Poloxamer-enhanced solubility of griseofulvin and its related antifungal activity against Trichophyton spp.

Abstract

Poorly water-soluble drugs, such as the antifungal drug griseofulvin (GF), exhibit limited bioavailability, despite their high membrane permeability. Several technological approaches have been proposed to enhance the water solubility and bioavailability of GF, including micellar solubilization. Poloxamers are amphiphilic block copolymers that increase drug solubility by forming micelles and supra-micellar structures via molecular self-association. In this regard, the aim of this study was to evaluate the water solubility increment of GF by poloxamer 407 (P407) and its effect on the antifungal activity against three Trichophyton mentagrophytes and two T. rubrum isolates. The GF water solubility profile with P407 revealed a non-linear behavior, well-fitted by the sigmoid model of Morgan-Mercer-Flodin. The polymer promoted an 8-fold increase in GF water solubility. Fourier-transform infrared (FT-IR) spectroscopy, differential scanning calorimetry (DSC), and 2D nuclear magnetic resonance (NMR Roesy) spectroscopy suggested a GF-P407 interaction, which occurs in the GF cyclohexene ring. These results were supported by an increase in the water solubility of the GF impurities with the same molecular structure. The MIC values recorded for GF ranged from 0.0028 to 0.0172 mM, except for T. Mentagrophytes TME34. Notably, the micellar solubilization of GF did not increase its antifungal activity, which could be related to the high binding constant between GF and P407.

Keywords:
Griseofulvin; Poloxamer 407; Micellar solubilization; Drug-polymer interaction; Antifungal activity

INTRODUCTION

Aqueous solubility is an essential property for drug formulation and targeted activity and thus represents a major challenge for technological development (Takagi et al., 2006; Kawabata et al., 2011; Buckley et al., 2013; Khadka et al., 2014). The Class II drugs of the Biopharmaceutics Classification System can preclude the development of effective dosage forms owing to their poor solubility in water and biological fluids (Aly et al., 1994; Amidon et al., 1995; Fujioka et al., 2007; Noomen et al., 2008). Griseofulvin (GF) (Figure 1), a fungistatic drug of choice for the treatment of dermatomycoses such as tinea capitis, especially infections caused by the genera Epidermophyton, Trichophyton, and Microsporum, is an example of such drug (Finkelstein, Amichai, Grunwald, 1996; Shishu, Aggarwal, 2006; Aggarwal, Shishu, Khurana, 2013; Gupta et al., 2018).

FIGURE 1
Chemical structure of griseofulvin (GF).

Several pharmaceutical approaches have been adopted to increase the aqueous solubility and bioavailability of GF, such as self-emulsifying drug delivery systems, solid dispersions, cocrystals, and cyclodextrin complexation (Dhanaraju et al., 1998; Arida, Al-Tabakha, Hamoury, 2007; Aitipamula et al., 2012; Cheng et al., 2015). Micellar solubilization by polymers is another alternative for overcoming problems that arise from poorly soluble drugs and hydrophobic molecules, including drug formulation and bioavailability (Lee et al., 2008; Liveri et al., 2012). Poloxamers are triblock copolymers consisting of ethylene oxide (EO) and propylene oxide (PO) units in an amphiphilic arrangement (Rowe, Sheskey, Owen, 2005; Dumortier et al., 2006). Their structure enables self-association from simple to more complex micelles with hydrophobic (PO) and hydrophilic (EO) domains (Kabanov, Alakhov, 2002). Poloxamer 407 (P407) is one of the most studied poloxamers due to its water solubility and excellent capacity to interact with hydrophobic drugs (Lau et al., 2004; Rowe, Sheskey, Owen, 2005; Dumortier et al., 2006). Studies on the micellar solubilization of GF, including di- and triblock copolymers, have been presented in the literature; however, these studies are restricted to technological issues, with no experimental evidence of the reflex on antifungal activity (Rekatas et al., 2001; Ribeiro et al., 2009; Oliveira et al., 2011). The formation of polymer micelles by P407 alone and its effect on GF aqueous solubility and antifungal activity are yet to be explored.

