Formulation and development of Serratiopeptidase enteric coated tablets and analytical method validation by UV Spectroscopy

Serratiopeptidase (SRP) is a proteolytic enzyme that emerged as one of the most potent anti-inflammatory and analgesic drugs. The purpose of the present study was to formulate and evaluate enteric-coated tablets for SRP and investigate their stability using a simple and validated analytical method by ultraviolet (UV) spectroscopy. The colloidal silicon dioxide (2.50%), sodium starch glycolate (3.44%), and crospovidone (2.50%) were used as appropriate excipients for the development of core part of tablets. To protect the prepared tablets from acidic environment in the stomach, white shellac, castor oil, HPMC phthalate 40, and ethyl cellulose were used. The seal coating and enteric coating attained were 2.75% and 6.74%, respectively. SRP was found to be linear at 265 nm in the concentration range of 25–150 µg/mL. The results revealed that our developed method was linear (R2 = 0.999), precise (RSD % = 0.133), and accurate (% recovery = 99.96–103.34). The formulated SRP tablets were found to be stable under accelerated conditions as well as under room temperature for 6 months (assay %: >97.5%). The in vitro drug release study demonstrated that enteric-coated tablets were able to restrict SRP release in both acidic environments: 0.1 N HCl and simulated gastric fluid (pH 1.2). Moreover, at 60 minutes, the formulated SRP tablets revealed 13.0% and 8.98% higher drug release in phosphate buffer (pH 6.8) and simulated intestinal fluid (pH 6.8), respectively, compared to the marketed tablet formulation. This study concludes that enteric-coated tablets of SRP with higher drug release in the intestine can be prepared and examined for their stability using validated analytical technique of UV spectroscopy.


Introduction
A wide range of proteolytic enzymes mixtures have been used as supportive therapy in clinical condition such as trauma and orthopedic.
ere are several reports supporting the use of these proteolytic enzymes for the treatment of inflammatory disorders [1]. Moreover, these enzymes linked to metalloprotease family have been profitably assessed for their anti-inflammatory properties, which include trypsin, chymotrypsin, and serratiopeptidase (SRP) [2]. Chemically, SRP is an extracellular metalloprotease derived from the nonpathogenic enterobacteria Serratia E15 [3]. It consists of a polypeptide chain of 470 residues and a catalytic zinc ion per molecule with molecular weight of 45-60 kDa. SRP is normally recommended for oral administration at a dose of 5-10 mg three times a day [1]. is enzyme is rapidly and readily absorbed through the intestine and transported directly into the blood circulation [4]. SRP has been extensively used in Europe and Asia for more than 30 years but is relatively new in the United States and Canada. In addition, its anti-inflammatory property was first studied in Japan in 1967. Later, during the 1970s, these parenteral enzyme preparations were replaced by oral enteric-coated tablet form. During the 1980s and 1990s, this research was proposed to separately be conducted in Europe and Japan and demonstrated that SRP is the most effective agent in diminishing inflammation among all available enzyme formulations [3,5]. Currently, SRP has been broadly used in Japan and Europe as the anti-inflammatory and analgesic agent of choice [6]. e most common problem associated with SRP oral delivery is high risk of enzymatic degradation in the gastrointestinal tract due to its proteinaceous nature. In addition, hydrophilic nature of SRP leads to low intestinal membrane permeability, due to which a very high dosage of SRP needs to be orally administered to elicit significant antiinflammatory responses [7]. In order to increase the stability of SRP (reduced acid hydrolysis) and improve the oral bioavailability simultaneously, several techniques like delivering the SRP entrapped in Eudragit S100 microspheres, liposomal formulations, alginate gel encapsulated with SRP, chitosan-coated ceramic nanocores containing SRP, in situ cubic phase transforming system of glyceryl monooleate containing SRP, tetracycline-SRP-containing periodontal gel, and polar lipid-based lipospheres were approached previously [1]. Oral tablet dosage form with enteric coating and combination with controlled and sustained release property could be an effective way to decrease the frequency of dosing and increase the bioavailability of SRP [8][9][10]. erefore, in vitro release profiles and in vivo efficacy are considered as important parameters to be studied for developing suitable delivery system. Another major challenge in developing a formulation of SRP is to retain its structural backbone, inhibiting the folding tendency during manufacturing, storage, digestion, and absorption in the stomach and intestines [11].
In order to determine the qualitative and quantitative evaluation of SRP, different analytical techniques have been advised including thin layer chromatography (TLC), X-ray powder diffractometry (XRPD), enzyme-linked immunosorbent assay (ELISA), high-performance liquid chromatography (HPLC), and ultraviolet (UV) spectroscopy. Meanwhile, some drawbacks still exist behind the successful application of these techniques. Although TLC technique is easy and fast for the qualitative measurement and identification of SRP, it has demerits like long plate running time and laboriousness. Furthermore, XRPD is very expensive, and the cost involved in purchase of the instrument and its upkeep may prevent its use for estimation of SRP is a simple routine tool. Moreover, although ELISA appears to be simple, it is very difficult to receive the antibodies against SRP. e cost involved to carry out a single analysis is a factor for the technique being widely used. In addition, requirement of specific column and solvents may limit the adequate utilization of HPLC for SRP determination. On the contrary, many studies revealed that UV spectrophotometric method was found to be precise, accurate, robust, simple, and economical for the determination of SRP alone and in combination with other drugs including aceclofenac, diclofenac, and nimesulide [3]. In addition, one of the advantages of the application of UV method over other analytical techniques is that the UV method does not require time consuming treatments and procedures usually associated with chromatographic methods as well as rapid analytical techniques in the early phase of product development [12,13]. e main objective of this research was to formulate stable enteric-coated tablets of SRP to prevent the degradation in gastric environment and develop and validate simple and cost-effective UV spectroscopy method for the determination of SRP.

