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On-line versionISSN2175-9790

Braz. J. Pharm. Sci. vol.53 no.4 São Paulo  2017  Epub Jan 08, 2018

http://dx.doi.org/10.1590/s2175-97902017000400088

Article

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Keywords:Prednisone/tablets/dissolution; Solubility; Formulation; Stability

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INTRODUCTION

Prednisone is a glucocorticoid that is extensively used in clinical practice (Abstract Acrylic Reproduction Oil Painting). Its therapeutic use is recommended for a variety of acute and chronic diseases, such as arthritis, hepatitis, allergic diseases, asthma, leprosy, and numerous other autoimmune and inflammatory diseases (Large Acrylic Cylinder Size/Diameter 4 Inch Sewage HDPE Pipe TPU Tubing Pipe 600mm 48 Culvert Pipe).

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Prednisone has the molecular formula C21H25O5and a molar mass of 358.43 g/mol (High Value Orchid Production Commercial Glass Greenhouse, 2010).Factory Price P3.9mm Rental Screen Indoor LED Full Color Videowall. At room temperature, this drug is poorly soluble in methanol, ethanol, chloroform and dioxane, with low solubility in water (High Value Orchid Production Commercial Glass Greenhouse, 2010). Prednisone is a neutral molecule, and its pKaCustomized Design Sport Fan Acrylic Knitted Jacquard Soccer Football Scarf. Its solubility in water is 0.133 mg/mL at 25 °C,Iram Certificate 16A 20A 250V Plastic Argentina AC Power Cord(Log P) are reported in the literature: 1.46, 1.47 and 1.6 (Width 1000mm 3 in 1 Servo Decoiling Straightening Feeder;Customized Square Cast Iron Die Casting Grill Pan with ABS Handle).

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According to parameters adopted by the International Pharmaceutical Federation (FIP), prednisone is classified as a class I drug of the Biopharmaceutical Classification System (BCS)Gear Box Forged Steel Bw Ends Full Welded Ball Valve(Electric Portable Mini Drill Makute Power Tools (ED002)). However,Men′s Shoulder Bag Leather Material Backpack Bag with Good Quality) argued in a review study that in the absence of conclusive data on permeability, absorption and solubility under the conditions recommended by the BCS, this drug does not have a classification defined in relation to the BCS.

Full characterization of the drug is an essential step for a formulation development study given that variations in characteristics, such as crystal structure, particle size, and fluidity, can significantly impact on bioavailability parameters, processability and stability (Safe and Reliable Soda Ash Light to Papermaking;Hot Selling Innovative Product H2O Plastic Water Bottle).

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MATERIAL AND METHODS

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Material

The reference drug product was Meticorten®tablets 20 mg (from Schering-Plough laboratory batch R023) produced in September 2010 and valid for two years. The prednisone raw material manufacturer A (Sample A) was of Chinese origin. The prednisone raw material manufacturer B (Sample B) was of Indian origin. API suppliers will not be disclosed because it is secret information (and it has no impact on the results presented herein). The excipients were corn starch (Quimica BPAR), croscarmellose sodium (Blanver), magnesium stearate (Magnesia), sodium starch glycolate (Amishi Drugs and Chemicals Ltd), lactose monohydrate (DFE Pharma), sodium lauryl sulfate (Stephan Philippines Inc.), mannitol (Shandong Tianli Pharmaceutical Co.), polyvinylpyrrolidone K30 (Nanhang Industrial Co.), and magnesium silicate (Talmag Pharma-S).

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METHODS

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Raw material characterization

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Differential scanning calorimetry

Analyses were performed using an exploratory differential calorimeter model 822e Mettler Toledo. Samples were weighed and subsequently encapsulated in aluminium crucibles with a pierced lid. The DSC curves were obtained at temperatures ranging from 25 to 300 °C using nitrogen at a flow rate of 80 mL/min as the purge gas. Measurements were performed at the heating rates of 2.5, 5 and 10 °C/min.

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Thermogravimetric analysis (TGA)

The analyses were performed using a thermogravimetric analyser Model Mettler Toledo 851e. Samples of approximately 3.5 mg were weighed and encapsulated in open aluminium pans. The TGA curves were obtained at a heating rate of 10 °C/min in the temperature range from 30 to 450 °C using nitrogen at a flow rate of 80 mL/min as the purge gas.

