Molluskicidal nanoemulsion of Neomitranthes obscura (DC.) N. Silveira for schistosomiasis control

Schistosomiasis is caused by the parasite Schistosoma mansoni, which uses mollusks of the Biomphalaria genus as intermediate hosts. In 2020, approximately 241 million people worldwide underwent treatment for schistosomiasis. For this reason, the World Health Organization encourages research on alternative molluskicides based on plant species. The objective of this work was to investigate Neomitranthes obscura essential oil from leaf chemical composition and its essential oil nanoemulsion activity on intermediate hosts of schistosomiasis Biomphalaria glabrata control. The major chemical components of the Neomitranthes obscura essential oil were zonarene, seline-3,7(11)-diene, β-selinene, and α-selinene. The nanoemulsion tested using 24-well plate methodology showed lethality and juvenile mollusks with LC90 values of 53.9 and 25.0 ppm after 48 h, respectively, and on their spawning with an LC90 of 66.2 ppm after 48 h. Additionally, the nanoemulsion exhibited an LC90 value against the infective form of the parasite Schistosoma mansoni of 11.5 ppm after 4 h. This pharmaceutical formulation acted inhibiting the acetylcholinesterase activity and was not toxic for Mellanoides sp. This result suggests the use of this nanoformulation as a promising alternative in the control of Biomphalaria glabrata and the transmission of schistosomiasis.


Introduction
Schistosomiasis is a parasitic disease caused by the trematode species Schistosoma mansoni, which in 2020 affected approximately 240 million people worldwide to undergo treatment for schistosomiasis. Schistosoma mansoni requires aquatic intermediate hosts in its infection cycle, such as mollusks from the Biomphalaria genus (Neglected_diseases, 2022;Colley et al., 2014).
The World Health Organization (WHO) recommends improving the basic sanitation system and prevention methods, such as eradicating mollusk hosts using chemical pesticides, such as niclosamide, to control the disease (OMS-Organização Mundial da saúde, 1983). However, this substance is toxic to the environment and possesses cases of resistance to this agent, making it necessary to search for new substances (Inobaya et al., 2014). Therefore, the WHO encourages research into alternative molluskicides based on plant derivatives, since these are abundant in countries with endemic schistosomiasis. It is difficult for vegetal species and plant-based products to develop resistance because they are phytocomplex (Tavares et al., 2007;Ding-Feng, 2010).
Although several extracts and vegetable oils have intrinsic molluskicidal activity, they exhibit low solubility in aqueous media due to their hydrophobic characteristics. Nanotechnology has been used to circumvent this problem by promoting the solubility and stability of active substances. Currently, there are several drug nanocarriers, including nanoparticles, nanoemulsions (NEs), and liposomes (Donsì and Ferrar, 2016). Some important advantages of these nanocarriers are their easy preparation, simple composition, low production cost, possibility of industrial production, and high thermodynamic stability (Cornwell et al., 2000;Trommer and Neubert, 2006;Sagalowicz and Leser, 2010;Campos et al., 2012;Jaiswal et al., 2015).
Belonging to the Myrtaceae family, which is one of the families with the highest species richness in Brazilian Restingas, the species Neomitranthes obscura is known as "camboim-de-cachorro" and "pitanga-de-cachorro." The geographic distribution occurs only in Espírito Santo and Rio de Janeiro in Brazil and is popularly used as food and medicine, mainly for the treatment of intestinal disorders. Some biological activities are known, such as Trypanosoma cruzi proliferation and cholinesterase activity inhibition (Marques, 2001;Ramos et al., 2010;Faria et al., 2017). Therefore, we evaluated the N. obscura leaf essential oil nanoemulsion properties on B. glabrata mollusks and against the human infective form of S. mansoni to control the transmission of schistosomiasis.

Methodology Vegetal material
Fresh leaves of N. obscura were collected on 27 June 2018, in the Restinga de Jurubatiba National Park, Rio de Janeiro, Brazil (22°13′4.00625°and 41°35.919 W). The collection and research of plant material were authorized by Sisbio/ICMbio (13, and SisGen (A0D648D). The species was identified by botanist Dr. Marcelo Guerra Santos, and a voucher was deposited in the herbarium of the Faculty of Teacher Training (University of the State of Rio de Janeiro, Brazil).

