- *Corresponding Author:
- Paloma Torre-Iglesias
Institute of Industrial Pharmacy, Faculty of Pharmacy, Complutense University, 28040 Madrid, Spain
|Date of Submission||26 November 2018|
|Date of Revision||11 April 2019|
|Date of Acceptance||22 July 2019|
|Indian J Pharm Sci 2019;81(5):824-833|
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In the present study, new indomethacin formulations were developed in order to enhance the indomethacin dissolution rate by preparing solid dispersions using the freeze-drying method. The degree of alterations in the crystallinity of indomethacin was assessed according to the preparation method and by the addition of low-substituted hydroxypropyl cellulose. Solid dispersions improved the dissolution rate of indomethacin. Combined use of scanning electron microscopy, X-ray powder diffraction and differential scanning calorimetry revealed the basis of the increase in dissolution rate of indomethacin when formulated as low-substituted hydroxypropyl cellulose solid dispersions.
Indomethacin, solid dispersions, low-substituted hydroxypropyl cellulose, freeze-drying
Indomethacin (IND) is a non-steroidal antiinflammatory agent with antiinflammatory, analgesic and antipyretic activity. Its pharmacological effect is thought to be mediated through the inhibition of the enzyme cyclooxygenase (COX), which is responsible for catalysing the rate-limiting step in prostaglandin synthesis[1,2]. However, IND is relatively versatile, and further studies have pointed to the potential use in cancer prevention therapy. Some studies have reported activity on melanoma and non-melanoma skin cancers in animal and in vitro studies. Clinical studies have found that topical or oral non-steroidal antiinflammatory drugs may lead to the regression of skin neoplasms. A recent work reported that prostaglandin E2 (PGE2) is secreted by resistant tumour cells and inhibition of PGE2 production by IND eliminated the macrophage suppression factor from the supernatant and sensitized resistant tumour cells to macrophage cytotoxicity. This study emphasized the important role of tumoursecreted PGE2 in escaping macrophage surveillance, and justifies the use of COX inhibitors as an adjuvant for improving tumour immunotherapy.
IND is classified as class II due to its poor solubility and high permeability. According to the Biopharmaceutics Classification System, a drug compound is poorly soluble if the highest dose strength is not soluble in 250 ml aqueous media over the pH range at 37°. Over 40 % of active pharmaceutical ingredients in development pipelines are poorly water-soluble drugs, which limit the formulation approaches and their clinical application and marketability due to their low dissolution and bioavailability.
Various formulation techniques have been developed to enhance the water solubility of IND, such as salt formation, microemulsions, nanosuspensions, polymeric micelles, nanoemulsions, microspheres, particle size reduction, cyclodextrins, prodrug formation, solid-lipid nanoparticle and solid dispersion, which is considered one of the most successful strategies to improve the dissolution profile of poorly soluble drugs. The term solid dispersion refers to the dispersion of one or more active ingredients in an inert carrier or matrix in the solid state. Low-substituted hydroxypropylcellulose (L-HPC) and sodium dodecyl sulphate (SDS) have been used by several researchers as carriers to obtain solid dispersions of poorly soluble drugs. L-HPC, as an inert carrier, has properties as a disintegrant, and also improves the wettability and dispersibility of solid dispersions, which may influence the drug’s dissolution behaviour[23-25]. SDS is an anionic surfactant that enhances drug wetting. The objective of the present study was to evaluate the feasibility of L-HPC in altering the crystalline property of IND and enhancing its dissolution rate by preparing solid dispersions using a freeze-drying method.
Materials and Methods
IND was supplied by Fagron Iberica SAU, Spain. SDS was supplied by Fischer Scientific, England. L-HPC was supplied by Shin-Etsu®, Tokyo, Japan. All other chemical reagents were of pharmaceutical grade or higher.
