Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/30616
Title: Fabrication of Emulsion Loaded with Cyclosporine and Moringa Oleifera Oil Potentially for Topical Psoriasis Treatment
Authors: Siti Hajar Musa
Nurul Huda Heri
Fatin Atirah Borhan
Nurul Fatin Inani Mustaffa
Nabilah Rosman
Faizan Naeem Razali
(UniKL RCMP)
Keywords: Cyclosporine
Emulsion
Formulation
Moringa oleifera oil
Psoriasis
Topical
Issue Date: Sep-2022
Publisher: Oriental Scientific Publishing Company
Citation: Siti Hajar Musa, Nurul Huda Heri, Fatin Atirah Borhan, Mustaffa, Nurul Fatin Inani, Nabilah Rosman, & Faizan Naeem Razali. (2022). Fabrication of Emulsion Loaded with Cyclosporine and Moringa Oleifera Oil Potentially for Topical Psoriasis Treatment. Biomedical and Pharmacology Journal, 15(3), 1709–1720. https://doi.org/10.13005/bpj/2509 ‌
Abstract: Psoriasis is a widespread autoimmune inflammatory dermatological disease treated with oral cyclosporine to reduce the uneasiness of psoriasis. However, systemic therapy of cyclosporine is associated with high risk of side effect that limit the usage in psoriasis treatment. Topical delivery of cyclosporine is believed could overcome cyclosporine related toxicity issues. In this study, a new carrier for topical cyclosporine was developed, which cooperated with Moringa oleifera oil (MOO) that has been reported could enhance the moisture-retaining of the skin. Both high-shear homogenizer and overhead stirrer homogenizer were utilized in formulating a cyclosporine-loaded emulsion carrier. Two emulsions were prepared at different proportions of MOO, water and surfactant (Tween80:Span80) based on the constructed ternary phase diagram. Samples with different formulation (E1 and E2) were subjected to several tests including the stability, rheological, colony and in vitro release analysis. E1 and E2 possessed good stability against phase separation for 1 month at different storage temperatures (4, 25 and 40ºC), having pH values within the range of 4 to 5 as well as showing no mould and microbial growth after been incubated on nutrient agar plate at controlled conditions. Optimized formulations were found to be non-Newtonian and followed the pseudoplastic flow behaviour. Nonetheless, E2 exhibited highest permeation of cyclosporine (80.23%) through cellulose acetate membrane via Franz diffusion cell, which correspond to controlled release and best fitted to first order kinetic behaviour (R2=0.9819). This preliminary study suggested that the formulated emulsion has a promising potential as topical medicament for psoriasis.
URI: https://ir.unikl.edu.my/jspui/handle/123456789/30616
ISSN: 09746242
Appears in Collections:Journal Articles

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