Abstract

Biofunctionalized magnetic nanoparticles (FMNPs) were synthesized through in situ coprecipitations of Fe (II) and Fe (III) salts under air followed by the addition of amino acids (AA): serine (Ser), alanine (Ala), cysteine (Cys), histidine (His), and methionine (Met) via bottom-up approach without following any sophisticated route. However, the effect of amino acid side chain on the formation of γ-Fe2O3 (maghemite) and Fe3O4 (magnetite) was attained through XRD, HR-TEM, SEM, VSM, FTIR, DLS and Mercury Porosimeter (MP). Surprisingly, our study depicts that except His; Ser, Ala, Cys and Met produced more than 50% of magnetite phase and inhibited the oxidation of Fe3O4 in the presence of air. Furthermore, AA@MNPs were used for in vitro biological assessment such as salmon testes DNA (ST-DNA) binding efficiency, DPPH scavenging activity, antimicrobial and anticancer properties using UV–visible spectrophotometry and colorimeter respectively. The ST-DNA binding efficiency was observed at λmax 259 nm and quantitative interaction was determined using 15–125 µM AA@MNPs and 500 µg/ml DNA at physiological temperature, shows stacking interaction. The Cys@MNPs have exhibited highest DPPH scavenging activity with SC50 2.5 µg/mL at λmax 525 nm. Antimicrobial property of AA@MNPs was studied on gram-positive (B. subtilis), gram-negative (E. coli) bacteria and fungi (C. albicans) using disc diffusion assay by measuring zone of inhibition (ZOI) in mm, mentioned as a diameter. Alongside, minimum inhibition concentration (MIC) was estimated by the dilution method for those strains sensitive against AA@MNPs. Although, AA@MNPs showed ∼100% control growth of human lung cancer cell line (A549) with LC50, TGI and GI50 >80 µg/ml shown cells compatibility. These significant results revealed the impact of AA side chain with different surface activities of FMNPs.

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