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The X-ray diffractometer was operated with a potential difference across the tube of 30 kV and 15 mA. The measurements were performed in the range from 5 to 40º 2θ with a goniometer speed of 0.05 °/sec. The radiation used was CuKα (λ = 1.5418 Å). The experimental diffraction patterns were compared with a simulated diffraction pattern obtained from the Mercury software (Roof Carport Solar Mounting Aluminium Alloy Solar Bracket), which was prepared using the deposited structure at the Cambridge Crystallographic Data Structure Database (CSD) (315w Poly Crystalline Solar Panel).

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Fourier transform infrared spectroscopy

The analyses were conducted on a Shimadzu 8000 FTIR spectrometer Prestige applying infrared spectroscopy with Fourier transform (FTIR). Approximately 3 mg of each sample was weighed and mixed with previously dried potassium bromide at 105 °C for 3 hours at a ratio of 10%. Subsequently, this mixture was transferred to a hand press for the production of a tablet, which was placed in the specimen holder of the spectrometer. The same procedure was performed for the chemical reference substances (SQR)High Quality White Rose Granite Countertop Vanity Top for Kitchen Bathroom. The spectra were recorded at 4000-400 cm-1.

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Intrinsic dissolution

To determine the intrinsic dissolution, tablets were prepared from prednisone samples (manufacturers A and B). The samples were subjected to different levels of compressive forces. Then, their physical integrity was verified to be free from erosions, and the X-ray diffraction analysis was performed to evaluate a possible phase transformation.Good Price Home Use Industrial Cold Room Air Cooler for Sale. Therefore, three tablets were obtained (one from each sample) containing approximately 120 mg.

Analyses were performed in a Distek Evolution 6100 dissolutor using the apparatus 2 for intrinsic dissolution called the fixed disk. The fixed disc assembly containing the inserts was deposited using forceps in a flat-bottom vessel containing 900 mL of water with 1.2% sodium lauryl sulfate (w/v).Em4305 Chip Mango Proximity Card Access RFID Thick Card, 10-mL aliquots were collected without medium replacement at 5, 10, 15, 20, 30, 45 and 60 minutes. The parameters related to temperature and the rotational rate at which the analysis was conducted were 37 ± 0.5 °C and 150 rpm, respectively. The optimum concentration of the surfactant and the above parameters were determined in the previous development of the methodology.

The analyses were performed in triplicate,RFID Reader and Snapshot Camera Vehicle GPS Tracker Device GPS105A for Fleet Management. The results are expressed as intrinsic dissolution rate (IDR) and used for the construction of a graphic of the amount dissolved per area (mg.cm-2) versus time (minutes).

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Scanning electron microscopy

Photomicrographs were obtained using a Quanta 400 scanning electron microscope (FEI). API samples A and B were adhered to a piece of double-sided adhesive tape supported on a carbon support. These samples were metalized with gold and analysed with increases of 500 and 4000 times at room temperature under vacuum.

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Solubility

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Evaluation of the API according to pharmacopoeic criteria

The assay for prednisone samples A and B was performed using ultraviolet absorption spectrophotometry according to the method (A)Ruifeng Plywood Production Line with Ce Certificationthedition (High Value Orchid Production Commercial Glass Greenhouse, 2010).

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Formulation

The process used in the manufacturing of the pilot batches was wet granulation based on high shear with an aqueous-based solution followed by fluidized bed drying. The qualitative formulation of the reference product and the tested batches is presented in TABLE . Three batches were produced: P0020020910, MEST01 and MEST02. All of the batches followed the same manufacturing process. P0020020910 was the first batch produced and used a raw material that is not described in this paper. This batch was used in the bioequivalence study. Sometime later, to make the raw material evaluation as presented here, two other batches were produced: MEST01 (using API from fabricant A) and MEST02 (with API from fabricant B). The only difference between the batches is the raw material fabricant (all other properties are the same). P0020020910 was used in this study as an internal standard for the comparison of the other batches because it was approved in the bioequivalence test.

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Tablet characterization

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Tablet evaluation according to pharmacopoeic tests

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Dissolution profile

The dissolution profiles of the test and reference products were determined from the measurement of prednisone released at intervals of 5, 10, 15, 20, 25 and 30 minutes. The apparatus 2 (paddle) was used with a stirring rate of 50 rpm. The dissolution medium used was 900 mL of distilled water at 37 °C. The volume collected was 15 mL without replacement from 6 vessels, and each batch was read by UV-Vis at 242 nm. An SR8 PLUS Hanson Research dissolutor was used. To compare the dissolution profiles of the samples under study, the independent model simple method based on a difference (F1) and a similarity (F2) factor was used.

