GC/MS Analysis, Antioxidant Activity, and Antimicrobial Effect of Pelargonium peltatum (Geraniaceae)

In recent years, the increase in antibiotic resistance demands searching for new compounds with antimicrobial activity. Phytochemicals found in plants offer an alternative to this problem. The genus Pelargonium contains several species; some have commercial use in traditional medicine such as P. sinoides, and others such as P. peltatum are little studied but have promising potential for various applications such as phytopharmaceuticals. In this work, we characterized the freeze-dried extracts (FDEs) of five tissues (root, stem, leaf, and two types of flowers) and the ethyl acetate fractions from leaf (Lf-EtOAc) and flower (Fwr-EtOAc) of P. peltatum through the analysis by thin-layer chromatography (T.L.C.), gas chromatography coupled to mass spectrometry (GC-MS), phytochemicals quantification, antioxidant capacity, and antimicrobial activity. After the first round of analysis, it was observed that the FDE-Leaf and FDE-Flower showed higher antioxidant and antimicrobial activities compared to the other FDEs, for which FDE-Leaf and FDE-Flower were fractionated and analyzed in a second round. The antioxidant activity determined by ABTS showed that Lf-EtOAc and Fwr-EtOAc had the lowest IC50 values with 27.15 ± 1.04 and 28.11 ± 1.3 µg/mL, respectively. The content of total polyphenols was 264.57 ± 7.73 for Lf-EtOAc and 105.39 ± 4.04 mg G.A./g FDE for Fwr-EtOAc. Regarding the content of flavonoid, Lf-EtOAc and Fw-EtOAc had the highest concentration with 34.4 ± 1.06 and 29.45 ± 1.09 mg Q.E./g FDE. In addition, the minimum inhibitory concentration (M.I.C.) of antimicrobial activity was evaluated: Lf-EtOAc and Fwr-EtOAc were effective at 31.2 µg/mL for Staphylococcus aureus and 62.5 µg/mL for Salmonella enterica, while for the Enterococcus feacalis strain, Fwr-EtOAc presented 31.2 µg/mL of M.I.C. According to the GC-MS analysis, the main compounds were 1,2,3-Benzenetriol (Pyrogallol), with 77.38% of relative abundance in the Lf-EtOAc and 71.24% in the Fwr-EtOAc, followed by ethyl gallate (13.10%) in the Fwr-EtOAc and (Z)-9-Octadecenamide (13.63% and 6.75%) in both Lf-EtOAc and Fwr-EtOAc, respectively.


