Sonia
García-Jimeno
a,
Joan
Estelrich
a,
José
Callejas-Fernández
b and
Sándalo
Roldán-Vargas
*c
aSecció de Fisicoquímica, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Avda. Joan XXIII 17-31, E-08028, Barcelona, Catalonia, Spain
bGrupo de Física de Fluidos y Biocoloides, Departamento de Física Aplicada, Facultad de Ciencias, Universidad de Granada, E-18071, Granada, Spain
cMax Planck Institute for the Physics of Complex Systems, D-01187, Dresden, Germany. E-mail: sandalo@pks.mpg.de
First published on 26th September 2017
Understanding stabilization and aggregation in magnetic nanoparticle systems is crucial to optimizing the functionality of these systems in real physiological applications. Here we address this problem for a specific, yet representative, system. We present an experimental and analytical study on the aggregation of superparamagnetic liposomes in suspension in the presence of a controllable external magnetic field. We study the aggregation kinetics and report an intermediate time power law evolution and a long time stationary value for the average aggregate diffusion coefficient, both depending on the magnetic field intensity. We then show that the long time aggregate structure is fractal with a fractal dimension that decreases upon increasing the magnetic field intensity. By scaling arguments we also establish an analytical relation between the aggregate fractal dimension and the power law exponent controlling the aggregation kinetics. This relation is indeed independent on the magnetic field intensity. Despite the superparamagnetic character of our particles, we further prove the existence of a population of surviving aggregates able to maintain their integrity after switching off the external magnetic field. Finally, we suggest a schematic interaction scenario to rationalize the observed coexistence between reversible and irreversible aggregation.
A notable family among these new primary components is that constituted by those nano- and meso-sized particles able to respond to an external magnetic field. These “magnetic nanodevices” are usually categorized according to their remanent magnetization at a given temperature after having been exposed to an external magnetic field.8 Thus mesoscopic particles consisting of single magnetic domains9 can behave as permanent magnets due to their remanent (or even spontaneous) magnetization in the absence of an external magnetic field. This phenomenon is known as stable ferromagnetism.8 However, if thermal energy is able to cause the random orientation of the different single magnetic domains, the particle remanent magnetization after removing the external magnetic field will be negligible. These particles, which present no magnetic hysteresis, are known as superparamagnetic particles.8,10 These two behaviors (ferromagnetic and superparamagnetic) are nowadays exploited in several consolidated research lines with a special emphasis in nanomedical applications.11–19
Among the distinct mesoscopic particles, liposomes, i.e. mesosized lipid vesicles, have been recognized by their singular capabilities (e.g. as drug nanocarriers) due to their synthetically controllable size, surface electric charge, membrane elastic properties, and encapsulation efficiency.20–22 The superparamagnetic version of these highly tuneable particles results from our ability to encapsulate in their interior small (single domain) magnetite grains.23–30 These are the so-called magnetic liposomes. Thus these systems combine biocompatibility and vesicular structure31 with their superparamagnetic character, therefore being magnetically controllable agents with no side-effects on the organism. Fruitful applications using these systems are already amenable to experimentation covering specific areas in therapy and diagnostics such as chemotherapy,17,32 hyperthermia,33–37 magnetic resonance imaging,24,38,39 magnetic cell targeting,40–42 or magnetically driven delivery.30,43
Reaching an efficient functionality for these vesicular systems (and other magnetic nanoparticles) depends on our understanding of the distinct particle interactions. This understanding is intrinsically connected with those mechanisms controlling stabilization and aggregation. Indeed, magnetically induced aggregation not only provides us with an implicit understanding on the particle interactions but it is explicitly manifested in real applications. For instance, aggregates of superparamagnetic particles present an enhanced heating efficiency in hyperthermia as compared to that corresponding to non-aggregated samples.44–46 The presence of aggregates can also increase the sensitivity of some detection techniques such as Surface-Enhanced Raman Scattering (SERS), leading to a significant increase of the Raman intensity.47 Irreversible aggregates can also influence the system functionality when their size is comparable to those length scales defining the targeted microenvironment, e.g. in Enhanced Permeability and Retention (EPR)15,48 or in the subsequent particle excretion from the body.49 These functional implications demand a comprehensive study on the still poorly understood mechanisms controlling aggregation in magnetic nanoparticle systems. In this work we present such a study for a system of magnetic vesicles.
