Vol.1 , No. 4, Publication Date: Aug. 31, 2015, Page: 45-50
[1] | Ugoeze K. C., Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, University of Port Harcourt, Port Harcourt, Nigeria. |
[2] | Nkoro V. O., Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, University of Port Harcourt, Port Harcourt, Nigeria. |
[3] | Nwachukwu N., Department of Pharmaceutics and Pharmaceutical Technology, Faculty of Pharmaceutical Sciences, University of Port Harcourt, Port Harcourt, Nigeria. |
Ibuprofen has poor water solubility. Its direct compressibility into tablet is difficult due to poor flowability and compactibility. The suitability of a novel multicomponent Lentinus tuber regium based co-processed excipient (fizlent) as a directly compressible (DC) filler-binder and superdisintegrant in ibuprofen tablet was investigated. Ibuprofen (76.92% w/w) blended with fizlent (22.58 % w/w) and lubricated with 0.50 % w/w magnesium stearate was compressed at 8 tons in Erweka table top single punch tablet press fitted with 8.50 mm biconvex punch and die. Tablet weights, total drug content, crushing strength, friability and disintegration time were determined using the British Pharmacopoeia methods. The basket method in Erweka dissolution apparatus at 50 rpm was used for dissolution study in 900 ml phosphate buffer (pH 7.2) at 37 ± 1o C for 60 min. The absorbance of samples withdrawn at 5 min intervals were spectrophometrically determined at wavelength of 221nm. Glossy, intact, off-white, round and convex shaped tablets obtained disintegrated within 30.17 ± 1.94s. Other tablet properties complied within pharmacopoeia limit. The application of fizlent as filler-binder in DC of ibuprofen tablet solved problem of its poor compactability and flowability. The ability of the tablet to break down completely in 30.17 ± 1.94 s shows that fizlent has a superdisintegrant property. This aided the early release and dissolution of ibuprofen, hence its ability to achieve T50, T80 in less than 5 min and T90 in 12.50 min. Furthermore, the onset of action and attainment of peak plasma concentration of ibuprofen will not be prolonged, thus, resolving the issues with poor water solubility noted for ibuprofen.
Keywords
Lentinus tuber regium, Co-processed, fizlent, Directly Compressible, Filler-Binder-Superdisintegrant, Ibuprofen
Reference
[01] | Chein YW (2002). Oral Drug delivery and delivery systems. In: Novel drug delivery systems. Marcel Dekker, Inc., New York, Vol. 50; 3rd edition: 139-96. |
[02] | AnupamaKalia, shelly Khurana, Neena Bed (2009). Formulation and evaluation of mouth dissolving tablets of oxcarbazepine. International journal of pharmacy and pharmaceutical science 1(1):12-23. |
[03] | Avachat A, Ahire V (2007). Characterization and evaluation of spray dried co-processed excipients and their application in solid dosage forms. Indian J. Pharm. Sci. 69:85-90. |
[04] | Saha S, Shahiwala AF (2009). Multifunctional co-processed excipients for improved tabletting performance. Expert Opin. Drug Deliv. 6:197-208. |
[05] | Bolhuis GK, Armstrong AN (2006). Excipient for direct compaction-an update. Pharm. Dev. Technol. 11:111-124 |
[06] | Jacob S, Shirwaikar A, Joseph A, Srinivasan K (2007). Novel co-processed excipients of mannitol and microcrystalline cellulose for preparing fast dissolving tablets of glipizide. Indian J. Pharm. Sci. 69:633-639. |
[07] | Villanova JCO, Ayres E, Oréfice RL (2011). Design of prolonged release tablets using new solid acrylic excipients for direct compression. Eur. J. Pharm. BioPharm. 79: 664–673 |
[08] | Gowtham Kumar, Dokala, Ch. Pallavi (2013). Direct Compression - An overview. International Journal of Research in Pharmaceutical and Biomedical Sciences. Vol. 4 (1) 155-158. |
[09] | Gohel MC, Jogani PD (2005). A review of co-processed directly compressible excipients. J Pharm Sci. 8(1):76-93. |
[10] | Haware RV, Tho I, Bauer-Brandl A (2010). Evaluation of a rapid approximation method for the elastic recovery of tablets. Adv. Powder Technol. 202 (1-3):71-7. |
