3D Encapsulation Made Easy: A Coaxial-Flow Circuit for the Fabrication of Hydrogel Microfibers Patches

To fully exploit the potential of hydrogel micro-fibers in the design of regenerative medicinal materials, we designed a simple, easy to replicate system for cell embedding in degradable fibrous scaffolds, and validated its effectiveness using alginate-based materials. For scaffold fabrication, cells are suspended in a hydrogel-precursor and injected in a closed-loop circuit, where a pump circulates the ionic cross-linking solution. The flow of the cross-linking solution stretches and solidifies a continuous micro-scaled, cell-loaded hydrogel fiber that whips, bends, and spontaneously assembles in a self-standing, spaghetti-like patch. After investigation and tuning of process- and solution-related parameters, homogeneous microfibers with controlled diameters and consistent scaffolds were obtained from different alginate concentrations and blends with biologically favorable macromolecules (i.e., gelatin or hyaluronic acid). Despite its simplicity, this coaxial-flow encapsulation system allows for the rapid and effortless fabrication of thick, well-defined scaffolds, with viable cells being homogeneously distributed within the fibers. The reduced fiber diameter and the inherent macro-porous structure that is created from the random winding of fibers can sustain mass transport, and support encapsulated cell survival. As different materials and formulations can be processed to easily create homogeneously cell-populated structures, this system appears as a valuable platform, not only for regenerative medicine, but also, more in general, for 3D cell culturing in vitro.


Introduction
The therapeutic delivery of autologous cells to support the structure and functions of biological tissues is a core paradigm in regenerative medicine. In their infancy, cell-based approaches have been mainly based on the delivery of plain, high-density cell suspensions to the target site. This strategy, however, has generally shown to have a poor clinical outcome, due to major loss of cell viability, and a limited control over cell fate, both in terms of cell differentiation and site-specificity (with cells eventually migrating to other sites) [1,2]. To improve site-specific engraftment of transplanted cells, and achieve to clinically relevant outcomes, in most applications a scaffold or carrier material is essential [3][4][5][6].
Among other possible scaffolding options (seeding on preformed 3D porous structures, above all [7,8]), encapsulating cells in short-term degradable hydrogels is a particularly attractive strategy when mechanical properties are not critical. Hydrogels, in fact, offer a highly hydrated environment, and they can adapt to implantation sites and generally maintain graft volume. No less With the coaxial flow circuit developed, fibers with diameters ranging from 60 to about 400 μm were obtained in a relatively large range of alginate concentrations (Figure 2a). For each concentration, the microfiber diameter was strongly influenced by the syringe pump flow rate, and as reasonable expected, an increase was observed when the solution feed was raised. Increasing the alginate concentration had the same effect for up to 2%, but there was a tendency to a decrease in diameters that was observed for the 4% solutions. This finding is probably due to the high viscosity of the 4% solution, which appeared to have hindered the extrusion of the material, as only short fibers and elongated beads were collected in the strainer. The diameter of the needle also influenced, as expected, the dimensions of the microfibers (Figure 2b). A significant difference in fiber dimensions when using the 22 G or 26 G needle was observed for each pumping flow rate, except for 70 mm/hr.
Fibers generally appeared homogeneous in diameter and smooth in their surface, except for some combinations with low CaCl2 flow rates ( Figure 2c) and low alginate flow rates (10-30 mm/hr, Figure 2d), where the fiber surfaces appeared wrinkled.

Plain Alginate Fiber Fabrication and System Optimization
To prepare the hydrogel fibers, alginic acid sodium salt from brown algae (viscosity 15.0-25.0 cP, Mw = 120-190 kDa) was dissolved in Dulbecco's Modified Eagle's Medium (DMEM), and injected in the circulating CaCl 2 solution. To optimize the fabrication process, and evaluate the effect of solutionand processing-related parameters on fiber formation, the alginate concentration was varied from 1% to 4% (w/v), and the CaCl 2 molarity from 35 to 150 mM, and syringe pump advancing rate from 10 to 90 mm/h (1 mm/h, corresponding to 0.3 mL/h). To assess the effects of the syringe needle dimension, 22, 24, and 26 G diameters were compared for the injection of the alginate solution.
For each set of parameters, the extruded fibers were retrieved from the strainer, and their morphologies were evaluated by optical microscopy. Quantitative analyses on fiber diameter were performed on acquired images, using the image-processing software ImageJ [36], based on 30 different measures in random points from at least three different images.

