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Print version ISSN 1984-8250
Braz. J. Pharm. Sci. vol.47 no.3 São Paulo July/Sept. 2011
Lara Alexandre de OliveiraI, II; Tatiana Maria de Souza-MoreiraII; Letícia Caramori CefaliII; Bruna Galdorfini ChiariII; Marcos Antonio CorrêaII; Vera Lucia Borges IsaacII; Hérida Regina Nunes SalgadoII; Rosemeire Cristina Linhari Rodrigues PietroII, *
IFaculty of Pharmacy, University Center of Araraquara, UNIARA,
IIFaculty of Pharmaceutical Sciences, São Paulo State University, UNESP
The leaves of the Brazilian species Plinia cauliflora were used to obtain active hydroalcoholic extract and fractions enabling the development of efficient antiseptic pharmaceutical formulations. A chemical composition of 70% ethanol extract, aqueous and ethyl acetate fractions was analyzed by thin-layer chromatography and for phenol content. Antimicrobial activity was tested against Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Lactobacillus acidophilus and Candida albicans by the agar diffusion method and the minimum inhibitory concentration was assayed by broth microdilution. Extract microbiological quality was tested to avoid contamination in the formulations. A mouthwash and a topical cream containing the extract were developed and antiseptic activity was assessed by agar diffusion. Sensory and physicochemical stability of the formulations were assayed. Chromatography indicated the presence of terpenes, flavonoids and tannins in the extract and fractions and total phenol content were found to be high. The plant samples were active against all the microorganisms tested, except for Lactobacillus acidophilus. Both topical formulations showed antiseptic activity and stability. Thus, these may be used as antimicrobials in skin infections, but would be more useful in the treatment of candidiasis.
Uniterms: Antiseptic formulations/design. Plinia cauliflora/antimicrobial activity. Plinia cauliflora/antiseptic activity. Mouthwash. Plant extract. Topical cream.
As folhas da espécie brasileira Plinia cauliflora foram utilizadas a fim de se obter um extrato hidroalcoólico e frações ativas proporcionando o desenvolvimento de eficazes formulações farmacêuticas antissépticas. A composição química do extrato etanólico 70%, fração aquosa e acetato de etila foi analisada por cromatografia em camada delgada e teor de fenóis. A atividade antimicrobiana foi testada frente a Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli, Lactobacillus acidophilus e Candida albicans por difusão em ágar e a concentração inibitória mínima foi determinada por microdiluição. A qualidade microbiológica do extrato foi avaliada para evitar a contaminação das formulações. Foram desenvolvidos um enxaguatório bucal e um creme tópico contendo o extrato sendo que a atividade antisséptica foi ensaiada por difusão em ágar. A estabilidade sensorial e físico-química foram testadas. A cromatografia indicou a presença de terpenos, flavonóides e taninos no extrato e frações, observando-se alto teor de fenóis totais. As amostras vegetais foram ativas contra todos os micro-organismos testados, exceto Lactobacillus acidophilus. Ambas as formulações apresentaram atividade antisséptica e estabilidade. Desta forma, infere-se que as formulações desenvolvidas podem ser utilizadas como antissépticas em infecções de pele, podendo ser mais eficazes no tratamento de candidíase.
Unitermos: Formulações antissépticas/planejamento. Plinia cauliflora/atividade antimicrobiana. Plinia cauliflora/atividade antisséptica. Enxaguatório bucal. Extrato vegetal. Creme tópico.
Antimicrobial agents have been used since the seventeenth century for the treatment of infectious diseases. Over the past 20 years, there has been a growing interest in screening natural products as a potential source of new antimicrobial substances (Silva et al., 2005; Suffredini et al., 2006). The antimicrobial properties of many substances extracted from plants have been scientifically proven. Thus, research conducted in several countries, including Brazil, where the plant diversity is exceptional, has shown a variety of substances to be effective in controlling the growth of microorganisms, as reported in the work of Pessini et al. (2003), Souza et al. (2003), Fiuza et al. (2008) and many others.