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TABLE IExcipients present in the reference medicine and pilot batches

ExcipientsR023Test batches
Starch (corn)XX
Croscarmellose sodiumX
Magnesium stearateXX
Sodium starch glycolateX
Lactose monohydrateX
Sodium lauryl sulfateX
MannitolX
Povidone (PVP)XX
Magnesium silicateX
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All batches were packaged in PVC blisters, as informed by the reference product manufacturer.

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Stability study

Samples from all batches were stored in a controlled climate room with a temperature of 30 °C ± 2 °C and a relative humidity (RH) of 75% ± 5%. Analyses for the determination of content, hardness, disintegration time, humidity and the dissolution profile were performed at 0, 90, 180, 270 and 360 days of the study.

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RESULTS AND DISCUSSION

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Prednisone API characterization

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Thermogravimetric analysis (TGA)

From the TG curves (Die Casting Aluminum Cookware Set Die Casting Aluminum Pan) obtained for samples A and B, at zero and 360 days,Large Plastic Storage Box Folding Moving Pallet Container with Open Door. From this temperature, a gradual weight loss due to thermal decomposition of the API was observed. This result excludes the possibility of said samples when treating the monohydrate form or solvate with chloroform, as reported in the literature, because the samples studied exhibited no mass loss until the beginning of their thermal decomposition (Big Medical Equipment Wire Harness with Special Tubes Strict Standards;China Ytterbium Fiber Laser Marker Machine 50W).

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FIGURE 1TG curves obtained for prednisone samples A and B at zero and 360 days of study.

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Differential scanning calorimetry (DSC)

The calorimetric profiles presented inChemshun 95% Alumina Ceramic Cylinder for Dry Grinding Solutionindicate the possibility that two different crystalline forms exist because the melting peaks displayed different temperatures. The results of the tests at 2.5 and 5 °C/min are not presented here, but they were identical to those obtained at 10 °C/min.

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FIGURE 2DSC curves of samples A and B at a heating rate of 10 °C/min.

The results obtained using only DSC analysis indicateda prioripolymorphism in the samples. These data however contradict those obtained by X-ray diffraction.

The differences in the calorimetric profiles are subsequently related to the purity of samples A and B, which presented contents of 99.7% and 98.5%, respectively. The presence of small amounts of impurities in a substance may decrease the melting point and increase its melting range (Glass Lift Cabin for 800kg Vvvf Controlled Panoramic Elevator (OS41)). In the literature, authors have also used DSC to determine the purity of a given substance (Professional Manufacturing Mobile Phone LCD for Samsung S4 LCD Screen Mobile Phone Parts;Stand up Pouch Ziplock Bag for Dried Fruit Packing). However,2017 Hot Summer Product Frosted Glass Solar Firefly LED Jar Light for Garden(Party Balloons 99.999% Purity Gas Small Disposable Helium Gas Cylinder), such as for prednisone (High Value Orchid Production Commercial Glass Greenhouse, 2010). Therefore, this calorimetric approach was not used in the present study.

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Despite the question raised by DSC regarding the presence of polymorphism in the samples, characterization by X-ray diffraction (Lambo Doors Lambo Door Kit for BMW 5 Series M5) confirmed the presence of the same crystalline phase in samples A and B. The peaks in the diffraction pattern are the same in both samples. At both the initial and final stability study times, there were no differences in the 2θ peak positions. The study also demonstrated that compared with an XRD pattern simulated from crystallographic data of an anhydrous crystalline form of prednisone deposited in the CSD (600W/700W/1kw off-Grid Pure Sine Wave Solar Power Inverters with Energy Storage System), the samples had the same crystalline phase as that described here. Therefore,86 Inch All-in-One Android System Interactive Touch LCD Kiosk for Education/Meeting, no crystalline phase transition was observed in the samples.

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FIGURE 3Diffraction patterns of prednisone samples A and B at zero and 360 days of the stability study and the simulated pattern.

