Next Article in Journal
Approaches in Animal Proteins and Natural Polysaccharides Application for Food Packaging: Edible Film Production and Quality Estimation
Previous Article in Journal
Recent Progress in Antimicrobial Strategies for Resin-Based Restoratives
Previous Article in Special Issue
Effect of Printing Parameters on Dimensional Error, Surface Roughness and Porosity of FFF Printed Parts with Grid Structure
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

PCL/Andiroba Oil (Carapa guianensis Aubl.) Hybrid Film for Wound Healing Applications

by
Debora F. Silva
1,
Klinsmann T. Lima
2,
Gilmara N. T. Bastos
2,
Johnatt Allan R. Oliveira
3,
Luís Adriano S. do Nascimento
1,
Carlos Emmerson F. Costa
1,
Geraldo N. R. Filho
1,
Viktor O. C. Concha
4 and
Marcele F. Passos
1,*
1
Laboratory of Oils of the Amazon, Federal University of Pará, Belém 66075-750, PA, Brazil
2
Laboratory of Neuroinflammation, Federal University of Pará, Belém 66075-110, PA, Brazil
3
Department of Nutrition, Federal University of Pará, Belém 66073-040, PA, Brazil
4
Department of Chemical Engineering, Federal University of São Paulo, Diadema 09913-030, SP, Brazil
*
Author to whom correspondence should be addressed.
Polymers 2021, 13(10), 1591; https://doi.org/10.3390/polym13101591
Submission received: 4 February 2021 / Revised: 4 March 2021 / Accepted: 13 March 2021 / Published: 14 May 2021
(This article belongs to the Special Issue Porous Polymer Scaffolds and Their Applications)

Abstract

:
Developing a biomimetic material to wound care is an emerging need for the healing process. Poly (ε-caprolactone) (PCL) is a polymer with the necessary dressing’s requirements often used in medicine. Their surface, physic-chemical and biological properties can be modified by adding bioactive compounds, such as andiroba seed oil (Carapa guianensis). This Amazonian natural plant has medicinal and pharmacological properties. For this purpose, PCL polymeric films incorporated with andiroba oil were investigated. The synthesis of hybrids materials was carried out in the solvent casting method. Thermal properties were evaluated using thermogravimetric analysis (TGA/DTGA) and differential scanning calorimetry (DSC). The solvent type on the surface and hydrophilicity of samples was studied using a scanning electron microscope (SEM). Additionally, contact angle measurements, functional groups analysis, fluid absorption capacity, and cell viability were performed. The results demonstrated the influences of andiroba oil under the morphology and thermal properties of the polymeric matrix; the hydrophilicity of the hybrid film obtained by acetic acid was reduced by 13%; the porosity decreased as the concentration of oil increased, but its higher thermal stability. The L929 cell line’s proliferation was observed in all materials, and it presented nontoxic nature. It was demonstrated the ability of PCL hybrid film as a matrix for cell growth. Then, the materials were proved potential candidates for biomedical applications.

Graphical Abstract

1. Introduction

Researchers have aroused interest in using biomimetic dressings, with bioactive properties and as carriers of medicines, mainly for exudative wounds or resulting from prolonged pressure on the skin [1,2]. These sterile therapeutics covers may interact and imitate harmful tissue, reducing the time for treating the lesion, with cell regeneration and proliferation in the affected region; they have adequate porosity and fluid absorption capacity. Dressings must also avoid complications for the patient, differentiating themselves in physical and chemical terms to meet different biological and mechanical needs. Thus, they need to be easy to apply and remove; they must have nontoxic, nonallergenic, and biocompatible properties.
Hydrogels and silicones are commonly used as smart dressings for exudative wounds due to the high potential for swelling [3,4]. However, they have been causing inflammation and harmful monomers’ release during treatment [5,6]. Thus, the search for bioactive materials with good biological properties and low-cost becomes essential. Moreover, technological advances in wound dressings are no longer restricted to producing materials with static purposes of mechanical protection and gas exchange through the membrane. The transport of therapeutic compounds such as hormones, anticancer agents, drugs, and other assets has enabled patients to be more independent and practical [7,8,9,10].
Poly (ε-caprolactone) (PCL) has been applied in conjunction with other additives for use in biomedical applications. It is an acyclic polyester with excellent elastic, biodegradable, and bioabsorbable properties [11]. The Food and Drug Administration has approved PCL to use in drug delivery devices and various structures as nanospheres, nanofibers, foams, meshes, membranes, and scaffolds [12,13]. Furthermore, as a temporary substitute (scaffold) of the cell-matrix, the PCL allows cell adhesion and stimulates new ones’ growth [14]. Muwaffak et al. [15] produced polycaprolactone filaments interspersed with antimicrobial metals using a hot-melt extruder and 3D printing techniques, obtaining potent antibacterial dressings. Poly (ε-caprolactone) nanofibers coated with chitosan and gamma oryzanol also showed results for wound healing in mice [16]. On the other hand, incorporating vegetable oils in hybrid nanocarriers has decreased cytotoxicological effects and increased the dressing’s antimicrobial properties [17]. Cardoso et al. [18] evaluated the effect on molar mass distribution of jojoba and andiroba oil encapsulation by miniemulsion polymerization. Uscátegui et al. [19] studied the cytotoxicity and antibacterial activity of polyurethanes based on modified castor oil and polycaprolactone. However, few studies on the intercalation of vegetable oils under alpha-hydroxy ester polymeric matrices and their potential for wound healing have been discussed in the literature via solvent casting technique. The possibility of adding bioactive natural compounds to PCL molecular chains represents a springboard to produce new dressings with different therapeutic qualities and low-cost.
Several oils and extracts of medicinal plants and dressings of animal origin [20] are currently used in regenerative medicine to stop bleeding, to reduce the effects of contamination on injuries, to modulate the healing process, and to promote better esthetic results with reduced scar formation [21,22]. The andiroba (Carapa guianensis) seed oil is widely used in traditional medicine for its pharmacological properties. It is extracted from the seed and has anti-inflammatory, analgesic, antiallergic, antimicrobial, and healing properties, which are derived from its biologically active constituents such as limonoids and triterpenes [23,24,25]. Thus, the present study aimed to develop PCL films incorporated with andiroba oil (hybrids) like a scaffold to the wound healing process, using the solvent casting technique. This technique is commonly used to synthesize PCL, and PCL-based films for wound dressings purposes, where porous and bio-resorbable materials have been obtained in an accessible manner [26]. It does not require specific equipment and is suitable for the large-scale production of low cytotoxicity and cost wound dressings [27]. Here, we focus on PCL’s hybridization, using andiroba oil as an active compound to create a multifunctional wound dressing. The objective was to assess these materials’ thermal, surface, and biological properties, to a more natural and straightforward treatment.

2. Materials and Methods

2.1. Materials

Poly (ε-caprolactone) (PCL) (Mn = 45,000 and δ = ((9.65 cal cm−3)1/2)), dimethyl sulfoxide, phosphate-buffered saline (PBS) and amphotericin B were supplied by Sigma-Aldrich (Barueri, Brazil). Andiroba oil (AO) was provided by Amazon Oil (Belém, Brazil). Its physic-chemical characteristics are listed in Table 1. Acetone ((δ* = 9.77 (cal cm−3)1/2), acetic acid ((δ* = 10.5 cal cm−3)1/2) and dichloromethane (δ* = 9.70 (cal cm−3)1/2) were purchased from Neon Comercial (Belém, Brazil). Penicillin-streptomycin was supplied by Nacalai Tesque (Kyoto, Japan). The L929 cell line was obtained from American Type Culture Collection (Rockville, MD, USA). *δ = solubility parameter [28,29,30].

