Physico-chemical and pro-wound healing properties of microporous cellulosic sponge from Gleditsia triacanthos pods functionalized with Phytolacca americana fruit extract

This study aimed to exploit two invasive plant species to develop a novel, multifunctional, bioactive wound dressing based on a microporous cellulosic sponge (CS) from Gleditsia triacanthos pods and functionalizing them with Phytolacca americana fruit extract. The CS was functionalized, lyophilized, and characterized by Attenuated total reflectance–Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, contact angle, water absorption, and retention capacity. In addition, two parameters were evaluated in temporal dynamics: controlled release of phenolic compounds and antioxidant activities. The hemolytic index, blood clotting kinetics, lactate dehydrogenase release, and wound scratch assays proved their hemo- and biocompatibility, as well as their ability to promote cell proliferation and migration promoting-activity and to inhibit microbial growth. Furthermore, the obtained spongious material exhibited an anti-inflammatory effect by modulating the macrophages’ secretion profile of IL-6 and IL-10. In conclusion, the microporous cellulosic sponge obtained from G. triacanthos could be used as a vehicle to ensure the controlled release of bioactive principles with pro-wound healing activities extracted from invasive plants.


Introduction
Currently, wound management poses significant economic and clinical challenges, which explain the considerable interest in wound healing research and the development of more efficient therapeutic approaches.The wound healing could be impaired or delayed by the development of microbial biofilms, hyper or chronic inflammation, accumulation of free radicals (especially reactive oxygen species), and decreased mitogenic activity, inhibiting progression to proliferation and re-epithelialization (Shedoeva et al. 2019).
Along with technological progress, different wound dressings, such as hydrogels, hydrocolloids, alginates, tissue adhesives, porous adhesive films, and dressings containing silver and/or collagen, have been obtained (Dhivya et al. 2015).Many recent studies showed cellulose materials are appropriate for biomedical purposes due to their high biocompatibility (Dowsett and Newton 2005;Vartiainen et al. 2011;Alexandrescu et al. 2013;Rees et al. 2015).Being one of the most widespread compounds in nature, cellulose can be extracted from a wide range of sources (Moon et al. 2011;Fernandes et al. 2013), which mainly include plants and vegetal food waste, such as rice straw (Jianan et al. 1996), cannabis (Virtanen et al. 2012), cotton (Reddy and Yang 2009), wood (Cara et al. 2006), potato tubers (Abe and Yano 2009), banana peels (Phirom-on and Apiraksakorn 2022), pineapple (Fareez et al. 2018), etc.The performance characteristics of cellulose, such as its molecular chain length (degree of polymerization), size, degree of crystallinity, and thermal stability, depend on the plant source species, as well as the extraction method, including pre-treatment, post-treatment, and disintegration steps (Siqueira et al. 2010;Jeong et al. 2015;Lee et al. 2015;Trache et al. 2016).Although bacterial and vegetal cellulose's chemical structure is similar, bacterial cellulose has a higher degree of crystallinity (> 80%) (Long et al. 2018).
Cellulose has a high chemical reactivity, allowing to obtain different derivatives, many of them multifunctional, using flexible preparation and numerous modification methods.The three main ways to modify cellulosic materials are: (i) adding active principles to the cellulose solution/suspension (Gawryla et al. 2009); (ii) depositing coatings on the cellulose gel surface using a sol-gel method; (iii) modifying the surfaces of cellulose aerogels by using a silanetype coupling agent and/or atomic layer deposition (Long et al. 2018).
Invasive plants, which pose significant risks to biodiversity, the structure and functions of ecosystems, and the conservation of protected areas, could represent a cheap, readily available source of cellulose and active principles offering alternative and almost unlimited therapeutic options and, at the same time helping to limit their uncontrolled spread (Holloran 2006;Kumar Rai and Singh 2020).Among the invasive species, Phytolacca americana contains toxic compounds, especially in leaves and roots, that could cause pokeweed poisoning after oral administration.Symptoms include stomach burning, nausea, vomiting, and diarrhea (Ravikiran et al. 2011).However, the fruits are less toxic due to phytolaccatoxin and related triterpenes (Hamissou and Kurdmongkoltham 2015).As a result of their anti-inflammatory, antitumoral, and antimicrobial activity, P. americana extracts are used in folk medicine from Central and South America for treating inflammation, syphilisassociated pain, and other diseases (Gomes et al. 2008;Ravikiran et al. 2011).In addition, according to Patra et al. (2014), the crude extract of P. americana contains active substances that can inhibit the bacterial growth responsible for various oral diseases (Patra et al. 2014).
The mitogenic properties of P. americana extracts due to compounds such as the pokeweed mitogen lectin (PWM) isolated by saline extraction from pokeweed roots (Bodger et al. 1979;Bekeredjian-Ding et al. 2012) have been demonstrated since the 1960s by in vitro (Farnes et al. 1964) and in vivo assays (Barker et al. 1966).
However, for P. americana plant extracts, a release system is needed to avoid hemolysis which occurs at high concentrations.In this study, we address this limitation by using a cellulose matrix extracted from another invasive species, G. triacanthos, to encapsulate and release of the active principles contained in the P. americana fruit extract.This could lead to a cost-effective, circular bioeconomy and ecological approach to stop the uncontrolled spread of these two invasive species.
In this context, the present study characterizes cellulosic spongious materials from G. triacanthos pods that were functionalized with active principles from P. americana fruit extract.The potential of this bioactive spongious material was established based on the in vitro determination of the wound healing accelerating effect, cytocompatibility, hemocompatibility, antimicrobial, antioxidant properties, and immunomodulatory activity.