Introduction
Plants' primary metabolism is essential for their survival, characterized by synthesizing the necessary metabolites for their growth and functionality, such as sugars, fatty acids, and amino acids, among others. On the other hand, secondary metabolism is not essential for their survival; it is generated in response to chemical, physical, and biological factors resulting from the interaction between the plant and the environment. Secondary metabolism confers defense to biotic and abiotic stress, triggering a synthesis response of secondary metabolites that activates the plant's defense mechanism [1,2].
It has been estimated that plants can produce more than 200,000 secondary metabolites; among them, terpenes, alkaloids, and polyphenols are the most diverse [3,4]. Polyphenols are a well-known group of compounds with antioxidant properties present in plants among the secondary metabolites. Polyphenols are present in more significant quantities in epidermal and sub-epidermal cells' walls and vacuoles. The basic structure of polyphenols is composed of a phenyl ring with a hydroxyl group attached to it. This basic structure allows polyphenols to be classified into different subfamilies, including flavonoids and tannins [5][6][7].
Flavonoids have a 15-carbon phenyl benzopyran skeleton [5]. They are synthesized in all parts of the plant and are responsible for the pigmentation of flowers. Polyphenols protect the plant from certain insects and ultraviolet radiation [8]. Tannins are molecules with high molecular weight (500 to 20,000 Daltons), produced in seeds, roots, bark, wood, and leaves. They are characterized by an astringent taste [9] that generates protection against predators such as birds, herbivores, and some insects [5].
Tannins are classified as hydrolyzable and condensed tannins. Hydrolyzable tannins can be hydrolyzed with acids, bases, and hot water. This class of tannins is divided into gallotannins with a central structure of glucose, and ellagitannins result from the oxidation of penta-galloylglucose. Condensed tannins, also called proanthocyanidins are flavonoid oligomers with varying degrees of polymerization [9]. These metabolites are characterized by their ability to scavenge free radicals, such as reactive oxygen species (R.O.S.), reactive nitrogen species (R.N.S.), and reactive sulfur species (R.S.).
These radical species affect cells through various mechanisms, such as destabilization of cell membrane structure, interference in signaling pathways, alteration of D.N.A. integrity, disruption of homeostasis, and induction of imbalance in organisms. All these mechanisms can lead to cardiovascular and chronic degenerative diseases and some types of cancer [10].
Many patients in clinics present complications caused by microorganisms since the treatments are not as efficient as required because bacteria have developed resistance to certain antibiotics, causing complications and delays in the recovery of health in patients [11]. In fact, we are going through a stage that may become critical since antibiotics are becoming less effective and common bacterial infections that were easily cured are now more complicated to treat. These complications are due to the increasing antibiotic resistance in bacterial strains. This phenomenon worsens, and many people could risk losing their lives due to a lack of adequate and effective treatment. Therefore, the search for new active ingredients with antimicrobial activity is required, and one primary source is plants.
Plants are an excellent renewable source of chemical compounds with various properties beneficial to humans. However, plants produce a wide variety of compounds, making it difficult to identify specific compounds associated with a given property. To solve this challenge, various chromatographic techniques have been developed to separate and identify the compounds of a complex sample, such as gas chromatography coupled to mass spectrometry (GC-MS), used in several studies for the identification of different compounds with antimicrobial activity obtained through the extraction of various parts of the plant and with different types of solvents [12][13][14][15][16].
Several studies researched the composition of the aerial parts of plants by GC/MS to characterize the volatile compounds in the extracts. For example, 77 compounds were found accumulated in mint extract, within which menthol and p-mentahn3-one had the highest antimicrobial activity [17]. Some studies relate antioxidant activity and the profile of volatiles in plants [18][19][20][21]. On the other hand, there are few studies of characterization by GC/MS in the genus Pelargonium, including P.graveolens [21], P. quercetorum [18], and P. capitatum [22].
In traditional medicine, the use of plant extracts is common. An example of this is the standardized extract [23] from the Pelargonium sidoides plant, an auxiliary in treating respiratory tract complications [24]. To this extract, it is attributed antimicrobial activity [25,26], antiviral activity [27], antitumor activity [28], and antioxidant synergistic potential [29]. Antimicrobial and antiviral activities have been attributed to gallic acid, its methyl ester derivatives, and coumarins such as 5,6,7-trimethoxycoumarin and 6,8-dihydroxy-5,7dimethoxycoumarin [25,30]. P. sidoides belong to the Geraniaceae family, most of which are native to Africa and comprise 11 genera, including the genus Pelargonium, which comprises more than 7500 species [31,32].
However, the diverse biological activities are not exclusive to the species P. sidoides; for example, antimicrobial activity has been reported against Staphylococcus aureus in extracts of P. graveolens. In this study, the antimicrobial activity of essential oil from P. graveolens was attributed to compounds such as β-citronellol, β-caryophyllene, and caryophyllene oxide [33,34]. In the case of P. peltatum, biological activity against Streptococcus mutans and Streptococcus tanguinis has also been reported. Nevertheless, more studies are needed to demonstrate the potential of the compounds present in P. peltatum, both in their antimicrobial properties and antioxidant potential. Therefore, the purpose of this research was to perform a phytochemical, antioxidant, and GC-MS profile of hydroalcoholic extracts of root, stem, leaf, and flower of P. peltatum, seeking to compare the differences in the concentration of antioxidant compounds among the different tissues and to evaluate which of the extracts obtained had the highest antioxidant and antimicrobial activity and the possible semi-volatile compounds related to them. Table 1 shows the dry weight of each part of the plant and the weight obtained from the freeze-dried extracts (FDE). The freeze-dried flower extract (FDE-Bicolour) showed the highest recovery with a 28.47% yield, while the freeze-dried stem extract (FDE-Stem) showed the lowest with a 6.65% yield. From now on, we will refer to the freeze-dried extracts as FDE-Root, FDE-Stem, FDE-Leaf, FDE-Flower, and FDE-Bicolour. The lyophilized extracts were subjected to solubility tests. Most of the extracts were soluble in polar solvents, as shown in Supplementary Table S1.

Phytochemical Profiling by High-Performance Thin Layer Chromatography
The FDEs of P. peltatum were analyzed by thin-layer chromatography (T.L.C.) using a mobile phase of water: methanol: ethyl acetate (10:14:76) for their separation. The chromatoplates were developed using specific reagents for each group of compounds and exposure to ultraviolet light at two wavelengths (254 and 366 nm). For the development of tannins, we used a 1% ferric chloride solution; the chromatoplates showed the presence of bands in all the FDE. In particular, two bands (with RF = 0.015 and RF = 0.036) were present in all extracts, suggesting that the compounds found in these retention factors are common in all plant tissues. Similarly, a 1% aluminum chloride developer was used for flavonoids. In this case, all extracts presented bands reactive to this solution, where FDE-Flower showed the highest complexity of banding pattern (13 bands). Table 2 summarizes the retention factors (R.F.) for the bands detected in each experiment. In the case of the chromatoplates visualized at 254 nm, very few bands were observed in only two extracts, while the banding patterns visualized at a wavelength of 366 nm presented complex banding patterns in all extracts (see Supplementary Figure S1). We were unable to detect compounds with the alkaloid developer.