2.2. Fabrication of PCL Casting Films

PCL hybrids films were obtained from the solvent casting technique (Figure 1), using different solvents (acetic acid, acetone, and dichloromethane). The polymer solution concentration was kept constant at 5% w/v. Andiroba oil was added to the polymeric solution at room temperature until homogenized, without phase separation. Two concentrations were evaluated to hybrids films, 1.7% w/w and 2.7% w/w (g of andiroba oil/g of PCL). After 10 min stirring, the mixture (PCL solution/oil) was applied to the cylindrical silicone mold, with a volume constant (5 mL). The films were dried for one week at room temperature and another four days in a vacuum oven at 40 °C to remove the solvent’s residual traces. PCL without oil was synthesized as a control film under the same conditions. Table 2 summarizes the compositions of each sample.

2.3. Fatty Acid Composition of Andiroba Oil (Carapa guianensis)

The fatty acid composition of andiroba oil was determined by the American Oil Chemists’ Society’s official methods [31,32]. It was used a Varian CP 3800 gas chromatograph system (GC) (São Paulo, Brazil), equipped with a capillary column Agilent (30 m × 0.32 mm CP WAX 52 CB) (Santa Clara, CA, USA) and a hydrogen flame ionization detector (Varian, São Paulo, Brazil). The analysis was performed under the following conditions: helium as a carrier gas, adjusted at a flow rate of 1 mL min−1; programmed temperature to ramp from 50–250 °C at 10 °C. min−1; detector temperature set to 270 °C; split mode injection for 1 µL (1:10); and injector temperature at 250 °C. The quantitative data were performed by peak area normalization. The fatty acid methyl esters were identified by comparing their retention indices with fatty acid methyl ester standards (Table 3). The analyses were performed in triplicate.

2.4. Thermal Analysis

A Shimadzu DTG-60H thermogravimetric analyzer (TGA) (Kyoto, Japan) was used to evaluate samples’ thermal stability. Approximately 5–8 mg of samples were weighed into an aluminum pan. The experiments were done from 25 to 550 °C at a heating rate of 10 °C. min−1, under dynamic nitrogen atmosphere (50 mL min−1). The glass transition temperature (Tg) and melting temperature (Tm) were determined using a differential scanning calorimeter, model DSC60 plus (Kyoto, Japan, Shimadzu Corporation). The specimens were scanned from 35 to 250 °C, with isotherms for 5 min, cooling from 250 to 35 °C, isothermal for 5 min, and heated again from 35 to 250 °C. The films’ thermal history was eliminated in heating and cooling consecutive programs, and the second run measured the transition temperatures. TGA and DSC thermograms were evaluated by Origin pro 9.1 software (Originlab Corporation, Northampton, MA, USA). Enthalpy of fusion (ΔHm) was determined by the area under the endothermic peak (integrating the melting peak below the baseline). The degree of crystallinity (xc) of films was calculated using Equation (1)
x c   % = Δ H m Δ H m φ   ×   100
where ΔHm, ΔHm, and φ are the experimental endothermic enthalpy of fusion (J g−1), the theoretical enthalpy of 100% crystalline PCL, taken 136.5 J g−1 [33] and the weight fraction of the PCL.

2.5. Fourier-Transform Infrared Spectroscopy (FTIR)

FTIR absorption spectra were recorded using a Agilent spectrophotometer, model cary 630 (Hanover, Germany), equipped with ATR to evaluate specimens’ vibrational mode. IR analysis was carried out in the range from 4000 to 650 cm−1, with a resolution of 8 cm−1 and 32 scans.

2.6. Surface Characterization

The surface morphology (porosity and roughness) was investigated using a Jeol JSM-6610LV scanning electron microscope (SEM) (Tokyo, Japan). The samples were covered with a thin gold layer (Denton Vacuum, model Desk V, Moorestown, NJ, USA) and evaluated with accelerating voltage 1 kV and magnification 1000×. The hydrophilicity property of polymer film was investigated using angle contact angle measurements. The sessile drop method was used at room temperature. The average angle of deionized water droplets on the material’s surface was obtained from six measurements for each sample. Water drop images were recorded using Nikon b500 16 mp/40× photographic camera and analyzed by Image J. software. The thickness of the pieces was determined using the micrometer.

2.7. In Vitro Tests

2.7.1. 3D Cell Culture

Fibroblast lineage cells (L929) (Rockville, MD, USA) were incubated in 96-well plates at a density of 2 × 104 cells/well. The experiment was performed in an incubator at 37 °C, humidified, 5% CO2/95% air environment at 24 h. The Dulbecco’s modified Eagle’s medium (DMEM) with 10% bovine fetal serum (SBF)(GibcoTM, Sao Paulo, Brazil), contained 100 units/mL penicillin, and 50 μg/mL streptomycin was used for cell nutrition and maintenance.

2.7.2. Cell Viability Assay

The films were placed at the bottom of the well covering all surfaces, and cell viability was performed using the 3-(4,5-dimethyl-thiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay [34]. The methodology consists of soluble chromogen (MTT) conversion to slightly soluble formazan via dehydrogenases present in viable cells. Then, dimethyl sulfoxide (100 ul) was added to each well to measure the MTT product (formazan). After, the content of formazan crystals was evaluated at 570 nm by a scanning multi-well spectrophotometer plate reader (ELISA reader, Bio-Rad 2550 EIA, Hercules, CA, USA). The blue color intensity in control (only cells) wells was designated as 100% viability. The groups evaluated were: (1) control (cell only); (2) PAcA-control; (3) PAcA-1.7, and (4) PAcA-2.7. All further comparisons were based on this reference level to determine the percentage of cell viability. The experiments were performed in quadruplicate, and the results are presented as mean ± standard deviation.

2.7.3. Fluid Absorption Capacity/Degree of Swelling

The phosphate-buffered saline (PBS) and protein milk-based solution, both with pH = 6.3, were used for the assessment of biomaterial as a function of macromolecule permeability. The materials were previously cut into pieces of 1 cm2 and weighted. Through the differences in the weight of the materials, the absorption volume was quantified by Equation (2). Ws is the swollen sample weight, and Wd is the dry sample weight. The immersion was done at 37 °C (body temperature) for 1 h.
D e g r e e   o f   s w e l l i n g   % = W s W d W d   × 100

2.7.4. Statistical Analysis

The significance of the difference between the mean concentration of material absorption and standard control was tested using the Mann-Whitney U procedure for nonparametric data sets. The meaning of cell viability was performed by ANOVA One-Way, with a significance level of p < 0.05. The GraphPad Prism software (version 6.01, La Jolla, San Diego, CA, USA) was used.