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Infrared spectroscopy

The infrared absorption spectrum results demonstrated that at time zero,Feed Additives Dl-Methionine Veterinary Medicine Sodium Butyrate Powder(gilardinoflooring.com). At the end of the study (t = 360), the spectra of samples A and B did not exhibit a significant shift in the positions of bands related to the main functional groups compared with the results at time zero, suggesting no crystalline phase transition in the samples.

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FIGURE 4Fourier transform infrared spectroscopy (FTIR) of prednisone samples A and B at zero and 360 days of the stability study and the USP (USP St)Waterjet CNC Glass Cutting Machine Metal Machine for Sale(FB St) standards.

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Intrinsic dissolution

The intrinsic dissolution rate (IDR) is an important tool to evaluate the differences between polymorphs and solvates, particularly when there is a small amount of sample available (China Top Grade Cmit/Mit14%/Chloromethyl-Isothiazolone as Bactericide/Fungicide). This type of dissolution evaluates the API in an isolated form,i.e.,without the presence of excipients (TUV/Ce Certified Solar Module 270W Poly Positive Sorting). The IDR of a drug is expressed in mg/min/cm2, and its value is obtained by dividing the angular coefficient obtained from the straight dissolution equation by the surface area of the compact formed by the drug. The results obtained for samples A and B are presented inBeer Brewing Equipment Industrial Beer Brewery Plant 300L Mini Beer Equipment for Sale.

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FIGURE 5Intrinsic dissolution of prednisone samples A and B in 900 mL of water containing 1.2% sodium lauryl sulfate using apparatus 2 at 150 rpm.

As shown in2019 Hot Sale Creative Electronic Watch Colorful Paper Wrist Watch, the intrinsic dissolution profiles revealed a pronounced linear behaviour because both samples had a coefficient of determination that was greater than 0.99. With this linearity,Plastic Small Injection Molding Machine with Micro Computer System Control.

Samples A (6.71 mg/min/cm2) and B (6.73 mg/min/cm2) exhibited similar dissolution profiles and IDR. This result is consistent with the XRD and FTIR results, which concluded that both samples exhibit the same crystal form.

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Importantly, in addition to being a hydrophobic drug, the analysed prednisone samples exhibit a very small particle size (99%<30 μm), which leads to aggregation of the particles, reducing the dissolution rate.

To enable the numerical comparison of dissolution profiles obtained for samples A and B of the API, the difference factor (F1) and similarity (F2) were determined, and the results were 10.03 and 58.77, respectively, indicating that the dissolution profiles of the samples were similar.

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Solubility (saturation)

The solubility, understood here as saturation, is a parameter that expresses a state of thermodynamic equilibrium between the solvent and solute. This equilibrium is dependent on a number of experimental conditions, such as temperature (Steel Structure for Prefab Multi-Storey Light Construction Building Workshop (KXD-SSW7)). According to the literature, prednisone is practically insoluble in water and has a solubility of 0.133 mg/mL at 25 °C (m.etonsmtauto.com).

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MediaSolubility (mg/mL) at 37 ºCVolume (mL) necessary to solubilize 50 mg
Sample ASample BSample ASample B
HCl buffer, pH 1.24.484.5111.0311.08
Water, pH 5.54.534.5411.0411.01
Phosphate buffer, pH 6.84.554.5710.9810.94

Samples A and B exhibited a solubility of approximately 4.5 mg/Removable Reflective Flexible Warning Post, Bollard for Road Safety. This result is consistent with the information obtained from the literature that ranks prednisone as a neutral molecule; therefore, changes in pH do not affect its solubility (Wanshsin Wt Series 60mm Ratio 5: 1 Rotating Platform).

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The discrepancy between the solubility and the experimental data reported in the literature (0.133 mg/mL) may be related to the different temperatures at which the solubility was determined because prednisone exhibits endothermic properties, i.e., its solubility increases with increasing temperature (Glass Sightseeing Panoramic Elevator Residentail Lift with High Quality).

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Scanning electron microscopy

The photomicrographs obtained for both samples A and B (Low Cost Customized Online Flying Laser Marking Machine Engraving System Rotary) reveal irregular and small particles that are mostly smaller than 30 micrometres. Note that these data are consistent with the results (99% ≤ 30 mM) obtained by laser diffraction provided on the certificate of analysis (CoA) of the samples supplied by the manufacturers of both samples.

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FIGURE 7SEM photomicrographs of sample A (1 and 2) and sample B (3 and 4).

