Droplet-Based Microfluidic Preparation of Shape-Variable Alginate Hydrogel Magnetic Micromotors.

This article introduces a facile droplet-based microfluidic method for the preparation of Fe3O4-incorporated alginate hydrogel magnetic micromotors with variable shapes. By using droplet-based microfluidics and water diffusion, monodisperse (quasi-)spherical microparticles of sodium alginate and Fe3O4 (Na-Alg/Fe3O4) are obtained. The diameter varies from 31.9 to 102.7 µm with the initial concentration of Na-Alginate in dispersed fluid ranging from 0.09 to 9 mg/mL. Calcium chloride (CaCl2) is used for gelation, immediately transforming Na-Alg/Fe3O4 microparticles into Ca-Alginate hydrogel microparticles incorporating Fe3O4 nanoparticles, i.e., Ca-Alg/Fe3O4 micromotors. Spherical, droplet-like, and worm-like shapes are yielded depending on the concentration of CaCl2, which is explained by crosslinking and anisotropic swelling during the gelation. The locomotion of Ca-Alg/Fe3O4 micromotors is activated by applying external magnetic fields. Under the rotating magnetic field (5 mT, 1-15 Hz), spherical Ca-Alg/Fe3O4 micromotors exhibit an average advancing velocity up to 158.2 ± 8.6 µm/s, whereas worm-like Ca-Alg/Fe3O4 micromotors could be rotated for potential advancing. Under the magnetic field gradient (3 T/m), droplet-like Ca-Alg/Fe3O4 micromotors are pulled forward with the average velocity of 70.7 ± 2.8 µm/s. This article provides an inspiring and timesaving approach for the preparation of shape-variable hydrogel micromotors without using complex patterns or sophisticated facilities, which holds potential for biomedical applications such as targeted drug delivery.

1. Introduction

Micromotors are microdevices capable of converting the energy from the environment into autonomous motion. Micromotors show promising aspects for applications in biomedical engineering and environmental remediation [1,2,3,4,5]. Magnetic micromotors are propelled by external magnetic fields. Compared with other types of micromotors, magnetic micromotors have advantages such as remote control, fuel-free, recyclability, etc. [6]. In addition, magnetic micromotors are demonstrated to be excellent candidates for long-term navigation [7]. Various methods have been reported for the preparation of magnetic micromotors with different shapes. Spherical magnetic micromotors can be prepared via the template-assisted method with sputtering or incorporating magnetic materials [8,9,10]. Helical magnetic micromotors can be prepared by two-photon polymerization lithography [11] and 3D printing [12]. Other shapes are produced by using a specific pattern [10,13]. However, these methods require sophisticated facilities and are usually time-consuming. Therefore, they are difficult to be replicated in normal laboratories. On the other hand, these micromotors are commonly composed of rigid materials which are not biodegradable in aqueous environments [14,15]. Thus, facile fabrication methods are in demand for magnetic micromotors using soft biodegradable materials.

Droplet-based microfluidics is widely used for the preparation of monodisperse microparticles. Recently, it attracted much researchers’ attention for the fabrication of magnetic micromotors due to its low-cost and easy-to-use platform. Typically, magnetic nanoparticles are incorporated within micromotors by means of photopolymerization or crosslinking. Both spherical [14,15,16,17,18,19] and helical [20] shapes can be produced. It allows fabricating micromotors with narrow size distribution, which is essential for biomedical applications such as drug delivery.

As for the material of micromotors, alginate is a natural polysaccharide extracted mainly from brown algae. Alginate hydrogel has been extensively used in drug delivery and tissue engineering because of its biocompatibility and biodegradability [21,22]. Besides, alginate hydrogel is easily synthesized through ionic crosslinking by divalent cations such as Ca2+.