3. Results and Discussion

3.1. Fatty Acid Composition of Andiroba Seed Oil (Carapa guianensis)

Andiroba oil (AO) has often been studied as an insect repellent [35]. However, their physic-chemical properties can offer new opportunities for use in wound care. Table 3 shows the chemical composition of the fatty acids in the andiroba seed oil, and the profile agrees with that described in the literature [36,37]. In total, twelve methyl esters were identified, and about 60.5% account for the averaged composition of unsaturated fatty acids. The major compounds found were oleic acid (48.67%), palmitic acid (26.89%), linoleic acid (10.79%), and stearic acid (8.80%). In smaller percentage following acids can be seen: lauric (0.89%), myristic (0.68%), palmitoleic (0.81%), arachidic (1.30%), behenic (0.25%), heptadecanoic (0.29%) and lignoceric acid (0.20%). These acids play a key role in wound care, with emollient action and biological properties [37,38]. Cutaneous dressings need to act as a bacterial barrier and prevent dehydration of the skin. Linoleic acid integrates the stratum corneum and prevents transepidermal water loss, ensuring its integrity [39,40]. This compound favors autolytic debridement in the wound and accelerates the healing process.
Additionally, oleic acid (Omega 9) and linoleic acid (Omega 6) are essentials fatty acids (AGE), which participate in human metabolism and nutrition. AGE induces the tissue granulation process, facilitates cell proliferation, and increases the membrane’s cell permeability, protecting the lesion [40]. The presence of non-fatty acid components (tocopherols, carotene, and tetranortriterpenoids) also attributes other medicinal properties and anti-inflammatory effects to the AO [37,41,42,43].

3.2. Surface Characterization

3.2.1. Optical and SEM Imaging of PCL Casting Films

The type of solvent and their evaporation rate are some critical parameters that affect the surface, physic-chemical and biological properties of films on the solvent casting method [44]. Figure 2 shows the optical and microscopic images of PCL control and hybrids film, respectively. Three different solvents were evaluated: acetone, dichloromethane, and acetic acid to determine an optimum solvent system. All polymer solutions formed opaque films. No macroscopic phase separation was observed after casting of samples, which suggests high PCL molecular weight and enough Van der Waals forces to aggregate the solution’s polymer chains [45]. Figure 2A shows optical images of samples dissolved in dichloromethane (DCM). The high solvent evaporation rate (boiling point 39.6 °C) induced specimens with body deformation, air bubbles, inhomogeneous surfaces, irregular shape, and dimensional shrinkage [44]. The solvent molecules diffusion fast generated smooth and dense surfaces, as can be seen in Figure 2D. Although nonpolar organic solvent facilitates the PCL solubilization process due to higher solvent-polymer chemical affinity, the low difference between its solubility parameters ((δ = 0.05 (cal cm−3)½) can make difficult the mass transport of volatile and the use of DCM as a porogen [46].
On the other hand, porous structures were observed on films formed by acetone (boiling point 56.0 °C, Figure 2E) and acetic acid (boiling point 118 °C, Figure 2F). Volatile species (solvent) escaped from the film surface and allowed pores’ organization to different diameters (0.5 to 19.8 μm). This characteristic plays a role in inducing cell penetration and proliferation, the mass transport of nutrients, and tissue growth [47]. Additionally, acetone vapor trapping under solidified samples was observed (central region, Figure 2B). Factors as room temperature, drying environment, humidity [48] and Amazonian climate affected the solvent’s gradual evaporation kinetics (low evaporation rate). Acetic acid was observed to possess excellent film-forming properties. The samples presented a regular surface, uniform thickness, and good mechanical handling strength (Figure 2C). This behavior may have been influenced by viscoelasticity, the degree of entanglement of the chains in solution, and the solvent molecules’ size [49]. An acidic solvent can decrease the PCL polymeric chain by breaking of ester linkages, affecting the viscosity of solution and morphology on the surface [50]. Considering its potential to inhibit bacteria colonization, such as Escherichia coli and Staphylococcus aureus [45], the acetic acid was selected as the optimum solvent system to obtain PCL hybrids films (PCL/AO). By adding AO, in the case of samples PAcA-1.7 (Figure 2G) and PAcA-2.7 (Figure 2H), a decrease in the number and size of pores was observed. From the SEM micrograph, AO partially filled the empty spaces on the material surface. The porosity decreases as the concentration of oil increases. Visually, there are no significant differences between the oil-loaded film and the control sample; only an increase in the film’s initial thickness was detected (>50%). No migration of oil to the surface was observed, suggesting good interaction to system PCL/AO.

3.2.2. Water Contact Angle Measurement

Table 4 displays the water contact angle measurements for control and hybridized polycaprolactone film, and the results were reported as mean values and standard deviation. Andiroba oil content and surface morphology affected the hydrophilic property of samples, decreasing their interaction with water. This behavior can be explained by the nonpolar group content on the film’s surface and triglycerides’ chemical structure. The contact angle values were observed as 80.26° (PAcA-control), 87.25° (PAcA-1.7), and 91.39° (PAcA-2.7), and are according appropriate range for adhesion cell of scaffolds [51,52].

3.3. Fourier-Transform Infrared Spectroscopy (FTIR) Analysis

FTIR spectroscopy is a useful technique to investigate the chemical structure of organic molecules and understanding changes in their band position and vibrational modes. Clearly, the IR visual inspection showed great similarities and overlapping of the data in samples’ spectral profiles (Figure 3). In the spectrum of andiroba oil, the fingerprint region at 2900–2850 cm−1 is assigned to stretching vibration of CH2 groups; peaks at 1746 cm−1 and 1464 cm−1 are attributed to -C=O stretching (saturated aliphatic ester) and -C-H bending vibrations, respectively; bands in the range 1200–1160 cm−1 are related to the—C-O stretching [35,53]. PCL typical bands were observed for all casting films: in the region 3000–2860 cm−1, which represents the C-H asymmetric and symmetric stretching vibration of aliphatic carbons and peaks at 1720 cm−1, due to the presence of the ester carbonyl group (C=O stretching) [54,55,56,57]. Some differences in the peak intensity and position also may be observed for hybrid samples (PAcA-1.7 and PAcA-2.7), according to the increasing amount of andiroba oil. Bands at 1160 and 1165 cm−1 are assigned to -C-O stretching of andiroba oil [53] and to the -C-O stretching vibration in the amorphous phase of PCL [57].

3.4. Thermogravimetric Analysis and Its Derivates (TGA and DrTGA)

Figure 4 displays the TGA curves and their derivates (DrTGA) for PCL control and hybrid film and andiroba oil. The maximum decomposition (Tdmax), onset degradation temperatures (Tonset), mass loss, and the percentage of residues are given in Table 5. The thermal degradation of the PAcA-control sample occurs between 242.7 °C (Tonset) and 450 °C, in a single mass loss step (96.5%) and maximum degradation temperature (Tdmax) of 249.8 °C. This event can be attributed to the chemical bond cleavage of polyester chains by the pyrolysis reaction. In Figure 4a, it was observed four stages of weight loss for andiroba oil (AO), which began to degrade at 150 °C (Tonset) and are entirely decomposed above 531.3 °C with 99.9% of weight loss. The first step can be attributed to the evaporation and/or pyrolysis of smaller carbon chain fatty acids (C12—C16:1) at the maximum degradation temperature (Tdmax) of 249.8 °C. Triglycerides with long-carbon chains tend to be thermally decomposed above 288.1 °C (Tonset) due to the higher boiling point. Around 404 °C and 482 °C (Tonset) probably occur the decomposition of stearic, oleic, linoleic, linolenic fatty acids, and others [38]. From Figure 4b, we also observed that incorporating higher levels of andiroba oil in PCL film tends to shift the Tonset and Tdmax to higher values and reduces the mass residue percentage (0.5%). This increase in the degradation temperatures may be related to the barrier effect caused by polymer chains to the AO molecules, making it difficult to diffusion volatile compounds and increase the thermal stability of hybrid materials.

