Development of enteric coated tablets from spray dried extract of feverfew (Tanacetum parthenium L: )

ARTICLE

Development of enteric coated tablets from spray dried extract of feverfew (Tanacetum parthenium L.)

Juliana Siqueira Chaves; Fernando Batista Da Costa; Luís Alexandre Pedro de Freitas^*

Department of Pharmaceutical Sciences, Faculty of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo

ABSTRACT

Tanacetum parthenium (feverfew) is an herb that is commercialized worldwide as a therapeutic treatment for migraine. Its pharmacological effect is mainly due to the presence of the sesquiterpene lactone parthenolide as well as of flavonoids. So far, there are no studies on standardization of pre-formulations or phytomedicines containing this herb. The present study aimed at developing a pre-formulation using a standardized spray-dried extract of feverfew and further designing and standardizing enteric coated tablets. In this work, the spray-dried extract of feverfew was evaluated for its parthenolide, santin and total flavonoid content, parthenolide solubility, particle size, tapped density, hygroscopicity, angle of repose and moisture content. Tablets containing the spray-dried extract were tested for their average weight, friability, hardness, and disintegration time. The total flavonoid and parthenolide contents in the spray-dried extract were 1.31 % and 0.76% w/w, respectively. The spray-dried extract presented consistent pharmacotechnical properties and allowed its tableting by direct compression. Tablet properties were in accordance with the proposed specifications. The procedures described herein can be used to prepare and evaluate pre-formulations of feverfew with adequate properties for the development of a high-quality phytomedicine.

Uniterms: Enteric coated tablets. Flavonoids. Parthenolide. Phytomedicine. Spray-dried extract. Tanacetum parthenium.

RESUMO

Tanacetum parthenium (tanaceto) é uma planta medicinal comercializada no mundo todo para tratamento de enxaqueca. Seu efeito farmacológico é creditado principalmente à lactona sesquiterpênica partenolídeo e flavonóides. Até o momento não existem estudos sobre a padronização de pré-formulações ou o desenvolvimento de fitoterápicos com tanaceto. Logo, o objetivo deste trabalho foi obter comprimidos de revestimento entérico a partir de extrato seco e padronizado de tanaceto. Neste trabalho, o extrato seco do tanaceto obtido pelo método de spray drying foi avaliado quanto ao teor de partenolídeo, presença da santina, teor de flavonóides totais, solubilidade do partenolídeo, tamanho de partícula, ângulo de repouso, densidade, análise higroscópica e teor de umidade. A partir do extrato seco obtiveram-se comprimidos que foram revestidos em leito de jorro. Os comprimidos revestidos foram avaliados com relação ao peso médio, friabilidade, dureza e desintegração. O teor de flavonóides totais e de partenolídeo no extrato seco foram 1,31% e 0,76% (p/p), respectivamente. O extrato seco apresentou características farmacotécnicas satisfatórias permitindo a obtenção de comprimidos pelo método de compressão direta. As propriedades dos comprimidos revestidos estão de acordo com as especificações da literatura. Os procedimentos utilizados nesse trabalho podem ser utilizados para obter extrato seco e fitoterápicos de T. parthenium com alto padrão de qualidade.

Unitermos: Comprimidos de revestimento entérico. Extrato seco. Fitoterápicos. Flavonóides. Partenolídeo. Tanacetum parthenium.

