Synthesis, characterization and antibacterial activity of juglone encapsulated PLGA nanoparticles

Aims The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l‐lactide co‐glycolide) amount, polyvinyl alcohol volume and polyvinyl alcohol concentration on encapsulation of juglone to poly(d,l‐lactide co‐glycolide) nanop...

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Published inJournal of applied microbiology Vol. 123; no. 6; pp. 1407 - 1419
Main Authors Arasoglu, T., Derman, S., Mansuroglu, B., Yelkenci, G., Kocyigit, B., Gumus, B., Acar, T., Kocacaliskan, I.
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.12.2017
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Abstract Aims The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l‐lactide co‐glycolide) amount, polyvinyl alcohol volume and polyvinyl alcohol concentration on encapsulation of juglone to poly(d,l‐lactide co‐glycolide) nanoparticles. Methods and Results The synthesized nanoparticle formulations were analyzed for reaction yield, encapsulation efficiency, particle size, polydispersity, zeta potential and juglone release. In conjunction with the highest encapsulation rate, the highest amount of juglone release was obtained for F4 formulation, which has 281·8 nm particle size, 0·217 polydispersity index, and −19·55 mV zeta potential. After the detailed physicochemical characterization of this formulation, the four different kinetic models were used and it was found that juglone release mechanism controlled by Fickian diffusion method. According to antimicrobial activity results, minimal inhibitory concentration (MIC) values of both F4 and free juglone is higher for Gram negative bacteria than Gram positive bacteria. Inhibition zone diameters in the quantitative methods are found 15 and 16 mm for Staphylococcus aureus, 9 and 7 mm for Bacillus cereus, respectively, for F4 and free juglone. Moreover, the MIC values for qualitative methods were found 31·5 μg ml−1 for two bacteria strains. Conclusions It was found that the antibacterial activity of the juglone nanoparticles was higher and longer than the free juglone. Additionally, a similar antimicrobial effect with a lower juglone amount (obtained from controlled release study) indicates that nanoparticle formulation is more effective. Significance and Impact of the Study The use of nanoparticle formulations of juglone in biological systems and applications could be more beneficial than its free form due to its toxicity.
AbstractList Aims The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l‐lactide co‐glycolide) amount, polyvinyl alcohol volume and polyvinyl alcohol concentration on encapsulation of juglone to poly(d,l‐lactide co‐glycolide) nanoparticles. Methods and Results The synthesized nanoparticle formulations were analyzed for reaction yield, encapsulation efficiency, particle size, polydispersity, zeta potential and juglone release. In conjunction with the highest encapsulation rate, the highest amount of juglone release was obtained for F4 formulation, which has 281·8 nm particle size, 0·217 polydispersity index, and −19·55 mV zeta potential. After the detailed physicochemical characterization of this formulation, the four different kinetic models were used and it was found that juglone release mechanism controlled by Fickian diffusion method. According to antimicrobial activity results, minimal inhibitory concentration (MIC) values of both F4 and free juglone is higher for Gram negative bacteria than Gram positive bacteria. Inhibition zone diameters in the quantitative methods are found 15 and 16 mm for Staphylococcus aureus, 9 and 7 mm for Bacillus cereus, respectively, for F4 and free juglone. Moreover, the MIC values for qualitative methods were found 31·5 μg ml−1 for two bacteria strains. Conclusions It was found that the antibacterial activity of the juglone nanoparticles was higher and longer than the free juglone. Additionally, a similar antimicrobial effect with a lower juglone amount (obtained from controlled release study) indicates that nanoparticle formulation is more effective. Significance and Impact of the Study The use of nanoparticle formulations of juglone in biological systems and applications could be more beneficial than its free form due to its toxicity.
