FORMULATION AND EVALUATION OF DILTIAZEM HCl FAST DISSOLVING TABLETS USING DIFFERENT CO-PROCESSED EXCIPIENTS BY DIRECT COMPRESSION METHODHTML Full Text
FORMULATION AND EVALUATION OF DILTIAZEM HCl FAST DISSOLVING TABLETS USING DIFFERENT CO-PROCESSED EXCIPIENTS BY DIRECT COMPRESSION METHOD
M. Sunitha Reddy*, Niveditha Kore and S. Muhammad Fazal Ul Haq
Centre for Pharmaceutical Sciences, Institute of Science and Technology, Jawaharlal Nehru Technological University, Kukatpally, Hyderabad - 500085, Telangana, India.
ABSTRACT: The aim of present work was to prepare Diltiazem HCl Fast Dissolving tablets by Direct compression method because of their convenience in administration and suitability for patients having dysphagia using Co-processed excipients-Disintequik MCC25, Disintequik MCC, Lubritose MCC, Lubritose SD, Lubritose AN, NF Fast flow Lactose Monohydrate modified spray dried. The Prepared powdered blend and tablets were evaluated for Pre compression parameters such as Angle of repose, Bulk density, Tapped density, Compressibility index, Hausners ratio and Post compression parameters such as weight variation, thickness, hardness, disintegration time, content uniformity, in-vitro dissolution studies and stability studies. All the parameters were within the limits. IR and DSC study showed that drug and excipients were compatible with each other. Twelve formulations were prepared by direct compression method in which F10 was the best formulation using Disintequik MCC25 at a concentration of 4% as it was disintegrated with in 30 sec and drug release was 99.88% over a period of 15 min. The wetting time and disintegration time decreases considerably with the increase in co-processed excipients.
Fast dissolving tablets, Diltiazem HCl, Co-processed excipients, Direct compression method
INTRODUCTION: US FDA defined fast dissolving or disintegrating tablets (FDT) as “A solid dosage form containing medicinal substances, which disintegrates rapidly, usually within a matter of seconds, when placed upon the tongue”. Fast disintegrating tablets (FDT) are also known as ‘Fast Dissolving’, ‘Mouth Dissolving’, ‘Rapid Dissolving’, ‘Quick Dissolving’, ‘Orally Disintegrating’, ‘Rapid melt’, Oro Dispersible’, ‘Porous Tablets’.
Salient Features of Fast Dissolving Tablets:
- Ease of administration to patients who refuse to swallow tablets such as pediatric, geriatric and psychiatric patients
- No need of water to swallow the dosage form, which is highly convenient feature for patients who are travelling and do not have access to water.
- Rapid dissolution and absorption of drug, which will produce quick onset of action.
- Some drugs are absorbed from the mouth, pharynx and oesophagus as the saliva passes down into the stomach; in such cases bioavailability of drug is increased.
- Pre-gastric absorption can result in improved bioavailability.
MATERIAL AND METHODS:
Equipment: Bruker Alpha FTIR Spectrophotometer; Shimadzu U.V Spectrophotometer; Tablet Compression machine, USP type II Dissolution apparatus; Mansanto hardness tester, vernier calipers, Sonicator, Roche friabilator.
Chemicals and Reagents: Diltiazem Hydrochloride, pH 6.8 Phosphate buffer, Disintequik MCC25, Disintequik MCC, Lubritose MCC, Lubritose SD, Lubritose AN, NF Fast flo lactose monohydrate modified spray dried, Magnesium stearate as lubricant, Mannitol was used as diluent, Talc as a glidant.
Preparation of Diltiazem HCl fast dissolving tablets: Diltiazem HCl Fast dissolving tablets are prepared for F1 to F12 batches by using different concentration (mentioned in Table 1) of co-processed excipients like Disintequik MCC 25, Disintequik MCC, Lactose monohydrate NF spray dried, Lubritose anhydrous AN, Lubritose MCC, Lubritose SD by direct compression method. Keeping total weight (100mg) of tablet constant in all the formulations. All the ingredients are passed through sieve no. 40 to ensure better mixing. All ingredients were mixed in motar and pestle then magnesium stearate and talc were added. The resulting mixture is compressed into tablet and then tablets were evaluated.
