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Tropical Journal of Pharmaceutical Research , Vol. 2, No. 1, June, 2003 pp. 147-153 Research Article Effects of interacting variables on the tensile strength and the release properties of paracetamol tablets Oluwatoyin A Odeku Φ and Oludele A Itiola Department of Pharmaceutics & Industrial Pharmacy, University of Ibadan, Ibadan,
Nigeria Code Number: pr03004 Abstract Purpose: The individual and interaction effects of nature of
binder (N), concentration of binder (C) and the relative density (D) on
the tensile strength and release properties of paracetamol tablets have
been studied using a 23 factorial experimental design. Keywords: Binding agent, khaya gum, release properties, paracetamol tablets, tensile strength Introduction The tensile strength, which is a measure of the bond strength of tablets, is an indicator of the ability of the tablet to withstand the rigours of handling involved in manufacture, transportation, dispensing and usage of pharmaceutical tablets. However, the tablet must be able to release the drug content in the GIT for absorption. Thus, the tensile strength of a tablet plays a vital role in the release of the drug from the formulations. The release properties of drug from the tablet formulations can be quantified by the disintegration and the dissolution times of the tablet. It is well known that, for disintegrating tablets, considerable dissolution of drug can take place before complete disintegration of the tablets, a phenomenon which depends largely on the mechanism of disintegration and certain physicochemical properties of the drug, such as its solubility. The physicochemical properties of tablets have been shown to depend considerably on the nature and concentration of the binding agent employed in the formulation and also on the relative density of the tablet1-4. Thus, the relationship between these parameters for particular drugs is of interest and the quantitative effects of important formulation and processing variables on these parameters are very important. In an effort to produce tablets of important drugs such as paracetamol from locally available materials, khaya gum obtained from the incised trunk of the tree Khaya grandifolia (also called Khaya grandifoliola), Family Meliaceae, has been investigated as a binding agent in tablet formulations4,5. The gum has been found to be useful as a binding agent for particular tablet formulations but the quantitative effects of important formulation and processing variables on the tensile strength and release properties of the tablet appear to be largely uninvestigated. In the present work, a study has been made of the relative quantitative effects of nature (khaya gum and PVP) and concentration of binding agent, and the relative density of the tablets on the tensile strength (T), the disintegration time (DT) and dissolution parameters - t50 and t90 (the time required for 50% and 90% of paracetamol to be dissolved respectively) of paracetamol tablets using a factorial experimental design6 which has already proved useful in the analysis of the quantitative individual and interaction effects of various formulation factors on the disintegration and dissolution rate of tablets3,7. Paracetamol, a widely used analgesic and antipyretic agent, cannot be made into satisfactory tablets due to its capping and lamination tendencies. It is normally produced commercially as tablets containing 500 mg of the drug with added excipients such as a binding agent to modify its plastic and elastic properties8. Materials and methods MaterialsThe materials used were paracetamol BP and corn starch BP (BDH Chemicals Ltd., Poole, U.K), lactose (DMV Veghel, Netherlands), gelatin BP (Hopkin & Williams, Chadwell Heath, Essex, U.K), PVP (mw, 40,000; Aldrich Chemicals Co. Ltd, Gillingham, Dorset, U. K) and khaya gum from Khaya grandifolia (Botanical Gardens, University of Ibadan, Ibadan, Nigeria). A description of the collection and purification of khaya gum has been given elsewhere4. Preparation of granules Batches (250g) of a basic formulation of paracetamol (83% w/w), lactose (10% w/w) and corn starch (7% w/w) were dry-mixed for 5 min in a Kenwood planetary mixer and then moistened with either 31 ml of distilled water or the prepared binder solutions of PVP or mucilages of Khaya gum to produce granules containing different concentrations of the binders. Massing was continued for 5 min and the wet masses were granulated by passing them manually through a number 12 mesh sieve (1400 µm), dried in a hot air oven for 18 hr at 50o C and then resieved through a number 16 mesh sieve (1000 µm). The moisture content of the granule formulations as determined with an Ohaus moisture balance (Ohaus Scale Corporation, USA) was between 1.1 and 1.8% w/w. Particle densities were determined by the pycnometer method with xylene as the displacement fluid. The degree of mixing of the granules from three different regions of each formulation batch was determined by spectrophotometric assay of paracetamol in quadruplicate at 249 nm. In each case, the degree of mixing was found to be > 0.95. Preparation of tablets Quantities (500 mg) of granules of the formulations, giving a tablet thickness of 4.37 ± 0.02 mm at zero porosity as calculated from particle density values, were compressed for 1 min with predetermined loads using a Carver hydraulic hand press (Model C, Carver Inc., Menomonee falls, Wisconsin, USA). Before each compression, the die (10.5 mm diameter) and the flat-faced punches were lubricated with a 2% w/v dispersion of magnesium stearate in ethanol: ether (1:1). After