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Memórias do Instituto Oswaldo Cruz

Print version ISSN 0074-0276On-line version ISSN 1678-8060

Mem. Inst. Oswaldo Cruz vol.114  Rio de Janeiro  2019  Epub Apr 08, 2019

http://dx.doi.org/10.1590/0074-02760180489 

ORIGINAL ARTICLES

Nanoemulsion containing essential oil from Xylopia ochrantha Mart. produces molluscicidal effects against different species of Biomphalaria (Schistosoma hosts)

Fernanda de Paula Araújo1  5 

Ricardo Diego Duarte Galhardo de Albuquerque1  + 
http://orcid.org/0000-0002-8442-3849

Leonardo da Silva Rangel2  3  5 

Gabriel Rocha Caldas1 

Luís Armando Cândido Tietbohl1 

Marcelo Guerra Santos4 

Eduardo Ricci-Júnior6 

Silvana Thiengo7 

Monica Ammon Fernandez7 

José Augusto Albuquerque dos Santos2 

Robson Xavier Faria3  5 

Leandro Rocha1  5 

1Universidade Federal Fluminense, Laboratório de Tecnologia de Produtos Naturais, Niterói, RJ, Brasil

2Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Avaliação e Promoção da Saúde Ambiental, Rio de Janeiro, RJ, Brasil

3Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Toxoplasmose e Outras Protozooses, Rio de Janeiro, RJ, Brasil

4Universidade do Estado do Rio de Janeiro, Faculdade de Formação de Professores, Departamento de Ciências, Rio de Janeiro, RJ, Brasill

5Universidade Federal Fluminense, Programa de Pós-Graduação em Ciências e Tecnologia, Niterói, RJ, Brasil

6Universidade Federal do Rio de Janeiro, Centro de Ciências da Saúde, Departamento de Medicamentos, Rio de Janeiro, RJ, Brasil

7Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Malacologia, Rio de Janeiro, RJ, Brasil

ABSTRACT

BACKGROUND

This work describes a chemical study of the essential oil from leaves of Xylopia ochrantha, an endemic Annonaceae species from Brazil, and its activity against Biomphalaria species. Considering its poor solubility in aqueous medium, the essential oil was nanoemulsified to evaluate its action on controlling some mollusc species of genus Biomphalaria, snail hosts of Schistosoma mansoni that causes schistosomiasis, which mainly affects tropical and subtropical countries.

OBJECTIVES

The main aims of this work were to analyse the chemical composition of essential oil from X. ochrantha, and to evaluate the effect of its nanoemulsion on molluscs of genus Biomphalaria and their oviposition.

METHODS

Chemical analysis was performed by gas chromatography coupled to mass spectrometry. Nanoemulsions were prepared by a low energy method and characterised by particle size and polydispersity index. Biological assays evaluating the mortality of adult species of B. glabrata, B. straminea and B. tenagophila and their ovipositions upon contact with the most stable nanoemulsion during 24 and 48 h were performed.

FINDINGS

Chemical analysis by mass spectrometry revealed the majority presence of bicyclogermacrene and germacrene D in the essential oil. The formulation with a hydrophilic-lipophilic balance (HLB) of 9.26 was the most suitable for the oil delivery system. This nanoemulsion caused the mortality in B. tenagophila, B. straminea and B. glabarata of different sizes at levels ranging from 50 to 100% in 48 h. Additionally, the formulation could inhibit the development of deposited eggs.

CONCLUSION

Thus, these results suggest the use of nanoemulsified essential oil from X. ochrantha as a possible alternative in controlling some Biomphalaria species involved in the schistosomiasis cycle.

Key words: essential oil nanoemulsion; Xylopia ochrantha; mollusc control; Biomphalaria; schistosomiasis

Schistosomiasis is an acute and chronic parasitic disease caused by trematode worms of the genus Schistosoma and is transmitted by several types of snails. It affects people along 78 countries mainly in tropical and subtropical regions. Schistosomiasis is the second largest infectious-parasitic disease in the world after malaria. In 2014, at least 61.6 million people in the world have been treated for schistosomiasis.1 The acute form of this disease causes symptoms like fever, fatigue, myalgia, malaise, non-productive cough, whereas later stages show abdominal pathologies such as diarrhoea, diffuse abdominal pain, and hepatosplenomegaly. A chronic condition occurs when Schistosoma deposits its eggs and reactions from the host immune system lead to urinary, intestinal, hepatic, and ectopic forms of the disease.2