INTRODUCTION

Herbal medicines have a long history of traditional use and play an important role in the primary health care of developing countries (Calixto, 2000). Nonetheless, in many developed countries, herbal medicinal products - or phytomedicines - are widely used and retail sales surpass billions of dollars (Barnes, 2003). The aerial parts of feverfew [Tanacetum parthenium L. Shultz Bip., Asteraceae] have been used since ancient times for a variety of medicinal purposes because of its anti-inflammatory, analgesic and antipyretic properties. Nowadays it is a recommended therapeutic treatment for migraine prophylaxis (Khan et al., 2003). Although the pathophysiology of migraine is not yet fully understood, its symptoms are reported by 15% of females and 6% of males in the adult age, from 35 to 45 years (Pfaffenrath, 2002). Clinical trials have demonstrated the high effectiveness of feverfew against headache and other symptoms linked to migraine (Palevith, 1997). Amongst feverfew constituents are sesquiterpene lactones, flavonoids and spiroketal enol ethers (Bolhmann, Zdero, 1982; Long et al., 1999; Williams et al., 2003). Parthenolide, a sesquiterpene lactone, is the major constituent of the herb and accounts for many of its biological activities. For instance, it has been shown that parthenolide presents in vitro inhibitory effect on the release of serotonin from blood platelets (Vogler, 1998; Weber et al., 1997), in vivo antinociceptive and anti-inflammatory effects and in vitro and in vivo inhibition of several eicosanoids (Hwang et al., 1996; Fukuda, 2000; Kwok et al., 2001). Furthermore, other studies have shown that the feverfew flavonoids also present anti-inflammatory activity (Long et al., 1999; Williams et al., 2003).

Parthenolide is usually employed as a chemical marker in quality control of feverfew products. Due to the importance of this compound, besides the evaluation of its biological activities, many studies describing its quantification by HPLC methods have been published (Zhou et al., 1999; Abourashed, Khan, 2000).

Despite of its importance in the herbal medicine market, several feverfew products are still sold as hard gelatine capsules containing grinded aerial parts of the plant, which substantially increases the difficulties of standardization and quality control as well as the establishment of therapeutic effectiveness of this herbal medicine.

Over the last few years, the industrial manufacture of phytomedicines has grown considerably. For this reason, organizations like the World Health Organization (WHO), the European Union (EU) and the European Scientific Co-operative on Phytotherapy (ESCOP) have been demanding regulatory guidelines and conclusive studies on chemical, physical and pharmacological properties of herbal drugs for their approval (Barnes, 2003; Silano et al., 2004). Moreover, the market demand for plant medicines is based on reliable products, obtained by validated methods and standardized. One of the most used methods for extracts stabilization and standardization is the spray drying using technological carriers (Senna et al., 1997; Linden et al., 2000).

Dry extracts show a number of advantages over the conventional fluid forms, including higher amounts of active compounds, higher stability, easier standardization and quality control, which therefore increase the therapeutic efficacy and product value (Runha et al., 2001). Furthermore, the design and formulation of herbal medicine tablets is a challenging task due to poor tableting properties of plant extracts (Palma et al., 2002).

Therefore, the aim of the present study was to develop enteric coated tablets of feverfew using its spray dried extracts.

MATERIAL AND METHODS

Chromatographic standards

Parthenolide was isolated from Talauma ovata ST. HIL (Magnoliaceae) according to a previously reported method (Stefanello, Alvarenga, 1997).

Santin was isolated from the T. parthenium powder (aerial parts) according to a previously reported method (Chaves, Da Costa, 2008).

Solvents, reagents and pharmaceutical excipients

Solvents for HPLC analysis (HPLC grade) were supplied by Mallinckrodt Baker (USA); solvents for UV analysis, reagents and salts were supplied by Merck (Rio de Janeiro, Brazil). The water was purified using a Milli-Q system (Millipore^®, USA). Phosphate buffer pH 7.5 and HCl buffer pH 1.2 were prepared according to the United States Pharmacopoeia (1995) specifications. The pharmaceutical ingredients, colloidal silicon dioxide (Aerosil 200^®), lactose monohydrate (lactose), microcrystalline cellulose (PH 102), magnesium stearate, sodium starch glicolate, polyvinylpyrrolidone (PVP) K30, and talc were supplied by Henrifarma (Brazil). Eudragit L 30 D 55^® (Rohm, Germany) and triethyl citrate were supplied by Almapal (Brazil). Simethicone (Dow Corning^®, Belgium), titanium dioxide and polysorbate 80 were supplied by Gerbras (São Paulo, Brazil).