Combining these two points mentioned above in terms of the choice of the preparing method and material, here we describe a facile droplet-based microfluidic method for the preparation of alginate hydrogel magnetic micromotors. First, a droplet-based microfluidic system is built for the generation of droplets of Na-alginate and Fe3O4 (Na-Alg/Fe3O4) in dimethyl carbonate (DMC). After water diffusion (details in Section 2.3), monodisperse (quasi-spherical) Na-Alg/Fe3O4 microparticles are obtained. An aqueous solution of calcium chloride (CaCl2) is used to achieve the gelation, transforming Na-Alg/Fe3O4 microparticles into Ca-Alginate hydrogel microparticles incorporating Fe3O4 nanoparticles (Ca-Alg/Fe3O4 micromotors). Spherical, droplet-like, and worm-like shapes are produced depending on the concentration of CaCl2, which avoids the use of complex patterns or sophisticated facilities. Besides, gelation being immediate makes the method timesaving. The mechanism of deformation is proposed based on the competition between crosslinking and anisotropic swelling during the gelation. Finally, both rotating magnetic field and magnetic field gradient are employed to activate the locomotion of Ca-Alg/Fe3O4 micromotors, showing their potentials for micro/nano-motors based drug delivery systems.

2. Materials and Methods

2.1. Chemical Materials

Na-Alginate (90%, M/G 1:2), DMC (99%), CaCl2 (96%), FeSO4·7H2O, fluorescein isothiocyanate isomer I (FITC, 90%) were all obtained from MACKLIN (Shanghai, China). FeCl3·6H2O, trisodium citrate dihydrate and NH3·H2O were obtained from BAISHI (Tianjin, China), DAMAO (Tianjin, China) and ALADDIN (Shanghai, China), respectively. All chemical materials are of analytical grade and used without further purification.

2.2. Synthesis of Fe3O4@Trisodium Citrate Nanoparticles

A total of 100 mL of DI water was heated in a three-neck flask at 80 °C for 20 min with the protection of nitrogen. An amount of 10 mL of FeCl3 solution (100 mg/mL), 5 mL of FeSO4 solution (100 mg/mL), 4.5 mL of NH3·H2O and 5 mL of trisodium citrate solution (400 mg/mL) were successively added into the flask. The mixture was blended at 1000 rpm for 90 min. Fe3O4@trisodium citrate nanoparticles (named for short as Fe3O4 nanoparticles thereafter) were collected by centrifugation (12,000× rpm, 10 min). Fe3O4 nanoparticles were cleaned 3 times with DI water.

2.3. Preparation of Na-Alg/Fe3O4 Microparticles via Droplet-Based Microfluidics and Water Diffusion

A droplet-based microfluidic system was built by connecting a microchip (cubic channel, side length 500 µm) fabricated by 3D-printing with commercially available fluorinated ethylene propylene (FEP) capillary tubes (external diameter 1/16′′, internal diameter 500 µm) (Figure 1). The dispersed fluid was an aqueous solution of Na-Alginate (0.09, 0.9, 9 mg/mL) mixed with Fe3O4 nanoparticles (0.36 mg/mL), abbreviated as Na-Alg/Fe3O4. The continuous fluid was DMC. No surfactant was used because it created problems for further observation (Figure S1) and removal. With the pressure of nitrogen (50 mbar), the solution of Na-Alg/Fe3O4 and DMC were, respectively, injected into the microchip through two inlets. The flowrate of each fluid was controlled by a gas pump (ELVEFLOW). Due to the immiscibility between these two fluids, at the T-junction on chip (position 1 on the microchip in Figure 1), droplets of Na-Alg/Fe3O4 were generated in DMC, followed by droplet shrinkage. The principle of droplet shrinkage has been reported in our previous article [23]. Briefly, despite the immiscibility between DMC and water, DMC has a low solubility of water (3 wt%) [24]. Thus, after the droplet generation, water diffused gradually from each droplet to DMC, causing droplet shrinkage. It was observed by comparing the droplet at the T-junction (position 1 on chip in Figure 1) and that near the outlet of microchip (position 2 on chip in Figure 1). This process is called on-chip droplet shrinkage to indicate that it happens in the microchip. Droplets were collected with the yield of 1 droplet/s in a glass Petri dish filled with DMC through a capillary tube (length 46 cm). Note that the yield varies with experimental parameters, such as the gas pressure, the microchannel dimension, etc. Droplet shrinkage continued out of the microchip (off-chip droplet shrinkage) until the equilibrium was reached. Finally, Na-Alg/Fe3O4 microparticles were obtained.

Figure 1

Schematic illustration of the preparation of Ca-Alg/Fe3O4 micromotors, with optical microscopic images of a droplet (outlined in white) generated right after the T-junction at Position 1 (insert microscopic image 1) and a droplet near the outlet of microchip at Position 2 (insert microscopic image 2).

