*Corresponding Author:
R. P. Swain
Drug Development and Analysis Laboratory, School of Pharmaceutical Sciences, Siksha O Anusandhan University, Bhubaneswar-751003, India
E-mail: ranjit.prasad797@gmail.com
Date of Submission 24 March 2018
Date of Revision 22 September 2018
Date of Acceptance 15 February 2019
Indian J Pharm Sci 2019;81(2):317-325  

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Poor aqueous solubility and slow dissolution rate adversely affects bioavailability of pioglitazone hydrochloride. This study was undertaken to improve dissolution and bioavailability of pioglitazone hydrochloride through preparation of stable solid dispersions by melting and solvent evaporation method using Solutol HS 15. Solubility of pioglitazone hydrochloride was enhanced by 9 to 49 fold as the drug-carrier ratio was increased in solid dispersions as compared to pure drug. Furthermore, compared to pure drug or physical mixture, solid dispersions significantly improved the dissolution rate and the extent of drug release. Solid dispersions at 1:7 drug:solutol HS 15 weight ratio showed complete and rapid drug release within 15 min at pH 1.2. The Fourier-transform infrared spectrum revealed the chemical compatibility with solutol HS 15. Differential scanning calorimetry and X-ray powder diffraction pattern revealed a change in crystallinity to amorphous state that supported the enhancement of solubility of pioglitazone hydrochloride with Solutol HS 15. In vivo test showed that Solutol HS 15-based solid dispersions showed higher AUC0-t and Cmax, which was ~4 times higher than that of pure pioglitazone (p<0.05) implying solid dispersions could be effective in increasing the bioavailability. In conclusion, solid dispersions with Solutol HS 15 prepared using solvent evaporation method appeared to be a promising technique to improve the dissolution, bioavailability and stability of pioglitazone hydrochloride.


Pioglitazone HCl, Solutol HS 15, pharmacokinetic, recrystallization, solid dispersion

Oral route is the most preferred route of administration for majority of the drugs [1]. Unfortunately many drug candidates suffer from poor pharmacokinetics and bioavailability, following oral delivery due to poor solubility [2]. Biopharmaceutics classification system (BCS) class II drugs often exhibit dissolution ratelimited absorption leading to low and variable oral bioavailability. There is a need to enhance the solubility without compromising for stability and activity of the drugs.

Pioglitazone hydrochloride (HCl), a BCS class II drug is used as a potent and highly selective agonist for peroxisome proliferator-activated receptor gamma in type II diabetes [3-5]. The poor aqueous solubility and dissolution rate of Pioglitazone HC is a major hurdle in its bioavailability and therapeutic application [6,7]. To enhance its solubility, approaches including inclusion complexation [8-10], micellar solubilization [11], co-solvent solubilisation [12], solid dispersion [13-15] (SD) and spray drying [16] have been evaluated. High thermodynamic stability of the first and second generation polymeric carriers lowers the dissolution rate, recrystallization and precipitation, which were the limitations of the SDs. Amorphous SDs is a promising strategy to increase the bioavailability of poorly soluble drugs by improving their rate and extent of dissolution [17]. However the earlier reported SDs of pioglitazone had stability issues due to precipitation and recrystallization, which negatively impacted solubility leading to inadequate dissolution. Besides, there are not enough reports to correlate the in vitro dissolution to in vivo bioavailability. Hence, there is an unmet need to properly adopt the SDs to improve stability, solubility and bioavailability of Pioglitazone HCl. Amorphous SDs with classical surfactant carriers have attracted attention of many researchers. However, in many instances, the amorphous form is thermodynamically unstable and tends to crystallize during storage leading to decreased solubility [18]. Thus careful choice of carriers and methods of preparation of SDs are critical for enhancing the solubility of Pioglitazone HCl while overcoming the limitations of previous approaches. Solutol HS 15 is a third generation surfactant carrier used to improve the solubility and bioavailability [18,19]. Thus its use was optimised to achieve the desired attributes. Surface active carriers (non-polymeric) like Cremophor RH 40, Poloxamers were proposed to influence the rate and extent of drug absorption by altering the thermodynamic activity, solubility, diffusion, disintegration and dissolution rate of a drug. Furthermore, surface active carriers can exert direct effects on biological membranes leading to modulation of drug transport across the membrane [20]. Melting (MM) and solvent evaporation (SM) methods are the most scalable industrial technologies for manufacture of SDs. Homogeneous mixing of the drug and carrier in molten state without any solvent is the advantage of MM [21,22]. Prevention of decomposition of the drug and carrier at high temperature and molecular mixing in solution stage are the advantages of SM [21,22]. The influence of carriers on crystallization behaviour, impact on in vitro dissolution and in vivo performance has not been investigated to the best of our knowledge. Therefore, this study was aimed to evaluate the prepared SDs using a surfactant carrier and Pioglitazone HCl. The prepared formulations were thoroughly evaluated to understand the impact on in vitro and in vivo performance to justify their application in oral drug delivery.