Plinia cauliflora (Mart.) Kausel is a tree of the Myrtaceae family, widely distributed in Brazil, where its popular edible fruit is known as jaboticaba and the bark is used as a source of astringent (Lorenzi, 2000). This tree occurs in alluvial plains and open rain forests, being found in forests in Brazil, Argentina and Paraguay. P. cauliflora produces abundant delicious fruits two or more times a year (Barros et al., 1996; Lorenzi, 2000). The bark is astringent and used by Brazilians to treat diarrhoea and skin irritations (Lorenzi, 2000). Extracts of the leaves were shown to have antimicrobial activity in previous work (Souza-Moreira et al., 2010). These promising results prompted this study to assess the antimicrobial activity of extracts and fractions from leaves of Plinia cauliflora against several species of microorganisms and to develop a topical cream for skin and genital administration as well as a mouthwash containing the extract, which should be effective, stable and of good quality.
Some mouthwashes are responsible for reducing the microbial load in the oral cavity (Shapiro et al., 2002). Bacterial and fungal infections are prevalent in critically ill and immunocompromised patients, and there is a high prevalence of oral candidiasis in immunocompromised patients and patients with dentures (Abu-Elteen and Abu-Alteen, 1998; Webb et al., 1998), especially when denture hygiene is poor (Webb et al., 2005). Alcohol and chlorhexidine are frequently used as oral cavity antimicrobials but show significant irritant potential. Sensitive and inflamed mucosa, especially that of cancer, is more susceptible to the unpleasant taste and irritant property of these products (Bahna et al., 2007).
Creams are well tolerated formulations because they interact mildly with the skin (Xhauflaire-Uhoda et al., 2008). They provide a barrier effect and improve permeation of active compounds into the human epidermis. Several topical formulations were prepared with Melaleuca alternifolia essential oil, a potent antimicrobial agent, at concentrations up to 5% (Biju et al., 2005; Reichling et al., 2006). Emulsion, ointment and cream proved to enhance essential oil permeation through the skin where this is important in the treatment of some subcutaneous infections such as candidiasis (Reichling et al., 2006).
The purpose of the present study was to develop, for the first time, two antiseptic phytopharmaceutical formulations with extract of the Brazilian native leaves of P. cauliflora to help control infections in oral and vaginal mucous membranes.
MATERIAL AND METHODS
Media, chemicals and reagents
Brain-Heart Infusion broth, Sabouraud broth, Sabouraud Dextrose agar and microbiological quality control media besides agar were acquired from Acumedia (Lansing, Michigan, USA); MRS broth was acquired from Fluka (Steinheim, Switzerland); Müeller Hinton agar was acquired from Himedia (Mumbai, India) and RPMI-1640 broth was acquired from Sigma (St. Louis, Missouri, USA). Solvents (glycerol, ethanol, ethyl acetate, chloroform, methanol, n-propanol, dimethyl sulfoxide, propylene glycol, sorbitol), glucose, sodium saccharine and p-anysaldehide-sulphuric acid were purchased from Labsynth (Diadema, São Paulo, Brazil). Emulsifying wax and methylparaben were obtained from Volp (Osasco, São Paulo, Brazil); grape seed oil and propylparaben were obtained from Deg (São Paulo, São Paulo, Brazil); octyl stearate and carbomer were acquired from PharmaSpecial (Santana de Parnaíba, São Paulo, Brazil); and butylhydroxy toluene was acquired from Makeni Chemicals (Diadema, São Paulo, Brazil). The Folin-Ciocalteau reagents were obtained from Imbralab (Ribeirão Preto, São Paulo, Brazil); tannic acid was acquired from Ecibra (Santo Amaro, São Paulo, Brazil); sodium carbonate, resazurin and 2,3,5-triphenyltetrazolium were obtained from Vetec (Duque de Caxias, Rio de Janeiro, Brazil).