The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l-lactide co-glycolide) amount, polyvinyl alcohol volume and polyvinyl alcohol concentration on encapsulation of juglone to poly(d,l-lactide co-glycolide) nanoparticles. The synthesized nanoparticle formulations were analyzed for reaction yield, encapsulation efficiency, particle size, polydispersity, zeta potential and juglone release. In conjunction with the highest encapsulation rate, the highest amount of juglone release was obtained for F4 formulation, which has 281·8 nm particle size, 0·217 polydispersity index, and -19·55 mV zeta potential. After the detailed physicochemical characterization of this formulation, the four different kinetic models were used and it was found that juglone release mechanism controlled by Fickian diffusion method. According to antimicrobial activity results, minimal inhibitory concentration (MIC) values of both F4 and free juglone is higher for Gram negative bacteria than Gram positive bacteria. Inhibition zone diameters in the quantitative methods are found 15 and 16 mm for Staphylococcus aureus, 9 and 7 mm for Bacillus cereus, respectively, for F4 and free juglone. Moreover, the MIC values for qualitative methods were found 31·5 μg ml for two bacteria strains. It was found that the antibacterial activity of the juglone nanoparticles was higher and longer than the free juglone. Additionally, a similar antimicrobial effect with a lower juglone amount (obtained from controlled release study) indicates that nanoparticle formulation is more effective. The use of nanoparticle formulations of juglone in biological systems and applications could be more beneficial than its free form due to its toxicity.
Aims The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l-lactide co-glycolide) amount, polyvinyl alcohol volume and polyvinyl alcohol concentration on encapsulation of juglone to poly(d,l-lactide co-glycolide) nanoparticles. Methods and Results The synthesized nanoparticle formulations were analyzed for reaction yield, encapsulation efficiency, particle size, polydispersity, zeta potential and juglone release. In conjunction with the highest encapsulation rate, the highest amount of juglone release was obtained for F4 formulation, which has 281·8 nm particle size, 0·217 polydispersity index, and -19·55 mV zeta potential. After the detailed physicochemical characterization of this formulation, the four different kinetic models were used and it was found that juglone release mechanism controlled by Fickian diffusion method. According to antimicrobial activity results, minimal inhibitory concentration (MIC) values of both F4 and free juglone is higher for Gram negative bacteria than Gram positive bacteria. Inhibition zone diameters in the quantitative methods are found 15 and 16 mm for Staphylococcus aureus, 9 and 7 mm for Bacillus cereus, respectively, for F4 and free juglone. Moreover, the MIC values for qualitative methods were found 31·5 µg ml-1 for two bacteria strains. Conclusions It was found that the antibacterial activity of the juglone nanoparticles was higher and longer than the free juglone. Additionally, a similar antimicrobial effect with a lower juglone amount (obtained from controlled release study) indicates that nanoparticle formulation is more effective. Significance and Impact of the Study The use of nanoparticle formulations of juglone in biological systems and applications could be more beneficial than its free form due to its toxicity.
Author Yelkenci, G.
Kocyigit, B.
Gumus, B.
Acar, T.
Kocacaliskan, I.
Arasoglu, T.
Mansuroglu, B.
Derman, S.
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Keywords Staphylococci
biodegradation
E. coli
antimicrobials
biopolymers
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Snippet Aims The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l‐lactide...
The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l-lactide co-glycolide)...
Aims The aim of the study was to examine the effect of different process parameters which including; initial juglone amount, initial poly(d,l-lactide...
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SubjectTerms Alcohols
Anti-Bacterial Agents - chemistry
Anti-Bacterial Agents - pharmacology
Antibacterial activity
Antimicrobial activity
Antimicrobial agents
antimicrobials
Bacteria
Bacteria - drug effects
biodegradation
biopolymers
Chemical synthesis
Controlled release
Drug Compounding
E. coli
Encapsulation
Formulations
Free form
Gram-negative bacteria
Gram-positive bacteria
Juglone
Microbial Sensitivity Tests
Minimum inhibitory concentration
Nanoparticles
Nanoparticles - chemistry
Naphthoquinones - chemistry
Naphthoquinones - pharmacology
Particle Size
Polydispersity
Polyglycolic Acid - chemistry
Polylactide-co-glycolide
Polyvinyl alcohol
Process parameters
Staphylococci
Toxicity
Zeta potential
Title Synthesis, characterization and antibacterial activity of juglone encapsulated PLGA nanoparticles
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjam.13601
https://www.ncbi.nlm.nih.gov/pubmed/28980369
https://www.proquest.com/docview/1963844933/abstract/
Volume 123
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