Gabriella Baki

Dr. Gabriella Baki

orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 November 2016 in Journal of Pharmaceutics
Verified
Journal Article
Open access
PDF file
MCMei X. Chen
Mei X. Chen
KAKenneth S. Alexander
Kenneth S. Alexander
GBGabriella Baki
Gabriella Baki
Background. Skin infections occur commonly and often present therapeutic challenges to practitioners due to the growing concerns regarding multidrug-resistant bacterial, viral, and fungal strains. The antimicrobial properties of zinc sulfate and copper sulfate are well known and have been investigated for many years. However, the synergistic activity between these two metal ions as antimicrobial ingredients has not been evaluated in topical formulations. Objective. The aims of the present study were to (1) formulate topical creams and gels containing zinc and copper alone or in combination and (2) evaluate the in vitro antibacterial activity of these metal ions in the formulations. Method. Formulation of the gels and creams was followed by evaluating their organoleptic characteristics, physicochemical properties, and in vitro antibacterial activity against Escherichia coli and Staphylococcus aureus. Results. Zinc sulfate and copper sulfate had a strong synergistic antibacterial activity in the creams and gels. The minimum effective concentration was found to be 3 w/w% for both active ingredients against the two tested microorganisms. Conclusions. This study evaluated and confirmed the synergistic in vitro antibacterial effect of copper sulfate and zinc sulfate in a cream and two gels.

28 November 2020 in Journal of Cosmetic Dermatology
Verified
Journal Article
Closed access
PDF file
JCJahnna G. Coats
Jahnna G. Coats
BMBriana Maktabi
Briana Maktabi
MAMariam Abou-Dahech
Mariam Abou-Dahech
GBGabriella Baki
Gabriella Baki

2 July 2019 in Pharmaceutics
Verified
Journal Article
Open access
PDF file
SZStella Zsikó
Stella Zsikó
KCKendra Cutcher
Kendra Cutcher
AKAnita Kovacs
Anita Kovacs
MBMária Budai-Szűcs
Mária Budai-Szűcs
AGAttila Gácsi
Attila Gácsi
SBSzilvia Berkó
Szilvia Berkó
The aim of this research was to investigate the stability of a lidocaine-loaded nanostructured lipid carrier dispersion at different temperatures, formulate a nanostructured lipid carrier gel, and test the penetration profile of lidocaine from the nanostructured lipid carrier gel using different skin penetration modeling methods. The formulations were characterized by laser diffraction, rheological measurements and microscopic examinations. Various in vitro methods were used to study drug release, diffusion and penetration. Two types of vertical Franz diffusion cells with three different membranes, including cellulose, Strat-M®, and heat separated human epidermis were used and compared to the Skin-parallel artificial membrane permeability assay (PAMPA) method. Results indicated that the nanostructured lipid carrier dispersion had to be gelified as soon as possible for proper stability. Both the Skin-PAMPA model and Strat-M® membranes correlated favorably with heat separated human epidermis in this research, with the Strat-M® membranes sharing the most similar drug permeability profile to an ex vivo human skin model. Our experimental findings suggest that even when the best available in vitro experiment is selected for modeling human skin penetration to study nanostructured lipid carrier gel systems, relevant in vitro/in vivo correlation should be made to calculate the drug release/permeation in vivo. Future investigations in this field are still needed to demonstrate the influence of membranes and equipment from other classes on other drug candidates.

4 September 2020 in International Journal of Cosmetic Science
Verified
Journal Article
Closed access
PDF file
AHA. Huynh
A. Huynh
AGAndrew G. Garcia
Andrew G. Garcia
LYLisa K. Young
Lisa K. Young
MSMihaly Szoboszlai
Mihaly Szoboszlai
MLMatthew W. Liberatore
Matthew W. Liberatore
GBGabriella Baki
Gabriella Baki

5 June 2018 in Cosmetics
Verified
Journal Article
Open access
PDF file
KMKyle Douglas McIntosh
Kyle Douglas McIntosh
ASAmber Smith
Amber Smith
LYLisa K. Young
Lisa K. Young
MLMichael A. Leitch
Michael A. Leitch
ATAmit K Tiwari
Amit K Tiwari
GBGabriella Baki
Gabriella Baki
The move toward green, sustainable, natural products has been growing in the cosmetic and personal care industry. Ingredients derived from marine organisms and algae are present in many cosmetic products. In this study, a new green ingredient, a wax (i.e., long-chain alkenones) derived from Isochyrsis sp., was evaluated as an alternative for cosmetic waxes. First, the melting point was determined (71.1–77.4 °C), then the alkenones’ thickening capability in five emollients was evaluated and compared to microcrystalline wax and ozokerite. Alkenones were compatible with three emollients and thickened the emollients similarly to the other waxes. Then, lipsticks and lip balms were formulated with and without alkenones. All products remained stable at room temperature for 10 weeks. Lipstick formulated with alkenones was the most resistant to high temperature. Finally, alkenones were compared to three cosmetic thickening waxes in creams. Viscosity, rheology, and stability of the creams were evaluated. All creams had a gel-like behavior. Both viscosity and storage modulus increased in the same order: cream with alkenones < cetyl alcohol < stearic acid < glyceryl monostearate. Overall, alkenones’ performance was comparable to the other three waxes. Alkenones can thus offer a potential green choice as a new cosmetic structuring agent.

1 February 2016 in Journal of Pharmaceutical and Biomedical Analysis
Verified
Journal Article
Closed access
PHPatrick Hooper
Patrick Hooper
JLJason Lasher
Jason Lasher
KAKenneth S. Alexander
Kenneth S. Alexander
GBGabriella Baki
Gabriella Baki