Preparation of formulations:
IND solid dispersions were prepared using the freezedrying method using L-HPC as a carrier. Solid dispersions were prepared with ratios of IND-SDSL- HPC, 1:0.06:0; 1:0.12:0; 1:0.12:5; 1:0.12:10 and 1:0.12:20 (w/w/w). The required amounts of IND and L-HPC were co-dissolved in 20 ml of solution with 0.125 mg/ml of SDS, except for SD-1:0.06:0, which was co-dissolved in 20 ml of solution with of 0.075 mg/ml of SDS, in a pH 8.4 buffer (prepared as described in the United States Pharmacopeia). The samples were then frozen at –40° for at least 24 h and freeze-dried using a Liolabar 7 (Telstat Inc., Madrid, Spain). They were loaded on the freeze-dryer shelf at 5°. After thermal equilibration, the shelf temperature was lowered to –40° and the product was maintained at this temperature for 2 h. The system was then evacuated to a pressure of 0.04 mbar and the shelf temperature was adjusted to –35° and maintained for 4 h, before being raised to –20° (2 h). After the freeze-drying process, each formulation was ground and sieved to obtain a particle size fraction of 0.125-0.500 mm; the vials were capped within 5 min and stored at room temperature (22-24°) in a desiccator containing silica gel. The physical mixture (PM) containing an INDSDS- L-HPC ratio of 1:0.12:20 (w/w/w) was prepared by manually mixing the appropriate amount of IND with particle size fractions of 0.125-0.500 mm and carrier in a ceramic bowl using a polymeric spatula. SD-0:0.12:0 was obtained by the same preparation method as for the solid dispersions but without IND.
Wetting property measurement:
The contact angles on the powder compacts were measured on a Dataphysics OCA contact angle system equipped with a conventional goniometer and a highperformance video camera controlled by the OCA20 software provided by the manufacturer. A syringe connected to a Teflon capillary with an inner diameter of approximately 2 mm was used to supply liquid from above to measure the drops. Briefly, 200 mg of sample was weighed and compressed using a circular stainlesssteel punch and die assembly (diameter 1 cm) in an infrared tablet press (dwell time of 30 s and pressure of 8 tons). A drop of deionized water (2.5 μl) was placed on the compressed plate and the measurement of the contact angle was initiated in the dynamic mode. The camera captures images with a frame size of 640×480 pixels at a maximum rate of 60 frames per second. The images are analysed using the axisymmetric drop shape analysis profile (ADSA-P) to obtain the contact length and height of the droplet. Finally, these parameters are used to estimate the contact angle of the droplet. At least two measurements were made per sample to ensure reproducibility. All the measurements were made at room temperature.
In vitro dissolution studies:
Dissolution assays of IND powder, SD-1:0.06:0, SD- 1:0.12:0, SD-1:0.12:5, SD-1:0.12:10, SD-1:0.12:20 and PM-1:0.12:20 were carried out using the DT80 dissolution system (Erweka GMBH, Germany). Initially, the dissolution rate of different formulations was studied in simulated gastric fluid without enzyme (0.1 N HCl), and the dissolution data showed low drug release (less than 12.7 %). Other authors have reported that less than 6.2 % of IND was dissolved at pH 1.2, hence phosphate buffer of pH 6.8 was used as a dissolution medium in this method. Other authors have achieved satisfactory results at a similar pH. However, at pH 6.8 the drug dissolves so rapidly that it is impossible to observe differences between the dissolution profiles of the various solid dispersions. Dissolution assays were therefore also performed at pH 4.5 in order to obtain slower dissolution profiles and allow the observation of differences in the dissolution rates between the different formulations. A USP apparatus 2 (paddle) was set up with a rotational speed of 50 rpm and 900 ml of dissolution medium. The temperature was maintained at 37.0±0.1° throughout the dissolution study. An amount of solid dispersion equivalent to 10 mg of IND was introduced into the vessel. At predetermined times, a 5 ml sample was withdrawn and filtered through a 0.45 μm filter (Minisart®). The quantity of IND was determined at 266 nm using a UV/Vis 1700 spectrophotometer (Shimadzu, Japan).
