Evidence map›Paper›PMID 38344440›Full record

ArticleInternational journal of nanomedicine2024

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.

Sammar Fathy Elhabal, Nashwa Abdelaal, Saeed A S Al-Zuhairy, Mohamed Fathi Mohamed Elrefai, Mohamed Mansour Khalifa, Mohammad Ahmad Khasawneh, Ahmed Mohsen Elsaid Hamdan, Passant M Mohie, Rania A Gad, Soad L Kabil and 7 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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  20. Green Synthesis of Zinc Oxide Nanoparticles fromInternational journal of nanomedicine · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 11 institutions in 5 countries.

Sammar Fathy ElhabalDepartment of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Modern University for Technology and Information (MTI), Mokattam, Cairo, Egypt.ORCID 0000-0002-7970-2288
Nashwa AbdelaalDepartment of Integrative Physiology, Baylor College of Medicine, Houston, TX, USA.
Saeed A S Al-ZuhairyDepartment of Pharmacy, Kut University College, Kut, Wasit, Iraq.ORCID 0000-0002-7871-3313
Mohamed Fathi Mohamed ElrefaiDepartment of Anatomy, Histology, Physiology, and Biochemistry, Faculty of Medicine, The Hashemite University, Zarqa, Jordan.ORCID 0000-0002-4442-9867
Mohamed Mansour KhalifaDepartment of Human Physiology, Faculty of Medicine, Cairo University, Cairo, Egypt.ORCID 0000-0002-2966-835X
Mohammad Ahmad KhasawnehDepartment of Chemistry, College of Science, U.A.E. University, Al-Ain, United Arab Emirates.ORCID 0000-0001-5853-8311
Ahmed Mohsen Elsaid HamdanDepartment of Pharmacy Practice, Faculty of Pharmacy, University of Tabuk, Tabuk, Saudi Arabia.
Passant M MohieDepartment of Clinical Pharmacology, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Rania A GadDepartment of Pharmacology and Toxicology, Faculty of Pharmacy, Nahda University, Beni-Suef, Egypt.
Soad L KabilDepartment of Clinical Pharmacology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Mohamed Kandeel El-AsheryPharmaceutical Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Bhaskara R JastiDepartment of Pharmaceutics and Medicinal Chemistry, Thomas J. Long School of Pharmacy & Health Sciences, University of the Pacific, Stockton, CA, USA.ORCID 0000-0002-6893-1237
Nahla A ElzohairyAir Force Specialized Hospital, Cairo, Egypt.
Nehal ElfarDepartment of Pharmaceutical Technology, Faculty of Pharmacy, Horus University, New Demiette, Egypt.
Tayseer ElnawawyDepartment of Pharmaceutics, Egyptian Drug Authority, Cairo, Egypt.
Fatma E HassanMedical Physiology Department, Kasr Alainy, Faculty of Medicine, Cairo University, Giza, Egypt.
Mohamed Ahmed El-NabarawiDepartment of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Cairo University, Cairo, Egypt.
Cairo University · EGModern University for Information and Technology · EGAin Shams University · EGAlexandria University · EGBaylor College of Medicine · USEgyptian Government · EGNahda University · EGUniversity of Tabuk · SAUniversity of the Pacific · USUniversity of Wasit · IQZagazig University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

AnthralinPsoriasisAdministration, CutaneousAnimalsCeramidesCyclosporineDisease Models, AnimalHumansMicePhospholipidsSkinAnthralinCeramidesCyclosporinePhospholipidsBCS IIbiopharmaceutics classification system class IIcerosomesimiquimodIMQniosomesniosomes based on ceramide IIIBPASI scoreproinflammatory cytokinespsoriasispsoriasis area and severity index

Identifiers

PMID38344440
PMCPMC10859058
OpenAlexW4391613812

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.