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Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite

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Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite. / Khan, A.S.; Aziz, M.S.; Paul, D. et al.
In: Journal of Bionanoscience, Vol. 2, No. 2, 2008, p. 75-88.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Khan, AS, Aziz, MS, Paul, D, Wong, F & Rehman, IU 2008, 'Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite', Journal of Bionanoscience, vol. 2, no. 2, pp. 75-88. https://doi.org/10.1166/jbns.2008.033

APA

Khan, A. S., Aziz, M. S., Paul, D., Wong, F., & Rehman, I. U. (2008). Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite. Journal of Bionanoscience, 2(2), 75-88. https://doi.org/10.1166/jbns.2008.033

Vancouver

Khan AS, Aziz MS, Paul D, Wong F, Rehman IU. Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite. Journal of Bionanoscience. 2008;2(2):75-88. doi: 10.1166/jbns.2008.033

Author

Khan, A.S. ; Aziz, M.S. ; Paul, D. et al. / Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite. In: Journal of Bionanoscience. 2008 ; Vol. 2, No. 2. pp. 75-88.

Bibtex

@article{23b560157a2248fc94bdb03f37513f94,
title = "Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite",
abstract = "The biostability of the polymer is one of the critical parameters to use them for biomaterial application. Polyurethane being one of the most compliant polymer but there are concerns regarding its resistance to degradation, particularly from hydrolysis and oxidation. The aim of this study is to synthesise a novel bioactive composite by creating a covalent linkage between polyurethane and nano-apatites and to analyse the in-vitro hydrolytic degradation of a series of newly synthesised polyurethane (PU) and polyurethane/nano-hydroxyapatite (PU/n-HA) composites. Nano-apatite powder was produced through sol-gel technique. A novel polyurethane composite material was prepared by chemically bonding the n-HA to the diisocyanate component in the polyurethane backbone by utilising solvent polymerisation. The concentration of nano-apatite was 5, 10, 15 and 20% wt/wt in polyurethane. Hydrolytic degradation of the PU and PU/n-HA composites were carried out both in deionised water and in phosphate buffer solution (PBS) having (pH 7.4) at 37 °C for a predetermined time interval of 90 days. The PU and PU/ n-HA composites were physically and chemically characterised by using contact angle measurement, weight loss, Fourier Transform Infrared spectroscopy couples with Photoacoustic Sampling Cell (FTIR-PAS), Raman Spectroscopy, X-ray Diffraction (XRD) and Scanning electron microscopy (SEM). These characterisations showed that with the addition of n-HA the composite exhibits hydrophobic behaviour and degradation rate reduces due to covalent linkage between n-HA and PU. Hence it has been concluded that the degradation rate of the newly developed PU/n-HA composites can be controlled, which helps in tailor making the biomaterial for specific applications. Copyright {\textcopyright} 2008 American Scientific Publishers All rights reserved.",
keywords = "Bioactive nano-composites, Degradation, FTIR, Hydroxyapatite, Polyurethanes, Raman spectroscopy, Angle measurement, Apatite, Biological membranes, Biomaterials, Composite materials, Composite micromechanics, Contact angle, Deionized water, Fourier transform infrared spectroscopy, Fourier transforms, Gelation, Hydroxylation, Nanocomposites, Phosphate minerals, Photoacoustic spectroscopy, Photodegradation, Polymers, Raman scattering, Scanning electron microscopy, Spectroscopic analysis, Spectrum analysis, Bioactive composites, Biomaterial applications, Biostability, Concentration of, Contact-angle measurements, Covalent linkages, Critical parameters, Degradation rates, Diisocyanate, Fourier transform infra-red spectroscopies, Ftir salp, Hydrolytic degradations, In-vitro, In-vitro analysis, Nano apatites, Phosphate buffer solutions, Polymerisation, Polyurethane composites, Sampling cells, Sem, Sol-gel techniques, Time intervals, Weight loss, X-ray diffractions",
author = "A.S. Khan and M.S. Aziz and D. Paul and F. Wong and I.U. Rehman",
year = "2008",
doi = "10.1166/jbns.2008.033",
language = "English",
volume = "2",
pages = "75--88",
journal = "Journal of Bionanoscience",
issn = "1557-7910",
publisher = "American Scientific Publishers",
number = "2",

}

RIS

TY - JOUR

T1 - Synthesis and in-vitro analysis of degradative resistance of a novel bioactive composite

AU - Khan, A.S.

AU - Aziz, M.S.

AU - Paul, D.

AU - Wong, F.

AU - Rehman, I.U.

