Formulation and evaluation of glipizide-loaded fast-dissolving tablets using husk of Plantago ovata as a superdisintegrant
Main Article Content
Abstract
respectively. The tablet blends were converted into tablets by using direct compression method. The tablets were evaluated for disintegration test, hardness test, friability test, drug entrapment efficiency, content uniformity tests and drug release study. Formulations, which contained pregelatinized husk of P. ovata as a superdisintegrant, showed faster disintegration, higher percentage friability and lesser hardness than formulations containing husk of P. ovata as a superdisintegrant. Drug entrapment efficiency was found to be uniform among different batches of the tablets and ranged from 97.53±0.52 to
99.72±0.45.The results of content uniformity test of all the batches were found in the official range.The batches containing husk of P. ovata as a superdisintegrant released 15%–27% of glipizide per minute and those containing pregelatinized husk of P. ovata as a superdisintegrant released more than 95% of the drug within a minute.These results revealed that pregelatinized
husk of P. ovata can be used as a superdisintegrant for obtaining FDTs.
Downloads
Article Details
This is an Open Access article distributed under the terms of the Attribution-Noncommercial 4.0 International License [CC BY-NC 4.0], which requires that reusers give credit to the creator. It allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, for noncommercial purposes only.
References
Ciper M, Bodmeier R. Modified conventional hard gelatin capsules as
fast disintegrating dosage form in the oral cavity. Eur J Pharm Biopharm
;62:178-84.
Mizumoto T, Masuda Y, Yamamoto T, Yonemochi E, Terada K.
Formulation design of a novel fast-disintegrating tablet. Int J Pharm
;306:83-90.
Seager H. Drug-delivery products and the Zydis fast-dissolving dosage
form. J Pharm Pharmacol 1998;50:375-82.
Sastry SV, Nyshadham JR, Fix JA. Recent technological advances in oral
drug delivery- a review. Pharm Sci Technolo Today 2000;3:138-45.
Dobetti L. Fast-melting tablets: developments and technologies. Pharm
Technol (North Am) Suppl., 2001:44-50.
Jeong SH, Park K. Development of sustained release fast-disintegrating
tablets using various polymer-coated ion-exchange resin complexes.
Int J Pharm 2008;353:195-204.
Sweetman, SC. Martindale: The complete drug reference. 36th ed.
London: Pharmaceutical Press; 2009. p. 441.
Allen LV. Rapid-dissolve technology: an interview with Loyd V. Allen.
Int J Pharm Technol 2003;7:449-50.
Fu Y, Yang S, Jeong SH, Kimura S, Park K. Orally fast disintegrating
tablets: developments, technologies, taste-making and clinical studies.
Crit Rev Ther Drug Carrier Syst 2004;21:433-76.
Rawas-Qalaji MM, Simons FE, Simons KJ. Fast-disintegrating sublingual tablets: effect of epinephrine load on tablet characteristics. AAPS PharmSciTech 2006;7:E41.
Monif T, Malhotra AK, Kapoor VP. Cassia fistula seed galactomannan:
Potential binding agent for pharmaceutical formulation. Indian J Pharm
Sci 1992;54:234-40.
Kapoor VP, Banerji R, Prakash D. Leguminous seeds: Potential industrial sources for gum, fat and protein. J Sci Ind Res 1992;51:1-22.
Baveja SK, Gupta BM. Rheology of aqueous dispersion of Plantago ovata seed husk-II. Indian J Pharm Sci 1968;30:247-51.
Cooper J, Gunn C. Powder flow and compaction. In: Carter SJ, editor.
Tutorial Pharmacy. New Delhi, India: CBS Publishers and Distributors;
p. 211-33.
Shah D, Shah Y, Rampradhan M. Development and evaluation of
controlled release diltiazem hydrochloride microparticles using cross-
linked poly (vinyl alcohol). Drug Dev Ind Pharm 1997;23:567-74.
Aulton ME, Wells TI. Pharmaceutics: The science of dosage form design.London, England: Churchill Livingstone; 1988.
United States Pharmacopeia 24/NF19. The Official Compendia of
Standards. Asian ed. Rockville, MD: United States Pharmacopoeial
Convention Inc. 2000. p. 1913-4.
Qureshi SA. Tablet testing. In: Swarbrick J, Encyclopedia of
pharmaceutical technology. 3rd ed. New York. London: Informa
Healthcare 2007. p. 3707-16.
Patel JK, Patel RP, Amin AF, Patel MM. Formulation and Evaluation
of Mucoadhesive Glipizide Microspheres. AAPS PharmSciTech
;20;6:E49-55.
Khan S, Kataria P, Nakhat P, Yeole P. Taste masking of ondansetron
hydrochloride by polymer carrier system and formulation of rapid-
disintegrating tablets. AAPS PharmSciTech 2007;8:Article 46.
Morita Y, Tsushima Y, Yasui M, Termoz R, Ajioka J, Takayama K. Evaluation of disintegration time of rapidly disintegrating tablets via a novel method utilizing a CCD camera. Chem Pharm Bull (Tokyo) 2002;50:1181-6.
Shibata Y, Yamamoto Y, Fujii M, Kondoh M, Watanabe Y. A novel method
for predicting disintegration time in the mouth of rapid disintegrating
tablet by compaction analysis using Tab AII. Chem Pharm Bull (Tokyo)
;52:1394-5.
Narazaki R, Harada T, Takami N, Koto Y, Ohwaki T. A new method for
disintegration studies of rapid disintegrating tablets. Chem Pharm Bull
(Tokyo) 2004;52:704-7.
Ishikawa T, Mukai B, Shiraishi S, Utoguchi N, Fujii M, Matsumoto M,
et al. Preparation of RDT using new type of microcrystalline cellulose
(PH-M series) and low substituted-hydroxypropyl cellulose or spherical
sugar granules by direct compression method. Chem Pharm Bull (Tokyo)
;49:134-9.
Shin SC, Oh IJ, Lee YB, Choi HK, Choi JS. Enhanced dissolution of
furosemide by coprecipitating or cogrinding with crospovidone. Int J
Pharm 1998;175:17-24.
Martin A. Micromeritics. In: Martin A, editor. Physical Pharmacy.
Baltimore, MD: Lippincott Williams & Wilkins; 2001. p. 423-54.
Banker GS, Anderson LR. Tablets. In: Lachman L, Liberman HA, Kanig JL,et al. The Theory and Practice of Industrial Pharmacy. Mumbai, India:
Varghese Publishing House; 1987. p. 293-345.