The present work aimed to evaluate GF solubilization using P407 and their reflex on the antifungal activity of GF against Trichophyton mentagrophytes and Trichophyton rubrum isolates.

MATERIAL AND METHODS

Material

Griseofulvin (98% purity) and acetone-d ₆ were purchased from Sigma Aldrich (St. Louis, MO, USA). Poloxamer 407 (Pluronic® F127) was kindly provided by BASF (Ludwigshafen am Rhein, Germany). Acetonitrile (Merck Millipore, Darmstadt, Germany), formic acid (Tedia, Fairfield, USA), and ultrapure water obtained from a Milli-Q® system (Millipore Merck, Darmstadt, Germany) were used for the mobile phase in LC analysis. Sterilizing filters (0.22-µm membrane) were obtained from Sartorius (Goettingen, Germany). For the antifungal assay, RPMI 1640 culture medium and potato dextrose agar were purchased from Sigma Aldrich.

Quantification and characterization by HPLC-PDA

GF quantification was performed using an HPLC instrument (Prominence, Shimadzu, Kyoto, Japan) equipped with an FCV-AL 10 system controller, LC-20 AT pump, SIL-20 A autosampler, and a photodiodo array detector (PDA) SPD-M20A. The stationary phase was a Kinetex^® Phenomenex C18 100A column (150 × 4.6 mm ID, 5 µm) coupled with a SecurityGuard ULTRA Phenomenex C18 guard column (4.6 mm ID, sub-2 μm). An isocratic system was employed, with a mixture of 0.1% (v/v) formic acid in water (A) and acetonitrile (B) (65:35%, v/v) as the mobile phase. The flow rate (1.1 mL/min) and temperature (35±1 °C) were kept constant throughout the analysis, and absorption was detected at 290 nm. All samples were appropriately diluted with mobile phase and filtered through a 0.45-μm membrane (Millipore^®, Merck Millipore, Darmstadt, Germany). The method was previously validated according to ICH guidelines (data not shown).

Solubilization assay

P407 aqueous dispersions in the 0.02-4.8 mM concentration range were prepared and maintained overnight at 10 °C. Separately, a GF excess above water saturation was added to the dispersions. Thereafter, the mixtures were stirred magnetically for 24 h at 37±1 °C (MULTISTIRRER Velp, Usmate, MB, Italy). The samples were centrifuged for 20 min at 3.600 G, and the supernatant was filtered through a 0.45-µm membrane. An aliquot of each solution was diluted with the mobile phase for subsequent analysis by HPLC-PDA. The intrinsic solubility of GF was determined using ultrapure water under the same experimental conditions. The impurities present in GF samples were analyzed by HPLC and their solubilization profiles were recorded. All analyses were performed in triplicate.

Physicochemical characterization

Fourier-transform infrared spectroscopy (FT-IR)

The FT-IR spectra of GF, P407, and GF-P407 physical mixture (1:1, w/w) were recorded in the scanning range of 4000 - 600 cm^-1, using a resolution of 4 cm^-1 and 40 accumulations (Spectrum BX FTIR, PerkinElmer, Waltham, USA).

Differential scanning calorimetry (DSC)

Thermograms were recorded using a Shimadzu DSC-60 calorimeter, and data analysis was performed using TA Analysis Software (Shimadzu, Kyoto, Japan). Accurately weighed amounts of approximately 1 - 2 mg of GF, P407, and GF-P407 physical mixture (1:1, w/w) were analyzed in crimped aluminum pans. The operating conditions were a heating rate of 10 °C/min (25 to 250 °C) and a dynamic nitrogen atmosphere of 50 mL/min.