The following reference strains were used in the study: Staphylococcus aureus ATCC 25923, Staphylococcus epidermidis ATCC 12228, Escherichia coli ATCC 10536, Lactobacillus acidophilus INCQS 00076 and Candida albicans ATCC 64548. Bacteria were maintained in Brain-Heart Infusion (BHI) broth and L. acidophilus in MRS broth, both containing 20% (v/v) glycerol at -20 °C. Before testing, the bacteria were transferred to fresh BHI medium and left to grow aerobically for 24 h at 37 °C. The inocula for the tests were prepared by diluting these bacterial suspensions in saline to the turbidity of the 0.5 McFarland standard (108 CFU mL-1) (CLSI, 2003a), except in the case of L. acidophilus, which was diluted to match the 5 McFarland standard (109 CFU mL-1) (Ocaña et al., 2006). C. albicans was maintained by culturing on Sabouraud Dextrose Agar (SDA) and, for the tests, transferred to Sabouraud broth and grown at 35 °C for 48 h. The inoculum was prepared by adjusting the suspension turbidity to match the 0.5 McFarland standard (106 CFU mL-1), in saline (CLSI, 2009).
Leaves of Plinia cauliflora were collected in São Carlos city, state of São Paulo (22º01'16.6" N, 47°53'57.0" W).
Specimens of this species were identified by Marcos Sobral and a copy was deposited in the herbarium of Escola Superior de Agricultura "Luiz de Queiroz" (ESALQ), USP at Piracicaba (São Paulo, Brazil) (ESA No. 96038).
Preparation of leaf extract and fractions
The leaves were dried for four days at 40 °C, powdered in a knife mill and stored. The dried and powdered leaves of P. cauliflora were extracted to exhaustion with 70% ethanol (v/v) in a percolating apparatus at room temperature (Farmacopéia Brasileira, 1988). The extract was dried under reduced pressure at 40 °C and weighed. This extract was subjected to liquid-liquid partition with water and ethyl acetate. The fractions were dried under reduced pressure at 40 °C and weighed.
Thin-layer chromatography: Preliminary pharmacognostic analysis was performed by comparative thin-layer chromatography (TLC), applying the 70% ethanol extract and fractions to a silica gel 60 F254 plate. The mobile phase consisted of the organic phase of chloroform:methanol:n-propanol:water (5:6:1:4, v/v). The spots were observed under UV and visible light and after being sprayed with p-anisaldehyde-sulfuric acid reagent.
Phenolics content: Total phenolic compounds in the extract were determined by the Folin-Ciocalteau method (1927), adapted by Monteiro et al. (2006). Results were expressed in terms of a standard curve for tannic acid. To prepare this, several aliquots of a 1.0 mg mL-1 tannic acid aqueous solution were diluted in 7.5 mL of distilled water, 0.5 mL 10% Folin-Ciocalteau reagent and 1.0 mL 0.75% Na2CO3 were added and the volume completed to 10 mL with water. Extract was treated similarly, but to a final concentration of 10 µg mL-1. After 3 h, the absorbance was measured at 760 nm with a Shimadzu UV-1603 spectrophotometer.
Microbiological quality control of the extract
In order to avoid further contamination in the formulations the extract microbiological assay was performed. The numbers of viable aerobic microorganisms (Salmonella sp, Escherichia coli, Pseudomonas aeruginosa and Staphylococcus aureus) in the extract were determined by methods recommended by the Farmacopeia Brasileira (1988) and Pinto et al. (2003), performed in triplicate.
Agar diffusion method
Bacteria: Except for lactobacilli, the test was performed in Müller Hinton agar (MHA) following the Guideline M2-A8 from the Clinical and Laboratory Standards Institute (CLSI, 2003a). Plates were seeded separately, with each bacterial cell suspension at 1% (v/v), giving 106 CFU mL-1. L. acidophilus was inoculated at 1% (v/v) (107 CFU mL-1) in MRS agar (Ocaña et al., 2006).
Yeast: The test was performed in MHA supplemented with 0.05 mg mL-1 methylene blue and 2% glucose, inoculated with 1% of the cell suspension (104 CFU mL-1) as in Guideline M44-A2 from the CLSI (2009). In all tests, a steel template was placed on the seeded agar and separately, in each 6 mm, 100 µL of the extract, ethyl acetate fraction or aqueous fraction was added at a concentration of 50 mg mL-1, in dimethyl sulfoxide (DMSO) diluted in saline (1:5, v/v, or 100 µL of the positive control: ampicillin (50 µg mL-1) for all bacteria and amphotericin B (64 µg mL-1) for yeast. A negative solvent control, DMSO:BHI (1:5, v/v), was also used on all plates. The tests were performed in triplicate.