As the carrier L-HPC, SDS, and the solvent components (NaOH, H3BO3 and KCl) do not absorb UV, these do not interfere at the chosen wavelength. The cumulative amount of IND released from the system was determined from the following calibration curves at pH 1.2, 6.8 and 4.5, respectively, y=0.0517x+0.0068 (r2=0.9999), y=0.0526x+0.0166 (r2=0.9993) and y=0.0587x+0.0027 (r2=0.9995). The results obtained from the dissolution assays of different formulations were analysed using one-way analysis of variance (ANOVA), followed by Fisher’s least statistical difference for multiple comparisons. A p-value of less than 0.05 was considered significant.
Scanning electron microscopy (SEM) studies:
IND powder, SD-0:0.12:0, SD-1:0.12:0, SD-1:0.12:5, SD-1:0.12:10, SD-1:0.12:20, PM-1:0.12:20 and L-HPC were placed on an aluminium sample mount. After coating with a thin layer of gold-palladium, the samples were analysed with a Jeol® 6400 SEM. All the micrographs were produced by secondary electron imaging used for surface morphology identification at magnifications of 500× and an accelerating voltage of 20 kV.
X-ray powder diffraction (XRPD): crystal structure characterization:
The structure of the material was characterized by means of conventional θ-2θ powder X-ray diffraction with Cu-kα radiation (Philips X’Pert-MPD) in several of the samples (IND powder, SD-1:0.12:0, SD- 1:0.12:10, SD-1:0.12:20, PM-1:0.12:20 and L-HPC) in the study at room temperature. The 5-35° 2θ range was scanned at a 0.04° step size and 1 s time per step in all cases. Approximately 20 mg of sample was dispersed on a zero-background Si sample holder, taking care was not to introduce a preferential orientation of the crystals.
Differential scanning calorimetry (DSC):
The thermal behaviour of the pure IND; SD-1:0.12:0, SD-1:0.12:10, SD-1:0.12:20, PM-1:0.12:20 and L-HPC was characterized by means of DSC analysis. DSC thermograms were obtained with an automatic thermal analyser system (Mettler Toledo TC15, TA controller). Temperature was calibrated using the Indium Calibration Reference Standard (transition point: 156.60°). Samples of about 2 mg were accurately weighed into aluminium pans, then hermetically sealed with aluminium lids and heated from 30 to 220° at a heating rate of 10°/min under constant purging of dry nitrogen for 20 ml/min. An empty pan, sealed in the same way as the sample, was used as a reference.
Results and Discussion
The deionized water contact angle was measured on SD tablets (SD-1:0.12:0; SD-1:0.12:5 and SD-1:0.12:20), a PM tablet (PM-1:0.12:20) and a tablet of compacted pure drug. Surface roughness and potential polymer swelling are known to potentially influence wetting behaviour. As can be seen in fig. 1, the water contact angle on the tablets gradually decreased between 1 s and 4 s. The IND tablet had the highest water contact angle (107±2° after 1 s), which was attributed to the stronger hydrophobicity of IND; while the PM produced much smaller contact angle values (39±2° after 1 s), probably due to its composition L-HPC and SDS, which increases its wettability. The solid dispersion SD-1:0.12:20 had the smallest contact angle (15±2° after 1 s), much less than the PM with the same IND:L-HPC ratio, which may be due to an increase in the wettability of the formulation after the lyophilization process. It was also observed that the solid dispersion without carrier, SD-1:0.12:0, has a contact angle of over SD-1: 0.12:5; this difference becomes greater as the L-HPC loading in the formulation increases (SD-1: 0.12:20), which may be due to the hydrophilicity of L-HPC. In view of these results, it can be concluded that L-HPC has a significant influence on the wettability of the samples.
The use of acidic medium (pH 1.2), and two intestinal media (pH 4.5 and pH 6.8, respectively) is proposed to evaluate the differences in the dissolution rate of various IND formulations. These media have been used by different authors to compare various drug formulations that present substantial changes in solubility during their gastro-intestinal transit[29-31].
