Global Journal of Pharmacology 9 (3): 278-281, 2015 ISSN 1992-0075 © IDOSI Publications, 2015 DOI: 10.5829/idosi.gjp.2015.9.3.95226 Comparative Study among the Different Formulation of Antacid Tablets by Using Acid-Base Neutralization Reaction 1 Md. Jakaria, 1Rashaduz Zaman, 1Mohammad Parvez, 1Minhajul Islam, 2 Md. Areeful Haque, 1Mohammed Abu Sayeed and 1Md. Hazrat Ali Department of Pharmacy, Faculty of Science and Engineering, International Islamic University Chittagong (IIUC), Chittagong 4203, Bangladesh 2 Drug and Herbal Research Centre, Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur, Malaysia 1 Abstract: Antacids were the mainstay of treatment for acid-peptic disorders until the advent of Hreceptor antagonist and proton pump inhibitors. We attempted to compare the activity of the different antacid tablets formulation by using acid-base neutralization reaction studies. This experiment based on acid-base neutralization reaction studies between independent variable (sample of antacid) and dependent variable (amount of acid needed to neutralize the antacid). The tablet code no. D neutralizes highest (7 ml) of acid solution and lowest (1.2 ml) was neutralizing by antacid code no. C. The sequences of antacid according to amount of acid required to neutralization was D> E> B> A> C. This in-vitro study may help in the deepest research works such as design and discovery of new antacid formulation. Key words: Antacids Acid Solution Neutralization INTRODUCTION In vitro aluminium hydroxide, aluminium phosphate, magnesium trisilicate, magnesium hydroxide, magnesium carbonate and calcium carbonate [5, 6]. The systemic antacid most commonly used is sodium bicarbonate. There occurs no systemic absorption of the bases among non systemic antacids, because the salt formed with combination of the gastric acid combines with the bicarbonate in the intestine to form the original base which will be excreted in the feces [7, 8]. Table 1 shows some the most common active ingredients in antacid tablets. These compounds neutralize stomach acid to produce salts and water [9]. Complex antacids are major type of antacids other than systemic and non-systemic antacids e.g., magaldrate, almagate and hydrotalcite etc. Magaldrate is a hydroxymagnesium aluminate. It contains the equivalent of 28-39% magnesium oxide and 17-25% aluminum oxide. It has a homogenous material since the aluminium and magnesium components dissolve concurrently. It reacts with acid in stages; the hydroxymagnesium ion is relatively rapidly converted to magnesium ion and the aluminate to hydrated aluminium hydroxide and thence to aluminium salts. Antacids are commonly used world over as over the counter (OTC) or prescribed medications. They were the mainstay of treatment for acid-peptic disorders until the advent of H receptor antagonist and proton pump inhibitors. They have been used in the treatment for acid-peptic disorders such as peptic ulcers, gastritis, gastro-oesophageal reflux disease (GERD) and functional dyspepsia [1, 2]. Antacids are basic substances that reduce gastric acidity by neutralizing hydrochloric acid [3]. Therapeutic efficacy and adverse effects depend also on the metallic ion with which the base is combined. The metallic ion is usually aluminium, magnesium or sodium and hydroxide is the most common base, but trisillicate, carbonate and bicarbonate are also used [4]. The antacids can be classified into two major types one is systemic antacids and another one is non systemic antacids. Systemic antacid is the one that undergoes complete systemic absorption following oral ingestion. The non systemic antacids are the one that does not undergo systemic absorption following the oral ingestion. The most commonly used non systemic antacids are Corresponding Author: Md. Jakaria, Department of Pharmacy, International Islamic University Chittagong, Chittagong, 4203, Bangladesh. Tel: +8801823618436. 278 Global J. Pharmacol., 9 (3): 278-281, 2015 Table 1: Common antacids and it’s mechanism of action through neutralizing reaction with acid Compound Chemical formula Chemical Reaction Aluminum hydroxide Calcium carbonate Magnesium carbonate Magnesium hydroxide Sodium bicarbonate Al(OH) 3 CaCO 3 MgCO 3 Mg(OH)3 NaHCO 3 Al(OH)3 (s) + 3 HCl (aq) = AlCl3 (aq) + 3 (H2 O)(l) CaCO 3 (s) + 2 HCl (aq) = CaCl2 (aq) + H2 O(l) + CO 2 (g) MgCO 3 (s) + 2 HCl (aq) = MgCl2 (aq) + H 2 O(1) + CO 2 (g) Mg(OH)3 (s) + 2 HCl (aq) = MgCl2 (aq) + 2 H 2 O(1) NaHCO 3 (aq) + HCl (aq) = NaCl2 (aq) + H2 O (l) + CO 2 (g) Alginic acid may be combined with the antacid to encourage the adherence of the antacid to the mucosa and it also acts like a protective to the gastric mucosa. Simethicone or dimethicone are included in the antacid as an foaming agent to reduce flatulence by lowering the surface tension and allowing the small bubbles of froth to coalesce into large bubbles that can be more easily be passed up from the stomach