Antioxidant Activity of Freeze-Dried Extract from P. peltatum
The antioxidant capacity of the FDEs samples were evaluated using the DPPH, ABTS, and FRAP methodologies. The results are shown in Table 3. In these experiments, we evaluated different concentrations of the FDEs (20-500 µg/mL), and the results were expressed as IC 50 (µg/mL) for ABTS and DPPH. FRAP measurements are reported in µM Trolox equivalent (T.E.).  Figure 1A.

Antimicrobial Activity of Freeze-Dried Extract from P. peltatum
The FDEs of P. peltatum were tested to inhibit bacterial growth using four strains: Staphylococcus aureus, Enterococcus faecalis (Gram + bacteria), Salmonella enterica, and Serratia marcescens (Gram-bacteria). The FDEs were diluted with sterile water to a 5 mg/mL Tannin concentration was determined by the vanillin method. The results were expressed in mg of catechin equivalents (Q.A.)/g of dry extract. The FDE-Root had the highest tannin content with 214.99 ± 21.3 mg Q.A. equivalents/g of FDE, being almost twice as high as the FDE-Flower extracts with 99.02 ± 8.2 and the FDE-Bicolour with 77.14 ± 8.2 mg Q.A. equivalents/g of FDE. In contrast, the FDE-Leaf had the lowest tannin concentration with 6.23 ± 7.5 mg Q.A. equivalents/g of FDE. These values are plotted in Figure 1B, where the significant differences between the samples can be observed with a confidence level of 95% using the ANOVA and Tukey test.
The flavonoid content was performed using the aluminum trichloride method. Results were expressed as mg quercetin equivalents (Q.E.)/g of FDE. The FDE-Root showed the highest amount of flavonoids with 743.5 ± 36.7 mg Q.E. equivalents/g of FDE ( Figure 1C) compared with the rest of the extracts, which showed about three times less. This time, the FDE-Stem was the sample with the lowest flavonoid content with 157.58 ± 24.6 mg Q.E. equivalents/g of FDE.

Antimicrobial Activity of Freeze-Dried Extract from P. peltatum
The FDEs of P. peltatum were tested to inhibit bacterial growth using four strains: Staphylococcus aureus, Enterococcus faecalis (Gram + bacteria), Salmonella enterica, and Serratia marcescens (Gram-bacteria). The FDEs were diluted with sterile water to a 5 mg/mL concentration and then assayed in the agar-well diffusion method. The FDEs exhibited microbial inhibitory activity in all strains tested ( Figure S2). However, FDE-Leaf, FDEbicolour, and FDE-Flower presented generally more considerable inhibition halos than FDE-Stem and FDE-root. Gram-positive strains were more susceptible to inhibition by FDEs than gram-negative strains. Notably, E. faecalis was highly susceptible to growth inhibition with FDE-Leaf. Generally, the FDEs with the highest activity are also those with the highest presence of polyphenols. The inhibition zones generated by FDEs against S. aureus, E. faecalis, S. enterica, and S. marcescens are presented in Supplementary Table S2.

GC-MS Analysis of FDEs from P. peltatum
In order to know the chemical composition of the five extracts, we decided to perform a screening of volatile and semi-volatile compounds by gas chromatography coupled with mass spectrometry (GC-MS). A total of 53 compounds were identified by GC-MS analysis of polar extracts (Table 4). These compounds were esters, carboxylic acids, aldehydes, benzene derivatives, phenolic compounds, aromatic compounds, and terpenes. The FDE-Root had the most diverse chemical composition with 32 compounds, of which eight were unique, while the leaf extract was the least diverse with 21 compounds, of which four were unique, and only eight compounds are shared among all five FDEs ( Figure 2).  The ethyl gallate and 1,2,3-Benzenetriol, also known as pyrogallol, are the most abundant compounds in the leaf, stem, flower, and bicolour extracts, while in the root, tridecanoic acid and 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one are the most abundant. This difference in chemical composition could be related to the nature of the samples, since the root is the underground part, while the leaf, stem, and flower are the aerial part of the plant.  (1) KIexp: Kovats indices calculated from retention time data on a HP-5ms capillary column. (2) KIlit: Kovats indices from literature (NIST). (3) The Kovats index was not reported on a HP-5ms capillary column, the identification was made by comparison with M.S. mass spectra. The ethyl gallate and 1,2,3-Benzenetriol, also known as pyrogallol, are the most abundant compounds in the leaf, stem, flower, and bicolour extracts, while in the root, tridecanoic acid and 2,3-dihydro-3,5-dihydroxy-6-methyl-4H-pyran-4-one are the most abundant. This difference in chemical composition could be related to the nature of the samples, since the root is the underground part, while the leaf, stem, and flower are the aerial part of the plant.