Materials and Methods

Pioglitazone HCl was obtained as a gift sample from Aurobindo Pharma Ltd. (Hyderabad, India). Cremophor RH40 (polyethoxylated castor oil), Solutol HS 15 (macrogol 15 hydroxystearate), Poloxamer 188, Poloxamer 407, hydroxypropyl methylcellulose (HPMC), polyethylene glycol (PEG) 4000, polyvinylpyrrolidone (PVP) K-15 were purchased from Yarrow Chem Products, Mumbai, India. Ammonium acetate was purchased from Merck Specialities Pvt., Ltd. (Mumbai, India). Acetonitrile was purchased from the Thermo Fisher Scientific India Pvt., Ltd. (Mumbai, India). All other chemicals and reagents were purchased from Lotus Enterprises, Andhra Pradesh, India.

SDs preparation:

Initially SDs were prepared using SM with HPMC, PEG 4000, PVP K-15, Cremophor RH 40, Solutol HS 15, Poloxamer 188 and 407 carriers in 1:5 weight ratio (drug:polymer). The aqueous solubility was determined for screening of carrier. After screening, SDs of Pioglitazone HCl were formulated with Solutol HS 15 in various drug/polymer weight ratios (1:1, 1:3, 1:5, 1:7 and 1:9) by physical mixing (PM), MM and SM. Pioglitazone HCl and Solutol HS 15 were mixed in a glass mortar for 10 min to obtain PMs. In MM, carrier was heated at 10° above the melting point of the carrier. Drug was dispersed in the melted carrier with continuous agitation. The blend mass was immediately transferred in crushed ice bath, so that the crystalline drug will convert amorphous. SDs were also developed by SM. Ethanol (10 ml) was used to solubilise the Pioglitazone HCl and carrier individually by continuous stirring with a glass rod at room temperature and mixed together. Solvent was removed under reduced pressure using a rotary evaporator (model R-215, Buchi, Switzerland) and kept at 40° in hot air oven (KOMS- 3, KEMI, India) for complete evaporation of ethanol. The products were scraped, pulverized gently with a mortar and pestle and sieved through 40# mesh sieve. The samples were stored in screw cap glass vials and kept in a desiccator until further uses [17, 21].

Solubility test:

Sample amount equivalent to 10 mg of Pioglitazone HCl was added in 10 ml of distilled water. The samples were sealed in triplicate and shaken for 48 h at 37±0.5° in a thermostatically controlled horizontal shaker (model: RSB12, Remi Elektrotechnik Ltd., India). The resulting samples were filtered through a Millipore filter (pore size 0.45 μm), suitably diluted and assayed by following a valid reversed-phase high pressure liquid chromatography (HPLC, Agilent 1220 infinity series, software: Ezichrome elite, Agilent Technologies, USA) method [23].