Essential oil extraction
Fresh leaves (1,810 g) were separated from the stem and ground in distilled water. Then, the plant material was placed in a 5 L roundbottomed flask and subjected to hydrodistillation for 4 h in a Clevenger-type apparatus. Then, the essential oil was dried with anhydrous sodium sulfate and stored in an amber glass vial at 4°C.

Essential oil characterization
The oil was characterized using a GC-MS QP2010 (Shimadzu) gas chromatograph equipped with a mass spectrometer and a GC-2014 (Shimadzu) gas chromatograph equipped with a flame ionization detector (FID). Gas chromatographic (GC) conditions were as follows: injector temperature, 260°C; ca, helium as carrier gas; flow rate, 1 mL/min and split injection with split ratio 1:40. The oven temperature was initially 60°C and then increased to 290°C at a 3°C/ min rate. One microliter of the sample dissolved in dichloromethane (1:100 mg/μL) was injected into an RTX-5 column (0.25 mm ID, 30 m in length, 0.25 μm, and film thickness). Mass spectrometry (MS) electron ionization was 70 eV, and the scan rate was one scan/s. The ionization gas chromatography GC-FID conditions were similar to those of the MS, except for the FID temperature at 290°C. The arithmetic index (AI) was calculated by interpolating the retention times of a mixture of aliphatic hydrocarbons (C9-C30) analyzed under the same conditions. The identification of substances was accomplished by comparing their retention indices and mass spectra with those reported in the literature (Adams, 2007). The MS fragmentation pattern of compounds was also compared with NIST mass spectrum libraries. The relative abundance of the chemical constituents was determined by flame GC-FID under the same conditions as GC-MS. The FID peak area normalization method obtained the analysis and percentages of these compounds.

Nanoemulsion preparation and characterization
Emulsification was performed by the low-energy input method by phase inversion in temperature (PIT) according to Feng et al. (2021). The oil-in-water (O/W) emulsions were composed of 5% (w/w) N. obscura essential oil, 5% (w/w) surfactant mixture, and 90% (w/w) water. Surfactants (Span 80 and Tween 80) with an hydrophiliclipophilic balance (HLB) range of 12-15 were used. For the preparation of NEs, the oily phase consisted of the essential oil of N. obscura, and a mixture of surfactants was homogenized by magnetic stirring (500 rpm) for 30 min. In sequence, the oil phase was heated to 40°C, the aqueous phase (distilled water) was heated to 40°C ± 2°C, and then the aqueous phase was slowly dripped onto the oil phase under constant magnetic stirring for another 60 min. The formulations were characterized by dynamic light scattering (DLS) in a Zetasizer (Malvern, United Kingdom). The NEs were diluted in distilled water (1:40), and the parameters analyzed were droplet size (nm) and polydispersity index (PdI). Additionally, the turbidity of the formulations was evaluated in a UV-visible spectrophotometer (T80 UV/VIS Spectrometer, PG Instruments Ltd.) at a wavelength of 570 nm using a quartz cuvette with an optical path of 1 cm and distilled water as a blank.

Molluskicidal assay
The bioassay was performed with B. glabrata mollusks by the method of Santos et al. (2017). For the test, the animals were separated into groups of three individuals for each evaluated developmental stage. Adult and juvenile snails with diameters of 10-12 mm and 6-8 mm, respectively, were individually placed in 24-well plates and exposed to NE at concentrations of 20-120 ppm with a 2 mL final volume. The mortality was compared with NE blank and distilled water and with niclosamide as a pharmacological control at 2 mg/L. Then, mortality was assessed at 24 and 48 h. The absence of retraction in the shell and hemolymph release were the criteria for assessing mortality. The test was performed in triplicate, on different days.

Ovicidal assay
Styrofoam plates were deposited in the water of the B. glabrata breeding tanks for oviposition After 48 h, the egg capsules were carefully removed from the Styrofoam and placed in 24-well plates using the adapted method of Araújo et al. (2019). Then, the viable eggs were counted at time zero, and 1 mL of NE was added to the wells at concentrations of 20-120 ppm. After 24 and 48 h of exposure, viable egg counts were repeated.