Kupchan Partitioning of FDE-Flower and FDE-Leaf
The GC-MS analysis of the FDEs yielded important information about their chemical composition. However, the number of identified compounds was relatively high, and the data obtained in the antimicrobial activity assay showed that this effect was observed at high concentrations, suggesting that the compound(s) associated with this activity were diluted in the samples. In order to define these compounds, the fractionation of the FDEs was carried out using solvents with different polarities. In this case, we decided to work exclusively with the flower and leaf samples because, in the antioxidant and antimicrobial activity experiments, both FDEs presented the highest activity in both analyses. Likewise, the FDE-flower and FDE-bicolour were worked together since the GC-MS data showed that both shared 85% of the compounds. Four solvents were used: hexane (Hx), chloroform (Chl), ethyl acetate (EtOAc), and methanol (MeOH), using a Kupchan partition sequence.
The FDE-Flower and FDE-Leaf samples were subjected to solvent partitioning. The yield with the Hx fraction was practically null, so it will no longer be reported during this study. On the other hand, we obtained sufficient yields for our experiments with the FDE partitioned with Chl, EtOAc, and MeOH.

Antioxidant Activity of FDE-Flower and FDE-Leaf Partitioned Extracts
We analyzed the fractions extracted with the solvents using the three aforementioned antioxidant capacity measurement techniques. In all three methods used, the fractions with the highest antioxidant activity were those of FDE-Leaf and FDE-Flower partitioned with EtOAc (Lf-EtOAc and Fwr-EtOAc, respectively Regarding the other antioxidant capacity measurement methodologies, the trend indicated that for both methodologies (DPPH and FRAP), the fractions with the highest antioxidant activity were Lf-EtOAc and Fwr-EtOAc. The graphs of the reported antioxidant activities can be seen in Figure 3A-C. We decided to evaluate also the content of total phenols and flavonoids in these fractions. Interestingly, total polyphenols ( Figure 3D

M.I.C. of Lf-EtOAc and Fwr-EtOAc Fractions against Pathogenic Bacteria
Once the fractions antioxidant activities and phytochemical content were verified, we decided to evaluate the minimum inhibitory concentration (M.I.C.) against the pathogenic bacteria evaluated in the experiment with the FDEs. However, this time, we took advantage of the decrease in the complexity of the compound mixtures achieved by solvent partitioning. Among the fractions evaluated, it was clear that Lf-EtOAc and Fwr-

M.I.C. of Lf-EtOAc and Fwr-EtOAc Fractions against Pathogenic Bacteria
Once the fractions antioxidant activities and phytochemical content were verified, we decided to evaluate the minimum inhibitory concentration (M.I.C.) against the pathogenic bacteria evaluated in the experiment with the FDEs. However, this time, we took advantage of the decrease in the complexity of the compound mixtures achieved by solvent partitioning. Among the fractions evaluated, it was clear that Lf-EtOAc and Fwr-EtOAc were by far the ones with the best minimum inhibitory concentration, reaching 31.2 µg/mL for S. aureus and 62.5 µg/mL for S. enterica. While for E. faecalis strain, the Fwr-EtOAc fraction presented 31.2 µg/mL of M.I.C. In contrast, the Lf-EtOAc fraction was twice as high at 62.5 µg/mL. It should be noted that the antimicrobial effect against S. marcescens was greatly diminished since both EtOAc fractions presented a M.I.C. of 500 µg/mL. The rest of the fractions presented high M.I.C. values; therefore, they were considered ineffective for antimicrobial inhibition. The data are summarized in Table 5.

GC-MS Analysis and IC 50 of Lf-EtOAC and Fwr-EtOAC Fractions
This time, nine compounds were identified in the leaf fraction and 12 compounds in the Lf-EtOAc fraction. The main compounds were 1,2,3-Benzenetriol (Pyrogallol), with 77.38% of relative abundance in the Lf-EtOAc's fraction and 71.24% in the Fwr-EtOAc fraction, followed by ethyl gallate (13.10%) in the Fwr-EtOAc fraction and (Z)-9-Octadecenamide (13.63% and 6.75%) in both fractions, Lf-EtOAc, and Fwr-EtOAc, respectively (Table 6). Additionally, we calculated the IC 50 values for the Lf-EtOAc and Fwr-EtOAc fractions. The IC 50 obtained for the Lf-EtOAc by ABTS was 27.15 ± 1.04 and 33.66 ± 1.50 µg/mL with the DPPH technique. On the other hand, values of 28.11 ± 1.3 and 52.69 ± 1.6 µg/mL of IC 50 were obtained for the Fw-EtOAc fraction by ABTS and DPPH technique, respectively.

