1. Introduction
Polymorphism, the ability of a molecule to exist in more crystal structures, is critical for the bioavailability of many drugs [
1], since polymorphic forms of a drug display different physico-chemical properties, such as, among many, solubility and stability. The fact that polymorphism and pseudopolymorphism of active pharmaceutical ingredients play a crucial role in their dissolution rate, is now well established [
2,
3,
4].
Rifaximin (
Figure S1 in Supplementary Materials) can be classified among highly (pseudo)polymorphic drugs, as at least eight crystal phases have been described so far (α, β, γ, δ, ε) [
5,
6] and (ζ, η, and ι) [
7,
8,
9]. It is a broad-spectrum antibiotic drug belonging to the family of rifamycins that acts on bacterial DNA-dependent RNA-polymerase [
10]. Being poorly water-soluble and poorly permeable through the intestinal mucosa, it is included in BCS class IV. In fact, the very low absorption in the human intestine is exploited for its local effect in the treatment of gastrointestinal diseases, such as traveller’s diarrhoea and irritable bowel syndrome, as well as in the management of hepatic encephalopathy; all these pathologies require a topical action upon oral administration, and absorption and systemic distribution are considered an undesirable side effect.
It has been reported that the crystallization of rifaximin in different conditions and solvents leads to different solvated forms [
11], with α, β, and amorphous being the most represented forms, impacting in a different manner on the antimicrobial activity of the drug [
12,
13], as well as on its bioavailability [
14]. The β and α forms contain between 3 and 4.5 and 0.5 and 1.5 water molecules in the formula unit, respectively [
6]. The amorphous form is reported to have pharmacokinetic behaviour similar to that of the poorly crystalline polymorph γ, which is the most soluble of the crystal forms, all exhibiting systemic absorption [
5].
In this respect, therefore, rifaximin represents a paramount example of the strict relationship between solid-state and biopharmaceutical properties.
The literature analysis affords the picture of a complex pattern of polymorphs, as clearly described by Viscomi and Braga [
5,
6]. In detail, the β form is obtained from wet rifaximin; when sprayed with water, α, γ, δ, and ε forms completely revert, with a different rate (faster for α, slower for γ), to the β form; their interconversion depends on the environmental conditions, in particular relative humidity. α and δ forms show the lowest water content but do not directly convert into one another.
Nonetheless, the conversion from one form to another is not straightforward and not yet fully understood, especially with respect to the role played by ambient humidity and aqueous dissolution media in this phenomenon.
Given these premises, the aim of this work is to investigate the dissolution behaviour of the most important solid phases of rifaximin, namely α, β, and amorphous, in relation to what is known about the relative thermodynamic stability and to contribute to clarifying any possible solvent- or humidity-mediated conversion pattern.
3. Results
As already reported, the β form represents the thermodynamically stable form in standard conditions and relative humidity >56%, while the other forms undergo a more or less rapid conversion [
5,
6]. Therefore, it was not surprising to observe that the β form afforded quite rapidly the lowest equilibrium solubility concentration of 2.73 ± 0.22 µg mL
−1 after an initial, limited, and short supersaturation phase (maximum concentration 3.65 ± 0.09 µg mL
−1), which may be ascribable to the presence of traces of amorphous rifaximin [
5]. The alpha form afforded a significantly higher initial concentration (6.30 ± 2.43 µg mL
−1), which was followed by a concentration decrease, slower than that observed for the β form, affording a final equilibrium value of 2.67 ± 0.19 µg mL
−1. As expected, the amorphous form gave rise to a significantly higher initial concentration, reaching a maximum value of 206.50 ± 22.55 µg mL
−1. The subsequent decrease was much slower than that observed for the α form (see insert in
Figure 1B) approaching the equilibrium value of 2.72 ± 0.07 µg mL
−1 only after 7 days.
The amount of rifaximin dissolved per surface unit from the compacts prepared with the different solid phases is represented as a function of time in
Figure 2. The linear regression of the experimental points between 15 and 120 min (linear portion of the dissolution curve) was performed to calculate the slope of the regression line which corresponds to the intrinsic dissolution rate expressed in mg cm
−2 min
−1. The values obtained are reported in
Table 1 as mean value ± standard deviation.
The amorphous form gave rise to an IDR more than one order of magnitude higher than that of the crystalline phases. On the contrary, and quite curiously, rifaximin β form did not afford the lowest IDR, as could be expected from the relative thermodynamical stability [
5]. However, the difference with the IDR with respect to the α form was not statistically significant (ANOVA,
p > 0.05). However, it was observed that the compact of α form gave rise to a progressive disintegration at the solid-liquid interface rather than a uniform dissolution as the β and amorphous forms did. The constancy of the surface area of the compact is a crucial requisite in the IDR measurement. Thus, the observed phenomenon invalidates the reliability of the measurement as the solid liquid interface area did not remain constant. The experimental points relevant to the α form showed an upward curvature and in fact the R
2 of the linear regression was only 0.87 vs. 0.98 for both the curves of β and amorphous form. The USP states that this type of curvature may be indicative of a systematic experimental problem such as compact delamination or disintegration.