Cercaricidal assay
In 24-well plates, the amount of S. mansoni cercariae present in 1 mL was initially estimated using 20 μL of Lugol's and counted under a stereomicroscope, where we obtain an average of 80 cercariae per plate well for these assays. Then, in another well of the plate, 1 mL of the suspension of S. mansoni cercariae and 1 mL of NE were added at concentrations of 20-120 ppm. Then, 20 μL of 0.1% Trypan Blue dye was added. The counting of dead cercariae, stained blue, was performed from 1 to 4 h.
For tests with mollusks of another genus, snails Mellanoides sp. with 15-20 mm in diameter (length), collected from the IOC/FIOCRUZ ditches, kept in dechlorinated water and fed with lettuce leaves for stabilization, at the Pavilion Lauro Travassos, at Instituto Oswaldo Cruz, in the state of Rio of January. We used the methodology adapted with 24-well plates, previously described for B. glabrata (Santos et al., 2017). The substances were tested at lethal concentrations for 50% and 90% (LC 50 and LC 90 ) of that obtained for B. glabrata. After the treatment for 48 h, the mollusks were recovered for 96 h in H 2 O. The mortality was compared with NE blank and distilled water and with niclosamide as a pharmacological control at 2 mg/L. The opercula opening and hemolymph release were the criteria for assessing mortality.

Acetylcholinesterase inhibition assay in 96well microplate
We use the enzyme acetylcholinesterase (AChE, E.C. 3.1.1.7 electric ell, code C3389) acquired by sigma Aldrich. A quantity of 30 mL of buffer A (Tris HCl pH: 7.8-50 mM) was used to dilute the AChE enzyme to obtain a final concentration of 66.6 U/ mL. We added 1% albumin for stabilization and stored at −2°C. Additionally, we prepared buffer B: 0.067 M sodium phosphate at pH 6.85. Acetonitrile was the solvent used to prepare the 1 mM paranitrophenyl acetate substrate. The nanoemulsion concentrations with and without the active were prepared in DMSO.
In the first step of the reaction: in the enzyme control (94 µL Buffer B, 6 µL enzyme with 1% albumin); enzyme control blank (94 µL buffer B, 6 µL tris HCl buffer with 1% albumin); to offer the same enzyme conditions, 94 µL buffer B containing inhibitor, 6 µL tris HCl buffer with 1% albumin were placed in the inhibitor blank and 94 µL buffer B containing inhibitor and 6 µL enzyme with 1% albumin at 2U in the inhibitor test/mL. Then we conditioned in the biological oxygen demand (B.O.D) at 25°C for 10 min to interact the inhibitor with the enzyme. In the second step, we completed the reaction volume with 98 µL Buffer B and 2 µL of 1 mM 4-Nitrophenyl acetate (PNPA) substrate, which was added for 20 to 20 s. After completing the reaction with a volume of 200 μL, we waited for 2 min and 30 s to start the readings on the Elisa plate reader for 20 to 20 s within a period of 5 min at a wavelength of 405 nm.

Toxicity hemocompatibility
The toxicity of Neomitranthes obscura was evaluated by the hemocompatibility test, according to Bauer et al. (2012), with modifications. The compound (100 μg/mL) or saline (control) was incubated with a 13% (v/v) red blood cell suspension for 3 h at 37°C. Then, the samples were centrifuged for 3 min at 1,800 rpm, and lysis of the cells was detected by measuring hemoglobin at an absorbance of 578 nm using a microplate reader (SpectraMax, Model M4, Molecular Devices, California, United Stated). One hundred percent hemolysis (pharmacological control) was achieved by adding Triton X-100 (1%, v/v) or water to the red blood cell suspension.

Single dose toxicity
Neomitranthes obscura toxicity was evaluated by the in vivo test, according to ANVISA. National Health Surveillance Agency (2013), with modifications. NE (1,000 mg/kg) or saline solution was injected intraperitoneally (i.p.) into the abdominal region of the mice. Then, behavior and mortality were observed for 24 h.

