Ca-Alginate-PEGMA Hydrogels for In Situ Delivery of TGF- β Neutralizing Antibodies in a Mouse Model of Wound Healing

: Hydrogels provide effective alternatives for drug delivery when therapeutics cannot be applied directly to a wound, or if adverse effects are associated with systemic administration. However, drug delivery vehicles need to be biocompatible and biodegradable and exhibit sufﬁcient mechanical strength to withstand handling and different physiological conditions, such as those encountered during topical administration of a therapeutic. Wound healing can be divided into three phases stimu-lated by transforming growth factor-beta (TGF- β ) and, subsequently, targeted therapeutics have been developed to inhibit this cytokine for the treatment of chronic wounds and to prevent scarring. In this study, the capacity of calcium alginate hydrogels plasticized with poly(ethylene glycol) methyl ether methacrylate (PEGMA) to deliver anti-TGF- β antibodies (1D11.16.8) to a wound was investigated in situ. Three levels of antibodies, 10, 50, and 100 µ g, were loaded into calcium-alginate-PEGMA hydrogels and evaluated in an excisional wound model in mice. Hydrogels containing 50 and 100 µ g 1D11.16.8 produced less inﬂammation, accompanied by a marked reduction in collagen deposition and cell inﬁltration. These ﬁndings demonstrate the capacity of calcium-alginate-PEGMA hydrogels to deliver larger proteins, such as antibodies, to the site of a wound. Contributions: Conceptualization, A.B.C.-C. and A.F.L.-N.; methodology, A.F.L.-N., T.C.-V., P.H.L.-F., A.B.C.-C., N.E.D.-M., R.E. and E.P.-C.; formal analysis, J.G.-B., T.C.-V., R.E. and P.H.L.-F.; investigation, J.G.-B., T.C.-V., P.H.L.-F.,


Introduction
Wound healing is a dynamic process comprised of three overlapping phases, including inflammation, proliferation, and matrix remodeling, where any imbalance can lead to aberrant tissue formation known as fibrosis [1]. Transforming growth factor-beta (TGF-β) is a cytokine that exists in mammals as three different isoforms (TGF-β1, 2, and 3) and plays critical roles in wound healing and fibrosis [2]. Although the three isoforms activate the same receptor complex, they have slight differences in the signal transduction pathway. TGF-β1 participates throughout the wound healing process, promoting epithelial cell cycle arrest, and with TGF-β2, recruiting fibroblast and immune cells and extracellular matrix (ECM) production [3,4], whereas TGF-β3 promotes epidermis migration and fetal scarless wounds [5,6]. The TGF-β signaling pathway is considered a promising target to improve wound healing outcomes in pathological wounds (such as hypertrophic scarring) or to prevent scarring in wounds produced by surgery or minor injuries [7]. Immunomodulatory treatments have been developed to target TGF-β signaling and prevent the action of this cytokine. Fresolimumab is one such treatment and a potent human monoclonal antibody that binds to and inhibits all isoforms of TGF-β. However, systemic administration of Fresolimumab is associated with adverse effects, such as keratoacanthomas, due to the complete neutralization of TGF-β [8,9]. To avoid adverse effects associated with systemic administration, therapies can be applied topically to elicit local effects. Hydrogels are one of the most attractive biomaterials for topical administration and are extremely useful when a therapy cannot be applied directly to a wound.
Polymeric matrices have been explored for the controlled release of proteins and other therapeutics, prolonging circulation half-life, and target-specific delivery [10,11]. One polymeric matrix is sodium alginate; a linear polysaccharide and copolymer derived from brown marine algae comprised of β-D-mannuronate (M) and α-L-guluronate (G) residues covalently linked in different alternating or random sequences, such as MMM, GGG, or MGM [12]. Alginate is used as a polymer in hydrogels because of its highly adsorptive capacity, high cost-effectiveness, biodegradability, and antibacterial characteristics [13]. Alginate hydrogels are also highly porous, contributing to the functionality of this matrix in wound dressings by keeping wounds moist without damaging newly formed tissue [14]. However, hydrogels based only on alginate exhibit poor structural stability that degrades further on contact with biological fluids due to loss of the crosslinker ion calcium (Ca 2+ ) [15]. To increase the handling and stability of alginate hydrogels, covalent or ionic crosslinking can be employed, or alginate can be combined with other biopolymers such as gelatin or chitosan [16][17][18]. Plasticizers are another excellent option to increase hydrogel stability because they reduce intermolecular forces between polymer chains, decrease brittleness, and increase flexibility, toughness, traction, and resistance; however, plasticizers also compromise the porosity of the resultant gel [19].
Recently, our group reported the impact of poly(ethylene glycol) methyl ether methacrylate (PEGMA) as a plasticizer in calcium alginate hydrogels. The addition of PEGMA created a spongious material composed of semispherical and interconnected 50-100 µm pores with increased stability in aqueous media and structural resistance to manipulation and bending [20]. To determine if Ca-alginate-PEGMA hydrogels (CAPH) could confer site-specific delivery of antibodies, a murine IgG1 pan-specific TGF-β neutralizing antibody, 1D11, was incorporated into CAPH [21]. The ID11 antibody was selected based on the capacity to neutralize the three isoforms of TGF-β and the implication of this cytokine in wound healing, and on previous studies reporting visible improvements in scarring, reduced infiltration of immune cells, less extracellular matrix (ECM) deposition of collagen fibers, and reduced vascularity observed following neutralization of TGF-β [22][23][24]. Therefore, the capacity of CAPH to release TGF-β neutralizing antibodies at the site of a wound and reduce the fibrotic effects of TGF-β was investigated in this study using a mouse model of dorsal bilateral excisional wound healing. Wound contraction ratio, collagen content, and wound healing assessment were determined to evaluate the activity of 1D11 and effectiveness of CAPH as a delivery vehicle.