Nuclear magnetic resonance spectroscopy (NMR) studies

One-dimensional ¹H NMR and homonuclear 2D-Roesy spectra were recorded using a Bruker 400 MHz spectrometer (Bruker, USA) operating at 400 MHz and room temperature. The data were processed using MestReNova^® 6.0 software (Mestrelab Research^©, Spain). Sample solutions of GF, P407, and GF-P407 physical mixture (3:1, w/w) were prepared using acetone-d ₆ .

Analysis by Zetasizer

The particle size and polydispersity index (PDI) of P407, alone and associated with GF, were determined by photon correlation spectroscopy. Zeta potential (ζ) and conductivity were measured by electrophoretic mobility (Zetasizer 3000HS, Malvern Instruments, Malvern, England). Samples were prepared in the same concentrations and experimental conditions described in the solubilization assay and analyzed at 37 °C.

Multivariate analysis

Hierarchical clusters (HCA) and principal component (PCA) analyses of particle size, PDI, ζ potential, conductivity, GF solubilization, and polymer concentration were performed using MINITAB^® 16 software (State College, PA, USA). The number of components was determined according to the magnitude of the eigenvalues following the Mahalanobis distance. Each variable was evaluated as per the set of data obtained in triplicate on three different days. For the non-unimodal samples, the particle size of the major population (> 90%) was selected for analytical purposes.

Fungal susceptibility tests

Microorganisms

The isolates of Trichophyton mentagrophytes (TME16, TME34, and TME40) and Trichophyton rubrum (TRU43, TRU51) were obtained from the culture collection of the Laboratory of Applied Mycological Research, Federal University of Rio Grande do Sul, Porto Alegre, Brazil. Fungal inocula were prepared according to the Clinical Laboratory Standard Institute protocol (M38-A2 document, CLSI, 2008). After incubation, the conidia suspension was prepared, and the concentration was adjusted in a counting chamber for 1x10³-3x10³ CFU/mL.

Work samples

Samples of the GF and GF-P407 mixtures at different polymer concentrations (0.04, 0.8, 1.6, 2.4, and 4.8 mM) were prepared as described in the solubilization assay. All work samples were prepared under laminar flow aseptic conditions and sterilized by filtration through a 0.22-µm membrane. GF alone was solubilized with ultrapure water, according to the intrinsic solubility assay, and filtered to eliminate the particles that were not soluble.

Minimum inhibitory concentration test (MIC)

The minimum inhibitory concentration values of each sample were determined by the microdilution broth method according to the Clinical Laboratory Standard Institute protocol (M38-A2 document - CLSI, 2008), with modifications. GF and GF-P407 solutions were tested against the isolates of T. mentagrophytes and T. rubrum at concentrations ranging from 5.56x10^-5 - 0.011 mM and 1.95x10^-4 - 0.039 mM of GF, respectively. For T. mentagrophytes (TME 34), the GF-P407 sample was tested in the concentration range of 3.89x10^-4 - 0.097 mM of GF and the plates were incubated at 32 °C for five days. The MIC was defined as the lowest concentration of GF where the tested isolate did not demonstrate visible growth. The assay was performed in triplicate for each sample on three different days. The viability of fungal growth, sterility of the culture medium and samples, and the effect of the sample containing only polymer were used as controls.