3.5. Differential Scanning Calorimetry (DSC) Nonisothermal Studies

Figure 5 shows the DSC thermograms for PCL control and hybrid samples. All materials revealed an endothermic peak between 56 and 58 °C, attributed to the polymeric matrix melting. The oil incorporation did not show a significant shift on Tm peak. However, more porous media (PAcA-control) can provide higher surface area contact and reduce the flow resistance, improving the heat transfer of scaffolds [58,59].
The melting enthalpy (areas of endothermic peaks) for the samples PAcA-control, PAcA-1.7, and PAcA-2.7 was 38.93 J g−1, 46.70 J g−1, and 61.31 J g−1 (Table 6). An increase in the degree of crystallinity (28.52 to 44.91) and ΔH was also observed as the oil content increases, decreasing the amorphous domain. The PAcA-2.7 sample showed an increase of 57.46% to the degree of crystallinity about PAcA-control. The oil dispersion within the PCL chain made it difficult to evaporate the solvent via casting technique, decreasing the evaporation rate of acetic acid. Thus, the polymer chains had more time to reorganize into a more crystalline conformation. Gomes [60] produced more crystalline PCL fibers, reducing the acetic acid content, using 95:5 acetic acid:water ratios. The low volatility and low chemical affinity of acetic acid with the PCL’s hydrophobic chain lead to less aggressive solubilization, affecting crystal domains’ formation [61,62].

3.6. Cell Viability Assays (MTT)

As shown in Figure 6, the PAcA-control and hybrids film did not demonstrate cell death 24 h after cell seed. L929 cells were grown on PAcA-control film, and PAcA-1.7 and PAcA-2.7 samples had a viability of 142.0 ± 29.85, 174.8 ± 41.72, and 203.8 ± 34.33, respectively. However, there was no statistical difference (p < 0.05) between the PAcA-control and hybrids compared to the control group (cell only). In all samples, the proliferation of L929 cells was observed, indicating the high-affinity of the cells for the polymer. Our results are following cytotoxic effects to biodegradable polyester films [63,64]. Both the PAcA-control polymer and the polymer incorporated with the andiroba oil (hybrids sample) do not induce a toxic response on the L929 cell line, demonstrating the ability of PCL casting film for cell viability and growth. The insertion of andiroba oil in the PCL matrix also helps in the high cell viability presented. The oil has anti-inflammatory, antimicrobial, and antiallergic potential effects [25], is widely used in traditional medicine to treat joint pain and treat muscle and skin injuries [65,66]. The oil still may have antioxidant activities that are important during the inflammatory phase of the healing process [67].

3.7. Biological Fluid Absorption Capacity

Dressings that assist in absorbing exudate, preventing infection, covering the wound, and promoting a moist environment, consequently improve the conditions of the wound bed and assist in its healing [68,69]. We evaluated the material’s degree of swelling in different test solutions to use the material as wound dressings, whether exudative or not. Our results suggest a statistically significant difference only between the group with the PAcA-control film, in which greater permeability of protein solution (milk) was observed compared to an aqueous solution (PBS). The swelling may have been influenced by the chemical interactions between solution and hybrid films, molecular diffusion, and surface characteristics. There was no statistically significant difference between the PAcA-1.7 and PAcA-2.7 (Figure 7).

4. Conclusions

In this study, PCL-based hybrid films were prepared by solvent casting technique for wound healing applications. Andiroba-oil-loaded PCL membranes were evaluated by surface morphology, water contact angle, functional groups, and thermal behavior. FTIR showed great similarities and overlapping of the data in samples’ spectral profiles. Water contact angle measurement and SEM images showed that the AO affects samples’ hydrophilicity and porosity, decreasing their interaction with water. DSC analyses showed that andiroba oil affects the evaporation rate of solvent and increases the crystals domains. TGA analysis suggested higher thermal stability of hybrid materials due to the barrier effect caused by polymer chains to the AO molecules. Viability tests demonstrated the absence of cytotoxicity and proliferation of L929 cells on PCL—AO film. Moreover, the absorption capacity presented by the material probably can make it suitable for biomedical applications, such as wound dressings, which can assist in covering, preventing infection, and, consequently, in the wound healing process. However, mechanical properties assays, antimicrobial and antioxidant activity, and degradation tests in the future should be performed for a successful application of scaffolds in medicine regenerative.

Author Contributions

D.F.S.: Investigation, methodology, validation, writing—original draft preparation. K.T.L.: investigation, validation, methodology, writing—original draft preparation. G.N.T.B.: methodology, data curation, formal analysis, supervision. J.A.R.O.: writing—review and editing, visualization. L.A.S.d.N.: writing—review and editing, visualization, funding acquisition. C.E.F.C.: funding acquisition, resources. G.N.R.F.: funding acquisition, writing—review and editing. V.O.C.C.: formal analysis, methodology. M.F.P.: Conceptualization, investigation, formal analysis, writing—review and editing, supervision, project administration. All authors have read and agreed to the published version of the manuscript.

Funding

This project received funding from The Dean of Research and Graduate Studies (PROPESP/UFPA, Brazil) and the Banco da Amazônia (BASA/UFPA n° 2018/212, Brazil).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

