THE EFFECT OF A NOVEL HYDROPHILIC BIOPOLYMER DERIVED FROM IPOMOEA BATATAS TUBER AS A GRANULATING AGENT IN PARACETAMOL TABLET FORMULATION
Abstract
A novel hydrophilic biopolymer, I-polygel (IP) derived from the tubers of Ipomoea batatas was evaluated as a granulating agent at 2.50-5.50 % w/w in paracetamol tablets. Its compatibility with paracetamol was investigated using differential scanning calorimetry (DSC).  The micromeritic properties of the granules prepared by wet granulation method were considered.  They were compressed into tablets with a 12.5 mm flat-faced punch‎ fitted in a single punch tabletting machine. The weight uniformity, mechanical properties, disintegration time, dissolution profile, dissolution efficiency (DE) and the organoleptic properties of the tablets were studied. Gelatin (GT) was employed as a standard granulating agent. From the results, DSC thermograms showed that paracetamol was compatible with IP. Flowability and compressibility of the granules generally improved with increasing concentrations of the granulating agents with GT yielding better results (p > 0.05). The uniformity of weight of all the batches of tablets exhibited a variation in tablet weight ranging between 0.37 – 0.87 %. A consistent increase in the  mechanical properties of the tablets along the line of increasing concentrations of IP or GT with a corresponding decrease in friability was recorded, with GT indicating better outcomes at each concentration (p<0.05). The batches of tablets containing IP disintegrated within 3.76 -7.62 min whereas those of GT disintegrated between 10.89-20.92 min. All the batches of tablets containing IP and only 2.5 % w/w GT released up to 80 % of paracetamol within 30 min. The highest values of DE of 71.32- 74.17 % was obtained within 2.50-4.0 % w/w of IP only (p<0.05). Tablets with acceptable mechanical strength were obtained with either IP or GT, but lower disintegration time (<<< 15.00 min) and highest DEs of tablets were obtainable only with IP at the concentrations of 2.50-4.00 % w/w, showing that IP was better than GT as a granulating agent.
Keywords: Hydrophilic biopolymer, I-polygel, Ipomoea batatas, granulating agent, paracetamol, tablet.
DOI
https://doi.org/10.22270/jddt.v8i2.1669References
Loyd V. Allen Jr, Popovich NG, Ansel HC. Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems. 8th ed. Baltimore, Md: Lippincott Williams & Wilkins; 2005. P. 228-245.
Augsburger LL, Hoag SW (eds). Pharmaceutical Dosage Forms. In: Tablets (3rd ed.), Volume 2: Rational Design and Formulation. New York, Informa Healthcare, 2008.
Gupta P, Nachaegari SK, Bansal AK. Improved excipient functionality coprocessing. In: Katdare KA, Chaubal MV, eds. Excipient developement for pharmaceutical biotechnology, and drug delivery systems. New York: Taylor & Francis, USA, 2006:109-126
Moreton RC. Excipient functionality, Pharm Technol, 2004; 28(98):99, 119.
Tousey MD. The manufacturing process: Tablet and capsule manufacturing. Solid dose Experts Techceuticals Training. 2015; (15):1-12.
Adedokun MO, Ayorinde JO, Odeniyi MA. Compressional, mechanical and release properties of a novel gum in paracetamol tablet formulations. Curr. Issues Pharm. Med. Sci., 2014; 27(3):187-194.
Ugoeze KC, Nwachukwu N, Nwodo CC. Excipient Functionality of a Novel Hydrophilic Biopolymer derived from Ipomoea batatas Tubers. Indo American Journal of Pharmaceutical Research, 2017; 7(7)360-368.
Ugoeze KC, Nwachukwu N, Evaluation of the Suspending Properties of a Novel Hydrophilic Biopolymer Derived from the Tubers of Ipomoea batatas on Sulphamethoxazole Suspension. Journal of Advances in Medical and Pharmaceutical Sciences, 2017; 15(2):1-8.
Carstensen JT, Chan FC. Flow rates and repose angle of wet-processed granulations. J. Pharm. Sci. 1977; 66:1235.
Odeku OA, Awe OO, Popoola B, Odeniyi MA, Itiola OA. Compression & mechanical properties of tablet formulations containing corn, sweet potato and cocoyam starches as binders. Pharm. Technol. 2005; 29(4):82-90.
Carr R. Classifying flow of solids. Chem. Eng. 1965; 72:69-72.
Hausner HH. Friction conditions in a mass of metal powder. Int. J. Powder Metal. 1967; 3:7-13.
British Pharmacopeia. Vols. 1 and 2; London, Her Majesty’s Stationary Office, 1980.
Fell JT, Newton JM. Determination of tablet strength by the diametral compression test. J. Pharm. Sci. 1970; 59:688-691.
Merck Index 39. Available from: https://www.rsc.org/merck-index. Retrieved on 5th August 2017.
Haynes WM (ed.). CRC Handbook of Chemistry and Physics. 94th Edition. Boca Raton, CRC Press LLC, FL 2013-2014, pp. 3-314.
United States Pharmacopeia. 30th Edition, National Formulary 25th ed., Rockville, MD, USA, United States Pharmacopeia Convection, 2007.
Published
Abstract Display: 695
PDF Downloads: 785 How to Cite
Issue
Section
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgment of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).

.