Human schistosomiasis is caused by Schistosoma mansoni that uses molluscs of genus Biomphalaria as its intermediate host. In many cases, prevention methods like Biomphalaria and Oncomelania eradication using chemical pesticides are relevant to control the disease. Niclosamide (Bayluscide, Bayer, Leverkusen, Germany) is the only commercially available molluscicide recommended by the World Health Organization (WHO) for large-scale use in Schistosomiasis Control Programs.3 However, this drug is toxic to other organisms, and resistance to niclosamide requires a search for new drugs and substances to be used in the vector control.4 Therefore, the WHO encourages a search for alternative drugs in schistosomiasis control. Natural products can be seen as a promising alternative as they are plentiful in schistosomiasis-endemic countries and have a large number of different substances in their extracts, which hinders the appearance of vectors-resistance.5

Essential oils are used to the control of snails, and plant species with high yields of essential oil as from genus Xylopia, showed activity against Biomphalaria glabrata, a relevant intermediate host of S. mansoni.6 However, essential oils have low solubility in water, which may compromise their activity against Biomphalaria. Therefore, they must be processed into a formulation capable of viable use in biological activity studies. Nanotechnology has been used to solve problems of hydrosolubility and stability for active substances. There are several nanocarriers of drugs including nanoparticles, liposomes, and nanoemulsions (NEs).7

Nanoemulsions have been widely used as nanocarriers of hydrophobic drugs and essential oils. The majority of NEs are dispersions of nanometric oil droplets in water stabilized by surfactants. The droplet size of a nanoemulsion is typically in the range of 20-200 nm.8,9 Some key advantages of these nanocarriers are easy preparation, simple composition, the possibility of industrial-scale production, low cost of production, and high thermodynamic stability.10,11

Xylopia ochrantha Mart. is an endemic Annonaceae species from Brazil and is popularly known as “imbiú-prego”. There is little information regarding the chemical, pharmaceutical, and biological activities from this species.12,13 Thus, this work aimed to identify the chemical composition of essential oil from X. ochrantha leaves and to evaluate the activity of a nanoemulsion produced with this oil on the developmental stages (oviposition) and mortality of different Biomphalaria species.

MATERIALS AND METHODS

Plant material - Three specimens of X. ochrantha Mart., Annonaceae, were collected at Restinga de Jurubatiba National Park (RJ), Brazil, in Clusia scrub vegetation (22º13’0.95’’S - 41º35’164”W, 22º13’685”S - 41º35’256”W, 22º12’420”S - 41º36’354”W) during the day on July 27, 2016. This species was identified by botanist Dr Santos MG and a voucher specimen was deposited at the Faculdade de Formação de Professores herbarium (Universidade do Estado do Rio de Janeiro, Brazil) under registration number RFFP 14.500.

Extraction of essential oil - A mixture of leaves (1000 g) from the three specimens collected was turbolised with distilled water. The material was then placed in a five L bottom flask and subjected to hydrodistillation for 4 h in a Clevenger-type apparatus. In the end, the oils were collected and stored at 4ºC for further analyses.

Gas chromatography/mass spectrometry analysis - The essential oil recovered was analysed using a GCMS-QP5000 (Shimadzu) gas chromatograph, equipped with a mass spectrometer using electron ionisation. Gas chromatographic (GC) conditions were as follows: injector temperature, 260ºC; flame ionisation detection (FID) temperature, 290ºC; carrier gas, Helium; flow rate, 1 mL/min; and split injection with split ratio 1:40. The oven temperature was initially 60ºC and was increased to 290ºC at a rate of 3ºC/min. One microliter of each sample, dissolved in dichloromethane (1:100 mg/μL), was injected into a DB-5 column (0.25 mm I.D, 30 m in length, and 0.25 μm film thickness). Mass spectrometry (MS) electron ionisation was at 70 eV and scan rate was 1 scan/s. Retention indices (RI) were calculated by extrapolating the retention times of a mixture of aliphatic hydrocarbons (C9-C30) analysed under the same conditions.14 Substances were identified by comparing their retention indices and mass spectra with those reported in literature.15 The MS fragmentation pattern of compounds was also compared with NIST mass spectra libraries. Quantitative analysis of the chemical constituents was performed by flame ionisation gas chromatography (CG/FID), under the same conditions as GC/MS analysis. Percentages of these compounds were obtained by FID peak area normalisation method.