Materials and Methods
2.1. Materials. Serratiopeptidase (SRP) powder was purchased from Biocon Limited, Bangalore, India. Isopropyl alcohol and methylene chloride were procured from ermo Fisher GmbH, Karlsruhe, Germany. Microcrystalline cellulose powder (MCCP) pH 101 and 102, colloidal silicon dioxide, crospovidone, magnesium stearate, and stearic acid were purchased from ermax Pvt. Ltd., India. Hydroxypropyl methyl cellulose (HPMC) phthalate 40 was obtained from Shandong Head Co., Ltd., China. e other coating materials were obtained as a gift sample from Colorcon Asia Pvt. Ltd, Industrial Estate, Goa, India. Marketed entericcoated tablet formulation of SRP was procured from local medical store and used as a reference sample. All the reagents and solvents used in the analysis were of analytical grade.

Determination of Wavelength of Maximum Absorption of SRP.
e 25-150 µg/mL of concentration range of SRP was dissolved in deionized (DI) water and the UV-visible spectrum of SRP was examined using UV spectrophotometer between 200 and 400 nm. Next, the derivative spectra of SRP at various concentrations were recorded. e interfering effect of all excipients on the maximum absorption was assessed by scanning the spectrum of each excipient alone and in combination with SRP. e maximum absorbance was observed at 265 nm.

Preparation of Standard Stock Solution of SRP.
Standard solution was prepared by weighing 50 mg of SRP accurately and then was transferred to a 100 mL volumetric flask and dissolved by adding 25 mL of DI water. e flask was allowed to sonicate for 15 minutes and volume was made up to the mark with DI water to give a solution containing 500 µg/mL of SRP.

Determination of Calibration Curve of SRP.
e required volume from the standard stock solution of SRP was withdrawn and transferred to a 10 mL volumetric flask. e final volume was adjusted up to the mark with DI water to obtain different concentration of SRP including 25, 50, 75, 100, 125, and 150 µg/mL. e calibration curve of concentration versus absorbance was plotted and then straight-line equation was determined.

Analysis of Formulated and Commercial Tablet
Formulation.
e developed method was also applied to determine SRP in formulated and marketed tablets. An average weight of SRP tablet equivalent to 50 mg was taken in 50 mL volumetric flask and volume was made up to the mark with diluents. From this, 5 mL was taken and transferred to a 50 mL volumetric flask and the final volume was made up to the mark with diluent to give a final concentration of 100 µg/mL. e absorption was recorded at 265 nm and the concentrations of the drug were calculated from the linear regression equation. e percentage assay and relative standard deviation (RSD %) of the SRP in tablets were calculated in triplicates.