The same measurement was repeated on four different batches (from two different manufacturers) of crystalline rifaximin α form (
Figure 3). The computed IDR values are summarized in
Table 2.
The IDR of the samples corresponding to the batches B1M1, B2M1, and B4M2 was comprised between 1.2 and 2.7 mg cm−2 min−1, being the differences among these values not statistically significant (ANOVA, p > 0.2).
The IDR of batch B3M2 was significantly higher (19.2 mg cm−2 min−1) relative to the other α rifaximin samples (ANOVA, p < 0.02).
The IDR values determined in this second set of measurements were compared to that of the α form reported in
Table 1: only the IDR of the batch B3M2 resulted to be significantly different (ANOVA,
p < 0.05). Moreover, all batches, but the B3M2 one, gave rise to a non-significantly different IDR compared to that of the β form reported in
Table 1.
Additionally, for all these measurements a progressive disintegration at the solid-liquid interface was observed. Thus, the same consideration made for data in
Table 1 and
Figure 1 applies.
The morphology of the particles of the four α rifaximin batches was investigated by scanning electron microscopy. As an example, pictures obtained at 3000× magnification for each powder are reported in
Figure 4.
Particles of the batches B1M1 and B2M1 (
Figure 4, panel A and B respectively) were very similar to each other being irregularly shaped and presenting a relatively large size distribution. Powders from the second manufacturer presented a different morphology; the particles of the batch B3M2 (panel C) were smoother with an apparently smaller size distribution compared to the particles of the batches of manufacture 1. In addition, besides some larger particles, the population contained a significant amount of very small particles. The fourth batch (B4M2, panel D) presented particles with a shape like that of batches B1M1 and B2M2 but smaller and more uniform in terms of size distribution.
The particle size distribution of these four batches was investigated in more detail by laser diffraction (
Table 3).
As it can be appreciated, the laser diffraction data confirmed what was already anticipated by the simple SEM images observation, namely the high similarity between B1M1 and B2M1, and the smaller particle size of the batches B3M2 and B4M2, the latter presenting a slightly larger size distribution (span 2.13 vs. 1.9).
As the size distribution data did not fully correlate with IDR data, a further evaluation of whether the differences in observed IDR among the four α rifaximin batches could be ascribed to morphological differences noticed in the SEM experiments, specific surface area measurements were carried out with the BET method. The obtained results are reported in
Table 4. The values of SSA scaled with the relevant IDR values, indicating that the observed IDR differences may be, at least in part, related to the different surface area stemming from the release of the single particles upon erosion of the compact. The largest surface area was presented by batch B3M2 which, however, was not the one with the smallest particle size distribution, suggesting that B3M2 could present a greater internal porosity of the particles compared to B4M2, which may justify the highest observed IDR.
Size and morphology variability of the α form is, however, not sufficient to explain the peculiar behavior reported in
Figure 2 and, in some instances, also the variability of the data in
Figure 3. Therefore, an in-depth investigation of the α -> β and amorphous -> β transitions in solution was carried out by coupling dissolution rate measurement by HPLC and solid-state monitoring with ATR-FT-IR. The FT-IR spectra of the three rifaximin forms are reported in
Figure S3; two spectral regions were of interest for discriminating the three rifaximin forms: between 1570 and 1600 cm
−1 and between 1220 and 1250 cm
−1. In the second region, the peaks appeared more resolved, thus, diagnostic peaks were selected at the following wavenumber: 1227 cm
−1 for the α form, 1241 and 1223 cm
−1 for the β form, and 1230 cm
−1 for the amorphous form. The dissolution test was carried out on 200 mg of rifaximin in 150 mL of phosphate buffer to improve the detectability. The obtained data are reported in
Figure 5 as both drug concentration profile in solution and height of the IR peak at 1241 cm
−1, as an indicator of the presence of β form in the suspended particles. In this experimental set-up, the α form (
Figure 5A) attained a higher maximum value of concentration compared to the one reported in
Figure 1A and reached the equilibrium concentration of the β form in about 1 h. The amorphous (
Figure 5C) form as well afforded a significantly higher metastable solubility value compared to that of
Figure 1B, while, despite the plateau reached by the IR signal relevant to the height of the 1241 cm
−1 peak, the transition to β form apparently was not completed in 75 min, as indicated by the still relatively high value of concentration (11.7 µg mL
−1). Nevertheless, for this form, as well as for the α form, the monitoring of the solid phase by IR spectroscopy, clearly indicated that the appearance of the diagnostic peak of the β form mirrored the kinetics of the dissolution curve. It is worth noting that the IR curve of the amorphous phase presented a larger initial lag time compared those of α and β forms. However, one can argue that the amount of rifaximin dissolved, especially in the case of the α form, does not seem to be sufficient to justify a complete (in the case of the α form) or almost complete (in the case of the amorphous form) solution mediated transition to β form as indicated by the values of rifaximin concentration recorded after 1 h.