Note that the serpentine channel in the microchip was specially designed to prolong the residence time of droplet (). With the straight channel, was relatively short. On-chip droplet shrinkage was not efficient. Large droplets were observed at the outlet of microchip. Besides, they were likely to stagnate there where a capillary tube was connected, probably due to the imperfect connection or a minor flaw in the capillary tube. With water diffusion, the stagnating droplets became condensed and at last clogged the channel. By using the serpentine channel, was prolonged. It allowed for an efficient on-chip droplet shrinkage. Droplets were smaller at the outlet of microchip. Therefore, they were less likely to stagnate or eventually cause clogging there. Moreover, with an elevated droplet shrinkage, the distance between two droplets was also prolonged. At the end of the capillary tube in the glass Petri dish, there was less tendency for droplet coalescence, which was advantageous for preparing monodisperse microparticles.

2.4. Preparation of Ca-Alg/Fe3O4 Micromotors via Ionic Crosslinking

Na-Alg/Fe3O4 microparticles were dried in air with the evaporation of DMC. An aqueous solution of CaCl2 (10, 1, 0.1, 0.01 wt%) was added, transforming Na-Alginate into Ca-Alginate hydrogel via ionic crosslinking. Fe3O4 nanoparticles were incorporated inside. The ensemble was used as the hydrogel magnetic micromotor and named for short as Ca-Alg/Fe3O4 micromotor thereafter. It should be mentioned that the gelation process is immediate. Thus, the production of Ca-Alg/Fe3O4 micromotors mainly depends on the microfluidic experimental parameters and the quantity of micromotors required.

2.5. Characterization of Na-Alg/Fe3O4 Microparticles and Ca-Alg/Fe3O4 Micromotors

2.5.1. Scanning Electron Microscope

Scanning electron microscope (SEM, Phenom ProX, Phenom-World, The Netherlands) was used to characterize the morphology of Na-Alg/Fe3O4 microparticles and Ca-Alg/Fe3O4 micromotors. The SEM sample was prepared by adhering dried particles to a copper sample-holder with a conductive tape. Some particles were broken after this step, which revealed information for the interior structure [23]. For a better resolution, all samples were coated by a thin layer of gold (Au) before SEM observation. The acceleration voltage of SEM was 15 kV. Energy-dispersive X-ray (EDX, Phenom) mapping analysis was conducted for element detection.

2.5.2. Confocal Laser Scanning Microscope

Confocal laser scanning microscope (CLSM, Nikon A1, Nikon Company Ltd., Tokyo, Japan) was used to characterize the distribution of Fe3O4 nanoparticles inside Ca-Alg/Fe3O4 micromotors. For this purpose, FITC was initially conjugated with Fe3O4 nanoparticles by surface modification to form FITC-labeled Fe3O4 nanoparticles. They were then mixed with the solution of Na-alginate. After the protocol described above for the preparation of Ca-Alg/Fe3O4 micromotors, samples were immerged in DI water and observed by CLSM. The distribution of FITC represented that of Fe3O4 nanoparticles inside Ca-Alg/Fe3O4 micromotors. The 3D-image reconstruction was carried out to characterize the spatial distribution of Fe3O4 nanoparticles.

2.5.3. Locomotion of Ca-Alg/Fe3O4 Micromotors in External Magnetic Fields

A home-made magnetic field generator was constructed [25]. It consisted of electromagnetic coils, a function generator (FY8300S) and a power amplifier (HSLFSun GLY-FP1000, Lab.Gruppen, Kungsbacka, Sweden). It allowed control of the magnetic field strength and orientation in the X, Y and Z axes by modulating the current in each electromagnetic coil. Sinusoidal function with a phase difference of 90° was used to generate the rotating magnetic field whose field vector varied regularly around the X axis in the Y-Z plane. Only one electromagnetic coil was activated to produce the magnetic field gradient at X axis. A glass slide was placed in the center of electromagnetic coils. A total of 20 µL of suspension consisting of Ca-Alg/Fe3O4 micromotors and water was added on the glass slide. Upon application of the external magnetic field, the movement of Ca-Alg/Fe3O4 micromotors was observed by an optical microscope (Leica DMi8, Leica Microsystems, Wetzlar, Germany) coupled with a CCD camera. The movement video was recorded and analyzed to calculate the advancing velocity of Ca-Alg/Fe3O4 micromotors.