Nanoemulsification method and determination of hydrophilic-lipophilic balance (HLB) - Emulsification was performed by modification of the low energy method described by Ostertag et al.16 Emulsions comprised 5% (w/w) of X. ochrantha oil, 5% (w/w) of surfactants, and 90% (w/w) water. Tween 20 and Span 80 were used as surfactants to prepare the nanoemulsions. Various emulsions with HLB values ranging from 4.3 to 16.7 were prepared by mixing the surfactants in different proportions. For preparation of nanoemulsions, oily phase constituted by X. ochrantha oil and surfactants was homogenised by magnetic stirring (400 rpm) for 30 min at room temperature. After this, the aqueous phase (distilled water) was added to the oily phase under the same continuous magnetic stirring (400 rpm) for 1 h. The formulations were analysed to verify their stability by analysis of droplet size and polydispersity index values. The formulation with the lowest values of droplet size and polydispersity index indicated the adequate oil HLB.

Nanoemulsion characterisation - Droplet size and polydispersity index (PDI) of the nanoemulsions were determined by photon correlation spectroscopy (Zetasizer ZS, Malvern, UK). Droplet measurements were performed in triplicate and average droplet size was expressed as the mean diameter ± standard deviation.

Molluscicidal assays - Nanoemulsion of essential oil from X. ochrantha (100 ppm) was diluted to three different concentrations (80 ppm, 60 ppm, and 40 ppm) in distilled water. For the assay, 10 adult snails of B. glabrata species (measuring 10-12 mm diameter, from Sumidouro, RJ, Brazil) were exposed to 2 mL of the nanoemulsion, in a 24-well plate for 48 h at room temperature, according to the bioassay adapted from WHO, 198317 (Fig. 1). Adult snails free of S. mansoni infection were kept in breeding grounds at the Laboratory for Analysis and Promotion of Environmental Health (LAPSA/IOC). Snail mortality was recorded over the following 48 h, and was compared with the nanoformulation control (formulation without oil at 100 ppm), positive control [Bayluscide WP 70® (Niclosamide) at 1 ppm], and negative control (distilled water). Absence of snail retraction into their shells after stimulation of the cephalopodal mass and/or release of haemolymph were the criteria of death. These assays were performed in triplicate.

Fig. 1: a 24-well plate divided into two groups of ten Biomphalaria molluscs. 

Complementary assessments of mortality and inhibition of posture development were performed with B. straminea, B. tenagophila, and B. glabrata from other locations (Ressaca, Belo Horizonte, MG, Brazil). For each analysis of mortality, according to a previous protocol, 2 mL of the DL25, DL50, and DL90 sample concentrations obtained in the previous analysis with B. glabrata were used, and the groups of molluscs were divided into 10 individuals, and were separated according to size (3-5 mm, 4-6 mm, and 8-10 mm). Analysis of postures viability of B. glabrata (Ressaca, MG) was performed by treating them (two and five days old) with 2 mL of DL25, DL50, and DL90 sample concentrations, and counting the number of eggs that were not viable in relation to the initial amount, at 24 and 48 h (Fig. 2). As in the previous assay, the results were compared with the positive, negative, and nanoformulation controls.

Fig. 2: egg postures of Biomphalaria species in extended size. 

Concentrations that killed 50% and 90% (LC50 and LC90) of the exposed snails in 24 h and 48 h (compared with the negative-control cultures) were expressed as the mean and standard deviation, and were statistically analysed using Student’s t-test (p ≤ 0.05), using the software R (MASS data package).

RESULTS

Essential oil - Essential oil obtained from fresh leaves (2.0 g) showed a bright green colour and a yield of 0.2%. Oil density was 0.8 g/mL and pH was equal to 5.0. In total, 27 substances were identified with the predominance of sesquiterpenes and hydrocarbons (68.55%). The main substances found in these analyses were bicyclogermacrene (25.18%), and germacrene D (20.90%). Substances such as β-pinene (8.07%), sylvestrene (6.50%), and E-caryophyllene (6.23%) were also present (Table I).

TABLE I Chemical composition of essential oil of leaves from Xylopia ochrantha (Mart.) 