RESULTS AND DISCUSSION

Solubility assay

The solubilization assay data revealed an approximately 8-fold increase in the solubility of GF in the highest P407 concentration. The GF-P407 solubilization profiles appeared as a sigmoid-shaped curve and were better fitted by the Morgan-Mercer-Flodin mathematical model (y = [ab + cx ^d]/[b + x ^d]) but with a discrete regression coefficient (R² = 0.90) (Figure 2). Notably, sigmoid-shaped curves are not always common in drug solubilization profiles. For instance, the GF solubilization disagrees with that reported for felodipine under similiar experimental conditions, in which the solubilization occurred as a linear function of P407 concentration (Lee et al., 2008). In addition, the GF-P407 sigmoid-shaped curve described above was unrelated to any experimental conditions applied in this work, as confirmed after five replications at different days. This might be linked to the formation and coexistence of globular, lamellar, cylindrical, hexagonal, and cubic micellar arrangements, after spontaneous self-association of the single poloxamer molecules (Lawrence, 1994; Alexandridis, Olsson, Lindman, 1998; Mortensen, 2001; Kabanov, Alakhov, 2002). The self-association of the poloxamer in different structures can occur at low concentrations, below its critical micelle concentration (CMC), depending on the surrounding temperature (Lin, Alexandridis, 2002; Lee et al., 2008; Ren et al., 2015). In fact, there is no consensus on the P407 CMC value being reported from 0.18% (25 °C) to 0.01% (37 °C). As a rule, the more complex the micelle structure, the higher the drug solubilization (Kabanov, Alakhov, 2002). In addition, a more intricate picture emerges following the addition of a solute that can contribute to a high structural polymorphism and the coexistence of distinct molecular arrangements in a dynamic manner. Thus, the coexistence of these structures, different stages of self-assembly with the addition of the copolymer, and the potential interaction of the drug could explain the decrease in GF solubility in some P407 concentrations (Alexandridis et al., 1994; Ivanova, Lindman, Alexandridis, 2000a; Ivanova, Lindman, Alexandridis, 2000b; Kabanov, Alakhov, 2002; Ren et al., 2015).

FIGURE 2
Curve of GF solubilized (µg/mL) versus P407 concentration (%) (A); and the curve of GF solubilized (mM) versus P407 concentration (mM) adjusted by the Morgan-Mercer-Flodin model (CurveExpertPro-2.6.3) (B).

FT-IR

The potential interactions between GF and P407 were investigated by FT-IR analysis by comparing the respective absorption spectra, considering specific functional groups of GF and P407 alone, and the GF-P407 physical mixture (1:1, w/w). The choice of this ratio between GF and P407 was based on studies of drug-excipient compatibility for maximizing the probability of observing any GF-P407 interaction.

The GF spectrum showed characteristic bands at 2945 cm^-1 (C=C─H stretching), 1704 cm^-1 and 1658 cm^-1 (stretching of the carbonyl group of benzofuran and cyclohexene, respectively), 1614 cm^-1 and 1584 cm^-1 (aromatic C=C), 1210 cm^-1 (C─O stretching attached in ring), 1135 cm^-1 (C=C─O stretching), and 800 cm^-1 (aromatic C─H) (Figure 3A). The P407 spectrum showed characteristic bands at 2881 cm^-1 (aliphatic C─H) and 1100 cm^-1 (C─O stretching) (Figure 3B) (Garg, Sachdeva, Kapoor, 2013).

FIGURE 3
Fourier-transform infrared (FT-IR) spectrum of (A) GF; (B) P407, and (C) GF-P407 physical mixture (1:1, w/w).

The spectrum of the GF-P407 physical mixture (Figure 3C) presented almost all characteristic bands of both substances, except the GF band at 2945 cm^-1. In addition, evident intensity and shape changes were recorded, mainly the decreased intensity of the GF bands at 1210 and 1135 cm^-1 and the shape and intensity change of the P407 band at 1100 cm^-1. These results suggest the involvement of the proton of the cyclohexene ring of GF in the molecular interaction between GF and P407.

DSC

The DSC curves of GF, P407, GF-P407 physical mixture (1:1, w/w), and the reanalysis after cooling of the previously melted physical mixture are shown in Figure 4. Both the GF (A) and P407 (B) curves matched the published data (Feng, Pinal, Carvajal, 2008; Garg, Sachdeva, Kapoor, 2013), showing endothermic peaks at 218 and 52 °C, respectively.

FIGURE 4
DSC curves of (A) GF; (B) P407; (C) GF-P407 physical mixture (1:1, w/w), (D) reanalysis of the physical mixture under the same experimental conditions.