3. Results and Discussion

3.1. Na-Alg/Fe3O4 Microparticles

Droplet-based microfluidic experiments were performed with three different initial concentrations of Na-Alginate in dispersed fluid (): 0.09, 0.9 and 9 mg/mL. The concentration of Fe3O4 () was fixed at 0.36 mg/mL for all experiments.

3.1.1. Diameter and Volume

Monodisperse (quasi-)spherical Na-Alg/Fe3O4 microparticles were observed in DMC with an optical microscope (Figure 2(a1,c1)). The diameter of Na-Alg/Fe3O4 microparticles in DMC () increases with (Table 1). varies from 31.9 to 102.7 µm with ranging from 0.09 to 9 mg/mL.

Figure 2

(a1,b1,c1) Optical microscopic images and (a2,b2,c2) SEM images of Na-Alg/Fe3O4 microparticles. The initial concentration of Na-Alginate in dispersed fluid ( ) for the preparation is (a1,a2) 0.09 mg/mL, (b1,b2) 0.9 mg/mL, (c1,c2) 9 mg/mL. The red arrow in b1 shows the neat cross section. SEM scale bar 20 µm. Relationship between and (d) Na-Alg/Fe3O4 microparticle volume, interior liquid volume, solid volume; (e) liquid portion in Na-Alg/Fe3O4 microparticles in DMC. (f) Evolution of the diameter of Na-Alg/Fe3O4 microparticles (prepared with at 9 mg/mL) in different media.

Table 1

Diameter of Na-Alg/Fe3O4 microparticles in DMC () in function of the initial concentration of Na-Alginate in dispersed fluid ().

C_i,Na-Alg (mg/mL)	d_particle,DMC (µm)
0.09	31.9 ± 1.4
0.9	48.2 ± 1.6
9	102.7 ± 1.7

The volume of Na-Alg/Fe3O4 microparticles in DMC () is calculated according to the Equation (1).

increases with (black symbols in Figure 2d), whose relationship is well fitted by a linear equation (written in black in Figure 2d). On the other hand, the diffusion of Na-Alginate and Fe3O4 from droplets to DMC is negligeable during the water diffusion [26]. Thus, the volume of Na-Alginate () and the volume of Fe3O4 () are the same as the corresponding volume in the initially generated droplet. is calculated by dividing the mass of Na-Alginate () with the density of Na-Alginate (). is calculated by multiplying with the initial droplet volume () (Equation (2)). is calculated the same way (Equation (3)). Finally, the solid volume in the Na-Alg/Fe3O4 microparticle (), sum of and is calculated with the Equation (4).

increases with (orange symbols in Figure 2d) with a leaner fitting equation (written in orange in Figure 2d). In fact, the linear relationship can be explained mathematically. In Equation (4), , and are constant. As for , since it varies little from 0.3 to 0.4 µL for all experiments, it can also be considered as constant. is the only variable. Consequently, Equation (4) gives a linear relationship for the function .

3.1.2. Interior Liquid

It can be seen from Figure 2d that there is an evident gap between and , indicating that the Na-Alg/Fe3O4 microparticle is not composed of condensed solid materials. In fact, flattened broken microparticles have been observed by SEM (Figure S2), which confirms the porous interior structure. For Na-Alg/Fe3O4 microparticles collected in DMC, there can be water trapped inside after water diffusion reaches equilibrium. DMC can also diffuse into Na-Alg/Fe3O4 microparticles. Thus, the difference between and is caused by the interior liquid which is water and DMC. The volume of the interior liquid () is simply calculated with Equation (5) and plotted with in Figure 2d (red symbols). shows a linear relationship with (fitting equation written in red in Figure 2d). The liquid portion, defined as the liquid volume percentage in the Na-Alg/Fe3O4 microparticle (), is calculated by Equation (6). It is found that about 50–70% of the Na-Alg/Fe3O4 microparticle is filled with liquid, despite used (Figure 2e).