Plant material
G. triacanthos pods and P. americana fruits (spontaneous flora) were harvested from Râmnicu Vâlcea and Bucharest, Romania, in September 2019.The voucher specimens are stored in Botanical Garden' Herbarium "Dimitrie Brândză" from the University of Bucharest (no. 40065 and no. 400712,respectively), where their taxonomic affiliation was certified too.The G. triacanthos pods were manually separated from other vegetative organs, slightly cleaned, and dried at 25 °C, while fresh P. americana fruits were used for extraction (on the same day after harvest).

Phenolic compounds extraction from P. americana fruits
An amount of 5 g of previously milled fresh fruits was weighed, ethanol was used as a solvent, and the ultrasound-assisted extraction method was applied to obtain the extract.The final volume of the extract was brought to 50 mL with the same solvent.The sonication was repeated (for 30 min) and after that, the extract was maintained at 25 °C for 20 days, then filtered and stored at − 20 °C until incorporation into cellulosic spongious material.

Total phenolic content (TPC)
The Folin-Ciocalteu method (Singleton and Rossi 1965) was applied to establish the TPC content, which was expressed as milligram gallic acid equivalent/mL extract (mg GAE/mL).Briefly, Folin-Ciocalteu reagent (0.1 mL) was mixed with extract, distilled water (1.8 mL), and saturated solution sodium carbonate (0.1 mL).After homogenization (15 s, at vortex), the solutions were kept in the dark for 60 min.Under the same conditions, the standard curve was drawn for different concentrations of gallic acid (R 2 = 0.9985).The absorbance was measured at 765 nm using a FlexStation 3 UV-VIS (Molecular devices Company, Sunnyvale, CA, USA) Spectrophotometer for samples or standard solutions.

Ultra-high-performance liquid chromatographyelectrospray ionization-high resolution mass spectrometry (UHPLC-ESI-HRMS)
The quantitative analysis of phenolic compounds in the extract was performed using an UltiMate 3000 UHPLC system coupled to a Q-Exactive Focus Hybrid Quadrupole-OrbiTrap mass spectrometer equipped with heated electrospray ionization (HESI) probe (Thermo Scientific, Germany) set as described by Ciucure and Geană (2019).Separations was performed using a Kinetex (C18, 100 × 2.1 mm, 1.7 µm, Phenomenex, USA) column and a binary solvent system (A: water with 0.1% formic acid and B: methanol with 0.1% formic acid).Also, a screening UHPLC-MS/MS analysis was done to identify specific compounds from P. americana fruit extract.Full scan data were acquired in negative mode covering a scan range of m/z 120-1800 at a resolving power of 70,000 FWHM at m/z 200, while variable data-independent analysis MS 2 (vDIA) was performed at the resolution of 35,000, isolation windows and scan set as follow: 120-305 m/z, 195-405 m/z, 295-505 m/z, 395-1000 m/z and 1000-1800 m/z.Data processing were performed with Compound Discoverer v. 2.1 Software, following an untargeted metabolomics working template.

The fabrication of CS and FCS
The cellulose extraction from 30 g Gleditsia triacanthos pods was carried out as presented by Zhuo et al. (2017), evaluating the presence of lignin after each cycle (n = 10).The extractable compounds were solubilized in toluene: ethanol (2:1, v:v) solution for 8 h at 90 ºC.A delignification cycle involved alternative reflux in the presence of sodium hypochlorite (70 ºC, heating on oil bath, 6 h) and NaOH 2% (90 ºC, 2 h).After each cycle, the biomass was centrifuged, washed with deionized water, and the total lignin content was quantified.The protocol used for total lignin (hydroxycinnamic acid method using lignin for calibration curve) content was done according to British Pharmacopoeia (Gaur et al. 2009).The supernatant was titrated with AgNO 3 to highlight the removal of chloride anions from the obtained cellulose solution.The washed cellulosic spongious material (approx. 2 g dry matter) was dispersed in the extract (4 mL) obtained previously, while for the control, ethanol (50%, 4 mL) was used.Then both were dispersed five times for ten minutes using IKA Ultra-Turax, followed by 30 min of sonication and freeze-drying to obtain the CS and the FCS, respectively.The schematic representation of the spongious materials fabrication stages is presented in Fig. 1.

Attenuated total reflectance-Fourier transform infrared (ATR-FTIR)
The Cary 630 FTIR Spectrometer in ATR mode and Agilent MicroLab Software FTIR System (Agilent Vol.: (0123456789) Technologies, Inc., USA) were used to record the FTIR spectra for CS, FCS, and dry extract.4000-650 cm −1 was the selected measurement range, with 400 scans and a resolution of 4 cm −1 .

X-ray diffraction
The X-ray diffraction (XRD) pattern was recorded using a laboratory Rigaku SmartLab (Osaka, Japan) X-ray diffractometer with nominal power of 9 kW, which provides monochromatic X-rays with wavelength, λ = 0.15418 nm.The XRD measurement was performed in grazing incidence configuration, for which the incidence angle of the source was kept at 0.5°, while the detector moved from 5 to 70°.During the acquisition, a speed of 2.5°/min was used, while the scan step was 0.05°.

Morphology of CS and FCS
The morphological features of CS and FCS were acquired using a Nova NanoSEM 630 Scanning Electron Microscope (FEI Company, Hillsboro, OR, USA) using an accelerating voltage of 10 kx.For the SEM images, all samples were coat-sputtered with Au to ensure the conductivity of the sample.