AI lit AI exp Substance (%)
932 934 ɑ-pinene 2.7
969 974 sabinene 1.0
974 978 β-pinene 8.1
1002 1007 ɑ-phellandrene 0.7
1022 1026 o-cymene 0.9
1025 1030 sylvestrene 6.5
1032 1037 Z-β-ocimene 0.4
1044 1048 E-β-ocimene 1.3
1335 1340 δ-elemene 5.4
1374 1378 ɑ-copaene 2.3
1389 1395 β-elemene 2.4
1417 1423 E-caryophyllene 6.2
1434 1436 λ-elemene 0.5
1452 1452 cis muurola-3,5-diene 0.6
1452 1458 ɑ-humulene 0.8
1458 1465 allo-aromadendrene 0.6
1478 1481 λ-muurolene 1.0
1480 1486 germacrene D 20.9
1500 1502 bicyclogermacrene 25.2
1506 1505 ɑ-bisabolene 0.4
1522 1528 δ-cadinene 0.9
1559 1562 germacrene B 1.4
1577 1586 spathulenol 4.0
1590 1591 globulol 0.8
1592 1600 viridiflorol 0.5
1649 1659 β-eudesmol 0.7
1652 1663 ɑ-cadinol 0.5
Total identified 96.6
Monoterpeneshydrocarbons 21.6
Sesquiterpeneshydrocarbons 68.6
Oxygenatedsesquiterpenes 6.5

Nanoemulsion - The droplet size and PDI were used to select the HLB of the NE (Table II). The formulation with a HLB of 9.26 (40% of Tween 20 and 60% of Span 80), showed values of droplet size as 114 ± 1 nm and a PDI of 0.1 ± 0.0, which in turn, are characteristic of a stable nanoemulsion. The selected NE exhibited a translucent and homogeneous appearance.

TABLE II Size droplet, polydispersity index (PDI) and hydrophilic-lipophilic balance (HLB) values of eleven formulations with essential oil from Xylopia ochrantha 

Formulation Sizedroplet (nm) PDI HLB
F1 329 ± 19 0.3 ± 0.2 16.70
F2 232 ± 4 0.3 ± 0.0 15.46
F3 168 ± 3 0.3 ± 0.0 14.22
F4 142 ± 3 0.2 ± 0.0 12.98
F5 112 ± 1 0.3 ± 0.0 11.74
F6 114 ± 1 0.2 ± 0.0 10.50
F7 114 ± 1 0.1 ± 0.0 9.26
F8 187 ± 1 0.3 ± 0.0 8.02
F9 227 ± 4 0.2 ± 0.0 6.78
F10 386 ± 13 0.2 ± 0.0 5.54
F11 323 ± 2 0.3 ± 0.0 4.30

Molluscicidal assays

Effects on B. glabrata juvenile and adults from Sumidouro and Ressaca regions - Molluscicidal activity was tested in juveniles (size of 3-5 mm), adults with 6-7 mm, and adults with 8-10 mm. Additionally, these specimens were collected from two regions, Sumidouro (RJ, Brazil) and Ressaca (MG, Brazil).

Lethal concentrations obtained from B. glabrata (Sumidouro, RJ) were used to test against B. glabrata (Ressaca, MG) of different age/size, and against other Biomphalaria species. Additionally, the same lethal concentrations were used in oviposition tests on Biomphalaria.

Nanoemulsion (NE) of the essential oil from X. ochrantha leaves exhibited molluscicidal activity against adult (size of 10-12 mm) B. glabrata (Sumidouro, RJ) with LC50/24 h = 50.91 ± 3.06 ppm, LC90/24 h = 85.46 ± 4.96 ppm, LC50/48 h = 47.41 ± 2.85 ppm, and LC90/48 h = 78.48 ± 4.35 ppm. Furthermore, in the complementary assay with B. glabrata (Ressaca, MG), NE was tested at three concentrations 32, 47, and 78 ppm. Among juvenile molluscs with a size of 3-5 mm, 96.7% and 100% mortality was observed at the concentrations of 47 ppm (LC90/48 h) and 78 ppm (LC50/48 h), respectively, within 24 h. The NE could cause a higher mortality rate among adults of size 6-7 mm (100% at the concentration of 47 ppm). When it was used at a concentration of 32 ppm, the NE caused mortality in 96.7% adults from this region. Adult molluscs (between 8-10 mm) were affected to a lesser extent, exhibiting mortality of 3.3% in 24 h at the concentration of 47 ppm (Table III).