or down from the colon [9]. In our present study, we attempted to compare the activity of the different antacid tablets formulation by using acid-base neutralization reaction studies. MATERIALS AND METHODS Reagents: Analytical grade reagents hydrochloric acid and distilled water. were 0.1N Glasswares: Volumetric flask, funnel, beakers, Measuring cylinder, burette, pipette and stirrer used were of Pyrex type and were washed followed by thorough washing with water. Instruments: Theses include: Weighing Balance: Precision balance, LF224DR, Shinko Denshi Co., ltd. pH Meter: HANNA Instruments, HI-98107, Europe (Romania) Sample Information: The five different antacid tablets formulation were purchased from a local drug shop located in Bayezid Bostami thana of Chittagong district. Shows label information of different brands (Table 2) and contents in each sample showing in Table 3. Experimental Design: This experiment based on acid-base neutralization reaction studies between independent variable (sample of antacid) and dependent variable (amount of acid needed to neutralize the antacid). The five beakers were filled with 200 ml of water each. Using the marker pen, the five beakers were labeled with code numbers A, B, C, D and E. Each tablet form of antacid was crushed first using the mortar and pestle then five types of antacids were mixed together with the water in their respective beakers, named according to the code number of sample. 40 ml 0.1N of hydrochloric acid was poured into the burette. The burette was placed over the beaker labeled for sample A. The acid in the burette is inserted, drop by drop fallen into the beaker. With every drop, the solution was mixed using a stirrer and the pH reading is taken, until it reaches at 7.0. The amount of acid required to neutralize the solution in the beaker is recorded in the table below. The burette was refilled with hydrochloric acid until 40 ml again for the next samples B, C, D and E. Titrations were performed repeatedly for each sample like sample A. Table 2: Label information of antacid tablets Sl. No Brand Name Batch No. Mfg. Lic. No DAR No Mfg. Date Exp. Date Manufactured by A. B. C. D. E. Entacyd Entacyd Plus Maganta Plus Algicid XCID 405001 T0514048 505002 14014 407004 33&114 250&115 33&114 193&108 33&114 012-947-50 036-162-50 012-1089-29 116-953-29 012-875-67 May, 2014 June, 2014 May, 2015 Sep, 2014 Jul, 2014 Apr, 2016 Oct, 2016 Apr, 2017 Aug, 2016 Jun, 2016 SquarePharma. Ltd. SquarePharma. Ltd. SquarePharma. Ltd. Incepta Pharma. Ltd. SquarePharma. Ltd. Table 3: Contents of sample of antacids Sl. No Brand Name A. Entacyd Contains Dried Aluminium Hydroxide Gel BP 250 mg (Al2 O3 47%, minimum) and Magnesium Hydroxide BP 400 mg B. Entacyd Plus Dried Aluminium Hydroxide Gel BP 425.53 mg (Al2 O3, 47% minimum) and Magnesium Hydroxide BP 400 mg and Simethicone USP 30 mg C. Maganta Plus Magaldrate USP 480 mg and Simethicone USP 20 mg D. Algicid Sodium Alginate BP 500 mg and Potassium Bicarbonate BP 100 mg. E. XCID Calcium Carbonate BP 1000 mg 279 Global J. Pharmacol., 9 (3): 278-281, 2015 Fig. 1: Acid neutralizing efficacy of different antacid tablet formulations RESULTS This capacity may vary due to the variation in the tablet formulation. It was observed that the tablet formulation Sodium Alginate BP 500 mg and Potassium Bicarbonate BP 100 mg had higher acid neutralizing capacity. The physician should use the antacids with the higher neutralizing capacity to obtain faster symptomatic relief from dyspepsia. This in-vitro study may help in the further research works such as design and discovery of new antacid formulation. All the tablet formulations have effect on pH of acid solution. The tablet code no. D neutralizes highest 7 ml of acid solution and lowest 1.2 ml neutralize by antacid code no. C. The sequences from greatest efficacy to lowest efficacy of antacid according to amount of acid neutralization was D> E> B> A> C (Figure 1). DISCUSSION ACKNOWLEDGEMENT The main properties of antacid are; a small dose of antacid should neutralize an adequate volume of gastric acid, the maximum neutralizing effect should be achieved rapidly, the action should be maintained for a sufficient length of time and an antacid should ideally produce prolonged neutralization when administered in acceptable amounts. The measure of the antacid “capacity” of a preparation in terms of hydrochloric acid units with which physician is familiar and also in terms of pH values [10]. Theoretically ideal neutralization is the maintenance of gastric contents at a pH of 3.0 to 5.0 at which level pepsin activity is considerably reduced [11-13]. Our study shows that among the all types of antacids, systemic antacid (Sodium Alginate BP 500 mg and Potassium Bicarbonate BP 100 mg) has the greatest effect. In terms of the non systemic antacid, Calcium Carbonate BP 1000 mg has greatest effect. 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