So far, magnetically induced aggregation has been experimentally investigated but being focused on the study of non-encapsulating superparamagnetic particles. For instance, light scattering has been used to probe aggregation kinetics and/or aggregate structure50–56 whereas two-dimensional microscopy images have been analyzed to look into the cluster morphology.51,52,55–58 Apart from studies on real systems, simulations and analytical approaches have also been proposed to rationalize the aggregation of ferro- and superpara-magnetic particles where magnetic interaction is treated in terms of a dipolar hard-sphere like model.59–63
Here we present a detailed study on the aggregation of magnetic liposomes in suspension in the presence of a controllable external magnetic field. By Dynamic Light Scattering (DLS) we explore the aggregation kinetics and find an intermediate time regime where the aggregate diffusion coefficient presents a power law evolution. This evolution, which can be controlled by changing the magnetic field intensity, reaches at sufficiently long times a stationary value as a result of a competition between cluster formation and fragmentation. This final steady-state of the diffusion coefficient allows us to investigate the aggregate structure by Static Light Scattering (SLS). This structure is fractal and results in increasingly linear aggregates upon increasing the magnetic field intensity. Interestingly, we can appeal to scaling arguments and establish a relation between the aggregate fractal dimension and the power law exponent governing the aggregation kinetics. With this analytical approach we create a link between structure and dynamics in our system. To extend the aggregate characterization, we directly observe the system by Transmission Electron Microscopy (TEM) and report a coexistence between reversible and irreversible aggregates (i.e. aggregates that survive despite switching off the external magnetic field). Finally, this coexistence is discussed in terms of an interplay between interactions of different origin. Our results and the general picture we offer are of particular interest for predicting and controlling those time and length scales that play a relevant role in real physiological applications.
The rest of the paper is organized as follows: in section II we introduce the system and present our methodologies. In section III we show and discuss our results on stabilization, aggregation kinetics, aggregate structure, and aggregate reversibility. Finally, in section IV we summarize our main findings and present our conclusions.
For both aggregating and non-aggregating samples we used purified aqueous suspensions of magnetic liposomes where the presence of salt in the medium was prevented by inverse osmosis using Millipore equipment. We prepared sufficiently diluted suspensions at 0.1% liposome volume fraction. This concentration avoids the effect of long-range interactions between liposomes in case of non-aggregating samples (section III.A) and gives us an optimal aggregation time for the magnetically induced aggregating samples. This time is sufficiently long compared with that needed for computing 〈I(θf;t)I(θf;t + τ)〉 (2 orders of magnitude greater) but sufficiently short to follow the complete aggregation process. We ensured statistical reliability by performing at least 10 independent experimental realizations of each DLS and SLS measurement for both aggregating and non-aggregating samples. In all the light scattering experiments temperature was kept constant at 25 °C.
The experimental set-up to induce liposome aggregation by means of an external magnetic field deserves further explanation. Fig. 1 shows a schematic view of this experimental set-up where the magnetic field intensity is controlled by adding or removing Nd2Fe12B magnets on the top of the scattering vessel containing the sample. To enhance the magnetic field intensity acting on the sample, we insert between the pile of magnets and the sample a cylindrical iron bar to promote magnetic field line confinement. Thus, the direction of the magnetic field is essentially perpendicular to the scattering plane. Fig. 1 also shows the magnetic field intensity acting on the sample as a function of the number of neodymium magnets. We see how upon increasing the number of magnets the magnetic field intensity increases, leading to an intensity field saturation which imposes an upper threshold for the magnetic field intensity of about 40 mT. Accordingly we performed DLS and SLS experiments for magnetically induced aggregating samples at Bscatt = 16.6(±0.7), 27.5(±0.7), and 38.8(±0.6) mT. No aggregation was detected for B < 16.6 mT.