Discussion
The extracts of root, stem, leaf, flower, and bicolour flower of Pelargonium peltatum were obtained by hydroalcoholic maceration at 70%, and the chromatographic profile was analyzed. The phytochemical profile with the highest complexity was FDE-flower, which has been mentioned in phytochemical studies of other species belonging to the Pelargonium genus. However, it is essential to emphasize that species belonging to the Pelargonium genus, such as P. sidoides, have a high demand because of their use as a constituent in the formulation of phytopharmaceuticals. Due to its exploitation and the unfavorable factors in its habitat, P. sidoides is experiencing a decrease in its natural population and a deterioration of its biological niche. Thus, this research on the phytochemical and antioxidant profile of P. peltatum contributes to producing information to offer an alternative in the future as a possible source of bioactive components [35].
Polyphenols are compounds whose basic structure is hydroxyl groups attached to a phenyl ring. One of its qualities is its antioxidant activity, and in this study, a high content was detected in the FDE-Flower and FDE-Leaf. In work by Mona M. and co-workers [36] showed high polyphenol content in the extract of P. sidoides, as did Malek Ennaifer in P. graveolens, [37] and GökçeŞeker Karatoprak and co-workers [38] in P. endlicherianum, indicating that a high content of polyphenolic compounds is a characteristic in common between the different species of the genus Pelargonium. Polyphenols are highly relevant for their beneficial impact on health since they inhibit factors that can cause cardiovascular diseases (v.g. hydroxytyrosol, quercetin, and resveratrol), give protection against different types of cancer (v.g. apigenin, quercetin, curcumin, resveratrol, EGCG, and kaempferol), and help inhibit inflammatory processes in chronic degenerative diseases (e.g., apigenin, epigallocatechin gallate, ellagic acid, and rutin) that have a high incidence in the world population [39,40]. The profiles obtained by GC/MS found that one of the major components of the polyphenols is pyrogallol, among others such as catechol, eugenol, vanillic acid, methyl, and ethyl gallate.
The antioxidant activities for the FDEs presented values of low antioxidant activity measured by IC 50 , except for those reported for FDE-Flower and FDE-Leaf, whose values ranged between (46.32-48.90 µg/mL for ABTS and 132.50-103.90 µg/mL for DPPH). IC 50 values for extracts and essential oils of P. graveolens have been reported in the literature ranging from 711-1280 µg/mL for oils and 12.24-44.24 µg/mL for extracts measured by DPPH [21]. This places our results below the values obtained for oils and above those obtained for extracts. In comparison with other species, the IC 50 values reported for Nepeta melissifolia (IC 50 = 13.5 ± 0.4 µg/mL) [41] and Mentha pulegium (IC 50 = 69.60 ± 1.72 µg/mL) [42] were in comparison to our measurements by DPPH much higher in their IC 50 . On the other hand, once the extracts were fractionated, the Lf-EtOAc and Fwr-EtOAc produced IC 50 values ranging from 27.15-33.66 µg/mL for ABTS and 28.11-52.69 µg/mL for DPPH. Those values are closer to those reported in extracts of other plants with broad antioxidant power [43,44] and even relatively close to references in antioxidants of pure compounds such as BHT (18.5 ± 0.4 ug/mL) [45] but still distant from classical antioxidants such as ascorbic acid (3.9 ± 0.3 µg/mL) [46].
At least two antimicrobial compounds were detected in the Lf-EtOAc and Fwr-EtOAc fractions in the GC-MS analysis, the first one is pyrogallol (1,2,3-trihydroxybenzene) which has been reported several times as an antimicrobial and antioxidant compound. In the work reported by [47], they demonstrate that a dimer of this compound can produce a MIC value for Staphylococcus aureus and Escherichia coli of (8 µg/mL) and in its non-polymerized form of 512 and 256 µg/mL, respectively. This study was performed with a pure compound, while in our analysis a MIC value of 31.2 µg/mL was found in the analyzed fractions of EtOAc against S. aureus and of the Fwr-EtOAc fraction against E. faecalis. In fact, pyrogallol is classified as an allelochemical [48,49] and other polyphenolic compounds in conjunction with pyrogallol have been evaluated to potentiate the effect of known antibiotics [50]. It is important to mention, that there are new studies regarding the possibilities of the use of pyrogallol, in material sciences, and due to the complexity of its synthesis, extractions from the plant kingdom are still a suitable option for its isolation [51]. The other compound found in our study from acetate fractions is ethyl gallate. This compound has been reported with a MIC of 0.24 and 0.48 mg/mL in extracts of R. crenulata, against E. coli and S. aureus strains. Although these MIC concentrations are very high compared to the highest MIC values obtained in this study for acetate fractions (500 ug/mL), other reports have indicated the potential of its antioxidant and antimicrobial activity [52][53][54][55][56][57].
Interestingly, our analysis showed the presence of (Z)-9-Octadecenamide, in the acetate fractions, this compound has been known by the common name oleamide and has neurological activities, in fact, it is a lipid-like molecule that induces sleep [58], but it also has activities that regulate memory processes and antinociception [59]. Other reports have associated it with an algaecidal and fungicidal agent [60].
Finally, in the food industry, many molecules of synthetic origin, such as BHT and its derivatives, are used to improve processed foods' quality and shelf life; however, these types of molecules can have adverse effects, leading to the development of tumor tissues [61]. That is why it is crucial to identify naturally occurring molecules with antioxidant activity. In this work, we detected 53 different compounds by GC/MS in the five FDE extracts, including furan derivatives, furfurans, polyphenols, fatty acids, and various esters of gallic acid. Interestingly, the fractions obtained by partitioning with ethyl acetate in flower and leaf reported excellent antimicrobial and antioxidant activities. Overall, the results obtained in this research suggest that P. peltatum is an excellent option for further studies, elucidating the compounds involved in the significant antioxidant capacity values and the promising potential of antimicrobial activities.

