Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing Inflammation

Mild to moderate pain for a few hours to several days post-piercing is normal, and the pain is usually accompanied by swelling, redness, and warmth due to the inflammatory response. Cool compresses and over-the-counter analgesics (e.g., NSAIDs) can ease mild discomfort. However, oral NSAIDs may have...

Full description

Saved in:
Bibliographic Details
Main Authors: Negar Ahmadi, Maria Rincón, Mireia Mallandrich, Joaquim Suñer-Carbó, Lilian Sosa, Mireya Zelaya, Sergio Martinez-Ruiz, Cecilia Cordero, Ana C. Calpena
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Gels
Subjects:
Online Access:https://www.mdpi.com/2310-2861/11/5/334
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849711539434553344
author Negar Ahmadi
Maria Rincón
Mireia Mallandrich
Joaquim Suñer-Carbó
Lilian Sosa
Mireya Zelaya
Sergio Martinez-Ruiz
Cecilia Cordero
Ana C. Calpena
author_facet Negar Ahmadi
Maria Rincón
Mireia Mallandrich
Joaquim Suñer-Carbó
Lilian Sosa
Mireya Zelaya
Sergio Martinez-Ruiz
Cecilia Cordero
Ana C. Calpena
author_sort Negar Ahmadi
collection DOAJ
description Mild to moderate pain for a few hours to several days post-piercing is normal, and the pain is usually accompanied by swelling, redness, and warmth due to the inflammatory response. Cool compresses and over-the-counter analgesics (e.g., NSAIDs) can ease mild discomfort. However, oral NSAIDs may have systemic side effects; for this reason, we propose a topical anti-inflammatory approach. Four pranoprofen-loaded gels were created using different gelling agents: Sepigel<sup>®</sup> 305 (PF-Gel-Sep), Carbopol<sup>®</sup> 940 (PF-Gel-Car), Pluronic<sup>®</sup> F-68 (PF-Gel-Plu), and Lutrol<sup>®</sup> F-127 (PF-Gel-Lut). The gels were assessed for pH, morphology, FT-IR spectroscopy, rheological properties, spreadability, swelling and degradation, drug release kinetics, skin permeation (cow and human skin), irritation potential (HET-CAM assay), and impact on skin barrier function (TEWL and SCH). The gels exhibited varied rheological properties with PF-Gel-Car showing high viscosity and PF-Gel-Plu very low viscosity. All gels had similar spreadability with PF-Gel-Lut showing the highest. PF-Gel-Car showed the highest amounts of PF released, whereas PF-Gel-Plu led to the highest amount of pranoprofen retained in human and bovine skin. The HET-CAM assay indicated that none of the PF-Gels were irritating. Additionally, PF-Gel-Car and PF-Gel-Plu showed no cytotoxic effects on HaCaT cells. In vivo testing on mice showed that PF-Gel-Car prevented inflammation, while the rest of the gels were able to revert it in 25 min. Skin tolerance tests revealed the gels did not affect TEWL, and some gels improved SCH. The study successfully formulated and characterized four PF-loaded topical gels with potential to be used as an alternative for treating inflammation from piercings and ear tags.
format Article
id doaj-art-1b240a94c2ff4fc99fd7badf20d8edcb
institution DOAJ
issn 2310-2861
language English
publishDate 2025-04-01
publisher MDPI AG
record_format Article
series Gels
spelling doaj-art-1b240a94c2ff4fc99fd7badf20d8edcb2025-08-20T03:14:36ZengMDPI AGGels2310-28612025-04-0111533410.3390/gels11050334Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing InflammationNegar Ahmadi0Maria Rincón1Mireia Mallandrich2Joaquim Suñer-Carbó3Lilian Sosa4Mireya Zelaya5Sergio Martinez-Ruiz6Cecilia Cordero7Ana C. Calpena8Department of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII 27-31, 08028 Barcelona, SpainDepartment of Materials Science and Physical Chemistry, Faculty of Chemistry, University of Barcelona, C. Martí i Franquès 1-11, 08028 Barcelona, SpainDepartment of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII 27-31, 08028 Barcelona, SpainDepartment of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII 27-31, 08028 Barcelona, SpainCentro Experimental en Biociencia (CENBIO), Facultad de Ciencias Químicas y Farmacia, Universidad Nacional Autónoma de Honduras (UNAH), Tegucigalpa 11101, HondurasLaboratorio de Técnicas Histológicas, Facultad de Ciencias, Universidad Nacional Autónoma de Honduras (UNAH), Tegucigalpa 