Linearity.
e linearity and range of the developed method were analyzed by measuring the absorption of a series of SRP standard solutions (25-150 µg/mL) at λ max of 265 nm. e absorption of these standard solutions was plotted against different concentration. e regression line equation and the square of the correlation coefficient (R 2 ) were calculated.

Accuracy.
In this research, the accuracy of the method was determined by addition of standard drug to the sample at three different concentration levels (50, 100, and 150%) taking into consideration percentage purity of added bulk drug samples. It was determined by calculating the recovery of SRP by standard addition method. In addition, accuracy of the developed method in SRP enteric-coated tablet formulation was studied by the analysis of spiked samples at different concentrations as mentioned above.

Precision.
Precision studies were performed by analyzing standard solutions containing 50, 100, and 150 µg/mL on three different days by two different analysts as an interday precision. e absorbance of the solutions was examined and then standard deviation (SD) and RSD % were calculated. Moreover, to determine intraday precision, standard solutions containing 50, 100, and 150 µg/mL of SRP were analyzed three times on the same day. Next, absorbance of the solutions was examined and standard deviation (SD) and RSD % were calculated.

Limit of Detection (LOD) and Limit of Quantitation (LOQ).
e calibration curve was repeated for 6 times and SD of the intercepts was calculated using the following formula: where SD is standard deviation of Y-intercept of 6 calibration curves. Furthermore, SD intercept � SE intercept * √N. N is number of test samples. Slope is the mean slope of the 6 calibration curves [14,15].

2.4.5.
Robustness. e robustness of the method was evaluated by examining the different mixture of same concentration of samples to find out the effect of slight changes on absorption at wavelengths of 265 ± 1.0, and then average mean, SD, and RSD % of absorbance were determined.

Formulation and Development of SRP Tablets.
e core part of SRP tablets was prepared by dry mixing process followed by slugging using roller compactor prior to improving the powder flow properties of granules.
is process was performed without applying heat to avoid thermal denaturation. Slugging is a dry granulation that uses mechanical compression (slugs) or compaction (roller compaction) to facilitate the agglomeration of dry powder particles. e conformational changes in proteins that occur when they are heated are referred to as denaturation [16,17]. Before commencement of manufacturing process, MCCP pH 101 and 102 and crospovidone were allowed to dry at 100°C for 30 minutes. After drying, MCCP pH 101 and 102 and crospovidone were sieved through 30 meshes and half quantities of three excipients (colloidal silicon dioxide, purified talc, and stearic acid) were sieved through 60 meshes and mixed properly for 10 minutes. Subsequently, mixed powder was sieved through roller compactor as a slugging process and materials were passed through 20 meshes. Finally, remaining amounts of colloidal silicon dioxide, purified talc, and stearic acid were sifted through 60 meshes for lubrication. Consequently, lubricated granules were compressed in 8-station rotary compression machine using dies and punch having 7.4 mm diameter without break line.
To seal-coat the tablet, white shellac was dissolved in isopropyl alcohol (IPA) with continuous stirring for about 30 minutes and then castor oil was added in it and it was allowed to stir for 10 minutes. For preparation of enteric coating solution, HPMC phthalate 40 was dispersed in IPA with continuous stirring for 10 minutes and then methylene International Journal of Analytical Chemistry chloride was added in it followed by stirring continuously for 30 minutes prior to dissolving. Subsequently, ethyl cellulose (EC), castor oil, titanium dioxide, and Lake Erythrosine were added in this solution with regular stirring approximately for 30 minutes. In this study, coating of tablets was done using a side-vented, perforated pan coating apparatus machine. Firstly, weighed quantity (about 1.0 kg) of tablets was kept in the coating pan which was preadjusted at 40°C for 5-10 minutes and actual weight of tablet was evaluated. Secondly, tube was put in the coating solution, and then the various parameters including spray rate (8-20 mL/min), inlet air temperature (20-50°C), atomizing air pressure (1-3 bar), and the rotating speed of coating pan (8-15 rpm) were adjusted and optimized. Furthermore, after completion of coating, tablets were kept in the pan at 37°C and 3 rpm for curing. Finally, coated tablets were taken from the pan and the various parameters were assessed. Although EC is not an enteric coating material, this excipient was used in this study owing to its binding properties to enhance the hardness of tablet as well as to avoid drug release in gastric region. EC is water-insoluble cellulose having various appealing characteristics including biocompatibility, gastroresistance, and degradation to nontoxic and readily excreted components.
is material is widely applied in pharmaceutical technology because it is convenient for processing alone or in combination with other excipients such as plasticizers or other polymers [18]. Furthermore, due to the potentiality of EC to modify release rate of drug, it is extensively utilized as a coating agent. A study done by Shah et al. developed a colon targeted multiunit formulation of metronidazole using EC and Eudragit® S 100 as coating polymers to prevent initial drug release in the gastric region. e drug release was remarkably hindered by the outer ECbased coating layer [19]. Moreover, EC, on the other hand, has ethoxy functional groups with a very low propensity to react chemically.
is polymer, then, could provide the formulator good binding characteristics with low chemical reactivity [20]. e detailed composition of the tablet formulation is mentioned in Table 1 and the overall procedure was illustrated in flowchart shown in Figure 1.