Reagents
All chemicals used were of analytical grade and were used as received without any further purification. All solutions were prepared with deionized water.

Harvesting and Identification of P. peltatum
Plant material was obtained from various nurseries in the city of Guadalajara Jalisco between February and June 2020, one of the specimens was used for taxonomic identification by Dr. Liberato Portillo of the Centro Universitario de Ciencias Biológicas y Agropecuarias (CUCBA) of the University of Guadalajara and stored in the IBUG (Herbarium Luz María Villareal de Puga) generating the ID: SIST-TRA-2020-2.

Cleaning and Drying of Collected Material
Plants were separated by their root, stem, leaf, and flower sections (in the case of flowers, they were subdivided into flowers of a single color and bicolored flowers), and then the general dirt was removed with potable water and rinsed with injectable water.
The plant material was dried at room temperature in the absence of light, and the help of printing paper was changed every 24 h to avoid the accumulation of humidity.

Extracts Preparation
The dried plant material of root (158 g), stem (290 g), leaf (200 g), flower (150), and bicolor (144 g) was deposited in amber flasks, and 2 L of 70% ethanol was added to each sample. These flasks were kept under agitation for 15 days. Subsequently, the extracts obtained were filtered through Whatman's paper three times. On each occasion, the filter was exchanged to remove the separated solids.

Concentration and Lyophilization of Extracts
The extracts were concentrated by rotary evaporation to obtain the aqueous phase in a Buchi R-200 equipment. The concentrated extracts were then placed in freeze-drying bottles, and with the help of acetone and CO 2 , the samples were frozen and immediately placed in a LABCONCO freeze-dryer for 24 h at −51 • C with a pressure of 0.090 mbar, protected from light. Once lyophilization was completed, the extracts were aliquoted in a laminar flow hood and stored under refrigeration at 4 • C until use.

Solubility Test
Next, 1 mg of the lyophilized material of the five hydroalcoholic extracts of P. peltatum were deposited in test tubes, and subsequently, the solubility was evaluated by adding 1 mL of different solvents (polar and non-polar). The results were expressed with the legend: (−) not soluble, (+) soluble (++), and very soluble.

Phytochemical Profiling by High-Performance Thin Layer Chromatography
The lyophilizates of each tissue were resuspended with distilled water to a concentration of 10 mg/mL. Then, 15 µL of these solutions were deposited in bands with a length of 8 mm each with a Camag syringe of 100 µL on aluminum support plates coated with silica gel 60F254 (20 × 10 cm) by an autosampler Camag Linomat 5.
The plates were then placed in a glass chamber previously saturated (30 min) with the mobile phase: water-methanol-ethyl acetate (10:14:76 v:v, respectively) [23]. Once the plates were dried, they were visualized in a U.V. chamber at two wavelengths of 254 and 366 nm. Additionally, T.L.C. plates were developed with specific solutions for each group of compounds: ferric chloride solution for tannin determination, trichloroacetic acid solution for glycosides, Dragendorff's reaction for alkaloids, and aluminum chloride solution for flavonoids.
The retention factor was calculated using the following equation:

Antioxidant Activity
The antioxidant activity of the hydroalcoholic extract of P. peltatum was determined by DPPH, ABTS, and FRAP techniques and dilutions of the freeze-dried extracts of P. peltatum were prepared from 13 to 1000 µg/mL. These samples were used for antioxidant and phytochemical determinations. The half-maximal inhibitory concentration (IC 50 ) was calculated with the statistical program Graph pad version 9 with simple ANOVA analysis.

