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      Gallium-containing mesoporous bioactive glass with potent hemostatic activity and antibacterial efficacy

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          Abstract

          Gallium-containing mesoporous bioactive glass can be considered as an efficient hemostatic material due to its merits of increased platelet adhesion and thrombin formation as well as antibacterial properties.

          Abstract

          Haemorrhage remains the leading cause of potentially survivable death in both military and civilian populations. Although a large variety of hemostatic agents have been developed, many of them have an inadequate capacity to induce hemostasis and are not effective in killing bacteria. In recent years, mesoporous bioactive glasses (MBGs) were found to be effective in inducing hemostasis. However, the materials may not be considered as ideal hemostats since they do not offer antimicrobial activity. The gallium ion (Ga +3) not only exhibits antibacterial properties but also accelerates the blood coagulation cascade. The aim of this study was to develop MBGs containing various concentrations of Ga 2O 3(1, 2 & 3 mol%) viathe evaporation-induced self-assembly (EISA) process and investigate whether the addition of Ga 3+would induce both hemostatic and antibacterial effects. The results indicated that the incorporation of lower Ga 2O 3content (1 mol%) into the MBG system improved structural properties including the specific surface area, mesopore size and pore volume as well as the release of silicon and calcium ions. The bioactive glass was found to stimulate blood coagulation, platelet adhesion and thrombus generation and exerted an antibacterial effect against both Escherichia coliand Staphylococcus aureus. Likewise, Ga-doped MBGs showed excellent cytocompatibility even after 3 days, with the 1% Ga 2O 3-containing MBG attaining the best biocompatibility that render them safe hemostatic agents for stopping bleeding. This study demonstrated that the lowest Ga 2O 3-substituted MBG can be a potent candidate for controlling haemorrhage and wound infection.

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          Most cited references61

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          Adsorption of Gases in Multimolecular Layers

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            The Determination of Pore Volume and Area Distributions in Porous Substances. I. Computations from Nitrogen Isotherms

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              The bacterial cell envelope.

              The bacteria cell envelope is a complex multilayered structure that serves to protect these organisms from their unpredictable and often hostile environment. The cell envelopes of most bacteria fall into one of two major groups. Gram-negative bacteria are surrounded by a thin peptidoglycan cell wall, which itself is surrounded by an outer membrane containing lipopolysaccharide. Gram-positive bacteria lack an outer membrane but are surrounded by layers of peptidoglycan many times thicker than is found in the gram-negatives. Threading through these layers of peptidoglycan are long anionic polymers, called teichoic acids. The composition and organization of these envelope layers and recent insights into the mechanisms of cell envelope assembly are discussed.
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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                JMCBDV
                Journal of Materials Chemistry B
                J. Mater. Chem. B
                Royal Society of Chemistry (RSC)
                2050-750X
                2050-7518
                2016
                2016
                : 4
                : 1
                : 71-86
                Affiliations
                [1 ]Department of Biomedical Engineering
                [2 ]Faculty of Engineering
                [3 ]University of Malaya
                [4 ]Kuala Lumpur 50603
                [5 ]Malaysia
                [6 ]Laboratori di Chimica Applicata
                [7 ]Dipartimento di Ingegneria Chimica
                [8 ]dei Materiali e della Produzione Industriale
                [9 ]Università Federico II
                [10 ]80125 Napoli
                [11 ]Tissue Engineering Group (TEG)
                [12 ]Department of Orthopedic Surgery
                [13 ]NOCERAL
                [14 ]Faculty of Medicine
                Article
                10.1039/C5TB02062J
                32262810
                9d359cf6-233a-43d8-91a7-b96c77ebf2af
                © 2016
                History

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