3.1.3. Stability

Na-Alg/Fe3O4 microparticles were stored in DMC and air (25 °C, humidity 40%), respectively, to assess the stability in terms of diameter in 72 h after the preparation. Na-Alg/Fe3O4 microparticles were observed by both optical microscope and SEM. The diameter of Na-Alg/Fe3O4 microparticles is measured in three different ways. (1) In DMC with optical microscopic observation: the diameter is stable around 100 µm (black symbols in Figure 2f). (2) In air with optical microscopic observation: the diameter reduces from 100 to 82 µm within the first 24 h and stays unchanged for the following 48 h (orange symbols in Figure 2f and Figure S3(a1–a5)). It can be explained by the evaporation of the interior liquid in air. After being dried in air for 72 h, the same sample is also observed by SEM (Figure S4). The diameter measured from SEM observation (green symbol in Figure 2f) shows no evident difference from that from optical microscopic observation, indicating that the observing tool does not contribute to the difference of measurement. (3) Samples are coated by a thin layer of Au once and observed by SEM. They are stored in air each time after observation. The diameter reduces from 100 to 89 µm within the first 24 h and stays unchanged for the following 48 h (blue symbols in Figure 2f and Figure S3(a1–a5)). The final diameter is higher than that observed in air. It is due to the presence of deposited Au layer on the surface of Na-Alg/Fe3O4 microparticles which hinders the evaporation of the interior liquid. Consequently, larger microparticles are observed.

Note that with the same at 9 mg/mL, (Figure 2d) gives an equivalent diameter of 70 ± 2 µm. It is still lower than the last diameter measured in air with optical microscope (82 µm). Thus, we assume that the interior liquid is not all evaporated.

3.1.4. Morphology

The morphology of Na-Alg/Fe3O4 microparticles was characterized by SEM. Different morphologies were observed depending on used for the preparation. When is extremely low at 0.09 mg/mL, the surface of Na-Alg/Fe3O4 microparticles is rough (Figure 2(a2)). By increasing to 0.9 mg/mL, the obtained Na-Alg/Fe3O4 microparticles have a smooth and porous surface with a neat cross section (Figure 2(c2) and Figure S5(a1–a3)). The fact that this structure is also observed by optical microscope for Na-Alg/Fe3O4 microparticles in DMC (red arrow in Figure 2(b1)), demonstrating that it is not caused by vacuum during SEM observation. For the highest at 9 mg/mL, Na-Alg/Fe3O4 microparticles have a smooth and porous surface with a tiny flat round trace (Figure 2(c2) and Figure S5(b1–b3)).

Since and are constant parameters for all experiments, the quantity of Fe3O4 is fixed in Na-Alg/Fe3O4 microparticles. Thus, the difference of morphology is caused by the quantity of Na-Alginate. Based on the results, the mechanism of the formation of Na-Alg/Fe3O4 microparticles is proposed as follows.

3.1.5. Mechanism of the Formation of Na-Alg/Fe3O4 Microparticles

Na-Alg/Fe3O4 droplets are collected in DMC in a glass Petri dish. As droplets fall in DMC, water diffuses from droplets into DMC though the interface (Figure 3a). The diffusion of water brings about the migration of alginate polymeric chains until the interface [27]. Progressively, a primary porous shell structure is formed. When a droplet lands on the glass bottom, the deformation depends on the resistance of the shell which is influenced by the alginate quantity () in the droplet (Figure 3b). When is extremely low (corresponding to = 0.09 mg/mL), the shell is not resistant enough to the shock upon landing, producing a spreading form. Since there is no sufficient alginate to form a full shell, the final structure is rather a random stock of Fe3O4 nanoparticles which is the major solid material in this case (Figure 3c). When is increased but still low (corresponding to = 0.9 mg/mL), the shell resists better the shock of glass. The droplet stays spherical with a neat cross section due to the contact with the glass, which explains the morphology observed by SEM. With the highest (corresponding to = 9 mg/mL), the shell is so strong that the droplet is hardly deformed. In the end, spherical microparticles are obtained with a tiny flat round trace left when touching the glass.

Figure 3

Illustration of the mechanism of the formation of Na-Alg/Fe3O4 microparticles in a glass Petri dish filled with DMC: (a) droplets fall with water diffusion; (b) droplets land on the glass bottom with a primary shell formed on the surface; (c) water diffusion reaches equilibrium and final microparticles are formed.

3.2. Ca-Alg/Fe3O4 Micromotors

An aqueous solution of CaCl2 (10, 1, 0.1, 0.01 wt%) was added to dried Na-Alg/Fe3O4 microparticles, transforming Na-Alg/Fe3O4 microparticles into Ca-Alg/Fe3O4 micromotors. Spherical, droplet-like, and worm-like shapes are obtained (Table 2). The influence of the concentration of CaCl2 () is studied.