Preparation of Composite Hydrogels
The CAPH solution was prepared as described elsewhere [20]. Briefly, 0.375% (v/v) PEGMA was homogenized with 1.5% (w/v) sodium alginate and cross-linked with 0.75% (w/v) calcium chloride with intensive stirring until a smooth solution was obtained. For hydrogel formation, CAPH solution was mixed with 1, 5, 10, 50, and 100 µg pan-specific anti-TGF-β mouse monoclonal antibody 1D11.16.8 (BioxCell, Lebanon, NH, USA) diluted in Phosphate Buffered Saline (PBS), before being poured into a 96-well plate, frozen for 48 h at −20 • C, and lyophilized for another 24 h at −52 • C in a FreeZone 1-Liter Freeze dryer (Labconco, Kansas City, MO, USA). Empty hydrogels without antibody were also prepared and stored at 4 • C. In the remainder of this study, empty hydrogels are referred to as CAPH, while 1D11.16.8-loaded hydrogels are referred to as CAPH-1D11. For the in vitro assays described in Section 2.2, 0.1 µg of 1D11 antibody is enough to neutralize 20 pM of TGF-β (data are not shown), so hydrogels of 1 and 5 µg CAPH-1D11 were used, while 10, 50, and 100 µg CAPH-1D11 were explored in situ, as described in Section 2.3. The higher doses of 50 and 100 µg are to mimic the doses employed in previous works where neutralizing antibodies were injected [22,24,25].