Plant material

Powdered aerial parts of T. parthenium were purchased from Galilee Herbal Remedies (Kibbutz Kfar Hanassi, Israel) and submitted to several analyses in order to certificate its authenticity (Chaves, Da Costa, 2008).

Preparation of feverfew hydroalcoholic extract

The hydroalcoholic extract was obtained by percolation of the T. parthenium powder in 70% ethanol according to the German Pharmacopoeia specifications, described by List and Schmidt (1989). Two parts of the extract were obtained from one part of the powder. This process was performed in three steps: 1) pre-swelling for 2 h with a 1:3 solvent to powder proportion; 2) intermediate maceration (24 h); 3) percolation (4-6 drops/min) per 100 g of powder (List, Schmidt, 1989).

Spray drying of extracts

The T. parthenium spray-dried powder was prepared from a suspension containing 55% of hydroalcoholic extract (w/w), 40% of water (w/w) and 5% of colloidal silicon dioxide. During the atomization procedure, the mixture was mixed with a magnetic stirring bar. The suspension was dried using a mini spray-drier model LM MSD 1.0 (Labmaq do Brasil Ltda., Brazil) with capacity of drying up to 1.0 litre per hour. The atomization was carried out with a two-fluid 1.2 mm pneumatic nozzle, and the dryer was operated in concurrent flow. A summary of operational conditions employed during spray-drying is shown in Table I.

Tablet compaction and coating

Tablets were obtained by a direct compression method in an eccentric compression machine (Fabbe^®, Brazil) using an 8 mm bi-concave punction regulated to obtain tablets of 200 mg. Excipients (Table II) were sieved and mixed in a geometric order. The spray-dried extract was mixed with sodium starch glicolate, cellulose and lactose. The magnesium stearate was mixed with talc and colloidal silicon dioxide, followed by PVP. Finally, the components were mixed thoroughly.

The tablets were coated in a lab scale Wurster bed coater model SBC 1.0 (Labmaq do Brasil Ltda., Brazil) with capacity of up to 1.0 kg of tablets. The equipment is a bottom spray fluid bed coater. The coating suspension (Table III) was applied in a proportion of 4:1 (w/v) tablets:suspension. The coating operational conditions are summarized in Table IV. The suspension components were mixed in a high shear mixer at 13,500 rpm during 5 min. Then, Eudragit^® L30 D55 was added and the mixture was stirred with a magnetic bar at 50 rpm for 1 h (Kfuri, Freitas, 2006).

Quantitative analysis of parthenolide

The parthenolide content was determined by HPLC according to a previously reported method (Chaves, Da Costa, 2008). In summary, the stock solution of parthenolide was prepared dissolving 5 mg of parthenolide in 5mL of acetonitrile (CH₃CN). Standard solutions with concentrations of 1, 2, 10, 50, 100, 250, 500, and 750 μg mL were prepared from the parthenolide stock solution (1 mg/mL) by means of sequential dilution with CH₃CN. 150 mg of the T. parthenium spray dried powder were extracted with 10 mL of CH₃CN:H₂O 9:1 (v/v), sonicated for 30 min and centrifuged for 12 min. The supernatant was passed through a 0.45 μm nylon membrane (Sartorius, Spain). The injection sample volume was always 20 μL. The analyses were performed in triplicate and the parthenolide content was calculated on the basis of the peak area against a calibration curve prepared by injecting standard solutions (Chaves, Da Costa, 2008).

Detection of santin in spray-dried extract

The santin content was determined by HPLC according to a previously reported method (Chaves, Da Costa, 2008). A clean-up step with a C-18 Sep-Pak cartridge (Waters Association, Milford, USA) was used to remove interfering material of the T. parthenium spray dried powder. The cartridge was preconditioned with 5 mL of methanol and 5 mL of water. An aliquot of the extract (1 g) was mixed with 2 mL of ethanol and eluted with 10 mL of methanol 60%. The solvent was evaporated and the residue was suspended in 1 mL of methanol 60%. Santin was suspended in 1mL of methanol 60% (1 mg/mL). The samples were filtered through a 0.45 μm nylon membrane and directly injected into the HPLC system. Injection volume was 50 μL.

