Azone analogues: classification, design, and transdermal penetration principles

被引:64
作者
Jampilek, Josef [1 ,2 ]
Brychtova, Katerina [2 ]
机构
[1] Zentiva Ks, Prague 10237 10, Czech Republic
[2] Univ Vet & Pharmaceut Sci Brno, Fac Pharm, Dept Chem Drugs, Brno 61242, Czech Republic
关键词
transdermal penetration principles; transdermal penetration enhancers; classification of enhancers; Azone-like enhancers; SAR; QSAR; IN-VITRO EVALUATION; HUMAN STRATUM-CORNEUM; PROTEIN-PARTITIONING THEORY; LOW-FREQUENCY SONOPHORESIS; SKIN PERMEATION ENHANCERS; O-ACYLMENTHOL DERIVATIVES; EXCISED HAIRLESS MOUSE; PORCINE EAR SKIN; PERCUTANEOUS-ABSORPTION; DRUG-DELIVERY;
D O I
10.1002/med.20227
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The development in the field of pharmaceutical dosage forms results in the discovery of additional highly sophisticated drug delivery systems that allow maintaining a constant level of the active substance in an organism. Transdermal therapeutic systems are an excellent alternative to conventional pharmaceutical dosage forms. However, the application of transdermal drug delivery faces the problem of insufficient or no penetration of active pharmaceutical substances through the skin. This review article describes the possible fundamental mechanisms of penetration through the skin barrier and refers to the classification of skin penetration enhancers. Azone-like enhancers are considered in detail and classified according to their structure on the basis of medicinal chemistry approaches. The article also provides a review of original transdermal penetration enhancers prepared in our laboratory and discusses the relationship between the chemical structure of the described Azone analogues and their penetration activity (SAR/QSAR).
引用
收藏
页码:907 / 947
页数:41
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