TABLE 1: FORMULATION OF 100MG DILTIAZEM HYDROCHLORIDE FAST DISSOLVING TABLETS
|Ingredients (taken in mg)|
|Disintequik MCC 25||-||-||-||-||-||-||-||-||2||4||-||-|
|NF Fast Flo Lactose Monohydrate
Modified Spray Dried
Preparation of pH 6.8 phosphate buffer: Dissolve 28.80 g of disodium hydrogen phosphate and 11.45 g of potassium dihydrogen phosphate in sufficient water to produce 1000 ml.
Preparation of Calibration Curve of Diltiazem HCl in pH 6.8 phosphate buffer: 100mg of Diltiazem HCl was weighed accurately and dissolved in pH 6.8 phosphate buffer, which resulted in 1000 µg/ml. Then from the stock solution 100 µg/ml solution was prepared from this 2, 4, 6, 8, 10 µg/ml were prepared.
The absorbance of the above dilutions were measured using UV-spectrophotometer at 236nm using 6.8 pH phosphate buffer as blank. The conc. of corresponding absorbance was given below table. standard curve was plotted by taking concentration on x-axis and absorbance on y-axis.
Drug-Excipient Compatibility study (FTIR): The study was designed to determine compatibility of drug with different co-processed excipients. Completely dried KBR and samples (drug and excipients) taken in 9:1 ratio and grinded for proper mixing. Sample was filled into the holes of stainless steel disk and sandwiched in the hydraulic press until pressure reaches 20,000 psi. After few seconds, pressure was released and pellet was collected. Then the pellet was inserted into the sample holder and run for the spectrum. FTIR spectra of pure drug and excipients separately done to determine the compatibility. FTIR spectra of drug and excipients were obtained on alpha-Bruker FTIR (Tokyo, Japan). The spectra were scanned over the wave number range of4000-400 cm-1.
X-Ray Diffraction studies (XRD): X-ray powder diffraction (XRD) is a rapid analytical technique
primarily used for phase identification of a crystalline material and can provide information on unit cell dimensions. The analyzed material is finely ground, homogenized, and average bulk composition is determined.
Differential Scanning Calorimetry: DSC is a thermoanalytical technique carried to know compatability between drug and excipient.
In which the difference in the amount of heat required to increase the temperature of a sample and reference is measured as a function of temperature. All the samples were run at a scanning rate of 10 ºC/min from 50-350 ºC.
Evaluation of mixed powder blend of drug and excipients:
Angle of Repose (θ): Angle of repose was determined by the fixed funnel and free standing cone method. This is the maximum angle possible between the surface of a pile of powder and the horizontal plane.
Formula: Tan θ = (h/r)
θ = tan-1 (h/r)
Where ’ h’ is the height of the cone
‘r’ is the radius of the cone.
Different ranges of flowability in terms of angle of repose was shown in Table 4.
Bulk density (g/ml): The bulk density of Precompressional blend was determined by three tap method. Weighed quantity of Precompressional blend was transferred into 100ml graduated cylinder and the cylinder was dropped onto a hard wooden surface 3times from a height of 2.5cm at an interval of 2sec.
Bulk density = weight of the sample/bulk volume of the sample
Tapped density (g/ml): The weighed quantity of dry Precompressional blend was taken in a graduated cylinder and the cylinder was allowed to tap for 100 times onto a hard wooden surface from a height of 2.5cm.
Tapped density = weight of the sample/Tapped volume of the sample
Carr’s Index or Compressibility: It is directly related to flow rate, cohesiveness and particle size.
Carr’s index = Tapped density-Bulk density/ Tapped density
Hausner’s Ratio: It is the ratio of tapped density to bulk density and was related to interparticle friction.
Hausner’s ratio = Tapped density/Bulk density.
Porosity (%): Ratio of total volume of void spaces to the bulk volume of material is referred to as porosity. It was calculated by using the formula:
Percentage porosity = 100 [1 – Vt/ Vb]
Where, Vt = true volume of powder
Vb = bulk volume of powder
Evaluation of Tablets:
Weight variation test: To find out weight variation, 20 tablets of each type of formulation were weighed individually using an electronic balance, average weight was calculated and individual tablet weight was then compared with average value to find the deviation in weight.
Thickness: The thickness of the tablets was determined using a Micrometer screw gauge. Five tablets from each type of formulation were used and average values were calculated. It is expressed in mm.