Table 2

Optical microscopic and schematic images of Ca-Alg/Fe3O4 micromotors with the indication of and for the preparation. Scale bar 100 µm.

C_CaCl_2	C_i,Na-Alg=0.09 mg/mL	C_i,Na-Alg=0.9 mg/mL	C_i,Na-Alg=9 mg/mL
	Optical   Schematic	Optical   Schematic	Optical   Schematic
10 wt%
1 wt%
0.1 wt%
0.01 wt%

For Na-Alg/Fe3O4 microparticles prepared with at 0.09 mg/mL

3.2.1. Influence of on the Shape of Ca-Alg/Fe3O4 Micromotors

is low in Na-Alg/Fe3O4 microparticles. The gelation does not produce any evident deformation with varying from 0.1 to 10 wt%. Ca-Alg/Fe3O4 micromotors stay quasi-spherical. When the solution of CaCl2 is too diluted ( = 0.01 wt%), Na-Alg/Fe3O4 microparticles are almost dissolved.

For Na-Alg/Fe3O4 microparticles prepared with at 0.9 and 9 mg/mL

These Na-Alg/Fe3O4 microparticles have a similar manner of deformation depending on . With a concentrated solution of CaCl2 (= 10 wt%), no deformation is produced. Ca-Alg/Fe3O4 micromotors are spherical. When Na-Alg/Fe3O4 microparticles are immerged in a solution with at 1 wt%, a tail is grown from the “defect” (neat cross section or tiny flat round trace, Figure 2(b2,c2)) on the surface of Na-Alg/Fe3O4 microparticles (Video S1). As a result, Ca-Alg/Fe3O4 micromotors have a droplet-like shape. By reducing to 0.1 wt%, a longer tail is grown, creating the worm-like shape. Finally, the use of a solution with at 0.01 wt% almost dissolves Na-Alg/Fe3O4 microparticles.

3.2.2. Mechanism of the Deformation

When adding an aqueous solution of CaCl2 for the gelation, calcium cations diffuse into Na-Alg/Fe3O4 microparticles, causing ionic crosslinking. It allows strengthening bonds between alginate polymeric chains, which impedes further deformation. Meanwhile, water also diffuses into Na-Alg/Fe3O4 microparticles, causing swelling. The swelling is anisotropic because of the anisotropic morphology of Na-Alg/Fe3O4 microparticles with “defect” on the surface (neat cross section or tiny flat round trace, Figure 2(b2,c2)). Overall, in our case, the gelation process is a competition of crosslinking which impedes the deformation and anisotropic swelling which encourages the deformation.

When is high at 10 wt%, calcium cations diffuse fast to Na-Alg/Fe3O4 microparticles to achieve crosslinking. The spherical shape is preserved with nearly no swelling. When is 1 wt%, calcium cations diffuse more slowly to Na-Alg/Fe3O4 microparticles, leading to a slower crosslinking. It leaves time for anisotropic swelling. According to the result, the swelling is more important at the “defect” on the surface, which explains the growth of the tail. A further reduction in to 0.1 wt% is more advantageous for anisotropic swelling, as there is more water and fewer calcium cations in the environment. A longer tail is grown. Furthermore, we note that with the anisotropic swelling, Na-Alg/Fe3O4 microparticle grow upwards from the glass bottom (Video S1) with a tail adhered to the glass. The tail bends when it can no longer bear the weight of the whole microparticle. It explains why certain tails are curved. Finally, when is too low at 0.01 wt%, there are no sufficient calcium cations for crosslinking. Anisotropic swelling takes over crosslinking totally. Na-Alg/Fe3O4 microparticles are almost dissolved.

3.2.3. Characterization of Fe3O4 Nanoparticles inside Ca-Alg/Fe3O4 Micromotors

By using FITC-labeled Fe3O4 nanoparticles, the fabricated micromotors were observed by CLSM. The fluorescent image (Figure 4(a1,a2)) indicates that Fe3O4 nanoparticles are incorporated in Ca-Alginate hydrogel successfully. It is also verified by EDX mapping analysis (Figure 4(b1,b2)). Moreover, the 3D-image reconstruction by CLSM shows that Fe3O4 nanoparticles are mostly located at the bottom half semi-sphere of the micromotor (Video S2).