HEK-Blue TGF-β SEAP Reporter Assay
The HEK-Blue TGF-β cell line (InvivoGen, San Diego, CA, USA) was used for in vitro assessment of TGF-β neutralization. Stimulation of these cells with TGF-β induces the Smad dependent pathway and secretion of secreted embryonic alkaline phosphatase (SEAP) into media that can be measured via QUANTI-Blue and spectrophotometry. Cells were maintained and assayed according to the manufacturer's protocol with modifications. Briefly, alginate hydrogels were incubated for 2 h in 1 mL Dulbecco's Modified Eagle Medium (DMEM) to release antibodies, then 2.5 × 10 4 cells (90 µL) were seeded into a 96-well plate before 20 pM (in 10 µL) recombinant human TGF-β1 (Peprotech, Cranbury, NJ, USA) was used to stimulate the cells. Next, 100 µL alginate hydrogels pre-conditioned media was added to the cells. Two activity controls included TGF-β treatment of cells with DMEM without hydrogels and cells incubated only with DMEM (without TGF-β). Cells were incubated for 24 h at 37 • C and 5% CO 2 . Media (10 µL) were transferred to a new plate and mixed with 90 µL QUANTI-Blue reagent and incubated for 1 h at 37 • C before absorbance was measured at 655 nm. The percentage of neutralization was estimated with the equation below, where absorbance of TGF-β control (A TGFβ ) was considered as 0% of neutralization (full effect of cytokine), and absorbance of media control without TGF-β (A media ) was considered as 100% of neutralization (no effect of cytokine).

Full-Thickness Excision Wound Model
Female BALB/c mice were housed individually in the Center for Research and Assistance in Technology and Design in the State of Jalisco A. C. (CIATEJ), maintained on a 12-h light/dark cycle, and allowed ad libitum access to food and water. Experimental conditions adhered to the requirements defined by the Guidelines of the Institutional Animal Care and Use Committee (CICUAL). All assays fulfilled the Mexican regulations NOM-062-ZOO-1999. The animal facility has SENASICA certification AUT-B-B1115-025.
Mice (23-26 g weight and 12 weeks old) were anesthetized with isoflurane before dorsal surfaces were shaved and bilateral surgical wounds performed under sterile conditions with aseptic and antiseptic techniques. Two circular full-thickness skin wounds (2 mm diameter) were created with a disposable biopsy punch on each side of the mouse dorsum to include the panniculus carnosus layer (Integra Miltex, York, PA, USA). The right dorsal wound of each mouse was treated with the hydrogel (i.e., CAPH, CAPH-1D11-10, CAPH-1D11-50, or CAPH-1D11-100) while the left side of the same animal was left untreated as the control.

Macroscopic Evaluation of Wound Healing
Body weight and general health were monitored throughout the experiment for 10 days. Wound healing was carefully monitored with digital photographs taken at days 0, 2, 4, 7, and 10, and by measuring wound diameter at each time-point. A semiquantitative four-point score-0 (none), 1 (scant), 2 (moderate), and 3 (abundant)-was used for evaluating macroscopic physiological healing parameters, including: exudation, re-epithelialization, papule, erythema, inflammation, granulation tissue, hemorrhage, and necrosis [26]. Re-epithelialization was scored as: (0) absent, bright-red wound; (1) moderate presence of epithelialization surrounding granulation tissue, pink wound; (2) the presence of epithelialization exceeds that of granulation tissue, pale wound; and (3) fully healed wound [27][28][29]. Inflammation of the wound was determined by the presence of tissue bulging accompanied by erythema, and scored as (0) absent, (1) scant presence in the wound surroundings, (2) moderate presence outside the edges of the wound, and (3) completely surrounding the wound [30]. Each parameter was presented as a global score calculated by averaging the scores of all evaluated time-points.

Histological Analysis
All mice were euthanized on day 10 with an intraperitoneal injection of sodium pentobarbital (120 mg/kg). The wounded area and 5 mm margin of surrounding intact skin were collected for RT-PCR and histological evaluation with hematoxylin and eosin (H&E) and Masson's trichrome (MT) stains. Samples were fixed in 10% formalin for 24 h before being embedded in a paraffin wax block and cross-sectioned (6-8 µm). H&E staining was observed under 100× magnification to evaluate re-epithelialization and inflammation (i.e., granulated tissue), while collagen deposits and fibrosis were visualized by MT staining (also under 100× magnification). Optical collagen density was quantified from MT-stained sections with FIJI/ImageJ (NIH, v 2.0.0), images were converted to RGB, and the blue channel was used to analyze the collagen fibers [31].

