Fanni Farner, L. Bors, Ágnes Bajza, G. Karvaly, I. Antal, F. Erdő
{"title":"咖啡因经皮给药的体内外测定系统的验证","authors":"Fanni Farner, L. Bors, Ágnes Bajza, G. Karvaly, I. Antal, F. Erdő","doi":"10.2174/2210303108666180903102107","DOIUrl":null,"url":null,"abstract":"\n\nIntroduction: Degree of skin penetration of topical drugs and cosmetics is a crucial point\nconcerning their effects and tolerability. For testing drug delivery across the dermal barrier different in\nvitro and in vivo assays have been developed. Caffeine has been shown to have beneficial effects\nagainst skin aging, sunburn and hair-loss, and it is protective against melanoma and non-melanoma\ntype skin cancers. Aim of our study was to set up an assay system to evaluate caffeine penetration from\ntopical formulation into the skin.\n\nMethods: Franz diffusion cells consisting of either a filter paper or an artificial membrane or rat skin\nwere used as in vitro/ex vivo test systems and transdermal microdialysis in anaesthetized rats was performed\nas an in vivo assay.\n\nResults: Results indicate that Franz diffusion cell studies provide a good approximation of the release\nof caffeine from the formulation but are not able to differentiate between 2% and 4% cream concentrations.\nThe maximum concentrations (Cmax) in case of the 2% cream formulation were 708.3 (2.7 μm\npore), 78.7 (0.8 µm pore), 45.3 (0.45 µm pore) and 44.9 (rat skin) µg/7.5 mL, respectively. The in vivo\nmicrodialysis experiments were in accordance with the in vitro and ex vivo results and gave more information\non the dynamics and follicular and transcellular phases of drug penetration through the layers\nof the skin.\n\nDiscussion and Conclusion: Taken together, Franz diffusion cell and transdermal microdialysis are a\ngood combination to evaluate caffeine release and penetration into the skin from the formulations\ntested. This system might also be used for rapid testing of other hydrophilic topical drugs and has a\nbenefit in the prediction for human skin absorption and tolerability studies, in an early phase of drug\ndevelopment.\n","PeriodicalId":11310,"journal":{"name":"Drug Delivery Letters","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2174/2210303108666180903102107","citationCount":"9","resultStr":"{\"title\":\"Validation of an In vitro-in vivo Assay System for Evaluation of Transdermal Delivery of Caffeine\",\"authors\":\"Fanni Farner, L. Bors, Ágnes Bajza, G. Karvaly, I. Antal, F. Erdő\",\"doi\":\"10.2174/2210303108666180903102107\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\\n\\nIntroduction: Degree of skin penetration of topical drugs and cosmetics is a crucial point\\nconcerning their effects and tolerability. For testing drug delivery across the dermal barrier different in\\nvitro and in vivo assays have been developed. Caffeine has been shown to have beneficial effects\\nagainst skin aging, sunburn and hair-loss, and it is protective against melanoma and non-melanoma\\ntype skin cancers. Aim of our study was to set up an assay system to evaluate caffeine penetration from\\ntopical formulation into the skin.\\n\\nMethods: Franz diffusion cells consisting of either a filter paper or an artificial membrane or rat skin\\nwere used as in vitro/ex vivo test systems and transdermal microdialysis in anaesthetized rats was performed\\nas an in vivo assay.\\n\\nResults: Results indicate that Franz diffusion cell studies provide a good approximation of the release\\nof caffeine from the formulation but are not able to differentiate between 2% and 4% cream concentrations.\\nThe maximum concentrations (Cmax) in case of the 2% cream formulation were 708.3 (2.7 μm\\npore), 78.7 (0.8 µm pore), 45.3 (0.45 µm pore) and 44.9 (rat skin) µg/7.5 mL, respectively. The in vivo\\nmicrodialysis experiments were in accordance with the in vitro and ex vivo results and gave more information\\non the dynamics and follicular and transcellular phases of drug penetration through the layers\\nof the skin.\\n\\nDiscussion and Conclusion: Taken together, Franz diffusion cell and transdermal microdialysis are a\\ngood combination to evaluate caffeine release and penetration into the skin from the formulations\\ntested. This system might also be used for rapid testing of other hydrophilic topical drugs and has a\\nbenefit in the prediction for human skin absorption and tolerability studies, in an early phase of drug\\ndevelopment.\\n\",\"PeriodicalId\":11310,\"journal\":{\"name\":\"Drug Delivery Letters\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-02-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.2174/2210303108666180903102107\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Drug Delivery Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/2210303108666180903102107\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Pharmacology, Toxicology and Pharmaceutics\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Delivery Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/2210303108666180903102107","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
Validation of an In vitro-in vivo Assay System for Evaluation of Transdermal Delivery of Caffeine
Introduction: Degree of skin penetration of topical drugs and cosmetics is a crucial point
concerning their effects and tolerability. For testing drug delivery across the dermal barrier different in
vitro and in vivo assays have been developed. Caffeine has been shown to have beneficial effects
against skin aging, sunburn and hair-loss, and it is protective against melanoma and non-melanoma
type skin cancers. Aim of our study was to set up an assay system to evaluate caffeine penetration from
topical formulation into the skin.
Methods: Franz diffusion cells consisting of either a filter paper or an artificial membrane or rat skin
were used as in vitro/ex vivo test systems and transdermal microdialysis in anaesthetized rats was performed
as an in vivo assay.
Results: Results indicate that Franz diffusion cell studies provide a good approximation of the release
of caffeine from the formulation but are not able to differentiate between 2% and 4% cream concentrations.
The maximum concentrations (Cmax) in case of the 2% cream formulation were 708.3 (2.7 μm
pore), 78.7 (0.8 µm pore), 45.3 (0.45 µm pore) and 44.9 (rat skin) µg/7.5 mL, respectively. The in vivo
microdialysis experiments were in accordance with the in vitro and ex vivo results and gave more information
on the dynamics and follicular and transcellular phases of drug penetration through the layers
of the skin.
Discussion and Conclusion: Taken together, Franz diffusion cell and transdermal microdialysis are a
good combination to evaluate caffeine release and penetration into the skin from the formulations
tested. This system might also be used for rapid testing of other hydrophilic topical drugs and has a
benefit in the prediction for human skin absorption and tolerability studies, in an early phase of drug
development.