Thus, the transition of the two metastable forms into the stable one was checked in a different experimental set-up, which implied the exposition of the three solid phases to room temperature and ambient humidity (64%), 70%, 75%, or 95% RH. The results relevant to the α form are reported in
Figure 6 as 3D IR spectra in the 1300–1180 cm
−1. It can be appreciated that the α form converted quite rapidly in all the tested humidity conditions. This conversion was practically complete after 15 min as indicated by disappearance of the peak at 1127 cm
−1 and the attainment of a plateau of the height of the two peaks at 1223 and 1241 cm
−1 (
Figure 7) The two profiles of the two curves were perfectly specular, suggesting that the conversion from one form to the other occurred without formation of any intermediate form.
The same experiments carried out on the amorphous form did not afford any significant change of the diagnostic peak at 1230 cm−1 indicating that apparently the amorphous -> β transition does not occur upon exposure to humidity or at least not within the experimental timeframe adopted.
Dynamic Vapor Sorption experiments were thus conducted to investigate in deeper detail the value of relative humidity at which the α -> β transition occurs.
Figure 8 reports the DVS profile at 25 °C of α (Panel A), and amorphous rifaximin (Panel B).
Amorphous rifaximin presented a quite uniform weight gain as a function of RH with a limited change in slope that increased above 60% RH; the decreasing curve was smooth and almost linear. X-ray diffraction on powder recovered upon exposure to 70% RH still presented the typical halo of the amorphous material without any crystalline peak (see
Supplementary Materials, Figure S5). Crystallization did not occur even after exposure to 95% R.H. for 20 days. Rifaximin α form afforded an ascending curve with a sharp slope change at 40% RH, while the descending curve decreased uniformly with a change in slope distributed between 40 and 20% RH. PXRD of the powder sample recovered upon stopping the measurement at RH > 40% clearly indicated the transformation in the β form (see
Supplementary material, Figure S6A). The process was reversible as indicated by the fact that the PXRD pattern of the powder recovered in the descending curve at 10% RH was back to that of the α form (see
Supplementary Materials, Figure S6B).
4. Discussion
Solubility is a general term for defining the maximum concentration that a compound (drug) can reach in a solvent at a given temperature. From the thermodynamical standpoint, it represents the equilibrium between the drug in the solid phase and the drug in solution. In general terms, therefore, the determination of the equilibrium solubility of metastable solid phased would be a paradox, being this, by definition, a non-equilibrium phase. In practice, the determination of pseudo-equilibrium solubility of metastable solid phases can be carried out provided that the energy barrier between the solid phase under investigation and its stable counterpart is sufficiently high to guarantee that the transition does not take place during the measurement time. In some cases, the solubility can be estimated by applying complex thermodynamical models [
15]. In other cases, such as in the case of rifaximin, the determination of the so-called kinetic solubility is commonly used. This type of measurement offers, however, only a partial picture of the real solubility value of the metastable form, since the attainment of the maximum concentration value and the rate of decrease are largely depending on the test conditions, such as the ratio between the amount of solid phase and the solvent volume, as well as the stirring rate, as demonstrated by the discrepancy between data of
Figure 1 and
Figure 5. Data reported in
Figure 1 clearly indicated that, irrespectively from the solid phase in the starting suspension, the concentration tended to a value of about 2.7 µg mL
−1, which corresponds to the concentration of the solution in equilibrium with the rifaximin stable solid phase. Rifaximin α and β forms afforded very low values of maximum concentration compared to the amorphous phase, with α slightly higher than β, confirming that these crystal phases can be considered practically insoluble. These data are in good agreement with the literature [
5,
7] that reported C
max in solution slightly higher for α relative to β. This is somehow an obvious observation considering that the solubility in water of hydrate forms is lower than that of the relevant form at a lower degree of hydration, due to the fact that the relative stability of two pseudo-polymorphic phases does not depend only on temperature and pressure, as it happens for anhydrous phases, but also on the activity of the water [
16]. The very low solubility of rifaximin α form implies a poor systemic absorption and is therefore strictly related to a favorable safety profile. In fact, pharmacokinetic studies both in dogs and humans have indicated that the absorption upon oral administration is less than 1% [
5,
11], while the fecal and urinary excretion represent 96.9 and 0.4%, respectively, of the administered dose [
17]. On the other hand, the local antimicrobial efficacy is not separated from the presence in the intestinal lumen of a minimal and transient concentration of rifaximin in solution, which is guaranteed by the dissolution of the α form. From this point of view, the ability of the α form with respect to the β to give rise to an initial slightly higher, though not insignificant
oversaturation is crucial.