TABLE III Mortality index (in percentage) of different Biomphalaria species in different sizes/ages treated with the nanoemulsionated essential oil from Xylopia ochrantha in 24 h 

mollusks 32 ppm 47 ppm 78 ppm Positive control Nano control Negative control
(%) mortality (24 h)
B. straminea (3-5 mm) - 90 100 100 0 0
B. tenagophila (3-5 mm) - 100 100 100 0 0
B. glabrata (3-5 mm) - 96.7 100 100 10 10
B. straminea (6-7 mm) 93.3 100 - 100 0 0
B. tenagophila (6-7 mm) 96.7 100 - 100 0 0
B. glabrata (6-7 mm) 96.7 100 - 100 0 0
B. straminea (8-10 mm) - 46.7 - 100 0 0
B. tenagophila (8-10 mm) - 26.7 - 100 0 0
B. glabrata (8-10 mm) - 3.3 - 100 0 0

NE treatment for 48 h basically maintained the results observed after 24 h (Table IV) for all sizes of B. glabrata (Ressaca, MG) tested.

TABLE IV Mortality index (in percentage) of different Biomphalaria species in different sizes/ages treated with the nanoemulsionated essential oil from Xylopia ochrantha in 48 h 

mollusks 32 ppm 47 ppm 78 ppm Positive control Nano control Negative control
(%) mortality (48 h)
B. straminea (3-5 mm) - 93.3 100 100 0 0
B. tenagophila (3-5 mm) - 100 100 100 0 0
B. glabrata (3-5 mm) - 96.7 100 100 10 20
B. straminea (6-7 mm) 100 100 - 100 0 0
B. tenagophila (6-7 mm) 96.7 100 - 100 0 0
B. glabrata (6-7 mm) 96.7 100 - 100 0 0
B. straminea (8-10 mm) - 100 - 100 0 0
B. tenagophila (8-10 mm) - 53.3 - 100 0 0
B. glabrata (8-10 mm) - 10 - 100 0 0

Effects on B. straminea adults - As in the evaluations on B glabrata (Ressaca, MG), NE caused mortality in molluscs of 3-5 mm in the range of 100% and 90% in 24 h when used at concentrations of 78 and 32 ppm, respectively. Adults of size 6-7 mm exhibited higher mortality of 100% at the concentration of 47 ppm and 93.3% at the concentration of 32 ppm, within 24 h. NE at the concentration of 47 ppm was evaluated in molluscs of 8-10 mm, which caused mortality in the range of 46.7% at 24 h.

NE treatment for 48 h in molluscs of 3-5 mm treated with 78 and 32 ppm caused 100%, and 93.3% mortality, respectively. When treated for 48 h, molluscs of 6-7 mm showed 100% mortality in the presence of 47 ppm NE (Figs 3,4). Molluscs of 8-10 mm showed mortality in the range of 100% when treated with 47 ppm (Table IV).

Fig. 3: Biomphalaria straminea in distilled water after 48 h (Photo: LRNEM/IOC). 

Fig. 4: Biomphalaria straminea dead in contact with 47 ppm nanoemulsion (NE) after 48 h (Photo: LRNEM/IOC). 

Effects on B. tenagophila adults - At the highest concentration tested (78 ppm), molluscs of 3-5 mm were totally affected after 24 h, with 100% mortality. Molluscs of 6-7 mm also showed 100% mortality at 24 h, when tested at the 47 ppm concentration. In this same period, 32 ppm NE caused 96.7% mortality. In larger molluscs (8-10 mm), 47 ppm NE caused a mortality rate of 26.7% in 24 h (Table III).

NE treatment for 48 h in molluscs of 3-5 mm and 6-7 mm caused 100% mortality in 47 ppm (Fig. 5). In molluscs of 8-10 mm, the concentration of 47 ppm resulted in 53.3% mortality (Tables IV).

In all these analyses, the positive control was fully effective for the three species in all sizes. NE free of essential oil did not cause mortality.

Fig. 5: Biomphalaria tenagophila dead in contact with 47 ppm nanoemulsion (NE) after 48 h (Photo: LRNEM/IOC). 

Effects on eggs posture development - In the analysis of eggs posture, NE was able to render the eggs from recent oviposition (two days) unfeasible in a period of 24 h with 100% inhibition for B. straminea, B. tenagophila, and B. glabrata (Ressaca, MG) at both concentrations (47 and 72 ppm) tested (Table V).