Total flavonoid content of spray-dried extract

The determination of total flavonoid content was carried out using a UV spectrophotometer model Kayak XA (Hewlett Packard, USA), according to the method described in the German Pharmacopoeia (De Paula, 1996). Analyses with samples of 0.4 g were performed in triplicate. The following formula was used to calculate the total flavonoid content:

TF = A . fd / 500 . p . (100 - t), where:

TF = total flavonoids calculated using quercetin as reference (%; w/w)

A = absorbance

p = weight (g)

t = loss on drying (0.41 %)

fd = dilution factor (62500)

Particle size measurements

The determination of particle size of the spray-dried powder was performed using an optical microscope (Olympus BX 60) coupled with an image capture system (Sony CCD-Iris, Japan). The powder was homogeneously dispersed on a slate using a vacuum device (vacuum-gage PD-10, Galai). The average particle diameter was calculated using the software Image Pro-Plus^® (Media Cybernetics Inc. All^®, USA). The analyses were performed in triplicate, counting 270 to 300 particles in each measurement.

Angle of repose

The powder sample was put carefully in a funnel with bottom stem of 4.5 mm internal diameter. The powder was allowed to flow freely and the diameter and height of the mound formed were measured (Swarosky, 1987). The analyses were performed in triplicate and the angle of repose was calculated by the arc tangent of the ratio of mound height to radius.

Tapped density

The powder (2.5 g) was carefully placed into a 25 mL graduated cylinder. The cylinder was tapped 200 times and the powder volume was measured at every 20 taps. This procedure was repeated three times (Kawashima et al., 1988).

Hygroscopicity evaluation

Spray-dried powder moisture uptake was determined using a method modified from the one described by Senna et al. (1997). Powder samples (300 mg) were conditioned at 25 ºC ± 1 ºC in four airtight glass flasks with different saturated salt solutions in water (magnesium chloride hexahydrate, potassium carbonate, sodium nitrate and zinc sulphate), corresponding to 33, 43.2, 64.5 and 90% relative humidity, respectively. The sample moisture content was gravimetrically determined at 24 h intervals during a 10-day period. These experiments were carried out in duplicate.

Scanning electronic microscopy (SEM)

The morphology of the spray-dried powders was evaluated by scanning electron microscopy (Field Emission Gun Philips 3000^®) at magnifications of 500, 1,000, 2,000 and 10,000x. Before the SEM, the samples were coated with gold/palladium under argon atmosphere using a Balzers evaporator (SCD 050, Bal-Tec, AU).

Moisture content

The residual moisture content of the spray-dried extracts was determined by weight loss in an oven at 105 ºC for 5 h using samples of 300 mg (Farmacopéia Brasileira, 2000). Analyses were performed in triplicate.

Parthenolide soluble content

The parthenolide soluble fraction in the spray-dried powder was determined by dissolving it at 12 different concentrations (20 - 100 mg/mL) in phosphate (pH 7.5) and hydrogen chloride (pH 1.2) buffers. Samples were stirred for 48 h, at 37 ºC and 500 rpm (Swarosky ,1987), filtered using 0.45 μm membranes and then analyzed by HPLC (see Quantitative analysis of parthenolide).

Evaluation of uncoated and coated tablets

The average weight, hardness, friability and disintegration time of the uncoated and coated tablets were determined according to the methods described in the Brazilian Pharmacopoeia (1988). The hardness was determined using a Tablet Tester 8M, the friability was measured with an Ética 300.1 friabilator and the disintegration time was measured in purified water at 37 ± 0.5 °C, in an Ética 301 AC apparatus.

Dissolution of coated tablets

The coated and uncoated tablets containing 0.2% of parthenolide were inserted into dialysis bags which were subsequently immersed in flasks containing 10 mL of phosphate buffer pH 7.4 under magnetic stirring at 100 rpm and 37 ºC. This procedure was adopted to guarantee that the dissolution test would be adequate for both sink conditions and the detectable range of parthenolide by the HPLC methodology adopted herein. Samples were collected at every 15 min for a 2 h period and then analyzed by HPLC (see Quantitative analysis of parthenolide).