2,2-diphenyl-1-picrylhydrazyl Hydroxyl Radical (DPPH) Activity
The DPPH radical scavenging assay was carried out according to the methodology of Brand-Williams [62] with minor modifications. Briefly, the working solution of DPPH was prepared at 0.04% (w/v) in methanol and protected from light. In a microplate, 20 µL of the sample and 280 µL of the working solution were added in triplicate. The mixtures were incubated for 30 min at room temperature under the dark, and the absorbance was measured at 515 nm. Trolox was used as a standard with a curve between 0 and 1280 µg/mL. The results were expressed as percentage inhibition using the following equation: 4.5.2. 2,2 -azino-bis-(3-ethylbenzothiazolin-6-sulfonic acid) (ABTS) Radical Scavenging Activity The ABTS radical scavenging assay was performed by the technique reported by Li et al. [63] with minor modifications. A stock solution of 7 mM ABTS was prepared with 4 mM ammonium persulfate (P.S.A.) in distilled water. The solution was kept at 4 • C for 12 h to allow radical formation. The working solution was then prepared by adjusting the optical density to 0.7 ± 0.02 units at 750 nm. In a microplate, 280 µL of the working solution was placed in triplicate with 20 µL of each sample. The reaction was monitored at 750 nm for 30 min. Trolox was used as a standard with a curve between 0 and 400 µg/mL. The results were expressed as mg Trolox equivalents per g of dry extract. When indicated IC 50 was determined.

Ferric Ion Reducing Activity (FRAP)
The ferric reducing antioxidant power was evaluated by the method described by Benzie et al. [64]. A working reagent was prepared by mixing: 2.5 mL of 2,4,6-Tris(2pyridyl)-s-triazine (TPTZ) at 10 mM, 2.5 mL of Ferric chloride (FeCl3) at 20 mM, and 25 mL of 0.1 M acetate buffer at pH 3.7. The reaction was carried out in a microplate by placing 40 µL of the sample, followed by 40 µL of acetate buffer pH 4.7 with 150 µL of working reagent. Readings were taken at 595 nm after 30 min, and each sample was analyzed by triplicate. Trolox was used as a standard with a curve between 0 and 400 µg/mL. The results were expressed as mg of Trolox equivalents per g of dry extract.

Total Polyphenol Content
Total polyphenol content was determined spectrophotometrically, using Folin-Ciocalteu reagent and gallic acid as standard, following the procedure reported by Singleton [65]. To 125 µL of each sample, 750 µL of distilled water and 62.5 µL of Folin-Ciocalteu reagent were added; after 5 min of incubation in the dark, 250 µL of distilled water and 187.5 µL of 20% (w/v) Na 2 CO 3 were added, and the mixture was incubated for 2 h in the dark. After that time, 200 µL of each reaction was placed in triplicate in microplates, and absorbance was measured at 750 nm. The calibration curve was made in the range 0 to 100 µg/mL of gallic acid. The results were expressed as mg of gallic acid equivalents per g of dry extract.

Total Tannin Content
The quantification of tannins was determined by the Broadhurst and Jones method [66]. A 4% vanillin solution in methanol (4 g/100 mL) was prepared. Then in an Eppendorf tube, 1 mL of the vanillin solution, 133 µL of extract, and 500 µL of concentrated hydrochloric acid were added. Solutions were mixed and incubated for 15 min and then 200 µL of the solution was dispensed by triplicate in a 96-well plate. Readings were taken at 500 nm of absorbance. A curve of catechin was made from 0 to 100 µg/mL. The results were expressed as mg of catechin equivalents per g of dry extract.

Total Flavonoid Content
The determination was performed by the aluminum trichloride (AlCl 3 ) method, as reported by Zhishen et al. [67]. To 125 µL of each extract, 500 µL of distilled water, and 37.5 µL of 5% (w/v) sodium nitrite (NaNO 2 ) was added and incubated at room temperature for 5 min. After this time, 37.5 µL of 10% (w/v) AlCl 3 was added and incubated for 6 min. Finally, 300 µL of distilled water and 250 µL of 1 M sodium hydroxide (NaOH) were added.
After 15 min, the mixture was homogenized, and 200 µL were transferred in triplicate to a microplate. Finally, the absorbance at 510 nm was determined. A quercetin standard curve was used in a range of concentrations between 0 and 1000 µg/mL. The results were expressed as µg quercetin equivalents per g of dry extract.