In addition, the curve of the GF-P407 physical mixture (C) revealed a slight displacement of the endothermic peak of P407 and the complete disappearance of the GF peak. This implies a clear modification of the crystalline structure of GF linked to a feasible molecular interaction between GF and P407; however, it can also be associated with the solubilization of GF in the mass of a previously melted polymer. The same behavior was observed in the DSC analysis of solid dispersions composed of felodipine and P407 (Kim et al., 2006). The reanalysis of the GF-P407 physical mixture (D) reinforced the postulation of a potential solubilization of GF in the polymer, taking into account the lack of any thermal variation event in the same temperature range.

NMR studies

Homonuclear 2D-Roesy is commonly used to elucidate the intermolecular interactions between two or more substances. The data obtained herein for the GF-P407 mixture did not enable us to draw a concrete conclusion regarding the interaction region. The Roesy spectrum showed a region of interaction that involved the proton of the GF cyclohexene ring (5.6 ppm) and some protons of P407 at the chemical shift region of 3.6 - 3.8 ppm. This result suggests that the interaction occurs with the CH₂ group of the poloxamer EO part, indicating that GF molecules are not exclusively located in the micelles. However, the high proximity of the signals of both substances in this region interferes with the ideal visualization of the phenomenon and exact confirmation of the protons involved in the process. Another interference could be the organic solvent choice owing to the low GF solubility, which prevents the use of deuterium oxide in the evaluation (Supplementary Material).

Analysis by Zetasizer

The initial concentrations of P407 (0.016 mM, 0.04 mM, and 0.08 mM), alone or combined with GF, showed bimodal and trimodal particle size populations. The polydispersity index ranging from 0.5 to 0.6 corroborated a clear heterogeneity among the particle size population. The population with the smallest particle size (approximately 2 nm) was assigned to small structures as polymer chains. Particles of intermediate size (25 nm) predominated over other populations and were ascribed to single micellar structures. Conversely, those with the largest size (100 nm) to more complex structures or the polymer aggregates did not completely disperse. However, a tendency toward a unimodal distribution accompanied by a decrease in PDI values (between 0.1 and 0.2) was observed after the P407 concentration was increased. Thus, particle size remained in the range of 20 to 30 nm, and no direct correlation was observed between the increase in P407 concentration and particle size. The obtained data reflected those previously reported by Chiappetta et al. (2011), who observed a similar behavior and the presence of micelle structures of approximately 20 nm in the P407 dispersions. The Zetasizer analysis carried out after GF addition showed similar particle size distribution and PDI, demonstrating that both variables were not affected by the presence of GF. The (zeta) ζ potential of the P407 dispersions varied from − -20 to -5 mV, according to the increase in P407 concentration, which may be due to the formation of micelle arrangements in different ways. The decrease in the ζ potential values indicates a higher aggregation tendency of the polymer molecules and lower stability of the polymeric micelles (Sezgin, Yüksel, Baykara, 2006; Ghaffari et al., 2011; Suksiriworapong et al., 2014). The GF-P407 dispersions showed the same behavior, but varied from -8 mV to -2 mV. Such finding suggests that GF molecules are interacting with the P407 micelles, in some extension, at least. Furthermore, the instability of the system indicated by the lower ζ potential values could explain the sigmoid profile of GF solubilization. The conductivities of the P407 dispersions and GF-P407 dispersions were very similar, ranging from 0.05 - 0.18 μS/cm to 0.02 - 0.15 μS/cm, respectively. This discrete conductivity value is associated with the nonionic nature of the poloxamer and can be ascribed to the increase in P407 concentration.