In silico assays
The prediction of the ecotoxicity profile of the major essential oil compounds was performed by ADMET Predictor ™ (version 9.5, Simulations Plus, Lancaster, CA). The terpenoids were compiled in the format of the simplified molecular-input line-entry system (SMILES) and entered into ADMET Predictor ™ . The endpoints analyzed were bioconcentration, biodegradation, impact at three different trophic levels (Tetrahymena pyriformis, water flea (Daphnia), and fathead minnow), and effects due to interference with sex hormones (estrogen and androgen disruptors).

Statistical analysis
Statistical analysis was performed using the Statgraph and Prism 6 GraphPad programs (GraphPad Software) using two-Frontiers in Pharmacology frontiersin.org 03 way ANOVA followed by Tukey's test with p < 0.001. Linear regression with p < 0.0001 The probit analysis was performed using Statgraphics Plus software v.5.1 (Stat Easy Co., Minneapolis, United States).

Nanoemulsion preparation and characterization
The required HLB of the most promising formulation containing the essential oil of N. obscura (NE) was 14.5, presenting a bluish color, turbidity of 95.25%, droplet size of 164.5 nm, and polydispersion index of 0.309. The selection criterion was a smaller droplet size, followed by the PdI value. The other formulations are described in Table 2.

Molluskicidal assay
Treatment with the essential oil nanoemulsion against adult (10-12 mm) B. glabrata caused a toxic effect, with LC 50 and LC 90 values of 39.4 (24.6-52.7) and 55.4 ppm (46.6-100.0), respectively, after 24 h. After 48 h, they reduced the LC 50 and LC 90 values to 34.0 ppm (12.6-47.7) and 55.4 ppm (43.2-109.5), respectively. Figure 2A shows the average mortality of adult mollusks after 48 h, showing a lethality of 100% of the population at 80 ppm in 24 h. The negative and blank controls of NE did not present mortality ( Figure 2B).
The essential oil nanoemultion was also evaluated against juvenile (6-8 mm) B. glabrata. The LC 50 value observed for B. glabrata juveniles was 20.6 ppm, and the LC 90 was 25.05 ppm after 48 h ( Figure 3A). The negative and blank controls of NE did not present mortality ( Figure 3B).

Ovicidal assay
The NE effect on the spawning viability of B. glabrata was tested in crescent concentrations for 24 and 48 h. After 48 h, the NE at 100 ppm presented a mortality rate higher than 90% of the viable eggs

Cercaricidal assay
The NE effect on S. mansoni cercariae viability was measured in crescent concentrations for up to 4 h. After 1 h of exposition, the concentration of 100 ppm NE eliminated more than 50% of cercariae, much higher than the pharmacological control. After 2 h of exposure, the concentrations of 60 ppm-100 ppm eliminated 100% of cercariae. After 4 h of exposure, all concentrations tested reduced the cercariae population by 100% ( Figure 5). The lethal concentrations for the cercaricidal test are shown in Table 3.

Mechanism action of the nanoemulsion
Additionally, we investigated the nanoemulsion effect on cholinesterase enzyme activity. The nanoemulsion dosedependently inhibited this enzyme activity ( Figure 6) with maximal inhibition about 80% in the concentration of 100 ppm. In contrast, the blanck nanoemulsion did not exhibit effect on this enzyme. Therefore, the hypothetical nanoemulsion effect is through of this enzyme inhibition. Effects of Neomitranthes obscura nanoemulsion on another snail species The N. obscura nanoemulsion toxicity was evaluated on Mellanoides sp for 48 h caused toxicity in concentrations higher than 100 ppm with maximal toxicity in 300 ppm (Figure 7). The nanoemulsion without the active (blanck nanoemulsion) did not caused relevant mortality until 300 ppm. In vitro Toxicity of Neomitranthes obscura.
The toxicity of N. obscura was evaluated by an in vitro hemocompatibility test with red blood cells. Treatment of cells with Triton X-100 or water lysed 100% of the red blood cells (positive groups), whereas treatment with saline solution (control) resulted in no lysis. NE (100 μg/mL) lysed approximately 5% of red blood cells (data not shown), and according to Bauer et al. (2012), hemolysis below 9% means that the compound or molecule is devoid of toxicity; thus, NE can be considered a non-hemolytic or non-toxic molecule.