PY - 2008

Y1 - 2008

N2 - The biostability of the polymer is one of the critical parameters to use them for biomaterial application. Polyurethane being one of the most compliant polymer but there are concerns regarding its resistance to degradation, particularly from hydrolysis and oxidation. The aim of this study is to synthesise a novel bioactive composite by creating a covalent linkage between polyurethane and nano-apatites and to analyse the in-vitro hydrolytic degradation of a series of newly synthesised polyurethane (PU) and polyurethane/nano-hydroxyapatite (PU/n-HA) composites. Nano-apatite powder was produced through sol-gel technique. A novel polyurethane composite material was prepared by chemically bonding the n-HA to the diisocyanate component in the polyurethane backbone by utilising solvent polymerisation. The concentration of nano-apatite was 5, 10, 15 and 20% wt/wt in polyurethane. Hydrolytic degradation of the PU and PU/n-HA composites were carried out both in deionised water and in phosphate buffer solution (PBS) having (pH 7.4) at 37 °C for a predetermined time interval of 90 days. The PU and PU/ n-HA composites were physically and chemically characterised by using contact angle measurement, weight loss, Fourier Transform Infrared spectroscopy couples with Photoacoustic Sampling Cell (FTIR-PAS), Raman Spectroscopy, X-ray Diffraction (XRD) and Scanning electron microscopy (SEM). These characterisations showed that with the addition of n-HA the composite exhibits hydrophobic behaviour and degradation rate reduces due to covalent linkage between n-HA and PU. Hence it has been concluded that the degradation rate of the newly developed PU/n-HA composites can be controlled, which helps in tailor making the biomaterial for specific applications. Copyright © 2008 American Scientific Publishers All rights reserved.

AB - The biostability of the polymer is one of the critical parameters to use them for biomaterial application. Polyurethane being one of the most compliant polymer but there are concerns regarding its resistance to degradation, particularly from hydrolysis and oxidation. The aim of this study is to synthesise a novel bioactive composite by creating a covalent linkage between polyurethane and nano-apatites and to analyse the in-vitro hydrolytic degradation of a series of newly synthesised polyurethane (PU) and polyurethane/nano-hydroxyapatite (PU/n-HA) composites. Nano-apatite powder was produced through sol-gel technique. A novel polyurethane composite material was prepared by chemically bonding the n-HA to the diisocyanate component in the polyurethane backbone by utilising solvent polymerisation. The concentration of nano-apatite was 5, 10, 15 and 20% wt/wt in polyurethane. Hydrolytic degradation of the PU and PU/n-HA composites were carried out both in deionised water and in phosphate buffer solution (PBS) having (pH 7.4) at 37 °C for a predetermined time interval of 90 days. The PU and PU/ n-HA composites were physically and chemically characterised by using contact angle measurement, weight loss, Fourier Transform Infrared spectroscopy couples with Photoacoustic Sampling Cell (FTIR-PAS), Raman Spectroscopy, X-ray Diffraction (XRD) and Scanning electron microscopy (SEM). These characterisations showed that with the addition of n-HA the composite exhibits hydrophobic behaviour and degradation rate reduces due to covalent linkage between n-HA and PU. Hence it has been concluded that the degradation rate of the newly developed PU/n-HA composites can be controlled, which helps in tailor making the biomaterial for specific applications. Copyright © 2008 American Scientific Publishers All rights reserved.

KW - Bioactive nano-composites

KW - Degradation

KW - FTIR

KW - Hydroxyapatite

KW - Polyurethanes

KW - Raman spectroscopy

KW - Angle measurement

KW - Apatite

KW - Biological membranes

KW - Biomaterials

KW - Composite materials

KW - Composite micromechanics

KW - Contact angle

KW - Deionized water

KW - Fourier transform infrared spectroscopy

KW - Fourier transforms

KW - Gelation

KW - Hydroxylation

KW - Nanocomposites

KW - Phosphate minerals

KW - Photoacoustic spectroscopy

KW - Photodegradation

KW - Polymers

KW - Raman scattering

KW - Scanning electron microscopy

KW - Spectroscopic analysis

KW - Spectrum analysis

KW - Bioactive composites

KW - Biomaterial applications

KW - Biostability

KW - Concentration of

KW - Contact-angle measurements

KW - Covalent linkages

KW - Critical parameters

KW - Degradation rates

KW - Diisocyanate

KW - Fourier transform infra-red spectroscopies

KW - Ftir salp

KW - Hydrolytic degradations

KW - In-vitro

KW - In-vitro analysis

KW - Nano apatites

KW - Phosphate buffer solutions

KW - Polymerisation

KW - Polyurethane composites

KW - Sampling cells

KW - Sem

KW - Sol-gel techniques

KW - Time intervals

KW - Weight loss

KW - X-ray diffractions

U2 - 10.1166/jbns.2008.033

DO - 10.1166/jbns.2008.033

M3 - Journal article

VL - 2

SP - 75

EP - 88

JO - Journal of Bionanoscience

JF - Journal of Bionanoscience

SN - 1557-7910

IS - 2

ER -