Topical Options For Erectile Dysfunction
Topical Options For Erectile Dysfunction
By Sarah Taylor, PharmD
Erectile
dysfunction (ED) is a common patient concern, and its prevalence is strongly
associated with age. Data from the US National Heath and Nutrition Examination
Survey suggests that 8.2% of men between ages 40-49 years and 77.5% of men
greater than 75 years old suffer from erectile dysfunction.1 The
prevalence of ED was also associated with other conditions such as diabetes
mellitus, smoking, cardiovascular disease, hypertension, and obesity.1
ED is most commonly managed with prescription phosphodiesterase-5 (PDE5)
inhibitors used orally such as sildenafil, tadalafil, or vardenafil.1
Commercially available injectables for ED such as alprostadil or phentolamine
mesylate injections are also sometimes used. Compounded options for ED often
include combination injectable products such as phentolamine
mesylate/papaverine HCl/alprostadil combinations, commonly referred to as “Tri-mix”.
Tri-mix injections can be associated with serious side effects. One study
evaluating trimix use and reasons for dropout in 189 patients noted that 30% of
patients discontinued Tri-mix due to lack of efficacy, 5.2% experienced
fibrosis or scarring, and 3.7% reported priapism.2 While Tri-mix
works well for many patients, adverse effects make this route inappropriate for
some patients creating a need for alternatives. In this newsletter, we will
discuss existing evidence for the use of topically administered treatments, for
the management of ED.
Alprostadil
is available in the United States as an injectable for ED as well as an
intraurethral suppository, but in other countries, there are alternatives such
as intraurethral alprostadil. Vitaros is an intraurethral cream available in
some European countries as well as Canada. It is 3mg/g alprostadil and is
packaged in single dose syringes carrying 100mg of cream, equivalent to 300mcg
alprostadil. Phase II and III trials demonstrated up to 83% efficacy with this
product with only 3% of the treated population reporting systemic adverse
effects.3 In addition to intraurethral administration, some studies
have also evaluated topical/transdermal use. One study of alprostadil 1% had
patients apply 0.25ml of alprostadil 1% or placebo gel to the glans penis. The
study reported better responses to the alprostadil treatment at all timepoints,
with greatest differences noted at 45 and 60 minutes after application. The
study noted that of the tested patients 38.9% in the treatment group and 6.9%
in the placebo group achieved an erection deemed sufficient for penetration.4
Some
studies have also evaluated papaverine HCl for transdermal use. One study of
drug release of papaverine HCl in a gel vehicle found an alcohol-containing
penetration enhancer resulted in drug penetration both in vitro and in vivo in
rabbits. The study suggested that their results supported the use of
penetration enhancer to deliver papaverine HCl transdermally.5 Another
study evaluated 15% and 20% papaverine HCl gel applied to the scrotum,
perineum, and penis. Patient response was evaluated 45 minutes after treatment.
The treatment was well tolerated and papaverine HCl was minimally systemically
absorbed, the researchers hypothesized that effects seen, mainly increase in
duration of erection compared to placebo, were a result of local rather than
systemic absorption.6 Phentolamine mesylate, while sometimes
included in transdermal erectile dysfunction combination products, has not
currently been studied in well controlled trials for its potentially efficacy
via the transdermal route.
Sildenafil
is a PDE5 Inhibitor commercially available for oral use for ED, but there is
some information to suggest that it may be efficacious transdermally as well.