RNA Isolation, Reverse Transcription, and Real-Time PCR Analysis
RNA was isolated from skin samples using a tissue homogenizer and RiboZol reagent (Amresco LLC, Solon, OH, USA) according to manufacturer's instructions. cDNA was synthesized from 500 ng RNA using the RevertAid First Strand cDNA Synthesis Kit (Thermo Fisher Scientific, Inc., Waltham, MA, USA). Real-time PCR was performed on the resultant cDNA using EvaGreen 5X qPCR mix (qARTA Bio Inc., Carson, CA, USA) and 10 pmol/µL forward and reverse primers in a LightCycler 96 (Roche Diagnostics, Mannheim, Germany). The amplification conditions consisted of 1 cycle of initial denaturation at 95 • C for 15 min followed by 40 cycles of denaturation at 95 • C for 15 s, annealing at 56 • C for 20 s, and extension at 72 • C for 20 s. The primers used to amplify Transforming growth factor beta 1 (Tgfb1), alpha-smooth muscle actin (Acta2), and hypoxanthine phosphoribosyltransferase (Hprt) are shown in Table 1. Hprt was used as an internal control to normalize gene expression data. The relative quantities of mRNA expression were determined using the 2 −∆∆Ct method.

Statistical Analysis
All statistical analyses were performed using Prism 8.0 (GraphPad Software, Inc., San Diego, CA, USA). Data were expressed as mean ± Standard Error of the Mean (SEM). For HEK-Blue reporter cell assays, differences between multiple groups were evaluated by a one-way analysis of variance (ANOVA) followed by a Tukey's test. Wound closure in response to anti-TGF-β loaded CAPH (i.e., CAPH-1D11) was compared with CAPH by a two-way ANOVA, followed by a Dunnett's test. The differences observed between treated and untreated wounds following macroscopic evaluation of epithelialization and inflammation, collagen density, and real-time PCR analysis were determined by t-test. In all statistical comparisons, differences were deemed significant when p values < 0.05.

HEK-Blue TGF-β SEAP Reporter Cells Assay
Previous studies reported increased stability in CAPH compared to Ca-alginate hydrogels [20], along with the capacity of CAPH to store antibodies due to simple electrostatic interactions facilitated by PEGMA that can form acid-ether hydrogen bonds and create hydrophobic associations [32,33]. In the study reported here, neutralization of TGF-β by 1D11 antibodies released from hydrogels was evaluated in vitro and is presented in Figure  1. The findings show that CAPH-1D11 retained viability of 1D11 and enabled antibody release after being suspended in media for two hours. This period of time was determined previously using a control antibody, where a plateau of liberation was reached at two hours (data not shown). The results show that 1D11 was stable in solution, following lyophilization, and after being released from the hydrogel. However, the TGF-β neutralizing activity of 1D11 antibodies released from CAPH-1D11-1µg was approximately 70% and significantly lower than the lyophilized and solution 1D11 controls. It is possible that this reduced activity may be due to limited release of 1D11 from CAPH-1D11 after only two hours in media. Interestingly, CAPH without antibodies showed slight neutralizing activity of approximately 30%. Previous studies have reported that alginate can prevent TGF-β signaling by downregulating Smad2 phosphorylation and TGF-β expression [34][35][36]. However, calcium release could be another factor contributing to the observed neutralizing activity. Organista-Juárez et al. [37] showed in vitro using hepatic C9 cells and transfected HEK293 cells that exogenous administration of calcium decreases TGF-β dependent transcriptional activity through the calcium-sensing receptor (CaSR), interfering with Smad2 phosphorylation and inducing proteasomal degradation of Smad2.

