This study determined the in vivo human bioavailability of topical estradiol, and the transfer of drug between dosed subject and naive recipient. In vivo bioavailability was determined in human volunteers by 14C urinary excretion following topical [14C]-estradiol (0.06%) dose administration and were adjusted by intravenous human excretion amounts to give absolute bioavailability amounts. Drug transfer was determined by volunteer skin contact/rubbing for 15minutes, 1hour after topical dosing. [14C]-estradiol bioavailability as percent dose absorbed (n=6) was 7.5±4.1 from protected dose site, 8.2±6.3 from non-protected dose site, 6.6±7.6 from dosed volunteers subjected to skin contact/rub and 4.3±3.8 from non-dosed volunteers subjected to ski...
Estradiol, the most important hormone in females, was complexed with hydroxypropyl-beta-cyclodextrin...
In vitro methods are commonly used in order to estimate the extent of systemic absorption of chemica...
Women experience the decline of estrogen levels during their menopausal transition between 45 and 55...
This study determined the in vivo human bioavailability of topical estradiol, and the transfer of dr...
Use of the percutaneous route may avoid some of the undesirable side effects that occur following or...
Assessment of the bioavailability of topically applied drugs designed to act within or beneath the s...
The overall goal of this study was to explore the potential of using stratum corneum (SC) tape-strip...
To investigate the effects of topically applied 17β-estradiol on the expression of extracellular mat...
Assessing the bioavailability of drug molecules at the site of action provides better insight into t...
To investigate the effects of topically applied 17beta-estradiol on the expression of extracellular ...
The OECD test guideline 428 for the assessment of dermal absorption in vitro has been in force for m...
The percutaneous absorption of genistein (GEN) and daidzein (DAI), whose oestrogenic-like activity i...
An open-label, randomised, crossover study was conducted with in healthy postmenopausal women to com...
The single-application bioavailability of estradiol from a new matrix (Climaderm(R)) versus a standa...
The percutaneous absorption of sH-betamethasone-17-valerate was studied in young domestic pigs. Our ...
Estradiol, the most important hormone in females, was complexed with hydroxypropyl-beta-cyclodextrin...
In vitro methods are commonly used in order to estimate the extent of systemic absorption of chemica...
Women experience the decline of estrogen levels during their menopausal transition between 45 and 55...
This study determined the in vivo human bioavailability of topical estradiol, and the transfer of dr...
Use of the percutaneous route may avoid some of the undesirable side effects that occur following or...
Assessment of the bioavailability of topically applied drugs designed to act within or beneath the s...
The overall goal of this study was to explore the potential of using stratum corneum (SC) tape-strip...
To investigate the effects of topically applied 17β-estradiol on the expression of extracellular mat...
Assessing the bioavailability of drug molecules at the site of action provides better insight into t...
To investigate the effects of topically applied 17beta-estradiol on the expression of extracellular ...
The OECD test guideline 428 for the assessment of dermal absorption in vitro has been in force for m...
The percutaneous absorption of genistein (GEN) and daidzein (DAI), whose oestrogenic-like activity i...
An open-label, randomised, crossover study was conducted with in healthy postmenopausal women to com...
The single-application bioavailability of estradiol from a new matrix (Climaderm(R)) versus a standa...
The percutaneous absorption of sH-betamethasone-17-valerate was studied in young domestic pigs. Our ...
Estradiol, the most important hormone in females, was complexed with hydroxypropyl-beta-cyclodextrin...
In vitro methods are commonly used in order to estimate the extent of systemic absorption of chemica...
Women experience the decline of estrogen levels during their menopausal transition between 45 and 55...