![]() | (1) |
![]() | (2) |
Aggregates with fractal structure (section III.C) present a power law behavior for S(q) within an intra-aggregate spatial scale which is constrained by the typical linear size of the aggregates and the linear size of the monomers (i.e. the liposomes) constituting the aggregates:69–71
S(q) ∼ q−df ; 1/Ragg ≪ q ≪ 1/ā | (3) |
Dynamics in aggregating and non-aggregating samples is probed by DLS experiments through the intensity autocorrelation function 〈I(q;t)I(q;t + τ)〉 at a fixed q. This autocorrelation function provides us with the corresponding electric field autocorrelation function, gE(τ), by means of Siegert relation.72 In its turn, gE(τ) is expanded into cumulants and interpreted in terms of a sample probability distribution of diffusion coefficients.72,73 The first cumulant, μ1, represents an inverse relaxation time containing both translational and rotational diffusive contributions:54,74
![]() | (4) |
![]() | (5) |
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Fig. 2 (a) Form factor, P(q), of a diluted (non-aggregating) sample of magnetic liposomes. Circles stand for the experimental values as obtained from a SLS measurement at B = 0 whereas solid line represents a fit according to a solid sphere RGD model and assuming a pseudo-Schulz distribution. Inset: TEM micrograph of a single magnetic liposome encapsulating a core of magnetite grains.30 (b) Magnetization as a function of the magnetic field intensity, B. Solid line with solid diamonds (empty circles) stands for the forward (backward) magnetization path. Both paths collapse into a single curve as a manifestation of no magnetic hysteresis. Dashed vertical lines signal the different field intensities (![]() |
At this point, one might ask for the repulsive interactions avoiding aggregation at B = 0. In this respect, two main interactions for stabilizing these and other lipid vesicle suspensions have been presented in the literature: Coulombic and hydration repulsions. On one hand, Coulombic repulsion, which is the main ingredient for stabilization in DLVO theory,81,82 seems to be present in our system despite the non-polar nature of PC as accounted for by the weak but still non-negligible liposome zeta-potential.30 On the other hand, short-range repulsive hydration forces have been associated to these and other lipid vesicles leading to stabilization even when Coulombic repulsion is not present.70,83–88 Nevertheless, we should stress that the repulsive interactions stabilizing the system in the absence of an external magnetic field do not create long-range structural correlations between the liposomes for the probed dilution as manifested through P(q) (which only contains correlations at the single particle level).
To place the magnetic field intensities at which we perform our light scattering experiments and obtain our TEM micrographs for the aggregating samples, we present in Fig. 2(b) the magnetization, M, of the magnetic liposomes as a function of B (see section II.C). A previous characterization of the liposome magnetization was already presented in ref. 30. We see how the forward and backward magnetization paths essentially collapse into a single curve: the magnetic liposomes do not present hysteresis. The absence of hysteresis represents a manifestation of the superparamagnetic nature of the magnetic liposomes which are indeed lipid vesicles encapsulating single-domain magnetite grains (linear size ≅10 nm) which recover their random field orientation as soon as the magnetic field is switched off.10 As also shown in Fig. 2b), magnetization saturates around ±100 mT. In this respect, we see how our light scattering experiments (sections III.B and C) are performed below the saturation threshold whereas the TEM micrographs obtained for the aggregating samples (section III.E) correspond to an almost magnetically saturated sample. We also note that the different magnetic fields at which we perform our experiments for the aggregating samples do not present a significant difference in magnetization. However, the potential magnetic energy between magnetic liposomes could be significantly different for the different magnetic fields shown in Fig. 2(b). In general, the potential magnetic energy between two magnetic particles (here liposomes) depends on the product of the dipole magnetic moments of the two particles, where each dipole magnetic moment is proportional to the particle magnetization.89–92 Therefore a given ratio between two different generic magnetizations, M1/M2, in Fig. 2(b) will in general re-scale the potential magnetic energy between two magnetic particles by a factor (M1/M2)2.