The five days old oviposition treated with 47 ppm NE showed 91.7% unviable eggs after 24 h of treatment in B. straminea molluscs. At the concentration of 78 ppm, a reduction of the effect in B. straminea (17.3%) was observed. The molluscs B. tenagophila treated with 47 ppm exhibited 49.4% unviable eggs, and 78 ppm caused a greater effect with 82.5% unviable eggs in 24 h.

TABLE V Inhibition of eggs development index (in percentage) of different species of Biomphalaria (two and five days old) after contacting with the nanoemulsionated essential oil from Xylopia ochrantha in 24 h 

mollusks 47 ppm 78 ppm Positive control Nano control Negative control
(%) unviable eggs (24 h)
B. straminea (two days old) 100 100 100 6.9 0
B. tenagophila (two days old) 100 100 100 0 0
B. glabrata (two days old) 100 100 83.3 2 0
B. straminea (five days old) 91.7 17.3 100 0 0
B. tenagophila (five days old) 49.4 82.3 100 0 0
B. glabrata (five days old) 62.7 73.5 100 0 0

The molluscs B. glabrata (Ressaca, MG) showed 62.7% unviable eggs with 47 ppm, and 73.5% with 78 ppm for the same egg stage and time (Table V).

In 48 h, all species eggs at two days were rendered unfeasible (Table VI). When the eggs were observed at late oviposition (five days), NE caused the maximal effect on B. straminea and B. glabrata (Ressaca, MG). In late oviposition, B. tenaghofila at 47 ppm and 78 ppm showed 70.4% and 95.2% unviable eggs, respectively.

TABLE VI Inhibition of eggs development index (in percentage) of different species of Biomphalaria (two and five days old) after contacting with the nanoemulsionated essential oil from Xylopia ochrantha in 48 h 

mollusks 47 ppm 78 ppm Positive control Nano control Negative control
(%) unviable eggs (48 h)
B. straminea (two days old) 100 100 100 6.9 0
B. tenagophila (two days old) 100 100 100 45 0
B. glabrata (two days old) 100 100 100 2 0
B. straminea (five days old) 100 100 100 0 0
B. tenagophila (five days old) 70.4 95.2 100 0 0
B. glabrata (five days old) 100 100 100 0 0

DISCUSSION

Bicyclogermacrene and germacrene D, two major substances of the leaf essential oil from X. ochrantha, are the main components in other species of the genus such as X. langsdorffiana A.St.-Hil. & Tul., X. aethiopica (Dunal) A.Rich., and X. aromatica (Lam.) Mart. Furthermore, high occurrence of sesquiterpenes in foliar essential oil is also observed in these species.6,18,19 The yield of leaf essential oil (0.20%) is similar to that in other species of the genus, in a range from 0.07% and 0.43%, relative to fresh leaves.19,20,21 Bicyclogermacrene is best known for its antimicrobial and fungicidal activities.22,23,24 Germacrene D is cited in literature as a simulator of insect pheromones, and is also involved in other important mechanisms of the insect-plant relationship.25,26 Additionally, a previous study demonstrated molluscicidal activity from the leaf essential oil of X. langsdorffiana against B. glabrata, in which, germacrene D was the major compound.6 This result can suggest an association with the activity found in the essential oil from X. ochrantha against B. glabrata, since these species are included in the same genus and have germacrene D as one of the two main constituents.