RESULTS AND DISCUSSION

Parthenolide quantification and flavonoids analyses

The grinded herb contained 0.49% of parthenolide and 0.54% of total flavonoids. The hydroalcoholic extract presented total flavonoid and parthenolide and total solid contents of 1.05, 1.06 and 10.8%, respectively. The total flavonoid and parthenolide contents in spray-dried extracts were 1.31% and 0.76% (w/w), respectively, with relative standard deviations (RSD) of 6.9% and 1.6% (Table V). The low RSD obtained for triplicate quantifications demonstrate the adequacy of the methods.

According to literature, ethanol extracts should be prepared with ethanol and water and contain 70% or less of alcohol. In this work the alcohol 70 was chosen to prepare the extract by percolation because it showed the better extraction of parthenolide than other alcohol/water mixtures (data not shown).

The analysis of parthenolide from the spray-dried extract and solid dosage form are important to evaluate the overall process efficiency and reproducibility because this metabolite can undergo thermal or chemical degradation during the process. Furthermore, these metabolites are essential for the pharmacological effects of T. parthenium (Williams et al., 2003). The HPLC/DAD chromatograms obtained for parthenolide and spray-dried extract are shown in Figures 1A and 1B, respectively. The chromatogram in Figure 1B demonstrates the excellent resolution of the method for parthenolide, which was detected at 210 nm after a retention time of about 15 min (in the middle of the chromatogram).

The calibration curve was obtained for the peak area as a function of the standard concentration in the solution (μg/mL). The variation coefficients ranged from 0.23 to 3.7% (data not shown). Analyses of UV spectra collected at the beginning, in the middle and at the end of the parthenolide peak showed that the method presents specificity. The quantification limit was 0.07 μg (70 μL of a 1 μg/mL solution) and the detection limit, based on three times the noise level, was 0.02 μg (20 μL of a 1 μg/mL solution). Acceptable intra and inter-assay precision were obtained for the method since the % RSD ranged from 0.34 - 4.1% for the intra-assays and 0.34 - 2.19 % for the inter-assay precision tests (data not shown). The accuracy ranged from 94.09 - 99.99 (data not shown). These results demonstrate that the HPLC and sample extraction methods were reproducible.

Figures 2A and 2B present the HPLC/DAD chromatograms for flavonoid santin and the spray-dried extract, respectively. Santin was detected at 241 nm after a retention time of about 4 min, and Figure 2B shows that a good resolution was obtained under the applied conditions. Besides the analysis of santin, experiments were performed in order to determine the total flavonoid content by spectrophotometry using quercetin as reference.

Pharmacological investigations of feverfew and parthenolide have demonstrated that both present anti-inflammatory effect through the inhibition of eicosanoids as well as the transcription nuclear kappa-B (NF-kB) (Gruenwald et al., 2000; Garcia-Piñeres et al., 2001; 2004). Further studies revealed that flavonoids such as santin are also important anti-inflammatory constituents of this species (Long et al., 2003; Williams et al., 1999).

Although parthenolide as well as feverfew have been subject to several chemical and pharmacological investigations, a study describing the standardization of its dried including flavonoids analysis as well as parthenolide quantification was still lacking.

Characterization of the spray-dried extract

Before spray drying, the liquid extracts were diluted in water to increase their fluidity and reduce the ethanol content, preventing explosion hazards and nozzle blocking during the atomization. The addition of colloidal silicon dioxide in the liquid extract reduces the adherence of the material to the equipment walls and improves the dry powder shape (spherical), size distribution and flowability (Runha et al., 2001).

