This study focused on the measurement of anthropogenic radionuclides such as americium (Am) and plutonium (Pu) in environmental samples. Plutonium isotopes, particularly ${}^{239}\mathrm{Pu}$, ${}^{240}\mathrm{Pu}$, and ${}^{241}\mathrm{Pu}$, originated from nuclear weapons testing, nuclear power plants, and accidents like Chernobyl and Fukushima Daiichi. Accurate measurement of these isotopes, considering their half-lives and trace concentrations, provides critical information about their persistence and environmental transport. Using the 1 MV Tandetron accelerator, we expanded the measurement capabilities to include ${}^{241}\mathrm{Pu}$, ${}^{241}\mathrm{Am}$. Chemical separation of these isotopes was achieved through ion chromatography, employing reference isotopes ${}^{242}\mathrm{Pu}$ and ${}^{243}\mathrm{Am}$ for method validation. Certified reference materials, including IAEA-410 (Bikini Atoll sediment) and Sample 05, were analyzed to ensure accuracy. We validated the ${}^{241}\mathrm{Am}$/${}^{243}\mathrm{Am}$ ratio in an Am standard (IFIN-STD-Am, our laboratory produced standard for Am), achieving a measured value of 0.158 at·at⁻¹ (3%), in good agreement with the nominal value of 0.154 at·at⁻¹. Additionally, we determined the ${(}^{241}\mathrm{Pu}$ + ${}^{241}\mathrm{Am}){/}^{242}\mathrm{Pu}$ ratio in the ColPuS standard to be equal to 0.029 at ·at⁻¹ (7%). These results demonstrate the potential of AMS for improved detection of actinides at low concentrations and contribute to understanding the behavior of Pu and Am isotopes.