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Tocopherol succinate-loaded ethosomal gel synthesized by cold method technique: Deeper biophysical characterizations for translational application on human skin.
Akhtar, Naheed; Menaa, Farid; Akhtar, Naveed; Javed, Nayla; Sethi, Aisha; Khan, Muhammad Shahzad.
Affiliation
  • Akhtar N; Department of Pharmaceutics, The Islamia University of Bahawalpur, Bahawalpur, Bahawalpur, Punjab, Pakistan.
  • Menaa F; Department of Nanomedicine, California Innovations Corporation, San Diego, California, USA.
  • Akhtar N; Department of Pharmaceutics, The Islamia University of Bahawalpur, Bahawalpur, Bahawalpur, Punjab, Pakistan.
  • Javed N; Department of Pharmaceutics, The Islamia University of Bahawalpur, Bahawalpur, Bahawalpur, Punjab, Pakistan.
  • Sethi A; Department of Pharmaceutics, Government College university Faisalabad, Faisalabad, Pakistan.
  • Khan MS; Abbas Institute of Medical Sciences, GC University Sub-Campus, Layyah, Pakistan.
J Cosmet Dermatol ; 23(3): 1015-1028, 2024 Mar.
Article in En | MEDLINE | ID: mdl-38268219
ABSTRACT

BACKGROUND:

Tocopherols are well-known antioxidant and moisturizing agent. Tocopherol succinate (TS) are widely used in many skin products especially used in anti-aging and skin whitening product formulation.

AIM:

We previously reported the successful synthesis and preliminary characterizations of stable TS ethosomal gels (TSEG) (DOI 10.1111/jocd.14907). Herein, we develop and further characterize TSEG to enhance the stability of the developed formulation with increased permeation through skin.

METHODS:

Cold method technique was used to prepare TS ethosomes. The developed ethosomal vesicle size was 250 nm, which allowed TS to penetrate through the stratum corneum layer and act on melanocytes. For stability study was assessed by thermogravimetric analysis (TGA) by placing TSEG and unloaded/control ethosomal gel (CEG) at various temperature conditions, that is, 8°C, 25°C, 40°C, and 40°C ± 75% RH for 3 months. Organoleptic evaluation was done in terms of color, odor, and phase separation. Transmission electron microscopy (TEM), Fourier Transform infrared spectroscopy (FTIR), x-ray diffraction spectroscopy (XRD), zeta potential (ZP) and particle size (PS) was used for TSEG physical characterizations. In vitro dissolution and ex-vivo permeation studies (using Franz diffusion cell) were performed for both TSEG and CEG formulations. Human women (N = 34) were used to evaluate in vivo biophysical parameters including erythema, melanin, moisture content, sebum level, and skin elasticity.

RESULTS:

Developed formulation was highly thermostable during the 3 months. Erythema, melanin, and sebum level decreased while marked improvement (p < 0.05) in moisture content and elasticity have been observed for the developed TSEG.

CONCLUSION:

The developed TSEG formulation was found to be efficient, safe (no adverse effects observed), stable (at least for 3 months), and easy to use for topical application with improved skin complexation and skin integrity.
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Full text: 1 Database: MEDLINE Main subject: Skin Absorption / Alpha-Tocopherol Limits: Female / Humans Language: En Journal: J Cosmet Dermatol Journal subject: DERMATOLOGIA Year: 2024 Type: Article Affiliation country: Pakistan

Full text: 1 Database: MEDLINE Main subject: Skin Absorption / Alpha-Tocopherol Limits: Female / Humans Language: En Journal: J Cosmet Dermatol Journal subject: DERMATOLOGIA Year: 2024 Type: Article Affiliation country: Pakistan