Hardness: It was determined using the Monsanto hardness tester. The tablet was held along its oblong axis in between the two jaws of the tester. At this point, reading should be zero kg/cm2. Then constant force was applied by rotating the knob until the tablet fractured.
Friability: Friability is the measure of tablet strength. Roche Friabilator was used for testing the friability. A sample of preweighed 6 tablets was placed in Roche friabilator which was then operated for 100 revolutions i.e. 4 minutes. The tablets were then dusted and reweighed. A loss of less than 1% in weight is generally considered acceptable.
Wetting Time: A piece of tissue paper folded twice containing amaranth powder on the upper surface was placed in a small Petri dish (ID =6.5 cm) containing 6 ml of pH 6.8 Phosphate buffer, a tablet was put on the paper and the time required for formation of pink color was measured as wetting time. The study was performed in triplicate.
Drug Content Uniformity: Five tablets were weighed and crushed with pestle in a motar. The fine powder was weighed to get a100mg (equivalent to 60mg Diltiazem HCl) and transferred to 250 ml conical flask containing 100 ml of 6.8 pH phosphate buffer stirred for 45 min in an sonicator then the solution was filtered and it was analyzed by UV spectrophotometrically at 236 nm and drug content was determined.
Disintegration Time: Disintegration time is the time required for a tablet to break into granules of specified size (or smaller), under carefully specified test conditions. Six tablets were placed in each of the tubes and run the apparatus using phosphate buffer 6.8 pH which is maintained at 37±2 ºC. The time required for complete passage of tablet fragments through the sieve #10 was considered as the disintegration time of the tablet.
In-vitro dissolution Studies: The release rate of Diltiazem HCl tablets was determined using USP Dissolution type II testing apparatus (paddle type). One tablet was placed in each of the six dissolution flasks containing 900 ml of dissolution medium previously maintained at 37 ± 0.5ºC and at 50 rpm. After completion of each specified time interval, aliquots of 5ml was withdrawn from the dissolution media and the samples were replaced with fresh dissolution medium. After filtration and samples are diluted and absorbance was noted at 236 nm using UV visible spectrophotometer and percentage of drug release was calculated.
RESULTS AND DISCUSSSION:
UV Absorbance Maxima of Diltiazem HCl: Standard calibration curve obeyed Beer`s law in the concentration range of 2-10 µg/ml and the value of regression coefficient was found to be 0.99948 which showed a linear relationship between concentration and absorbance as shown in the Fig.1
FTIR Compatibility studies FTIR spectra of Diltiazem HCl alone and with Co-processed excipients Disintequik MCC25, Disintequik MCC, Monohydrate NF spray dried, Lubritose MCC, Lubritose SD, Lubritose AN, Magnesium Stearate, Mannitol, Talc was done. Hence there was No Interaction between Diltazem HCl and Excipients.
XRD: The X- RAY diffraction studies of Diltiazem HCl show a characteristic sharp intensity peak at 2θ values of 10.1˚, 19˚, 22˚, which reflected the crystalline nature of drug. Both the formulations showed diffraction peaks at respective 2θ values of pure Diltiazem HCl although their relative intensities were reduced or there was a slight shift in their peaks, suggesting reduced degree of crystallinity of drug in Optimized formulation.
DSC: Melting point of Diltiazem HCl was found to be 216˚C and optimized formulation melting point was found to be 214˚C.
FIG. 1: CONCENTRATION VS ABSORBANCE
Micromeritic Properties of Powder Blend: The powder mixtures of all the batches (F1-F12) were evaluated for Bulk density, Tapped density, Carr’s index, Porosity, Hausners ratio, Angle of repose and showed in the Table 6. Bulk density ranged from 0.45 to 0.52g/ml, Tapped density ranged from 0.55 to 0.69 g/ml, Angle of repose ranged from 180 17’ to 200 42’, Hausners ratio ranged from 1.12 to 1.25 %. All these results indicated that the powder mixture possess Good flow property and compressibility index.
In vitro Drug Release Studies: In vitro dissolution studies were performed in pH 6.8 Phosphate buffer. The dissolution results showed gradient increase with the increase in the concentration of the coprocessed excipients. Among all the formulations F10 was found to show best results with 99.88% release and it is more suitable for Fast dissolving tablets by direct compression technique.
Stability studies: The results of stability was given in Table 5. After analysis it was found that there was no substantial changes in all parameter of optimized batch F10. The results revealed the product is stable for the period of one month at 40ºC±2ºC/RH75±5%.
