Frequently occurring skin irritancy and flare-up reactions impede the
use of topical tretinoin for acne vulgaris due to poor patient complia
nce. Liposome encapsulation improves penetration into the skin and loc
al tolerability in animals. We investigated efficacy and local tolerab
ility of liposomal tretinoin in man. In a double-blind study 20 patien
ts with uncomplicated acne vulgaris received liposomal tretinoin (0.01
%) on one side of the body and a commercial gel preparation with eithe
r 0.025% or 0.05% on the other once daily for 10 weeks. Comedones and
papules/pustules were counted every 2 (-4) weeks. Then also redness, s
caling, and burning were rated according to a four-point scale. Moreov
er, the patients noted skin irritancy in a diary on a daily base. With
conventional tretinoin the gels were equally efficacious and equally
well tolerated. Liposomal tretinoin also appeared equipotent to the re
ference gels. There may even have been a slightly more rapid clearing
of comedones following the liposome preparation. With respect to skin
irritancy, however, liposomal tretinoin was superior. As rated by the
patients, liposome encapsulated tretinoin induced less burning (mean c
umulative score 2.7 +/- 1.2) than the 0.025% gel (16.1 +/- 7.1) and th
e 0.05% gel (9.7 +/- 4.1) gel and less erythema (1.8 +/- 0.7) than the
0.025% gel (11.4 +/- 3.8; (P < 0.05). Liposomal tretinoin was also be
tter tolerated according to the rating by the investigator. Liposomal
encapsulation of tretinoin allows reduction of the concentration of th
e active agent without a decline in efficacy for acne vulgaris. Since
local tolerability is thus increased, liposomal tretinoin should favor
the acceptance of this treatment by the patient.