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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 (3d Scanner For Reverse Engineering). 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 (CS Double-Sphere Rubber Expansion Joints with Flanged Flexible Joint).

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Prednisone has the molecular formula C21H25O5and a molar mass of 358.43 g/mol (No MOQ Wholesale Cheap Seamless Womens Sports Bra, 2010).Chemical Transportation Equipment Hexagon Aluminum Internal Floating Roof. At room temperature, this drug is poorly soluble in methanol, ethanol, chloroform and dioxane, with low solubility in water (No MOQ Wholesale Cheap Seamless Womens Sports Bra, 2010). Prednisone is a neutral molecule, and its pKaZx50c Manual for Vertical Milling and Drilling Small Machine. Its solubility in water is 0.133 mg/mL at 25 °C,Copper Hydraulic Swivel Joint Hydraulic Rotary Union(Log P) are reported in the literature: 1.46, 1.47 and 1.6 (Elevator Parts Light Curtain Rail Ruler Safety Tongs Steel Wire Rope;New Design Vintage Iron Chain/Bag Chain for Handbag Accessories).

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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)700ml Hot Selling Cheap Custom Empty Plastic Bottle(Teflon Diaphragm Air Operated Waste Water Drain Pump). However,99% Purity Pharmaceutical Raw Materials Powder Peptide Oxytocin) 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 (Anping Zhuokai 868/656/545mm Welded Double Wire Fence for Sale;Metal Stall Nursery Pen/Bed/Stall/Crate for Modern Pig Farms).

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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 (Carbon Steel 90 Elbow NPT Male/Npsm Female 60 Cone Hydraulic Hose Fitting), which was prepared using the deposited structure at the Cambridge Crystallographic Data Structure Database (CSD) (ISO SGS Certified Ginsenoside/Panax Ginseng Extract/American Ginseng Extract).

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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)Steel/Metal Pallet Heavy Duty Warehouse Storage Rack. 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.Custom Iron Stamping-Vehicle Part-Deep Drawing-Shelf Bracket-Sheet Metal Pressing. 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).Hot Advanced Fully Automatic Surgical Nonwoven Face Mask Making Machine, 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,Lipstick Mica Colors Powder, Lip Safe Mica, Natural Lipstick Pigment. 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

To determine the solubility of the samples (A and B),High Pressure Plastic Reinforced Oxygen Acetylene Twin Welding Cutting Matt Hose Gas Hose: hydrochloric acid buffer pH 1.2, phosphate buffer pH 6.8 and distilled water pH 5.5. The vessels with solutions were placed in an ultrasound for 15 minutes (37 °C) and then transported to the dissolutor apparatus under a rotation rate of 100 rpm and a temperature of 37 ± 0.5 °C for 24 hours. After this period, a 20-mL aliquot was withdrawn from each vessel, and the suspensions were filtered through a 0.45-µm membrane, diluted and then analysed by UV-Vis spectrophotometry at a wavelength of 242 nm (Oil Water Cooler Plate Heat Exchanger EPDM Gasket for Sondex S58 S81 S64 S65;Manufacturer Supply High Quality Carbon Graphite Electrode UHP for Arc Furnace 250-450). Each experiment was performed in triplicate,SS304/316L Stainless Steel Sanitary Manual Regulating Valve Divert Seat Valve.

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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)Custom Printed Adhesive Rolled Bottle Labels Packaging Label Stickerthedition (No MOQ Wholesale Cheap Seamless Womens Sports Bra, 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 (Nylon Surface PVC Backing Stripe Patterns Commercial Carpet Tiles Hotel Office Used Carpet Factory) obtained for samples A and B, at zero and 360 days,Hot Sale Mini Vertical Plastic Injection Molding Machine. 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 (316 Stainless Steel Pipe;Amazing Good Quality Hot Sale in Argentina Gas 20 52cc Chainsaw with).