Figure 3 presents the scanning electronic microscopy (SEM) of the spray-dried extract powder showing that the particles are spherical in shape, which is a common feature of the spray drying process. The particles sphericity is one of the advantages of spray-dried pharmaceutical powders, since this shape is associated with adequate flowability and bulk density. The results on particle size measurements (PSM) are shown in Figure 4, representing the cumulative size distribution. The PSM in Figure 4 showed that the powder sizes are homogenously distributed, and the cumulative size distribution fits to the Rosin-Rammler distribution with an acceptable squared correlation coefficient (R² = 0.9976). The average diameter based on 50% cumulative weight was 4μm.

Other important physicochemical properties of the spray-dried powder are presented in Table V. The "poured" angle of repose was 35.7º, which can be related to "intermediate" powder flow properties. Considering that this powder is obtained from a plant extract it is expected to have angle of repose higher than 30º (Endale et al., 2002; Stariff et al., 2007; Von Eggelkraut et al., 2002).

The dried extract presents low bulk density and moisture content, which are indicatives of good fluidity and chemical/microbiological stability, respectively. These properties are essential for the development of tablets (Senna et al., 1997).

Besides the determination of spray-dried extract moisture content, their hygroscopic properties were also determined by water uptake under different relative humidity conditions. The curves of water uptake or powder weight gain as function of time obtained for the relative humidity of 33, 43, 65 and 90% are shown in Figure 5. As can be seen, except at the relative humidity of 90%, the spray-dried extracts showed very low water adsorption during the entire experiment (240 h). This can be explained by the non-hygroscopic characteristic of the drying aid used (colloidal silicon dioxide). However, under extreme relative humidity conditions (90%), the powder absorbs water in the initial 72 h and then the moisture content remains constant, attaining the balanced moisture content.

The solubility of parthenolide from the spray-dried extract was assayed in phosphate buffer solution pH 7.5 at different powder concentrations, as presented in Figure 6. The graph demonstrates that there is a maximum in the percentage of parthenolide solubilised for the concentration of 50 mg/mL of spray-dried extract. However, in all concentrations only a fraction, 25 to 40%, of parthenolide was solubilized.

Experiments were also run to determine parthenolide solubility in HCl buffer pH 1.2, but the amounts solubilized were not detectable by HPLC/DAD (data not shown). Based on these results, experiments were carried out to determine the dry extract n-octanol-water partition coefficient (log P). Nevertheless, it was not possible to determine this parameter since parthenolide was almost entirely found in the n-octanol phase. These results suggest that the feverfew pre-formulation may be absorbed through the intestinal mucosa. Previous work showed that parthenolide is effectively absorbed through the intestinal mucosa via a passive diffusion mechanism (Khan et al., 2003).

Recently, there has been an increasing interest in dry extracts of natural products. The dry extracts present obvious advantages in pharmaceutical formulations, such as the possibility of easy preparation of tablets and capsules and better conditions of stability. Moreover, we showed that the content of parthenolide and total flavonoids in the spray-dried extract of T. parthenium are higher than the powder of the plant (Chaves, Costa, in Press)

Feverfew tablets

The properties of the feverfew dry extract presented in the previous section demonstrated that it is fairly adequate for direct compression, although this is not the usual characteristic of dry herbal extracts (Palma et al., 2002). The direct compression method is faster and simple, but requires the use of excipients with good flow and compressibility properties, such as microcrystalline cellulose PH 102, PVP 30, magnesium stearate and colloidal silicon dioxide. The amount of spray-dried extract in tablets was established according to literature information of parthenolide therapeutical doses, ranging from 0.1 to 0.4 mg daily (Gruenwall et al., 2000). The formulation in this work presents a total parthenolide content of 0.4 mg. The formulation used is shown in Table II, and during the whole compression process it showed none of the problems associated with unsatisfactory tableting.

Some important properties of the tablets obtained are presented in Table VI, demonstrating that the cores have adequate hardness, friability and weight uniformity. On the other hand, the tablets rapidly disintegrate in simulated gastric fluid (8 min).

