Dubey Astita, Salamon Soma, Attanayake Supun B, Ibrahim Syaidah, Landers Joachim, Castillo Marianela Escobar, Wende Heiko, Srikanth Hari, Shvartsman Vladimir V, Lupascu Doru C
Institute for Materials Science and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Essen, Germany.
Faculty of Physics and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Duisburg, Germany.
Front Bioeng Biotechnol. 2022 Oct 18;10:965146. doi: 10.3389/fbioe.2022.965146. eCollection 2022.
Ionic engineering is exploited to substitute Bi cations in BiFeMnO NPs (BFM) with rare-earth (RE) elements (Nd, Gd, and Dy). The sol-gel synthesized RE-NPs are tested for their magnetic hyperthermia potential. RE-dopants alter the morphology of BFM NPs from elliptical to rectangular to irregular hexagonal for Nd, Gd, and Dy doping, respectively. The RE-BFM NPs are ferroelectric and show larger piezoresponse than the pristine BFO NPs. There is an increase of the maximum magnetization at 300 K of BFM up to 550% by introducing Gd. In hyperthermia tests, 3 mg/ml dispersion of NPs in water and agar could increase the temperature of the dispersion up to ∼39°C under an applied AC magnetic field of 80 mT. Although Gd doping generates the highest increment in magnetization of BFM NPs, the Dy-BFM NPs show the best hyperthermia results. These findings show that RE-doped BFO NPs are promising for hyperthermia and other biomedical applications.
利用离子工程将稀土(RE)元素(钕、钆和镝)替代铋铁锰氧化物纳米颗粒(BFM)中的铋阳离子。对通过溶胶-凝胶法合成的稀土纳米颗粒的磁热疗潜力进行了测试。对于钕、钆和镝掺杂,稀土掺杂剂分别将BFM纳米颗粒的形态从椭圆形改变为矩形再到不规则六边形。稀土-BFM纳米颗粒具有铁电性,并且比原始的BFO纳米颗粒表现出更大的压电响应。通过引入钆,BFM在300K时的最大磁化强度增加了高达550%。在热疗测试中,纳米颗粒在水和琼脂中的3mg/ml分散液在80mT的外加交流磁场下可将分散液温度升高至约39°C。尽管钆掺杂使BFM纳米颗粒的磁化强度增加最多,但镝-BFM纳米颗粒显示出最佳的热疗效果。这些发现表明,稀土掺杂的BFO纳米颗粒在热疗和其他生物医学应用方面具有潜力。
Front Bioeng Biotechnol. 2022-10-18
Nanotechnology. 2023-10-19
Phys Chem Chem Phys. 2016-3-7
ACS Appl Mater Interfaces. 2016-5-10
IEEE Trans Ultrason Ferroelectr Freq Control. 2015-1
Rep Pract Oncol Radiother. 2013-11-1
Nanotechnology. 2013-8-6
Phys Chem Chem Phys. 2012-12-14