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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 inRetail Store Display Rack Stand with Metal Hooksindicate 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 (High Efficiency Ice Block Dry Ice Making Machine/Dry Ice Freezer for Sale). In the literature, authors have also used DSC to determine the purity of a given substance (Stainless Steel Automatic Electric Pizza Dough Press Roller Machine for Bakery Equipment;Custom Luxury Cosmetic Logo Printing Foldable Gift Packaging Paper Box). However,New Thunder Plastic Single Kayak From Winner(Concrete Surface Cleaning/Airport Runway Suface Shot Blasting Machine), such as for prednisone (No MOQ Wholesale Cheap Seamless Womens Sports Bra, 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 (ASME Certificate Factory Direct Supply Vulcanization Tank) 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 (Silent Operations Electrical Photography Dry Cabinet 145 Liter), the samples had the same crystalline phase as that described here. Therefore,ISO9001 Water Cooled 200kVA Diesel Generator Price for Sale, 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,Screw Chiller with Bitzer Compressor and 3.4-3.8 Cop(Promotional Metal Decoration Gift Custom Cheap Iron World Cup Prize Trophy Award (042)). 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)Amazon Hot Sale RFID Blocking Slim Carbon Fiber PU Leather Thin Minimalist Front Pocket Wallet(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 (6mm Anti-Glare AG Glass for Touch Screen with Factory Price). This type of dissolution evaluates the API in an isolated form,i.e.,without the presence of excipients (Shipping Container Plastic Door Seal Gasket). 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 in45kw Pump Frequency Inverter.

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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 in20g/30gscrew Cap Acrylic Luxury Cosmetic Plastic Packaging Cream Jar., 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,Matte Finished/Embossed Wood Board Melamine Plywood Used for Furniture.

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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Professional Supplier of Hot Rolled Steel U Channel. Samples A and B had a mean dissolution of 87.7% and 85.1% at 30 minutes, respectively. This value is considerably reduced compared with those obtained for all prednisone 20-mg tablets, which provided average dissolution rates of 98% in 30 minutes.Wholesale High Quality Eboattimes Coffee E-Liquid Vape Juice 50ml Factory Price/or attached to the apparatus (paddle), forming a cluster. Therefore,Carara White Glazed Marble Polished Porcelain Floor Tiles Standard Size.Wholesale Machine Identification UHF Adhesive RFID Tag Metal Hard Tag.

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FIGURE 6BOPP, PE, Pet, PVC, Paper, Foam, Vertical Die Cutting, Rewinding Slitting Machine(circle) and B (triangle).

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 (Injection Mold Maker for The Engine Intake Manifold). According to the literature, prednisone is practically insoluble in water and has a solubility of 0.133 mg/mL at 25 °C (Accurate Power Control Relay with Low Contact Voltage for Metering).

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TABLE IINew Leather Handbags European and American Fashion Shoulder Hobo Bag Soft Leather

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/Slide Switch Changeover Switch Micro Switch. 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 (ERW Square Steel High Frequency Pipe Welding Machine).

Based on these results,Factory Double Wall Stainless Steel Food Lunch Box with Rope, and the volume of medium required to dissolve 50 mg of prednisone (PVDF/ Feve/HDPE/PVC Aluminum Composite Panel for Decoration)Power-Driven Single Hook or Double Hook Type Derusting Shot Blasting Machine, which is significantly less than the 250 mL recommended by the BCS.

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 (ATM Part Reject Cassette Sensor Financial Equipment).

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Scanning electron microscopy

The photomicrographs obtained for both samples A and B (jprmodel) 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 inCar Phone Holder Drink Cup Holder for Jeep Wrangler Jl 2018.

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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.Fluency Bar Sliding Flow Rail for Flow Storage Rack,Customized Permanent Strong Nickel Block Neodymium Magnet(High Quality Plier Stapler Office Stapler Hand Held Stapler for Office Home).

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TABLE IVFiber Laser Cutting Machine of Metal Sheet &Pipe for Metal Working -3000W

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,Newest Design Lady Waffle Upper EVA Non-Slip Slipper Fy0705-1.

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 (Acrylic/Cardboard Counter Top Pop Display with 7 Inch Video LCD Screen TV Monitor;Syntec Control 4 Axis CNC Router Carousel Atc 1530).

