TY - JOUR
T1 - Evaluation of the toxicities of silver and silver sulfide nanoparticles against Gram‐positive and Gram‐negative bacteria
AU - Subramaniyan, Siva Bala
AU - Megarajan, Sengan
AU - Vijayakumar, Santhosh
AU - Mariappan, Mariappan
AU - Veerappan, Anbazhagan
PY - 2019/5
Y1 - 2019/5
N2 - In this study, the endogenous lipid signalling molecules, N -myristoylethanolamine, were explored as a capping agent to synthesise stable silver nanoparticles (AgNPs) and Ag sulphide NPs (Ag2 S NPs). Sulphidation of the AgNPs abolishes the surface plasmon resonance (SPR) maximum of AgNPs at 415 nm with concomitant changes in the SPR, indicating the formation of Ag2 S NPs. Transmission electron microscopy revealed that the AgNPs and Ag2 S NPs are spherical in shape with a size of 5–30 and 8–30 nm, respectively. AgNPs and Ag2 S NPs exhibit antimicrobial activity against Gram-positive and Gram-negative bacteria. The minimum inhibitory concentrations (MIC) of 25 and 50 μM for AgNPs and Ag2 S NPs, respectively, were determined from resazurin microtitre plate assay. At or above MIC, both AgNPs and Ag2 S NPs decrease the cell viability through the mechanism of membrane damage and generation of excess reactive oxygen species.
AB - In this study, the endogenous lipid signalling molecules, N -myristoylethanolamine, were explored as a capping agent to synthesise stable silver nanoparticles (AgNPs) and Ag sulphide NPs (Ag2 S NPs). Sulphidation of the AgNPs abolishes the surface plasmon resonance (SPR) maximum of AgNPs at 415 nm with concomitant changes in the SPR, indicating the formation of Ag2 S NPs. Transmission electron microscopy revealed that the AgNPs and Ag2 S NPs are spherical in shape with a size of 5–30 and 8–30 nm, respectively. AgNPs and Ag2 S NPs exhibit antimicrobial activity against Gram-positive and Gram-negative bacteria. The minimum inhibitory concentrations (MIC) of 25 and 50 μM for AgNPs and Ag2 S NPs, respectively, were determined from resazurin microtitre plate assay. At or above MIC, both AgNPs and Ag2 S NPs decrease the cell viability through the mechanism of membrane damage and generation of excess reactive oxygen species.
U2 - 10.1049/iet-nbt.2018.5221
DO - 10.1049/iet-nbt.2018.5221
M3 - Article
C2 - 31053697
SN - 1751-875X
VL - 13
SP - 326
EP - 331
JO - IET Nanobiotechnology
JF - IET Nanobiotechnology
IS - 3
ER -