One placebo-controlled study compared sildenafil 1% gel to sildenafil 100mg
tablets. The topical gel group applied 0.5g of sildenafil 1% gel to the glans
of the penis approximately 5 minutes before sexual activity and the tablet
group took a 100mg tablet 1 hour before sexual activity. In the gel group, 25%
of patients achieved complete or moderate erections compared to 75% of the
tablet group. Though oral tablets demonstrated increased likelihood of complete
or moderate erection, both groups did see benefit and onset of erection in the
patients who applied sildenafil gel was 7.4 ±3.6 minutes, but was 37.8 ± 14.9
minutes in the group who used oral tablets.7 Though there aren’t
many other studies on sildenafil cream topical for erectile dysfunction, other
studies for conditions such as Raynaud’s have demonstrated benefit and
increased blood flow as a result of local administration of sildenafil 5%
cream, further suggesting that sildenafil may be absorbed from topical
administration.8 Though currently information regarding other in
vivo studies on other PDE5 inhibitors topically for erectile dysfunction are not
available, some studies have found benefit for tadalafil used topically for
Raynaud’s, suggesting transdermal penetration and potential local efficacy.9
Future studies are needed to confirm the potential of tadalafil as a topical
treatment for erectile dysfunction.
Other
active ingredients used transdermally to increase blood flow are sometimes also
considered for combination topical ED mediations. Arginine, sometimes used at
3-6% in female sexual dysfunction creams, was found in a study of diabetic
patients to improve blood flow. These patients applied transdermal arginine
12.5% cream to the feet and noted improved blood flow with a doppler flow meter
and with an infrared thermometer 30 minutes after application.10 Despite
this promising information, not enough data yet exists to suggest that arginine
transdermal is appropriate for the management of ED.
Though
there is limited information to support transdermal application of medication
for ED, some data exists to suggest efficacy. The transdermal route could be
considered for patients who prefer not to use oral or injectable medications.
Check out the Fagron Academy site for related formulas. If you have further
questions, feel free to reach out to Fagron Academy Technical Support Services!
Sources:
1.
Mulhall J, Luo X, Zou K, Stecher V,
Galaznik A. Relationship between age and erectile dysfunction diagnosis or
treatment using real-world observational data in the United States. Int J Clin
Pract. 2016; 70(12)1012-1018. doi: 10.1111/ijcp.12908.
2.
Casabe A, Bachra A, Cheliz G, Romano S,
Rey H, Fredotovich. Drop-out reasons and complications in self-injection triple
vasoactive drug mixture in sexual erectile dysfunction. International Journal
of Impotence Research. 1998; 10:5-9.
3.
Cuzin B. Alprostadil cream in the
treatment of erectile dysfunction: clinical evidence and experience. Ther Adv
Urol. 2016; 8(4):249-256.
4.
Goldstein I, Payton T, Schechter P. A
double-blind, placebo-controlled, efficacy and safety study of topical gel
formulation of 1% alprostadil (Topiglan) for the in-office treatment of
erectile dysfunction. Adult urology. 2001;57)2):301-305.
DOI:https://doi.org/10.1016/S0090-4295(00)00936-5.
5.
Ming Wen M El-Kamel A, Khalil S.
Systemic enhancement of papaverine transdermal gel for erectile dysfunction.
Drug Dev Ind Pharm. 2012; 38(8): 912-922. doi: 10.3109/03639045.2011.633262.
6.
Kim E, el-Rashidy R, McVary K.
Papaverine topical gel for treatment of erectile dysfunction. J Urol. 1995;
153(2):361-5. doi: 10.1097/00005392-199502000-00019.
7.
Yonessi M, Saeedi M. A double-blind
placebo-controlled evaluation of the effect of topical sildenafil on erectile
dysfunction. The Journal of Applied Research. 2005;5(2):289-294.
8.
Research Letter. Nifedipine cream
versus sildenafil cream for patients with secondary Raynaud phenomenon: a
randomized double-blind, controlled pilot study. J Am Acad Dermatol:78(1):189
9.
Fernández-Codina, A., Kazem, M. &
Pope, J.E. Possible benefit of tadalafil cream for the treatment of Raynaud’s
phenomenon and digital ulcers in systemic sclerosis. Clin Rheumatol 39, 963–965
(2020). https://doi.org/10.1007/s10067-020-04966-z
10.
Fossel E. Improvement of temperature
and flow in feet of subjects with diabetes with use of a transdermal
preparation of L-arginine: a pilot study. Diabetes Care. 2004; 27(1): 284-285. https://doi.org/10.2337/diacare.27.1.284.
Comments
Post a Comment