Ahmad M. Eid’s research while affiliated with An-Najah National University and other places

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Publications (1)


Schematic illustration showing the structure of transethosomal nanovesicular carrier
AFM image of clindamycin transethosomal system showing the closed spherical structure of the nanovesicles
In vitro release profile of clindamycin from three transethosomal systems containing various HPC concentrations, expressed as A cumulative released amount and B percentage of clindamycin released amount
HPLC calibration curve of clindamycin over a concentration range of 1–200 µg/mL
Clindamycin amounts penetrated into the skin (µg/cm²) from the topical transethosomal system as compared to conventional ointment
Transethosomal System for Enhanced Dermal Delivery of Clindamycin
  • Article
  • Publisher preview available

February 2025

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40 Reads

BioNanoScience

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Ahmad M. Eid

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Maisam Metani

Overcoming the skin barrier is crucial for the treatment of skin infections affecting the deep skin layers. Delivery of therapeutics to these layers is considered the key to efficient treatment. The objective of this study is to develop and investigate a nanovesicular system to improve the penetration of the antibacterial drug, clindamycin, into the skin. The carrier employed in this investigation is a transethosomal carrier consisting of phospholipid nanovesicles that possess flexible and adaptable characteristics due to the inclusion of surfactants and cosolvents like ethanol and propanediol. System characterization by atomic force microscopy and dynamic light scattering revealed the presence of enclosed, spherical nanovesicles. Additional pH measurements indicated that the system is appropriate for topical application. The drug release rate in the in vitro tests was shown to be dependent on the viscosity of the system. The results indicated that higher concentrations of the thickening agent, hydroxypropyl cellulose, led to sustained release characteristics. Furthermore, in vitro penetration experiments indicated an enhanced penetration of clindamycin into the skin tissue as compared to traditional formulations. These findings point towards the significance of the transethosomal carrier in facilitating the penetration of drugs into the epidermis leading to better management of bacterial skin infections.

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