Loss on Drying (LOD) of Granules.
After successful drying, approximately 5 gm sample was taken from tray dryer and poured in moisture analyzer (Sartorius MA37) containing weighing pan and distributed over its surface area and finally allowed to heat at 80°C. en LOD value of dried granules was reported from moisture analyzer.

Carr's Index and Hausner Ratio of Lubricated Granules.
After complete drying of moistened granules, lubricants were added and mixed properly for 5 minutes in order to enhance the flow properties of lubricated granules. e 10 gm sample of lubricated granules was poured in 100 mL measuring cylinder and tapped 100 times. Next, Carr's index and Hausner ratio of lubricated granules were determined. e ratio of tapped density to bulk density of the powders is called the Hausner ratio [21].

Weight Variation and Physical Specification.
Weight variation of the formulated tablets was evaluated according to USP method recommended for uncoated tablets. is parameter is performed by weighing 20 tablets separately and if it satisfies the criteria approved by official pharmacopoeia, test will be considered successful [15]. Tablet physical specifications such as hardness were evaluated by digital portable hardness tester (Electrolab, Model EH-01P), while thickness and diameter were examined by Vernier caliper (Electronic Express, model: 0604CAL6++). e test was performed on ten tablets; the average reading was assigned as the tablet hardness, thickness, and diameter specifications of the formulated tablets. In addition, for appearance examination, twenty tablets of each formulation were randomly selected to check any discoloration or degradation of drug in the tablets by visual method. If any discoloration or black spots appear, it shows the degradation or decomposition of drug in the tablet formulation [22].