Broth microdilution method
Minimum inhibitory concentrations (MIC) were determined as recommended in Guidelines M7-A6 of the Clinical and Laboratory Standards Institute (CLSI, 2003b) for bacteria and M27-A2 for yeast (CLSI, 2002). The test was performed in sterile 96-well microplates. The test solutions of extract and fractions in DMSO:medium (1:10 v/v) were transferred to microplate wells so as to obtain two-fold serial dilutions in a concentration range from 2.5 to 0.039 mg mL-1, with diluted ampicillin from 12.5 to 0.019 µg mL-1 and amphotericin B from 16 to 0.01 µg mL-1, as positive controls. The inocula (100 µL), containing 2.5x105 CFU mL-1 of bacteria or 2.5x103 CFU mL-1 of yeast (in BHI or RPMI-1640 broth),were added to each well. A number of wells were reserved in each plate to check sterility (without inoculum), inoculum viability (without extract) and DMSO inhibitory effect. Plates were incubated aerobically with shaking (100 rotates per min) at 35 °C, for 24 h for bacteria and 48 h for yeast. After incubation, microbial growth was observed by the addition of a 0.5% aqueous solution of resazurin for bacteria and 1% aqueous solution of 2,3,5-triphenyltetrazolium for yeast. MIC was deûned as the lowest concentration that inhibited growth (Gabrielson et al., 2002; Duarte et al., 2005). The minimum bactericidal and fungicidal concentrations (MBC and MFC) were determined by subculturing from microplate wells on MHA and Sabouraud agar plates, respectively, which were incubated for 24 h at 37 °C for bacteria and 48 h at 35 °C for yeast. MBC and MFC were the lowest concentrations without viable cells. The tests were performed in triplicate.
In the topical cream (O/W) formula, the following materials were used: emulsifying wax (1.5%), octyl stearate (2.0%), grape seed oil (2.0%), methylparaben (0.002%), propylparaben (0.018%), butylhydroxy toluene (0.02%), propylene glycol (4.0%), carbomer (30%), extract of P. cauliflora (0.25%) and aqua q.s. 100% by weight. The extract was incorporated in the cream at 40 °C and homogenized. The mouthwash was prepared from the following materials: sorbitol (3.0-5.0%), methylparaben (0.20%), sodium saccharin (q.s.), extract of P. cauliflora (0.25%) and aqua q.s. 100%. Extract of Plinia cauliflora was dissolved in sorbitol and incorporated into the prepared solution of mouthwash. The concentration of extract used in these preparations was determined from the MIC values. The cream and mouthwash were also prepared without the extract, for comparison with the activity of antiseptic preparations containing extract.
Determination of antimicrobial activity of pharmaceutical formulations
The antiseptic activity of preparations was tested by the agar diffusion method. The density of microorganisms and preparation of the plates were as in the test for antimicrobial activity described above. The mouthwash samples (200 µL) were placed in steel templates on the solidified inoculated agar (Ocaña et al., 2006), but the samples of topical cream were added by the pour-plate method in the culture medium. Tests were performed on the mouthwash with and without extract and the topical cream with and without extract. The positive controls were ampicillin (50 µg mL-1) for bacteria and amphotericin B (64 µg mL-1) for yeast. The plates were incubated for 24 h at 37 °C for bacteria and 48 h at 35 °C for yeast. All tests were performed in triplicate and the mean diameters of the inhibition zones were recorded.
Physical stability tests
Physical stability was tested by subjecting the formulations to storage at 5 ± 2 °C, at 45 ± 2 °C and exposed to light at room temperature, with a control at room temperature (27 ± 2 ºC). Samples from each formulation container were tested at the start and after 1, 7, 15, 30, 60 and 90 d, by the following methods (Isaac et al., 2008; Ordoñez et al., 2009):
Centrifugation assays: Five grams of each sample was centrifuged three times at 3000 rpm for 30 min each time. Subsequently, preparations were placed in opaque containers and stored under the stress conditions described above.
pH measurements: One gram of each formulation was weighed and diluted to 10 mL with distilled water. The mixture was homogenized and its pH measured with a pH meter. All measurements were made at room temperature in triplicate for each analyzed sample.