Surface wettability
Static (equilibrium) CAs were carried out at 25 °C, and a drop shape analysis instrument, model DSA100 (Krüss GmbH, Hamburg, Germany), was used.The analysis was performed according to Stan et al. (2020).

Water absorption and retention properties
The method was adapted after Ngadaonye et al. (2013).Briefly, 0.1 g CS or FCS was submerged in phosphate buffer solution (PBS) (pH 7.4, 37 °C, for 15 min).The PBS excess was taken away with filter paper, and the material's wet mass was determined.Then, the swelling ratio (%) for CS and FCS was calculated according to Ngadaonye et al. (2013).
For fluid retention tests, the samples (CS and FCS) were taken in PBS for 24 h at 37 °C, and the excess solution was removed with filter paper.The samples were maintained at 37 °C and weighed at different time points (1, 2, 3, 4, 5, 6, 12, 24, and 48 h) (Lu et al. 2016).Finally, the equation applied was done according to Marinas et al. (2020).

In vitro release studies for phenolic compounds and their antioxidant activity
The FCS were immersed in PBS for five days at 37 °C in dark glass vessels containing 1 mL PBS to analyze phenolic compounds' release kinetics.The release studies were conducted by replacing the medium with fresh PBS at each sampling time point (at 2, 4, 6, 24, 48, and 72 h).The release of the active principles was quantified by Folin-Ciocalteu, 2,2-Diphenyl-1-picrylhydrazyl (DPPH), and Ferric Reducing Antioxidant Power (FRAP) methods with a FlexStation 3 UV-VIS Spectrophotometer (molecular devices company, Sunnyvale, CA, USA).Total phenolic content was determined according to 2.2.2.

DPPH assay
A previously reported method with slight changes was applied (Madhu et al. 2013).The reaction mixture consisted of 100 µL of sample and 100 µL DPPH solution, incubated for 30 min in the dark.The absorbance was measured at 517 nm.A Trolox solution (0-200 μM concentrations) was used for the standard curve (R 2 = 0.9982).The antioxidant activity was expressed as mM TE (Trolox Equivalent)/g material.

Sterilization of CS and FCS
The CS and FCS were sterilized by irradiation, the doses absorbed by the samples ranging between D min = 33.2± 1.6 kGy and D max = 35.7 ± 1.6 kGy.The used dosimetry system consisted in ethanol chlorobenzene (ECB) mixture.Gamma irradiation (Co-60) was performed for around 12 h at a dose greater than 25 kGy using SVST Co-60/B irradiator (Institute of Isotopes Co. Ltd.Budapest, Hungary).The sterility verification was done at 10% CS in peptone water and maintained at 37 °C for 24 h, and 100 µL was inoculated on tryptone soy agar and Sabouraud agar.Finally, the Petri plates were incubated at 30 °C for 72 h for the enumeration of aerobic and mesophilic microorganisms and seven days for fungi.

Evaluation of the antimicrobial activity
The following strains were used: Escherichia coli ATCC 11229; Staphylococcus aureus ATCC 6538; Enterococcus faecium DMS 13590, Pseudomonas aeruginosa ATCC 27853; Candida parapsilosis ATCC 22019 and Candida albicans ATCC 10231 as well as clinical, multi-drug resistant isolates, i.e., Staphylococcus aureus, Pseudomonas aeruginosa, Acinetobacter baumannii and Enterobacter cloacae, from the microbial collection of Microbiology Laboratory from Faculty of Biology, University of Bucharest (Ong et al. 2008).The CS and FCS samples were submerged with microbial suspension (10 4 CFU/mL) and vortexed.The viable cell counts (CFU/mL) were determined on solid media (Muller-Hinton agar for bacteria and Sabouraud for yeasts) at initial (around 10 min) and one-day contact times.The method was adapted from SR EN ISO 11737-1 (2006) Sterilization of medical devices-Microbiological methods-Part 1: Determination of a population of microorganisms on products.The logarithmic reduction of microbial growth was calculated as follows: (1) Assessment of the anti-inflammatory effect and biocompatibility

Cytotoxicity and cell proliferation
Hep-2 (Human Epithelial Cell Line, ATCC) and RAW 264.7 (macrophage-like, Abelson leukemia virus-transformed cell line derived from BALB/c mice, ATCC) cells were cultured in Gibco Dulbeccoʼs Modified Eagle Medium (DMEM) supplemented with 10% fetal bovine serum and Penicillin-Streptomycin (100 U/mL) and Amphotericin B (25 µg/mL).CS and FCS were weighted in sterile saline buffer.The tested concentrations were 25, 50, 150, 250 and 500 µg material/mL.Cytotoxicity was assessed using the Cytotoxicity Detection Kit (Sigma-Aldrich) based on the measurement of the LDH released from damaged cells.Cell proliferation was analyzed with the Cell Proliferation Kit I (MTT, Sigma-Aldrich) (Serbezeanu et al. 2019).

Pro-wound healing activity
Using a previously described method, the standard Hep-2 cell line, recommended for routine testing of biomaterials cytocompatibility, was used to test the new materials effect on wound healing (Muniandy et al. 2018).The Hep-2 cell line is also recommended for the scratch assay (Takumi-Tanimukai et al. 2022) because these cells easily form a confluent monolayer.The CS and FCS were tested at 100 µg/mL concentration, for which they show the highest level of biocompatibility.Image analysis was performed using the Image J software.

