Fabrication and efficacy assessment of combination of brimonidine and ivermectin for treatment of papulopustular rosacea

Author:

Pakdaman Samin Fallah1ORCID,Samadi Aniseh2ORCID,Fattahi Mahsa2ORCID,Naeimifar Atefeh3ORCID,Ardehali Fatemeh Amiri2ORCID,Ketabi Yasaman4ORCID,Nasrollahi Saman Ahmad2ORCID,Firooz Alireza2ORCID

Affiliation:

1. Pharmaceutical Sciences Branch, Islamic Azad University Tehran Iran

2. Center for Research & Training in Skin Diseases & Leprosy Tehran University of Medical Sciences Tehran Iran

3. Department of Pharmaceutics, Faculty of Pharmacy Tehran University of Medical Sciences Tehran Iran

4. Shahid Beheshti University of Medical Science Tehran Iran

Abstract

AbstractBackground & AimRosacea is a chronic inflammatory, multifactorial disease for which combination therapy could be an effective treatment.In this study, we evaluate the effect of the combination therapy of brimonidine 0.33% and ivermectin 1% as a single cream for the treatment of papulopustular rosacea.MethodA stable and appropriate formulation was prepared by adding the aqueous phase to the lipid phase while being stirred. The stability and physicochemical properties of the formulation were evaluated under accelerated conditions. Twelve patients (36–60 years) with mild to moderate papulopustular rosacea and a Demodex count of five or more were treated with the combination of brimonidine 0.33% and ivermectin 1% cream. Clinician's Erythema Assessment (CEA), Patients Self‐Assessment (PSA), skin erythema (ΔE) and lightness (ΔL), and skin biophysical parameters including transepidermal water loss (TEWL), skin hydration, pH, and sebum content, as well as erythema and melanin index and ultrasound parameters, were measured before treatment and 4 and 8 weeks after. Adverse drug reactions were also recorded.ResultsCEA and PSA decreased significantly from 3 to 2 after 8 weeks, respectively (p‐value = 0.014 for CEA and 0.010 for PSA). ΔE and ΔL, as well as skin erythema index and TEWL improved after 8 weeks of treatment (p < 0.05). Two patients withdrew from the study in the first week because of local adverse effects; one developed flushing following treatment and left the investigation after 4 weeks and another patient withdrew from the study after 4 weeks due to deciding to become pregnant.ConclusionEight‐week treatment with the combination of brimonidine 0.33% and ivermectin 1% was shown to be effective for improvement of erythema and inflammatory lesions in mild to moderate papulopustular rosacea.

Funder

National Institute for Medical Research Development

Publisher

Wiley

Reference21 articles.

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5. Efficacy and safety of once‐daily topical brimonidine tartrate gel 0.5% for the treatment of moderate to severe facial erythema of rosacea: results of two randomized, double‐blind, and vehicle‐controlled pivotal studies;Fowler J;J Drugs Dermatol,2013

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