Sensory properties: Color, odor and appearance were monitored at the same time intervals as the other parameters.
Viscosity: Minimum apparent viscosity was determined with a cone and plate Haake rheometer (Rheostress1), equipped with a recirculating water-bath, to control the sample container temperature, and Rhcowin-3 software. Viscosity was measured at progressively higher shear rates (speed of rotation 0-100 s-1) for the upward curve and the procedure was repeated in reverse, with progressively slower rates (100-0 s-1) for the descending curve, both for 120 s. All tests were performed in triplicate for each sample analyzed.
The results are expressed as mean ± SD. MIC, MBC and MFC are expressed as mode values. Statistical significance was tested using Student's t test. A difference was taken to be significant at P < 0.05.
The present study was conducted to investigate the antimicrobial activity of P. cauliflora leaf extract and fractions and to use this extract to prepare pharmaceutical formulations with antimicrobial properties. The extract was chosen for its good activity (Souza-Moreira et al., 2010) and with the aim of providing cheaper formulations.
The dried 70% ethanol extract and its aqueous and ethyl acetate fractions yielded 24 g, 1.65 g and 4.22 g, respectively. The TLC indicated the presence of terpenes, flavonoids and tannins in the hydroethanolic extract, as described in the work of Souza Moreira et al. (2010). Tannins were mainly found in the aqueous fraction and terpenes and flavonoids in the ethyl acetate. The extract showed 70% phenolic content.
The microbiological quality control showed that there was no growth of the four pathogenic microorganisms, Salmonella, E. coli, S. aureus and P. aeruginosa, in the leaf extract. The total viable count of microorganisms was 17 CFU g-1 of extract, which allows its approval, according to the official limit of not more than 5x103 CFU g-1 or mL for non-sterile products (Farmacopeia Brasileira, 1988).
In the agar diffusion tests, the aqueous fraction and whole extract were the samples that showed the best antimicrobial activity against the bacterium S. aureus and the yeast Candida albicans, while the acetate fraction showed the smallest inhibition zones (Table I). No samples showed inhibitory activity against Lactobacillus acidophilus. Table I also shows the values of MIC, MBC and MFC for the extract and fractions. It can be seen that the yeast was more sensitive, with smaller MICs, although the minimum fungicidal concentrations were higher. The negative control using only DMSO did not inhibit the microbial growth.
The preparations were formulated with crude extract as antiseptic agent, not as preservative agent. Though not the best inhibition zones, the extract showed considerable antiseptic activity and was chosen since this material was much cheaper than the fractions. The topical cream and mouthwash containing the extract proved to be effective antiseptics in the agar diffusion tests, against all four microorganisms tested, as shown in Table II. Control preparations without extract did not show growth inhibition zone so they are not shown in Table II. A product is classed as an antiseptic when it produces an inhibition zone of 8 mm or more (using steel templates with 6 mm diameter wells) (Roessler, 1983).
Preparations showed no phase separation when centrifuged repeatedly and their sensory parameters of appearance, color and odor did not change throughout the period of exposure to stress conditions. Moreover, no significant changes in physical and chemical properties were observed, attesting to the stability of the preparations of topical cream and mouthwash with the extract of P. cauliflora.
The initial pH of the mouthwash and the topical cream was 6.50. These values did not vary by more than 0.5 during the period under stress conditions so that the pH remained compatible with mucosal and cutaneous pH and the formulations could be considered stable (Isaac et al., 2008).
The results of the viscosity tests can be seen in Figure 1 for the mouthwash (A) and for the topical cream (B).
It was observed that the viscosity of the emulsion (Figure 1 (B)) decreased slightly from initial value when subjected to stress conditions, but the overall variation was less than 10% and the emulsion is thus considered stable, according to Isaac et al. (2008). No significant change was observed in the viscosity of mouthwash (Figure 1 (A)). Its value was close to zero, as the main constituent of the formulation was water, which has this viscosity profile (Schramm, 2006). Since viscosity is a physicochemical parameter that reveals the flow properties of a fluid (Schramm, 2006), it was concluded that both preparations were stable with respect to this property.