ejection, tablets were stored over silica gel for 24 hr to allow for elastic recovery and hardening and prevent falsely low yield values. The weights, W, and dimensions were then determined to within ± 1mg and 0.01 mm respectively, and the relative densities, D, were calculated using the equation: D = W / Vt. ρs (3) where Vt is the volume of tablet (including the hole when present) in cm3 and φs is the particle density of the solid material in g/cm3. Tensile strength of tablets The tensile strengths, T, of the tablets were determined at room temperature by diametral compression using a PTB 301 hardness tester (Pharmatest, Switzerland) and applying the equation9: T = 2F / π dt (4) where T is the tensile strength of the tablet (MNm-2), F is the load (MN) needed to cause fracture, d is the tablet diameter (m), and t is the tablet thickness (m). Results were taken only from tablets which split cleanly into two halves without any sign of lamination. All measurements were made in triplicate or more and the results given are the mean of several determinations. Disintegration test The disintegration times, DT, of the tablets were determined in distilled water at 37 ± 0.5o C using an Apex disintegration testing apparatus (Apex Construction Ltd.; Northflect gravesent and Dartford, Kent, UK). The time taken for all the tablets to disintegrate and go through the wire mesh was recorded. Determinations were made in triplicate. Dissolution test The dissolution rates of the tablets were determined at 37 ± 0.5o C in 1 litre of 0.1 M HCl using an Erweka dissolution rate machine (Erweka Apparatabau, Gmbh Heusenstamm kr. Offenbach/Main, Germany) and a stirring speed of 100 revolutions per min (USP XX). The amount of paracetamol that had dissolved after a certain period was determined spectrophotometrically at 249 nm using a Lambda 3B UV/visible spectrophotometer (Perkin -Elmer, USA) replacing the sample with an equal volume of 0.1 M HCl at the same temperature in order to keep the volume of the dissolution medium constant during the course of the test. All determinations were made in triplicate or more and the results given are the means of several determinations. Experimental design To study the effect of nature of binding agent (denoted by N), concentration of binding agent (denoted by C) and relative density of the tablet (denoted by D) on the tensile strength, and the disintegration and dissolution times of the tablets, the experiments were performed in a factorial design, which involved the application of simple statistics7. The basis of the experimental design was that each of the three variables was utilized at a "high"level (denoted by the subscript, H) and a "low"level (denoted by the subscript, L). The number of experiments in the design was 23 i.e, 8. Using the above nomenclature the various combinations between the variables used in the design were; NLCLDL, NLCHDL, NLCHDH, NLCLDH NHCLDL, NHCHDL, NHCHDH, NHCLDH NL = Nature of binding agent (khaya gum) By grouping the results into a number of sets it was possible to assess the effects that each of the three variables had separately on the tensile strength, and the disintegration and dissolution times of the tablets and also to determine whether the variables were interacting or acting independently of each other. The effects of increasing N, from its "low"level to its "high"level on the tensile strength, and the disintegration and dissolution times were found by summing all tensile strength (or the disintegration or dissolution time) results of samples containing "high"level of N and subtracting the sum of the results of samples containing "low"levels of N. That is; 1/4 [(NHCLDL + NHCHDL + NHCHDH + NHCLDH) -(NLCLDL + NLCHDL + NLCHDH + NLCLDH ) ] (5) The amount by which the result of this treatment departed from zero (irrespective of whether positive or negative) was a quantitative measure of the effect of N tensile strength (or the disintegration or dissolution times) of the tablet. Similar expressions were used for finding the effects of C and P. To determine whether there was any interaction between two variables, the result of the combinations in which they appear together at either "high"or "low"levels were summed and the sum of other combinations subtracted from this to obtain the interaction coefficient. For N and C: 1/4[(NLCLDL + NLCLDH + NHCHDH + NHCHDL) -(NLCHDL + NLCHDH + NHCLDL + NHCLDH)] (6) A result of zero indicates no interaction, but if the interaction coefficient was significantly removed from zero, it is concluded that the two variables concerned were interacting with each other. The extent of removal from zero is a measure of the magnitude of interaction7. Similar expressions were used for estimating the interaction between N and D, and between C and D Results and Discussion Representative plots of tensile strength (T) and disintegration time (DT) versus relative density (D) for paracetamol tablets containing 4% w/w of the binders are presented in Figures 1 and 2 respectively while the plots of percentage of paracetamol dissolved versus time for paracetamol tablets compressed at relative density 0.9 are presented in Figure 3. The values of tensile strength and the disintegration and dissolution times at two selected relative densities of 0.8 and 0.9, which is representative of the range of relative density normally achieved for commercial paracetamol tablets, for the factorial experiments are given in Table 1. These values were used to calculate the individual and interaction coefficients for the variables using equations (5) and (6). The coefficient values are presented in Table 2. The