Abstract
Introduction: The development of magnetic agents for magnetic fluid hyperthermia application is a complex task requiring simultaneous optimization of chemical, biomedical, magnetic, and, in particular, thermal properties of magnetic nanoparticles (MNPs). In the majority of papers, the magnetothermal measurements are carried out on bare MNPs suspended in deionized water with subsequent optimization of the required physiological and medical properties, including toxicity and biocompatibility. However, in real hyperthermia practice, the stable fluids or colloids of magnetic MNPs are used, and the colloidal stabilization can significantly modify their magnetic properties, including magnetothermal ones.
Methods: This paper is focused on the study of ZnxMn1-xFe2O4 MNPs stabilized by oleic acid/sodium oleate in this context.
Results and Discussion: Our research demonstrates the crucial changes in the magnetic properties and magnetothermal response of ZnMn ferrite MNPs after the colloidal stabilization: while bare MNPs demonstrate significant coercivity, nonzero remanent magnetization, and superquadratic dependence of heat generation on the magnetic field amplitude, the magnetic properties of colloidal ZnMn ferrite MNPs are typical for superparamagnetic ones and their magnetothermal response is described by a conventional quadratic dependence on magnetic field amplitude. Various factors such as size distribution, magnetic anisotropy, and interparticle dipole–dipole interaction are considered as the origins of such an impact on magnetic MNPs’ properties.
1 Introduction
Magnetic hyperthermia has been widely investigated in recent years as an advanced clinical method for cancer treatment (). Magnetic hyperthermia is now considered a general-purpose method by regulatory agencies (FDA, EMA—European Medical Association—equivalent to the FDA). Deeply located tumors that are impossible to treat with the existing laser technology can be treated by magnetic hyperthermia. In addition, tumors with poorly developed blood networks can be treated with magnetic hyperthermia when chemotherapy is ineffective. Laboratory and clinical studies have shown that, in most cases, tumors stop growing and decay ().
On the one hand, the improvement of the efficiency of magnetic nanoparticles’ (MNPs) magnetic energy conversion into thermal energy is the key factor of this technology, whose efficiency is quantified as the specific absorption rate (SAR) that increases with the amplitude and frequency of magnetic field (; ). On the other hand, some physiological and patient safety issues should be taken into account. In addition to the well-known Brezovich limit [the product of frequency and magnetic field should not exceed 5×108A/(m*s)] (), for real clinical application, the stable nontoxic and biocompatible fluids or colloids of MNPs are needed. The other factors to be considered are the shape and size of the MNPs, whether they have a shell, the stability of the suspension, whether the protein is recognized, the viability of the cells, whether the MNPs can be eliminated through the kidneys, etc. (; ; ; ; ). Thus, the magnetothermal properties of MNP colloids depend not only on the amplitude and frequency of alternating magnetic fields but also on a number of physical–chemical characteristics, including those related to the technology of preparation of colloids of MNPs as well as physiological properties of cancer cells in Petri dish culture, mice tumor tissues, and eventually, human malignant neoplasms (). All aforementioned factors generally lead to the situation that the in vitro studies of MNPs in deionized water may not be directly applicable in vivo and need future additional investigations.
Scientists and radio engineers working in this field have to solve the magnetic hyperthermia trilemma (field–size–composition), which is similar to magnetic memory recording, but is much more complicated. For example, to make heating more efficient, it is necessary to optimize the SAR value while maintaining the product of frequency and amplitude within the Brezovich limit. In the case of superquadratic dependence of SAR on magnetic field amplitude, it enables reducing the operating frequencies to avoid technical difficulties with high-frequency source production. A decrease in field frequency leads to an increase in the optimal value of the relaxation time (satisfying the condition 2πfτ = 1) and implies modification of size distribution and the anisotropy constant of the MNP. In magnetic memory media, to increase magnetic anisotropy, Co and Cr are widely used, but magnetic hyperthermia is restricted in the choice of materials: toxic Co and Cr cannot be used here.
Achieving optimal heat distribution in magnetic hyperthermia has also been investigated by (). For example, the advantages of using spherical magnetic nanocapsule assemblies composed of metallic iron MNPs covered with a non-magnetic shell of sufficient thickness in magnetic hyperthermia was demonstrated. Based on numerical simulations, the size and geometry of the biocompatible spherical capsules were optimized to minimize the effects of strong magnetic dipole interactions between closely spaced MNPs. Under alternating magnetic fields of moderate amplitude H0 = 50–100 Oe and frequency f = 100–200 kHz, the assembly of capsules can provide sufficiently high SAR values of the order of 250–400 W/g for usage in clinical practice ().