Hemocompatibility
The hemolysis test was made according to Jiang et al. (2011) with few modifications.A 4 mL volume of whole bovine blood treated with 10% citric acid dextrose (CDA) was diluted with 5 mL of 0.9% PBS.An amount of 10 mg CS and FCS respectively, was incubated in PBS for 30 min at 37 °C.After adding diluted blood (0.05 mL) to each sample the tubes were incubated for 60 min at 37 °C.
Positive and negative controls were performed by adding 0.05 mL of bovine blood to 0.5 mL of distilled water (negative control) and PBS (positive control), respectively.All tubes were centrifuged for 5 min.The absorbance (A) of the supernatant was measured at 545 nm.Hemolysis was calculated as follows (Reshmi et al. 2018): For the blood clotting tests, a 5 μL volume of bovine blood was spotted over 10 mg of material.The blood was allowed to coagulate on the substrates for 60 min, and the free hemoglobin concentration was measured at 10 min.To measure the concentration of free hemoglobin lysis, the substrates were immersed in 500 μL of deionized water (DI).The substrates were gently shaken and left in DI water for 5 min to lyse free hemoglobin.The absorbance was measured at a wavelength of 540 nm.The absorbance value increases with the concentration of free hemoglobin (Smith et al. 2010).

Statistical analysis
Data were expressed as means ± SD determined by triplicate analysis.The GraphPad Prism v9 software was used for statistical analysis.Ordinary two-way ANOVA with two-stage linear step-up procedure with individual variances method was assessed for comparison between CS and FCS (for water retention, phenols release, antioxidant activity, antimicrobial activity, hemolysis, blood clotting, wound closure, LDH release, cell proliferation, and cell migration).For immunomodulatory activity, the results were analyzed using ordinary twoway ANOVA with main effects by Tukey's multiple comparisons assay for each comparison between native cells stimulated with E. coli and CS or FCS.The significant level was set to p-values < 0.05. (2)

