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Electrospun Antibacterial Composites for Cartilage Tissue Engineering

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Electrospun Antibacterial Composites for Cartilage Tissue Engineering. / Samie, Muhammad; Khan, Ather; Hardy, John et al.
In: Macromolecular Bioscience , Vol. 22, No. 9, 2200219, 30.09.2022.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Samie, M, Khan, A, Hardy, J & Yameen, M 2022, 'Electrospun Antibacterial Composites for Cartilage Tissue Engineering', Macromolecular Bioscience , vol. 22, no. 9, 2200219. https://doi.org/10.1002/mabi.202200219

APA

Samie, M., Khan, A., Hardy, J., & Yameen, M. (2022). Electrospun Antibacterial Composites for Cartilage Tissue Engineering. Macromolecular Bioscience , 22(9), Article 2200219. https://doi.org/10.1002/mabi.202200219

Vancouver

Samie M, Khan A, Hardy J, Yameen M. Electrospun Antibacterial Composites for Cartilage Tissue Engineering. Macromolecular Bioscience . 2022 Sept 30;22(9):2200219. Epub 2022 Jul 22. doi: 10.1002/mabi.202200219

Author

Samie, Muhammad ; Khan, Ather ; Hardy, John et al. / Electrospun Antibacterial Composites for Cartilage Tissue Engineering. In: Macromolecular Bioscience . 2022 ; Vol. 22, No. 9.

Bibtex

@article{fcad65c317c342549ab19f9bafa37f6e,
title = "Electrospun Antibacterial Composites for Cartilage Tissue Engineering",
abstract = "Implantation of biomaterials capable of the controlled release of antibacterials during articular cartilage repair may prevent postoperative infections. Herein, biomaterials are prepared with biomimetic architectures (nonwoven mats of fibers) via electrospinning that are composed of poly(ɛ-caprolactone), poly(lactic acid), and Bombyx mori silk fibroin (with varying ratios) and, optionally, an antibiotic drug (cefixime trihydrate). The composition, morphology, and mechanical properties of the nanofibrous mats are characterized using scanning electron microscope, Fourier transform infrared spectroscopy, and tensile testing. The nonwoven mats have nanoscale fibers (typical diameters of 324–725 nm) and are capable of controlling the release profiles of the drug, with antibacterial activity against Gram +ve and Gram −ve bacteria (two common strains of human pathogenic bacteria, Staphylococcus aureus and Escherichia coli) under in vitro static conditions. The drug loaded nanofiber mats display cytocompatibility comparable to pure poly(ɛ-caprolactone) nanofibers when cultured with National Institutes of Health (NIH) NIH-3T3 fibroblast cell line and have long-term potential for clinical applications in the field of pharmaceutical sciences.",
keywords = "antibacterial, cartilage, composite, drug delivery, electrospinning",
author = "Muhammad Samie and Ather Khan and John Hardy and Muhammad Yameen",
year = "2022",
month = sep,
day = "30",
doi = "10.1002/mabi.202200219",
language = "English",
volume = "22",
journal = "Macromolecular Bioscience ",
issn = "1616-5187",
publisher = "Wiley-VCH Verlag",
number = "9",

}

RIS

TY - JOUR

T1 - Electrospun Antibacterial Composites for Cartilage Tissue Engineering

AU - Samie, Muhammad

AU - Khan, Ather

AU - Hardy, John

AU - Yameen, Muhammad

PY - 2022/9/30

Y1 - 2022/9/30

N2 - Implantation of biomaterials capable of the controlled release of antibacterials during articular cartilage repair may prevent postoperative infections. Herein, biomaterials are prepared with biomimetic architectures (nonwoven mats of fibers) via electrospinning that are composed of poly(ɛ-caprolactone), poly(lactic acid), and Bombyx mori silk fibroin (with varying ratios) and, optionally, an antibiotic drug (cefixime trihydrate). The composition, morphology, and mechanical properties of the nanofibrous mats are characterized using scanning electron microscope, Fourier transform infrared spectroscopy, and tensile testing. The nonwoven mats have nanoscale fibers (typical diameters of 324–725 nm) and are capable of controlling the release profiles of the drug, with antibacterial activity against Gram +ve and Gram −ve bacteria (two common strains of human pathogenic bacteria, Staphylococcus aureus and Escherichia coli) under in vitro static conditions. The drug loaded nanofiber mats display cytocompatibility comparable to pure poly(ɛ-caprolactone) nanofibers when cultured with National Institutes of Health (NIH) NIH-3T3 fibroblast cell line and have long-term potential for clinical applications in the field of pharmaceutical sciences.

AB - Implantation of biomaterials capable of the controlled release of antibacterials during articular cartilage repair may prevent postoperative infections. Herein, biomaterials are prepared with biomimetic architectures (nonwoven mats of fibers) via electrospinning that are composed of poly(ɛ-caprolactone), poly(lactic acid), and Bombyx mori silk fibroin (with varying ratios) and, optionally, an antibiotic drug (cefixime trihydrate). The composition, morphology, and mechanical properties of the nanofibrous mats are characterized using scanning electron microscope, Fourier transform infrared spectroscopy, and tensile testing. The nonwoven mats have nanoscale fibers (typical diameters of 324–725 nm) and are capable of controlling the release profiles of the drug, with antibacterial activity against Gram +ve and Gram −ve bacteria (two common strains of human pathogenic bacteria, Staphylococcus aureus and Escherichia coli) under in vitro static conditions. The drug loaded nanofiber mats display cytocompatibility comparable to pure poly(ɛ-caprolactone) nanofibers when cultured with National Institutes of Health (NIH) NIH-3T3 fibroblast cell line and have long-term potential for clinical applications in the field of pharmaceutical sciences.

KW - antibacterial

KW - cartilage

KW - composite

KW - drug delivery

KW - electrospinning

U2 - 10.1002/mabi.202200219

DO - 10.1002/mabi.202200219

M3 - Journal article

VL - 22

JO - Macromolecular Bioscience

JF - Macromolecular Bioscience

SN - 1616-5187

IS - 9

M1 - 2200219

ER -