Antibacterial Porous Systems Based on Polylactide Loaded with Amikacin

Three porous matrices based on poly(lactic acid) are proposed herein for the controlled release of amikacin. The materials were fabricated by the method of spraying a surface liquid. Description is given as to the possibility of employing a modifier, such as a silica nanocarrier, for prolonging the...

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Main Authors: Marta Glinka, Katerina Filatova, Justyna Kucińska-Lipka, Tomáš Šopík, Eva Domincová Bergerová, Veronika Mikulcová, Andrzej Wasik, Vladimir Sedlařík
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/27/20/7045
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author Marta Glinka
Katerina Filatova
Justyna Kucińska-Lipka
Tomáš Šopík
Eva Domincová Bergerová
Veronika Mikulcová
Andrzej Wasik
Vladimir Sedlařík
author_facet Marta Glinka
Katerina Filatova
Justyna Kucińska-Lipka
Tomáš Šopík
Eva Domincová Bergerová
Veronika Mikulcová
Andrzej Wasik
Vladimir Sedlařík
author_sort Marta Glinka
collection DOAJ
description Three porous matrices based on poly(lactic acid) are proposed herein for the controlled release of amikacin. The materials were fabricated by the method of spraying a surface liquid. Description is given as to the possibility of employing a modifier, such as a silica nanocarrier, for prolonging the release of amikacin, in addition to using chitosan to improve the properties of the materials, e.g., stability and sorption capacity. Depending on their actual composition, the materials exhibited varied efficacy for drug loading, as follows: 25.4 ± 2.2 μg/mg (matrices with 0.05% <i>w</i>/<i>v</i> of chitosan), 93 ± 13 μg/mg (with 0.08% <i>w</i>/<i>v</i> SiO<sub>2</sub> amikacin modified nanoparticles), and 96 ± 34 μg/mg (matrices without functional additives). An in vitro study confirmed extended release of the drug (amikacin, over 60 days), carried out in accordance with the mathematical Kosmyer–Pepas model for all the materials tested. The matrices were also evaluated for their effectiveness in inhibiting the growth of bacteria such as <i>Staphylococcus aureus</i>, <i>Escherichia coli</i>, <i>Klebsiella pneumoniae</i>, and <i>Pseudomonas aeruginosa</i>. Concurrent research was conducted on the transdermal absorption, morphology, elemental composition, and thermogravimetric properties of the released drug.
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spelling doaj.art-f13c901f665246718cebc6717266640d2023-11-24T01:36:19ZengMDPI AGMolecules1420-30492022-10-012720704510.3390/molecules27207045Antibacterial Porous Systems Based on Polylactide Loaded with AmikacinMarta Glinka0Katerina Filatova1Justyna Kucińska-Lipka2Tomáš Šopík3Eva Domincová Bergerová4Veronika Mikulcová5Andrzej Wasik6Vladimir Sedlařík7Department of Analytical Chemistry, Faculty of Chemistry, Gdańsk University of Technology, 11/12 G. Narutowicza Street, 80-233 Gdańsk, PolandCentre of Polymer Systems, University Institute, Tomas Bata University in Zlín, Tomáše Bati 5678 Street, 760 01 Zlín, Czech RepublicDepartment of Polymer Technology, Faculty of Chemistry, Gdańsk University of Technology, 11/12 G. Narutowicza Street, 80-233 Gdańsk, PolandCentre of Polymer Systems, University Institute, Tomas Bata University in Zlín, Tomáše Bati 5678 Street, 760 01 Zlín, Czech RepublicCentre of Polymer Systems, University Institute, Tomas Bata University in Zlín, Tomáše Bati 5678 Street, 760 01 Zlín, Czech RepublicCentre of Polymer Systems, University Institute, Tomas Bata University in Zlín, Tomáše Bati 5678 Street, 760 01 Zlín, Czech RepublicDepartment of Analytical Chemistry, Faculty of Chemistry, Gdańsk University of Technology, 11/12 G. Narutowicza Street, 80-233 Gdańsk, PolandCentre of Polymer Systems, University Institute, Tomas Bata University in Zlín, Tomáše Bati 5678 Street, 760 01 Zlín, Czech RepublicThree porous matrices based on poly(lactic acid) are proposed herein for the controlled release of amikacin. The materials were fabricated by the method of spraying a surface liquid. Description is given as to the possibility of employing a modifier, such as a silica nanocarrier, for prolonging the release of amikacin, in addition to using chitosan to improve the properties of the materials, e.g., stability and sorption capacity. Depending on their actual composition, the materials exhibited varied efficacy for drug loading, as follows: 25.4 ± 2.2 μg/mg (matrices with 0.05% <i>w</i>/<i>v</i> of chitosan), 93 ± 13 μg/mg (with 0.08% <i>w</i>/<i>v</i> SiO<sub>2</sub> amikacin modified nanoparticles), and 96 ± 34 μg/mg (matrices without functional additives). An in vitro study confirmed extended release of the drug (amikacin, over 60 days), carried out in accordance with the mathematical Kosmyer–Pepas model for all the materials tested. The matrices were also evaluated for their effectiveness in inhibiting the growth of bacteria such as <i>Staphylococcus aureus</i>, <i>Escherichia coli</i>, <i>Klebsiella pneumoniae</i>, and <i>Pseudomonas aeruginosa</i>. Concurrent research was conducted on the transdermal absorption, morphology, elemental composition, and thermogravimetric properties of the released drug.https://www.mdpi.com/1420-3049/27/20/7045poly(lactic acid)amikacindrug delivery systemsporous matricestissue engineering
spellingShingle Marta Glinka
Katerina Filatova
Justyna Kucińska-Lipka
Tomáš Šopík
Eva Domincová Bergerová
Veronika Mikulcová
Andrzej Wasik
Vladimir Sedlařík
Antibacterial Porous Systems Based on Polylactide Loaded with Amikacin
Molecules
poly(lactic acid)
amikacin
drug delivery systems
porous matrices
tissue engineering
title Antibacterial Porous Systems Based on Polylactide Loaded with Amikacin
title_full Antibacterial Porous Systems Based on Polylactide Loaded with Amikacin
title_fullStr Antibacterial Porous Systems Based on Polylactide Loaded with Amikacin
title_full_unstemmed Antibacterial Porous Systems Based on Polylactide Loaded with Amikacin
title_short Antibacterial Porous Systems Based on Polylactide Loaded with Amikacin
title_sort antibacterial porous systems based on polylactide loaded with amikacin
topic poly(lactic acid)
amikacin
drug delivery systems
porous matrices
tissue engineering
url https://www.mdpi.com/1420-3049/27/20/7045
work_keys_str_mv AT martaglinka antibacterialporoussystemsbasedonpolylactideloadedwithamikacin
AT katerinafilatova antibacterialporoussystemsbasedonpolylactideloadedwithamikacin
AT justynakucinskalipka antibacterialporoussystemsbasedonpolylactideloadedwithamikacin
AT tomassopik antibacterialporoussystemsbasedonpolylactideloadedwithamikacin
AT evadomincovabergerova antibacterialporoussystemsbasedonpolylactideloadedwithamikacin
AT veronikamikulcova antibacterialporoussystemsbasedonpolylactideloadedwithamikacin
AT andrzejwasik antibacterialporoussystemsbasedonpolylactideloadedwithamikacin
AT vladimirsedlarik antibacterialporoussystemsbasedonpolylactideloadedwithamikacin