In our previous papers (; ; ), the extensive studies of various factors affecting the SAR value of bare ZnxMn1-xFe2O4 MNPs suspended in deionized water were carried out within the aforementioned optimal magnetic field amplitude and frequency range (H = 50–100 Oe, f = 100–200 kHz). The superquadratic, up to 5th power, dependence on amplitude was observed for medium-sized MNPs (13–17 nm). This unusual property enables one to reduce the operating frequency to values more suitable for clinical application and to reduce the economic cost of the instrument (; ; ; ). Since the size of MnZn ferrite MNPs obtained by the co-precipitation method depends on Zn content, the optimum Zn concentration corresponding to the maximum SAR value at constant magnetic field amplitude shifts from 25% to 15% while the frequency decreases from 300 kHz to 100 kHz (). The magnetothermal measurements of the MnZn ferrite MNP suspension in glycerol enabled ruling out the Brown mechanisms of heating while the dependence of coercivity on Zn content showed that for the average particle size larger than 13 nm, the hysteresis mechanism of heating dominates (). These studies raised the question of whether the small superparamagnetic MNPs (<10 nm) are the best choice for magnetic hyperthermia, as was widely believed before ().
It should be noted, however, that the aforementioned results were obtained on bare MNPs while their clinical usage requires coating MNPs with the agent preventing opsonization of the MNPs introduced to an organism and their subsequent elimination by phagocytes. The colloidal stabilization of iron oxide MNPs with oleic acid/sodium oleate was shown to exert therapeutic effects for curing tumors via magnetic hyperthermia (). Negligible toxicity, low local irritant effect, and no effect on the morphology of the internal organs were found. The efficiency of magnetic hyperthermia for the treatment of transplanted Walker 256 carcinoma with a survival rate of 85% was demonstrated in the studied therapy group of seven animals, while in the control group (without treatment), all animals died.
In this context, the magnetothermal properties of oleic acid/sodium oleate-coated MNPs are of special interest. The effect of colloidal stabilization on individual MNPs’ magnetic and magnetothermal properties, as well as on the interparticle interaction, is insufficiently studied. This paper is focused on the comparison of SAR and the mechanisms of heating for coated and bare MNPs on the example of ZnxMn1-xFe2O4 (x = 0,15 and 0,2) MNPs that were previously shown to have the largest SAR value (; ; ) in the prospective class of MnZn ferrite-based MNPs for hyperthermia application.
2 Material preparation and characterization
2.1 Magnetic nanoparticle synthesis
The schematic diagram of the synthesis of colloidal MNPs is presented in Figure 1. The process consists of two stages: nanoparticle synthesis and stabilization. ZnxMn1-xFe2O4 MNPs were obtained by co-precipitation of iron (III), manganese (II), and zinc salts from aqueous solutions in an alkaline environment of sodium hydroxide ():
FIGURE 1
MnCl2*4H2O, ZnCl2 (in certain proportions), and FeCl3*6H2O (3.5 g) were dissolved in 30 mL of deionized water preheated to 90°C. Then, 20 mL of aqueous NaOH (2.5 g) was added rapidly to the solution with vigorous stirring. The resulting ferrite particle suspension was stirred for a further 1 h at a temperature of 90°C and then purified by magnetic decantation and washed 10 times with deionized water and ethanol at a volume ratio of 4:1. After every two washing procedures, the magnetic particles were sonicated (low-power ultrasonic bath) (35 kHz, 200 W) for 20 min.
The temperature and time of the ZnMn ferrite MNPs in this fabrication process are the same as those of the MNPs fabricated in our previous work ().
0.16 g NaOH was dissolved in a solution containing 2 mL deionized water and 3 mL ethanol. 1.75 mL of oleic acid was added to the basic solution, and the mixture was stirred. Thus, a solution containing sodium oleate and free oleic acid was obtained for the peptization and stabilization of purified particles.
A freshly prepared hydro-alcoholic solution of the stabilizer was added to the purified ferrite particle suspension, and the resulting suspension was vigorously stirred at 100°C for 1 h in a stream of argon. During the heat treatment, the ethanol evaporates. In the final stage, the suspension was centrifuged at 10,000 RPM for 10 min to remove large aggregates.
