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In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications
Journal of Dispersion Science and Technology, Pages: 1 - 11
Swansea University Author:
Andrew Morris
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DOI (Published version): 10.1080/01932691.2025.2542342
Abstract
Curcumin obtained from Curcuma longa has shown anticancer activities against many types of cancers including melanoma. Tocotrienol is a chemosensitizer, and combining curcumin with tocotrienol may potentiate the anti-cancer activity with less harm to healthy cells. However, due to low aqueous solubi...
| Published in: | Journal of Dispersion Science and Technology |
|---|---|
| ISSN: | 0193-2691 1532-2351 |
| Published: |
Informa UK Limited
2025
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| URI: | https://cronfa.swan.ac.uk/Record/cronfa70181 |
| first_indexed |
2025-08-14T14:09:01Z |
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| last_indexed |
2026-02-03T05:30:16Z |
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2026-02-02T14:12:51.8977819 v2 70181 2025-08-14 In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications 3d7a7f540a5143114fcaf67e4c68d151 0000-0002-6315-7553 Andrew Morris Andrew Morris true false 2025-08-14 MEDS Curcumin obtained from Curcuma longa has shown anticancer activities against many types of cancers including melanoma. Tocotrienol is a chemosensitizer, and combining curcumin with tocotrienol may potentiate the anti-cancer activity with less harm to healthy cells. However, due to low aqueous solubility and poor skin permeation, topical delivery of these drug combinations is challenging. Therefore, this study aimed to develop a transethosomal formulation containing curcumin and tocotrienol for enhanced topical applications. Zetasizer analysis of the transethosomal formulation (Cu-TRF Ets) showed an average particle size of 129.3 ± 3.0 nm and a zeta potential (ZP) of − 87.5 ± 3.0 mV. The scanning transmission electron microscopy (STEM) analysis revealed spherical shapes, with sizes corroborating with Zetasizer results. Fourier transform infrared spectroscopy (FTIR) analysis ensured the compatibility of the drugs within the formulations, while differential scanning calorimetry (DSC) and X-ray diffraction (XRD) analyses confirmed the solid-state nature of curcumin in the formulation. The drug release from the formulations followed a release pattern closely fitting the Korsmeyer-Peppas release model. Permeation studies across synthetic Strat-M® membrane and full-thickness human skin demonstrated an enhanced transdermal flux of curcumin and tocotrienol from the Cu-TRF Ets compared to their pure drug solutions (p < .05). The rheological evaluation of the transethosome-loaded hydrogel demonstrated a pseudoplastic behavior, and the data approximated the Hershel-Buckley model. The study concludes that co-delivering curcumin and tocotrienol in transethosomal formulations can address the formulation issues associated with both curcumin and tocotrienol, while also enhancing skin permeation. Journal Article Journal of Dispersion Science and Technology 0 1 11 Informa UK Limited 0193-2691 1532-2351 Curcumin, tocotrienol, transethosomes, topical, skin permeation 19 8 2025 2025-08-19 10.1080/01932691.2025.2542342 COLLEGE NANME Medical School COLLEGE CODE MEDS Swansea University SU Library paid the OA fee (TA Institutional Deal) University of Nottingham Malaysia; Swansea University 2026-02-02T14:12:51.8977819 2025-08-14T15:06:15.6007804 Faculty of Medicine, Health and Life Sciences Swansea University Medical School - Pharmacy Rajesh Sreedharan Nair 0000-0002-8540-5044 1 Nashiru Billa 0000-0002-8496-1882 2 Andrew Morris 0000-0002-6315-7553 3 70181__35272__deb3ab9ff98548d8b1d17c526cd11d5a.pdf 70181.VOR.pdf 2025-10-07T14:32:46.2291882 Output 2005947 application/pdf Version of Record true © 2025 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution License (CC BY). true eng http://creativecommons.org/licenses/by/4.0/ |
| title |
In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications |
| spellingShingle |
In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications Andrew Morris |
| title_short |
In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications |
| title_full |
In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications |
| title_fullStr |
In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications |
| title_full_unstemmed |
In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications |
| title_sort |
In vitro skin permeation and rheological evaluation of a transethosomal formulation containing curcumin-tocotrienol combinations for enhanced topical applications |
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3d7a7f540a5143114fcaf67e4c68d151_***_Andrew Morris |
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Andrew Morris |
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Rajesh Sreedharan Nair Nashiru Billa Andrew Morris |
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Curcumin obtained from Curcuma longa has shown anticancer activities against many types of cancers including melanoma. Tocotrienol is a chemosensitizer, and combining curcumin with tocotrienol may potentiate the anti-cancer activity with less harm to healthy cells. However, due to low aqueous solubility and poor skin permeation, topical delivery of these drug combinations is challenging. Therefore, this study aimed to develop a transethosomal formulation containing curcumin and tocotrienol for enhanced topical applications. Zetasizer analysis of the transethosomal formulation (Cu-TRF Ets) showed an average particle size of 129.3 ± 3.0 nm and a zeta potential (ZP) of − 87.5 ± 3.0 mV. The scanning transmission electron microscopy (STEM) analysis revealed spherical shapes, with sizes corroborating with Zetasizer results. Fourier transform infrared spectroscopy (FTIR) analysis ensured the compatibility of the drugs within the formulations, while differential scanning calorimetry (DSC) and X-ray diffraction (XRD) analyses confirmed the solid-state nature of curcumin in the formulation. The drug release from the formulations followed a release pattern closely fitting the Korsmeyer-Peppas release model. Permeation studies across synthetic Strat-M® membrane and full-thickness human skin demonstrated an enhanced transdermal flux of curcumin and tocotrienol from the Cu-TRF Ets compared to their pure drug solutions (p < .05). The rheological evaluation of the transethosome-loaded hydrogel demonstrated a pseudoplastic behavior, and the data approximated the Hershel-Buckley model. The study concludes that co-delivering curcumin and tocotrienol in transethosomal formulations can address the formulation issues associated with both curcumin and tocotrienol, while also enhancing skin permeation. |
| published_date |
2025-08-19T05:30:43Z |
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11.095862 |