In vitro dissolution study:

In vitro dissolution studies were performed in triplicate using the USP II dissolution test apparatus (Electrolab, Mumbai, Model no. TDT-08L) maintained at temperature of 37±0.5° at 75 rpm speed in 900 ml of 0.1 N HCl. Pure drug and SD containing an equivalent to 15 mg of the Pioglitazone HCl were introduced into dissolution medium. At the predetermined time (5, 10, 15, 30, 45, 60 min) intervals, 5 ml samples were withdrawn, filtered through membrane filter (0.45 μm, Millipore). Immediately 5 ml of fresh medium maintained at 37±0.5° was replaced to maintain its constant volume. The samples were suitably diluted wherever necessary and analysed for Pioglitazone HCl using HPLC method.

Fourier-transform infrared spectroscopy (FTIR):

FTIR spectra can be used to detect drug-polymer interactions by following the shift in vibrational or stretching bands of key functional groups. FTIR spectra were obtained by using diamond ATR spectrophotometer (Model: Cary 630, Agilent technologies, Germany). All the samples (2-5 mg) were placed in diamond ATR sample holder and scanned over a wave number range of 500-4000 cm-1.

Differential scanning calorimetry (DSC):

DSC was performed for the pure drug pioglitazone, pure polymers, PMs and SDs using a DSC apparatus (Pyris Diamond thermo gravimetry/differential thermal analysis, PerkinElmer, Singapore). The powdered sample (3-5 mg) was hermetically sealed in aluminium pans and lids were crimped using a TA crimper and heated at a constant rate of 10°/min over a temperature range of 30-250°, using nitrogen as purge gas at a flow rate of 150 ml/min. Platinum crucible was used with alpha alumina powder as reference.

X-ray diffraction (XRD):

XRD of pure drug, carrier and formulations were performed at room temperature with an X-ray diffractometer (Ultima-III, Rigaku, Japan). Monochromatic Cu Kα radiation (λ=1.5418 Ǻ) was obtained with a Ni-filtration and a system of diverging and receiving slides of 0.5° and 0.1 mm, respectively. The diffraction pattern was measured with a voltage of 40 kV and current of 30 mA over a 2θ range of 0-55° using a step size of 0.02° at a scan speed of 1 s/step.

Stability test:

Stability testing (25° and 60 % RH) of SDs (SM) were performed as per the ICH guidelines in the stability chamber (Remi Instruments, India) [24]. Samples were analysed periodically for 3 mo and subjected to solubility and XRD analysis to explore the changes in the system.

Quantification/determination of Pioglitazone HCl:

A valid reversed-phase HPLC method was followed for quantification of Pioglitazone HCl for in vitro studies [25]. For in vivo analysis the same method was modified and verified before quantification of Pioglitazone HCl from plasma. A reversed-phase Agilent-TC- C18, (250×4.6; 5 μ) column was used for separation. The mobile phase was 0.1 M ammonium acetate (pH 4.0, adjusted with acetic acid):acetonitrile (70:30, v/v). The effluent was observed at 254 nm after a retention time of 3 min with a flow rate of 1.0 ml/min. The assay was linear for Pioglitazone HCl in the concentration range of 0.5- 80 μg/ml and the limit of detection was 0.05 μg.

In vivo studies:

The procedure for the in vivo study was approved by the Institutional Animal Ethical Committee (Approval No: 02/IAEC/CIPS/2016-17) and appropriate guidelines for the use of animals were followed during the study. The objective of this study was to characterize the bioavailability of Pioglitazone HCl from optimized SD as compared with the pure drug. Six male New Zealand rabbits (body weight 1.83±0.08 kg) divided randomly into two groups (n=3), were fasted for 18 h prior to the experiments and given free access to the water. Pure Pioglitazone HCl (2.5 mg/ml suspended in 0.5 % methyl-cellulose prepared in water for injection) and SD of Pioglitazone HCl:Solutol HS 15 prepared by SM at a dose equivalent to 2.5 mg/kg of Pioglitazone HCl were administered orally [26]. Blood samples (1 ml) were collected from marginal ear vein at time points of 0.5, 1, 2, 4, 8, 12 and 24 h post dose and transferred to ethylenediaminetetraacetic acid (EDTA)-coated tubes to prevent coagulation. Then blood samples were centrifuged at 5000 rpm for 10 min and the obtained plasma samples were stored at –80° until analysis.

