Optimization, Preparation, and Cytotoxic Potential of Pyrus communisExtract Loaded Ethosomes on Skin Cancer Cell Lines

Preliminary phytochemical screening results suggest that PCHE contains a significant amount of phenolic compounds compared to other extracts (PCEA and PCAE). The presence of these phenolic compounds contributes to the strong antioxidant and cytotoxic effects of PCHE, which are observed in a dose-dependent manner. Analysis through GC-MS has identified chlorogenic acid, arbutin, ursolic acid, quercetin, and epicatechin are present in PCHE. Based on the initial testing of the extracts, PCHE was chosen for the preparation of ethosomes. The optimized ethosomes were found to have a particle size of 699 nm and a zeta potential of -16.07. Transmission Electron Microscopy illustrated a closed, spherically symmetrical structure of the ethosomes. Additionally, the Franz diffusion cell analysis for percutaneous absorption using egg membrane indicated a steady-state flux of the drug from the ethosomes. The formulation's cytotoxicity potential was assessed using the epidermoid carcinoma cell line (A431) through the MTT assay. The results show that the ethosome formulations exhibit cytotoxic activity better than PCHE extract. 1 Conclusion: In sum, the result of this study clearly points out that Pyrus communis extract entrapped in ethosomes, prepared by hot method, displayed a cytotoxic potential against skin cancer cell lines. This ethosomal formulation can be harnessed for skin cancer therapy through further mechanistic analysis and animal studies.

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Journal
Current Topics in Medicinal Chemistry
Published
2025-05-02
DOI
https://doi.org/10.2174/0115680266349097250418135927
Primary Topic
Biological Activity of Diterpenoids and Biflavonoids
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article
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article

Optimization, Preparation, and Cytotoxic Potential of Pyrus communisExtract Loaded Ethosomes on Skin Cancer Cell Lines

Anju Dhiman, Vandana Garg, Kiran Kangra, Rohit Dutt
1 links
Current Topics in Medicinal Chemistry
Biological Activity of Diterpenoids and Biflavonoids
article

Optimization, Preparation, and Cytotoxic Potential of Pyrus communisExtract Loaded Ethosomes on Skin Cancer Cell Lines

Anju Dhiman, Vandana Garg, Kiran Kangra, Rohit Dutt
article en

Abstract

Preliminary phytochemical screening results suggest that PCHE contains a significant amount of phenolic compounds compared to other extracts (PCEA and PCAE). The presence of these phenolic compounds contributes to the strong antioxidant and cytotoxic effects of PCHE, which are observed in a dose-dependent manner. Analysis through GC-MS has identified chlorogenic acid, arbutin, ursolic acid, quercetin, and epicatechin are present in PCHE. Based on the initial testing of the extracts, PCHE was chosen for the preparation of ethosomes. The optimized ethosomes were found to have a particle size of 699 nm and a zeta potential of -16.07. Transmission Electron Microscopy illustrated a closed, spherically symmetrical structure of the ethosomes. Additionally, the Franz diffusion cell analysis for percutaneous absorption using egg membrane indicated a steady-state flux of the drug from the ethosomes. The formulation's cytotoxicity potential was assessed using the epidermoid carcinoma cell line (A431) through the MTT assay. The results show that the ethosome formulations exhibit cytotoxic activity better than PCHE extract. 1 Conclusion: In sum, the result of this study clearly points out that Pyrus communis extract entrapped in ethosomes, prepared by hot method, displayed a cytotoxic potential against skin cancer cell lines. This ethosomal formulation can be harnessed for skin cancer therapy through further mechanistic analysis and animal studies.

Current Topics in Medicinal ChemistryVol. 25
Maharshi Dayanand University (IN)
Good health and well-being
Openalex Percentile: Top 91%
Biological Activity of Diterpenoids and Biflavonoids
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Optimization, Preparation, and Cytotoxic Potential of Pyrus communisExtract Loaded Ethosomes on Skin Cancer Cell Lines — Anju Dhiman, Vandana Garg, et al. · Current Topics in Medicinal Chemistry (2025) | TGRS Research Map | TGRS