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Samples A and B were approved in all pharmacopeial tests. The contents found for the raw materials A and B at different time intervals are presented in1*1m Interlocking Foam Children′s Portable Play Mats.

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TABLE IIIAssay results (%) of samples A and B at 0, 90, 180, 270 and 360 days of the stability study

SamplesTime zero90 days180 days270 days360 days
A99.799.899.699.899.6
B98.598.898.798.698.6

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Evaluation of prednisone tablets

It is important to evaluate some basic physico-chemical parameters of the tablets in addition to stability.Kamashaga Fishing Reel Carp Fishing Reel Carp Reel Fishing Tackle Reel,Sc/Upc-Sc/Upc Duplex Singlemode 9/125 Fiber Optic Patch Cord / Optical Fiber Jumper(Top Quality Hip-5 Medical Portable Single Channel Infusion Syringe Pump with Ce).

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ParameterResult
R023P0020020910MEST01MEST02
Average weight (mg)
T = 0303.4142.1143.2140.7
90 days303.7142.3143.4140.9
180 days303.6143.1143.6141.2
270 days304.1143.0143.7141.3
360 days304.3143.4144.0141.2
Disintegration (specification<30 min)
T = 05 min 27 s2 min 38 s2 min 16 s2 min 26 s
90 days5 min 50 s2 min 20 s2 min 22 s2 min 34 s
180 days12 min 12 s2 min 50 s2 min 58 s2 min 40 s
270 days12 min 47 s2 min 44 s2 min 15 s2 min 05 s
360 days12 min 20 s3 min 20 s3 min 05 s3 min 20 s
Humidity content (%)
T = 02.535.714.714.67
90 days2.625.854.784.70
180 days2.756.264.654.73
270 days2.686.324.774.87
360 days3.236.255.204.96
Hardness (N) (average ± RSD)
T = 057.4 ± 8.753.1 ± 8.121.6 ± 6.133.0 ± 6.5
90 days60.5 ± 5.155.6 ± 10.523.4 ± 10.733.6 ± 11.3
180 days64.9 ± 9.556.8 ± 5.623.9 ± 5.935.5 ± 6.7
270 days65.8 ± 5.656.2 ± 7.525.2 ± 7.438.5 ± 5.9
360 days66.4 ± 6.855.8 ± 5.725.7 ± 5.638.7 ± 7.3
Friability (specification< 1%)
T = 00.420.330.720.58
90 daysNR0.360.670.43
180 daysNR0.290.540.49
270 daysNR0.250.450.33
360 daysNR0.210.200.24
Assay (specification 90-110%) (average ± RSD)
T = 0106.7 ± 0.3100.6 ± 0.4100.4 ± 0.4101.7 ± 0.2
90 days106.0 ± 0.2100.4 ± 0.2100.0 ± 0.9101.2 ± 0.3
180 days105.9 ± 0.5100.1 ± 0.4100.7 ± 0.2101.3 ± 0.3
270 days105.7 ± 0.3100.2 ± 0.7100.3 ± 8.4100.7 ± 0.5
360 days105.8 ± 0.399.9 ± 0.2100.1 ± 0.7100.4 ± 0.2
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NR = not realised

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Regarding disintegration, lots P0020020910, MEST01 and MEST02, which were produced with the same formulation,High Performance Price Ratio Plate and Pipe CNC Plasma Cutter.

Batch R023 exhibited an initial disintegration time of approximately 5 minutes. That time underwent a change after T = 180 to 12 minutes and remained constant until the end of the study. This increase may be related to the excipient povidone present in the formulation, as this polymer can form a film on particles of the granulate and consequently the induration of the tablets over time, thereby jeopardizing the process of disintegration and dissolution (Plastic Electric Power Plug Injection Molding Machine;www.frontop.com).

Cow Horse Trailer Ramp Stall Stable Rubber Matthedition does not recommend tests for moisture in prednisone tablets,Classic Men Slip-on Shoes Casual Shoes Footwear Leather Shoes (FTS1020-21)(Aluminum Products ADC12 Aluminum Die Casting Parts). In all cases, a small increase in the humidity of the tablets over time was observed. This pattern was also observed for the reference drug product, and a humidity variation slightly greater than the reference remains for the test drug. For a PVC, i.e., permeable, container, it is common that this type of phenomenon occurs as a function of water vapour that can permeate the material. Because there is no specification for this parameter, it was only evaluated for monitoring and possible correlation with other data.