11101, HondurasDepartament de Bioquímica i Fisiologia, Facultat de Farmàcia i Ciències de l’Alimentació, University of Barcelona, 08028 Barcelona, SpainDepartament de Bioquímica i Fisiologia, Facultat de Farmàcia i Ciències de l’Alimentació, University of Barcelona, 08028 Barcelona, SpainDepartment of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Av. Joan XXIII 27-31, 08028 Barcelona, SpainMild to moderate pain for a few hours to several days post-piercing is normal, and the pain is usually accompanied by swelling, redness, and warmth due to the inflammatory response. Cool compresses and over-the-counter analgesics (e.g., NSAIDs) can ease mild discomfort. However, oral NSAIDs may have systemic side effects; for this reason, we propose a topical anti-inflammatory approach. Four pranoprofen-loaded gels were created using different gelling agents: Sepigel<sup>®</sup> 305 (PF-Gel-Sep), Carbopol<sup>®</sup> 940 (PF-Gel-Car), Pluronic<sup>®</sup> F-68 (PF-Gel-Plu), and Lutrol<sup>®</sup> F-127 (PF-Gel-Lut). The gels were assessed for pH, morphology, FT-IR spectroscopy, rheological properties, spreadability, swelling and degradation, drug release kinetics, skin permeation (cow and human skin), irritation potential (HET-CAM assay), and impact on skin barrier function (TEWL and SCH). The gels exhibited varied rheological properties with PF-Gel-Car showing high viscosity and PF-Gel-Plu very low viscosity. All gels had similar spreadability with PF-Gel-Lut showing the highest. PF-Gel-Car showed the highest amounts of PF released, whereas PF-Gel-Plu led to the highest amount of pranoprofen retained in human and bovine skin. The HET-CAM assay indicated that none of the PF-Gels were irritating. Additionally, PF-Gel-Car and PF-Gel-Plu showed no cytotoxic effects on HaCaT cells. In vivo testing on mice showed that PF-Gel-Car prevented inflammation, while the rest of the gels were able to revert it in 25 min. Skin tolerance tests revealed the gels did not affect TEWL, and some gels improved SCH. The study successfully formulated and characterized four PF-loaded topical gels with potential to be used as an alternative for treating inflammation from piercings and ear tags.https://www.mdpi.com/2310-2861/11/5/334topical gelsNipagin (methyl 4-hydroxybenzoate)Nipasol (propyl 4-hydroxybenzoate)pranoprofen (PF)NSAIDinflammation reduction
spellingShingle Negar Ahmadi
Maria Rincón
Mireia Mallandrich
Joaquim Suñer-Carbó
Lilian Sosa
Mireya Zelaya
Sergio Martinez-Ruiz
Cecilia Cordero
Ana C. Calpena
Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing Inflammation
Gels
topical gels
Nipagin (methyl 4-hydroxybenzoate)
Nipasol (propyl 4-hydroxybenzoate)
pranoprofen (PF)
NSAID
inflammation reduction
title Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing Inflammation
title_full Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing Inflammation
title_fullStr Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing Inflammation
title_full_unstemmed Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing Inflammation
title_short Novel Gels for Post-Piercing Care: Evaluating the Efficacy of Pranoprofen Formulations in Reducing Inflammation
title_sort novel gels for post piercing care evaluating the efficacy of pranoprofen formulations in reducing inflammation
topic topical gels
Nipagin (methyl 4-hydroxybenzoate)
Nipasol (propyl 4-hydroxybenzoate)
pranoprofen (PF)
NSAID
inflammation reduction
url https://www.mdpi.com/2310-2861/11/5/334
work_keys_str_mv AT negarahmadi novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT mariarincon novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT mireiamallandrich novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT joaquimsunercarbo novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT liliansosa novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT mireyazelaya novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT sergiomartinezruiz novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT ceciliacordero novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation
AT anaccalpena novelgelsforpostpiercingcareevaluatingtheefficacyofpranoprofenformulationsinreducinginflammation