Antimicrobial Activity
Gram-negative (Salmonella enterica/Serratia marcescens) and Gram-positive (Enterococcus faecalis/Staphylococcus aureus) bacterial strains were used for the antimicrobial assays. Then, 5 mL of inoculum of each bacterial strain grown on Tripticasein Broth (T.S.B.) medium were placed at 37 • C in an incubator until reaching an optical density at 600 nm of 0.5 ± 0.02 units. Subsequently, 200 µL of these cultures were inoculated into 25 mL of molten T.S.B. agar. This agar was placed in Petri dishes and kept at room temperature until completely solidified. Each plate had 0.8 cm diameter wells, and each well was filled with 50 µL of each sample at a concentration of 5 mg/mL. As a positive control, 50 µL of kanamycin at 35 µg/mL was placed in the center. The plates were kept at 4 • C for 16 h to allow diffusion of the samples in agar. Subsequently, the plates were incubated at 37 • C for 36 h, and the inhibition halo was observed.

Gas Chromatography-Mass Spectrometry Analysis
The analysis of volatile and semi-volatile compounds of P. peltatum extracts was carried out with an Agilent 7890B gas chromatograph (G.C.), coupled with an Agilent 5977A mass selective detector (M.S.D.) (Agilent Technologies, Inc., Santa Clara, CA, USA), which used helium as the carrier gas with a flow of 1 mL/min. Then 20 mg of the samples were weighed and dissolved in 1 mL of HPLC-grade methanol, then filtered with a 45 µm PTFE microfilter, and 1 µL was injected into the G.C. inlet at 240 • C in splitless mode. The compounds were separated on a HP-5ms Ultra Inert capillary column (30 m × 250 µm × 0.25 µm), using the following G.C. oven temperature program: 3 min at 40 • C up to 280 • C during 2 min at 10 • C/min. The MS used electron ionization energy of 70 eV, scanning range of 30-550 uma, scan rate of 13.8 spectra/s, solvent delay of 3 min, ionization chamber temperature of 200 • C, and transfer line temperature of 250 • C. Data were processed with MassHunter Workstation software (Agilent Technologies, Inc., Santa Clara, CA, USA). Compounds were identified based on their mass spectra fragmentation patterns with the spectral database of the National Institute of Standards and Technology (NIST) and by comparing their Kovats indices (K.I.), calculated in relation to the retention times of a series of alkanes (C 7 -C 40 ) using the calculator described by [68]. The relative quantities of each compound were expressed as the area percentage.

Kupchan Partitioning and Fractionation
The fractionation of the FDE-Leaf and Flower was performed by Emran et al.'s method [69] with minor modifications, 5 g of each extract were resuspended in 200 mL of ethanol 70%, then the solution was divided into four parts with 200 mL of different organic solvents varying its polarity (hexane, chloroform, ethyl acetate, and methanol). These new solutions were put under agitation for 10 min, and poured into a decantation funnel for the separation of their phases. Each found fraction was concentrated by the use of a rotary evaporator (Buchi-R200 Alemania) to remove the solvents. Once the fractions were concentrated, they were taken into a LABCONCO freeze-dryer for 24 h at −51 • C with a pressure of 0.090 mbar, and stored at 4 • C until further use.

Minimum Inhibitory Concentration
The minimum inhibitory concentration (MIC) was determined with a 96-well plate microdilution method based on resazurin (Elshikh et al., 2016). In a 96-well plate, 300 µL of the sample were placed by triplicate at 1 mg/mL dissolved in LB medium with DMSO at 2% (v/v), from this sample serial dilutions were made with 150 µL of the previous concentration and 150 µL of fresh medium until reaching a final concentration of 15.62 µg/mL. Subsequently, 15 µL of culture at 1 × 10 6 CFU/mL of the aforementioned bacteria was added. The mix was incubated at 37 • C for 18 h. After this period, 30 µL of resazurin 0.015% was added to each well, and the plates were incubated for 1 h at 37 • C. The MIC was the lower concentration with no color change of resazurin, at the lowest concentration in which the color change of resazurin did not occur.

Statistical Analysis
One-way analysis of variance (ANOVA) was employed for analyzing the data and the mean difference between given treatments was intended for significance test at p > 0.05 level by Tukey's HSD. The software GraphPad Prism 9 was used to statistical analysis.
Supplementary Materials: The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/molecules27113436/s1, Figure S1: Thin layer chromatography of different freeze-dried extracts from P. peltatum; Figure S2: Evaluation of the antimicrobial activity of P. peltatum FDE against; Figure S3: Evaluation of the antimicrobial activity of FDE-flowers and FDE-Leaf fractions; Table S1: Solubility of P. peltatum freeze-dried extracts; Table S2: Inhibition zone growth (mm) of FDEs against different strains.