Single dose toxicity
We performed an assessment of mortality resulting from the probability of survival for the 1,000 mg/kg dose (ANVISA. National Health Surveillance Agency, 2013). This demonstrated that there was no lethal or behavioral toxic effect after inoculation of N. obscura compounds during the 24 h of observation.
The in silico data indicate some potential environmental toxicity for the major essential oil compounds, especially the bioccumulative potential and biodegradability. On the other hand, the two essential oil compounds with the highest percentage (zonarene and selina-3,7(11)diene) are not predicted to disrupt the endocrine receptors.

Discussion
Currently, schistosomiasis control includes methods such as prophylaxis, mollusk control, and the use of antiparasitics in the treatment of the disease (Neglected_diseases, 2022). The control of intermediate hosts of parasites of the Schistosoma genus, such as Biomphalaria glabrata, is widely used, but it is dependent on the few registered molluskicidal agents commercially available that have limitations, such as the occurrence of biological resistance to these chemical pesticides. In addition, they present high environmental residual effects, generating a negative impact on the local ecosystem (Colley et al., 2014;Neglected_diseases, 2022). Therefore, studies involving the search and development of new drugs with molluskicidal and/or antiparasitic potential against Schistosoma are necessary. Plants are a good source of active metabolites that can generate bioproducts with effectiveness, economic viability, and low environmental impact (Ramos et al., 2010;Amaral et al., 2014;Araújo et al., 2019).
Plants of the Myrtaceae family are described in the literature despite their pharmacological and biological activities, such as FIGURE 2 (A) Molluskicidal effect of the Neomitranthes obscura nanoemulsion on Biomphalaria glabrata adults exposed for 48 h. (B) Controls. These tests were repeated three times in three different periods (n = 9). R2: 0.9994, p-value: <0.0001.