Alginate-Blended Microfiber Production
To confirm the possibility of creating scaffolds from different compositions, two biological macromolecules were blended with 2% (w/v) alginate. Gelatin (from porcine skin, Type A) and hyaluronic acid sodium salt (HA, from Streptococcus equi, Mw = 1.5-1.8 × 10 6 g/mol) were blended in at the ratios in Table 1, and processed with the flow circuit, to fabricate microfibers patches.

Rheological Properties
Rheological properties of hydrogel-forming solutions are critical for fiber formation, and hence, they were evaluated using a CVO 120 stress-controlled Rotational Rheometer (Bohlin Instruments, cone/plate geometry with cone diameter = 40 mm and cone angle = 1 • ). The gap was automatically set to 0.03 mm. A Peltier plate was used to thermostat the solutions at 25 or 37 • C. Steady shear measurements were performed by increasing the shear stress from zero to a maximum of 300 Pa.

Swelling and Weight Loss
Swelling and weight loss of microfibers at 37 • C in phosphate buffer saline (PBS), or in complete cell culture medium were evaluated for up to 21 days, to appraise their kinetics. At selected time-points (1, 2, 3, 5, 7, 24, 48, 72 h, and 7, 14, 21 days), microfibers were strained from the medium, centrifuged to eliminate the excess of water, and weighted with a precision balance. The weight variation (∆W%) was calculated as: where W t is the measured weight of a swollen sample at time t and W 0 its initial weight.
To increase the stability of the fibers, two different methods were investigated: (i) a post-treatment of fibers in high molarity CaCl 2 solution (150 mM) for 5 min, and (ii) a combination of external and internal alginate gelation. In this latter case, 5 mM CaCO 3 was mixed with the cell suspension, and fibers were treated in D-gluconic acid-δ-lactone (GDL, 5 mM, pH 3.4) solution for five seconds.

Cells Encapsulation in Microfibers
For cell experiments, a CaCl 2 solution was sterile-filtered (0.2 µm), sodium alginate and gelatin powders were disinfected by soaking in ethanol and HA powder, and all of the flow-loop components were sterilized by autoclaving.
After fabrication, cell-loaded patches were placed in cell strainers and cultured in a 12-well multiwell plate with DMEM, supplemented with 10% (v/v) fetal bovine serum (FBS) with 1% penicillin/streptomycin at 37 • C and 5% CO 2 .

Evaluation of Cell Viability
Cell survival immediately after encapsulation was investigated by double staining with propidium iodide (20 µM) and calcein-AM (2 µM) in a serum-free cell culture medium. After rinsing in PBS, samples were incubated in the staining solution at 37 • C for 40 min and rinsed again before imaging. Fluorescence images were acquired by using a Zeiss Axioplan microscope, using 490/515 nm (excitation/emission) filters for calcein-AM, and 535/617 nm (excitation/emission) for propidium iodide. ImageJ [36] image processing software was used to merge the images and count cells.
Longer-term viability of embedded cells in alginate-based fibers was measured after 1, 3, 8, and 10 days, using an Alamar Blue ® assay according to the manufacturer's indications.

In Vitro Cell Release
The number of cells released from the alginate-based patches was estimated by acquiring daily microscopic images of the bottom of the wells, and counting cells in five randomly selected areas (0.7 mm 2 ). To evaluate the progression of cell release, strainers containing patches were moved daily to a new plate, in order to account only for cells released in the previous 24 h.

Statistical Analysis
Results are presented as mean ± standard deviation (SD). Statistical analyses were performed using GraphPad Prism software (GraphPad Software Inc., version 6). Statistically significant differences were determined by one-way analysis of variance (ANOVA), followed by Tukey's post-test for pairwise comparisons, and p < 0.05 was considered statistically significant.