The dissolution data showed low release in acidic medium (pH 1.2); less than 12.84±0.48 % of IND was dissolved from the pure drug at 24 h and only 5.22± 0.71 % at 120 min. PM-1:0.12:20 had a similar dissolution profile, and no statistically significant differences were found between the two (fig. 2a). The addition of SDS to solid dispersions produced an increase in IND dissolution profiles, so SD-1:0.06:0 and SD-1:0.12:0 showed 28.76±1.18 % and 37.80± 1.10 % of dissolved IND respectively at 120 min. This significant increase in the dissolution rate of the solid dispersions with a higher quantity of SDS could be attributed to the presence of SDS on the surface of the IND particles, as this ratio (IND:SDS 1:0.12) is required to produce a quicker interaction between IND and the dissolution medium. The IND dissolution rate was significantly improved in all the solid dispersions at this pH; the amount of IND dissolved (SD-1:0.12:0, SD-1:0.12:5, SD-1:0.12:10 and SD- 1:0.12:20) was between 37.80±1.10 and 41.79± 1.72 % at 120 min, and between 41.67±2.88 and 44.67± 2.68 % at 24 h, respectively. No significant differences were observed among the four solid dispersions at these times. However, after short time periods (15 min) in this acidic medium, statistically significant differences were observed between solid dispersions with higher (SD-1:0.12:10, SD-1:0.12:20) and lower (SD-1:0.12:0, SD-1:0.12:5) L-HPC loadings. These low dissolution percentages in acidic medium had previously been observed by other authors, who reported that less than 6.2 % of IND was dissolved at 24 h.
Figure 2: Release profiles of IND formulations at 37° and at different pH levels
Release profiles of IND formulations at 37° at pH levels of a. 1.2, b. 6.8, and c 4.5 IND powder (▬▲▬); SD-1:0.06:0 (▬◊▬); SD-1:0.12:0 (▬○▬); SD-1:0.12:5 (▬●▬); SD-1:0.12:10 (▬×▬); SD-1:0.12:20 (▬■▬) and PM-1:0.12:20 (▬▬)
The dissolution profiles of IND powder, the PM- 1:0.12:20, and the different solid dispersions at pH 6.8 (intestinal medium) are shown in fig. 2b. IND alone and PM-1:0.12:20 had the lowest dissolution rates. The amounts of IND dissolved from the drug powder compared to the amount released from PM-1:0.12:20 at 5 (25.23±3.05 and 49.75±0.80 % respectively) and at 120 min (76.56±5.60 and 93.90±5.53 %) were found to be significantly different. The presence of SDS in the PM (PM-1:0.12:20) can be associated to a substantial improvement in the dissolution properties in comparison to the pure drug, and could also be seen in the percentage of IND dissolved from SD- 1:0.06:0 and SD-1:0.12:0. There was a significant difference between both formulations at 120 min (83.33±1.16 and 90.23±1.28 %, respectively), while both finally attained 100 % of drug dissolved at 24 h. SD-1:0.12:0 also showed a high initial burst effect at 5 min (90.55±1.31 %), which is similar to the amount of IND dissolved from the PM-1:0.12:20 at 120 min (93.90±5.53%). This increase in the dissolution rate after the lyophilization process could be related to the increase in wettability observed in the contact angle measurements. The presence of higher amounts of L-HPC induces an increase in the quantity of IND dissolved from SD-1:0.12:10 and SD-1:0.12:20 at 5 min (95.21±1.16 and 93.83±2.40 %, respectively) in comparison to SD-1:0.12:0 (90.55±1.31 %). Increase in the amount of IND dissolved from the solid dispersions containing higher amounts of hydrophilic carrier (L-HPC) could be attributed to a lowering of the surface tension of the medium by L-HPC, resulting in improved wetting of the hydrophobic drug surface[32,33], according to the results obtained in the wettability measurements. At this pH (6.8), all solid dispersions showed higher dissolution rates, so when using this medium, no significant differences were seen between the dissolution profiles for the various solid dispersions. Other authors reported similar results using a buffer of pH 7.4, and obtained 72.5±1.0 % of IND dissolved from their solid dispersions at 90 min. The use of buffer media with a pH close to the IND pKa value (4.5) leads to lower IND solubility. Dissolution assays were therefore done at pH 4.5 (fig. 2c) in order to obtain slower dissolution profiles and allow the observation of differences in the dissolution rates among the various formulations.