In an early comparative study of the antioxidant and antimicrobial activities of 50% ethanol, 70% ethanol, acetone:water (7:3, v/v) and chloroform extracts obtained from the leaves of P. cauliflora by percolation, the best results were shown by the non-apolar extracts (Souza-Moreira et al., 2010). Some phytochemical characterization and biological activity were described previously by Souza-Moreira et al. (2010) while the present study has reproduced the standardized obtention of the 70% extract and provided pharmaceutical formulations confirming the activity of the extract in topical products.
Chemical compositions of the extract and fractions were confirmed by TLC and quantitative analysis. Choi et al. (2006) suggested that many biological activities in plants are due to the content of total phenols, such as flavonoids and tannins. The quantitative analysis of phenolic compounds demonstrated that the 70% ethanol extract of P. cauliflora standardized as 70% phenolic compounds may be sufficient to produce an inhibitory effect on the growth of pathogenic bacteria and yeasts.
The extract showed no growth of the specific pathogenic microorganisms and a low total viable count of microorganisms, ensuring that the microbial load in the final product does not lower its quality or endanger the patient (Pinto et al., 2003).
Serafin et al. (2007), working with Plinia glomerata leaves, found MIC values for the aqueous and ethyl acetate fractions ranging from 500 to 1000 µg mL-1 against E. coli and S. aureus, whereas against C. albicans the aqueous fraction had a MIC of 250 µg mL-1, showing that this yeast was more susceptible than the bacteria, as in the present study of the leaf extract of P. cauliflora, belonging to the same genus.
An important issue to be considered in relation to the fight against infection is the maintenance of the normal bacterial population in people, such as Lactobacillus spp bacteria in the human vaginal mucosa, which can protect against pathogens (Sobel, 2000; Reid, 2003; Andreu, 2004) by producing acids, hydrogen peroxide, bacteriocins and biosurfactants (Hillier et al., 1992). Since in this study the yeast C. albicans showed a greater susceptibility to the extract, it was especially interesting to note that the exemplary vaginal microorganism, L. acidophilus, was not sensitive to the plant extract, which may justify the development of pharmaceutical formulations containing extract or fractions of leaves of P. cauliflora to assist in the treatment of candidiasis by acting on the pathogen without disturbing the balance of the mucosal microbiota. Also, it was observed that the formulations provided antisepsis against the microorganisms tested, especially against the yeast. Candida albicans is a common commensal microorganism in skin and the genital area, but becomes pathogenic under predisposing conditions. To treat skin and the genital area it was important to develop a viscous topical cream with the active extract (Calderone, 2002). Another interesting finding of the present work is that, while M. alternifolia essential oil is used in creams at 5% (Biju et al., 2005; Reichling et al., 2006), the present study showed an efficient antiseptic formulation using 0.25% of a vegetal sample.
Cordeiro et al. (2006) observed that mouthwashes containing the plant species Rosmarinus officinalis, Plantago major, Tabebuia impetiginosa, Achillea millefolium and Nasturtium officinale also showed some activity, but there was no difference between the results produced by the mouthwashes with or without the plant extracts at 2% or 4%, while in our study a clear difference can be seen between the mouthwash containing the extract at 0.25% and the control.
Besides effectiveness, it is necessary to assess the stability of a formulation. The stability study provides information on the performance of the product after any given time intervals, taking into account the environmental conditions to which it may be subjected from production to expiry date (Isaac et al., 2008). In the accelerated stability test, it was observed that the formulations did not change significantly when subjected to stress conditions. Thus, these preparations show promise for the treatment of infections, especially candidiasis, since they possess activity against several pathogens, but none against the lactobacilli present in the normal mucosal microbiota, and are within the reference limits of quality and stability.
The authors acknowledge the technical assistance of Luis Eduardo dos Santos and Maria de Fátima Rodrigues and the financial support of FAPESP and PADC-UNESP.
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Received for publication on 11st November 2010
Accepted for publication on 14th April 2011
* Correspondence: R. C. L. R. Pietro. Department of Drugs and Medicines, School of Pharmaceutical Sciences, São Paulo State University - UNESP. Rod. Araraquara-Jaú km 1 - 14801-902 - Araraquara - SP, Brazil. E-mail: firstname.lastname@example.org