Multivariate analysis

To clarify the potential correlations between the variable P407 concentration, particle size, PDI, ζ potential, conductivity, and amount of solubilized GF, HCA and PCA analyses were performed. Both multivariate methods revealed two clusters (Figure 5A), with approximately 90.8% of the variability explained by the factor extractions, PC1 and PC2 (Figure 5B). The two groups demonstrated an antagonistic relationship, as displayed by the separation between both clusters and the location of the descriptive vectors in opposing camps. The first cluster included polymer concentration, conductivity, and solubilized GF. Thus, a high similarity between these variables can be inferred, confirming the correlation between the increase in P407 concentration and the amount of solubilized GF and the conductivity. The second cluster was comprised of particle size, PDI, and ζ potential. Thus, the three measures showed clear opposition for the first cluster, indicating that there is no linear relationship between the variation in these values and an increase in P407 concentration and GF solubility. Within the second cluster, a high similarity existed between particle size and PDI, which was expected as these measures are correlated. A further multivariate analysis omitting the solubilized GF data was carried out to infer its effect on GF-P407 behavior; however, no tangible changes were observed in the dendrograms described below (Figure 6A). Briefly, the variability explained by PC1 and PC2s remained at 93.3% (Figure 6B), and slight changes in the angle between some vectors were demonstrated, without characterizing significant changes. Thus, multivariate analysis revealed a correlation between the variables of interest but did not allow a clear visualization of the role of GF in this dynamic system.

FIGURE 5
HCA and PCA analyses of samples with GF - (A) dendrogram of the GF-P407 mixture samples using the single linkage method and Mahalanobis distance; (B) Loading plots (PC1 versus PC2) from variables. Group 1: P407 (polymer concentration), conductivity, GF solubilized; Group 2: particle size, PDI (polydispersity index), and ζ potential.

FIGURE 6
HCA and PCA analyses of samples without GF - (A) dendrogram of the P407 samples using the single linkage method and Mahalanobis distance; (B) Loading plots (PC1 versus PC2) from variables. Group 1: P407 (polymer concentration) and conductivity; Group 2: particle size, PDI (polydispersity index), and ζ potential.

Analysis of GF-P407 interaction via an evaluation of its synthesis impurities

Some of the GF impurities derived from its fermentation or chemical degradation have been identified and described (Townley, 1979; Kahsay et al., 2013). In the present study, these impurities were also observed in the GF sample in the absence of P407. Notably, in the GF solubilization study, changes were noted to occur for the peak area of some impurities as the P407 concentration increased. Thus, the evaluation of a potential GF-P407 interaction was performed by considering the impurity solubilization profile and its structural differences (Figure 7).

FIGURE 7
Solubilization profile of the GF impurity synthesis/degradation - (Impurity 1: griseofulvinic acid; Impurity 2: dechlorogriseofulvin; Impurity 3: deidrogriseofulvin).

According to Kahsay et al. (2013), the main impurities related to GF were griseofulvin acid (impurity 1), dechlorogriseofulvin (impurity 2), and deidrogriseofulvin (impurity 3) (Figure 8). The solubilization of the impurities, dechlorogriseofulvin and deidrogriseofulvin, revealed a strong correlation with the profile presented for GF (r_Pearson 0.9156 and 0.9142, respectively). However, the griseofulvinic acid solubilization was different to GF profile (r_Pearson 0.1166), and to dechlorogriseofulvin (r_Pearson 0.2286) and deidrogriseofulvin (r_Pearson 0.3848) profiles.

FIGURE 8
GF and impurity chromatogram in the presence of P407 - 1: griseofulvinic acid; 2: dechlorogriseofulvin; GF: griseofulvin; and 3: dechlorogriseofulvin.

Through multivariate analysis, the correlation between the solubilization profiles was confirmed as the HCA and PCA analyses revealed the presence of two groups. GF, dechlorogriseofulvin, and deidrogriseofulvin constitute the first group, with similar solubility profiles. Griseofulvin acid is composed of the second group, demonstrating a different behavior for GF and the other two impurities. In contrast to GF and the other two impurities, the griseofulvin acid molecule did not exhibit cyclohexene ring unsaturation. In conjunction with the data obtained from the FT-IR and NMR analyses, it is plausible to propose that the increased solubility of GF can be attributed to the interaction between the sp ² unsaturation of GF and P407.