Preparation of sample:

Frozen plasma samples were thawed at ambient temperature prior to extraction. In polypropylene tubes 0.1 ml of sample and 3 ml of tetra butyl methyl ether was added for extraction. Then, the mixture was vortexed for 15 min and centrifuged at 8000 rpm for 5 min. The supernate was transferred to new polypropylene tubes and dried at 70° for 20 min in a turbo evaporator (TurboVap LV, Biotage, NC USA). The residues were reconstituted with mobile phase and injected (10 μl) into HPLC for analysis by a validated reversed-phase HPLC method.

Pharmacokinetic analysis:

The primary pharmacokinetic parameters were performed by non-compartmental analysis. Maximum plasma concentration (Cmax), time to reach the peak plasma concentration (Tmax) and area under the plasma concentration-time curve (AUC0-t) were obtained from plasma data analysis using the software program PKSolver [27].

Statistical analysis:

All the mean values were presented with their standard deviations (mean±SD). Statistically significant difference was determined using t-test at 0. 05 level of significance and p value <0.05 was considered statistically significant [28].

Results and Discussion

SDs of Pioglitazone HCl was prepared by SM using non-polymeric (Poloxamers, Solutol HS 15, Cremophor RH 40) and polymeric carriers (HPMC, PEG 4000, Povidone K-15) at the drug-carrier ratio of 1:5 and then their effectiveness in improving the solubility of Pioglitazone HCl was evaluated (Table 1). Solutol HS 15 was the most effective to increase the solubility of Pioglitazone HCl by approximately 33 fold whereas Cremophor RH 40 increased approximately 27 folds. Suitability of Solutol HS 15 has earlier been demonstrated with its physiological compatibility and safety [29]. Entrapment of drugs in the loose and porous spherical micelles has been the major contributor to its high solubilisation capacity. In contrast to this, HPMC was least effective polymer for improving solubility of Pioglitazone HCl (Table 1). Poloxamer 188 and 407 due to surface active nature of carrier and swelling effect in water [30] showed ~17 fold increase in solubility of Pioglitazone HCl. Appreciable enhancement of solubility was also observed with PEG 4000 and povidone K-15. Nevertheless, Solutol HS 15 was selected for further study as hydrophilic carrier due to higher solubilisation capacity.

Formulations (w/w) Solubility (mg/l)
Pioglitazone HCl (untreated powder) 8.22±2.63
Pioglitazone HCl: Solutol HS 15 276. 81±3.5
Cremophor RH 40 219.93±4.68
Poloxamer 188 136.05±3.51
Poloxamer 407 149.26±4.53
PEG 4000 86.44±4.43
Povidone K- 15 104.31±3.21
HPMC 37.80±4.69