Determination of Content
Uniformity. According to European Pharmacopeia (Ph. Eur.), for the assessment of content uniformity, 10 tablets were subdivided and ten different subdivided parts were randomly selected. e active content in each part was determined using a suitable analytical method. Ten tablets were finely powdered; amount of the powder equivalent to 10.0 mg of SRP was accurately weighed and transferred to a 100 mL of volumetric flask. Subsequently, the flask was filled with phosphate buffer pH 6.8 and mixed thoroughly. e volume make-up was done up to the mark with the diluent to give a final concentration of 100 µg/mL and filtered. Moreover, the absorbance of the resulting solution was measured at 265.0 nm using UV spectroscopy. Finally, the linearity equation obtained from calibration curve as mentioned previously was used for the estimation of SRP in the tablet formulations. e preparation complies with the test if each individual content is between 85.0% and 115.0% of the average content.  e dissolution of formulated SRP enteric-coated tablets was examined as per the USP and International Conference on Harmonization (ICH) guidelines. is study was performed using USP apparatus 2 (paddle). e drug release study was carried out in two different dissolution media, 0.1 N HCl (pH 1.2) and phosphate buffer (pH 6.8), according to USP. After temperature reached 37 ± 0.5°C, single tablet was added individually to separate dissolution dishes containing 900 mL of dissolution medium and run for 60 minutes at 50 rpm. Subsequently, 5 mL of the solution was withdrawn using syringes from each dissolution container at predetermined time intervals of 15, 30, 45, and 60 minutes. After each withdrawal, 5 mL of fresh dissolution media was added to maintain sink condition. e mean value obtained from triplicate measurements was taken to assess the percentage of dissolved SRP using the following formula [24]: % of dissolved SRP � actual amount of released SRP theoretical amount of SRP × 100. (3) e comparative evaluation of dissolution was established on the readings of the evaluated similarity factor (f2) and dissimilarity factor (f1) of the dissolution profile for the formulated and marketed SRP tablets. Moreover, the values for f1 and f2 were examined using (4) and (5), respectively. e f2 factor evaluates the vicinity between two release profiles and similarly f1 also calculates the difference between two profiles. R t and T t in the equations represent the percentages of drug dissolved at each time point for the reference (market tablet) and test (formulated tablet), respectively. e f1 value higher than 15 demonstrates significant dissimilarity, while the f2 value more than 50 reveals significant similarity [15,[24][25][26]. e release assessment of SRP enteric-coated tablets applied a calibrated dissolution apparatus with paddles at 50 rpm, and the bath temperature was maintained at 37 ± 0.5°C. It is suggested that, for all the enteric-coated tablets, they must tolerate simulated gastric fluid (pH 1.2) in the initial 2h followed by 1 h in simulated intestinal fluid (pH 6.8) according to the standard method, since SRP will hydrolyze in aqueous solution. erefore, in this study, we employed simulated intestinal fluid (pH 6.8) that consisted of 0.25% sodium dodecyl sulphate (SDS) as release medium. For  International Journal of Analytical Chemistry preparation of simulated gastric fluid, NaCl (3 g) was dissolved in about 1450 mL of DI water with continuous stirring and then pH was adjusted to 1.2 ± 0.1 with diluted HCl. Furthermore, the simulated intestinal fluid was also composed by dissolving potassium phosphate monobasic (10.2 g) and SDS (3.75 g) in a same 1000 mL of DI water and then pH adjusted to 6.8 ± 0.1 with 1 N NaOH. Finally, the volume make-up of each prepared fluid was done up to 1500 mL with DI water [27].
(a) Tolerance test in simulated gastric fluid (i) Tolerance test of SRP enteric-coated tablets was performed in 250 mL simulated gastric fluid (pH 1.2) with a paddle rotation of 50 rpm and with the bath temperature of 37°C. After 2 h, 5 mL sample was taken by syringes from each vessel and filtered through a nylon filter (0.45 m, 25 mm). After each withdrawal, same volume (5 mL) of fresh dissolution media was added to maintain sink condition. e mean value obtained from triplicate measurements was taken to assess the percentage of dissolved SRP using the formula mentioned in equation (1)

Accelerated Stability Studies.
Stability studies were carried out on optimized formulation according to ICH guidelines. e formulated tablet packed in blister strips was subjected to accelerated stability testing for 6 months as per ICH norms at a temperature of 40 ± 2°C and relative humidity of 75 ± 5%. Samples were taken at regular time intervals of 1 month for over a period of 6 months and analyzed for the change in color, hardness, drug content, and in vitro drug release in acid media (0.1 N HCl) by procedure stated earlier. Any changes in evaluation parameters, if observed, were noted [28]. Tests were carried out in triplicates and mean value of the observed values was noted along with standard deviation.

Statistical Analyses
Statistical analyses were performed with GraphPad Prism 5.0 (GraphPad Software, Inc., San Diego, CA). e data were evaluated using one-way analysis of variance (ANOVA) followed by Tukey's multiple comparison test. P < 0.05 was considered to indicate statistical significance. All results are expressed as mean ± standard deviation.

Linearity.
e SRP was found to be linear at 265 nm in the concentration range of 25-150 µg/mL in water, which was demonstrated in calibration curve. e obtained correlation coefficient (R 2 ) and regression equation were 0.999 and Y � 0.001x + 0.005, respectively. e linearity range of SRP is shown in Figure 2. Furthermore, Nirale and Menon in 2010 studied the stability of SRP over a period of 12 h in DIW and Tris and phosphate buffer at room temperature and 37°C. e study that measured enzyme activity using proteolytic activity measurement method demonstrated retention of SRP enzyme activity of higher than 90% in Tris and phosphate buffer at both temperatures for at least 8 h. However, the stability of SRP was significantly decreased in DIW [2].