Figure 4

(a1) Bright-field and (a2) fluorescence microscopic image of micromotors with incorporated FITC-labeled Fe3O4 nanoparticles. (b1) SEM image and (b2) corresponding EDX mapping analysis of a Ca-Alg/Fe3O4 micromotor for iron (scale bar 20 µm). (c) Relationship between the advancing velocity of spherical micromotors (prepared with at 9 mg/mL for the microfluidic experiment and at 10 wt% for the gelation) and the frequency at 5 mT. Video snapshots (scale bar 200 µm) at different time intervals of a (d) spherical and (e) worm-like micromotor under the rotating magnetic field at 5 mT around X axis in Y-Z plane; (f) droplet-like micromotor under the X-axis magnetic field gradient of 3 T/m.

3.2.4. Locomotion of Ca-Alg/Fe3O4 Micromotors

The locomotion of all three types of micromotors is always observed at the bottom of the glass Petri dish. For spherical and worm-like Ca-Alg/Fe3O4 micromotors, the locomotion is activated by applying a rotating magnetic field at 5 mT around X axis in Y-Z plane. The frequency () varies from 1 to 15 Hz. We observe that spherical micromotors move forward by rotation-enabled rolling (Figure 4d, Video S3). The advancing velocity () increases with until the step-out frequency ( = 6 Hz) is reached (Figure 4c). Then, declines with the frequency. The maximum is 158.2 ± 8.6 µm/s with at 6 Hz. However, as for worm-like micromotors, with the application of rotating magnetic field, rotation behavior is observed, which can be further developed for advancing movement based on their helical structure (Figure 4e, Video S4).

With the symmetric structure, droplet-like Ca-Alg/Fe3O4 micromotors cannot move forward under the rotating magnetic field. The locomotion of a droplet-like Ca-Alg/Fe3O4 micromotor is activated by applying an X-axis magnetic field gradient. At 2 T/m, the micromotor is not actuated at all. At 3 T/m, a torque is first produced and turns the micromotor to align with the direction of the external magnetic field. Then, the micromotor is pulled forward (Figure 4f, Video S5) with an average velocity of 70.7 ± 2.8 µm/s.

Although all micromotors are not actuated in the same type of external magnetic field, we note that with the same current input in the electromagnetic coil, micromotors are more likely to be actuated by the rotating magnetic field than the magnetic field gradient. It can be explained by the fact that the friction force is generally higher when a micromotor is pulled forward than when it advances by rotation. Thus, the rotating magnetic field is preferably reported in the literature, whereas it demands a certain shape of micromotors, such as spherical and helical shapes. The present method allows producing the spherical shape. We hope that with further modification and precise control during gelation, the worm-like shape can be transformed into the well-defined shape such as helical structured motors.

4. Conclusions and Perspective

In conclusion, we present herein a facile droplet-based microfluidic preparation of Fe3O4-incorporated alginate hydrogel micromotors with variable shapes. First, monodisperse (quasi-)spherical Na-Alg/Fe3O4 microparticles are obtained by using droplet-based microfluidics and water diffusion. The diameter of Na-Alg/Fe3O4 microparticles varies from 31.9 to 102.7 µm, depending on the initial concentration of Na-Alginate in dispersed fluid. The mechanism of the formation of Na-Alg/Fe3O4 microparticles is proposed to explain different morphology observed by SEM. Second, an aqueous solution of CaCl2 is used for gelation, transforming Na-Alg/Fe3O4 microparticles into Ca-Alg/Fe3O4 micromotors. Spherical, droplet-like, and worm-like shapes are obtained, which is mainly affected by the concentration of CaCl2. The mechanism of deformation is proposed considering the crosslinking and anisotropic swelling during the gelation. Finally, Ca-Alg/Fe3O4 micromotors are actuated by applying external magnetic fields, showing their potential of developing functional micro/nano-motors.

This article provides an idea for producing different shapes of hydrogel micromotors without using complex patterns or sophisticated facilities. The method is timesaving and easy to be realized. In terms of the stability of micromotors, the size has been measured for 14 days consecutively and no evident change was found. Stored in pure water, micromotors demonstrated a decreasing locomotion probably due to the diffusion of Fe3O4 nanoparticles. Nevertheless, the advancing velocity of spherical micromotors was estimated to be stable within 2 days. For long-term utility or storage, work should be done to conserve the locomotion of micromotors. Future work will focus on integrating biomedical or biological agents, such as medical molecules and cells to achieve on-demand tasks such as drug delivery and cell transportation.