Table 1: Solubility of Pioglitazone HCl from Different SD Formulations

Crystallinity and aqueous solubility of drug is affected by the preparation techniques and drug-carrier ratio [31]. Considering this, the effect of amount of Solutol HS 15 on the solubility of Pioglitazone HCl is illustrated in figure 1. The solubility of Pioglitazone HCl significantly (p<0.05) increased in PMs, SMs and MMs with increase in concentration of the carrier. Concentration of Solutol HS 15 used in this study was higher than its critical micelle concentration [32]. So, there was simultaneous increase in concentration of micelles along with increase in concentration of Solutol HS 15. SMs showed significant (p<0.05) higher enhancement of solubility of Pioglitazone HCl than its corresponding PMs. Formulations (1:3) showed approximately 2.40 fold more solubility enhancement than 1:1 formulations. However 1:5 formulations showed approximately 1.30 fold more Pioglitazone HCl solubility (figure 1). Approximately 1.80 fold solubility was decreased as the concentration of the Solutol increased twice. Pioglitazone HCl and Solutol HS 15 (1:7 weight ratio) showed significant enhancement (p<0.05) of solubility than lower ratios. In higher ratios (1:7, 1:9), SMs showed approximately twice higher solubility than PMs and almost similar in the lower ratios. MMs and SMs showed almost similar enhancement of solubility of Pioglitazone HCl in all the chosen ratios. In comparison, solubility of Pioglitazone HCl was increased up to 1:7 ratio but further there was no significant enhancement of solubility as the amount of Solutol was added (1:9) and further it become constant. Enhancement of solubility might be due to the conversion of crystalline to amorphous state. Thus, SD with 1:7 weight ratio was found to be optimum for further exploration.


Figure 1: Solubility of Pioglitazone HCl from PM and SDs containing Solutol HS 15 in various proportions
Solubility of Pioglitazone HCl in physical mixture (PM) and solid dispersions (SDs) prepared by melting method (MM) and solvent evaporation method (SM) with Solutol HS 15 in various drug:carrier ratios. Mean±SD, n=3, *p<0.05, image PM, image MM, image SM

This formulation was meant for the oral drug delivery. It comes across different pH conditions from oral cavity to intestine to systemic circulation. Thus, the progression of in vivo dissolution will be far more complicated than the results of in vitro dissolution studies with USP dissolution apparatus due to the pH changes. Consequently, the in vitro dissolution results may not predict in vivo dissolution profile. The gastrointestinal simulator (GIS) is the in vitro dissolution apparatus to understand the in vivo dissolution phenomena of those drugs. The buffer solution with different pH in each compartment of the GIS will be transferred from one chamber to the next chamber with various transit rates. So it is important to understand the effect of different pH buffers (1.2, 1.5, 4.5, 6.8 and 7.4) on the solubility of the Pioglitazone HCl. With increase in pH of the buffer medium, the solubility of Pioglitazone HCl decreased up to the pH 6.8 may due to precipitation [33]. The solubility of pioglitazone is found to decrease drastically after pH 1.2. Further slight enhancement of solubility was observed at pH 7.4, which may due to the supersaturation and recrystallization of drug [33,34]. Similar pattern was also seen in the three different samples. As seen from the figure 2, SM showed highest solubility in all pH conditions among three different formulations. Higher amount of conversion of crystalline form of Pioglitazone HCl into amorphous form might be the reason for the above. MM showed slightly better solubility of Pioglitazone HCl than its corresponding PM. This may due to partial conversion into amorphous form during formulation in which some part of Pioglitazone HCl was dissolved in the melted Solutol HS 15.


Figure 2: Solubility of Pioglitazone HCl from PMs and SDs in various pH buffers
Solubility of Pioglitazone HCl from physical mixture (PM) and solid dispersions (SDs) prepared by melting method (MM) and solvent evaporation method (SM) in various pH buffers Mean±SD, n=3, *p<0.05, image pioglitazone, image1:7 PM, image 1:7 MM, image 1:7 SM

The dissolution profiles of pure drug, 1:7 PM and SDs prepared by MM and SM were evaluated in 0.1 N HCl as depicted in the figure 3. The dissolution of crystalline Pioglitazone HCl was incomplete with only 43.7 % after 60 min. The PM showed 85 % of drug dissolution within 45 min and incomplete drug release profile within 60 min of dissolution study. The enhancement of dissolution might be due to the solubilization of Pioglitazone HCl by micellization.