References

  1. Wang, X.; Cheng, F.; Liu, J.; Smått, J.-H.; Gepperth, D.; Lastusaari, M.; Xu, C.; Hupa, L. Biocomposites of Copper-Containing Mesoporous Bioactive Glass and Nanofibrillated Cellulose: Biocompatibility and Angiogenic Promotion in Chronic Wound Healing Application. Acta Biomater. 2016, 46, 286–298. [Google Scholar] [CrossRef]
  2. Zhang, H.; Peng, M.; Cheng, T.; Zhao, P.; Qiu, L.; Zhou, J.; Lu, G.; Chen, J. Silver Nanoparticles-Doped Collagen-Alginate Antimicrobial Biocomposite as Potential Wound Dressing. J. Mater. Sci. 2018, 53, 14944–14952. [Google Scholar] [CrossRef]
  3. Kamoun, E.A.; Kenawy, E.-R.S.; Chen, X. A Review on Polymeric Hydrogel Membranes for Wound Dressing Applications: PVA-Based Hydrogel Dressings. J. Adv. Res. 2017, 8, 217–233. [Google Scholar] [CrossRef]
  4. Rogers, V.; George, M.; Luk, A. Silicone Hydrogel Contact Lenses Having Improved Lubricity. U.S. Patent Application n. 16/066,680, 23 May 2019. [Google Scholar]
  5. Panpisut, P.; Toneluck, A. Monomer Conversion, Dimensional Stability, Biaxial Flexural Strength, and Fluoride Release of Resin-Based Restorative Material Containing Alkaline Fillers. Dent. Mater. J. 2020, 39, 608–615. [Google Scholar] [CrossRef] [Green Version]
  6. Tervaert, J.W.C. Silicone. In Mosaic of Autoimmunity; Elsevier: Amsterdam, The Netherlands, 2019; pp. 297–305. [Google Scholar]
  7. Sadeghianmaryan, A.; Yazdanpanah, Z.; Soltani, Y.A.; Sardroud, H.A.; Nasirtabrizi, M.H.; Chen, X. Curcumin-Loaded Electrospun Polycaprolactone/Montmorillonite Nanocomposite: Wound Dressing Application with Anti-Bacterial and Low Cell Toxicity Properties. J. Biomater. Sci. Polym. Ed. 2020, 31, 169–187. [Google Scholar] [CrossRef]
  8. Parashar, P.; Rathor, M.; Dwivedi, M.; Saraf, S.A. Hyaluronic Acid Decorated Naringenin Nanoparticles: Appraisal of Chemopreventive and Curative Potential for Lung Cancer. Pharmaceutics 2018, 10, 33. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Biswas, S.; Kumari, P.; Lakhani, P.M.; Ghosh, B. Recent Advances in Polymeric Micelles for Anti-Cancer Drug Delivery. Eur. J. Pharm. Sci. 2016, 83, 184–202. [Google Scholar] [CrossRef] [PubMed]
  10. Luo, Y.Y.; Xiong, X.Y.; Tian, Y.; Li, Z.L.; Gong, Y.C.; Li, Y.P. A Review of Biodegradable Polymeric Systems for Oral Insulin Delivery. Drug Deliv. 2016, 23, 1882–1891. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  11. Li, X.; Zhang, Q.; Ye, D.; Zhang, J.; Guo, Y.; You, R.; Yan, S.; Li, M.; Qu, J. Fabrication and Characterization of Electrospun PCL/Antheraea Pernyi Silk Fibroin Nanofibrous Scaffolds. Polym. Eng. Sci. 2017, 57, 206–213. [Google Scholar] [CrossRef]
  12. Song, R.; Murphy, M.; Li, C.; Ting, K.; Soo, C.; Zheng, Z. Current Development of Biodegradable Polymeric Materials for Biomedical Applications. Drug Des. Devel. Ther. 2018, 12, 3117. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Iaquinta, M.R.; Mazzoni, E.; Manfrini, M.; D’Agostino, A.; Trevisiol, L.; Nocini, R.; Trombelli, L.; Barbanti-Brodano, G.; Martini, F.; Tognon, M. Innovative Biomaterials for Bone Regrowth. Int. J. Mol. Sci. 2019, 20, 618. [Google Scholar] [CrossRef] [Green Version]
  14. Abdal-hay, A.; Raveendran, N.T.; Fournier, B.; Ivanovski, S. Fabrication of Biocompatible and Bioabsorbable Polycaprolactone/Magnesium Hydroxide 3D Printed Scaffolds: Degradation and in Vitro Osteoblasts Interactions. Compos. Part B Eng. 2020, 197, 108158. [Google Scholar] [CrossRef]
  15. Muwaffak, Z.; Goyanes, A.; Clark, V.; Basit, A.W.; Hilton, S.T.; Gaisford, S. Patient-Specific 3D Scanned and 3D Printed Antimicrobial Polycaprolactone Wound Dressings. Int. J. Pharm. 2017, 527, 161–170. [Google Scholar] [CrossRef]
  16. Hajilou, H.; Farahpour, M.R.; Hamishehkar, H. Polycaprolactone Nanofiber Coated with Chitosan and Gamma Oryzanol Functionalized as a Novel Wound Dressing for Healing Infected Wounds. Int. J. Biol. Macromol. 2020, 164, 2358–2369. [Google Scholar] [CrossRef]
  17. Ghitman, J.; Stan, R.; Cecoltan, S.; Chifiriuc, M.C.; Iovu, H. Hybrid Nanocarriers Based on PLGA-Vegetable Oil: A Novel Approach for High Lipophilic Drug Delivery. J. Drug Deliv. Sci. Technol. 2018, 46, 162–172. [Google Scholar] [CrossRef]
  18. Cardoso, P.B.; Araújo, P.H.H.; Sayer, C. Encapsulation of Jojoba and Andiroba Oils by Miniemulsion Polymerization. Effect on Molar Mass Distribution. In:Macromolecular Symposia; WILEY-VCH Verlag: Weinheim, Germany, 2013; Volume 324, pp. 114–123. [Google Scholar]
  19. Uscátegui, Y.L.; Díaz, L.E.; Gómez-Tejedor, J.A.; Vallés-Lluch, A.; Vilariño-Feltrer, G.; Serrano, M.A.; Valero, M.F. Candidate Polyurethanes Based on Castor Oil (Ricinus Communis), with Polycaprolactone Diol and Chitosan Additions, for Use in Biomedical Applications. Molecules 2019, 24, 237. [Google Scholar] [CrossRef] [Green Version]
  20. McIntyre, M.K.; Peacock, T.J.; Akers, K.S.; Burmeister, D.M. Initial Characterization of the Pig Skin Bacteriome and Its Effect on in Vitro Models of Wound Healing. PLoS ONE 2016, 11, e0166176. [Google Scholar] [CrossRef] [PubMed]
  21. Lima Júnior, E.M.; De Moraes Filho, M.O.; Costa, B.A.; Rohleder, A.V.P.; Sales Rocha, M.B.; Fechine, F.V.; Forte, A.J.; Alves, A.P.N.N.; Silva Júnior, F.R.; Martins, C.B. Innovative Burn Treatment Using Tilapia Skin as a Xenograft: A Phase II Randomized Controlled Trial. J. Burn Care Res. 2020, 41, 585–592. [Google Scholar] [CrossRef]
  22. Piriz, M.A.; Lima, C.A.B.; Jardim, V.M.R.; Mesquita, M.K.; Souza, A.D.Z.; Heck, R.M. Medicinal Plants in the Wound Healing Process: A Literature Review. Rev. Bras. Plantas Med. 2014, 16, 628–636. [Google Scholar] [CrossRef]
  23. Krist, S. Andiroba Oil BT-Vegetable Fats and Oils; Krist, S., Ed.; Springer International Publishing: Cham, Switzerland, 2020; pp. 57–60. ISBN 978-3-030-30314-3. [Google Scholar]
  24. Milhomem-Paixão, S.S.R.; Fascineli, M.L.; Roll, M.M.; Longo, J.P.F.; Azevedo, R.B.; Pieczarka, J.C.; Salgado, H.L.C.; Santos, A.S.; Grisolia, C.K. The Lipidome, Genotoxicity, Hematotoxicity and Antioxidant Properties of Andiroba Oil from the Brazilian Amazon. Genet. Mol. Biol. 2016, 39, 248–256. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Wanzeler, A.M.V.; Júnior, S.M.A.; Gomes, J.T.; Gouveia, E.H.H.; Henriques, H.Y.B.; Chaves, R.H.; Soares, B.M.; Salgado, H.L.C.; Santos, A.S.; Tuji, F.M. Therapeutic Effect of Andiroba Oil (Carapa Guianensis Aubl.) against Oral Mucositis: An Experimental Study in Golden Syrian Hamsters. Clin. Oral Investig. 2018, 22, 2069–2079. [Google Scholar] [CrossRef]
  26. Malikmammadov, E.; Tanir, T.E.; Kiziltay, A.; Hasirci, V.; Hasirci, N. PCL and PCL-Based Materials in Biomedical Applications. J. Biomater. Sci. Polym. Ed. 2018, 29, 863–893. [Google Scholar] [CrossRef] [PubMed]
  27. Aliah, N.N.; Ansari, M.N.M. Thermal Analysis on Characterization of Polycaprolactone (PCL)-Chitosan Scaffold for Tissue Engineering. Int. J. Sci. Res. Eng. Technol 2017, 6, 2278–2882. [Google Scholar]
  28. Gorrasi, G.; Guadagno, L.; Vittoria, V. Solvent Induced Polymorphism of Quenched Syndiotactic Polypropylene in Different Liquids. Colloid Polym. Sci. 2003, 281, 469–475. [Google Scholar] [CrossRef]
  29. Bordes, C.; Fréville, V.; Ruffinb, E.; Marotea, P.; Gauvrita, J.Y.; Briançon, S.; Lantéria, P. Determination of Poly(_-Caprolactone) Solubility Parameters: Application to Solvent Substitution in a Microencapsulation Process. Int. J. Pharm. 2010, 383, 236–243. [Google Scholar] [CrossRef]
  30. Canevarolo, S.V., Jr. Ciência Dos Polímeros.Um Texto Básico Para Tecnólogos e Engenheiros; Artliber Editora: São Paulo, Brazil, 2002. [Google Scholar]
  31. Warner, K.; Eskin, M. Methods to Access Quality and Stability of Oils and Fat-Containing Foods; AOCS Publishing: Urbana, IL, USA, 1995; ISBN 143983198X. [Google Scholar]