Although the constituents of essential oils from X. ochrantha are related to relevant biological activities, they have low solubility in water, which hinders their dispersion into the environment in aquatic media. Thus, delivery in aqueous carriers as nanoemulsions (NEs) is required. NEs were successfully produced using a low energy method of spontaneous emulsification. This method is simple and only uses magnetic stirring.8 The aqueous phase was dripped over the organic phase under continuous magnetic stirring for 1 h. The transition of surfactants from the oil phase to aqueous phase produces interfacial turbulence and spontaneous formation of nanometric oil droplets that are involved and stabilised by surfactants27 (Table II). The following criteria were used for the analysis and selection of the formulation: size < 200 nm; PDI < 0.25; and organoleptic characteristics: absence of phase separation and precipitation. The formulation with HLB of 9.26 (40% of Tween 20 and 60% of Span 80) showed low values of droplet size and polydispersity index, which in turn, are characteristic of a nanoemulsion system. Development of a system to provide a suitable nanoformulation with a size below 200 nm for essential oil from X. ochrantha allows a more efficient aqueous dispersibility, stability, and delivery of actives in the target of action. NEs as delivery systems for essential oils permit interaction between the active principles and biological membranes. In general, this occurs through one of four main routes: 1-increased surface area and passive transport across the plasma membrane of cells; 2-fusion of the droplets with the cell membrane occurring specifically upon delivery of the substances at the site of action; 3-reservoir effect with sustained release of essential oil; 4-electrostatic interaction between positively charged droplets and negatively charged biological membrane favouring bioadhesion and biological effects.8 These facts highlight the relevance of bionanotechnology as an effective alternative for the control of diseases through inhibition of intermediate hosts of parasites present in the environment. Moreover, the biodegradability of the formulation is another factor that minimises residual toxicity problems of molluscicidal agents to the environment.

Molluscicidal activity of the nanoemulsion containing the essential oil from X. ochrantha against Biomphalaria molluscs could be observed in all evaluated species, including individuals of different ages/sizes and at different stages of egg development. According to the observed effects on mortality of B. glabrata of size 10-12 mm (Sumidouro, RJ), the LC90/24h (85.46 ppm) of the oil is considered satisfactory, as the value recommended by the WHO for a plant sample to be considered active is DL90/48h < 100 ppm.3 Differences in action on individuals of different species could be observed, so that comparing the NE concentration (47 ppm) at 24h, B. tenaghofila appeared to be more susceptible to NE, though all species with sizes of 3-5 mm and 6-7 mm presented a high mortality rate. Adult individuals of B. glabrata (8-10 mm) exhibited resistance. Treatment for 48 h at the concentration of 47 ppm caused an effect similar to that at 24 h. In contrast to old specimens (8-10 mm) that increased the susceptibility at B. straminea.

Another observation can be noted when comparing the sizes of individuals within the same species, wherein smaller/younger molluscs were found to be less resistant to NE action, suggesting that older individuals may have a more developed resistance system against the active components of NE.

NE also acts on oviposition with an inhibitory effect at the concentrations of 47 ppm and 78 ppm. All eggs, from more recent oviposition (two days), presented 100% mortality in 24 h. In eggs from older oviposition (five days), 100% inhibition of development was observed only in a period of 48 h, although inhibition was also observed at 24 h, at varying degrees. These results suggest a higher resistance to oil compounds by the more developed eggs of B. tenaghofila species.

Finally, these biological assays demonstrated the molluscicidal activity of the nanoemulsified essential oil from X. ochrantha and the inhibition of different stages of development in Biomphalaria molluscs, which denotes the biological importance of a species with poor scientific information regarding controlling disease transmitters.

In conclusion - This study reported the molluscicidal activity and chemical composition of essential oil from leaves of X. ochrantha, a Brazilian endemic species. This is the first report on the activity of this species in the control of molluscs that are part of infectious diseases cycles, more specifically against Biomphalaria that are involved in the transmission of schistosomiasis. Thus, this result suggests the use of nanoemulsified essential oil from X. ochrantha as a promising alternative for Biomphalaria control, as this plant species is endemic to a country affected by schistosomiasis.

ACKNOWLEDGEMENTS

To Henrique dos Santos Almeida for statistical analysis.

REFERENCES

1. WHO - World Health Organization. Epidemiology and control of schistosomiasis. Technical report series 728. Geneva: WHO; 2016. [ Links ]

2. Colley DG, Bustinduy AL, Secor WE, King CH. Human schistosomiasis. Lancet. 2014; 383(9936): 2253-64. [ Links ]

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Financial support: This study was financed in part by the CAPES (Finance Code 001).

Received: October 15, 2018; Accepted: February 21, 2019

+ Corresponding author: ricardo-diego-cf@hotmail.com

FPA, RDDGA, LSR, MAF and JAAS performed the biological experiments; ST, MAF, JAAS and RXF were responsible for the development of biological experiments; GRC worked on the nanoemulsion activities; RDDGA wrote the manuscript and performed the chemical analysis; RXF, ER and LACT reviewed the manuscript; MG collected the plant material and performed the botanical identification; LR coordinated the overall project. All authors have read and approved the manuscript. The authors declare no conflicts of interest.

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