Wound Contraction
To determine if CAPH-1D11 could retain the viability of 1D11 and enable antibody release in situ, CAPH and CAPH-1D11 were assessed in a mouse model of dorsal bilateral excisional wound healing [38][39][40] to observe the impact of TGF-β neutralization on wound healing parameters. Wound closure was evaluated for ten days to ensure a comprehensive assessment of the impact of TGF-β neutralization on wound healing. During this period, it was assumed wound healing would progress through the fibroblast and keratinocyte proliferation phase and enter the first stage of matrix remodeling (on day seven), characterized by ECM formation and collagen deposition [11,41]. Figure 2 illustrates the progress of wound closure over the course of the ten-day study. The findings show that the application of CAPH-1D11-10 resulted in the lowest wound diameter at day ten, while delays in wound closure were observed in response to CAPH-1D11-100. Overall, wound sizes did not vary significantly between groups at any experimental time point (Figure 2b). Expansion of the wound was observed in the first day and is often described in the early stages of excisional wound healing models as a result of tissue loosening [31,42].

Wound Contraction
To determine if CAPH-1D11 could retain the viability of 1D11 and enable release in situ, CAPH and CAPH-1D11 were assessed in a mouse model of dorsa excisional wound healing [38][39][40] to observe the impact of TGF-β neutralization o healing parameters. Wound closure was evaluated for ten days to ensure a comp assessment of the impact of TGF-β neutralization on wound healing. During th it was assumed wound healing would progress through the fibroblast and ker proliferation phase and enter the first stage of matrix remodeling (on day seven terized by ECM formation and collagen deposition [11,41]. Figure 2 illustrate gress of wound closure over the course of the ten-day study. The findings show application of CAPH-1D11-10 resulted in the lowest wound diameter at day t delays in wound closure were observed in response to CAPH-1D11-100. Overa sizes did not vary significantly between groups at any experimental time poin 2b). Expansion of the wound was observed in the first day and is often describ early stages of excisional wound healing models as a result of tissue loosening [ Macroscopic assessment of the wounds showed no papule, exudation, hem or necrosis, and granulation tissue was similar across all groups (data not show roscopic epithelialization and inflammation were also assessed (Figure 2c,d). T potent inhibitor of keratinocyte proliferation through the induction of G1 cell cy [43,44]. After treatment with CAPH-1D11-10 and CAPH-1D11-50, epithelializat increased, coinciding with a reversal in the proliferative arrest of keratinocytes moting epidermal recovery. These findings agree with a study by Mandapalli Dry-1D11 is a reconstituted antibody that was lyophilized and 1D11 is a soluble antibody without any drying. Each bar represents the mean ± SEM of 3 independent assays conducted in triplicate. Significance denoted by ** p < 0.01 and **** p < 0.0001.
Macroscopic assessment of the wounds showed no papule, exudation, hemorrhage, or necrosis, and granulation tissue was similar across all groups (data not shown). Macroscopic epithelialization and inflammation were also assessed (Figure 2c,d). TGF-β is a potent inhibitor of keratinocyte proliferation through the induction of G1 cell cycle arrest [43,44]. After treatment with CAPH-1D11-10 and CAPH-1D11-50, epithelialization scores increased, coinciding with a reversal in the proliferative arrest of keratinocytes and promoting epidermal recovery. These findings agree with a study by Mandapalli et al. [45], where treatment with a TGF-β siRNA or crocodile oil accelerated re-epithelialization and reduced TGF-β1 and Smad3 protein and mRNA levels [46]. However, in the study presented here, epithelialization scores of wounds treated with CAPH-1D11-100 were similar to control wounds. This effect was possibly due to the negative impact of excessive TGF-β neutralization in the wound environment, resulting in non-healing chronic wounds where the ECM is not organized for efficient keratinization [47,48]. This assumption may also explain the delay in wound closure observed following CAPH-1D11-100 treatment.
