Modified Bacterial Cellulose Dressings to Treat Inflammatory Wounds

Natural products suited for prophylaxis and therapy of inflammatory diseases have gained increasing importance. These compounds could be beneficially integrated into bacterial cellulose (BC), which is a natural hydropolymer applicable as a wound dressing and drug delivery system alike. This study pr...

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Main Authors: Uwe Beekmann, Paul Zahel, Berit Karl, Lisa Schmölz, Friedemann Börner, Jana Gerstmeier, Oliver Werz, Stefan Lorkowski, Cornelia Wiegand, Dagmar Fischer, Dana Kralisch
Format: Article
Language:English
Published: MDPI AG 2020-12-01
Series:Nanomaterials
Subjects:
Online Access:https://www.mdpi.com/2079-4991/10/12/2508
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spelling doaj-348eba18d68b473d97f5441602640d862020-12-15T00:02:59ZengMDPI AGNanomaterials2079-49912020-12-01102508250810.3390/nano10122508Modified Bacterial Cellulose Dressings to Treat Inflammatory WoundsUwe Beekmann0Paul Zahel1Berit Karl2Lisa Schmölz3Friedemann Börner4Jana Gerstmeier5Oliver Werz6Stefan Lorkowski7Cornelia Wiegand8Dagmar Fischer9Dana Kralisch10Pharmaceutical Technology and Biopharmacy, Institute of Pharmacy, Friedrich Schiller University, Lessingstraße 8, 07743 Jena, GermanyPharmaceutical Technology and Biopharmacy, Institute of Pharmacy, Friedrich Schiller University, Lessingstraße 8, 07743 Jena, GermanyPharmaceutical Technology and Biopharmacy, Institute of Pharmacy, Friedrich Schiller University, Lessingstraße 8, 07743 Jena, GermanyNutritional Biochemistry and Physiology, Institute of Nutritional Sciences, Friedrich Schiller University, Dornburger Straße 25, 07743 Jena, GermanyPharmaceutical and Medicinal Chemistry, Institute of Pharmacy, Friedrich Schiller University, Philosophenweg 14, 07743 Jena, GermanyPharmaceutical and Medicinal Chemistry, Institute of Pharmacy, Friedrich Schiller University, Philosophenweg 14, 07743 Jena, GermanyPharmaceutical and Medicinal Chemistry, Institute of Pharmacy, Friedrich Schiller University, Philosophenweg 14, 07743 Jena, GermanyNutritional Biochemistry and Physiology, Institute of Nutritional Sciences, Friedrich Schiller University, Dornburger Straße 25, 07743 Jena, GermanyDepartment of Dermatology, Jena University Hospital, Erfurter Str. 35, 07743 Jena, GermanyPharmaceutical Technology and Biopharmacy, Institute of Pharmacy, Friedrich Schiller University, Lessingstraße 8, 07743 Jena, GermanyPharmaceutical Technology and Biopharmacy, Institute of Pharmacy, Friedrich Schiller University, Lessingstraße 8, 07743 Jena, GermanyNatural products suited for prophylaxis and therapy of inflammatory diseases have gained increasing importance. These compounds could be beneficially integrated into bacterial cellulose (BC), which is a natural hydropolymer applicable as a wound dressing and drug delivery system alike. This study presents experimental outcomes for a natural anti-inflammatory product concept of boswellic acids from frankincense formulated in BC. Using esterification respectively (resp.) oxidation and subsequent coupling with phenylalanine and tryptophan, <i>post</i>-modification of BC was tested to facilitate lipophilic active pharmaceutical ingredient (API) incorporation. Diclofenac sodium and indomethacin were used as anti-inflammatory model drugs before the findings were transferred to boswellic acids. By acetylation of BC fibers, the loading efficiency for the more lipophilic API indomethacin and the release was increased by up to 65.6% and 25%, respectively, while no significant differences in loading could be found for the API diclofenac sodium. <i>Post</i>-modifications could be made while preserving biocompatibility, essential wound dressing properties and anti-inflammatory efficacy. Eventually, in vitro wound closure experiments and evaluations of the effect of secondary dressings completed the study.https://www.mdpi.com/2079-4991/10/12/2508bacterial cellulosewound dressinganti-inflammatorydrug delivery systemdiclofenacindomethacin
collection DOAJ
language English
format Article
sources DOAJ
author Uwe Beekmann
Paul Zahel
Berit Karl
Lisa Schmölz
Friedemann Börner
Jana Gerstmeier
Oliver Werz
Stefan Lorkowski
Cornelia Wiegand
Dagmar Fischer
Dana Kralisch
spellingShingle Uwe Beekmann
Paul Zahel
Berit Karl
Lisa Schmölz
Friedemann Börner
Jana Gerstmeier
Oliver Werz
Stefan Lorkowski
Cornelia Wiegand
Dagmar Fischer
Dana Kralisch
Modified Bacterial Cellulose Dressings to Treat Inflammatory Wounds
Nanomaterials
bacterial cellulose
wound dressing
anti-inflammatory
drug delivery system
diclofenac
indomethacin
author_facet Uwe Beekmann
Paul Zahel
Berit Karl
Lisa Schmölz
Friedemann Börner
Jana Gerstmeier
Oliver Werz
Stefan Lorkowski
Cornelia Wiegand
Dagmar Fischer
Dana Kralisch
author_sort Uwe Beekmann
title Modified Bacterial Cellulose Dressings to Treat Inflammatory Wounds
title_short Modified Bacterial Cellulose Dressings to Treat Inflammatory Wounds
title_full Modified Bacterial Cellulose Dressings to Treat Inflammatory Wounds
title_fullStr Modified Bacterial Cellulose Dressings to Treat Inflammatory Wounds
title_full_unstemmed Modified Bacterial Cellulose Dressings to Treat Inflammatory Wounds
title_sort modified bacterial cellulose dressings to treat inflammatory wounds
publisher MDPI AG
series Nanomaterials
issn 2079-4991
publishDate 2020-12-01
description Natural products suited for prophylaxis and therapy of inflammatory diseases have gained increasing importance. These compounds could be beneficially integrated into bacterial cellulose (BC), which is a natural hydropolymer applicable as a wound dressing and drug delivery system alike. This study presents experimental outcomes for a natural anti-inflammatory product concept of boswellic acids from frankincense formulated in BC. Using esterification respectively (resp.) oxidation and subsequent coupling with phenylalanine and tryptophan, <i>post</i>-modification of BC was tested to facilitate lipophilic active pharmaceutical ingredient (API) incorporation. Diclofenac sodium and indomethacin were used as anti-inflammatory model drugs before the findings were transferred to boswellic acids. By acetylation of BC fibers, the loading efficiency for the more lipophilic API indomethacin and the release was increased by up to 65.6% and 25%, respectively, while no significant differences in loading could be found for the API diclofenac sodium. <i>Post</i>-modifications could be made while preserving biocompatibility, essential wound dressing properties and anti-inflammatory efficacy. Eventually, in vitro wound closure experiments and evaluations of the effect of secondary dressings completed the study.
topic bacterial cellulose
wound dressing
anti-inflammatory
drug delivery system
diclofenac
indomethacin
url https://www.mdpi.com/2079-4991/10/12/2508
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