  32. American Oil Chemists’ Society (AOCS). Official Methods and Recommended Practices of the AOCS, 4th ed.; AOCS: Urbana, IL, USA, 1995. [Google Scholar]
  33. Delgado-Lima, A.; Botelho, G.; Silva, M.M.; Machado, A. V Durability of PCL Nanocomposites under Different Environments. J. Polym. Environ. 2013, 21, 710–717. [Google Scholar] [CrossRef]
  34. Mosmann, T. Rapid Colorimetric Assay for Cellular Growth and Survival: Application to Proliferation and Cytotoxicity Assays. J. Immunol. Methods 1983, 65, 55–63. [Google Scholar] [CrossRef]
  35. Senhorini, G.A.; Zawadzki, S.F.; Farago, P.V.; Zanin, S.M.W.; Marques, F.A. Microparticles of Poly(Hydroxybutyrate-Co-Hydroxyvalerate) Loaded with Andiroba Oil: Preparation and Characterization. Mater. Sci. Eng. C 2012, 32, 1121–1126. [Google Scholar] [CrossRef]
  36. Dhorm Pimentel de Moraes, A.R.; Tavares, G.D.; Soares Rocha, F.J.; de Paula, E.; Giorgio, S. Effects of Nanoemulsions Prepared with Essential Oils of Copaiba- and Andiroba against Leishmania Infantum and Leishmania Amazonensis Infections. Exp. Parasitol. 2018, 187, 12–21. [Google Scholar] [CrossRef] [PubMed]
  37. Novello, Z.; Scapinello, J.; Magro, J.D.; Zin, G.; Di Luccio, M.; Tres, M.V.; Oliveira, J.V. Extraction, Chemical Characterization and Antioxidant Activity of Andiroba Seeds Oil Obtained from Pressurized n-Butane. Ind. Crops Prod. 2015, 76, 697–701. [Google Scholar] [CrossRef]
  38. Dos Santos Costa, M.N.F.; Muniz, M.A.P.; Negrão, C.A.B.; da Costa, C.E.F.; Lamarão, M.L.N.; Morais, L.; Silva Júnior, J.O.C.; Ribeiro Costa, R.M. Characterization of Pentaclethra Macroloba Oil. J. Therm. Anal. Calorim. 2014, 115, 2269–2275. [Google Scholar] [CrossRef]
  39. Manhez, A.C.; Bachion, M.M.; Pereira, Â.L. The Use of Essential Fatty Acids in the Treatments of Wound. Rev. Bras. Enferm. 2008, 61, 620–629. [Google Scholar]
  40. Ferreira, A.M.; de Souza, B.M.V.; Rigotti, M.A.; Loureiro, M.R.D. The Use of Fatty Acids in Wound Care: An Integrative Review of the Brazilian Literature. Rev. Esc. Enferm. USP 2012, 46, 752–760. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  41. Kimura, V.T.; Miyasato, C.S.; Genesi, B.P.; Lopes, P.S.; Yoshida, C.M.P.; Silva, C.F.d. The Effect of Andiroba Oil and Chitosan Concentration on the Physical Properties of Chitosan Emulsion Film. Polímeros 2016, 26, 168–175. [Google Scholar] [CrossRef] [Green Version]
  42. Tappin, M.R.R.; Nakamura, M.J.; Siani, A.C.; Lucchetti, L. Development of an HPLC Method for the Determination of Tetranortriterpenoids in Carapa Guianensis Seed Oil by Experimental Design. J. Pharm. Biomed. Anal. 2008, 48, 1090–1095. [Google Scholar] [CrossRef] [PubMed]
  43. Pardauil, J.J.R.; de Molfetta, F.A.; Braga, M.; de Souza, L.K.C.; Filho, G.N.R.; Zamian, J.R.; da Costa, C.E.F. Characterization, Thermal Properties and Phase Transitions of Amazonian Vegetable Oils. J. Therm. Anal. Calorim. 2017, 127, 1221–1229. [Google Scholar] [CrossRef]
  44. Taherkhani, S.; Moztarzadeh, F. Fabrication of a Poly(ɛ-Caprolactone)/Starch Nanocomposite Scaffold with a Solvent-Casting/Salt-Leaching Technique for Bone Tissue Engineering Applications. J. Appl. Polym. Sci. 2016, 133. [Google Scholar] [CrossRef]
  45. Chee, T.Y.; Yusoff, A.R.M.; Malek, N.A.N.N. Characterization of Poly(Vinyl Alcohol)-Polycaprolactone Hybridized Scaffold for Potential Skin Tissue Regeneration. Malaysian J. Fundam. Appl. Sci. 2020, 16, 6–9. [Google Scholar] [CrossRef]
  46. Safaei, F.; Khalili, S.; Khorasani, S.N.; Ghasemi-Mobarakeh, L.; Neisiany, R.E. Porogen Effect of Solvents on Pore Size Distribution of Solvent-Casted Polycaprolactone Thin Films. J. Polym. Sci. Eng. 2018, 1. [Google Scholar] [CrossRef]
  47. Thi Hiep, N.; Chan Khon, H.; Dai Hai, N.; Byong-Taek, L.; Van Toi, V.; Thanh Hung, L. Biocompatibility of PCL/PLGA-BCP Porous Scaffold for Bone Tissue Engineering Applications. J. Biomater. Sci. Polym. Ed. 2017, 28, 864–878. [Google Scholar] [CrossRef]
  48. Lucero, J.M.; Jasinski, J.B.; Song, M.; Li, D.; Liu, L.; Liu, J.; De Yoreo, J.J.; Thallapally, P.K.; Carreon, M.A. Synthesis of Porous Organic Cage CC3 via Solvent Modulated Evaporation. Inorg. Chem. Acta 2020. [Google Scholar] [CrossRef]
  49. Costa, R.G.F.; de Oliveira, J.E.; de Paula, G.F.; de S. Picciani, P.H.; de Medeiros, E.S.; Ribeiro, C.; Mattoso, L.H.C. Electrospinning of Polymers in Solution. Part I: Theoretical Foundation. Polímeros 2012, 22, 170–177. [Google Scholar] [CrossRef]
  50. Das, P.; Remigy, J.-C.; Lahitte, J.-F.; van der Meer, A.D.; Garmy-Susini, B.; Coetsier, C.; Desclaux, S.; Bacchin, P. Development of Double Porous Poly (ε-Caprolactone)/Chitosan Polymer as Tissue Engineering Scaffold. Mater. Sci. Eng. C 2020, 107, 110257. [Google Scholar] [CrossRef] [PubMed]
  51. Rahmati Nejad, M.; Yousefzadeh, M.; Solouk, A. Electrospun PET/PCL Small Diameter Nanofibrous Conduit for Biomedical Application. Mater. Sci. Eng. C 2020, 110, 110692. [Google Scholar] [CrossRef]
  52. Arima, Y.; Iwata, H. Effects of Surface Functional Groups on Protein Adsorption and Subsequent Cell Adhesion Using Self-Assembled Monolayers. J. Mater. Chem. 2007, 17, 4079–4087. [Google Scholar] [CrossRef]
  53. De Santana, F.B.; Mazivila, S.J.; Gontijo, L.C.; Neto, W.B.; Poppi, R.J. Rapid Discrimination Between Authentic and Adulterated Andiroba Oil Using FTIR-HATR Spectroscopy and Random Forest. Food Anal. Methods 2018, 11, 1927–1935. [Google Scholar] [CrossRef]
  54. Herrera-Kao, W.A.; Loría-Bastarrachea, M.I.; Pérez-Padilla, Y.; Cauich-Rodríguez, J.V.; Vázquez-Torres, H.; Cervantes-Uc, J.M. Thermal Degradation of Poly(Caprolactone), Poly(Lactic Acid), and Poly(Hydroxybutyrate) Studied by TGA/FTIR and Other Analytical Techniques. Polym. Bull. 2018, 75, 4191–4205. [Google Scholar] [CrossRef]
  55. Obasi, H.C.; Chaudhry, A.A.; Ijaz, K.; Akhtar, H.; Malik, M.H. Development of Biocomposites from Coir Fibre and Poly (Caprolactone) by Solvent Casting Technique. Polym. Bull. 2018, 75, 1775–1787. [Google Scholar] [CrossRef]
  56. Augustine, R.; Kalarikkal, N.; Thomas, S. Effect of Zinc Oxide Nanoparticles on the in Vitro Degradation of Electrospun Polycaprolactone Membranes in Simulated Body Fluid. Int. J. Polym. Mater. Polym. Biomater. 2016, 65, 28–37. [Google Scholar] [CrossRef]
  57. Abdelrazek, E.M.; Hezma, A.M.; El-khodary, A.; Elzayat, A.M. Spectroscopic Studies and Thermal Properties of PCL/PMMA Biopolymer Blend. Egypt. J. Basic Appl. Sci. 2016, 3, 10–15. [Google Scholar] [CrossRef]
  58. Liang, M.; Fu, C.; Xiao, B.; Luo, L.; Wang, Z. A Fractal Study for the Effective Electrolyte Diffusion through Charged Porous Media. Int. J. Heat Mass Transf. 2019, 137, 365–371. [Google Scholar] [CrossRef]
  59. Kasaeian, A.; Daneshazarian, R.; Mahian, O.; Kolsi, L.; Chamkha, A.J.; Wongwises, S.; Pop, I. Nanofluid Flow and Heat Transfer in Porous Media: A Review of the Latest Developments. Int. J. Heat Mass Transf. 2017, 107, 778–791. [Google Scholar] [CrossRef]
  60. Gomes, S.; Querido, D.; Ferreira, J.L.; Borges, J.P.; Henriques, C.; Silva, J.C. Using Water to Control Electrospun Polycaprolactone Fibre Morphology for Soft Tissue Engineering. J. Polym. Res. 2019, 26, 222. [Google Scholar] [CrossRef]
  61. Del Ángel-Sánchez, K.; Borbolla-Torres, C.I.; Palacios-Pineda, L.M.; Ulloa-Castillo, N.A.; Elías-Zúñiga, A. Development, Fabrication, and Characterization of Composite Polycaprolactone Membranes Reinforced with TiO2 Nanoparticles. Polymers 2019, 11, 1955. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Boucher, D.S. Solubility Parameters and Solvent Affinities for Polycaprolactone: A Comparison of Methods. J. Appl. Polym. Sci. 2020, 137, 48908. [Google Scholar] [CrossRef]
  63. Boyandin, A.; Dvoinina, L.; Sukovatiy, A.; Sukhanova, A. Production of Porous Films Based on Biodegradable Polyesters by the Casting Solution Technique Using a Co-Soluble Porogen (Camphor). Polymers 2020, 12, 1950. [Google Scholar] [CrossRef] [PubMed]