FIGURE 3
Molluskicide test on juvenile Biomphalaria glabrata for 48 h using NE (A,B). The test was performed in triplicate on different days using 27 specimens/triplicate. These data are expressed as the mean ± S.D. Linear regression analysis, R 2 : 0.8924, p-value: 0.0025.
In our work, the chemical EO from leaves of N. obscura showed the highest fraction of sesquiterpenes, corresponding to 78.8%, thus corroborating the highest fractions described by other authors 25-28). The major terpenoid was zonarene (22%), followed by selina-3.7(11)diene (16.2%). The metabolites β-selinene, α-selinene, βcaryophyllene, and germacrene B also appeared in the N. obscura EO analyzed, corroborating the results of the aforementioned authors. The constituent zonarene, a compound that until then had not been described as a chemical component of N. obscura oil, may play a key role in molluskicidal activity since it is present in greater quantities. The production of this skeleton-type of sesquiterpene is common in the biosynthetic pathway in Myrtaceae. Likewise, minor substances such as the monoterpenes α-pinene and β-pinene are possibly relevant to the chemical profile and bioactivity of the species. Variations between products of metabolism among individuals of the same species are common due to different environmental pressures, which result in different metabolic expression pathways (Amaral et al., 2013;Amaral et al., 2014).
Chemical analysis of the essential oil of N. obscura allowed the identification of 90.18% of its components. Of these, 78.82% were shown to be hydrocarbon sesquiterpenes, 10.95% hydrocarbon monoterpenes and only 0.41% oxygenated monoterpenes. The 4 major components of the essential oil are all hydrocarbon sesquiterpenes: zonarene (22.38%), selin-3,7(11)-diene (16.18%), beta-selinene (8.59%) and alpha-selinene (5.87%). These four majority substances together add up to more than half of the essential oil components (53.02%). Therefore, we could affirm that the sesquiterpene hydrocarbons are responsible, at least in part, for the activity presented by the essential oil of N. obscura".
The nanoemulsion is a product of operational simplicity, is effective, has a low cost of production, and allows the dispersion of lipophilic agents, such as essential oils, in aquatic environments, presenting itself ideally for the control of mollusks of medical interest. The extremely low droplet size provides greater resistance to the effects of cremation and sedimentation, suggesting good physicochemical stability (Victório et al., 2018;Araújo et al., 2019;Feng et al., 2021).
The PIT method (Mustafa and Hussein, 2020;Feng et al., 2021) was used because it forms low interfacial tension between the nonionic surfactants and the oil phase, favoring emulsification together with a reduced drip velocity of the aqueous phase and constant homogenization by magnetic stirring. In addition, this method does not use organic solvents and allows reproducibility on an industrial scale (El-Ekiaby, 2019; Mustafa and Hussein, 2020;Feng et al., 2021;Marhamati et al., 2021). The most promising formulation with N. obscura essential oil presented a proportion of surfactants of 0.2335% for Span 80, 4.766% for Tween 80, 5% for essential oil, and 90% for distilled water. The required HLB of 14.5 suggests that the essential oil Effect of NE on the spawning of Biomphalaria glabrata in the period from 24 to 48 h. The test was repeated three different times in triplicate (n = 9). A range of 20-25 spawns was used per well. These data are expressed as the mean ± S.D. The statistical test used was ANOVA 2-way, R 2 : 0.9793, p-value: <0.0001. has some hydrophilic characteristics. Additionally, the HLB 14.5 formulation showed a translucent bluish color characteristic of light scattering in colloidal systems with reduced particle size defined by the Tyndall effect (El-Ekiaby, 2019; Marhamati et al., 2021). In addition, the turbidity evaluates the transparency of the system; values close to 100% indicate a lower scattering and absorption of light. All formulations in table 2 presented values that indicate the presence of reduced-size droplets. For a dispersion to be classified as a nanoemulsion, it must have a droplet size of 20-200 nm and PdI values below 0.3 to be considered a monodisperse system (El-Ekiaby, 2019; Matos et al., 2020). Within this context, the most promising formulation fits as a nanoemulsion with a particle size of 164.5 nm and 0.309 PdI.
NE showed molluskicidal activity with an LC 50 of 35.3 ppm and an LC 90 of 53.9 ppm after 48 h. The WHO classifies a plant extract with molluskicidal properties if the LC 90 value is below 100 ppm after 48 h (OMS-Organização Mundial da saúde, 1983). In this way, NE can be classified as a promising agent for the control of B. glabrata, and since the nanoemulsion is stable, operationally simple and low cost, industrial production is possible, making it an alternative for use in large portions of water.
The NE estimated for 24 h showed a reduction of 80% in B. glabrata egg viability at 100 ppm, and at 48 h, it was reduced by more than 90% at 60 ppm. Watanabe (Watanabe, 1997) reported the great importance of tests on embryonic stages in Biomphalaria sp. serving as bioindicators in polluted waters and tests performed as biomarkers in tests and mutagenicity.
In the cercaricidal assay, NE presented a mortality of more than 90% of the cercariae in the second hour at a concentration of 60 ppm, and after 4 h, even the lowest concentration of 20 ppm eliminated all cercariae (LC 90 = 11.5 ppm), proving to be effective when compared to the control groups (p-value: <0.0001). The data obtained in this work showed experimental similarity with the study published by Albagouri et al. (2014), who demonstrated the cercaricidal activity of different Sudanese plants, such as the LC 50 and LC 90 found in this study, with N. obscura presenting values below 20 ppm.
Organophosphate pesticides and carbamates cause toxicity acting on AChE (Garate et al., 2020). Additionally, niclosamide possess a FIGURE 5 NE activity against Schistosoma mansoni cercariae for 4 h. The test was performed in triplicate on different days using a range of 80 cercariae per well during the testing of the samples. These data are expressed as the mean ± S.D. ANOVA 2-way, R 2 : 0.9813, p-value: <0.0001.