Accuracy.
For accuracy determination, the mean recovery % (n � 3) of SRP were 99.9% (50% level), 100.3% (100% level), and 100.2% (150% level). Results demonstrate that the recovery of SRP in spikes standard solution at different concentration range was between 99.9 and 100.3% with lower relative standard deviation (≤2%), ensuring the accuracy of the established method (Table 2). In addition, spike recovery in prepared formulation at 50%, 100%, and 150% spike level with RSD percentage of 0.190% also demonstrated the accuracy of the developed method in the real samples. Next, spike of blank tablet matrix with three different concentrations of SRP of 25, 50, and 75 µg/mL at 50%, 100%, and 150% of SRP spike level also demonstrated the percentage recovery of 98.0-101.0%, demonstrating the accuracy of the method as well as no interference of matrix (data not shown).
e RSD values lower than 2.0% ensure the precision of the method [29].

Determination of LOD and LOQ.
e sensitivity of method was assessed by determining LOD and LOQ according to the formula mentioned in Section 2.4.4. e LOD and LOQ of SRP were found to be 5.28 and 16.00 µg/ mL, respectively. e results obtained are presented in Table 6. 6 International Journal of Analytical Chemistry 4.1.5. Robustness. Despite the same concentration (100 µg/ mL) of SRP, the three different wavelengths showed robustness below 2.00 RSD %, which is within the acceptance criteria. e obtained results are illustrated in Table 7.

LOD of Granules.
Among five formulations, F4 demonstrated low LOD (1.72), followed by F5. F1 and F3 revealed nearly same LOD. ere were not any noticeable difficulties for the compression of tablets in each composition. e detailed value of LOD is shown in Table 8.

Carr's Index and Hausner Ratio of Lubricated
Granules. F4 and F5 showed Carr's index of 9.40 and 9.75, respectively, which means that powder flow was excellent as compared to other formulations ( Figure 3). Moreover, F3 exhibited 17.2 (fair flow), followed by good flow properties of F1 and F2 [30]. e flow characteristics of granules were significantly improved after adding MCC pH 102 instead of MCC pH 101. Furthermore, F2 also showed Hausner ratio of 1.09, which illustrates its flow superiority as compared to other formulations (Table 8).      International Journal of Analytical Chemistry

Optimization of Formulation.
All five formulations were compressed at same weight (160.00 mg) followed by seal coating and enteric coating. In formulation F1, the tablets were prepared using single superdisintegrants, that is, sodium starch glycolate (SSG), but disintegration time and the powder flow from hopper were not satisfactory, while rest of the compression parameters were appropriately good. In F2, the ratio of disintegrant was increased and MCCP pH 102 was included in the formulation instead of MCCP pH 101 to overcome the previous issue. e flow properties of granules were improved and tablet was completely disintegrated within 10 minutes. However, tablet appearance was not smooth. Furthermore, glidant, disintegrant, and lubricant proportion were increased in F3 along with another disintegrant (crospovidone). Although each tablet parameter was in the desired range and F3 was shifted for coating, formulation F3 demonstrated drug release in acid media. Moreover, concentration of white shellac was increased in F4 but seal coating layer was not sufficiently attached and started to crack. To address coating issue in previous approach, the ratio of white shellac, ethyl cellulose, and castor oil was added more in F5 (Table 1). e SRP tablets attained 2.75% seat coat and weight gain was found to be in the range of 3.95 to 4.45 mg. Core tablets containing 2.75% were fully coated with barrier coating without any kind of coating defect. So, this proportion of coating on core tablet was optimized concentration of seal coating [30,31]. Moreover, tablets attained 6.74% as enteric coating and weight gain was observed to be between 9.82 and 10.48 mg. is ratio in F5 gave sufficient protection of core tablet in 0.1 N HCl and did not release approximately more than 1.50% drug. So, enteric coating formula of F5 was optimized for further study. e final appearance of tablets was pink colored, round, biconvex, and enteric-coated ( Figure 4). us, only F5 was preceded further including detailed examination of tablets from day 1 to 6 months as accelerated analysis.