In the inflammation phase of wound healing, TGF-β has dual roles as a pro-inflammatory stimulus early in the phase and as a potent anti-inflammatory chemoattractant of immune cells, such as neutrophils or monocytes, towards the end of this phase [49]. In Figure 2d, reduced inflammation scores in wounds following treatment with CAPH-1D11 may be explained by a decrease in immune cell infiltration through neutralization of the chemoattractant activity of TGF-β. also explain the delay in wound closure observed following CAPH-1D11-100 treatment.
In the inflammation phase of wound healing, TGF-β has dual roles as a pro-inflammatory stimulus early in the phase and as a potent anti-inflammatory chemoattractant of immune cells, such as neutrophils or monocytes, towards the end of this phase [49]. In Figure  2d, reduced inflammation scores in wounds following treatment with CAPH-1D11 may be explained by a decrease in immune cell infiltration through neutralization of the chemoattractant activity of TGF-β. Figure 2. Wound contraction and assessment in response to application of Ca-alginate-PEGMA hydrogels with and without pan-specific anti-TGF-β mouse monoclonal antibody 1D11.16.8, evaluated over ten days. (a) Representative photographs of excisional wounds before and after application of Ca-alginate-PEGMA hydrogel (CAPH) loaded without or with 10, 50, and 100 μg anti-TGF-β antibody (CAPH-1D11-10, CAPH-1D11-50, and CAPH-1D11-100, respectively), evaluated over 10 days. (b) Comparison of wound size over 10 days with initial wound size being 2 mm for all groups. Graphic presented as the mean of wound diameter size in mm ± SEM, n = 5/group. (c) Epithelization. (d) Inflammation score of mice treated with CAPH with and without anti-TGF-β antibody. A four-point score was used (with 0 score (none), 1 score (scant), 2 score (moderate), and 3 score (abundant)), and is presented as a mean ± SEM. n = 5/group. Significance is denoted as * p < 0.05 and ** p < 0.01. Figure 2. Wound contraction and assessment in response to application of Ca-alginate-PEGMA hydrogels with and without pan-specific anti-TGF-β mouse monoclonal antibody 1D11.16.8, evaluated over ten days. (a) Representative photographs of excisional wounds before and after application of Ca-alginate-PEGMA hydrogel (CAPH) loaded without or with 10, 50, and 100 µg anti-TGF-β antibody (CAPH-1D11-10, CAPH-1D11-50, and CAPH-1D11-100, respectively), evaluated over 10 days. (b) Comparison of wound size over 10 days with initial wound size being 2 mm for all groups. Graphic presented as the mean of wound diameter size in mm ± SEM, n = 5/group. (c) Epithelization. (d) Inflammation score of mice treated with CAPH with and without anti-TGF-β antibody. A four-point score was used (with 0 score (none), 1 score (scant), 2 score (moderate), and 3 score (abundant)), and is presented as a mean ± SEM. n = 5/group. Significance is denoted as * p < 0.05 and ** p < 0.01.

Histological Observations
Histological analysis of wounds at day ten was performed by H&E and MT staining. In Figure 3, staining revealed the formation of thin epidermal layers in all samples. Furthermore, the application of CAPH-1D11-50 and CAPH-1D11-100 produced epidermal layers with irregular appearances compared to other groups. Previous studies have shown that alginate based wound dressings can promote fibroblast proliferation and collagen Appl. Sci. 2021, 11, 1164 8 of 12 deposition [35,50,51]. In this study, the application of CAPH combined with a low anti-TGF-β dose, such as CAPH-1D11-10, improved wound epithelialization (evidenced by a tighter epidermis), but without loss of collagen deposition similar to CAPH. However, experimental observations should be performed for longer than ten days to determine if CAPH-1D11-10 could prevent scarring.

