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Revolutionizing Psoriasis Topical Treatment: Enhanced Efficacy Through Ceramide/Phospholipid Composite Cerosomes Co-Delivery of Cyclosporine and Dithranol: In-Vitro, Ex-Vivo, and in-Vivo Studies.
Elhabal, Sammar Fathy; Abdelaal, Nashwa; Al-Zuhairy, Saeed A S; Mohamed Elrefai, Mohamed Fathi; Khalifa, Mohamed Mansour; Khasawneh, Mohammad Ahmad; Elsaid Hamdan, Ahmed Mohsen; Mohie, Passant M; Gad, Rania A; Kabil, Soad L; El-Ashery, Mohamed Kandeel; Jasti, Bhaskara R; Elzohairy, Nahla A; Elfar, Nehal; Elnawawy, Tayseer; Hassan, Fatma E; El-Nabarawi, Mohamed Ahmed.
Afiliação
  • Elhabal SF; Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Modern University for Technology and Information (MTI), Mokattam, Cairo, Egypt.
  • Abdelaal N; Department of Integrative Physiology, Baylor College of Medicine, Houston, TX, USA.
  • Al-Zuhairy SAS; Department of Pharmacy, Kut University College, Kut, Wasit, Iraq.
  • Mohamed Elrefai MF; Department of Anatomy, Histology, Physiology, and Biochemistry, Faculty of Medicine, The Hashemite University, Zarqa, Jordan.
  • Khalifa MM; Department of Anatomy and Embryology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
  • Khasawneh MA; Department of Human Physiology, Faculty of Medicine, Cairo University, Cairo, Egypt.
  • Elsaid Hamdan AM; Department of Chemistry, College of Science, U.A.E. University, Al-Ain, United Arab Emirates.
  • Mohie PM; Department of Pharmacy Practice, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia.
  • Gad RA; Department of Clinical Pharmacology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
  • Kabil SL; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Nahda University, Beni-Suef, Egypt.
  • El-Ashery MK; Department of Clinical Pharmacology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
  • Jasti BR; Pharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
  • Elzohairy NA; Medicinal Chemistry Department, Faculty of Pharmacy, King Salman International University, Ras-Sedr, South Sinai, Egypt.
  • Elfar N; Department of Pharmaceutics and Medicinal Chemistry, Thomas J. Long School of Pharmacy & Health Sciences, University of the Pacific, Stockton, CA, USA.
  • Elnawawy T; Air Force Specialized Hospital, Cairo, Egypt.
  • Hassan FE; Department of Microbiology and Immunology, Faculty of Pharmacy, Modern University for Technology and Information (MTI), Mokattam, Cairo, Egypt.
  • El-Nabarawi MA; Department of Pharmaceutical Technology, Faculty of Pharmacy, Horus University, New Demiette, Egypt.
Int J Nanomedicine ; 19: 1163-1187, 2024.
Article em En | MEDLINE | ID: mdl-38344440
ABSTRACT

Purpose:

Improving the treatment of psoriasis is a serious challenge today. Psoriasis is an immune-mediated skin condition affecting 125 million people worldwide. It is commonly treated with cyclosporine-A (CsA) and dithranol (DTH). CsA suppresses the activation of T-cells, immune cells involved in forming psoriatic lesions. Meanwhile, DTH is a potent anti-inflammatory and anti-proliferative drug that effectively reduces the severity of psoriasis symptoms such as redness, scaling, and skin thickness. CsA and DTH belong to BCS class II with limited oral bioavailability. We aim to develop a drug delivery system for topical co-delivery of CsA and DTH, exploring its therapeutic potential.

Methods:

Firstly, we developed a niosomal drug delivery system based on ceramide IIIB to form Cerosomes. Cerosomes were prepared from a mixture of Ceramide, hyaluronic acid, and edge activator using a thin-film hydration technique. To co-deliver CsA and DTH topically for the treatment of psoriasis. These two hydrophobic drugs encapsulated into our synthesized positively charged particle cerosomes.

Results:

 Cerosomes had an average particle size of (222.36 nm± 0.36), polydispersity index of (0.415±0.04), Entrapment Efficiency of (96.91%± 0.56), and zeta potential of (29.36±0.38mV) for selected formula. In vitro, In silico, in vivo, permeation, and histopathology experiments have shown that cerosomes enhanced the skin penetration of both hydrophobic drugs by 66.7% compared to the CsA/DTH solution. Imiquimod (IMQ) induced psoriatic mice model was topically treated with our CsA/DTH cerosomes. We found that our formulation enhances the skin penetration of both drugs and reduces psoriasis area and severity index (PASI score) by 2.73 times and 42.85%, respectively, compared to the CsA/DTH solution. Moreover, it reduces the levels of proinflammatory cytokines, TNF-α, IL-10, and IL-6 compared to CsA/DTH solution administration.

Conclusion:

The Cerosomes nano-vesicle-containing CsA/DTH represents a more promising topical treatment for psoriasis, giving new hope to individuals with psoriasis, compared to commercial and other conventional alternatives.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase / Antralina Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Int J Nanomedicine / Int. j. nanomed. (Online) / International journal of nanomedicine (Online) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Psoríase / Antralina Tipo de estudo: Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Int J Nanomedicine / Int. j. nanomed. (Online) / International journal of nanomedicine (Online) Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Egito