Fig. 3 shows the time evolution of at different magnetic field intensities (eqn (5)). At short times
: our aggregation process starts from a monomeric initial condition. At intermediate times
, where α is a B-dependent kinetic exponent which increases upon increasing magnetic field intensity. Finally, at long times
reaches a plateau with a final stationary value,
, which decreases upon increasing magnetic field intensity (from
at B = 16.6 mT to
at B = 38.8 mT).
The intermediate time power law behavior is a common feature in aggregation of mesoscopic particles which has been rationalized by different analytical approaches93,94 being usually expressed in terms of the average aggregate size evolution Ragg(t) ∼ tα. Depending on the system, this power law evolution will in principle continue without reaching a final stationary value69,95,96 or it will present (like in our system) a final constant value for
(or Ragg(t)) at sufficiently long times.52,54,59 This second case has in general been interpreted as a balance between aggregation and fragmentation where the sample reaches a steady-state for the cluster-size distribution.97,98
Balance between aggregation and fragmentation in magnetically induced aggregation processes has been discussed in terms of the so-called magnetic coupling parameter, Γ, defined as the ratio (competition) between magnetic dipole–dipole potential energy (which helps to retain particle bonds) and thermal energy (which tends to break particle bonds):59
![]() | (6) |
![]() | (7) |
Thus, at constant temperature, re-scaling particle magnetization by a factor γ will re-scale the final stationary diffusion coefficient by a factor 1/γ2, therefore connecting an individual particle property, M, with the final aggregate stability given by . For instance, (M(B3scatt)/M(B1scatt))2 ≅ (1.55)2 (Fig. 2(b)) to be compared with
(Fig. 3). This result, however, is satisfied by our system due to the low particle concentration where the influence of the liposome packing fraction is negligible.59
To conclude this section we briefly anticipate the discussion on aggregation reversibility in our system when the magnetic field is switched off. Fig. 4 shows the time evolution of at B = 38.8 mT (i.e. the highest field intensity in our DLS experiments) for times smaller than 2700 s and at B = 0 for times greater than 2700 s. Contrary to Fig. 3 where B is maintained, Fig. 4 shows how, as soon as the magnetic field is unplugged,
tends to D0eff as a manifestation of aggregation reversibility where the sample almost recovers its initial monomeric condition. However, for this magnetic field intensity, we cannot exclude by our DLS measurements and TEM micrographs the presence of some small surviving aggregates after switching off the magnetic field (note that
). We will come back to this point in sections III.E and F.
Fig. 5 shows the structure factor, S(q), for the aggregated samples at different magnetic field intensities. We see how the different S(q)'s present a power law fractal behavior within a certain intra-aggregate q-range according to eqn (3). On one hand this range is right-side limited by the monomer (liposome) linear size, where q < 2/. On the other hand we need an a priori estimation for the left-side limit based on the linear size of the aggregates given by Ragg (eqn (3)). To estimate the left-side limit we consider Stokes–Einstein relation
, where here Ragg is, formally speaking, the average hydrodynamic aggregate radius.
![]() | ||
Fig. 5 Log–log plot of the Structure Factor, S(q), of an aggregated sample for different magnetic field intensities. Measurements are performed at long times, that is, when ![]() |
Apart from using an interpolation range based on the average liposome and aggregate radii, we should also consider the size polydispersity of the liposomes forming the aggregates as well as the aggregate size polydispersity. Concerning the liposome polydispersity, our q interpolation range defines a length scale which is larger than all the liposome length scales (radii) associated to the populations obtained from our characterization of P(q) (see ESI†). Indeed, with this q constraint previous studies both theoretical and experimental have shown no effect on the aggregate fractal dimension due to the primary particle polydispersity.99,100 Large aggregate size polydispersity could also lead to spurious values of the measured fractal dimensions.101 However aggregation processes mainly controlled by diffusive motion such as that presented here (see ESI†) show a uniform aggregate distribution.96 This aggregate uniformity seems indeed to be present in the TEM micrographs that we will discuss in section III.E.