Histological Observations
Histological analysis of wounds at day ten was performed by H&E and MT staining. In Figure 3, staining revealed the formation of thin epidermal layers in all samples. Furthermore, the application of CAPH-1D11-50 and CAPH-1D11-100 produced epidermal layers with irregular appearances compared to other groups. Previous studies have shown that alginate based wound dressings can promote fibroblast proliferation and collagen deposition [35,50,51]. In this study, the application of CAPH combined with a low anti-TGF-β dose, such as CAPH-1D11-10, improved wound epithelialization (evidenced by a tighter epidermis), but without loss of collagen deposition similar to CAPH. However, experimental observations should be performed for longer than ten days to determine if CAPH-1D11-10 could prevent scarring.  Two excisional wounds were created on each dorsal side before Ca-alginate-PEGMA hydrogels (CAPH), or CAPH loaded with 10, 50, and 100 µg anti-TGF-β antibody (CAPH-1D11-10, CAPH-1D11-50, and CAPH-1D11-100, respectively) were applied to the right side. The wound on the left side received only standard disinfection treatment (Control). Micrographs of stained tissues were captured under 100X magnification. Application of CAPH-1D11-10 produced a tighter epidermis than other treatments (black arrowheads), while treatment with CAPH-1D11-50 produced irregular epidermal layers. Application of CAPH-1D11-100 produced epidermis and collagen fragmentation (white arrowheads and black arrows, respectively). Edematous zones (asterisks) are also indicated in CAPH-1D11-50 and CAPH-1D11-100 treated wounds. (b) Quantitative analysis of collagen density from blue channel of MT-stained sections. CAPH-1D11-100 treated wounds exhibit the lowest collagen density, presented as a mean ± SEM. n = 5/group. Significance is denoted as * p < 0.05 and ** p < 0.01.
In fibroblasts, the main promoter of collagen synthesis is TGF-β [52]. In Figure 3, MT staining of collagen fibers (in blue) revealed advanced collagen synthesis and remodeling with color intensity proportional to levels of deposited collagen [31,53]. Wounds treated with CAPH-1D11-100 showed reduced collagen deposition (Figure 3b) and fragmented epidermal layers. In wound healing, TGF-β not only promotes collagen synthesis, but is also responsible for preventing collagen degradation by regulating the synthesis of several ECM proteases and inducing the secretion of specific protease inhibitors [54,55]. The appearance of fragmented collagen following the application of CAPH-1D11-50 and CAPH-1D11-100 could be attributed to enhanced collagen protease activity caused by TGFβ neutralization. However, the 1D11 antibody's affinity is biased towards TGF-β3 [56], the denominated "scarless" isoform of TGF-β. Lu et al. [24] described that a better response in wound healing is more associated with the temporary effect of TGF-β than with the specific neutralization of an isoform. They showed that neutralization of the three isoforms of TGF-β on the same day of wounding showed delayed wound healing without a reduction in hypertrophic markers. However, neutralization of TGF-β one-week post-wounding improved the hypertrophy. This effect correlates with the impaired wound healing showed in CAPH-1D11-100, which was administered the same day of wounding.