TABLE 2: STABILITY STUDIES OF OPTIMIZED FORMULATION
|Long term||25±2oC,RH 60±5%||12 months|
|Intermediate||30±2oC, RH 65±5%||6 months|
|Accelerated temperature||40±2oC, RH 75±5%||6 months|
TABLE 3: LIMITS FOR WEIGHT VARIATION ACC TO IP
|Average Tablet Weight (mg)||Percentage Deviation (%)|
|Up to 80 mg||5|
|> 80mg,<250 mg||7.5|
|250mg or more||10|
TABLE 4: RELATIONSHIP BETWEEN ANGLE OF REPOSE AND FLOW PROPERTY
|Angle of repose (degrees)||Flow property|
FIG. 2: FTIR SPECTRA OF DILTIAZEM HCl
FIG. 3: FTIR SPECTRA OF DISINTEQUIK MCC 25
FIG. 4: COMPATIBILITY OF DILTIAZEM HCl AND DISINTEQUIK MCC 25
FIG. 5: FTIR SPECTRA OF DILTIAZEM HCl OPTIMIZED FORMULATION
FIG. 6: X-RAY DIFFRACTION PATTERN OF DILTIAZEM HCl AND DILTIAZEM HCl FORMULATION
DSC Thermogram of Diltiazem HCl
DSC Thermogram of Diltiazem HCl formulation
FIG. 7: DSC THERMOGRAM OF DILTIAZEM HCl AND DILTIAZEM HCl FORMULATION
TABLE 5: CUMULATIVE PERCENTAGE DRUG RELEASE OF DILTIAZEM HYDROCHLORIDE F1 TO F12
|Cumulative percentage drug release (%)|
Values ± SD, n = 3
TABLE 6: EVALUATION PARAMETERS OF PRECOMPRESSIONAL POWDER BLEND
|S.no||Formulation Code||Bulk Density
|Compressibilty Index (%)||Hausner’s
Values ± SD, n = 3
TABLE 7: EVALUATION PARAMETERS OF FORMULATED TABLETS
|Content Uniformity (%)||Disintegration time(sec)||Wetting time
Values ± SD, n= 3
FIG. 8: CUMULATIVE PERCENTAGE DRUG RELEASE PROFILES OF DILTIAZEM HCl FAST DISSOLVING TABLET FORMULATIONS (F1-F6)
FIG. 9: CUMULATIVE PERCENTAGE DRUG RELEASE PROFILES OF DILTIAZEM HCl FAST DISSOLVING TABLETS FORMULATIONS (F7-F12)
CONCLUSION: Diltiazem HCl Fast Dissolving tablets were prepared by direct compression method using Disintequik MCC25, Disintequik MCC, Lactose monohydrate NF spray dried, Lubritose anhydrous AN, Lubritose MCC, Lubritose SD. The tablets disintegrated rapidly and had acceptable hardness and friability. In-vitro drug release from the tablets shows significantly improved drug dissolution. Hence it could be concluded that the Co-processed excipient based Diltiazem HCl Fast Dissolving tablets would be quite effective in providing quick onset of action without need for water for swallowing or administration.
ACKNOWLEDGEMENT: Sincere Thanks to Dr. M. Sunitha Reddy for her valuable guidance throughout the tenure of the project and It is my privilege to express my gratitude to Centre for Pharmaceutical Sciences, Institute of Science and Technology, Jawaharlal Nehru Technological University, for providing appropriate facilities to carry on the above research.
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How to cite this article:
Reddy MS, Kore N and Fazal Ul Haq SM: Formulsation and evaluation of diltiazem HCl fast dissolving tablets using different co-processed excipients by direct compression method. Int J Pharm Sci Res 2017; 8(7): 2853-61.doi: 10.13040/IJPSR.0975-8232.8(7).2853-61.
All © 2013 are reserved by International Journal of Pharmaceutical Sciences and Research. This Journal licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License.
M. Sunitha Reddy*, Niveditha Kore and S. Muhammad Fazal Ul Haq
Centre for Pharmaceutical Sciences, Institute of Science and Technology, Jawaharlal Nehru Technological University, Kukatpally, Hyderabad, Telangana, India.
06 December, 2016
10 June, 2017
21 June, 2017
01 July, 2017