At low magnetic field intensities (B = 16.6 mT), the small aggregate linear size significantly restricts our q-range (see Fig. 5). Thus for q/2 ≲ 0.5 we already start to abandon the typical aggregate scale entering into the Guinier regime,71 therefore losing the details of the intra-aggregate structure whose spatial scale would be smaller than our q−1 observational window. Although not reliable, the fractal dimension (df ≊ 1.78) of the small aggregates at B = 16.6 mT would be compatible with that expected from a Diffusion Limited Cluster Aggregation (DLCA).96
Once we increase the magnetic field intensity the power law fractal behavior extends to smaller q values due to the increasing aggregate size, therefore permitting a more reliable estimation of df. The effect is apparent: df decreases upon increasing the magnetic field intensity. Thus, the increasing magnetic field intensity induces a highly directional magnetic liposome interaction which results in more linear fractal structures (df → 1). In particular, we see how at B = 38.8 mT the resulting fractal dimension is df = 1.33. This value, which is far from the typical ramified aggregates reported in DLCA processes, is comparable with those obtained for magnetic polystyrene particles in the presence of a magnetic field with added electrolyte51,52 and compatible with simulations of dipolar hard-sphere fluids.102,103 Finally, we conclude this section by addressing the following question: how is the kinetic exponent, α, connected with the aggregate fractal dimension, df?
kai,aj = aλki,j ; ∀i,j ; a∈![]() ![]() | (8) |
![]() | (9) |
![]() | (10) |
Table 1 shows the homogeneity parameter, λ, for the different magnetic field intensities at which we previously discussed the aggregation kinetics and the aggregate structure (included in the table are α, Fig. 3, and df, Fig. 5). It is interesting to note from the table how λ is almost independent (λ ≅ −0.4) on the applied magnetic field intensity. As a result, here all the aggregation processes at intermediate times present a connection between their corresponding α and df values which leads to a common (t) behavior given by eqn (9). According to our previous discussion, we can reach a physical intuition for the negative λ value by considering that the decreasing aggregate diffusivity is not compensated by the increasing aggregate collision cross section as
(t) increases. Indeed, the very geometry of the magnetic field lines around an aggregate results in an almost constant (elongated) cross section which will not depend on
(t).57 However, diffusivity will decrease upon increasing
(t) with an expected power law evolution.57 These scaling behaviors therefore lead to a more efficient reaction between small–small aggregates as compared with that between large–large aggregates.