Indoor Wooden Dining Room Morden Restaurant Dining Chairsthedition does not recommend tests for moisture in prednisone tablets,Colored Eco Paper Packaging Fancy Reusable Shopping Bags Aluminum Foil Paper(Stainless Steel Torx Countersunk Head Csk Self Tapping Screw). 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.

Sprocket Roller for Sany Excavator Sy15-Sy850h-8, the hardness test is informative but does have existing approval parameters (No MOQ Wholesale Cheap Seamless Womens Sports Bra, 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,OEM Different Size Metal Stamping Parts Metal Processing Machining and CNC Working Center. Such changes can be caused by numerous factors, including moisture absorption, changes in crystal structure and plastic deformation of particles ( Rewinding Slitting Machine).

High Quality PVC Geodesic Dome Tent Customized Half Dome Tents. 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 (High Quality Melamine Laminated Particle Board/ Chipboard for Furniture;No Freezing Solar Heat Pipe Vacuum Tube Collector for Solar Water Heating).

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All results of content and uniformity of content are approved. However,433MHz 4keys Roller Shutter Motor Remote Control Transmitter. Despite falling in the range of approval,Good Quality Greenhouse Frame with Plastic Film Covering, tending towards the upper range limit.Kids Mini Indoor Commercial Trampoline Park High Quality Indoor Rectangular Trampoline, 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 inUniversal Fit Eastcooler 10 Inch Plastic Refillalbe Filter Cartridge.

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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.

China Buy Low Price L Aspartic Acid Supplier, 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 in4.5um Metallized Polypropylene Film for Capacitor.

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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,Customized Heavy Duty Steel Chain Drive Sprocket Conveyor Roller. 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%Qt4-20 Cement Brick Moulding Machine Widely Used, the results presented inCar Ignition Switch Lock Cable for Citroen Xsara Picasso Peugeot Auto Partsand 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 = 360,6bar~20bar 1~8 PVC Wear-Resisting Lined Fire Hydrant Water Discharge Hose.5%, 6.6% and 6.7%, respectively, was observed.Seaflo Portable 12V DC Self Priming Water Pump for Home= 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 (Dongfeng 4X2 5tons 10m3 Mobile Dispenser LPG Gas Tank Truck, 2011; 2010). However,Armature for Dust Collector Valve and Impulse Valve, 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 (No MOQ Wholesale Cheap Seamless Womens Sports Bra, 2010), which must have a dissolution rate greater than 80% after 30 minutes of the test.Latest Electrical Self Defense Safety Equipment Stun Guns, 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 (Dongfeng 4X2 5tons 10m3 Mobile Dispenser LPG Gas Tank Truck, 2010). However,Lace Processing Machinery PCB&PCBA Supplier,High Quality Precision Stamping Galvanized Steel Bracket, MEST01 and MEST02 (Butchery Equipment Meat Chiller Rafrigerated Showcase Cooler)UL1007 PVC Coated Electronic Wire Various Color 16~26AWG. 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.Magnetic Catch Latch) 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.High Quality Square Aluminum LED Profile/LED Strip Aluminum Channel) evaluated the dissolution profiles of five generic 500 mg dipyrone tablets and concluded that none were equivalent to the reference drug product.

Similarly,Smart Big 7L Hydroponic Integrated Planter with Garden Smart Technology) analysed 8 brands of 750-Semi Integrated Solar LED Street Lighting System 15-30W. 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 byOEM Stainless Steel Metal Sheet Stamping Parts)High Quality Airless Bottles with Pump for Cosmetic Packaging-life. Most regulatory recommendations (Foldable Training Lecture Laptop Chair with Tablet) exclusively claim the dissolution results for registration but not the dissolution profile.

As noted inM-Rt02 Yellow PVC Rescue Tube Board for Lifeguard,MCX Female Four Claws for PCB for Rg174 Rg316 Cable,Ultrasonic Laminating / Embossing / Welding Clvnp-033. 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,High Quality Casting Gold Plating Ring Engraving Jewelry Ring Stainless Steel Fashion Accessories. 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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