Cyano-phycocyanin loaded enriched transfersomes for enhanced topical skin delivery and antioxidant protection

This study aimed to develop and evaluate cyano-phycocyanin (C-PC)-loaded enriched transfersomes for topical application, improved skin delivery, and antioxidant protection. The main objective was to overcome the limitations associated with C-PC's instability and poor skin permeability due to its high molecular weight and hydrophilicity. Six formulations were prepared using an organic solvent-free two-step method: glycerol-enriched transfersomes (Gly-transfersomes),glycerol and cholesterol-enriched transfersomes (Gly-chol-transfersomes),hyaluronate-enriched transfersomes (Hyal-transfersomes),hyaluronate and cholesterol-enriched transfersomes (Hyal-chol-transfersomes),glycerol and hyaluronate-enriched transfersomes (Hyal-gly-transfersomes), anda combination of all three (Hyal-gly-chol-transfersomes). Empty vesicles were prepared via direct sonication, then C-PC was gently loaded using mild sonication in a temperature-controlled ultrasonic bath. All formulations demonstrated properties suitable for skin delivery, with mean diameters <115 nm, polydispersity indexes <0.2, and zeta potential below -30 mV. Cryo- transmission electron microscopy confirmed spherical, unilamellar or oligolamellar morphology. Gly- and Gly-chol-transfersomes exhibited the highest encapsulation efficiency (∼52 %) and remained stable for up to 8 months at 4 °C. Antioxidant activity of C-PC (∼23-27 μmol TE/g of dry C-PC) was confirmed via DPPH assay. Biological tests on HaCaT cells exposed to H<sub>2</sub>O<sub>2</sub>-induced oxidative stress showed ∼80 % cell viability after treatment with C-PC formulations, compared to ∼60 % in untreated cells, indicating cytoprotective activity. Ex vivo skin penetration studies revealed significantly higher C-PC accumulation in the epidermis especially for Gly- and Gly-chol-transfersomes versus aqueous C-PC. These findings confirm the potential of enriched transfersomes as effective carriers to improve the skin delivery and bioactivity of C-PC in antioxidant skin care formulations.

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Publication Details

Journal
International Journal of Pharmaceutics
Published
2025-08-15
DOI
https://doi.org/10.1016/j.ijpharm.2025.126079
Citations
1
Primary Topic
Transgenic Plants and Applications
Type
article
Field-Weighted Citation Impact
1.23
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article

Cyano-phycocyanin loaded enriched transfersomes for enhanced topical skin delivery and antioxidant protection

Dainius H. Pauža, Modestas Žilius, Matteo Aroffu, María Letizia Manca et al.
1 citations
International Journal of Pharmaceutics
Transgenic Plants and Applications
1.23
article

Cyano-phycocyanin loaded enriched transfersomes for enhanced topical skin delivery and antioxidant protection

Dainius H. Pauža, Modestas Žilius, Matteo Aroffu, María Letizia Manca, Arūnas Savickas, Kristina Rysevaitė-Kyguolienė, Nijolė Savickienė, Jūratė Karosienė, Vitalis Briedis, Maria Manconi, Daiva Galinytė, Judita Koreivienė, Elvira Escribano Ferrer
article en
1 citations

Abstract

This study aimed to develop and evaluate cyano-phycocyanin (C-PC)-loaded enriched transfersomes for topical application, improved skin delivery, and antioxidant protection. The main objective was to overcome the limitations associated with C-PC's instability and poor skin permeability due to its high molecular weight and hydrophilicity. Six formulations were prepared using an organic solvent-free two-step method: glycerol-enriched transfersomes (Gly-transfersomes),glycerol and cholesterol-enriched transfersomes (Gly-chol-transfersomes),hyaluronate-enriched transfersomes (Hyal-transfersomes),hyaluronate and cholesterol-enriched transfersomes (Hyal-chol-transfersomes),glycerol and hyaluronate-enriched transfersomes (Hyal-gly-transfersomes), anda combination of all three (Hyal-gly-chol-transfersomes). Empty vesicles were prepared via direct sonication, then C-PC was gently loaded using mild sonication in a temperature-controlled ultrasonic bath. All formulations demonstrated properties suitable for skin delivery, with mean diameters <115 nm, polydispersity indexes <0.2, and zeta potential below -30 mV. Cryo- transmission electron microscopy confirmed spherical, unilamellar or oligolamellar morphology. Gly- and Gly-chol-transfersomes exhibited the highest encapsulation efficiency (∼52 %) and remained stable for up to 8 months at 4 °C. Antioxidant activity of C-PC (∼23-27 μmol TE/g of dry C-PC) was confirmed via DPPH assay. Biological tests on HaCaT cells exposed to H<sub>2</sub>O<sub>2</sub>-induced oxidative stress showed ∼80 % cell viability after treatment with C-PC formulations, compared to ∼60 % in untreated cells, indicating cytoprotective activity. Ex vivo skin penetration studies revealed significantly higher C-PC accumulation in the epidermis especially for Gly- and Gly-chol-transfersomes versus aqueous C-PC. These findings confirm the potential of enriched transfersomes as effective carriers to improve the skin delivery and bioactivity of C-PC in antioxidant skin care formulations.

International Journal of PharmaceuticsVol. 683
Lithuanian University of Health Sciences (LT), University of Cagliari (IT), Istituto Nazionale di Fisica Nucleare, Sezione di Cagliari (IT), Nature Research Centre (LT), Institute for Bioengineering of Catalonia (ES)
Openalex Percentile: Top 19%
Transgenic Plants and Applications
1.23
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