Evidence map›Paper›PMID 39428942›Full record

ArticleCurrent pharmaceutical biotechnology2025

Comparative Study on Enhanced Skin Permeation Efficiency of Phenylephrine via Novel Lipid Vesicles: A Promising Approach in Preventing Chemotherapy-induced Alopecia Management.

Ravi Shankar, Manish Kumar, Prabhat Kumar Upadhyay

Abstract readComparative Study
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Article in Current pharmaceutical biotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ravi ShankarInstitute of Pharmaceutical Research, GLA University, Mathura, 281406, (UP), India.ORCID 0000-0002-9586-5861
Manish KumarDepartment of Pharmaceutics, ISF College of Pharmacy, Moga, Punjab, India.ORCID 0000-0003-2042-1243
Prabhat Kumar UpadhyayInstitute of Pharmaceutical Research, GLA University, Mathura, 281406, (UP), India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemotherapy-induced alopecia (CIA) significantly impacts patients' emotional and psychological well-being and treatment regimen. Phenylephrine, a topical vasoconstrictor, can potentially reduce hair loss by limiting chemotherapy drug delivery to hair follicles. However, effective delivery of Phenylephrine through the skin remains challenging. This study investigates lipid vesicles as delivery vehicles to enhance Phenylephrine's skin permeation and sustained release due to their biocompatibility and encapsulation capabilities.

objectiveThis study aimed to formulate and compare different lipid vesicles of Phenylephrine HCl for enhanced permeation through the skin for deep dermal delivery with sustained release of the drug so as to achieve local vasoconstriction.

methodsPhenylephrine-loaded ethosomes, invasomes, and transfersomes were prepared and characterized for particle size (PS), polydispersity index (PDI), and entrapment efficiency (EE %). These lipid vesicles were incorporated into hydrogels to facilitate sustained drug release to deep dermal layers where they could target local vasculature and cause vasoconstriction. The prepared vesicular gels were evaluated for various permeation parameters.

resultsThe entrapment efficiencies of the developed vesicles ranged from 49.51 ± 3.25% to 69.09 ± 2.32%, with vesicle sizes ranging from 162.5 ± 5.21 nm to 321.32 ± 3.75 nm. Statistical analysis revealed significantly higher flux values (Jss, μg/cm

conclusionThe results demonstrate that ethosomal and invasomal formulations were efficient in delivering the drug to deep dermal layers of skin in a sustained manner. These findings suggest that these Lipidic vesicles would be able to target the local vasoconstrictor to vasculature, causing reduced hair loss by limiting chemotherapy drug delivery to hair follicles and managing chemotherapy-induced alopecia.

Indexed as

AlopeciaAntineoplastic AgentsLipidsPhenylephrineSkin AbsorptionVasoconstrictor AgentsAdministration, CutaneousAnimalsDelayed-Action PreparationsDrug LiberationHydrogelsLiposomesParticle SizeSkinSwineAntineoplastic AgentsDelayed-Action PreparationsHydrogelsLipidsLiposomesPhenylephrineVasoconstrictor AgentsChemotherapy-induced alopeciadrug delivery.ethosomesinvasomeslipid vesiclesphenylephrinetransfersomes

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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.