R. Marks et P. Dykes, PLASMA AND CUTANEOUS DRUG LEVELS AFTER TOPICAL APPLICATION OF PIROXICAM GEL - A STUDY IN HEALTHY-VOLUNTEERS, Skin pharmacology, 7(6), 1994, pp. 340-344
Two studies in healthy male and female volunteers (aged 18-65 years) w
ere undertaken to determine plasma and cutaneous levels of drug follow
ing topical application of piroxicam gel. Twelve subjects applied piro
xicam gel to the knee(l g of 0.5% Feldene gel) at baseline and then af
ter 6, 12 and 24 h. Plasma was collected after 1, 2, 4, 6, 14, 24, 28
and 48 h and piroxicam content determined by high-pressure liquid chro
matography (HPLC). For the majority of samples collected, piroxicam le
vels were below the limit of detection (LOD) of the assay and the maxi
mum recorded plasma level in any subject at any time point was 75.4 ng
/ml. A single application of gel was administered to the forearms of f
our groups each of 6 subjects, and biopsy samples of the stratum corne
um (skin surface biopsy, SBB) and epidermis/dermis were taken after 0.
5, 1, 2 and 4 h. The levels of piroxicam were again measured in each s
ample by HPLC. The highest levels of piroxicam were found in the super
ficial skin surface biopsy with the lowest levels recorded in the skin
surface biopsies nearest the viable epidermis. The mean tissue concen
trations ranged from 160 to 640 ng per sample (calculated to be 80-320
mu g/g of tissue), The mean levels of piroxicam in a 4-mm punch biops
y showed an increase with time after application, rising from 60.3 to
94.6 ng per biopsy (calculated to be 2.4 to 3.8 mu g/g of tissue). It
may be concluded that piroxicam rapidly permeates through the stratum
corneum into the epidermis/dermis after application of the gel. Low an
d often undetectable plasma levels of drug were observed after topical
application of piroxicam gel in a manner comparable to clinical usage
.