Therefore, the capability of discriminating the dissolution behavior of the two forms represents a fundamental element in the formulation development and quality control of medicines containing rifaximin and intended to act locally in the intestine. The use of a compendial test such as the measurement of the IDR may be the solution to avoid the variability generated by the experimental conditions used in the kinetic solubility tests. However, data reported in
Figure 2 and
Table 1, as well as those in
Figure 3, demonstrate that the intrinsic dissolution rate of rifaximin form α may be impossible to measure in a reliable manner, even in controlled and compendial test conditions. These phenomena can be considered responsible of the variability observed in
Figure 3. The differences in morphology and particle size distribution shown in
Figure 4 can only partly justify such variability. The thermodynamically driven α -> β transformation can be considered the main cause of the peculiar and variable behavior reported in
Figure 2 and
Figure 3. The disintegration of the compact at the solid-liquid interface that was already observed by Viscomi and collaborators [
5] can be ascribed to the increase in the volume of the crystal cell due to the incorporation of water molecules stemming from the α -> β transition; in fact, as reported by Braga and collaborators, the volume of the cell can be estimated in 4445 and in 4580 Å
3 for the α and β form, respectively [
6]. The volume increase, in turn, determines the development of a disintegration force that breaks the compacts layers as already demonstrated for compacts of a poorly soluble compound such as nitrofurantoin [
18]. As a further element supporting this interpretation, the data reported in
Figure 2 shows a slightly positive deviation from linearity of the experimental points relevant to α form. In addition, for these points the recorded concentration values were lower than those of β form, although not in a statistically significant manner. According to USP, the positive deviation may be ascribed to a physical phenomenon such as disintegration, which was in fact observed. However, the compact disintegration led to an increase of the surface area exposed to the dissolution medium. Therefore, one should expect higher concentration values from α form relative to β form also considering the relative thermodynamic stability of the two crystalline forms. Again, referring to USP it must be remembered that for IDR experimental point also downward curvature of the dissolution profile may be observed because of a transformation of the solid form of the compact at the surface when a less thermodynamically stable crystalline form converts to a more stable form, such as in the case of the transition from an anhydrous form to a hydrate form. Therefore, one may speculate that the measured concentration values obtained from the intrinsic dissolution of the α form are the result of the superimposition of two phenomena, namely the disintegration, which leads to a progressive increase in the dissolution rate and the α -> β transition, which, on the contrary, reduces the dissolution rate over time. The result is that the data obtained could not be considered reliable and representative of the actual dissolution behaviour of the α form.
Real-time monitoring of solid-state during dissolution represents a tool to obtain a more accurate picture of the solution-mediated transition phenomena [
19]; in this respect, the contemporary measurement of the amount of dissolved rifaximin and the appearance of the β form in suspension reported in
Figure 5 and
Figure 6 clearly evidence the transition mediated by the dissolution. However, the process appears to be not completed, likely due in part to the limit of the experimental set-up, which can detect only solid particles near to the probe, and in part to the complex process of dissolution/reprecipitation in β form.
In addition, DVS data offer a new element on what was already known on the interval of relative humidity at which the α form can be considered stable. Previous reports [
5,
6] indicated the limit of stability of β form > 56% RH; here, we show that the conversion α -> β occurs just above 40% RH while higher water activity is required to trigger the transition of the amorphous form.
Obviously, the transition from a less stable anhydrous (or less hydrated) metastable phase to the more stable and more hydrated stable one is thermodynamically driven by the presence of water or of a certain amount of humidity. However, the data relevant to the transition occurring upon humidity exposure (
Figure 6 and
Figure 7) offer further interesting elements to explain the articulated transition process that leads to the β form of rifaximin starting from its metastable solid phases and can be interpreted based on the thermodynamic and kinetic aspects discussed by Carstensen regarding the rate of conversion in moist storage [
20]. In fact, it is well known that moisture is one of the main drivers for polymorphic conversion, and the mechanism behind this transition is the saturation of the moisture layer on the surface of the metastable solid phase which creates a supersaturated solution relative to the stable one that eventually nucleates leading the conversion. The conversion rate is a function of the nucleation rate, that according to the Classical Nucleation Theory [
21], is inversely related to the supersaturation ratio, which represents the quotient of the concentration in solution and the concentration at the equilibrium. This ratio is high for poorly soluble compounds and represents a strong driver for the conversion. This consideration allows explaining both the observed very high conversion rate of the α form as well as the low tendency of the more soluble amorphous phase to transform into β form.