B (mT) | 16.6 ± 0.7 | 27.5 ± 0.7 | 38.8 ± 0.6 |
λ | −0.40 ± 0.12 | −0.42 ± 0.11 | −0.45 ± 0.10 |
α | 0.40 ± 0.03 | 0.44 ± 0.03 | 0.52 ± 0.03 |
d f | 1.78 ± 0.07 | 1.60 ± 0.06 | 1.33 ± 0.05 |
Fig. 6 shows different TEM micrographs of the liposome suspension for different control regions within the sample and different magnifications. The first message is obvious: despite having evolved without the presence of an external magnetic field, the sample shows the existence of several surviving aggregates (Fig. 6(b)). From now on we will refer to these aggregates as irreversible aggregates. Despite we cannot discard the existence of small surviving aggregates after applying lower magnetic field intensities, the presence of these irreversible aggregates seems to contrast with the almost complete reversible aggregation reported at the end of section III.B (Fig. 4). Micrographs also support a second structural message: irreversible aggregates show an almost linear structure (Fig. 6(a), (c), (d) and (f)) compatible with the fractal dimension (df → 1) that would be expected after having aggregated under the influence of an intense magnetic field (see section III.C). Indeed, the only non-linear (branched) structures we see (albeit scarce) correspond to “Y-like” shaped aggregates where one of the liposomes acts as a junction point between two branches (Fig. 6(e)).62
![]() | ||
Fig. 6 TEM micrographs of a sample of magnetic liposomes which was first exposed to an intense magnetic field of B = 80 mT. The sample then evolved for several minutes without the presence of an external magnetic field before capturing the images (see sections II.B and III.A, and Fig. 2b). The micrographs correspond to different control regions and different magnifications. |
We now discuss some specific but still significant details. On one hand, aggregate size polydispersity seems to be rather low (with an average number of liposomes per aggregate of the order of 10). On the other hand, irreversible aggregates seem to be constituted by rather monodisperse liposomes, that is, the size polydispersity of the liposomes forming the irreversible aggregates seems to be lower than that corresponding to the whole sample (section III.A). This rather monodisperse aggregate composition is compatible with theoretical predictions for chain-like aggregates in polydisperse ferrofluids where the presence of small magnetic particles as part of the aggregates is not favorable.107,108 On this theoretical basis, we could understand the presence of small magnetite spots in our TEM micrographs as a manifestation of small dried magnetic liposomes which were not able of being part of the irreversible aggregates.
Aggregate shape also deserves further discussion. Magnetic particles with remanent magnetization in the absence of an external magnetic field can in principle self-assemble into closed aggregates. In particular, computational studies on dipolar hard-spheres61 and experimental investigations with microscopic ferromagnetic particles109 show the emergence of ring shaped aggregates. However, our irreversible aggregates do not show (at least from the current TEM micrographs) ring structures. The absence of rings (whose presence is expected for particles with a high remanent magnetization) can represent a manifestation of the superparamagnetic nature of the magnetic liposomes for which no magnetic hysteresis was detected (Fig. 2(b)). In this respect, and giving that we cannot appeal to particle remanent magnetization, what is the interaction mechanism responsible for maintaining the integrity of our irreversible aggregates in the absence of an external magnetic field?
Coexistence between reversible and irreversible aggregation in mesoscopic particle systems has been rationalized by the existence of primary and secondary minima of the particle potential energy.110 Thus, when aggregation is promoted by a certain mechanism (e.g. here by applying an external magnetic field), particles can in principle aggregate in a permanent (irreversible) state which is associated to a primary minimum where the aggregated state will be maintained despite canceling the mechanism provoking aggregation (e.g. by switching off the external magnetic field). However, particles can also aggregate in a secondary minimum being restored to their non-aggregated state as soon as the mechanism promoting aggregation is canceled.
