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Updated: Jan 24, 2026

Fabrication and Characterization of a Conformal Skin-like Electronic System for Quantitative, Cutaneous Wound Management
Published on: September 2, 2015
Betamethasone dipropionate compounding for cutaneous T-cell lymphoma management
Patrícia Trindade1, Alice Gelpi2, Ana Salgado1
1Department of Pharmacy, Instituto Português de Oncologia de Lisboa Francisco Gentil EPE, Lisbon, Portugal.
Background:
Primary cutaneous lymphomas (extranodular non-Hodgkin lymphomas) are rare (incidence 1:100 000). Mycosis fungoides is the most common cutaneous T-cell lymphoma (CTCL) subtype. Treatment options are based on the diagnosis and the stage of the disease. Skin-directed therapies are useful for the initial stages and include topical treatments such as corticosteroids. Betamethasone dipropionate (BD) is a synthetic glucocorticoid with high anti-inflammatory activity, potency and immunosuppressant effects. It is used for topical treatment of CTCL within the following dosage 0.025-0.1% (w/w). In the Portuguese market only one topical cream contains BD at 0.05% (w/w).
Objectives:
To develop a new and stable emulsion containing 0.1% of BD.
Methods:
To accomplish this aim, development, stability, in vitro release and clinical studies of a new topical water-in-oil emulsion containing BD 0.1% w/w were assessed for the topical treatment of CTCL.
Results:
The three batches prepared were physically, chemically and microbiologically stable over a period of 90 days. 40% of BD was released over 6 hours and evaluation of skin lesions showed a favourable clinical effect (less itching, less infiltration, fewer patches and a reduced area of plaque).
Conclusions:
The clinical results show the effective cutaneous improvement of skin barrier conditions during the study.
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