[11] | John R, Julian A, Manuel H (2013). Screening of several excipients for direct compression of tablets: A new perspective based on functional properties. Journal of Basic and Applied Pharmaceutical Sciences 34(1):17-23. |
[12] | Lawrence H Block RC, Moreton PS, Apte RH, Wendt EJ, Munson JR, Creekmore IV, Persaud CS, Hong W (2009). Co-processed excipients. Pharmacopoeial forum, 35(4): 1026-1028. |
[13] | B. Shravani NG, Raghavendra Rao (2014).Formulation and Evaluation of Fast Dissolving tablets of Montelukast sodium using Co-Processed Superdisintegrants. Int. J. Drug Dev. & Res. 6 (1): 125-134 |
[14] | Chang D, Chang R (2007). Review of current issues in pharmaceutical excipients. Pharm Technol 31:56. |
[15] | Larner G, Schoneker D, Sheehan C, Uppoor R, Walsh P, Wiens R (2006). Pharmaceutical excipient testing and control strategies. Pharm Technol. 1:1-7. |
[16] | Block LH, Moreton RC, Apte SP, Wendt RH, Munson EJ, Creekmore JR, Persaud IV, Sheehan C, Wangc H (2009). Co-processed excipients. Pharm Forum 35:1026-1028. |
[17] | Nachaegari SK, Bansal AK (2004). Co-processed excipients for solid dosage forms. Pharm Technol, 28(1): 52-64. |
[18] | Marwaha M, Sandhu D, Marwaha R (2010). Co-processing of excipients: A review on excipient development for improved tableting performance. Int. J. Appl. Pharm. 2:41- 47. |
[19] | Ugoeze KC, Nkoro VO (2015). The physico-technical properties of a multicomponent Lentinus tuber regium based co-processed excipient (Fizlent). American Journal of Pharmacy and Pharmacology. 2(3):13-20. |
[20] | Halford GM, Lordkipanidzé M, Watson SP (2012). 50th anniversary of the discovery of ibuprofen: an interview with Dr. Stewart Adams. Platelets 23 (6): 415–22. |
[21] | Shailender Mohan (2012). Compression physics of pharmaceutical powders: a review. Int. J Pharm Sci. Res 3(6): 1580-1592. |
[22] | Aly Nada, Bernd W. Mueller, Saleh M. Al-Saidan (2005).Improving the physical and chemical properties of ibuprofen. Pharmaceutical Technology 29:11. |
[23] | Kirchheiner J, Brockmöller J (2005). Clinical consequences of cytochrome P450 2C9 polymorphisms. Clin. Pharmacol. Ther. 77: 1-16. |
[24] | Joe Tucci, Emily Bandiera, Rima Darwiche, Zeljko Medos, Robert Nashed, David Trinh (2009). Paracetamol and ibuprofen for paediatric pain and fever. Journal of Pharmacy Practice and Research Volume 39(3): 223-225. |
[25] | 18th WHO Model: List of Essential Medicines (April 2013) http://www.who.int/medicines/publications/essentialmedicines/en/ Retrieved 11th August, 2015. |
[26] | British Pharmacopeia. Her Majesty`s Stationery Office, University press, Cambridge. 2012. |
[27] | Promode RS (2014). An overview on bilayered tablet technology. Int. J. Pharm. Bio. Sci. 5 (2): (P) 113 - 128 |
[28] | Emeje M, Isimi C, Kunle O (2008). Effect of Grewia gum on the mechanical properties of Paracetamol tablet formulations. Afr. J. Pharm. Pharmacol. 2: 1-6. |
[29] | Mbah CC, Emosairue CO, Builders PF, Isimi CY, Kunle OO (2012). Effect of process parameters on the properties of some metronidazole tablet and capsule formulations. African Journal of Pharmacy and Pharmacology 6(24): 1719-1725. |
[30] | Odeku OA (2005). Assessment of Albiziazygia gum as binding agent in tablet formulations. Acta Pharm. 55: 263-276. |
[31] | Zhao N, Augsburger LL (2006). The influence of granulation on superdisintegrant performance. Pharm. Dev. Technol. 11:47-53 |
[32] | United States Pharmacopeia. 30th Edition, National Formulary 25th ed., United States Pharmacopeia Convection, Rockville, MD, USA. 2009. |
[33] | Okhuoya JA, Okogbo FO (1990). Induction of edible sclerotia of Pleurotus tuber-regium (FR) Singer in the laboratory. Ann. Appl. Biol. 117: 295-298. |
[34] | Isikhuemhen OS, Okhuoya JA 1995). A low cost technique for the cultivation of Pleurotus tuber-regium (FR.) Singer in developing tropical countries. The mushroom Growers’ Newsletter 4(6): 2 |