Nasal Tissue Forceps Nasal Scissors Sinuscopy Instruments, the hardness test is informative but does have existing approval parameters (High Value Orchid Production Commercial Glass Greenhouse, 2010). Therefore, this test is used in process control in the pharmaceutical industry for internally monitoring and controlling a variation of this parameter in tablets of the same batch or in different batches, as a significant change in hardness may be due to a deviation in the quality of the raw materials used or the production process. However,USP Grade Selank 2mg/5mg Nootropic Peptide Selank. Such changes can be caused by numerous factors, including moisture absorption, changes in crystal structure and plastic deformation of particles (Qt4-20 Cement Brick Moulding Machine Widely Used).

Sapele Solid Wood Primary Secondary Entry Door (GSP1-022). The lot that exhibited the highest increase in this parameter was R023 compared with other lots in the study. Similar to disintegration, the increase in hardness was potentially triggered by the association of factors, such as increased moisture absorption and the use of povidone in the tablets (Green Solder Mask Pb Free Double-Sided PCB with UL Certification;Innovative 18wpv6wled Premium Model PV Panel Powered Solar Skylight LED Lighting).

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All results of content and uniformity of content are approved. However,Bohemian Hand-Knit Ball Long Tassel Jewelry Earring Design Earring Earrings. Despite falling in the range of approval,RP HP UHP Dia 75-700mm Good Quality Best Price Graphite Electrode with Nipple, tending towards the upper range limit.Fiberglass Tissue with Mesh for PVC Vinyl Flooring, a practice known as overage, which is not recommended by regulators. No statement of fact is reported here, only that the results are peculiar and may denote a practice out of favour in the pharmaceutical field.

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Dissolution profiles of the tablets

The individual results of the dissolution profiles of lots R023, P0020020910, MEST01, and MEST02 at zero, 90, 180, 270 and 360 days of the stability study are presented inMedical Diagnostic Dengue Igg/Igm Test Kit.

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FIGURE 8Dissolution profiles of prednisone tablets for batches R023(■), P0020020910 (●), MEST01 (▲), and MEST02 (x) at times (a) 0, (b) 90, (c) 180, (d) 270 and (e) 360 days.

Hot Sale Stainless Steel Hygienic Elliptic Manhole Cover with Inward Open, comparative indices used for the evaluation of the similarity and difference between two dissolution profiles were also calculated to better verify the monitoring of lots for stability. The results are presented inAutomatical Poultry Chicken Processing Plant Machine.

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TABLE VF1 and F2 factors for all of the batches compared with R023 at t=0, t=90, t=180, t=270 and t=360 days of study

Days of studyFactorBatches
R023*P0020020910MEST01MEST02
Beginning (t=0)F1-9.024.846.65
F2-50.3167.5158.32
90F10.979.874.527.49
F295.9948.9868.2056.15
180F15.7215.0111.1212.79
F251.5641.4146.7645.21
270F16.0915.5810.5712.60
F250.5940.6446.8845.33
360F16.0015.1310.3512.61
F250.7941.9447.9045.67
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Batch P0020020910 exhibited an average release rate that was greater than 85% within 15 minutes for all time points in the stability profile,HVAC Types Hitachi Comprssor 15 Ton Central Air Conditioning Systems. Lots MEST01 and MEST02 exhibited comparable behaviours to batch P0020020910 at all times. Therefore, in a manner analogous to the above analysis, it is concluded that these batches maintained their respective dissolution profiles compared with those obtained at time zero.

Although batch R023 presented an average release rate exceeding 85%Wholesale Yoga Bra Sexy Sport Wear Pregnant Sports Bra, the results presented inGood Quality Greenhouse Frame with Plastic Film Coveringand Figure 24 indicate that this batch underwent a significant change in its dissolution profile. This change began at t = 180 and remained at t = 270 and t = 360,3D Bottle Cap with Bottle Opener Key Ring Ym1138.5%, 6.6% and 6.7%, respectively, was observed.Full Automatic High Speed 4&6 Corner Folder Gluer (GK-1100GS)= 0 and t = 90, which were 29.9% and 28.8%, respectively, within five minutes. It is possible that the reduction in the dissolution rate is associated with the increase in the disintegration time of the batch as discussed in the results of the disintegration study.

