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Article

Development of a Novel Drug Delivery System “Nanoemulfoam” for Topical Delivery of Terbinafine Hydrochloride as a Repurposed Therapy in Skin Cancer: Formulation, Optimization, In Vitro Characterization, Ex Vivo Transdermal Permeability, Cytotoxicity Studies, and In Silico Assessment

by
Abeer A. Musallam
1,*,
Reem A. Aldeeb
1,
Riham M. Mansour
2,
Manar Abd El-karim Kassem
3,
Doaa Fayez Saeed
4,
Mahmoud A. Mahdy
5,
Rana M. Abdelnaby
6,
Hanan M. Elnahas
5 and
Tarek M. Ibrahim
5
1
Department of Pharmaceutics, College of Pharmaceutical Sciences and Drug Manufacturing, Misr University for Science and Technology, 6th of October City, Giza 12582, Egypt
2
Department of Pharmacology and Toxicology, College of Pharmaceutical Sciences and Drug Manufacturing, Misr University for Science and Technology, 6th of October City, Giza 12582, Egypt
3
Department of Pharmaceutical Chemistry, College of Pharmaceutical Sciences and Drug Manufacturing, Misr University for Science and Technology, 6th of October City, Giza 12582, Egypt
4
Department of Biochemistry, College of Pharmaceutical Sciences and Drug Manufacturing, Misr University for Science and Technology, 6th of October City, Giza 12582, Egypt
5
Department of Pharmaceutics, Faculty of Pharmacy, Zagazig University, Zagazig 44519, Egypt
6
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Heliopolis University, Cairo 11785, Egypt
*
Author to whom correspondence should be addressed.
Pharmaceuticals 2025, 18(7), 972; https://doi.org/10.3390/ph18070972 (registering DOI)
Submission received: 1 May 2025 / Revised: 14 June 2025 / Accepted: 21 June 2025 / Published: 27 June 2025

Abstract

Background: Skin cancer has become a global health issue because of increasing exposure to environmental contaminants and UV radiation. Terbinafine hydrochloride (TRB), a broad-spectrum antifungal medication, has demonstrated notable anti-tumor properties in previous studies; however, its repurposing for skin cancer therapy remains underexplored. Objective: This study reports for the first time, the development of a new delivery system: a nanoemulsion (NE)–foam hybrid system, i.e., “nanoemulfoam” (NEF), designed to enhance the topical TRB delivery to the skin. The study applied this new hybrid system on TRB for managing skin cancer. Method: The TRB-loaded NEF was produced by loading TRB into a liquid NE. then this was incorporated into a liquid foam base and actuated into foam using a non-propellant mechanism. The NE was developed utilizing peppermint oil as the oil phase and Tween-20/ethanol as the surfactant/co-surfactant combination (Smix). The formulation underwent optimization using the D-optimal design that enabled the simultaneous evaluation of the impact of oil concentration and Tween 20 concentration in the Smix on the particle size (PS), zeta potential (ZP), and dissolution efficiency percent (DE%). Results: The optimal NE formula displayed a small PS of 186.60 ± 2.84 nm, ZP of −13.90 ± 0.99 mV, and DE% of 68.50 ± 1.78% (mean ± SD, n = 3). After incorporation into the foam system, the produced TRB-loaded NEF demonstrated a 7.43-fold increase in the drug transdermal flux in comparison with plain drug foam (p < 0.05). The TRB-loaded NEF showed no signs of inflammation or irritation when applied to abdominal rabbit skin, indicating its safety. The optimum formula exhibited a statistically significant 10-fold increase in cytotoxicity against A-431 skin cancer cells compared to TRB alone, along with a 1.54-fold increase in apoptosis (p < 0.05). Molecular docking studies targeting CDK2, a key regulator of cell proliferation and a known TRB target, revealed that TRB displayed highly favorable binding scores compared to the reference drug. Conclusions: The TRB-loaded NEF represents a promising nanotechnology-based approach for the topical treatment of skin cancer, supporting further investigation toward clinical translation.
Keywords: terbinafine hydrochloride; nanoemulfoam; D-optimal design; drug repurposing; ex vivo permeation; cell viability; skin cancer terbinafine hydrochloride; nanoemulfoam; D-optimal design; drug repurposing; ex vivo permeation; cell viability; skin cancer
Graphical Abstract

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MDPI and ACS Style

Musallam, A.A.; Aldeeb, R.A.; Mansour, R.M.; Kassem, M.A.E.-k.; Saeed, D.F.; Mahdy, M.A.; Abdelnaby, R.M.; Elnahas, H.M.; Ibrahim, T.M. Development of a Novel Drug Delivery System “Nanoemulfoam” for Topical Delivery of Terbinafine Hydrochloride as a Repurposed Therapy in Skin Cancer: Formulation, Optimization, In Vitro Characterization, Ex Vivo Transdermal Permeability, Cytotoxicity Studies, and In Silico Assessment. Pharmaceuticals 2025, 18, 972. https://doi.org/10.3390/ph18070972

AMA Style

Musallam AA, Aldeeb RA, Mansour RM, Kassem MAE-k, Saeed DF, Mahdy MA, Abdelnaby RM, Elnahas HM, Ibrahim TM. Development of a Novel Drug Delivery System “Nanoemulfoam” for Topical Delivery of Terbinafine Hydrochloride as a Repurposed Therapy in Skin Cancer: Formulation, Optimization, In Vitro Characterization, Ex Vivo Transdermal Permeability, Cytotoxicity Studies, and In Silico Assessment. Pharmaceuticals. 2025; 18(7):972. https://doi.org/10.3390/ph18070972

Chicago/Turabian Style

Musallam, Abeer A., Reem A. Aldeeb, Riham M. Mansour, Manar Abd El-karim Kassem, Doaa Fayez Saeed, Mahmoud A. Mahdy, Rana M. Abdelnaby, Hanan M. Elnahas, and Tarek M. Ibrahim. 2025. "Development of a Novel Drug Delivery System “Nanoemulfoam” for Topical Delivery of Terbinafine Hydrochloride as a Repurposed Therapy in Skin Cancer: Formulation, Optimization, In Vitro Characterization, Ex Vivo Transdermal Permeability, Cytotoxicity Studies, and In Silico Assessment" Pharmaceuticals 18, no. 7: 972. https://doi.org/10.3390/ph18070972

APA Style

Musallam, A. A., Aldeeb, R. A., Mansour, R. M., Kassem, M. A. E.-k., Saeed, D. F., Mahdy, M. A., Abdelnaby, R. M., Elnahas, H. M., & Ibrahim, T. M. (2025). Development of a Novel Drug Delivery System “Nanoemulfoam” for Topical Delivery of Terbinafine Hydrochloride as a Repurposed Therapy in Skin Cancer: Formulation, Optimization, In Vitro Characterization, Ex Vivo Transdermal Permeability, Cytotoxicity Studies, and In Silico Assessment. Pharmaceuticals, 18(7), 972. https://doi.org/10.3390/ph18070972

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