Chemical characterization of P. americana fruit extract
The quantification of TPC was done using the calibration curve for gallic acid, obtaining a content of 477.86 ± 6.19 μg TPC (GAE, gallic acid equivalents)/ mL extract.
The screening UHPLC-Q-Orbitrap HRMS analysis allowed to identify many bioactive compounds and their metabolites present in the P. americana extract, which are also responsible for antioxidant activity.In addition, data processing using Compound Discoverer Software allowed the identification of the compounds found in the extract by searching in online libraries and databases, such as Chemspider, mzCloud, MzVault and mass list matches (Hohrenk et al. 2020).
Chemical compounds such as phenolic acids, flavonoids, isoflavones, anthocyanidin derivatives and gibberellin plant hormones, but also organic acids and vitamins, could be identified in P. americana fruit extract.Table 1 shows the molecular formula and the retention time of the main identified compounds based on the mass-to-charge ratio (m/z) and MS/MS fragment formed during ESI in negative mode.Most identified compounds showed antimicrobial and anti-inflammatory properties (Bailly 2021), and anti-allergic effects (Chen et al. 2022), suggesting their efficacy in the treating skin health problems.
Attempts were made to identify the saponins in the extract obtained from P. americana fruits based on a UHPLC-ESI-HRMS analysis.The total ion current (TIC) chromatogram of the P. americana fruit extract in the negative ion mode, covering a scan range between 120 and 1800 m/z, is shown in Fig. S1.The extracted chromatograms of the main saponin compounds identified in the P. americana extract using a 5 ppm mass accuracy window are presented in Fig. S2.The retention times, precursor ion mass, and fragment ion data of these compounds are summarized in Table 2.
Thus, nine esculentosides (A, B, H, M, S, R, L, G, and F) were identified in P. americana fruit extract, from which A, B, and H, were the most abundant.Esculentoside compounds show strong anti-inflammatory (Wei et al. 2015;Saleri et al. 2017), anti-allergic (Ci et al. 2015), anti-cancer (Saleri et al. 2017;Bailly and Vergoten 2020), antifungal and antiviral, including against SARS-COV-2 (Zeng et al. 2021) effects.In addition, the antifungal saponins phytolaccoside F and phytolaccasaponin N-5, but also phytolaccagenin, widely used to treat inflammatory conditions (Wei et al. 2015), as well as triterpene glycosides (desholothurin and holothurinoside) which have considerable antitumor and antiviral activities (Bordbar et al. 2011) were also identified in the P. americana fruit extract.Phytolaccagenin, desholothurin and holothurinoside, are biologically-active   Pods from different vegetables have high cellulose, hemicellulose, and lignin content.In our previous studies, we extracted cellulose (Marinas et al. 2020) and obtained microfibers.In this study, the pods' powder was submitted to ten cycles of delignification to remove the extractable substances, hemicellulose, and lignin.After extraction, the lyophilized cellulosic spongious material (15.33 ± 2.52% from total pods powder) was characterized and compared with the nanocellulose functionalized with phenolic compounds extracted from P. americana fruits (Fig. 1).
The ATR-FTIR spectra of the studied materials, CS and FCS, are presented in Fig. 2. According to Garside and Wyeth (2003), the absence of the C=O band observed in both spectra (at ∼ 1735 cm −1 ) shows the complete hemicellulose removal.The lack of bands at ∼ 1505 cm −1 and ∼ 1595 cm −1 (aromatic C=C vibrations in the plane) and 1263 cm −1 (C-O-C specific to etheric bonds) highlights the successful removal of lignin.The glycosidic ether bands C-O-C (∼ 1160 cm −1 ) are specific for the presence of cellulose.The band from ∼ 2900 cm −1 , detected in all samples, corresponds to the C-H stretching vibration from the organic content (Garside and Wyeth 2003).The OH group specific to primary alcohols comes from the ethanol solvent, tested at a similar concentration to that used to obtain the P. americana fruit extract.
According to the literature data (Edelmann et al. 2001;Fernández and Agosin 2007), the bands in the region 1680-900 cm −1 are specific to phenolic compounds from the extract.The specific aromatic C-H vibrations are attributed to the wavenumbers between 670-900 cm −1 and 950-1225 cm −1 (Laghi et al. 2011).Also, the wavenumber 902 cm −1 can be attributed to the saponoside components in the composition of P. americana fruit extract (Hajimohammadi et al. 2016).The presence of fruits-specific beta-cyanides can be identified at the wave numbers 3274 cm −1 (range O-H and N-H), 1712 cm −1 (range C=O), and 1516 cm −1 (range C=C) (Qin et al. 2020).Table S2 gives the main absorption bands and their assignments for CS, FCS and dry extract.
Further, structural features of the investigated sample were assessed using X-ray diffraction.In Fig. 3 is presented the experimental XRD pattern (black line), which exhibits a main diffraction peak located at 22.3°, accompanied by broad diffraction features at ~ 15°, 16.5°, 28.4° and 34.2°.Besides, diffraction peaks with small intensity can be observed.
A key structural parameter for cellulose is the crystallinity degree (index), which is closely related to the rigidity/flexibility of cellulose fibers.For instance, Gümüskaya et al. (2003) showed that the rigidity and flexibility are closely related by the crystallinity degree given by hemicelluloses and lignin (Carrión-Prieto et al. 2019).The degree of crystallinity (Cr.I) was evaluated using the empirical equation proposed by Segal et al. (1959) through the following equation: where I 200 represents the peak intensity correspond- ing to the crystalline domain and I am to the minimum intensity between ( 110) and ( 200) located at 18.4°.Accordingly, a degree of crystallinity of 66.7% has been obtained.
Another central structural aspect is related to the size of the crystalline domains, since the different crystallite sizes affect the thermal degradation temperature of natural fibers (Poletto et al. 2013).One of the most common ways to evaluate the crystal quality is based on the Scherrer's equation on the (200) main reflection that gives the correlation between the size of the crystalline domains and the Full Width at Half Maximum (FWHM) (Patterson 1939): where k is a shape factor usually taken as 0.93, λ is the wavelength of the incident X-ray beam (0.15418 nm), β is the Full Width at Half Maximum (FWHM) of the diffraction peak in radians and θ is the angular position.Based on the pseudo-Voigt fit of the (200) cellulose reflection, the FWHM is 2.8°, which implies a mean crystallite size of 3.3 nm.Further insights related to the mean crystallite size and the lattice strain were gained using the Whole Powder Pattern Fitting (Rietveld) method using PDXL: Integrated (4) = k cos X-ray powder diffraction software developed by Rigaku corporation (https:// www.rigaku.com/ techn iques/ rietv eld-analy sis).After publication of the crystal structure of I β by Nishiyama et al. (2002), the Rietveld method was applied by a number of researchers (Thygesen et al. 2005;Driemeier and Calligaris 2011;Driemeier 2014;Duchemin 2017).Here, the pattern fitting is performed over a broad angular range, based on information about the crystal system and lattice constants (Rietveld 1967(Rietveld , 1969)).Thus, it requires to have a reasonable initial approximation of some parameters, including peak shape, unit cell dimensions, or coordinates of all atoms in the crystal structure, to resolve a real structure (Pecharsky and Zavalij 2008;French 2020).In Fig. 3, an initial model (olive line) was proposed in the assumption of two well-defined phases: (1) crystalline Nishiyama cellulose I β with theoretical positions displayed with blue lines and (2) amorphous state with crystallinity index of 67.7%, contributing to background.In this framework, the Rietveld method includes the smaller peaks that are lost in what appears to be background or amorphous scattering (French 2020).Extensive reports were published related to the shape of the amorphous scattering in cellulose.So far, in the literature is no standard model for amorphous cellulose and common peak functions such as Gauss, Lorentz and Voigt functions do not fit the amorphous profile well.It was shown that the amorphous contribution to the diffraction pattern is more complex than a simple shape.For instance, (Thygesen et al. 2005 2020).In this work, the Rietveld refinement using PDXL: Integrated X-ray powder diffraction commercial software was used to refine the amorphous XRD scattering, as well as the entire XRD pattern.In fact, it implies fitting of the experimental data with a theoretical profile, y calc i with the following expression (Pecharsky and Zavalij 2008): (5) Here, s n is the scale factor, 2 h the Bragg angle, A(2 ) the absorption and irradiation correction, P n,h the preferred orientation correction, I n,h the inte- grated intensity function, T 2 i the angular correc- tion, and y b (2 i ) the background function.During the refinement, the background was modelled with a B-spline function, the peak shift with the shift axial displacement model, the peak shapes using pseudo-Voigt fits, while the preferred orientation with the March-Dollase function.One can notice that the initial approximation fits adequately the amorphous intensity of the experimental data (I am ), as well as the ( 