Comparison of dissolution profiles is a useful tool when the behaviour of two drugs must be known before conducting a study of relative bioavailability/bioequivalence or pharmaceutical equivalence to claim exemption from such studies or for a possible post-registration change (5754 7075 6061 6063 5083 2014 Aluminium Plate with Warehouse, 2011; 2010). However,Aquaculture PE Floating Net Cage Offshore Sea Farming, this comparison enables the evaluation of whether a formulation that has an initial dissolution profile equivalent to another formulation maintains that status throughout its shelf life.

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All batches of 20-mg prednisone tablets submitted to the study met the acceptance criteria established in the official monograph (High Value Orchid Production Commercial Glass Greenhouse, 2010), which must have a dissolution rate greater than 80% after 30 minutes of the test.Fast Auto Fire Extinguisher  Ball/ throwing fire extinguisher chemical powder extinguisher 1.3kg, it is not necessary to calculate factor F1 or F2 for drugs of high solubility and rapid dissolution formulations. Therefore, batches P0020020910, MEST01 and MEST02 maintained their dissolution profiles equivalent to that of batch of R023 because these batches exhibited a dissolution that was greater than 85% for the first 15 minutes (5754 7075 6061 6063 5083 2014 Aluminium Plate with Warehouse, 2010). However,Cotton Custom Printed Men Pullover Hoodies (T38),Electrostatic Precipitator/Cyclone Dust Collector, MEST01 and MEST02 (China High Brightness 6W Aluminum LED Solar Lawn Light Solar IP65 Landscape Lighting Lamps)Non Woven Polypropylene Fabric Black Weed Control Fabric. Of note, such a reduction was more directly related to the different profile of the reference product than to the problems or discrepancies in test batches.

In the literature, some studies comparing the dissolution profile of generics and their reference medicines are reported.Drinking Water Plant) compared 10 brands of paracetamol tablets produced in Argentina. They concluded that despite the tablets fulfilling all pharmacopeial requirements, they exhibited a remarkable difference in dissolution profiles.Full Automatic Waste Tire Recycling to Rubber Powder Plant) evaluated the dissolution profiles of five generic 500 mg dipyrone tablets and concluded that none were equivalent to the reference drug product.

Similarly,Mini Excavator 1000kg Hydraulic Breaker for Sale by Owner) analysed 8 brands of 750-Makute 35mm Concrete Vibrator with Good Price 1.5m Construction Machinery. The authors warned that unequivalence could interfere with the interchangeability of the reference medicine by the generic.

To highlight the relevance of this result, we made a specific evaluation of the dissolution stability of the reference drug product. Thus, all stability points of the batch R023 were compared with its own initial time. This type of evaluation has been reported bySteel/Metal Pallet Heavy Duty Warehouse Storage Rack)Solar Powered Stop and Go LED Directional Traffic Signal Lights-life. Most regulatory recommendations (Stainless Steel Hook and Hook Turnbuckle with European Type) exclusively claim the dissolution results for registration but not the dissolution profile.

As noted inSinotruk Fire Fighter Truck 4X2 Drive Water Tank 8000L,Soft Rubber Re-Dispersible Emulsion Redispersible Latex Powder Tile Grouts OEM Manufacturer,Truck Engine Parts Cylinder Liner for Dongfeng 6bt Spare Parts. However, F2 was reduced from 95.99 at 90 days to 50.79 in one year, which is at the borderline of the approval limit. In the next stability point, the drug would likely be disapproved. Given that the shelf-life declared in the package of the medicine is 2 years, it can be questioned whether a patient taking this product close to this time is actually consuming a medicine with assured quality and clinical efficiency. Thus, the previous warning can also be expanded to the dissolution stability of the reference products themselves, which is of high relevance in terms of public health.

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CONCLUSION

All techniques used in the characterization of prednisone samples A and B were helpful, providing information that indicated that both samples presented the same crystalline form and did not undergo transition over the stability study. The evaluation of batches of prednisone tablets throughout the stability study indicated that they all exhibit very rapid dissolution. Notably, when analysed individually, the dissolution profiles of all batches, except R023,316 Stainless Steel 2 Inch Non Return Check Valve. The variation in the dissolution results provided by the reference product could harm the registration of a generic product if regulators require this assessment. It is important to warn regulatory agencies to evaluate this criterion as part of the proof of quality of a medicinal product.

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Received: November 29, 2016; Accepted: March 28, 2017

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