M
Mina Ibrahim Tadros
Researcher at Cairo University
Publications - 50
Citations - 1601
Mina Ibrahim Tadros is an academic researcher from Cairo University. The author has contributed to research in topics: Bioavailability & Transdermal. The author has an hindex of 18, co-authored 46 publications receiving 1264 citations. Previous affiliations of Mina Ibrahim Tadros include The Chinese University of Hong Kong.
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Controlled-release effervescent floating matrix tablets of ciprofloxacin hydrochloride: Development, optimization and in vitro-in vivo evaluation in healthy human volunteers.
TL;DR: Developing a gastroretentive controlled-release drug delivery system with swelling, floating, and adhesive properties with promising systems exhibiting excellent floating properties, extended adhesion periods and sustained drug release characteristics was developed.
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Enhanced transdermal delivery of salbutamol sulfate via ethosomes
TL;DR: In vitro permeation studies of the prepared gels containing the selected vesicles showed that ethosomal systems were much more efficient at delivering SS into mice skin than were liposomes or aqueous or hydroalcoholic solutions.
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Promising ion-sensitive in situ ocular nanoemulsion gels of terbinafine hydrochloride: Design, in vitro characterization and in vivo estimation of the ocular irritation and drug pharmacokinetics in the aqueous humor of rabbits
TL;DR: F31 in situ NE gel showed the least ocular irritation potential and significantly (P<0.01) higher C(max, delayed T(max), prolonged mean residence time and increased bioavailability.
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Sucrose stearate-based proniosome-derived niosomes for the nebulisable delivery of cromolyn sodium.
TL;DR: A novel approach was developed for the preparation of controlled release proniosome-derived niosomes, using sucrose stearates as non-ionic biocompatible surfactants for the nebulisable delivery of cromolyn sodium, and offers an alternative approach to minimize the problems associated with conventional niosome like degradation, sedimentation, aggregation and fusion.
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Brain targeting of olanzapine via intranasal delivery of core–shell difunctional block copolymer mixed nanomicellar carriers: In vitro characterization, ex vivo estimation of nasal toxicity and in vivo biodistribution studies
TL;DR: Development of OZ-loaded micellar nanocarriers and investigation of their nose-to-brain targeting potential confirm the development of a promising non-invasive Oz-loaded nose- to-brain delivery system.