110) and ( 200) reflections.This fact clearly indicates that the calculated crystallization index by Eq. ( 3) was successfully incorporated in the initial approximation.On the other hand, the initial approximation fails in the description of the secondary reflections located at higher 2θ angles.In addition, the Rietveld refinement considers the actual main crystalline parameters, such as the unit cell parameters, mean crystallite size, lattice strain or preferential orientation.The observed discrepancies between the initial approximation and experimental data result from either preferential orientation along (200) or due to a non-negligible strain in the cellulose lattice, reflected in the relative intensities of the reflections related to the (200) and shift of the diffraction peaks, respectively.The shift between the initial approximation and the experimental data, Δθ is evidenced using black arrows, indicating that the actual interplanar distance of ( 110) and ( 200) atomic planes is slightly expanded, probably due to a non-negligible tensile lattice strain.By means of the Rietveld refinement, the diffraction feature positions are well-described, as well as the relative intensities of the secondary diffraction peaks (i.e,.others than ( 200)).During the least squares fit, four numerical figures of merit (FOMʼs) were used: reliability factor (R p ), the weighted parameter (R wp ), the expected profile residual, Re and the goodness of the fit, χ 2 , showing the reliability of the fit.For the present fit, the following FOM's were obtained: R p = 3.60%, R wp = 4.83%, R e = 2.98% and χ 2 = 2.62 .
The discrepancies between Rietveld and experimental data reside in: (1) the presence of the crystalline phase, ascribed to the cinnamic acid, as well as (2) unresolved overlapped diffraction peaks due to the presence of the amorphous phase.In fact, Rietveld analysis proves the existence of the type I β cellulose with monoclinic symmetry in the investigated sample, with lattice unit parameters a = 7.784 Å, b = 8.201 Å, c = 10.38 Å nm with γ = 90°.Based on the Rietveld fit, a mean crystallite size of 2.6 nm was obtained, and at the same time, a tensile lattice strain of 1.6%.At the same time, the Scherrer equation gave a mean crystallite size of 3.3 nm, both values being typically for cellulose (Thygesen et al. 2005).
Figure 4 shows the morphologies of microporous cellulosic sponge (CS-a and b) and functionalized microporous cellulosic sponge (FCS-c and d).In the insets are illustrated the histograms of the pore diameter (Fig. 4A and C) and the nanofibersʼ diameter (Fig. 4B and D).The SEM images show two areas in both samples: microporous material and a smaller area that presents cellulose nanofibers.The size distribution of the CS (Fig. 4a, b) and FCS (Fig. 4c, d) was obtained by measuring around 150 nanofibers, and the histograms' layout was best fitted with the Gauss function.
The SEM analysis for CS showed that the pore diameter (Fig. 4A) ranged from 1.13 to 10.42 µm, and the cellulose fibers size (Fig. 4B) varied from 9 to 114 nm.The highest percentage of cellulose pores was found between the 1.51 and 4.22 µm size having a mean size of 3.66 ± 2.02 µm and for the cellulose fibers size was found a 10-36 nm size range, with the mean size of 25.1 ± 16.8 nm.Thus, the small crystallites led to nanofibers with higher diameters of different values.In the case of FCS, it was observed that the impregnation of the extract produced an increase in pore and fiber sizes compared with the control sample (CS) and ranged from 1.53 to 13.32 µm (Fig. 4C) and from 16 to 163 nm (Fig. 4D), respectively.The highest percentage of cellulose pores was found to be within the 1.95-5.08µm size range, having a mean size of 4.16 ± 1.97 µm, and for the cellulose fibers size was found a 26-71 nm range, with the mean size 57.9 ± 28.2 nm.
The CS and FCS obtained in this work are comparable to other porous materials obtained from plant (or bacterial) raw materials with similar microscopic features (Liu et al. 2021) and water absorption capacity (Bian et al. 2022).Regarding biological activity, some studies reported absorbent cellulose sponges with similar applications (Paprskářová et al. 2021;Bian et al. 2022), biocompatible aerogels (Zhang  (Liu et al. 2022).
The spongious material wettability is given by its microscopic characteristics, namely the surface roughness, the surface energy of the materials and the thin surface coatings.Contact angle measurements investigated the hydrophilicity characteristics of the synthesized structures (Supplement Information: video files).The cellulosic spongious materials showed a super hydrophilic behavior (CA ~ 0°), the water droplets being instantly absorbed in the case of FCS, while for the CS, the absorption rate was 1920 ms/μL.
The percentage of PBS absorption was almost similar in case of CS (1463.51%)and FCS (1463.93%)materials, but the absorption capacity is very high, suggesting their usefulness in case of wounds with excess exudate (Abdelrahman and Newton 2011).Statistically significant differences were observed in terms of fluid retention capacity between CS and FCS (Fig. 5).Thus, for the control, the retention became constant after 2 h, while for the functionalized spongious material the retention was slightly higher, becoming constant after 4 h.The water evaporation rate in the first 4 h was 23.15% evaporated PBS/h for FCS, while for the control, the rate was 68.13% in the first 2 h.
The new spongious material retained a specific humidity when exposed to air in wear conditions for long periods.Thus, these dressings will be advantageous for moderate and high exudate wounds.In addition, water loss could allow uptake of exudates and edema fluid from the dressing through an upward-directed active process, as reported for some commercially available dressings (Kickhöfen et al. 1986;Ngadaonye et al. 2013).
The final materials presented a super hydrophilic surface with a relatively smooth surface that ensures good absorbency and fluid retention.In functionalized spongious material, the slower evaporation of fluids could be explained by hydrogen bonds forming between the mixture of phenols and hydroxyl cellulose groups, which could challenge water evaporation (Fig. 5).The investigated samples show a wicking behavior.In addition, this phenomenon is well-known due to the spontaneous flow of the liquid in a porous substrate, the liquid being driven by the capillary forces.Absorption is the result of natural wetting in a capillary system.The molecular interactions at the interface between a liquid and a solid are based on the physics of wetting and absorption.Quick-drying and wetting are specific phenomena in the processing and use of textiles coming into contact with water or other liquids that the fibrous structures could absorb.These parameters are of the greatest interest in formulating new materials with a degree of comfort and performance of clothing fabrics, hygiene products, medical swabs, etc. (Cotorobai et al. 2016).
To evaluate the release kinetics of the active principles, the total content of phenolic compounds was determined by the Folin-Ciocalteu method and the antioxidant activity was evaluated in temporal dynamics.The releasing profile of active principles varied considerably over time (Fig. 6a), in the first 48 h, the release was linear (R 2 = 0.9935) with a velocity of 0.8941 μg GAE/mL xh.Although the active principles migration from the cellulose-based dressings was relatively short, after 48 h, the release of the incorporated extract remains constant.The results were statistically relevant (p < 0.0001).
The Folin-Ciocalteu method is an antioxidant assay based on electron transfer, which measures the reductive capacity of an antioxidant (Lamuela-Raventós 2017).The antiradical properties of native cellulose has been previously described (Criado et al. 2015).The cellulose sponge antioxidant activity could be attributed to the presence of the anomeric hydroxyl group, as previously mentioned (Mahmoud et al. 2022).However, the antioxidant effect of cellulose sponge has been much lower compared to pure antioxidants or P. americana extract.
In both FRAP (Fig. 6b) and DPPH (Fig. 6c) assays, it was observed that a high concentration of phenolic compounds with antioxidant potential was released in the first release cycle, and then, was reducing overtime.
In the FRAP assay (Fig. 6b), it was observed that in the first 24 h, the highest concentration of antioxidants was released, and a statistically significant difference being observed between FCS and CS after 2 h, 4 h, 24 h (p < 0.01) and 12 h (p < 0.001).
The antioxidant activity measured by the DPPH assay is inversely proportional to the contact time, with a constant release value maintained after 24 h (Fig. 6c).A statistically significant difference was observed between FCS and CS after 2 h, 4 h, 12 h, 48 h, 72 h (p < 0.0001) and 24 h (p < 0.01).
The release of antioxidant compounds from the bioactive wound dressing could positively impact the healing process by limiting the ROS (Reactive oxygen species) release and, possibly contributing to the occurrence of an antimicrobial effect which will prevent wound infection (Schafer and Werner 2008).In this context, we aimed to study the antioxidant potential and the kinetics of the active compounds release from the functionalized cellulose matrix and further correlated these effects with those of antimicrobial activity assay.