individual and interaction effects provide a clear indication of the quantitative effects of the three variables studied on the tensile strength, the disintegration and dissolution times of the paracetamol tablets. In comparing the formulations, the ranking of the individual (independent) coefficient values (Table 2) for the formulations was D > N > C for T and C >> N > D for the disintegration and dissolution parameters. It can be seen that all the individual effects were positive indicating that all the values of the parameters increased. The effect of C indicates that increasing the concentration of the plastoelastic binder from 0.5% to 4.0% w/w led to an increase in the plastic deformation of the formulation during compression and subsequently to the formation of more solid bonds in the tablet leading to an increase in tensile strength and the disintegration and dissolution times of the tablet. In general, the concentration of binder, C had the lowest effect on T but the highest effect on the disintegration and dissolution times of the tablets. The manifestations of the effects of C concerning tablet properties usually tends to be strongly related to those other formulation variables and should therefore be given particular consideration when developing tablet formulations. The effect of D on all the parameters was positive although D had the highest effect on the tensile strength of the tablet but the east effect on the disintegration and dissolution times. Thus, increasing the relative density from 0.8 to 0.9 led to an increase in the tensile strength of the tablet and the disintegration and dissolution times. This can be due to the fact that as the relative density of the tablet increased, more solid bonds will be formed between the particles leading to an increase in tensile strength. Furthermore, the binding agents are forced into interparticular spaces, thereby increasing the area of contact between particles leading to the formation of additional solid bonds and thus an increase in the disintegration and dissolution times of the tablets. This can be attributed to the reduction in the size of the capillary spaces between the particles which reduced the rate of penetration of water into the tablet to effect bond separation10. The influence of N on the tensile strength of the tablets was positive which indicates that tablets containing PVP as binder had higher tensile strength than tablets containing khaya gum. On the other hand, the influence of N on the disintegration and dissolution times was negative indicating that khaya gum, which represented the "low"level produced tablets with longer disintegration and dissolution times than PVP, which represented the "high"level of N. Thus while tablets containing khaya gum as binding agent had lower tensile strength, it also had longer disintegration and dissolution times than those containing PVP. However, all the tablets complied with the BP (1980) requirement on disintegration (i.e. disintegration within 15 minutes). Thus, khaya gum could be useful as an alternative binding agent to produce tablets with particular tensile strength and drug release profiles. The interaction coefficient values (Table 2) indicate the effect of the variables in combination. For the formulations, the ranking of the effects on T and t50 was N -D >> N -C > C - D, on DT was N -C >> N -D>C -D, and on t90 was C -D > N -C >> N - D. The magnitude of the interaction effects show that there were generally considerable interactions between the concentration of binder, C and the other two variables, N and D. This is probably due to the fact that binding agents being plastoelastic in nature undergoes extensive plastic deformation under high compressional forces to form strong solid bonds between particles, the number of bonds formed depending considerably on the concentration of binder employed. The manifestations of the effect of C, concerning tablet properties, have been shown to be strongly related to the relative density of the tablet, D and the nature of the binding agent, N employed in the formulation3, 6, 10. Thus, the nature of binder (N), concentration of binder (C) and relative density (D) employed in a formulation need to be carefully chosen to enable the production of tablets with the adequate bond strength to withstand the rigors of handling and afford the release of the drug in the desired time period and with the desired disintegration/ dissolution profile. Conclusion The results suggest that khaya gum could be useful as an alternative binding agent to produce tablets with particular tensile strength and drug release profiles. Furthermore, there was considerable interaction between the variables for the different binding agents as evidenced by the magnitude of the individual and interaction coefficient employed on the tensile strength and the disintegration and dissolution times of paracetamol tablets. The concentration of binder, C, appears to be the most influential variable in this case, indicating that any attempt to manipulate the tensile strength or the disintegration and dissolution times of the tablets should start with a consideration of C. This study would be useful in developing tablet formulations for other drugs as well. References
Full text of this journal is also available online at http://www.tjpr.freehosting.net © Pharmacotherapy Group, Faculty of Pharmacy, University of Benin, Benin City, Nigeria The following images related to this document are available:Photo images[pr03004f2.jpg] [pr03004f1.jpg] [pr03004t2.jpg] [pr03004t1.jpg] [pr03004f3.jpg] |
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