Effect of hot or warm property on skin toxicity of essential oil as penetration enhancer and its mechanism.
10.19540/j.cnki.cjcmm.20201022.302
- Author:
Qi GU
1
;
Xue-Min ZHU
1
;
Xu-Chao WEI
1
;
Ying LIANG
1
;
Wei GU
1
;
Jun CHEN
2
Author Information
1. School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, China.
2. School of Pharmacy, Nanjing University of Chinese Medicine Nanjing 210023, China Collaborative Innovation Center for Industrialization Process of Traditional Chinese Medicine Resources in Jiangsu Province Nanjing 210023, China.
- Publication Type:Journal Article
- Keywords:
hot essential oil;
sesquiterpene reservoir effect;
skin cytotoxicity;
skin irritation;
warm essential oil
- MeSH:
Humans;
Monoterpenes/metabolism*;
Oils, Volatile/toxicity*;
Sesquiterpenes/metabolism*;
Skin/metabolism*;
Skin Absorption
- From:
China Journal of Chinese Materia Medica
2021;46(2):359-365
- CountryChina
- Language:Chinese
-
Abstract:
To compare the effect of hot or warm property of Chinese medicine(CM) on the skin toxicity of essential oils(EOs) as penetration enhancer in vitro and in vivo, and explore the mechanism. EOs were extracted from WIM of Bichengqie(Litseae Fructus), Dingxiang(Flos Syzygii Aromatici), Huajiao(Pericarpium Zanthoxyli Bungeani), and Xiaohuixiang(Fructus Foeniculi) with warm property, and Ganjiang(Rhizoma Zingiberis), Gaoliangjiang(Rhizoma Alpiniae Officinari), Hujiao(Fructus Piperis), and Wuzhuyu(Fructus Evodiae Rutaecarpae) with hot property, respectively. Then the in vitro toxicity was evaluated by human keratinocyte cytotoxicity. In vivo skin irritation potency was also evaluated through pathological observation after topical administration. The components, especially those located in stratum corneum, were analyzed by GC-MS. The main components, namely monoterpenes and sesquiterpenes, of EOs extracted from CM with hot property,were detected for the interaction with keratino-lipid ceramide 3 by molecular simulation technology; and the interaction energy value was calculated based on the optimal conformation. It was found that the skin cell toxicity of EOs from CM with hot property was significantly higher than that of EOs from CM with warm property. However, there was no significant difference between them by in vivo skin irritation evaluation. Whether from CM with hot property or warm property, EOs showed a significant reduced toxicity compared with azone. Sesquiterpenes(33.56%±19.38%) were found to be one of the main components in EOs from CM with hot property, while almost no sesquiterpenes was found in EOs from CM with warm property. After topical administration of EOs from CM with hot property, sesquiterpenes were demonstrated to be prone to locate in stratum corneum. The results of molecular simulation also revealed that the interaction between sesquiterpenes and ceramide 3 was significantly stronger than that of monoterpenes(P<0.01). In conclusion, the location of sesquiterpenes in stratum corneum resulted in the significant difference between in vitro skin cell toxicity and in vivo skin irritation potency. The EOs from CM with hot property shall be taken into account for further development of potent penetration enhancer.