Microbiological control and antimicrobial activity
The degree of contamination showed that sterilization by gamma irradiation using the recommended doses ensured the sterility of the obtained products.
Regarding the antimicrobial activity, the active compounds released from the cellulose matrix inhibited the MRSA strains growth by up to about 30%.A significant difference between CS and FCS was observed for MRSA (p < 0.0001) (Fig. S4), E. faecium (p < 0.0001), P. aeruginosa ATCC (p < 0.0.5) (Fig. S5), and C. parapsilosis (p < 0.01) (Fig. S3) strains (Fig. 7).The growth of A. baumannii strain was completely abolished (100%) by both CS and FCS after 15 min (considered 0 h) and 24 h of contact.The calculation of CFU/mL suggested that the functionalized cellulose exhibited a more intense antimicrobial effect as compared to cellulose control.
This antimicrobial activity could be attributed to the presence of: (i) gibberellins, which are known for their antimicrobial properties against phytopathogens and clinical pathogens (Ciucure et al. 2022); (ii) azelaic acid, which is an important moiety for the management of acne, inhibiting the excess follicular sebum and Propionibacterium acne growth and exhibiting anti-inflammatory and hyperproliferative activity, according to Kumar et al. (2020); (iii) medicarpin, which has been shown to exhibit anti-gonococcal activity (Williams et al. 2021).
The decrease of CFU/mL induced by CS has been observed in the case of some bacterial strains (S. aureus, P. aeruginosa, and E. cloacae) in the absence of the active compounds from P. americana.This effect could be due to the physical interaction of the spongious material with these bacterial cells, favoring the immobilization of the microbial cells on the material surface, and not necessarily to the presence of a compound with an antimicrobial effect.In exchange, other species, such as E. coli (Liu and Yu 2012), C. albicans (Chambers et al. 1993) and C. parapsilosis (Brexó et al. 2020) were found to produce cellulases that could degrade the cellulose fibers from the sponge material, thus explaining the inconsistency of the CS antibacterial effect for some microbial species.However, in the case of the FCS, cellulase activity could be inhibited by the active principles (the phenolic compounds) from the plant extract (Qin et al. 2016), explaining their antimicrobial effect (Marinas et al. 2021).