Plain Alginate Microfiber Fabrication and System Optimization
The injection of alginate-based solutions in a circulating CaCl 2 bath was confirmed to be an easy and effective method of preparing alginate-based microfibers, and it proved the effectiveness of the designed flow circuit, as schematized in Figure 1a. For most sets of parameters tested, a continuous fiber was extruded (Figure 1b,c) and, more interestingly, in a subset of cases, it was spontaneously assembled in the strainer as a consistent, self-standing fibrous scaffold, as is shown in Figure 1d, where the appearance of wet and dry microfiber patches is shown.
With the coaxial flow circuit developed, fibers with diameters ranging from 60 to about 400 µm were obtained in a relatively large range of alginate concentrations (Figure 2a). For each concentration, the microfiber diameter was strongly influenced by the syringe pump flow rate, and as reasonable expected, an increase was observed when the solution feed was raised. Increasing the alginate concentration had the same effect for up to 2%, but there was a tendency to a decrease in diameters that was observed for the 4% solutions. This finding is probably due to the high viscosity of the 4% solution, which appeared to have hindered the extrusion of the material, as only short fibers and elongated beads were collected in the strainer. The diameter of the needle also influenced, as expected, the dimensions of the microfibers (Figure 2b). A significant difference in fiber dimensions when using the 22 G or 26 G needle was observed for each pumping flow rate, except for 70 mm/h. Bioengineering 2019, 6, x FOR PEER REVIEW 6 of 13 The flow of CaCl2 solution, on the other hand, did not appear to have a distinct influence on the fiber diameter (Supplementary material - Figure S1), but it had a strong effect on the patch coherence, as for the lower-flow speed-separated fibers that were collected. On the contrary, for higher values, a good adhesion among fibers were obtained and coherent scaffolds that were easy to handle, were retrieved.
When the effect of calcium molarity was investigated, circulating the 150 mM solution resulted in an immediate obstruction of the initial portion of the silicone tubing at high alginate feeding rates, and in needle clogging at lower rates. When using the 70 mM CaCl2 solution, fibers were formed, but no adhesion among them was observed in the strainer, possibly due to the saturation of calcium ions in the external alginate shell at the time of collection. As a result, non-consistent and extremely difficult-to-handle structures were retrieved, and 35 mM was chosen for the production of continuous microfibers and coherent, consistent scaffolds.  The flow of CaCl 2 solution, on the other hand, did not appear to have a distinct influence on the fiber diameter (Supplementary material- Figure S1), but it had a strong effect on the patch coherence, as for the lower-flow speed-separated fibers that were collected. On the contrary, for higher values, a good adhesion among fibers were obtained and coherent scaffolds that were easy to handle, were retrieved.
When the effect of calcium molarity was investigated, circulating the 150 mM solution resulted in an immediate obstruction of the initial portion of the silicone tubing at high alginate feeding rates, and in needle clogging at lower rates. When using the 70 mM CaCl 2 solution, fibers were formed, but no adhesion among them was observed in the strainer, possibly due to the saturation of calcium ions in the external alginate shell at the time of collection. As a result, non-consistent and extremely difficult-to-handle structures were retrieved, and 35 mM was chosen for the production of continuous microfibers and coherent, consistent scaffolds.
Results suggest that an effective adhesion between fibers requires crosslinking that should not have proceeded too far as they reach the strainer, because this allows further crosslinking to involve molecules from different fibers, and create strong adhesions among them. For this reason, a low concentration of crosslinking ions and a short permanence in the flow before the collection will result in self-standing, easy-to-handle patches.
The use of a coaxial flow in a non-microfluidic device allows for the production of fiber diameters that are comparable to those obtained in microfluidic devices (150-500 µm [27]), but with a processing speed that is one order of magnitude higher (0.5 mL/min versus 50 µL/min typically observed in microfluidic devices [27]). Furthermore, cohesive scaffolds are prepared within a very short time, for the benefit of cell survival, with a one-step procedure, avoiding the need for an additional step that is required to assemble discrete fibers that are produced in similar systems [24,[37][38][39].

Blended Microfiber Fabrication
The addition of gelatin or HA, as qualitatively shown in Figure 3d, did not inhibit fiber formation, neither did it affect the general morphology of the microfibers. In the case of gelatin, even when its proportion in the blend was higher than alginate (3% vs. 2%) smooth and homogeneous fibers were obtained.
have proceeded too far as they reach the strainer, because this allows further crosslinking to involve molecules from different fibers, and create strong adhesions among them. For this reason, a low concentration of crosslinking ions and a short permanence in the flow before the collection will result in self-standing, easy-to-handle patches.
The use of a coaxial flow in a non-microfluidic device allows for the production of fiber diameters that are comparable to those obtained in microfluidic devices (150-500 μm [27]), but with a processing speed that is one order of magnitude higher (0.5 mL/min versus 50 μL/min typically observed in microfluidic devices [27]). Furthermore, cohesive scaffolds are prepared within a very short time, for the benefit of cell survival, with a one-step procedure, avoiding the need for an additional step that is required to assemble discrete fibers that are produced in similar systems [24,[37][38][39].