Figure 3: Dissolution profiles of Pioglitazone HCl, PM and SD formulations in 0.1 N HCl
Dissolution profiles of Pioglitazone HCl, physical mixture (PM) and solid dispersion (SD) formulations prepared by melting method (MM) and solvent evaporation method (SM) using 1:3, 1:5 and 1:7 weight ratios in 0.1 N HCl. Mean±SD, n=3, (▬■▬) pure drug, (▬●▬) 1:3 PM, (▬▲▬) 1:5 SD (MM), (▬▼▬) 1:5 SD (SM), (▬◄▬) 1:7 PM, (▬►▬) 1:7 SD (MM), (▬♦▬) 1:7 SD (SM)

In 15 min of dissolution, complete drug release was observed for the formulation of SM but it decreased to ~98 % at 30 min. The decrease in % of dissolution with increased in time interval could be due to precipitation of drug present in supersaturated state in buffer. Drug release (37 %) was observed for the formulation of MM within 15 min. Interestingly in PM, approximately 50 % of Pioglitazone HCl was released within a span of 15 min and it was slow and incomplete in the latter stage. Increased number of micellar concentration of the polymer might be the reason for sudden increase of Pioglitazone HCl.

At 15 min of dissolution, initial dissolution rate of Solutol HS 15-based SD (SM) and pure drug Pioglitazone HCl 5.95 and 2.43 %/min, respectively. This was significantly (p<0.05) higher than that of pure drug. The relative dissolution rate was found to be 2.44. The dissolution efficiency of the sample improved from 53.97 % (pure drug) to 60.13 %. This indicated enhancement in the dissolution rate of the drug with SD. The T50% of the Pioglitazone HCl and formulation prepared in SM was found to be >60 and 7.27 min. This indicates the significance difference (p<0.05). Difference factor (f1) and similarity factor (f2) was calculated between the Pioglitazone HCl and Solutol HS 15-based SD (SM) and found to be 123.93 (f1) and 16.17 (f2). Pioglitazone HCl is not similar to Solutol HS 15-based SD (SM) product as the f1 and f2 values are more than 15 and less than 50, respectively. The effect of preparation methods of Pioglitazone HCl in Solutol HS 15 increased the dissolution rate in the following order: SM>MM>PM>drug. Significant enhancement of dissolution rate observed in formulations of SM compared to PM and pure drug indicated Pioglitazone HCl was present predominantly in an amorphous state in SM and this was confirmed by the data obtained in the DSC and XRD studies. Dissolution enhancement from SDs could be attributed to hydrophilicity, wettability, and formation of particles with higher porosity and properties of the polymers themselves [35]. Hence, Solutol HS 15 was suitable choice of polymer and SM was suitable method for dissolution enhancement of Pioglitazone HCl.

The FTIR spectra of pure drug Pioglitazone HCl, Solutol HS 15 and different formulations of Pioglitazone HCl are depicted in figure 4. The FTIR spectra of pioglitazone HCl showed characteristics absorption peak at 3354.67 cm-1 (N-H stretching vibration), 3084.18 cm-1 (C-H aromatic vibration), 2927.94 cm-1 (C-H aliphatic stretching), 1741.72 cm-1 (C=O carbonyl stretching vibration) (capable to form hydrogen bond). C=C stretching vibration at 1680 cm-1, CH2 deformation at 1462.04 cm-1, C-O-Ar group at 1244.09 cm-1 and C-H bending at 1037.70 cm-1 are displayed by the pure drug [36,37]. The FTIR of Solutol HS 15 could favour the physical interaction with drug. PMs of drug and the Solutol HS 15 showed no new peaks or shifting of existing peaks, indicate no chemical interaction. This signifies the stability of the drug and polymers. SDs of Pioglitazone HCl showed shifting of carbonyl stretching vibration of Pioglitazone HCl to 1740.7 cm-1 (MM) and 1738.8 cm-1 (SM). This indicate the formation of hydrogen bonds between the Pioglitazone HCl and Solutol HS 15.