FIGURE 6
Inhibition percentage of NE against anti-cholinesterase activity. These experiments were performed in triplicate at least three distinct days.
Niclosamide treatment cause ambiental toxicity (Leaka et al., 2020). Interestingly, N. obscura nanoemulsion was not toxic for Mellanoides sp. Therefore, this nanoemulsion would be a satisfactory alternative for B. glabrata control.
N. obscura hemolysis below 10% means that the compound or molecule is devoid of toxicity and, therefore, NE is within the allowed limit of 5% and can be considered non-hemolytic or nontoxic molecules. In addition, the toxicity assessment was performed in vivo, observing the probability of mortality at a dose of 1,000 mg/kg. N. obscura did not cause lethal or induced toxic behavioral effects in mice during 24 h of observation. Regarding the in silico environmental toxicity assay, the major compounds of the Neomitranthes obscura essential oil (zonarene, selina-3,7(11)-diene, α-selineno, and β-selineno) are predicted to have a higher bioaccumulative potential than niclosamide. Nevertheless, none of them presented an alarming bioaccumulative risk. A substance is considered bioaccumulative for REACH if the BCF value is greater than 2,000 (Lombardo et al., 2010).
All the compounds tested are predicted not to be biodegradable. Therefore, attention must be paid to the amount of waste generated in the environment and its potential harm. In this way, we emphasize that the nanoemulsion presents very low amounts of the bioaccumulative compounds mentioned above, and even so, they are compounds with low environmental impact, being ideal for use in lakes, ponds, dams, streams. However, we need to perform environmental toxicity tests and quantify the level of nanoformulation by-product. After we get this information, we can have a clearer notion of how and in which situation we can use the nanoformulation.
From the analysis of the impact at three different trophic levels, the four major compounds presented similar potential to inhibit T. pyriformis growth than niclosamide. In the D. magna model, the 20% most toxic compounds presented an LC 50 less than approximately 3.0. Therefore, only the major compound zonarene presented a small toxicity prediction; indeed, niclosamide is predicted to be more toxic than zonarene for D. magna. The Pimephales promelas model showed that approximately 20% of the most toxic compounds presented an IGC 50 less than 2.0. Therefore, the FIGURE 7 NE effect on Mellanoides sp viability. The snails were exposed for 48 h with NE and blanck NE. These tests were repeated three times in three different periods (n = 9). R2: 0.9, p-value: <0.0001 .   TABLE 4 Results of the compound ecotoxicity. The endpoints legend evaluated for each compound are defined: BCF, bioconcentration factor value; BOD, biodegradation-categorize the compounds as positive (readily biodegradable) if %biodegradation is greater than or equal to 60% and as negative otherwise; Th_ pyr_pIGC50, concentration of toxicant needed to inhibit 50% growth (IGC50) of Tetrahymena pyriformis after approximately 40 h of exposure; Daphnia_LC50, concentration (mg/L) of compound required to kill 50% of a D. magna population; Minnow_LC50, concentration (mg/L) of a compound that kills 50% of a population of minnows; Andro_Filter and Estro_Filter, assess a compound's likelihood of binding to the androgen/estrogen receptor. compounds selina-3,7(11)-diene, α-selineno, and β-selineno presented potential toxicity. Zonarene is predicted to be 9 times more toxic to P. promela than niclosamide.

Compounds
Regarding the estrogen receptor, most of the tested compounds are predicted to have a non-toxic effect. On the other hand, α-selineno and β-selineno exhibited the potential to interact with the androgen receptor. Therefore, these compounds present a risk of adverse health outcomes, including cancer, reproductive impairment, cognitive deficits, and obesity.
The endocrine toxicological results indicated that zonarene presented a low potential to interact with the tested receptors. This result suggests a low endocrine toxicological effect of this compound compared to that of niclosamide. Indeed, some recent works report the inhibition of androgen receptors by niclosamide (Liu et al., 2014;Sobhani et al., 2018;Parikh et al., 2021).
Thus, the present study demonstrated the molluskicidal activity of the nanoemulsified essential oil from the leaves of N. obscura in embryos, adult, and juvenile forms of B. glabrata mollusks, as well as the cercaricidal activity. Consequently, the biotechnological product developed from N. obscura exhibited action at different stages of the schistosomiasis transmission cycle, thus being a promising alternative in the control of this disease.

Conclusion
This work demonstrated the potential of the nanoemulsion of the essential oil of Neomitranthes obscura as molluscicide agent against the host species Biomphalaria glabrata and the human infective form cercariae.

Data availability statement
The raw data supporting the conclusion of this article will be made available by the authors, without undue reservation.

Author contributions
LD: performed biological tests and wrote the manuscript, FP: produced and evaluated the nanoemulsion, RA, AC, and MS: identified the plant material and performed the exsiccate, JA: revised the manuscript, NL, CR, and LR: performed the in silico analysis and RF: idealized, revised, and wrote the manuscript.