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PDADMAC/Alginate-Coated Gold Nanorod For Eradication of Staphylococcus Aureus Biofilms.
Manimaran, Malarmugila; Teo, Yin Yin; Kah, James Chen Yong; Beishenaliev, Adilet; Loke, Yean Leng; Foo, Yiing Yee; Ng, Shiow-Fern; Chee, Chin Fei; Chin, Sek Peng; Faruqu, Farid Nazer; Chang, Chia-Yu; Misran, Misni; Chung, Lip Yong; Leo, Bey Fen; Chiou, Shih-Hwa; Chang, Chia-Ching; Tay, Sun Tee; Kiew, Lik Voon.
Afiliação
  • Manimaran M; Department of Pharmacology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Teo YY; Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Kah JCY; Department of Biomedical Engineering, College of Design and Engineering, National University of Singapore, Singapore, Singapore.
  • Beishenaliev A; Department of Pharmacology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Loke YL; Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Foo YY; Department of Pharmacology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Ng SF; Centre for Drug Delivery Technology and Vaccine, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
  • Chee CF; Nanotechnology Catalysis Research Centre, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Chin SP; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Faruqu FN; Department of Pharmacology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Chang CY; Department of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan, Republic of China.
  • Misran M; Department of Chemistry, Faculty of Science, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Chung LY; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Leo BF; Department of Molecular Medicine, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
  • Chiou SH; Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan, Republic of China.
  • Chang CC; Institute of Pharmacology, National Yang Ming Chiao Tung University, Taipei, Taiwan, Republic of China.
  • Tay ST; Department of Biological Science and Technology, National Yang Ming Chiao Tung University, Hsinchu, Taiwan, Republic of China.
  • Kiew LV; Department of Electrophysics, National Yang Ming Chiao Tung University, Hsinchu, Taiwan, Republic of China.
Int J Nanomedicine ; 19: 3697-3714, 2024.
Article em En | MEDLINE | ID: mdl-38681091
ABSTRACT

Introduction:

Over 75% of clinical microbiological infections are caused by bacterial biofilms that grow on wounds or implantable medical devices. This work describes the development of a new poly(diallyldimethylammonium chloride) (PDADMAC)/alginate-coated gold nanorod (GNR/Alg/PDADMAC) that effectively disintegrates the biofilms of Staphylococcus aureus (S. aureus), a prominent pathogen responsible for hospital-acquired infections.

Methods:

GNR was synthesised via seed-mediated growth method, and the resulting nanoparticles were coated first with Alg and then PDADMAC. FTIR, zeta potential, transmission electron microscopy, and UV-Vis spectrophotometry analysis were performed to characterise the nanoparticles. The efficacy and speed of the non-coated GNR and GNR/Alg/PDADMAC in disintegrating S. aureus-preformed biofilms, as well as their in vitro biocompatibility (L929 murine fibroblast) were then studied.

Results:

The synthesised GNR/Alg/PDADMAC (mean length 55.71 ± 1.15 nm, mean width 23.70 ± 1.13 nm, aspect ratio 2.35) was biocompatible and potent in eradicating preformed biofilms of methicillin-resistant (MRSA) and methicillin-susceptible S. aureus (MSSA) when compared to triclosan, an antiseptic used for disinfecting S. aureus colonisation on abiotic surfaces in the hospital. The minimum biofilm eradication concentrations of GNR/Alg/PDADMAC (MBEC50 for MRSA biofilm = 0.029 nM; MBEC50 for MSSA biofilm = 0.032 nM) were significantly lower than those of triclosan (MBEC50 for MRSA biofilm = 10,784 nM; MBEC50 for MRSA biofilm 5967 nM). Moreover, GNR/Alg/PDADMAC was effective in eradicating 50% of MRSA and MSSA biofilms within 17 min when used at a low concentration (0.15 nM), similar to triclosan at a much higher concentration (50 µM). Disintegration of MRSA and MSSA biofilms was confirmed by field emission scanning electron microscopy and confocal laser scanning microscopy.

Conclusion:

These findings support the potential application of GNR/Alg/PDADMAC as an alternative agent to conventional antiseptics and antibiotics for the eradication of medically important MRSA and MSSA biofilms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polietilenos / Staphylococcus aureus / Biofilmes / Nanotubos / Alginatos / Ouro / Compostos de Amônio Quaternário / Antibacterianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Polietilenos / Staphylococcus aureus / Biofilmes / Nanotubos / Alginatos / Ouro / Compostos de Amônio Quaternário / Antibacterianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article