Weight Variation and Physical
Specification. Some of the physical parameters of formulated tablet including appearance, weight, hardness, thickness, and diameter were determined as tablet specification. e average value of the tested parameters will be considered as tablet specification. e physical appearance and hardness of formulated tablet were observed for 6 months at both 25°and 40°C (with 75% humidity). e detailed data of the tested parameters are shown in Tables 9 and 10.
From the evaluation of weight variation, the observed average, minimum, and maximum weight of formulated SRP were 172.77, 171.50, and 178.10 mg, respectively, which were within the limit of 170.00 mg ± 7.50%. e average thickness and diameter were 3.97 and 7.42 mm, respectively (Table 9). Furthermore, no noticeable physical change of tablet was observed till 6 months of stability for both room temperature and accelerated stability. In addition, during day 1, hardness of formulated tablets was 23.02 and 22.87 kgf at 25°and 40°(with 75% humidity), respectively, and until 6 months this parameter is not significantly declined as compared to day 1 (P > 0.05). erefore, unchanged color of tablets and insignificant decline of hardness revealed that the formulated SRP tablet was physically stable until 6 months of stability in accelerated conditions. e overall findings are revealed in Table 10. Moreover, thickness of tablets was observed to be 3.94 ± 0.011 mm in 6 months' analysis of accelerated stability which was very close to initial measurements which further signified that formulated tablets were not gaining the moisture because tablets were not swelling during the stability period. In addition, crushed tablets demonstrated LOD 1.82 which was also almost same as original value. ese findings exhibited that the hydrolysis   problem may not appear in formulated tablets. Furthermore, to avoid the chances of hydrolysis, the tablets were prepared by dry granulation followed by alcoholic coating and packed in blister packaging. For products which are susceptible to hydrolysis, packaging may deliver an appropriate alternative for enhancing the stability of product. Previous study suggested that many blister packaging materials that were proper for moisture were poor for oxygen. Due to the higher surface area of a blister package per dose, permeation of moisture will be considered an issue under challenging conditions with all the blisters except foil [32]. However, still few studies are necessary for the confirmation of hydrolysis.

Content
Uniformity. e uniformity content test was also performed according to the Ph. Eur. e results showed that no tablet assay % was out of the limit (85-115%) [33]. e determined content uniformity % of 10 tablets is presented in Figure 5.