Hemocompatibility and biocompatibility
The hemolysis index for CS and FCS was below 5%, i.e., 2.68 ± 0.29% and 3.28 ± 0.72%, respectively.The presence of saponosides in the FCS conferred to the functionalized cellulose a higher degree of hemolysis, although not statistically significant (p > 0.05), compared to the control.Although the complex processes involved in the four phases of wound healing, i.e. hemostasis, inflammation, proliferation, and regeneration, have been well characterized histologically, the cellular and molecular pathways that control normal and pathological wound healing are not fully elucidated.It is well known that red blood cells hemolyze in contact with deionized water.Considering the hemolysis rate values obtained for the used samples, the proposed materials can be classified as medical devices with possible applications as wound dressings for open wounds, for which a hemolysis rate of less than 5% is allowed (Jiang et al. 2011;Reshmi et al. 2018).
The whole blood clotting kinetics is important for evaluating the long-term success of biomaterials in contact with blood.The results indicated that the blood coagulated after 20 min in the case of CS, while for FCS, the blood clotting occurred after 30 min (Fig. 8).The delay in blood clotting may also be due to the slightly higher hemolysis index in the case of FCS.The differences between CS and FCS were not significant after 40 min (p > 0.05).However, the difference between CS and FCS was significant statistically after 10 min (p < 0.05), 20 min (p < 0.01), and 30 min (p < 0.01).
Cytotoxicity measured by the LDH assay on the Hep-2 cell line incubated with CS and FCS at different concentrations of 25, 50, 100, 250, and 500 µg/ mL is shown in Fig. 9a.The highest biocompatibility was for CS at 100 µg/µL, demonstrated by the increased cell proliferation rates (Fig. 9b, p < 0.0001) and similar LDH release with the control (p > 0.05).The results are correlated with those provided by the MTT method (Fig. 9b, c).It was observed that the plant extract significantly increases cell proliferation at 100 µg/mL (Fig. 9c, p < 0.001) while inhibiting the release of the LDH cytoplasmic enzyme, an indicator of disrupted membrane integrity.
Wound closure is a dynamic mechanical process depending on the proliferation and migration of skin cells.Therefore, the cytocompatibility of novel Fig. 8 The concentration of free hemoglobin expressed as absorbance in the presence of CS and FCS for 50 min of blood clotting spongious materials is compulsory to achieve optimal wound healing.The LDH cytotoxicity test provides multiple information on cell viability, allowing the selection of the appropriate concentration for future treatments, which in this case was 100 µg/mL.
Cell migration plays a vital role in wound healing (Muniandy et al. 2018); thus, the monolayer scratch test was performed to observe the extract's influence on cell migration and extrapolate it on wound closure.The wound scratch test is an in vitro assay that mimics the cell migration process during wound healing, and the obtained results demonstrate that the materials positively impact the wound closure process (Agyare et al. 2011;Muniandy et al. 2018) at the optimal concentration that ensures cell viability (100 µg/ mL).The values calculated according to the scratch coverage rate reached in 24 h are presented in Fig. 9d.
The migration analysis shows that, for CS, the treated cells showed a significant increase in migration by 15.39% (p < 0.05), compared to the control group, which is only 4.9%, while for FCS, cell migration increased to 26.33% (p < 0.001).Furthermore, a significant increase in migration was highlighted by comparing the functionalized spongious material with the non-functionalized one (p < 0.05).
A balanced inflammatory response provides the essential factors for wound healing and tissue regeneration during recovery (Eming et al. 2007).
In the present study, the FCS has significantly decreased the production of the pro-inflammatory cytokine IL-6 (p < 0.01) and stimulated the production of the anti-inflammatory cytokine IL-10 (p < 0.001) in the RAW macrophage cell line, in comparison with CS (Fig. 10a, b).In fact, macrophages' enhanced pro-inflammatory cytokines (such as IL-6) production which can negatively affect tissue repair rate, impairing the normal functions and extracellular matrix production in injured tissues (Eming et al. 2007;Albaayit et al. 2020).On the other part, IL-10 is an anti-inflammatory cytokine produced by several cell types that inhibits IL-1, TNF-α, IL-6, IL-8, and COX-2 production by macrophages, thus protecting cells and tissues from oxidative/nitrosative stress (Figueroa et al. 2015;Albaayit et al. 2016).
The anti-inflammatory response triggered by the functionalized spongious materials represents a strong argument that they deserve further attention for developing novel bioactive dressings that would facilitate tissue healing and recovery.
The high hydrophilic character of microporous cellulosic sponge from G. triacanthos pods functionalized with the P. americana fruit extract ensures wound fluids absorption.In addition, the obtained material shows antimicrobial, antioxidant and immunomodulatory properties, which are important for wound healing.Furthermore, the hemolysis rate of less than 5% is within legally acceptable limits.All these results suggest that FCS is an excellent candidate for developing bioactive dressings that could ensure cell proliferation and migration, and simultaneously limit microbial contamination, excessive inflammation, and ROS release.All these effects could increase the skin wounds' healing process.This option also represents a cost-effective and ecological approach to reduce the uncontrolled invasion of non-native plant species and exploit them for novel biomedical applications.

Fig. 4
Fig. 4 The SEM images of the reference CS surface (a 100 K × magnification, inset A-pore size histogram; b 500 × magnification, inset B-fibers size histogram) and the

Fig. 9
Fig. 9 The comparative biocompatibility of CS vs. FCS: a Cell cytotoxicity measured by LDH test-Hep-2 cells co-cultured in the presence of CS and FCS at different concentrations of 25, 50, 100, 250, and 500 µg/mL; b, c evaluation of cell proliferation and d, e cell migration.Statistical analysis was performed by reference to the control, represented by cells without any treatment ◂

Table 1
The chemical compounds identification in P. americana fruit extract based on UHPLC-ESI-HRMS analysis combined with data processing using compound discoverer software (Chen et al. 2022)nts, acting as bacterial growth inhibitors(Chen et al. 2022).Characterization of microporous cellulosic sponge (CS) and functionalized microporous cellulosic sponge(FCS)

Table 2
Identification of triterpenoid saponins in P. americana fruits based on UHPLC-ESI-HRMS analysis combined with data processing using Compound Discoverer Software R.T.-retention time