Figure 4: FTIR spectra of Pioglitazone HCl, Solutol HS 15, PM and SDs
Physical mixture (PM) and solid dispersions (SDs) were prepared using 1:7 weight ratio melting method (MM) and solvent evaporation method (SM). image Pioglitazone HCl, image Solutol HS 15, image PM (1:7), image SD (1:7, MM) and image SD (1:7, SM)

DSC thermogram of pure Pioglitazone HCl, Solutol HS 15, PM and SD formulations are shown in figure 5. The free Pioglitazone HCl exhibited a single sharp endothermic peak at 180.9° corresponding to its melting point accompanied by an enthalpy of fusion (ΔH) of 33.7 J/g confirming its crystallinity. The endotherm of Solutol HS 15 displayed melting peak at 32.2° [30]. The DSC thermogram of the PMs showed individual broad endothermic peaks corresponding to melting points of Solutol HS 15 and Pioglitazone HCl indicating crystallinity of the drug was remained in the PMs. In the thermograms of SDs in MM, the endotherms of Solutol HS 15 were remain unchanged, while melting peak of Pioglitazone HCl appeared with broad and less intensity at 1:5 and disappeared at 1:7 ratio indicating its partial and complete conversion into amorphous state, respectively (figure 5). The absence of melting peak of Pioglitazone HCl in the DSC thermogram of the prepared SDs (SM) at 1:5 and 1:7 ratio indicates a complete conversion of crystalline drug into amorphous form [23,29]. The results revealed that Solutol HS 15 have greater ability to form SDs in SM, which may result in higher dissolution rate and bioavailability.


Figure 5: DSC thermograms
A. Pioglitazone HCl, B. Solutol HS 15, C. Solutol HS 15-based PM (1:3), D. Solutol HS 15-based SD (1:5, MM), E. Solutol HS 15-based SD (1:5, SM), F. Solutol HS 15-based PM (1:7), G. Solutol HS 15-based SD (1:7, MM), H. Solutol HS 15-based SD (1:7, SM)

The XRD pattern of Pioglitazone HCl, Solutol HS 15, PM, MM and SM formulations were examined and depicted in figure 6. Sharp and intense diffraction peak at 2θº equivalent to 6.87°, 10.33°, 13.8°, 15.5°, 15.85°, 16.99°, 17.83°, 18.95°, 20.75°, 21.72°, 23.6°, 24.21°, 25.42°, 31.3° showed the strong evidence of crystallinity of Pioglitazone HCl in agreement to those of previous reports [15]. Solutol HS 15 exhibited no characteristics peaks as shown in figure 6. The XRD peaks of Pioglitazone HCl at 13.78º, 15. 85º, 21.72º disappeared in PMs and 18.95º, 25.42º peaks become shorter, implying that, drug was partially converted into amorphous form. The 2θ XRD peaks at 6.87°, 16.99°, 17.83°, 24.21°, 25.42° of Pioglitazone HCl was appeared in the 1:5 SDs indicating drug still retained its crystallinity. The amount of Solutol HS 15 was not sufficient to solubilise the drug completely in both the techniques. The melting mixture at 1:7 ratio showed similar peaks as 1:5 SDs. On other hand, SDs (SM) at 1:7 ratio, didn’t show any characteristics peaks of Pioglitazone HCl, suggesting complete change of drug crystallinity to amorphous state.


Figure 6: X-ray diffraction patterns
A. Pioglitazone HCl, B. Solutol HS 15, C. Solutol HS 15-based PM (1:3), D. Solutol HS 15-based SD (1:5, MM), E. Solutol HS 15-based SD (1:5, SM), F. Solutol HS 15-based PM (1:7), G. Solutol HS 15-based SD (1:7, MM), H. Solutol HS 15-based SD (1:7, SM)

The higher solubility of SDs is primarily attributed to its conversion to amorphous state. This state being thermodynamically unstable, might convert to lower energy state by recrystallization during storage. Hence, rate of recrystallization and its effect of solubility of 1:7 SD prepared by SM was investigated by periodic evaluation under 25° storage conditions according to the ICH guidelines. As shown in figure 7 (I), 1: 7 SD showed 385 μg/ml solubility of Pioglitazone HCl in 0 day and it was maintained at this level during 3 mo of storage period. This indicates no significance difference (p>0.05). This indicated that amorphous state of Pioglitazone HCl in SD almost remained unchanged within the study period. After 3 mo of storage, XRD pattern figure 7 (II), of SD formulation did not show any additional peaks, indicated drug remaining in the amorphous state. This confirmed that there is no recrystallization, which suggests its good physical stability.


Figure 7: Effect of storage at 25° for 3 months on solubility and X-ray diffraction patterns of Pioglitazone HCl from SDs
(I) Solubility of Pioglitazone HCl from SDs prepared by solvent evaporation method (SM) during 3 months storage at 25°, Mean±SD, n=3, *p<0.05; (II) X-ray diffraction patterns, A. Solutol HS 15-based SD (1:7) at 0 day, B. Solutol HS 15-based SD (1:7) after 1 month, C. Solutol HS 15-based SD (1:7) after 2 months, D. Solutol HS 15-based SD (1:7) after 3 months at 25°

To assess whether the in vitro dissolution parameters could be used to predict in vivo performance, a pharmacokinetic study was performed for the selected formulation and pure drug in rabbits. The plasma concentration-time curves after oral administration of pure drug and formulation were shown in figure 8 and the essential pharmacokinetics parameters were summarized in the Table 2. No significant difference was observed for Tmax and T1/2 between pure drug and Solutol HS 15-based 1:7 SD after oral administration. In contrast to this, Cmax of SD formulation was significantly higher (approximately 4 fold) than that of crystalline Pioglitazone HCl (p<0.05). This revealed the increase in bioavailability of Pioglitazone HCl from SD preparation. In agreement with this, AUC0-t of the SD was found to be about 2.4 fold higher than that of pure drug (p<0.05). These findings suggest the improvement in oral bioavailability of Pioglitazone HCl after administration of SD. This may due to excellent solubilization capacity of Solutol HS 15 and conversion to amorphous state during SD preparation by SM. Mean residence time of formulations showed more than the pure drug.

Parameter Pioglitazone HCl Solutol HS 15-based SD
Tmax (h) 1.00±0.001 0.83±0.02
Cmax (ng/ml) 16.78±6.81 64.37± 5.18*
AUC0-t (ng h/ml) 91.52±37.18 216.37±52.61*
AUC0-∞ (ng h/ml) 99.54±38.19 221.51±53.60*
MRT (h) 8.52±0.87 4.71±0.45*
T1/2 (h) 5.73±0.40 4.07±0.29

Table 2: Pharmacokinetic Parameters of Pioglitazone HCl and Solutol HS 15-Based SD (1:7) in Rabbits


Figure 8: Plasma concentration of Pioglitazone HCl with time from Pioglitazone HCl and SD of pioglitazone
Plasma concentration profile of Pioglitazone HCl and SD of Pioglitazone HCl with Solutol HS 15 prepared by solvent evaporation method (SM) Mean±SD, n=6, (▬■▬) pure drug, (▬●▬) 1:7 SD (SM)

This study revealed that Solutol HS 15 is an effective carrier in enhancing solubility and stability of the Pioglitazone HCl. Pioglitazone HCl in the SD prepared by SM with Solutol HS 15 at weight ratio of 1:7 existed in amorphous state and was stable under tested storage condition. This has resulted in significant improvement in the bioavailability. Thus, the present study showed an effective way of overcoming problems of solubility, stability and oral bioavailability of Pioglitazone HCl. Considering the simplicity of this approach, it could further be utilized to design capsules in higher scale for industrial application.


The authors would like to thank Aurobindo Pharma Ltd., Hyderabad, India for providing the pure drug Pioglitazone HCl as gift sample.

Conflict of interest

The authors declare no conflict of interest.