Dissolution
Profile. Drug release percentage in 0.1 N HCl was measured in different stability schedules including day 1, 1st month, 3rd month, and 6th month as accelerated stability analysis and its release % were compared with day 1. e ranges of dissolution in acid media were 0.85-1.59% (day 1), 1.45-2.47% (1st month), 1.56-2.55% (3rd month), and 1.95-3.34% (6th month). In acid media, from day 1 to 6 months of stability, SRP demonstrated the release profile within the limit of no     International Journal of Analytical Chemistry more than (NMT) 15.00%. No significant difference (P > 0.05) in acid uptake was observed until the 3rd month, while in 6th month the acid uptake % was remarkably higher (P < 0.05) as compared to day 1 which is considered as statistically significant, meaning that acid release was enhancing periodically but slowly ( Figure 6). Moreover, acid release was significantly higher in 6 months of accelerated stability but the overall release value was sufficiently within the limit (NMT 15%) which can be considered as a gradual degradation. e data observed in acid release demonstrated that the formulated SRP tablet was physically stable until the 6th month in accelerated stability. In addition, drug release in acidic medium becomes higher with lapses of time when stored under accelerated condition as revealed in Figure 6. is may be due to the weakening of polymer matrix present in the coating part of tablets as evidenced by the decline in hardness during stability studies as shown in Table 10. Although such changes are increased periodically, they can be considered as acceptable because observed values were within the range [34]. Furthermore, release rate of SRP formulated tablet in pH 6.8 phosphate buffer was compared with market sample excluding accelerated analysis. Both formulations revealed remarkable release profile until 60 minutes. e corresponding figures of formulated tablet and market sample were 106.00% and 93.00%, respectively ( Figure 7). However, the dissolution profile of the SRP formulated tablet revealed a slight dissolution improvement (13.00% higher) over the marketed SRP tablet. us, the dissolution findings exhibited that there was no statistical significance (P > 0.05) from 15 to 60 minutes between the formulated tablet and the marketed one.
In addition, in vitro release profile of SRP from entericcoated tablets was carried out in simulated gastric fluid (pH 1.2) for 2 h and findings are revealed in Table 11. e percentage of the residual content of SRP in enteric-coated tablets was determined in accordance with its initial amount. e results demonstrated that little amount of SRP was released from formulated enteric-coated tablets within 2 h of agitation. However, percentage of SRP released in simulated gastric fluid (pH 1.2) was 1.023-fold lower than market sample. Furthermore, no evidence of disaggregation, cracking, or melting was observed at the surface of enteric-coated tablets in simulated gastric fluid solution. Moreover, release profile of SRP from enteric-coated formulation and market sample over the period of 60 minutes in simulated intestinal fluid (pH 6.8) is revealed in Figure 8. Both samples showed significant release profile until 60 minutes. At 60 min, the formulated SRP tablets and market sample demonstrated 98.22% and 89.24% of drug release, respectively. In this medium, SRP tablets showed 8.98% higher dissolution as compared to market sample at 60 minutes. Interestingly, there was no significant variation in release profile of both formulated SRP and market sample in both phosphate buffer (pH 6.8) and simulated intestinal fluid (pH 6.8). us, the dissolution data showed that there was no statistical significance of drug release (P > 0.05) from 15 to 60 minutes between the formulated tablets and the marketed one in simulated intestinal fluid (pH 6.8) medium. Moreover, in this study, similarity factor (f2) and dissimilarity factor (f1) of optimized SRP entericcoated tablets and market sample were determined in both phosphate buffer (pH 6.8) and simulated intestinal fluid (pH 6.8).
e results of similarity factor (f2) applied in phosphate buffer (pH 6.8) and simulated intestinal fluid (pH 6.8) were 51.14 and 54.22, respectively. erefore, it was concluded that optimized formulation of SRP entericcoated tablets has shown good similarity (more than 50) with market sample. Furthermore, findings of dissimilarity factor (f1) in phosphate buffer (pH 6.8) and simulated intestinal fluid (pH 6.8) were 16.61 and 16.67, respectively. us, it was also further justified that an f1 value greater than 15 indicates significant dissimilarity between optimized SRP formulation and reference sample. In addition, SRP is soluble in water; therefore, in order to prevent it from hydrolysis during the preparation of enteric-coated tablets, it is suggested to adopt dry granulation or ethanol granulation method.

Determination of Assay.
e assay percentage of SRP was analyzed as per the procedure mentioned in Section 2.3.4. During day 1, the calculated assay for room temperature and accelerated analysis were 101.82 and 101.64%, respectively. Until 6 months of stability, both room temperature and accelerated stability analysis exhibited assay % within the limit. ere was no significant degradation in assay throughout the stability period. e corresponding figures for room temperature and accelerated stability were 99.32 and 97.91%, respectively, in 6th month's analysis. e overall mean RSD % was 1.51%. e detailed observations of assay are demonstrated in Figure 9.

Conclusions
In this study, enteric-coated tablet formulation of SRP was prepared and a simple validated UV method was developed for analytical determination and quantification of SRP in formulated tablets. e drug release profile of our formulated tablet at phosphate buffer (pH 6.8) and simulated intestinal fluid (pH 6.8) was relatively higher than the marketed sample of SRP tablet. e results of initial and accelerated stability until 6 months revealed that the formulated tablets were both physically and chemically stable. However, still adequate studies based on biological stability and hydrolysis are suggested to verify the stability and efficacy. From this study, it was concluded that, by employing commonly available pharmaceutical excipients such as diluents, superdisintegrants, and hydrophilic and hydrophobic polymers, a commercial enteric-coated tablet of SRP could be developed successfully. is study can contribute as a guide to the pharmaceutical companies to manufacture SRP containing dosage forms and apply validated analytical methods to assess its product quality.

Data Availability
No external data were used to support this study.

Conflicts of Interest
e authors declare that they have no conflicts of interest.