The previous reports on gastrointestinal irritation, abdominal pain and heartburn of feverfew preparations (Johnson et al., 1985; Murphy et al., 1988; O'Hara et al., 1998) indicate that enteric coating of the solid dosage form to allow release only in the intestine would be more adequate. Aqueous polymeric dispersions have gained popularity and are replacing solvent-based systems due their lower toxicity level and environment friendly standpoint. Acrylate polymers and their derivates such Eudragit L30 D-55 Ò in a form of aqueous dispersion are widely used in the pharmaceutical industry as coating materials (Zhang et al., 2007)

The spouted bed and its variants have been extensively studied for diverse unit operations such drying of granules and pastes and particle coating. In the pharmaceutical field, spouted bed coating has been used for tablets, capsules and granule coating with excellent results (Kfuri, Freitas, 2006) The recent development of the new aqueous polymeric emulsions for pharmaceutical coating has generated interest in alternative equipment, since the traditional pan coaters were shown to be ineffective in this case, due to their low aeration profiles and consequently low drying capacity. Fluidized and spouted beds have been the choice to overcome this limitation, due to their high level of aeration and good gas-solid contact. The previous studied published by our group (Kfuri, Freitas, 2006) showed that the fluidized bed conditions used here, presented good coating quality without problems of agglomeration, picking or any other factor related to poor drying conditions and that these operational conditions can be applied for the coating of tablets.

The properties of coated tablets can be seen in TABLE VI, showing an increase in hardness and decrease in friability, as expected for Eudragit^® L30 D55 coated cores. The tablets weight variation also decreased, which is indicative of the good coating uniformity provided by the fluid bed process. The disintegration test showed that tablets do not disintegrate in HCl solution, and totally disintegrate after 19 min in phosphate buffer.

According to literature specifications, 70-75% of the drug should be released in 45-60 min (United States Pharmacopoeia, 1995). However, the release profile can be limited by the physicochemical properties of parthenolide, such as the low solubility, as well as by the tablet formulation. Due to the poor parthenolide solubility and to the limit of detection of the HPLC method used in this work, the dissolution test was performed with modifications, as detailed in the materials and methods section. The dissolution profile is presented in Figure 7.

The dissolution profile demonstrates a linear rate until it reaches the maximum amount of parthenolide released in approximately 60 min. The linear section of parthenolide release, or zero order models, fitted to the dissolution data with squared correlation coefficient of 0.9916 and is adequate for this formulation. The release rate was 0.47% per minute, which corresponds to 1.88 μg of parthenolide per minute. However, due to the already mentioned poor solubility of the parthenolide, only a small fraction (30%) of this compound was released during the tests, which corresponds to 0.12 mg of parthenolide. The tablet formulation based on the feverfew spray-dried extract was demonstrated to be adequate for this phytomedicine.

CONCLUSIONS

The procedures described herein can be used to prepare and evaluate a pre-formulation of feverfew with essential properties for the development of a high-quality phytomedicine. The spray-dried extract demonstrated adequate properties, such as particle size and shape, bulk density, flowability, and compressibility. Furthermore, it was possible detect parthenolide and flavonoids after drying process. The characteristics of the tablets obtained confirmed the good compressibility of the spray-dried extract and showed adequate pharmacotechnical properties. However, the assays on parthenolide solubility showed that efforts should be directed towards the development of T. parthenium inclusions or complexes with solubility helpers.

ACKNOWLEDGEMENTS

The authors are grateful to FAPESP/Brazil (Contract/grant #01 12638-2) for financial support. We thank Dr. Élida A. Stefanello (UFPR, Brazil) for providing parthenolide, Antonio M. L. Prieto (UFSCar, Brazil) for SEM analysis, Dr. Mônica L. Aguiar (UFSCar, Brazil) for PSM analysis, Giovanna Bonfante Borini (FCFRP-USP, Brazil) for suggestions and Dr. Paul Gates (University of Bristol, UK) for English revision.

Received for publication on 19^th December 2007

Accepted for publication on 29^th April 2009

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Publication Dates

• Publication in this collection
  01 Dec 2009
• Date of issue
  Sept 2009

History

• Received
  19 Dec 2007
• Accepted
  29 Apr 2009