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Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release
A poloxamer 407 (P407)—Casein hydrogel was chosen to carry polycaprolactone nanoparticles carrying terbinafine (PCL-TBH-NP). In this study, terbinafine hydrochloride (TBH) was encapsulated into polycaprolactone (PCL) nanoparticles, which were further incorporated into a poloxamer-casein hydrogel in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056099/ https://www.ncbi.nlm.nih.gov/pubmed/36986702 http://dx.doi.org/10.3390/pharmaceutics15030841 |
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author | Tundisi, Louise Lacalendola Ataide, Janaína Artem da Fonseca, Jéssica Heline Lopes Silvério, Luiza Aparecida Luna Lancellotti, Marcelo Paiva-Santos, Ana Cláudia d’Ávila, Marcos Akira Kohane, Daniel S. Mazzola, Priscila Gava |
author_facet | Tundisi, Louise Lacalendola Ataide, Janaína Artem da Fonseca, Jéssica Heline Lopes Silvério, Luiza Aparecida Luna Lancellotti, Marcelo Paiva-Santos, Ana Cláudia d’Ávila, Marcos Akira Kohane, Daniel S. Mazzola, Priscila Gava |
author_sort | Tundisi, Louise Lacalendola |
collection | PubMed |
description | A poloxamer 407 (P407)—Casein hydrogel was chosen to carry polycaprolactone nanoparticles carrying terbinafine (PCL-TBH-NP). In this study, terbinafine hydrochloride (TBH) was encapsulated into polycaprolactone (PCL) nanoparticles, which were further incorporated into a poloxamer-casein hydrogel in a different addition order to evaluate the effect of gel formation. Nanoparticles were prepared by the nanoprecipitation technique and characterized by evaluating their physicochemical characteristics and morphology. The nanoparticles had a mean diameter of 196.7 ± 0.7 nm, PDI of 0.07, negative ζ potential (−0.713 mV), high encapsulation efficiency (>98%), and did not show cytotoxic effects in primary human keratinocytes. PCL-NP modulated terbinafine was released in artificial sweat. Rheological properties were analyzed by temperature sweep tests at different addition orders of nanoparticles into hydrogel formation. The rheological behavior of nanohybrid hydrogels showed the influence of TBH-PCL nanoparticles addition in the mechanical properties of the hydrogel and a long-term release of the nanoparticles from it. |
format | Online Article Text |
id | pubmed-10056099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100560992023-03-30 Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release Tundisi, Louise Lacalendola Ataide, Janaína Artem da Fonseca, Jéssica Heline Lopes Silvério, Luiza Aparecida Luna Lancellotti, Marcelo Paiva-Santos, Ana Cláudia d’Ávila, Marcos Akira Kohane, Daniel S. Mazzola, Priscila Gava Pharmaceutics Article A poloxamer 407 (P407)—Casein hydrogel was chosen to carry polycaprolactone nanoparticles carrying terbinafine (PCL-TBH-NP). In this study, terbinafine hydrochloride (TBH) was encapsulated into polycaprolactone (PCL) nanoparticles, which were further incorporated into a poloxamer-casein hydrogel in a different addition order to evaluate the effect of gel formation. Nanoparticles were prepared by the nanoprecipitation technique and characterized by evaluating their physicochemical characteristics and morphology. The nanoparticles had a mean diameter of 196.7 ± 0.7 nm, PDI of 0.07, negative ζ potential (−0.713 mV), high encapsulation efficiency (>98%), and did not show cytotoxic effects in primary human keratinocytes. PCL-NP modulated terbinafine was released in artificial sweat. Rheological properties were analyzed by temperature sweep tests at different addition orders of nanoparticles into hydrogel formation. The rheological behavior of nanohybrid hydrogels showed the influence of TBH-PCL nanoparticles addition in the mechanical properties of the hydrogel and a long-term release of the nanoparticles from it. MDPI 2023-03-04 /pmc/articles/PMC10056099/ /pubmed/36986702 http://dx.doi.org/10.3390/pharmaceutics15030841 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 Tundisi, Louise Lacalendola Ataide, Janaína Artem da Fonseca, Jéssica Heline Lopes Silvério, Luiza Aparecida Luna Lancellotti, Marcelo Paiva-Santos, Ana Cláudia d’Ávila, Marcos Akira Kohane, Daniel S. Mazzola, Priscila Gava Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release |
title | Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release |
title_full | Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release |
title_fullStr | Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release |
title_full_unstemmed | Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release |
title_short | Terbinafine Nanohybrid: Proposing a Hydrogel Carrying Nanoparticles for Topical Release |
title_sort | terbinafine nanohybrid: proposing a hydrogel carrying nanoparticles for topical release |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10056099/ https://www.ncbi.nlm.nih.gov/pubmed/36986702 http://dx.doi.org/10.3390/pharmaceutics15030841 |
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