  64. Patrício, T.; Domingos, M.; Gloria, A.; Bártolo, P. Characterisation of PCL and PCL/PLA Scaffolds for Tissue Engineering. Procedia CIRP 2013, 5, 110–114. [Google Scholar] [CrossRef]
  65. Das Graças Henriques, M.; Penido, C. The Therapeutic Properties of Carapa Guianensis. Curr. Pharm. Des. 2014, 20, 850–856. [Google Scholar] [CrossRef] [PubMed]
  66. Costa-Silva, J.H.; Lima, C.R.; Silva, E.J.R.; Araújo, A.V.; Fraga, M.; E Ribeiro, A.R.; Arruda, A.C.; Lafayette, S.S.L.; Wanderley, A.G. Acute and Subacute Toxicity of the Carapa Guianensis Aublet (Meliaceae) Seed Oil. J. Ethnopharmacol. 2008, 116, 495–500. [Google Scholar] [CrossRef]
  67. Araujo-Lima, C.F.; Fernandes, A.S.; Gomes, E.M.; Oliveira, L.L.; Macedo, A.F.; Antoniassi, R.; Wilhelm, A.E.; Aiub, C.A.F.; Felzenszwalb, I. Antioxidant Activity and Genotoxic Assessment of Crabwood (Andiroba, Carapa Guianensis Aublet) Seed Oils. Oxid. Med. Cell. Longev. 2018. [Google Scholar] [CrossRef] [Green Version]
  68. Wasiak, J.; Cleland, H.; Campbell, F.; Spinks, A. Dressings for Superficial and Partial Thickness Burns. Cochrane Database Syst. Rev. 2013, CD002106. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. De Smaniotto, P.H.; Ferreira, M.C.; Isaac, C.; Galli, R. Systematization of Dressings for Clinical Treatment of Wounds. Rev. Bras. Cir. Plástica 2012, 27, 623–626. [Google Scholar]
Figure 1. Schematic diagram of poly (ε-caprolactone) (PCL) film synthesis by the solvent casting technique.
Figure 1. Schematic diagram of poly (ε-caprolactone) (PCL) film synthesis by the solvent casting technique.
Polymers 13 01591 g001
Figure 2. The optical images (OI) and microscopic (SEM) of PCL casting film at magnification 1000×, respectively: (A) PD-control OI; (B) PAC-control OI; (C) PAcA-control OI; (D) PD-control SEM; (E) PAC-control SEM; (F) PAcA-control SEM; (G) PAcA-1.7 SEM; (H) PAcA-2.7 SEM.
Figure 2. The optical images (OI) and microscopic (SEM) of PCL casting film at magnification 1000×, respectively: (A) PD-control OI; (B) PAC-control OI; (C) PAcA-control OI; (D) PD-control SEM; (E) PAC-control SEM; (F) PAcA-control SEM; (G) PAcA-1.7 SEM; (H) PAcA-2.7 SEM.
Polymers 13 01591 g002
Figure 3. Fourier-transform infrared spectroscopy (FTIR) of andiroba oil and control and hybrids film of PCL.
Figure 3. Fourier-transform infrared spectroscopy (FTIR) of andiroba oil and control and hybrids film of PCL.
Polymers 13 01591 g003
Figure 4. (a) TGA (b) and DrTGA analysis of andiroba oil and PCL films in acetic acid (PAcA-control, PAcA-1.7, PAcA-2.7).
Figure 4. (a) TGA (b) and DrTGA analysis of andiroba oil and PCL films in acetic acid (PAcA-control, PAcA-1.7, PAcA-2.7).
Polymers 13 01591 g004
Figure 5. DSC (second heat) analysis of andiroba oil and PCL films in acetic acid (PAcA-control, PAcA-1.7, PAcA-2.7).
Figure 5. DSC (second heat) analysis of andiroba oil and PCL films in acetic acid (PAcA-control, PAcA-1.7, PAcA-2.7).
Polymers 13 01591 g005
Figure 6. Cell viability of L929 cells on PAcA-control and hybrids (PAcA 1.7 and PAcA-2.7) film after 24 h in culture. p < 0.05, n = 4. The asterisk (*) indicates a significant difference between the control and treated groups.
Figure 6. Cell viability of L929 cells on PAcA-control and hybrids (PAcA 1.7 and PAcA-2.7) film after 24 h in culture. p < 0.05, n = 4. The asterisk (*) indicates a significant difference between the control and treated groups.
Polymers 13 01591 g006
Figure 7. Evaluation of the fluid absorption capacity of PCL control polymeric films (PAcA-control) and incorporated with andiroba oil (PAcA-1.7 and PAcA-2.7) immersed for one hour in aqueous or protein solution. The data were plotted in the average format and standard error of the mean. The analysis was performed by 2-way ANOVA followed by Bonferroni’s test, with p < 0.05, n = 4. The asterisk (*) indicates a significant difference between the control and treated groups.
Figure 7. Evaluation of the fluid absorption capacity of PCL control polymeric films (PAcA-control) and incorporated with andiroba oil (PAcA-1.7 and PAcA-2.7) immersed for one hour in aqueous or protein solution. The data were plotted in the average format and standard error of the mean. The analysis was performed by 2-way ANOVA followed by Bonferroni’s test, with p < 0.05, n = 4. The asterisk (*) indicates a significant difference between the control and treated groups.
Polymers 13 01591 g007
Table 1. Physicochemical properties of commercial andiroba oil.
Table 1. Physicochemical properties of commercial andiroba oil.
Physicochemical DataUnitsValues *
Acidity level% weight<15.0
Density25 °C g/mL0.9261
Iodine indexgI2/100 g55–80
Melting point°C22
Peroxide content10 meq O2/kg<10.0
Saponification indexmg KOH/g190–210
Unsaponifiable matter (bioactive)%3–5
* Data obtained by the Amazon Oil supplier.
Table 2. Samples identification and composition.
Table 2. Samples identification and composition.
Sample NameSolventAndiroba oil (AO)
(% wt OIL/wt PCL)
PAcA-controlAcetic Acid-
PAcA-1.7Acetic Acid1.7
PAcA-2.7Acetic Acid2.7
PAC-controlAcetone-
PAC-1.7Acetone1.7
PAC-2.7Acetone2.7
PD-controlDichloromethane-
PD-1.7Dichloromethane1.7
PD-2.7Dichloromethane2.7
Table 3. Fatty acids composition of andiroba seed oil (Carapa guianensis) determined by gas chromatography.
Table 3. Fatty acids composition of andiroba seed oil (Carapa guianensis) determined by gas chromatography.
NomenclatureChainComposition * (%)
Lauric acidC12:00.89 ± 0.38
Myristic acidC14:00.68 ± 0.25
Palmitic acidC16:026.89 ± 0.98
Palmitoleic acidC16:10.81 ± 0.06
Heptadecanoic acidC17:00.29 ± 0.34
Stearic acidC18:08.80 ± 0.10
Oleic acidC18:1 (ω-9)48.67 ± 1.19
Linoleic acidC18:2 (ω-6)10.79 ± 0.39
Linolenic acidC18:3 (ω-3)0.22 ± 0.02
Arachidic acidC 20:01.30 ± 0.16
Behenic acidC22:00.25 ± 0.14
Lignoceric acidC24:00.20 ± 0.04
* Average values and standard derivations of the three andiroba oil (AO) samples studied.
Table 4. Water contact angle measurements (average ± standard deviation) for control and hybrid samples of PCL.
Table 4. Water contact angle measurements (average ± standard deviation) for control and hybrid samples of PCL.
SamplesWater Contact Angle/Degrees
PAcA-control80.26 ± 5.72
PAcA-1.787.25 ± 6.05
PAcA-2.791.39 ± 5.10
Table 5. TGA and DrTGA curves parameters of the PCL casting films and andiroba oil: degradation onset temperature (Tonset), maximum degradation temperature (Tdmax), weight loss (%), and the percentage of residues.
Table 5. TGA and DrTGA curves parameters of the PCL casting films and andiroba oil: degradation onset temperature (Tonset), maximum degradation temperature (Tdmax), weight loss (%), and the percentage of residues.
SamplesTonset (°C)Tdmax (°C)Weight Loss (%)Residue (%)
1° Stage2° Stage3° Stage4° Stage1° Stage2° Stage3° Stage4° Stage
PAcA-control242.7---402.4---96.53.5
PAcA-1.7262.9---401.5---99.10.9
PAcA-2.7269.9---408.9---99.50.5
AO150.0288.1404.0482.0249.8386.0413.5531.399.90.1
Table 6. DSC curves parameters of the PCL casting films: onset melting temperature (Tm onset), peak melting temperature (Tm peak), enthalpy for melting (ΔH), and degree of crystallinity (xc%).
Table 6. DSC curves parameters of the PCL casting films: onset melting temperature (Tm onset), peak melting temperature (Tm peak), enthalpy for melting (ΔH), and degree of crystallinity (xc%).
Parameters
SamplesTm Onset (°C)Tm Peak (°C)ΔH (J g−1)xc (%)
PAcA-control54.4056.5438.9328.52
PAcA-1.754.2357.2246.7034.21
PAcA-2.754.1558.7961.3144.91
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Silva, D.F.; Lima, K.T.; Bastos, G.N.T.; Oliveira, J.A.R.; do Nascimento, L.A.S.; Costa, C.E.F.; Filho, G.N.R.; Concha, V.O.C.; Passos, M.F. PCL/Andiroba Oil (Carapa guianensis Aubl.) Hybrid Film for Wound Healing Applications. Polymers 2021, 13, 1591. https://doi.org/10.3390/polym13101591