Fig. 2c shows the dissolution profiles of IND powder, the PM 1:20 (PM-1:0.12:20) and the various solid dispersions (SD-1:0.12:0, SD-1:0.12:5, SD-1:0.12:10, and SD-1:0.12:20) at pH 4.5. IND powder and PM- 1:0.12:20 had the poorest dissolution rates in this medium. 7.06±0.46 and 20.26±0.80 % of IND were dissolved from the pure drug and from PM-1:0.12:20 respectively at 120 min, and 23.07±2.33 and 29.88± 1.25 % respectively at 24 h. As occurred at pH 6.8, the PM showed a statistically significant improvement in the dissolution properties compared to the pure drug at 120 min. This high amount of drug dissolved from PM- 1:0.12:20 could be due to the presence of SDS in this formulation, and to the wetting properties of LHPC, as seen in the wettability measurements.
IND amount dissolved from SD-1:0.12:0 at 120 min was 42.84±2.59 %. As occurred at pH 6.8, SD-1:0.12:0 significantly improves the dissolution properties of the IND powder and PM-1:0.12:20. All the solid dispersions had substantially better dissolution profiles than PM-1:0.12:20, the same as at pH 6.8. Also similar to the results at pH 6.8, at pH 4.5 29.01±0.43 % of the drug was dissolved from SD-1:0.06:0 after 24 h and 41.67±2.88 % of IND from SD-1:0.12:0 after the same amount of time. At this pH there is therefore a statistically significant increase in the amount of IND dissolved from solid dispersions with a higher quantity of SDS. Formulations with higher L-HPC loadings (SD-1:0.12:10 and SD-1:0.12:20) showed a statistically significant increase in their dissolution profile compared to formulations with lower L-HPC loadings. These results suggested that L-HPC itself might act as a weak solubilizer in these formulations, and might prevent drug aggregation[35,36]. These results provided evidence that all the solid dispersions were superior in achieving 100 % dissolution more rapidly than the PM, i.e., over 40 % of IND dissolved in the 1:0.12:10 and 1:0.12:20 solid dispersions at 120 min.
The addition of small quantities of L-HPC to the solid dispersions did not produce any significant increments in the percentages of drug dissolved at 120 min (42.84±2.59 % from SD-1:0.12:0 and 42.87±3.56 % from SD-1:0.12:5, respectively). These small amounts of L-HPC might not prevent the agglomeration of IND particles during the dissolution process. However, solid dispersions with a higher quantity of L-HPC (SD- 1:0.12:10 and SD-1:0.12:20) increased wettability and favour a faster dissolution at the initial dissolution times, as seen in the contact angle measurements. Thus, at 5 min the amounts of IND dissolved from SD-1:0.12:5, SD-1:0.12:10 and SD-1:0.12:20 were 32.47±2.95, 45.69±4.26 and 54.01±2.26 %, respectively. Statistically significant differences observed among the different solid dispersions at this pH could be attributed to the poor solubility of the drug in this medium, possibly because IND solubility is pH-dependent, at a low pH (1.2) it has poor solubility properties, while its solubility is greatly increased at a high pH (6.8). However, the use of L-HPC in solid dispersions would be justified at a duodenal pH of 4.5, critical for IND, since it significantly increases the dissolution rate of formulations with high L-HPC loadings. These results also allow us to consider pH 4.5 as a discriminating medium that can be used to distinguish the dissolution profiles of our solid dispersions with different amounts of L-HPC. The presence of L-HPC reduced the surface tension of the medium, resulting in better wetting of the hydrophobic drug surface[32,33], according to the contact angle measurements.
