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Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique

The application of enzyme-based therapies has received significant attention in modern drug development. Lipases are one of the most versatile enzymes that can be used as therapeutic agents in basic skin care and medical treatment related to excessive sebum production, acne, and inflammation. The tr...

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Autores principales: Balogh-Weiser, Diána, Molnár, Alexandra, Tóth, Gergő D., Koplányi, Gábor, Szemes, József, Decsi, Balázs, Katona, Gábor, Salamah, Maryana, Ender, Ferenc, Kovács, Anita, Berkó, Szilvia, Budai-Szűcs, Mária, Balogh, György T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143802/
https://www.ncbi.nlm.nih.gov/pubmed/37111659
http://dx.doi.org/10.3390/pharmaceutics15041174
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author Balogh-Weiser, Diána
Molnár, Alexandra
Tóth, Gergő D.
Koplányi, Gábor
Szemes, József
Decsi, Balázs
Katona, Gábor
Salamah, Maryana
Ender, Ferenc
Kovács, Anita
Berkó, Szilvia
Budai-Szűcs, Mária
Balogh, György T.
author_facet Balogh-Weiser, Diána
Molnár, Alexandra
Tóth, Gergő D.
Koplányi, Gábor
Szemes, József
Decsi, Balázs
Katona, Gábor
Salamah, Maryana
Ender, Ferenc
Kovács, Anita
Berkó, Szilvia
Budai-Szűcs, Mária
Balogh, György T.
author_sort Balogh-Weiser, Diána
collection PubMed
description The application of enzyme-based therapies has received significant attention in modern drug development. Lipases are one of the most versatile enzymes that can be used as therapeutic agents in basic skin care and medical treatment related to excessive sebum production, acne, and inflammation. The traditional formulations available for skin treatment, such as creams, ointments or gels, are widely applied; however, their use is not always accompanied by good drug penetration properties, stability, or patient adherence. Nanoformulated drugs offer the possibility of combining enzymatic and small molecule formulations, making them a new and exciting alternative in this field. In this study polymeric nanofibrous matrices made of polyvinylpyrrolidone and polylactic acid were developed, entrapping lipases from Candida rugosa and Rizomucor miehei and antibiotic compound nadifloxacin. The effect of the type of polymers and lipases were investigated, and the nanofiber formation process was optimized to provide a promising alternative in topical treatment. Our experiments have shown that entrapment by electrospinning induced two orders of magnitude increase in the specific enzyme activity of lipases. Permeability investigations indicated that all lipase-loaded nanofibrous masks were capable of delivering nadifloxacin to the human epidermis, confirming the viability of electrospinning as a formulation method for topical skin medications.
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spelling pubmed-101438022023-04-29 Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique Balogh-Weiser, Diána Molnár, Alexandra Tóth, Gergő D. Koplányi, Gábor Szemes, József Decsi, Balázs Katona, Gábor Salamah, Maryana Ender, Ferenc Kovács, Anita Berkó, Szilvia Budai-Szűcs, Mária Balogh, György T. Pharmaceutics Article The application of enzyme-based therapies has received significant attention in modern drug development. Lipases are one of the most versatile enzymes that can be used as therapeutic agents in basic skin care and medical treatment related to excessive sebum production, acne, and inflammation. The traditional formulations available for skin treatment, such as creams, ointments or gels, are widely applied; however, their use is not always accompanied by good drug penetration properties, stability, or patient adherence. Nanoformulated drugs offer the possibility of combining enzymatic and small molecule formulations, making them a new and exciting alternative in this field. In this study polymeric nanofibrous matrices made of polyvinylpyrrolidone and polylactic acid were developed, entrapping lipases from Candida rugosa and Rizomucor miehei and antibiotic compound nadifloxacin. The effect of the type of polymers and lipases were investigated, and the nanofiber formation process was optimized to provide a promising alternative in topical treatment. Our experiments have shown that entrapment by electrospinning induced two orders of magnitude increase in the specific enzyme activity of lipases. Permeability investigations indicated that all lipase-loaded nanofibrous masks were capable of delivering nadifloxacin to the human epidermis, confirming the viability of electrospinning as a formulation method for topical skin medications. MDPI 2023-04-07 /pmc/articles/PMC10143802/ /pubmed/37111659 http://dx.doi.org/10.3390/pharmaceutics15041174 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Balogh-Weiser, Diána
Molnár, Alexandra
Tóth, Gergő D.
Koplányi, Gábor
Szemes, József
Decsi, Balázs
Katona, Gábor
Salamah, Maryana
Ender, Ferenc
Kovács, Anita
Berkó, Szilvia
Budai-Szűcs, Mária
Balogh, György T.
Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique
title Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique
title_full Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique
title_fullStr Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique
title_full_unstemmed Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique
title_short Combined Nanofibrous Face Mask: Co-Formulation of Lipases and Antibiotic Agent by Electrospinning Technique
title_sort combined nanofibrous face mask: co-formulation of lipases and antibiotic agent by electrospinning technique
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10143802/
https://www.ncbi.nlm.nih.gov/pubmed/37111659
http://dx.doi.org/10.3390/pharmaceutics15041174
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