Blended Microfiber Fabrication
The addition of gelatin or HA, as qualitatively shown in Figure 3d, did not inhibit fiber formation, neither did it affect the general morphology of the microfibers. In the case of gelatin, even when its proportion in the blend was higher than alginate (3% vs 2%) smooth and homogeneous fibers were obtained.
When increasing solution flow rate, the trend in microfiber diameter for blends was consistent with that observed for pure alginate, but the introduction of gelatin into the polymer solution determined a significant increase of microfiber diameter for all flow rates and concentrations ( Figure  3a,b). This finding is consistent with an increase in solution viscosity, as revealed by rheological measurements (Figure 4a), imputable to the increased overall concentration of the solution.
Contrarily, HA did not have the same effect at both of the concentrations chosen for blending (0.1% and 0.2% (w/v), Figure 3c) [40,41]. Due to the high molecular weight, HA was added in at lower percentages, and the increase in viscosity at room temperature was less pronounced ( Figure  4a).  When increasing solution flow rate, the trend in microfiber diameter for blends was consistent with that observed for pure alginate, but the introduction of gelatin into the polymer solution determined a significant increase of microfiber diameter for all flow rates and concentrations (Figure 3a,b). This finding is consistent with an increase in solution viscosity, as revealed by rheological measurements (Figure 4a), imputable to the increased overall concentration of the solution. < 0.05, ** p < 0.01 and *** p < 0.005).
Rheological measurements (Figure 4) also showed a distinct influence of temperature on the viscosity changes in both blends. While the alginate curve was substantially unchanged, the addition of both gelatin and HA caused a substantial increase in the viscosity at room temperature, while the effect was significantly less noticeable at 37 °C, where the curves of instantaneous viscosity were largely overlapped (Figure 4b).

Microfiber Swelling and Weight Loss
Swelling and weight loss of microfibers in PBS and in the cell culture medium at 37 °C for up to 21 days are shown in Figure 5. Plain alginate patches (Figure 5a,b) without any further crosslinking lost the majority of their weights within the first 48 h.
Based on the rapidity of weight loss and the degree of swelling, it is reasonable to assume that, due to the low concentration of CaCl2 a weakly cross-linked shell forms around a nearly liquid core [42]. As the shell breaks because of mechanical stress caused by swelling, the release of the liquid core accounts for the steep weight loss. Accordingly, when CaCO3 is added to the alginate solution to create a denser core, a higher persistence of fibers is observed, and the greatest weight loss takes place between 7 and 14 days. When the patches underwent a post treatment by immersion in concentrated CaCl2 solution (150 mM), a considerably higher PBS stability was observed, and swelling was still prevailing over degradation after 14 days. This large delay in swelling is likely to be due to both a denser (in shell) and deeper (in core, for the higher chemical gradient) amount of crosslinking. In this case, in fact, no relevant effects of calcium carbonate appeared.
The effects of post-treatment in a high molarity CaCl2 solution also had an important effect on the adhesion between fibers, as patches were more consolidated and resistant to handling. For this latter reason, together with it being less of a threat for cell viability (compared to internal gelation), this method was preferred for its increased fiber stability.
Interestingly, a very different mode of behavior was observed when post-treated patches were aged in complete medium (Figure 5b). Here, alginate patches lost a considerable percent of their weight (around 30%) within the first hour. After this initial contraction, a weight increase was observed for up to 7 days, followed by a progressive loss. As the swelling of ionic gels is controlled by the osmotic pressure in the gel and the elastic reaction of its network [43], it is not surprising to observe different behaviors in volume change after its immersion in solutions with different ionic strengths. In calcium alginate gels, in particular, swelling and degradation are regulated on an exchange mechanism between cross-linked Ca 2+ ions and Na + ions in the ageing media. When this exchange involves Ca 2+ that are bound to COO − groups of polymannuronate blocks, the resulting Contrarily, HA did not have the same effect at both of the concentrations chosen for blending (0.1% and 0.2% (w/v), Figure 3c) [40,41]. Due to the high molecular weight, HA was added in at lower percentages, and the increase in viscosity at room temperature was less pronounced (Figure 4a).
Rheological measurements (Figure 4) also showed a distinct influence of temperature on the viscosity changes in both blends. While the alginate curve was substantially unchanged, the addition of both gelatin and HA caused a substantial increase in the viscosity at room temperature, while the effect was significantly less noticeable at 37 • C, where the curves of instantaneous viscosity were largely overlapped (Figure 4b).