SEM was used to clarify the surface and shape characteristics of different samples (IND powder, SD- 0:0.12:0, SD-1:0.12:0, SD-1:0.12:5, SD-1:0.12:10, SD- 1:0.12:20, PM-1:0.12:20 and L-HPC). The IND powder presented heterogeneous crystals of different sizes with edges (fig. 3a). The original morphology of all the components disappeared in the solid dispersions, while the SD-1:0.12:0 observed at the same magnification (500×) (fig. 3b) had fine crystals covering their surface, possibly generated during the lyophilization process. SD-0:0.12:0 also presented acicular crystals that can be attributed to SDS and phosphate buffer components (fig. 3c). In a comparison of the PM-1:0.12:20 and the solid dispersion SD-1:0.12:20 (fig. 3d) the smooth particles of L-HPC (fig. 3e) could easily be distinguished from the heterogeneous crystals with edges, possibly related to IND, in the PM, but not in the solid dispersion. In contrast, solid dispersions with different L-HPC loadings (SD-1:0.12:5, SD-1:0.12:10 and SD-1:0.12:20) resembled a matrix (figs. 3f, g and h, respectively). In these L-HPC solid dispersions, the higher the loading of L-HPC, the lower the porosity of the matrix. These results demonstrated that IND was dispersed homogeneously in the L-HPC polymer matrix of the solid dispersions, where it could possibly exist in an amorphous form.
Fig. 4 shows the XRPD patterns of the pure IND powder, SD-1:0.12:0, SD-1:0.12:10, SD-1:0.12:20, PM-1:0.12:20, PM-1:0.12:5 and L-HPC. IND powder has low-intensity values in its diffraction peaks, typical of a substance with low crystallinity (see fig. 4). The crystal structure of the pure drug with low intensity peaks at angles of 11.6°, 17.2°, 19.5°, 21.6° and 29.3° (2θ) almost matches polymorph γ, as reported by other authors. This low drug crystallinity may be related to the heterogeneous shape of its crystals with edges and different sizes observed in SEM studies (fig. 3).
HPC is a semi-crystalline polymer with amorphous and crystalline domains[20,25]. The XRPD pattern of L-HPC (fig. 4) exhibited a characteristic semi-crystalline halo diffraction pattern with low intensity values similar to pure IND between 19.8° and 28.4° (2θ), and a majority diffraction intensity at 20.1° (2θ). Only one formulation excipient, boric acid (used in the 8.4 buffer), had a crystalline structure, with diffraction peaks at angles of 14.7°, 27.7°, 32.29° and 40.3° (2θ). In both PMs (PM-1:0.12:5 and PM-1:0.12:20) the diffraction peaks of the IND can still be seen at diffraction angles of 19.5° and 21.6° (2θ) (figs. 4a and b). The intensity of the peaks decreases with increasing amounts of L-HPC in the PM (PM-1: 0.12: 20). A reduction in drug crystallinity of nearly 55 % could be seen in PM-1: 0.12:5, and IND crystallinity declined by approximately 88 % in the PM with the highest amount of LHPC (PM-1:0.12:20). This result can be attributed to the dilution effect with higher amounts of carrier. As expected, the PM-1: 0.12: 20 showed higher intensity values for the semi-crystalline halo of the carrier (between 19.8° and 28.4° (2θ)). The high L-HPC loadings in this PM justified the presence of this halo (fig. 4b). Moreover, SD-1:0.12:0 (fig. 4) showed practically the same peaks at 15.9°, 28.3°, 32.3° and 40.4° (2θ), related to the boric acid, component of pH 8.4 buffer. The diffraction peaks of the IND could not be seen in this sample. The absence of crystallinity in the IND in this formulation could be caused by the freeze-drying process. This decrease in crystallinity after the freeze-drying process could be related to improvements in the dissolution profiles, as observed in the dissolution assays. Solid dispersions with different proportions of L-HPC (fig. 4) present a similar result to SD-1:0.12:0, and do not show any of the peaks attributed to IND.
Both formulations, SD-1:0.12:10 and SD-1:0.12:20, presented a semi-crystalline halo diffraction pattern from L-HPC, with lower intensities at 20.1° (2θ). The lower crystallinity in the halo attributed to the carrier for the solid dispersions may confirm that the freeze-drying process decreases the crystallinity in these formulations. The inferior sensitivity of the XRPD method also makes it difficult to determine the crystallinity peaks of samples with low-intensity values such as IND. Similar results were obtained by other authors. DSC studies will be necessary to complete these studies on the decline in crystallinity.
