A. Salimi, Behzad Sharif Makhmalzadeh, Ghazal Davood Baharvandi, Saeed Mohammad Soleymani
{"title":"植物油和挥发油对吡罗康皮肤渗透性影响的机理研究","authors":"A. Salimi, Behzad Sharif Makhmalzadeh, Ghazal Davood Baharvandi, Saeed Mohammad Soleymani","doi":"10.5812/jkums-126619","DOIUrl":null,"url":null,"abstract":"Background: Piroxicam is a non-steroidal anti-inflammatory medication for treating fever, discomfort, and inflammation. In addition, Piroxicam inhibits cyclooxygenase and lowers prostaglandin synthesis, resulting in analgesic and anti-inflammatory effects. Objectives: This study used Franz diffusion cells made from rat skin primed with sesame, eucalyptus, olive, menthol, clove, and sunflower oils. Methods: Control was hydrated rat skin. Permeability measurements include steady-state flux (Jss), permeability coefficient (Kp), and diffusion coefficient (D). FT-IR was used to compare changes in peak position, DSC, mean transition temperature, and the permeability enhancement methods of the penetration enhancer (Tm). The skin acted as a barrier to Piroxicam permeability throughout the whole surface, indicating that drug flux was limited by diffusion into the skin. Results: The steady-state flux (Jss) of all penetration enhancers were not significantly different from control, except for clove and menthol oil (4 hours treated) and olive oil (2 and 4 hours treated). Conclusions: Penetration enhancers improved drug permeability through rat skin. Sesame oil, Menthol oil, and Sesame oil were found to have higher ERflux, ERD, and ERP ratios than water-hydrated skin due to lipid fluidization, lipid structure disruption, and irreversible keratin denaturation.","PeriodicalId":16201,"journal":{"name":"Journal of Kermanshah University of Medical Sciences","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-08-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"The Effect of Vegetable and Volatile Oils on the Piroxicam Skin Permeability: A Mechanistic Study\",\"authors\":\"A. Salimi, Behzad Sharif Makhmalzadeh, Ghazal Davood Baharvandi, Saeed Mohammad Soleymani\",\"doi\":\"10.5812/jkums-126619\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Piroxicam is a non-steroidal anti-inflammatory medication for treating fever, discomfort, and inflammation. In addition, Piroxicam inhibits cyclooxygenase and lowers prostaglandin synthesis, resulting in analgesic and anti-inflammatory effects. Objectives: This study used Franz diffusion cells made from rat skin primed with sesame, eucalyptus, olive, menthol, clove, and sunflower oils. Methods: Control was hydrated rat skin. Permeability measurements include steady-state flux (Jss), permeability coefficient (Kp), and diffusion coefficient (D). FT-IR was used to compare changes in peak position, DSC, mean transition temperature, and the permeability enhancement methods of the penetration enhancer (Tm). The skin acted as a barrier to Piroxicam permeability throughout the whole surface, indicating that drug flux was limited by diffusion into the skin. Results: The steady-state flux (Jss) of all penetration enhancers were not significantly different from control, except for clove and menthol oil (4 hours treated) and olive oil (2 and 4 hours treated). Conclusions: Penetration enhancers improved drug permeability through rat skin. Sesame oil, Menthol oil, and Sesame oil were found to have higher ERflux, ERD, and ERP ratios than water-hydrated skin due to lipid fluidization, lipid structure disruption, and irreversible keratin denaturation.\",\"PeriodicalId\":16201,\"journal\":{\"name\":\"Journal of Kermanshah University of Medical Sciences\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-08-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Kermanshah University of Medical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5812/jkums-126619\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Kermanshah University of Medical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5812/jkums-126619","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The Effect of Vegetable and Volatile Oils on the Piroxicam Skin Permeability: A Mechanistic Study
Background: Piroxicam is a non-steroidal anti-inflammatory medication for treating fever, discomfort, and inflammation. In addition, Piroxicam inhibits cyclooxygenase and lowers prostaglandin synthesis, resulting in analgesic and anti-inflammatory effects. Objectives: This study used Franz diffusion cells made from rat skin primed with sesame, eucalyptus, olive, menthol, clove, and sunflower oils. Methods: Control was hydrated rat skin. Permeability measurements include steady-state flux (Jss), permeability coefficient (Kp), and diffusion coefficient (D). FT-IR was used to compare changes in peak position, DSC, mean transition temperature, and the permeability enhancement methods of the penetration enhancer (Tm). The skin acted as a barrier to Piroxicam permeability throughout the whole surface, indicating that drug flux was limited by diffusion into the skin. Results: The steady-state flux (Jss) of all penetration enhancers were not significantly different from control, except for clove and menthol oil (4 hours treated) and olive oil (2 and 4 hours treated). Conclusions: Penetration enhancers improved drug permeability through rat skin. Sesame oil, Menthol oil, and Sesame oil were found to have higher ERflux, ERD, and ERP ratios than water-hydrated skin due to lipid fluidization, lipid structure disruption, and irreversible keratin denaturation.