Microfiber Swelling and Weight Loss
Swelling and weight loss of microfibers in PBS and in the cell culture medium at 37 • C for up to 21 days are shown in Figure 5. Plain alginate patches (Figure 5a,b) without any further crosslinking lost the majority of their weights within the first 48 h.
Bioengineering 2019, 6, x FOR PEER REVIEW 9 of 13 chain relaxation favors swelling, while degradation begins when egg-box-forming Ca 2+ ions in polyguluronate blocks start to exchange with Na + [44]. Accordingly, the different behaviors in swelling and weight loss in PBS and the complete media can be explained by the differences in the types and concentrations of the solutes. As the difference in weight loss stands out when comparing the results in Figure 5a and 5b, its implications for the cell release profiles should be taken into account.
In Figure 5c, the swelling profile of blended hydrogel is shown. As observed in plain alginate Based on the rapidity of weight loss and the degree of swelling, it is reasonable to assume that, due to the low concentration of CaCl 2 a weakly cross-linked shell forms around a nearly liquid core [42]. As the shell breaks because of mechanical stress caused by swelling, the release of the liquid core accounts for the steep weight loss. Accordingly, when CaCO 3 is added to the alginate solution to create a denser core, a higher persistence of fibers is observed, and the greatest weight loss takes place between 7 and 14 days. When the patches underwent a post treatment by immersion in concentrated CaCl 2 solution (150 mM), a considerably higher PBS stability was observed, and swelling was still prevailing over degradation after 14 days. This large delay in swelling is likely to be due to both a denser (in shell) and deeper (in core, for the higher chemical gradient) amount of crosslinking. In this case, in fact, no relevant effects of calcium carbonate appeared.
The effects of post-treatment in a high molarity CaCl 2 solution also had an important effect on the adhesion between fibers, as patches were more consolidated and resistant to handling. For this latter reason, together with it being less of a threat for cell viability (compared to internal gelation), this method was preferred for its increased fiber stability.
Interestingly, a very different mode of behavior was observed when post-treated patches were aged in complete medium (Figure 5b). Here, alginate patches lost a considerable percent of their weight (around 30%) within the first hour. After this initial contraction, a weight increase was observed for up to 7 days, followed by a progressive loss. As the swelling of ionic gels is controlled by the osmotic pressure in the gel and the elastic reaction of its network [43], it is not surprising to observe different behaviors in volume change after its immersion in solutions with different ionic strengths. In calcium alginate gels, in particular, swelling and degradation are regulated on an exchange mechanism between cross-linked Ca 2+ ions and Na + ions in the ageing media. When this exchange involves Ca 2+ that are bound to COO − groups of polymannuronate blocks, the resulting chain relaxation favors swelling, while degradation begins when egg-box-forming Ca 2+ ions in polyguluronate blocks start to exchange with Na + [44].
Accordingly, the different behaviors in swelling and weight loss in PBS and the complete media can be explained by the differences in the types and concentrations of the solutes. As the difference in weight loss stands out when comparing the results in Figure 5a,b, its implications for the cell release profiles should be taken into account.
In Figure 5c, the swelling profile of blended hydrogel is shown. As observed in plain alginate samples, a significant degree of weight loss (around 30%) was measured within the first few hours of incubation, for the three types of microfibers (alginate, alginate/gelatin 1.5% and alginate/HA 0.2%). After this initial contraction, the alginate microfibers started to swell, and they increased in weight for up to 7 days, and they decreased again thereafter, to reveal a progressive dissolution of fibers. Although it occurred to different extents, the sequence of contraction, swelling, and dissolution was observed for all types of microfibers.