Fig. 5 shows thermograms for pure IND; SD-1:0.12:0, SD-1:0.12:10, SD-1:0.12:20, PM-1:0.12:20 and L-HPC. IND powder (fig. 5a) has an endothermic peak at 160.99° with low crystallinity (116.05 J/g). Fig. 5 shows a small endothermic peak for L-HPC at 158.31° (onset 157.14°); the low enthalpy of fusion of this peak (52.34 mJ/g) was related to its semicrystalline structure. Among the other formulation excipients, only boric acid, used in the pH 8.4 buffer, had a crystalline structure with two endothermic peaks at 167.22° (minor) and 170.31° (major), in addition to characteristic changes in the baseline at higher temperatures; while SDS and the other excipients had no endothermic peaks characteristic of crystalline substances.
Two thermal events occur in PM-1: 0.12: 20 (fig. 5b), showing a minor peak at 144.84° and a major peak at 168.22°. The IND melting peak in the curve for this PM underwent a shift to a lower temperature (144.84°), while the melting peak for L-HPC and boric acid shifted to a higher temperature (168.22°). This dip in the IND melting point is a common effect in multicomponent mixtures and is considered a positive interaction with the L-HPC and other crystalline formulation excipients[44-46]. The sharper peak at 168.22° observed in PM-1:0.12:20 can be attributed to a combination of two of the components in the formulation: the first is L-HPC, which may have shifted to higher temperatures (from 158.31° to 168.22°); and the second is boric acid, a highly crystalline substance used in the buffer. The presence of high amounts of L-HPC produces a single endothermic peak at 168° where boric acid is included. A similar process of inclusion in a single peak has been observed by different authors.
In contrast, in the SD-1:0.12:0 thermogram (fig 5c), only a slight amorphous halo was observed between 154-166°, which may be related to a decrease in IND crystallinity, possibly due to the lyophilization process. No peaks attributed to buffer components were observed in this lyophilized sample. IND:SDS:L-HPC solid dispersions (SD-1:0.12:10 and SD-1:0.12:20) showed both an incipient decrease to lower temperatures and also a widening in the amorphous halo (between 126- 162° for SD-1:0.12:10 and 122-158° for SD-1:0.12:20, respectively, figs. 5d and e). The onset of the amorphous halo of the IND decreases as the proportion of L-HPC in the sample increases. These results confirm the existence of a positive interaction between the IND and the L-HPC excipient in lyophilized samples.
The amorphous character of IND in the solid dispersions observed in the DSC studies confirmed the hypothesis that amorphous species of IND are being formed in the XRPD studies. Solid dispersions could modify drug crystallinity and represent a suitable modification for improving its dissolution profiles. These results were also confirmed in the dissolution assays, where improvements were observed in the dissolution profiles of the various solid dispersions compared to the IND powder and PM-1:0.12:20. Amorphous substances generally have a higher solubility and dissolution rate than their corresponding thermodynamically stable crystalline forms, as their internal bonding forces are weak.
In summary, IND:SDS:L-HPC solid dispersions improve the dissolution rate of IND. Wettability measurements, SEM, XRPD and DSC techniques were used to study the reasons for this, and suggest that an increase in the IND dissolution rate is caused by a reduction in drug crystallinity related to the freezedrying process and the amount of L-HPC added to the formulations. The addition of a hydrophilic carrier altered the surface morphology of the formulations and also increased their wetting effect. The formation of a less porous L-HPC matrix could be observed by SEM, as the proportion of polymer increased. From all of the above, it can be deduced that all these factors could cause an important increase in the IND dissolution rate.
The authors would like to thank the Department of Biomedical Sciences, Alcalá University, Spain, and the Department of Physical Chemistry, Faculty of Chemical Sciences, Madrid Complutense University, Spain for their support.
Conflict of interest:
No conflict of interest between any of the authors.
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