2.2 Size distribution and morphology
Transmission electron microscopy (TEM) measurements were performed on a high-resolution transmission electron microscope JEOL JEM-2010 to obtain the particle size distribution and MNP morphology. The particles have been re-suspended in ethanol and deposited on a copper mesh covered with a carbon film for examination in TEM (TEM images are presented in Supplementary Figure SA1). For each type of MNPs, we collected 20 TEM images. These data were processed using Image-Pro Plus software.
It can be seen in Figure 2 that the size distribution of colloidal MNPs has been significantly changed compared with results for MNPs in deionized water. While the bare ZnxMn1-xFe2O4 MNPs show a narrow distribution and a tendency for a mean size increase with an increase in Zn content (see the work of ) for details), the colloidal MNPs for x = 0.15 and x = 0.2 have nearly the same mean value (14 and 15 nm, respectively) and wide size distribution with higher representation of small particles below 10 nm.
FIGURE 2
3 Magnetic measurements
Magnetic measurements were performed using a Lake Shore Model 7407 vibrating sample magnetometer (VSM) with a maximum magnetic field of 1.5 T and in the temperature range of 100 K–450 K.
The effective anisotropy constant according to Akulov’s law of approximation to saturation (for bulk samples) (
Taking into account the paraprocess, the tail of the hysteresis loop in the saturation region can be approximated with a linear function. The slope value is the coefficient b, and the intercept value is Ms. Approximation of the magnetization curve by this function will make it possible to obtain the values of the effective anisotropy constant:
The magnetization curve and hysteresis loop can be approximated by the Langevin function (taking into account the diamagnetic contribution):where h is a dimensionless magnetic field, P1, P2, P3, P4, and P5 are selected parameters of the function: P1 is saturation magnetization, P2 is susceptibility, P3 is coercivity, P4 is linear contribution, and P5 is the offset.
Figure 3 presents the hysteresis loops of ZnxMn1-xFe2O4 (x = 0.15, 0.2) bare colloidal MNPs. The saturation magnetizations of bare ZnMn ferrite MNPs suspended in ionized water are much higher than the saturation magnetization of colloidal MNPs. For bare MNPs, the magnetization for the x = 0.2 compound is somewhat higher than that for x = 0.15. On the contrary, for colloidal MNPs, the magnetization for the x = 0.15 compound is higher than that for the x = 0.2 one, and this tendency is even more pronounced at lower temperatures (See Supplementary Figure SA3; Supplementary Table S2).
FIGURE 3

Hysteresis loops of ZnxMn1-xFe2O4 (x = 0.15, 0.2) MNPs and colloidal MNPs at temperature Т = 293K. The inset is an enlarged region of the hysteresis loop.
Figure 4 presents typical hysteresis loops of ZnxMn1-xFe2O4 (x = 0.15, 0.2) MNPs and colloids MNPs at various amplitudes of a magnetic field. It can be seen that M(H) curves of colloidal MNPs are typical for superparamagnetic MNPs (the coercivity of the hysteresis loops is below 400 A/m), while for bare MNPs, the coercivity is more than an order higher. The corresponding hysteresis loop area under the same magnetic field amplitude for bare MNPs is almost two orders of magnitude higher than for the colloidal MNPs (see Supplementary Figure SA4).
FIGURE 4

Hysteresis loops of ZnxMn1-xFe2O4 bare and colloidal MNPs in different magnetic fields at temperature 300K. (A)x = 0.15, colloidal MNPs; (B)x = 0.2, colloidal MNPs; (C)x = 0.15, bare MNPs; and (D)x = 0.2, bare MNPs.
4 Magnetothermal measurement: specific absorption rate
To measure the magnetothermal properties of the MNPs, the AC magnetic field-calorimetry facility produced by the AMT&C Group (Moscow, Russia) has been used. A detailed description of the experimental conditions is given in our previous work (
The specific absorption rate is calculated based on the temperature derivative with respect to time (
The SAR values measured at various frequencies and magnetic field amplitudes are shown in Figure 5. Quite surprisingly, the SAR values for colloidal MNPs are comparable with the ones for bare MNPs, despite the six times lower saturation magnetization and more than an order lower value of hysteresis loop area. To explain this counterintuitive fact, one needs to explore the mechanisms of heating of both bare MNPs and colloidal ones.