Reverse Transcription and Real-Time PCR Analysis
Reverse transcription and real-time PCR were used to measure mRNA levels of TGF-β and ACTA2 genes at day ten ( Figure 4). TGF-β positively regulates its own expression in many cells [57], while TGF-β activation of fibroblasts to myofibroblast promotes expression of ACTA2 [58]. In this study, mRNA levels of Tgfb1 and Acta2 genes were significantly lower in lesions treated with CAPH-1D11-100 compared to control lesions. These findings indicate that CAPH-1D11-100 can release viable TGF-β neutralizing antibodies into wounds. Decreased TGF-β mRNA levels were also observed in response to CAPH, as previously described by Lee et al. (2009), but were not statistically different to the control. of collagen density from blue channel of MT-stained sections. CAPH-1D11-100 treated wounds exhibit the lowest collagen density, presented as a mean ± SEM. n = 5/group. Significance is denoted as * p < 0.05 and ** p < 0.01.
In fibroblasts, the main promoter of collagen synthesis is TGF-β [52]. In Figure 3, MT staining of collagen fibers (in blue) revealed advanced collagen synthesis and remodeling with color intensity proportional to levels of deposited collagen [31,53]. Wounds treated with CAPH-1D11-100 showed reduced collagen deposition (Figure 3b) and fragmented epidermal layers. In wound healing, TGF-β not only promotes collagen synthesis, but is also responsible for preventing collagen degradation by regulating the synthesis of several ECM proteases and inducing the secretion of specific protease inhibitors [54,55]. The appearance of fragmented collagen following the application of CAPH-1D11-50 and CAPH-1D11-100 could be attributed to enhanced collagen protease activity caused by TGF-β neutralization. However, the 1D11 antibody's affinity is biased towards TGF-β3 [56], the denominated "scarless" isoform of TGF-β. Lu et al. [24] described that a better response in wound healing is more associated with the temporary effect of TGF-β than with the specific neutralization of an isoform. They showed that neutralization of the three isoforms of TGF-β on the same day of wounding showed delayed wound healing without a reduction in hypertrophic markers. However, neutralization of TGF-β one-week postwounding improved the hypertrophy. This effect correlates with the impaired wound healing showed in CAPH-1D11-100, which was administered the same day of wounding.

Reverse Transcription and Real-Time PCR Analysis
Reverse transcription and real-time PCR were used to measure mRNA levels of TGFβ and ACTA2 genes at day ten ( Figure 4). TGF-β positively regulates its own expression in many cells [57], while TGF-β activation of fibroblasts to myofibroblast promotes expression of ACTA2 [58]. In this study, mRNA levels of Tgfb1 and Acta2 genes were significantly lower in lesions treated with CAPH-1D11-100 compared to control lesions. These findings indicate that CAPH-1D11-100 can release viable TGF-β neutralizing antibodies into wounds. Decreased TGF-β mRNA levels were also observed in response to CAPH, as previously described by Lee et al. (2009), but were not statistically different to the control. . Reverse transcription and real-time PCR of transforming growth factor beta 1 (Tgfb1) and alpha-smooth muscle actin (Acta2) genes in skin lesions. mRNA levels of Tgfb1 and Acta2 genes were measured in skin lesions 10 days after treatment with Ca-alginate-PEGMA hydrogel (CAPH) or CAPH loaded with 10 or 100 μg 1D11.16.8 antibody (CAPH-1D11-10 and CAPH-1D11-100, respectively). Data were normalized to hypoxanthine phosphoribosyltransferase (HPRT) mRNA and presented as mean of fold induction (n = 5/group) ± SEM. Significance denoted as * p < 0.05 and *** p < 0.001.

Conclusions
In this study, a mouse model of dorsal bilateral excisional wound healing confirmed the capacity of Ca-alginate-PEGMA hydrogels to store, transport, and release TGF-β neutralizing antibodies at the site of a wound. Macroscopic assessment of the treated wounds revealed that wound sizes did not vary significantly between groups, and there was no evidence of papule, hemorrhage, or necrosis. Erythema surrounding each wound was also similar across all groups. Macroscopic epithelialization and inflammation were also assessed, revealing significantly reduced inflammation scores following application of all CAPH-1D11 treatments, while epithelialization significantly increased followed treatment with CAPH-1D11-10 and CAPH-1D11-50. The observations also supported a concomitant inhibition of fibrotic factors, such as collagen deposition and fibroblast to myofibroblast transition. Overall, these findings suggest that Ca-alginate-PEGMA hydrogels possess sufficient mechanical strength for the topical delivery of therapeutics. However, further studies are needed to explore the impact of Ca-alginate-PEGMA hydrogels loaded with anti-TGF-β antibodies on wound healing long-term.