Preparation, characterization and in vitro release study of carvacrol-loaded chitosan nanoparticles

[Display omitted] ▶ Carvacrol-loaded chitosan particles were prepared through emulsion formation and ionic gelation. ▶ Particles exhibited spherical shape, 40-80nm-size and positively charged surfaces. ▶ Particles showed antimicrobial activity against S. aureus, B. cereus and E. coli. ▶ Release of c...

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Published inColloids and surfaces, B, Biointerfaces Vol. 84; no. 1; pp. 163 - 171
Main Authors Keawchaoon, Lalita, Yoksan, Rangrong
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.05.2011
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Abstract [Display omitted] ▶ Carvacrol-loaded chitosan particles were prepared through emulsion formation and ionic gelation. ▶ Particles exhibited spherical shape, 40-80nm-size and positively charged surfaces. ▶ Particles showed antimicrobial activity against S. aureus, B. cereus and E. coli. ▶ Release of carvacrol in an acidic solution was faster than alkaline and neutral media. The fabrication of carvacrol-loaded chitosan nanoparticles was achieved by a two-step method, i.e., oil-in-water emulsion and ionic gelation of chitosan with pentasodium tripolyphosphate. The obtained particles possessed encapsulation efficiency (EE) and loading capacity (LC) in the ranges of 14–31% and 3–21%, respectively, when the initial carvacrol content was 0.25–1.25g/g of chitosan. The individual particles exhibited a spherical shape with an average diameter of 40–80nm, and a positively charged surface with a zeta potential value of 25–29mV. The increment of initial carvacrol content caused a reduction of surface charge. Carvacrol-loaded chitosan nanoparticles showed antimicrobial activity against Staphylococcus aureus, Bacillus cereus and Escherichia coli with an MIC of 0.257mg/mL. The release of carvacrol from chitosan nanoparticles reached plateau level on day 30, with release amounts of 53% in acetate buffer solution with pH of 3, and 23% and 33% in phosphate buffer solutions with pH of 7 and 11, respectively. The release mechanism followed a Fickian behavior. The release rate was superior in an acidic medium to either alkaline or neutral media, respectively.
AbstractList Display Omitted a- Carvacrol-loaded chitosan particles were prepared through emulsion formation and ionic gelation. a- Particles exhibited spherical shape, 40-80nm-size and positively charged surfaces. a- Particles showed antimicrobial activity against S. aureus, B. cereus and E. coli. a- Release of carvacrol in an acidic solution was faster than alkaline and neutral media. The fabrication of carvacrol-loaded chitosan nanoparticles was achieved by a two-step method, i.e., oil-in-water emulsion and ionic gelation of chitosan with pentasodium tripolyphosphate. The obtained particles possessed encapsulation efficiency (EE) and loading capacity (LC) in the ranges of 14-31% and 3-21%, respectively, when the initial carvacrol content was 0.25-1.25g/g of chitosan. The individual particles exhibited a spherical shape with an average diameter of 40-80nm, and a positively charged surface with a zeta potential value of 25-29mV. The increment of initial carvacrol content caused a reduction of surface charge. Carvacrol-loaded chitosan nanoparticles showed antimicrobial activity against Staphylococcus aureus, Bacillus cereus and Escherichia coli with an MIC of 0.257mg/mL. The release of carvacrol from chitosan nanoparticles reached plateau level on day 30, with release amounts of 53% in acetate buffer solution with pH of 3, and 23% and 33% in phosphate buffer solutions with pH of 7 and 11, respectively. The release mechanism followed a Fickian behavior. The release rate was superior in an acidic medium to either alkaline or neutral media, respectively.
The fabrication of carvacrol-loaded chitosan nanoparticles was achieved by a two-step method, i.e., oil-in-water emulsion and ionic gelation of chitosan with pentasodium tripolyphosphate. The obtained particles possessed encapsulation efficiency (EE) and loading capacity (LC) in the ranges of 14-31% and 3-21%, respectively, when the initial carvacrol content was 0.25-1.25 g/g of chitosan. The individual particles exhibited a spherical shape with an average diameter of 40-80 nm, and a positively charged surface with a zeta potential value of 25-29 mV. The increment of initial carvacrol content caused a reduction of surface charge. Carvacrol-loaded chitosan nanoparticles showed antimicrobial activity against Staphylococcus aureus, Bacillus cereus and Escherichia coli with an MIC of 0.257 mg/mL. The release of carvacrol from chitosan nanoparticles reached plateau level on day 30, with release amounts of 53% in acetate buffer solution with pH of 3, and 23% and 33% in phosphate buffer solutions with pH of 7 and 11, respectively. The release mechanism followed a Fickian behavior. The release rate was superior in an acidic medium to either alkaline or neutral media, respectively.