FIGURE 5

SAR values and curves for ZnxMn1-xFe2O4 MNPs at various AC magnetic fields 2.4kA/m -16.7kA/m and at various frequencies 0.015–0.3 MHz. (A)x = 0.15, colloidal MNPS; (B)x = 0.15, bare MNPs in deionized water; (C)x = 0.2, colloidal MNPS; and (D)x = 0.2, bare MNPs in deionized water. Points correspond to the experimental values, and lines correspond to mathematical approximation by the method of least squares.
5 Discussion
To gain insight into the mechanisms of MNP heating, the field and frequency dependencies of SAR should be analyzed. It can be seen from Figure 5 that the magnetic field dependencies for the frequency range optimal for the hyperthermia procedure (∼75–150 kHz) are different: the colloidal MNPs demonstrate conventional quadratic dependence on the amplitude of magnetic field typical for superparamagnetic particles, while for bare MNPs, this dependence is essentially superquadratic, up to 5th power. This striking difference can be attributed to the fundamentally different mechanisms of heating: for colloidal MNPs, the dominant mechanism is Néel relaxation proportional to the energy of magnetic field radiation (∼H2) (
FIGURE 6

Hysteresis contribution to SAR values for ZnxMn1-xFe2O4 (x = 0.15, 0.2) at various AC magnetic fields 0-40kA/m (0-500 Oe) and at frequencies 0.1 MHz: (A) colloidal MNPs and (B) bare MNPs. The operating frequency is 0.1 MHz.
The disappearance of highly superquadratic 5th power dependence on magnetic field amplitude in the case of colloidal MNPs may be attributed to the stability of colloidal MNPs in suspension, while bare MNPs in deionized water aggregates into large clusters with modified surface and bulk anisotropy of the particles and enhanced dipole–dipole interactions between them. Furthermore, the TEM data show that the particle size distribution for colloidal MNPs is wider (Figure 2), with a higher percentage of small particles in the colloid, and their shapes are irregular (Supplementary Figure SA1 in the Supplementary Material) compared to the almost circular shape of the bare ZnMn ferrite MNPs (
The presence of colloidal suspension MNPs with small volumes leads to the significant contribution of superparamagnetic MNPs with the dominant Néel relaxation mechanisms resulting in quadratic field dependence of the SAR on the magnetic field amplitude. Changes in the morphology of MNPs may also impact the values of shape and surface anisotropy of the MNPs in colloids.
To support the conclusion about the dominant role of superparamagnetism in the difference between the bare MNPs and the colloidal ones, we measure their blocking temperatures. The field-cooled and zero-field-cooled (ZFC-FC) curves for ZnxMn1-xFe2O4 (x = 0.15, x = 0.2) colloidal and bare MNPs are presented in Figure 7. The blocking temperatures for colloidal and bare MNPs differ drastically: about 280K and 405K, respectively.
FIGURE 7

MZFC and MFC for ZnxMn1-xFe2O4 bare and colloidal MNPs. FC stands for field-cooled and ZFC stands for zero-field-cooled. The blocking temperatures for ZnxMn1-xFe2O4 compounds in colloid and bare MNPs forms are 282K and 406K, respectively. For colloids and bare MNPs with x = 0.2, they are 276K and 405K, respectively. In the inset, the ZFC-FC curve for colloidal MNP x = 0.2 in the vicinity of the blocking point is shown in an enlarged scale.
Since the blocking temperature of colloids is significantly lower than that of bare MNPs, at room temperature, they behave like superparamagnetic particles with conventional magnetic field dependence of SAR, while bare MNPs at room temperature are in a blocked state, and the hysteresis mechanisms are relevant for them.
There were reports in the literature that the dipole–dipole interaction plays a crucial role in modifying the blocking temperature of MNPs; the stronger the interaction between MNPs, the higher the blocking temperature (
To prove the hypothesis about the role of dipole–dipole interaction, we need to estimate and compare the strength of particle-to-particle interactions in bare MNPs and colloidal MNPs. A remanent map method based on the Stoner–Wohlfarth hysteresis model was applied (
FIGURE 8

IRM and DCD of colloidal and bare ZnxMn1-xFe2O4 (x = 0.15, 0.2) MNPs.
It should be noted that even if all samples contained similar MNPs, the bare MNPs aggregation leads to an increased effective particle diameter, which will enhance interparticle interaction, increase the blocking temperature, and increase hysteresis loss. In contrast, the aggregation was much smaller in the colloid MNPs, resulting in a lower blocking temperature and lower hysteresis loss.