The idea of an interaction mechanism based on the existence of primary and secondary minima to understand irreversible and reversible aggregation is schematically presented in Fig. 7 for a magnetically induced aggregation process. Thus, in the presence of an external magnetic field (blue line) some particles (purple) aggregate in a permanent (irreversible) primary minimum whereas other (blue particles) aggregate in a (reversible) secondary minimum. When the external magnetic field is switched off (red line), particles aggregating in the secondary minimum become separated. Theoretical approximations based on this underlying picture have been proposed in the past to understand the aggregation of superparamagnetic colloidal latex particles.110–112 In this context, the emergence of primary and secondary minima results from the interplay (or competition) between Coulombic repulsion (treated by a linear superposition approximation), London-van der Waals attraction (Derjaguin approach), and magnetic dipole–dipole attraction. This approach has indeed shown to be successful for predicting and controlling magnetic flocculation to concentrate or remove ultrafine magnetic particles (linear size smaller than 5 μm).113
![]() | ||
Fig. 7 Sketch of the total potential energy between two magnetic particles (here liposomes) based on the theoretical approximation of ref. 110–112. Blue line represents the total potential energy in the presence of an external magnetic field where particles can become stuck in a primary (purple particles) or in a secondary (blue particles) minimum. In the absence of an external magnetic field (red line) those particles that were in a secondary minimum become separated (reversible aggregation, red particles) whereas particles that were in a primary minimum retain their aggregated state (irreversible aggregation, purple particles). Distance can here be interpreted as the separation distance between the external surface of the particles (i.e. the distance between the external surface of two liposome membranes). Separation between particle sketches is merely illustrative in the figure: thus separation between non-aggregated particles (red) has been enhanced whereas that corresponding to the aggregated particles (blue and purple) has been intentionally reduced. |
These interactions110–112 (i.e. DLVO and magnetic dipole–dipole interactions) seem to play, a priori, a significant role by governing stabilization–aggregation in our magnetic liposome system. Thus, Coulombic repulsion is present in our system as manifested by the non-negligible zeta-potential30 whereas London-van der Waals interaction has been identified as the main short range attraction between lipid membranes.114 In addition, a non-DLVO ingredient widely reported in the liposome literature should presumably be considered to reach a complete theoretical description for the magnetic liposome aggregation mechanism: short range hydration repulsion.70,83–88
To calibrate whether or not this complete approach is consistent with a primary–secondary minimum scenario in the present system, additional experiments should be performed. In particular, a more refined control of the magnetic field intensity would help us to better quantify the emergence of primary and secondary minima. Moreover, further experiments in the presence of added electrolyte could also help us to judiciously manipulate Coulombic and hydration repulsions,70 therefore providing valuable quantitative information on the interplay between attractive and repulsive interactions. In the meantime, we are led to speculate on the primary–secondary minimum picture as a plausible mechanism to explain irreversibility–reversibility in our system suggesting future systematic experimental work to resolve this issue further.
Aggregation kinetics has been probed by DLS and followed by the time evolution of the aggregate diffusion coefficient. For a constant magnetic field intensity, the aggregate diffusion coefficient shows a stationary value at sufficiently long times which decreases upon increasing the external magnetic field intensity. We have proven how this stationary value, which is here interpreted as a balance between liposome cluster aggregation and fragmentation, scales with the inverse of the square of the liposome magnetization. Before reaching its stationary value, the diffusion coefficient follows a time dependent power law behavior with a kinetic exponent, α, which increases upon increasing magnetic field intensity. As a manifestation of aggregation reversibility, we have further shown how liposomes aggregating under the influence of a low magnetic field intensity (<40 mT) almost recover their initial (non-aggregated) state when the external magnetic field is switched off.
We have taken advantage of the long time stationary value of the liposome aggregate diffusion coefficient to probe the aggregate structure by SLS through the aggregate structure factor. Thus we have proven the aggregate structure to be fractal and shown how the fractal dimension, df, decreases upon increasing the external magnetic field intensity, resulting in the emergence of almost linear aggregate structures (df → 1). We have finally shown how structure and dynamics are connected in our system by finding a scaling relation between the kinetic exponent, α, and the aggregate fractal dimension, df, which allows us to understand aggregation kinetics and aggregate structure in terms of a single homogeneity parameter.
By TEM micrographs we have also shown the existence of irreversible liposome aggregates which result from an aggregation process in the presence of an intense external magnetic field (80 mT). These irreversible aggregates show an open linear structure and survive despite switching off the external magnetic field. To rationalize the coexistence between reversible and irreversible aggregates, we have suggested a schematic picture based on the existence of primary and secondary minima of the liposome potential energy.
In conclusion, we have revealed the rich interaction scenario involved in the magnetically induced aggregation of superparamagnetic liposomes in suspension. Understanding the mechanisms controlling the aggregation of these (and other) biocompatible magnetic nanodevices is a cornerstone for exploiting their singular capabilities as functional agents in promising medical and biotechnological applications.
Footnote |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/C7NR05301K |
This journal is © The Royal Society of Chemistry 2017 |