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A Novel Substrate Based on Electrospun Polyurethane Nanofibers and Electrosprayed Polyvinyl Alcohol Microparticles for Recombinant Human Erythropoietin Delivery Publisher Pubmed



Ghanbari E1 ; Solouk A1 ; Mehdinavaz Aghdam R2 ; Haghbin Nazarpak M3 ; Ahmadi Tafti SH4
Authors
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Authors Affiliations
  1. 1. Department of Biomedical Engineering, Amirkabir University of Technology (Tehran Polytechnic), Tehran, Iran
  2. 2. School of Metallurgy and Materials Engineering, College of Engineering, University of Tehran, Tehran, Iran
  3. 3. New Technologies Research Center, Amirkabir University of Technology (Tehran Polytechnic), Tehran, Iran
  4. 4. Department of Medicine, Tehran University of Medical Science, Tehran, Iran

Source: Journal of Biomedical Materials Research - Part A Published:2022


Abstract

After myocardial infarction caused by a heart attack, endothelial cells need to be preserved in order to regenerate new capillaries. Moreover, sufficient mechanical support is necessary for the infarcted myocardium to pump the blood. Herein, we designed a novel substrate containing polyurethane (PU) nanofibrous layers and recombinant human erythropoietin (rhEPO)-loaded microparticles for both controlled releases of rhEPO and mechanical support of myocardium. In this system, the single-layer (SL) and double-layer (DL) PU nanofibers were electrospun, and then microparticles with different rhEPO:polyvinyl alcohol (PVA) ratios were electrosprayed on the layers. The in vitro release behavior of rhEPO from SL substrates was not satisfactory, and then the study focused on DL patches in which the release profile was in accordance with Korsmeyer–Peppas model. The release exponent of 0.89 for the DL PU/120PVA:1rhEPO represented zero-order release. The results inferred that these substrates possessed highly tailored mechanical properties; Young's modulus and ultimate tensile strength of the substrates were 74–172 kPa and 7.4–9.9 MPa, respectively. The rhEPO release from the substrates was leading to the proper adhesion of endothelial cells and more than 95% cell viability. The results indicated that the patch of elastic nanofibers and microparticles offered a potential substrate for simultaneous rhEPO delivery to endothelial cells and also mechanically supporting the infarcted myocardium. © 2021 Wiley Periodicals LLC.
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