The fabrication of carvacrol-loaded chitosan nanoparticles was achieved by a two-step method, i.e., oil-in-water emulsion and ionic gelation of chitosan with pentasodium tripolyphosphate. The obtained particles possessed encapsulation efficiency (EE) and loading capacity (LC) in the ranges of 14–31% and 3–21%, respectively, when the initial carvacrol content was 0.25–1.25g/g of chitosan. The individual particles exhibited a spherical shape with an average diameter of 40–80nm, and a positively charged surface with a zeta potential value of 25–29mV. The increment of initial carvacrol content caused a reduction of surface charge. Carvacrol-loaded chitosan nanoparticles showed antimicrobial activity against Staphylococcus aureus, Bacillus cereus and Escherichia coli with an MIC of 0.257mg/mL. The release of carvacrol from chitosan nanoparticles reached plateau level on day 30, with release amounts of 53% in acetate buffer solution with pH of 3, and 23% and 33% in phosphate buffer solutions with pH of 7 and 11, respectively. The release mechanism followed a Fickian behavior. The release rate was superior in an acidic medium to either alkaline or neutral media, respectively.
[Display omitted] ▶ Carvacrol-loaded chitosan particles were prepared through emulsion formation and ionic gelation. ▶ Particles exhibited spherical shape, 40-80nm-size and positively charged surfaces. ▶ Particles showed antimicrobial activity against S. aureus, B. cereus and E. coli. ▶ Release of carvacrol in an acidic solution was faster than alkaline and neutral media. The fabrication of carvacrol-loaded chitosan nanoparticles was achieved by a two-step method, i.e., oil-in-water emulsion and ionic gelation of chitosan with pentasodium tripolyphosphate. The obtained particles possessed encapsulation efficiency (EE) and loading capacity (LC) in the ranges of 14–31% and 3–21%, respectively, when the initial carvacrol content was 0.25–1.25g/g of chitosan. The individual particles exhibited a spherical shape with an average diameter of 40–80nm, and a positively charged surface with a zeta potential value of 25–29mV. The increment of initial carvacrol content caused a reduction of surface charge. Carvacrol-loaded chitosan nanoparticles showed antimicrobial activity against Staphylococcus aureus, Bacillus cereus and Escherichia coli with an MIC of 0.257mg/mL. The release of carvacrol from chitosan nanoparticles reached plateau level on day 30, with release amounts of 53% in acetate buffer solution with pH of 3, and 23% and 33% in phosphate buffer solutions with pH of 7 and 11, respectively. The release mechanism followed a Fickian behavior. The release rate was superior in an acidic medium to either alkaline or neutral media, respectively.
Author Yoksan, Rangrong
Keawchaoon, Lalita
Author_xml – sequence: 1
  givenname: Lalita
  surname: Keawchaoon
  fullname: Keawchaoon, Lalita
– sequence: 2
  givenname: Rangrong
  surname: Yoksan
  fullname: Yoksan, Rangrong
  email: rangrong.y@ku.ac.th
BackLink https://www.ncbi.nlm.nih.gov/pubmed/21296562$$D View this record in MEDLINE/PubMed
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Keywords Nanoparticles
Carvacrol
Bioactive compound
Antimicrobial activity
Chitosan
Controlled release
Language English
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Snippet [Display omitted] ▶ Carvacrol-loaded chitosan particles were prepared through emulsion formation and ionic gelation. ▶ Particles exhibited spherical shape,...
The fabrication of carvacrol-loaded chitosan nanoparticles was achieved by a two-step method, i.e., oil-in-water emulsion and ionic gelation of chitosan with...
Display Omitted a- Carvacrol-loaded chitosan particles were prepared through emulsion formation and ionic gelation. a- Particles exhibited spherical shape,...
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SubjectTerms acetates
Anti-Infective Agents - chemistry
Anti-Infective Agents - pharmacology
anti-infective properties
Antimicrobial activity
Bacillus cereus
Bioactive compound
Buffer solutions
Carvacrol
Charged particles
Chitosan
Chitosan - chemistry
colloids
Controlled release
Drug Carriers - chemistry
Emulsions
Emulsions - chemistry
encapsulation
Escherichia coli
Gelation
Gels - chemistry
Hydrogen-Ion Concentration
Media
Microbial Sensitivity Tests
Models, Biological
Monoterpenes - chemistry
Monoterpenes - pharmacology
Nanoparticles
Nanoparticles - chemistry
Particle Size
Staphylococcus aureus
Surface chemistry
tripolyphosphates
zeta potential
Title Preparation, characterization and in vitro release study of carvacrol-loaded chitosan nanoparticles
URI https://dx.doi.org/10.1016/j.colsurfb.2010.12.031
https://www.ncbi.nlm.nih.gov/pubmed/21296562
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https://search.proquest.com/docview/853222262
https://search.proquest.com/docview/869813146
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