Fungal susceptibility tests

The fungal susceptibility tests for samples containing GF-P407 association against Trichophyton mentagrophytes and Trichophyton rubrum isolates showed MIC values ranging from 0.0028 to 0.0172 mM, except for Trichophyton mentagrophytes - TME 34, which was not inhibited. For samples containing GF alone, the MIC values against isolates of T. mentragrophytes and T. rubrum were 0.0028 and 0.0056 mM, respectively (Table I). By comparing the MIC values obtained for GF alone and GF-P407 dispersions, a decrease in drug activity was noted for samples containing P407. This finding is more than evident for Trichophyton mentagrophytes - TME 34, which was not susceptible when exposed to a 10-fold higher concentration of the drug with P407 at 4.76 mM. Under the same experimental conditions, P407 showed no antifungal activity at the concentrations tested.

TABLE I
MIC values (µg/mL) of GF alone and GF-P407 association sample

Isolates/Samples	MIC (μg/mL)
	GF	Sample 1	Sample 2	Sample 3	Sample 4	Sample 5
T. mentragrophytes
TME16	1.0	1.2	1.0	1.5	1.2	-
TME40	1.0	1.3	1.9	1.5	2.0	-
TME34	NI	NI	NI	NI	NI	NI
T. rubrum
TRU51	2.0	2.6	3.8	6.2	4.0	-
TRU43	2.0	1.3	3.8	5.3	4.0	-

• *Sample 1 = 0.5% P407; Sample 2 = 1.0% P407; Sample 3 = 2.0% P407; Sample 4 = 3.0% P407; Sample 5 = 6.0% P407. NI = not inhibition.

To calculate the binding constant or apparent stability constant (K _S ) between GF and P407, the linear region of the sigmoid solubilization curve was analyzed using a regression model (y = 0.0511x + 0.000003; r² = 0.9957). Subsequently, the K _S value was calculated using equation 1 (Higuchi, Connors, 1965; Brewster, Loftsson, 2007):

$K_S=Slope/S_0\left(1-Slope\right)$ (1)

where S ₀ is the solubility of GF in the absence of polymer.

The high value observed (2,100 M^-1) indicates the formation of a stable complex between GF and P407 (Lee, Shin, Oh, 2003; Loftsson, Brewster, 2009; Changdeo et al., 2011; Parmar, Shah, Sheth, 2011). This result might explain the low antifungal activity of GF-P407; this is because GF must be free from the polymer to permeate the fungal membrane and exert its activity on microtubule assembly (Odds, Brown, Gow, 2003).

The formulation with poloxamer 407 resulted in a critical increase in the amount of solubilized GF. Although some techniques enable a higher increase in GF solubility, the advantages of micellar solubilization are far beyond solubilization (Al-Obaidi et al., 2019). Polymeric micelles are also employed to enhance stability and control wetting, bioavailability, and the controlled release of drugs. P407 presents low toxicity, good compatibility with chemical substances and biological media, and allows the development of different pharmaceutical formulations (Torchilin, 2001; Bodratti, Alexandridis, 2018). Different P407 supra-micellar structures could participate in the distinct behavior of GF solubilization, as suggested by the stepped sigmoid shape gained while the polymer amounts were increased. The molecular interaction between the two substances was inferred by physicochemical tests and might involve the cyclohexene ring of GF. Notably, no relationship was observed between the increase in the solubilized amount of griseofulvin and the enhancement of its antifungal activity. In this context, a more detailed approach of the relationship between poloxamer-induced solubilization of GF and the improvement of its therapeutic response might be a reasonable scope for examination, especially in the development of new pharmaceutical forms of GF administration.

ACKNOWLEDGMENTS

The authors are grateful to Brazilian Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES (finance code 001) for financial support to conduct this study.

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Publication Dates

• Publication in this collection
  08 Aug 2022
• Date of issue
  2022

History

• Received
  06 Sept 2019
• Accepted
  29 May 2020