575
EP - 581
JO - Biophysical Journal
JF - Biophysical Journal
IS - 4
ER -