AMA Style

Silva DF, Lima KT, Bastos GNT, Oliveira JAR, do Nascimento LAS, Costa CEF, Filho GNR, Concha VOC, Passos MF. PCL/Andiroba Oil (Carapa guianensis Aubl.) Hybrid Film for Wound Healing Applications. Polymers. 2021; 13(10):1591. https://doi.org/10.3390/polym13101591

Chicago/Turabian Style

Silva, Debora F., Klinsmann T. Lima, Gilmara N. T. Bastos, Johnatt Allan R. Oliveira, Luís Adriano S. do Nascimento, Carlos Emmerson F. Costa, Geraldo N. R. Filho, Viktor O. C. Concha, and Marcele F. Passos. 2021. "PCL/Andiroba Oil (Carapa guianensis Aubl.) Hybrid Film for Wound Healing Applications" Polymers 13, no. 10: 1591. https://doi.org/10.3390/polym13101591

APA Style

Silva, D. F., Lima, K. T., Bastos, G. N. T., Oliveira, J. A. R., do Nascimento, L. A. S., Costa, C. E. F., Filho, G. N. R., Concha, V. O. C., & Passos, M. F. (2021). PCL/Andiroba Oil (Carapa guianensis Aubl.) Hybrid Film for Wound Healing Applications. Polymers, 13(10), 1591. https://doi.org/10.3390/polym13101591

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop