Modification of the Release of Poorly Soluble Sulindac with the APTES-Modified SBA-15 Mesoporous Silica

The effectiveness of oral drug administration is related to the solubility of a drug in the gastrointestinal tract and its ability to penetrate the biological membranes. As most new drugs are poorly soluble in water, there is a need to develop novel drug carriers that improve the dissolution rate and increase bioavailability. The aim of this study was to analyze the modification of sulindac release profiles in various pH levels with two APTES ((3-aminopropyl)triethoxysilane)-modified SBA-15 (Santa Barbara Amorphous-15) silicas differing in 3-aminopropyl group content. Furthermore, we investigated the cytotoxicity of the analyzed molecules. The materials were characterized by differential scanning calorimetry, powder X-ray diffraction, scanning and transmission electron microscopy, proton nuclear magnetic resonance and Fourier transformed infrared spectroscopy. Sulindac loaded on the SBA-15 was released in the hydrochloric acidic medium (pH 1.2) and phosphate buffers (pH 5.8, 6.8, and 7.4). The cytotoxicity studies were performed on Caco-2 cell line. The APTES-modified SBA-15 with a lower adsorption capacity towards sulindac released the drug in a less favorable manner. However, both analyzed materials improved the dissolution rate in acidic pH, as compared to crystalline sulindac. Moreover, the SBA-15, both before and after drug adsorption, exhibited insignificant cytotoxicity towards Caco-2 cells. The presented study evidenced that SBA-15 could serve as a non-toxic drug delivery system that enhances the dissolution rate of sulindac and improves its bioavailability.


Introduction
Since 2017, the Food and Drug Administration (FDA) has noted a growing trend in the number of new drugs approved. In 2017-2020, 46, 59, 48, and 53 new active substances were approved as medicines each year, respectively [1]. Most of the newly approved drugs

Synthesis and Functionalization of Mesoporous Materials
We obtained the SBA-15 materials in accordance with the previously presented report [18]. We adapted the methodology presented by Zhao with modifications [8]. Briefly, we carried out the synthesis at 35 • C, and 24.0 g of poly(ethylene glycol) and poly(propylene glycol) block copolymer (Pluronic P123) (Merck Life Science Sp.z.o.o., an affiliate of Merck KGaA, Darmstadt, Germany, Poznań, Poland) was dissolved in 900 mL of aqueous HCl (1.6 M). Afterwards, we added 51.0 g of tetraethyl orthosilicate (TEOS) into the solution and magnetically stirred for 20 h. Next, the mixture was aged at 110 • C (24 h). Further, we filtered the suspension and washed using distilled water. Eventually, the precipitate was air dried, and the final product was calcined at 500 • C (6 h with heating rate 1 • C/min). We obtained the APTES ((3-aminopropyl) triethoxysilane) modified SBA-15 silica (Merck Life Science Sp.z.o.o., an affiliate of Merck KGaA, Darmstadt, Germany, Poznań, Poland) by grafting method in accordance with methodology presented by Geszke-Moritz and Moritz [19]. Using different molar ratios (0.05 and 0.20) of the trialkoxysilane to the SBA-15 silica, two different functionalized materials were obtained (SBA-15-A 0.05 and SBA-15-A 0.20 , respectively).

Sulindac Adsorption Studies
SBA-15 material modified with 3-aminopropyl groups was used for the tests. Adsorption of sulindac was carried out at 25 • C in 2-propanol (Avantor Performance Materials Poland, Gliwice, Poland). To obtain each sample, we used 5 mL of 3.0 mg/mL SUL solution and 50.0 mg of SBA-15-A 0.05 or SBA-15-A 0.20 . After stirring the mixture for 48 h, the suspension was centrifuged at 6000 rpm for 15 min. The precipitate was air dried. The obtained material was designated as SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL [18].
The amount of adsorbed SUL was calculated as the difference in the concentrations of the solutions before and after adsorption using a UV/VIS LAMBDA 20 Perkin Elmer spectrophotometer (PerkinElmer, Inc., Waltham, MA, USA) at 396 nm. The amount of SUL adsorbed in SBA-15-A 0.05 and SBA-15-A 0.20 was 90.5 mg/g and 221.3 mg/g, respectively [18].

Powder X-ray Diffraction (XRD)
The small angle XRD patterns were collected with Bruker D8 Advance (Billerica, MA, USA) in the range of 0.6 < 2θ < 8.0 • . The wide-angle XRD patterns were acquired with Bruker D2 Phaser (Billerica, MA, USA) in the range of 5.0 < 2θ < 45.0 • . The measurements were performed with a 0.02 • step width associated with a step time of 1-2 s.

Differential Scanning Calorimetry (DSC)
DSC thermograms were obtained using DSC 214 Polyma Netzsch (Netzsch Group, Selb, Germany) in a nitrogen atmosphere (30 mL/min). The samples were heated up to 250 • C with a scanning rate of 5 • C/min. The weight of each sample was approximately 5.0 mg. The FTIR analyses were performed on Bruker FTIR IFS 66/s spectrometer (Billerica, MA, USA) using the KBr pellet technique in the wavenumber range 400-4000 cm −1 with the resolution of 1 cm −1 . Tablets were formulated by mixing 1 mg of the studied substance with 200 mg of potassium bromide until a homogeneous mixture was obtained.

Proton Nuclear Magnetic Resonance ( 1 H-NMR)
The proton spin-lattice relaxation times T 1 in the laboratory frame were measured on a pulse spectrometer operating at a frequency of 25 MHz (El-Lab Tel-Atomic, Jackson, MI, USA) using the standard saturation recovery sequence ending with a solid echo [20][21][22].
All measurements were carried out with 3% error. The samples of SUL, SBA-15-A 0.05 :SUL, and SBA-15-A 0.20 :SUL were sealed in glass tubes and degassed in order to remove humidity effects and paramagnetic oxygen. Measurements were performed in a wide temperature range from 80 K to 300 K. The temperature of the sample was stabilized within 15 min and controlled using a gas-flow cryostat and monitored with a Pt resistor to an accuracy of 0.5 K. Due to a weak signal in the SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL samples that was related to a small number of protons, multiple-signal accumulation was applied. The T 1 values were extracted by fitting the magnetization recovery to the one or be-exponential function for SUL, and SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL samples, respectively.

Drug Release Studies
The release studies of sulindac from mesoporous silicas and the dissolution tests of pure sulindac were carried out on an Electrolab EDT 08Lx apparatus (Electrolab, Janki Impex, Gujarat, India) using the rotating paddle method at 37 ± 0.5 • C. Samples corresponding to 4 mg of sulindac were used for each analysis. The release volume was reduced to 500 mL under sink conditions, and the rotation speed was set at 70 rpm. During the test, the following media were used: a hydrochloric acidic medium at pH = 1.2 ± 0.1 and phosphate buffers at pH = 5.8 ± 0.1, 6.8 ± 0.1, and 7.4 ± 0.1 (European Pharmacopoeia 10th Edition). After the specified time (5,15,30,45,60,90, and 120 min), 4 mL of liquid was collected and then filtered through a 0.22 µm PTFE filter (Bionovo, Legnica, Poland), and the sulindac concentration was assessed by UV spectrophotometry at 333 nm for the hydrochloric acidic medium and 327 nm for the phosphate buffers. The removed volume of dissolution fluid was immediately replaced by 4 mL of fresh medium (37 ± 0.5 • C). All samples were analyzed in triplicate.
A method based on the calculation of the similarity index f 2 was used to compare the release profiles. The similarity coefficients f 2 were calculated according to the formula below [23]: where n is number of sample points, R t and T t are the percentage of dissolved/released SUL from the reference and test samples, respectively, at time t.

Cell Viability
Caco-2 cells were cultivated under the standard conditions in a humidified atmosphere containing 95% air and 5% CO 2 at 37 • C. To evaluate the effects of SUL, SBA-15-A 0.20 , and SBA-15-A 0.20 :SUL on cell viability, confluent stock cultures were detached using trypsin and seeded in 96-well plates at a density of 2 × 10 4 cells/well in 150 µL of growth medium. After attachment, the cells were left for 48 h and analyzed compounds were added. We analyzed the concentrations of SBA-15-A 0.20 of 0.125-1.0 mg/ mL and the SUL concentrations, which corresponded to the amount of the SUL adsorbed on the SBA-15-A 0.20 used for the tests. We measured the cell viability after 2 h of incubation using CellTiter-Glo Luminescent Cell Viability Assay (Promega, Madison, WI, USA), in accordance with the manufacturer's instructions.

Powder X-ray Diffraction (XRD)
The XRD analysis allowed us to distinguish between the crystalline and amorphous nature of the samples. Figure 1A presents the small-angle XRD profile of SBA-15-A 0.20 . The diffractogram reveals well-resolved peaks that correspond to (100), (110), and (200) planes and prove an ordered structure and hexagonal symmetry with the space group p6mm of analyzed silica [8].

Differential Scanning Calorimetry (DSC)
We applied the DSC method in order to analyze the thermal properties of samples and to evaluate their physical state. DSC allows the determination of glass transitions and the investigation of the crystallization and melting behavior of the analyzed materials. The DSC curves for SUL, SBA-15-A0.20, SBA-15-A0.05:SUL, and SBA-15-A0.20:SUL are presented in Figure 2. The DSC curve for SUL presents one endothermic peak at 186.6 °C, which is assigned to the melting temperature of the substance. Above the temperature of 205 °C, an exothermic peak begins, indicating the decomposition of the drug [26].
The DSC curve for SBA-15-A0.20 shows a peak correlated with glass transition at 65 °C. The presence of this peak proves the amorphous state of the carrier. In the analyzed temperature range, the SBA-15-A0.20 is thermally stable as there are no melting or degra-   [24]. The XRD patterns for both APTES-modified silicas present one wide peak with the maximum located at ≈22.5 • , corroborating the amorphous nature of the materials. Similarly, for samples with adsorbed SUL, we observe only one peak characteristic for the carrier. Those diffractograms show no peaks typical for crystalline sulindac, which proves that the adsorbed drug is in an amorphous state. Previous studies have also reported the transition of the drug from crystalline to amorphous state during the adsorption process on SBA-15 [25].

Differential Scanning Calorimetry (DSC)
We applied the DSC method in order to analyze the thermal properties of samples and to evaluate their physical state. DSC allows the determination of glass transitions and the investigation of the crystallization and melting behavior of the analyzed materials. The DSC curves for SUL, SBA-15-A 0.20 , SBA-15-A 0.05 :SUL, and SBA-15-A 0.20 :SUL are presented in Figure 2. The DSC curve for SUL presents one endothermic peak at 186.6 • C, which is assigned to the melting temperature of the substance. Above the temperature of 205 • C, an exothermic peak begins, indicating the decomposition of the drug [26].

Differential Scanning Calorimetry (DSC)
We applied the DSC method in order to analyze the thermal properties of samples and to evaluate their physical state. DSC allows the determination of glass transitions and the investigation of the crystallization and melting behavior of the analyzed materials. The DSC curves for SUL, SBA-15-A0.20, SBA-15-A0.05:SUL, and SBA-15-A0.20:SUL are presented in Figure 2. The DSC curve for SUL presents one endothermic peak at 186.6 °C, which is assigned to the melting temperature of the substance. Above the temperature of 205 °C, an exothermic peak begins, indicating the decomposition of the drug [26].
The DSC curve for SBA-15-A0.20 shows a peak correlated with glass transition at 65 °C. The presence of this peak proves the amorphous state of the carrier. In the analyzed temperature range, the SBA-15-A0.20 is thermally stable as there are no melting or degradation peaks [27].
Likewise, the DSC curve for SBA-15-A0.20:SUL presents no endothermic or exothermic peaks, which serves to corroborate the amorphous state of the SUL adsorbed inside the mesopores of the SBA-15-A0.20 [28].
For SBA-15-A0.05:SUL, we obtained the curve with one endothermic peak at 191.6 °C. The presence of this peak suggests that the crystalline SUL has partially adsorbed on the surface of SBA-15-A0.05 [28]. However, our XRD study showed conflicting results.

Transmission and Scanning Electron Microscopy (TEM and SEM)
The TEM and SEM micrographs enable the evaluation of the structure and the morphology of mesoporous materials. The TEM images present the structure of the SBA-15- The DSC curve for SBA-15-A 0.20 shows a peak correlated with glass transition at 65 • C. The presence of this peak proves the amorphous state of the carrier. In the analyzed temperature range, the SBA-15-A 0.20 is thermally stable as there are no melting or degradation peaks [27].
Likewise, the DSC curve for SBA-15-A 0.20 :SUL presents no endothermic or exothermic peaks, which serves to corroborate the amorphous state of the SUL adsorbed inside the mesopores of the SBA-15-A 0.20 [28].
For SBA-15-A 0.05 :SUL, we obtained the curve with one endothermic peak at 191.6 • C. The presence of this peak suggests that the crystalline SUL has partially adsorbed on the surface of SBA-15-A 0.05 [28]. However, our XRD study showed conflicting results.

Transmission and Scanning Electron Microscopy (TEM and SEM)
The TEM and SEM micrographs enable the evaluation of the structure and the morphology of mesoporous materials. The TEM images present the structure of the SBA-15-A 0.05 :SUL, SBA-15-A 0.20 :SUL, SBA-15-A 0.05 , and SBA-15-A 0.20 (Figure 3). The TEM micrographs show the parallel mesoporous channels, indicating the two-dimensional structure of the mesoporous silica. Noteworthy, too, is that the structure of SBA-15-A 0.20 and of SBA-15-A 0.05 remains unchanged after SUL adsorption. Similar results were reported in the literature data [29,30].
All SEM images ( Figure 4) present well-formed, rod-like particles of about 1 μm in length, which aggregated into larger linear, chain-like structures. The SEM micrographs of the samples after incorporation present no sulindac crystals, which indicate the adsorption of the sulindac inside the mesopores. Our observations are consistent with the results of Letchmanan et al. [29].

Fourier Transformed Infrared Spectroscopy (FTIR)
The FT-IR spectroscopy allowed the determination of the functional groups in the sample and the identification of the chemical bonds occurring in the molecule. Figure 5 presents the FT-IR spectra of SUL, APTES-modified SBA-15, and its SUL-loaded forms.

Fourier Transformed Infrared Spectroscopy (FTIR)
The FT-IR spectroscopy allowed the determination of the functional groups in the sample and the identification of the chemical bonds occurring in the molecule. Figure 5 presents the FT-IR spectra of SUL, APTES-modified SBA-15, and its SUL-loaded forms.

Proton Nuclear Magnetic Resonance 1 H-NMR
The nuclear magnetic resonance technique (NMR) is a very useful tool for studying the molecular dynamics of a drug molecule. The analysis of the temperature dependence of spin-lattice relaxation times T1 provided essential information about the physicochemical properties of the investigated substances [34,35]. Figure 6 presents the proton spin-lattice relaxation times T1 in the laboratory frame as a function of reciprocal temperature for SUL, SBA-15-A0.05:SUL, and SBA-15-A0.20:SUL, respectively.
For SUL, the recovery of magnetization Mz(t) was one exponential in the entire temperature range. The spin-relaxation time T1 was estimated from fitting the following equation to the experimental data: where M0 is the equilibrium magnetization and T1 is the relaxation time.
The temperature dependence of the longer component of the relaxation times for a drug incorporated into mesoporous silica had a similar course to the relaxation times for SUL. However, due to its small contribution to and its large dispersion of the experimental data, its interpretation was rejected. The existence of this component for both samples SBA-15-A0.05:SUL and SBA-15-A0.20:SUL indicated that some of the drug was not adsorbed to the interior of the silica and remained on its surface. Based on the experimental data, it was determined that less than 10% of the drug was localized outside the pores and about 90% inside. Obtained results are consistent with our DSC analysis, which confirmed partial adsorption on the silica's surface.
The temperature dependence of T1 relaxation times of SUL, SBA-15-A0.05: SUL and SBA-15-A0.20: SUL was analyzed, taking into account the dipole-dipole interactions modulated by molecular motions as described by Bloembergen-Purcell-Pound (BPP) theory [36]. It was assumed that the T1 values were determined by dipolar interactions modulated by two different molecular processes: the hindered rotation of methyl CH3 groups around the threefold axes C3 and the jumping of hydrogen atoms in hydrogen bonds at low temperature. To obtain the activation parameters of the two distinctive processes, the Our results are in line with the previously reported data. In the spectra of the APTESmodified SBA-15, the bands around 3430 cm −1 and 1630 cm −1 are identified as the stretching and bending vibrations of the OH groups (Si-OH), respectively [31]. The broad band in the range 1200-1080 cm −1 can be assigned to the Si-O-Si asymmetric stretching vibrations. The symmetric stretching and bending vibrations of Si-O-Si are located at 800 cm −1 and 460 cm −1 , respectively [31,32]. The band around 2920 cm −1 is attributed to stretching vibrations from the propyl chain and the band at 1550 cm −1 is associated to the N-H bending vibrations. The presence of those bands confirms the functionalization of SBA-15 silica [33].
In the spectrum of SUL, the band at 3064 cm −1 is related to the C-H fundamental stretching vibrations of the aromatic ring. The bands at 2994 cm −1 and 2911 cm −1 are assigned to the asymmetric stretching vibrations of CH 3 and CH 2 groups, respectively. The peaks at 2768 cm −1 , 2582 cm −1, and 2512 cm −1 correspond to the stretching vibrations of the OH group. The band at 1701 cm −1 is associated with the stretching vibrations of the C=O group. The stretching vibrations of the C-C bonds in the aromatic ring appear at 1602 cm −1 , 1588 cm −1 , and 1469 cm −1 . The peak identified at 1155 cm −1 is related to the stretching vibrations of C-F. The S-O bonds can be localized at 1010 cm −1 and 1005 cm −1 [26].
The comparison of FT-IR spectra of SUL, SBA-15-A 0.05 , and SBA-15-A 0.20 with its loaded forms proves the presence of the characteristic peak at 1469 cm −1 originating from SUL on the SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL spectra. It confirms the successful adsorption of sulindac.

Proton Nuclear Magnetic Resonance 1 H-NMR
The nuclear magnetic resonance technique (NMR) is a very useful tool for studying the molecular dynamics of a drug molecule. The analysis of the temperature dependence of spin-lattice relaxation times T 1 provided essential information about the physicochemical properties of the investigated substances [34,35]. Figure 6 presents the proton spin-lattice relaxation times T 1 in the laboratory frame as a function of reciprocal temperature for SUL, SBA-15-A 0.05 :SUL, and SBA-15-A 0.20 :SUL, respectively.

Drug Release Studies
Sulindac belongs to BCS class II and is characterized by high permeability but low solubility, which hinders its absorption, but its absorption may be improved by increasing its dissolution rate. Sulindac is a drug of arylalkanoic acid with a pKa of 4.27 [46], and as such, in the stomach where the pH is low, sulindac is poorly soluble, and its absorption is limited. In the small intestine, where the pH is higher, most of the drug molecules are ionized and partially dissolved [47].
The sulindac release profiles from SBA-15-A0.05:SUL and SBA-15-A0.20:SUL are presented in Figure 7. Our results confirmed a very low dissolution of sulindac at a low pH, mimicking the conditions in the stomach (hydrochloric acidic medium at a pH of 1.2). The increase of pH resulted in an increase of the amount of dissolved sulindac. The obtained results were consistent with the literature [46].
The dissolution tests at pH = 1.2 and pH = 5.8 proved that considerably more drug was released from SBA-15-A0.05:SUL and SBA-15-A0.20:SUL, respectively, than was dissolved from its crystalline form. In the hydrochloric acidic medium at pH = 1.2 and after 5 min of the test, 65.6% of sulindac was released from SBA-15-A0.20:SUL and almost 84% from SBA-15-A0.05:SUL. Only 1.2% of the crystalline sulindac was dissolved at the same time. After 2 h of the test, just 16.5% of the sulindac was dissolved while 72% of the drug For SUL, the recovery of magnetization M z (t) was one exponential in the entire temperature range. The spin-relaxation time T 1 was estimated from fitting the following equation to the experimental data: where M 0 is the equilibrium magnetization and T 1 is the relaxation time.
The recovery of the magnetization for SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL was bi-exponential, resulting in two magnetization fractions with a ratio of 1:9.
The temperature dependence of the longer component of the relaxation times for a drug incorporated into mesoporous silica had a similar course to the relaxation times for SUL. However, due to its small contribution to and its large dispersion of the experimental data, its interpretation was rejected. The existence of this component for both samples SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL indicated that some of the drug was not adsorbed to the interior of the silica and remained on its surface. Based on the experimental data, it was determined that less than 10% of the drug was localized outside the pores and about 90% inside. Obtained results are consistent with our DSC analysis, which confirmed partial adsorption on the silica's surface.
The temperature dependence of T 1 relaxation times of SUL, SBA-15-A 0.05 : SUL and SBA-15-A 0.20 : SUL was analyzed, taking into account the dipole-dipole interactions modulated by molecular motions as described by Bloembergen-Purcell-Pound (BPP) theory [36]. It was assumed that the T 1 values were determined by dipolar interactions modulated by two different molecular processes: the hindered rotation of methyl CH 3 groups around the threefold axes C3 and the jumping of hydrogen atoms in hydrogen bonds at low temperature. To obtain the activation parameters of the two distinctive processes, the temperature curves T 1 were determined by fitting the following Equations (3)-(5) to the experimental data [37,38]: 1 where γ is a gyromagnetic ratio of protons, ∆M 2k is a reduction of the second moment, and J k (ω) is the spectral density function for the angular frequency ω.
It was assumed that motions were thermally activated, and the temperature dependence of the correlation time τ c was expressed by the Arrhenius formula: where τ 0 is the pre-exponential factor corresponding to the correlation time at an infinite temperature, E a is the activation energy of molecular motion, and R is the universal gas constant. For the interpretation of the CH 3 motion, the classical BPP spectral density function was applied [39]: A sharp, symmetrical minimum of 128 ms at about 182 K (−91 • C), depicted in Figure 6, was attributed to the hindered rotation of methyl CH 3 groups around the threefold axes C3. For sulindac, the methyl group reorientation was characterized by the activation energy E a of 12.2 kJ/mol and a τ 0 value of 1.2 × 10 −12 s, which was confirmed by prior 1 H-NMR results [34,40,41]. In the low-temperature region, a decrease of the relaxation times T 1 was observed, and the contribution of another type of molecular motion was considered. The activation parameters of this motion are collected in Table 1. It was assumed that, at low temperatures, the relaxation was modulated by the jumping of hydrogen atoms in hydrogen bonds [42]. For the SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL samples, different temperature T 1 curves were obtained in comparison to SUL. The minima associated with the relaxation processes for sulindac incorporated into mesoporous silica appeared at the higher temperature, which implied that the molecular dynamics were hindered for molecules of SUL inside the pores. The analysis of 1 H-NMR data was performed according to the procedure described for SUL; however, to describe a low, wide temperature minimum of relaxation times T 1 , the spectral density function J(ω), given by Davidson and Cole, was used [43]: where τ c is the upper cut-off correlation time and β is the distribution width of the correlation times. The activation parameters of these molecular processes were extracted and collected in Table 1. The 1 H-NMR results showed that the activation energies of the hindered rotation of the CH 3 groups and of low temperature motion slightly increased for the drug adsorbed in the silica pores, as compared to SUL. In addition, a shorter relaxation time T 1 for the incorporated drug in the SBA-15 mesopores confirmed that the protons of the sulindac molecules incorporated into the silica were more mobile, which gave them a greater degree of freedom. The increased mobility of these systems evidenced the transfer of the crystalline structure to the amorphous one, which could improve the bioavailability of the drug [44,45].
Comparing 1 H-NMR data for the SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL samples, it can be stated that the relaxation times for the SBA-15-A 0.20 :SUL sample were the shortest, and, therefore, the mobility of protons in this system was the greatest. It can be assumed that an increase in the 3-aminopropyl groups in the silica structure may attenuate the interactions between the sulindac molecules.

Drug Release Studies
Sulindac belongs to BCS class II and is characterized by high permeability but low solubility, which hinders its absorption, but its absorption may be improved by increasing its dissolution rate. Sulindac is a drug of arylalkanoic acid with a pK a of 4.27 [46], and as such, in the stomach where the pH is low, sulindac is poorly soluble, and its absorption is limited. In the small intestine, where the pH is higher, most of the drug molecules are ionized and partially dissolved [47].
The sulindac release profiles from SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL are presented in Figure 7. Our results confirmed a very low dissolution of sulindac at a low pH, mimicking the conditions in the stomach (hydrochloric acidic medium at a pH of 1.2). The increase of pH resulted in an increase of the amount of dissolved sulindac. The obtained results were consistent with the literature [46].  What was noteworthy was that none of the analyzed conditions had allowed a complete release of the drug from the carriers. This could be due to the potential diffusion resistances or the sorption equilibrium of sulindac with the modified silica surfaces [48].
SBA-15-A0.20:SUL demonstrated a less favorable sulindac release profile at all of the studied pH values, as compared to SBA-15-A0.05:SUL. This may have resulted from the different pore sizes of the silicas. The larger pores in SBA-15-A0.05 allowed an easier diffusion of the drug molecules from the silica into the medium, resulting in a greater proportion of the released drug [32,49].  The dissolution tests at pH = 1.2 and pH = 5.8 proved that considerably more drug was released from SBA-15-A 0.05 :SUL and SBA-15-A 0.20 :SUL, respectively, than was dissolved from its crystalline form. In the hydrochloric acidic medium at pH = 1.2 and after 5 min of the test, 65.6% of sulindac was released from SBA-15-A 0.20 :SUL and almost 84% from SBA-12 of 16 15-A 0.05 :SUL. Only 1.2% of the crystalline sulindac was dissolved at the same time. After 2 h of the test, just 16.5% of the sulindac was dissolved while 72% of the drug was released from SBA-15-A 0.20 :SUL and almost 88% from SBA-15-A 0.05 :SUL. The increased dissolution rate of SUL adsorbed on the mesoporous silica was related to the amorphous state of the drug and the reduction in particle size of sulindac [29]. Substances in the amorphous form are characterized by reduced lattice energy and, therefore, higher dissolution rates and increased bioavailability. Moreover, the hydrophilic nature of the mesoporous silica surface facilitates the wetting and dispersion of the adsorbed SUL and accelerating its dissolution [10].
In a phosphate buffer at pH = 5.8, the differences in the release profiles of sulindac decreased, but remained significant. After 120 min, 59% of the crystalline form of sulindac dissolved, whereas 73.7% and almost 85% of the drug was released from SBA-15-A 0.20 :SUL and SBA-15-A 0.05 :SUL, respectively.
Based on the values of the similarity coefficient f 2 ( Table 2), we concluded that the observed drug release rate was higher than its dissolution rate. The improvement in the dissolution rate of sulindac may have resulted from its adsorption on mesoporous carriers in an amorphous state [31]. The amorphous state of the drug was confirmed in our DSC and XRD analyses. At higher pHs (6.8 and 7.4), an initially greater amount of sulindac was released from the silicas than that which was dissolved from the crystalline form. However, after 30 min at pH = 6.8 and after 15 min at pH = 7.4, the amount of dissolved sulindac exceeded the amount of released substance from both silica types. After 45 min of the test, the amount of the dissolved sulindac surpassed 98%.
In contrast to the pH-dependent dissolution of sulindac, the release of sulindac from the mesoporous materials remained constant under different pH conditions. The drug release profiles from both silicas were similar, as evidenced by the f 2 similarity coefficients above 50 (Table 3). The exception was the SBA-15-A 0.05 :SUL release profile in a phosphate buffer at pH = 6.8 and pH = 7.4. We observed a reduction in the amount of sulindac released from SBA-15-A 0.05 :SUL as the pH values increased. What was noteworthy was that none of the analyzed conditions had allowed a complete release of the drug from the carriers. This could be due to the potential diffusion resistances or the sorption equilibrium of sulindac with the modified silica surfaces [48].
SBA-15-A 0.20 :SUL demonstrated a less favorable sulindac release profile at all of the studied pH values, as compared to SBA-15-A 0.05 :SUL. This may have resulted from the different pore sizes of the silicas. The larger pores in SBA-15-A 0.05 allowed an easier diffusion of the drug molecules from the silica into the medium, resulting in a greater proportion of the released drug [32,49].

Cytotoxicity Studies
We assessed the biocompatibility of analyzed silica before and after sulindac loading. For this purpose, we used the cell visibility test, which assumes that the number of viable cells is proportional to the amount of ATP (adenosine triphosphate) produced by metabolically active cells [50]. To assess the cytotoxicity of analyzed samples, we used the Caco-2 cells (human colorectal adenocarcinoma cells) that resemble the human epithelial cells of the small intestine [51].  [28,52]. We also noted no differences between the cell viability of the samples between all analyzed concentrations. The results suggested that the adsorption of SUL to SBA-15-A 0.20 does not influence the silica's cytotoxicity.

Cytotoxicity Studies
We assessed the biocompatibility of analyzed silica before and after sulindac loading. For this purpose, we used the cell visibility test, which assumes that the number of viable cells is proportional to the amount of ATP (adenosine triphosphate) produced by metabolically active cells [50]. To assess the cytotoxicity of analyzed samples, we used the Caco-2 cells (human colorectal adenocarcinoma cells) that resemble the human epithelial cells of the small intestine [51].  [28,52]. We also noted no differences between the cell viability of the samples between all analyzed concentrations. The results suggested that the adsorption of SUL to SBA-15-A0.20 does not influence the silica's cytotoxicity.

Conclusions
Our study investigated the possibility of increasing the dissolution rate of the poorly soluble sulindac using adsorption on APTES-modified mesoporous silicas. Our SEM, DSC, XRD, and 1 H-NMR analyses proved that adsorption of the drug on the analyzed silicas provided the amorphous state of the adsorbed substance in 90% of the resulting specimens. We demonstrated that APTES-modified SBA-15 containing more 3-aminopropyl substituents, which are characterized by a higher adsorption capacity towards sulindac, released the drug in a less favorable manner, as compared to SBA-15-A0.05. We observed a higher dissolution rate of SUL when incorporated into SBA-15-A0.20 and SBA-15-A0.05 at acidic pH, as compared to the crystalline SUL. The cytotoxicity of the analyzed carrier before and after adsorption of SUL was insignificant. The presented study evidenced that mesoporous silica SBA-15 is applicable as a non-toxic, effective drug delivery system for the poorly soluble sulindac.

Conclusions
Our study investigated the possibility of increasing the dissolution rate of the poorly soluble sulindac using adsorption on APTES-modified mesoporous silicas. Our SEM, DSC, XRD, and 1 H-NMR analyses proved that adsorption of the drug on the analyzed silicas provided the amorphous state of the adsorbed substance in 90% of the resulting specimens. We demonstrated that APTES-modified SBA-15 containing more 3-aminopropyl substituents, which are characterized by a higher adsorption capacity towards sulindac, released the drug in a less favorable manner, as compared to SBA-15-A 0.05 . We observed a higher dissolution rate of SUL when incorporated into SBA-15-A 0.20 and SBA-15-A 0.05 at acidic pH, as compared to the crystalline SUL. The cytotoxicity of the analyzed carrier before and after adsorption of SUL was insignificant. The presented study evidenced that mesoporous silica SBA-15 is applicable as a non-toxic, effective drug delivery system for the poorly soluble sulindac.