Cell Encapsulation in Alginate Microfibers
Microfibers for cell embedding were produced using a 2% (w/v) alginate solution with the addition of 1.5% (w/v) or 0.2% (w/v) of gelatin and HA, respectively. Under these conditions, embedded cells were distributed as single cells uniformly along the microfibers, as shown in the optical micrographs (Figure 6a-c).
According to staining that was performed shortly after encapsulation (Figure 6d-f), the process allows for a good degree of viability to be preserved in all materials (75 ± 16% for alginate/gelatin blend, 71 ± 6% for alginate/HA blend and 79 ± 6% for plain alginate).
Over longer time spans, alginate-based microfibers were also confirmed to offer an adequate environment for the survival of embedded cells, as demonstrated from Alamar Blue ® results (Figure 6g). A progressive increase in fluorescence intensity is observed until day 8, but this is unchanged at the following time point. If this result is compared with the cell release profile (Figure 6h), it can be noticed that a large number of cells are actually released between day 8 and 10. As a consequence, proliferation and Alamar Blue ® reduction rely only on a lower number of cells. For all of the formulations, the released cells appeared to be viable, and they were well-adhered to the bottom of the well (Supplementary materials- Figure S2). Over longer time spans, alginate-based microfibers were also confirmed to offer an adequate environment for the survival of embedded cells, as demonstrated from Alamar Blue ® results ( Figure  6g). A progressive increase in fluorescence intensity is observed until day 8, but this is unchanged at the following time point. If this result is compared with the cell release profile (Figure 6h), it can be noticed that a large number of cells are actually released between day 8 and 10. As a consequence, proliferation and Alamar Blue ® reduction rely only on a lower number of cells. For all of the formulations, the released cells appeared to be viable, and they were well-adhered to the bottom of the well (Supplementary materials- Figure S2).

Conclusions
Designing a hydrogel scaffold for the in situ release of embedded cells raises many challenges, especially in terms of the compatibility of the fabrication with cell survival, adequate mass exchange, and the tuning of degradation profiles. For some types, however, the fiber-encapsulation system that has been designed in this work appears to offer some effective solutions.
Despite its simplicity (it can be built in a short period time, with readily available, inexpensive components), the system that has been designed in this study allows for the rapid (about 3 min) fabrication of large, cell-loaded fibrous scaffolds. The distribution of cells is very regular and homogenous within the fibers and throughout the scaffold. Furthermore, the two-step crosslinking process, by consolidating bonding between the fibers, results in cohesive, easy-to-handle scaffolds.
In the fibrous patch, only a thin layer of material separates the cells from the environment, and a uniform network of macro-pores is created in the structure as the fibers assemble. This favorable architecture, according to the viability results, appears to be a large benefit in terms of mass-exchange and cell survival, compared to bulk hydrogels.
In addition, the flow-circuit system demonstrated a significant degree of flexibility in terms of material composition, as fiber formation was possible for a relatively large range of parameters. As plain alginate might not always represent the ideal material [45], blending fiber-forming alginates with other molecules or macromolecules appears to be an interesting option for reducing alginate

Conclusions
Designing a hydrogel scaffold for the in situ release of embedded cells raises many challenges, especially in terms of the compatibility of the fabrication with cell survival, adequate mass exchange, and the tuning of degradation profiles. For some types, however, the fiber-encapsulation system that has been designed in this work appears to offer some effective solutions.
Despite its simplicity (it can be built in a short period time, with readily available, inexpensive components), the system that has been designed in this study allows for the rapid (about 3 min) fabrication of large, cell-loaded fibrous scaffolds. The distribution of cells is very regular and homogenous within the fibers and throughout the scaffold. Furthermore, the two-step crosslinking process, by consolidating bonding between the fibers, results in cohesive, easy-to-handle scaffolds.
In the fibrous patch, only a thin layer of material separates the cells from the environment, and a uniform network of macro-pores is created in the structure as the fibers assemble. This favorable architecture, according to the viability results, appears to be a large benefit in terms of mass-exchange and cell survival, compared to bulk hydrogels.
In addition, the flow-circuit system demonstrated a significant degree of flexibility in terms of material composition, as fiber formation was possible for a relatively large range of parameters. As plain alginate might not always represent the ideal material [45], blending fiber-forming alginates with other molecules or macromolecules appears to be an interesting option for reducing alginate quantities in favor of metabolically degradable components, instructions for cell behavior or tuning for cell release [42].
For all of the above-mentioned reasons, the developed fiber-encapsulating system appears to be a very powerful platform for in vivo cell delivery in regenerative medicine, but also, more generally, for in vitro cell culturing. For this latter technique in particular, a simple, widely available and effective technique for preparing effective cell-loaded scaffolds is highly desirable, as it represent an essential tool in the development of 3D cell cultures and more reliable in vitro models for many applications.
Funding: No financial support was received for this research.