Itraconazole-hydroxypropyl-β-cyclodextrin loaded deformable liposomes: In vitro skin penetration studies and antifungal efficacy using Candida albicans as model

2014 ◽  
Vol 121 ◽  
pp. 74-81 ◽  
Author(s):  
Abdullah H. Alomrani ◽  
Gamal A. Shazly ◽  
Amro A. Amara ◽  
Mohamed M. Badran
Author(s):  
Noha Saleh ◽  
Soha Elshaer ◽  
Germeen Girgis

Background: Fluconazole (FLZ), a potent antifungal medication, is characterized by poor water solubility that reduced its antifungal efficacy. Objective: This study aimed to prepare FLZ-loaded polymeric nanoparticles (NPs) by using different polymers and techniques as a mean of enhancing the antifungal activity of FLZ. Methods: NP1, NP2, and NP3 were prepared by the double emulsion/solvent evaporation method using PLGA, PCL, and PLA, respectively. The ionotropic pre-gelation technique was applied to prepare an alginate/chitosan-based formulation (NP4). Particle size, zeta potential, encapsulation efficiency, and loading capacity were characterized. FT-IR spectra of FLZ, the polymers, and the prepared NPs were estimated. NP4 was selected for further in-vitro release evaluation. The broth dilution method was used to assess the antifungal activity of NP4 using a resistant clinical isolate of Candida albicans. Results: The double emulsion method produced smaller-sized particles (<390 nm) but with much lower encapsulation efficiency (< 12%). Alternatively, the ionic gelation method resulted in nanosized particles with a markedly higher encapsulation efficiency of about 40%. The FT-IR spectroscopy confirmed the loading of the FLZ molecules in the polymeric network of the prepared NPs. The release profile of NP4 showed a burst initial release followed by a controlled pattern up to 24 hours with a higher percent released relative to the free FLZ suspension. NP4 was able to reduce the value of MIC of FLZ by 20 times. Conclusion: The antifungal activity of FLZ against C. albicans was enhanced markedly via its loading in the alginate/chitosan-based polymeric matrix of NP4.


Author(s):  
MAZAYA FADHILA ◽  
ABDUL MUN IM ◽  
MAHDI JUFRI

Objective: White mulberry (Morus alba) root extract has terpenoid, flavonoid, and stilbene compounds. The stilbenes, oxyresveratrol and resveratrol, have antioxidant and antityrosinase activities. Nanocarriers can help active ingredients to be delivered in a more efficient manner. The advantages of nanoemulsion on products include increased penetration, biocompatibility, and low toxicity due to its non-ionic properties and have the ability to combine the properties of lipophilic and hydrophilic active ingredients. The objective of this study was to prepare, characterize, and evaluate the in vitro skin penetration of M. alba root extract nanoemulsion. Methods: The M. alba root extract was prepared by ionic liquid-based microwave-assisted extraction method. Nanoemulsion was optimized and prepared using virgin coconut oil (VCO), Tween 80, and polyethylene glycol 400 (PEG 400) by aqueous phase-titration method to construct pseudoternary phase diagram. M. alba root extract nanoemulsion was characterized for droplet size, viscosity, zeta potential, and physical stability tests for 12 weeks. In vitro skin penetration of oxyresveratrol from nanoemulsion was determined by the Franz diffusion cell and was compared by macroemulsion preparation, then analyzed by high-performance liquid chromatography method. Results: Based on pseudoternary phase diagram, nanoemulsion of white mulberry root extract contained of 2% VCO and 18% mixture of surfactant Tween 80 and PEG 400 (1:1) was chosen. Nanoemulsion has average globule size of 81.61 nm, with polydispersity index 0.22, and potential zeta −1.56 mV. The cumulative penetration of oxyresveratrol from nanoemulsion was 55.86 μg/cm2 with flux of 6.53 μg/cm2/h, while regular emulsion was 32.45 μg/cm2 with flux of 3.5501 μg/cm2/h. Conclusion: Nanoemulsion of white mulberry root extract was penetrated deeper than regular emulsion.


2000 ◽  
Vol 23 (11) ◽  
pp. 1346-1351 ◽  
Author(s):  
Taro OGISO ◽  
Masahiro IWAKI ◽  
Tadatoshi TANINO ◽  
Akiko YONO ◽  
Akihiro ITO

2019 ◽  
Vol 572 ◽  
pp. 118793 ◽  
Author(s):  
C. Bellefroid ◽  
A. Lechanteur ◽  
B. Evrard ◽  
D. Mottet ◽  
F. Debacq-Chainiaux ◽  
...  

Química Nova ◽  
2012 ◽  
Vol 35 (11) ◽  
pp. 2312-2316 ◽  
Author(s):  
Renata F. J. Tiossi ◽  
Juliana C. Da Costa ◽  
Mariza A. Miranda ◽  
Fabíola S. G. Praça ◽  
Maria Vitória L. B. Bentley ◽  
...  

2006 ◽  
Vol 40 (5) ◽  
pp. 1187-1197 ◽  
Author(s):  
Edith Braun ◽  
Andreas Wagner ◽  
Eckhard Fürnschlief ◽  
Hermann Katinger ◽  
Karola Vorauer-Uhl

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