The influence of colloidal parameters on the SAR was especially discussed in the study by
Finally, both in the model of Néel relaxation and hysteresis model, the energy losses during remagnetization are related to the magnetic anisotropy of an MNP. The magnetic anisotropy for all considered types of MNPs estimated in Akulov’s law approximation of Eq. 2 is presented in Table 1. One can see that the anisotropy constants of colloidal MNPs are much smaller than those of bare MNPs. This fact also agrees with the superparamagnetic nature of colloidal MNPs.
TABLE 1
| x | Anisotropy constant K (×105) |
|---|---|
| x = 0.15 colloidal MNPs | 0.8 ± 0.1 |
| x = 0.2 colloidal MNPs | 0.7 ± 0.1 |
| x = 0.15 bare MNPs | 2.3 ± 0.3 |
| x = 0.2 bare MNPs | 2.3 ± 0.3 |
Anisotropy constants of colloidal and bare ZnxMn1-xFe2O4 (x = 0.15, 0.2) MNPs.
6 Conclusion
Summarizing, the ZnMn ferrite MNPs were obtained by the chemical co-precipitation method and then stabilized with oleic acid/sodium oleate. The particle distribution, morphology, and magnetic and magnetothermal properties of bare and colloidal MNPs were compared. It was shown that in contrast to the bare MNPs demonstrating the dominant hysteresis mechanisms of heating (the significant coercivity, superquadratic dependence of SAR on magnetic field amplitude, nonzero remanent magnetization, etc.), the magnetothermal properties of colloidal ZnMn ferrite MNPs were typical for superparamagnetic ones: the negligibly small coercivity, zero remanent magnetization, and the conventional quadratic SAR dependence on magnetic field amplitude. It was shown that the superparamagnetic behavior of colloid MNPs and their low blocking point (below room temperature) can be attributed to a number of factors such as wider size distribution, low magnetic anisotropy, and negligible interparticle dipole–dipole interaction.
Statements
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material; further inquiries can be directed to the corresponding author.
Author contributions
NL: methodology, data collection on magnetic hyperthermia and TEM, data analysis and interpretation, and article initial drafting, writing, and final draft. YA: collection of magnetic data and the methodology of data processing. AP: conception and design of the work, methodology, data analysis and interpretation, final draft, and final approval of the version to be published. MZ: sample preparation and data collection. DY: sample preparation and data collection. NP: data analysis and interpretation and final approval of the version to be published. GS: conception and general support to the work, critical revision of the article, and final approval of the version to be published. NP: data interpretation and critical revision of the final text. AT: conception of the work, data analysis and interpretation, critical revision of the article, and final approval of the version to be published. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the Russian Foundation for Basic Research (grant number 19-29-10013). NL acknowledges the China Scholarship Council for study support.
Conflict of interest
Author AT was employed by company AMT&C Group.
The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author AT declares that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors, and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fther.2023.1195740/full#supplementary-material
Footnotes
1.^This article was published in J. Magnetism Magnetic Mater, 555, Liu, N. N., Pyatakov, A. P., Saletsky, A.M., Zharkov, M. N., Pyataev, N. A., Sukhorukov, G. B., The “field or frequency” dilemma in magnetic hyperthermia: The case of Zn–Mn ferrite nanoparticles, 169379, Copyright Elsevier (2022).
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Summary
Keywords
magnetic hyperthermia, specific absorption rate, magnetic nanoparticles, colloidal MNPs, oleic acid
Citation
Liu NN, Alekhina YA, Pyatakov AP, Zharkov MN, Yakobson DE, Pyataev NA, Sukhorukov GB, Perov NS and Tishin AM (2023) Impact of colloidal stabilization of MnZn-ferrite nanoparticles by oleic acid on their magnetothermal properties. Front. Therm. Eng. 3:1195740. doi: 10.3389/fther.2023.1195740
Received
28 March 2023
Accepted
09 June 2023
Published
07 July 2023
Volume
3 - 2023
Edited by
Xiaohu Yang, Xi’an Jiaotong University, China
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© 2023 Liu, Alekhina, Pyatakov, Zharkov, Yakobson, Pyataev, Sukhorukov, Perov and Tishin.
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*Correspondence: N. N. Liu, nannan.liu@irlc.msu.ru
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.