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Hydrogel assisted synthesis of gold nanoparticles with enhanced microbicidal and in vivo wound healing potential

The present study reports a hydrogel-based sunlight-assisted synthesis of gold nanoparticles (Au NPs) with enhanced antimicrobial and wound healing potential. The hydrogel extracted from the seeds of Cydonia oblonga was used as a reducing and capping agent to synthesize Au NPs for the first time. Th...

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Detalles Bibliográficos
Autores principales: Batool, Zahra, Muhammad, Gulzar, Iqbal, Muhammad Mudassir, Aslam, Muhammad Shahbaz, Raza, Muhammad Arshad, Sajjad, Noreen, Abdullah, Muhammad, Akhtar, Naeem, Syed, Asad, Elgorban, Abdallah M., Al-Rejaie, Salim S., Shafiq, Zahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9023464/
https://www.ncbi.nlm.nih.gov/pubmed/35449438
http://dx.doi.org/10.1038/s41598-022-10495-3
Descripción
Sumario:The present study reports a hydrogel-based sunlight-assisted synthesis of gold nanoparticles (Au NPs) with enhanced antimicrobial and wound healing potential. The hydrogel extracted from the seeds of Cydonia oblonga was used as a reducing and capping agent to synthesize Au NPs for the first time. The as-synthesized Au NPs were characterized for an average size, shape, surface functionalization, antimicrobial, and wound healing capabilities. The cubic and rectangular-shaped Au NPs with an average edge length of 74 ± 4.57 nm depicted a characteristic surface plasmon resonance band at 560 nm. The hydrogel-based Au NPs inhibited the growth of microorganisms in zones with 12 mm diameter. In-vitro experiments showed that a minimum inhibitory concentration of Au NPs (16 µg/mL) was sufficient to mimic the 95% growth of pathogenic microorganisms in 24 h. In vivo treatment of wounds with Au NPs in murine models revealed a 99% wound closure within 5 days. Quantitative PCR analysis performed to decipher the role of Au NPs in enhanced wound healing showed an increase in the expression levels of NANOG and CD-34 proteins.