Formulation and Evaluation of Oro-Dispersible Tablets Using Modified Polysaccharides

Journal Title: Saudi Journal of Medical and Pharmaceutical Sciences - Year 2017, Vol 3, Issue 1

Abstract

Abstract: Orodispersible tablets (ODT) of levocetirizine was prepared using natural polysaccharides ipomoea batatas starch, amorphophalluscampanulatus starch and their modified form by direct compression method and evaluated for their superdisintegrant activity. Levocetirizinedihydrochloride was used as a model drug. The prepared formulations were compared with synthetic superdisintegrants such as crosspovidone and diluent Ludiflash for disintegration and other ODT parameters. FTIR study indicated no interaction between drug and excipients. Precompression parameters, studied for all the formulations were found to be satisfactory. Different concentrations of 2.5%, 5, 7.5% and 10% of modified and unmodified forms of both starches were studied for the improvement in the ODT parameters. The formulations LISN (10%), LISM (10%) (LIS-levocetirizinedihydrochloride+ ipomoea batatas starch; N-Natural; M-Modified) and LASN (10%), LASM (10%) (LAS-levocetirizinedihydrochloride+amorphophalluscampanulatusstarch; N-Natural; M-modified) of both the starches showed better DT than lower concentrations. Synthetic superdisintegrantcrosspovidone was compared with formulations of natural superdisintegrants. The formulation containing crospovidone 5% concentration showed better DT of 32 seconds compared to natural superdisintegrants, and was used for further comparison of modified polysaccharides. The tablets prepared with Ludiflash as diluent without crospovidone, showed no significant difference in disintegration time. The formulation LASMLU (LAS-Levocetirizinedihydrochloride + amorphophalluscampanulatus starch; M-Modified; Lu-Ludiflash) showed 95% of drug release compared to other formulations. The release profile of 10% of modified amorphophalluscampanulatus starch LASM or Ludiflash (LASMLU) formulations did not show any significant difference in release profile. Hence in conclusion starch citrate, a new modified starch at 10% or at 5% concentration with crosspovidone with or without Ludiflash as diluent can be used as superdisintegrant for the preparation of orodispersible tablets. Keywords: Levocetirizine-dihydrochloride, Oro-dispersible tablets, direct compression, ipomoea batatas starch, amorphophalluscampanulatus starch

Authors and Affiliations

P. K. Lakshmi, D. Vinod Kumar, K. Harini

Keywords

Related Articles

Chronic Consumption of ThermoxidizedPalm Oil Diet (TPO) Adversely Affects Haemostatic Status and Histology of Some Organs in Rabbit

Abstract:This study seeks to investigate the effects of chronic consumption of fresh palm oil(FPO) and thermoxidized palm oil (TPO) diets on indices of haemostasis and related organs.Eighteen male rabbits weighing 750–10...

Effect of Nutritional Status and Life Style on Type 2 Diabetes Mellitus Patients in Western Libya

Abstract:This study was descriptive cross-sectional study, aimed to study the effect of nutritional status, and lifestyle habit among type 2 DM patients in Surman, Western-Libya. A total of 130 type 2 DM patients were en...

Formulation and Evaluation of Flubiprofen Emulgel by Using Different Concentration CARBOPOL 974P

Abstract:The aim and objective of this study was to formulate and evaluate the Flurbiprofen emulgel as a topical drug delivery which is a novel and advantageous delivery system forhydrophobic drugs to systemic circulatio...

Biomarkers of Oxidative Stress and Inflammation in Patients with Rheumatoid Arthritis

Abstract:Rheumatoid arthritis (RA) is a chronic, autoimmune, systemic disease, characterized by polyarthritis, erosive synovitis and sometimes shows multi system involvement. Oxidative damage induced by reactive species...

Effect of hydrophobic polymer on release profile of DiltiazemHCl loaded gelatinous microsphere cross-linked with glutaraldehyde

Abstract: In this study, gelatin microspheres containing diltiazem hydrochloride (DTZ HCl) were prepared by the polymerization technique using glutaraldehyde as the cross-linking agent. The prepared microspheres were exa...

Download PDF file
  • EP ID EP389223
  • DOI -
  • Views 110
  • Downloads 0

How To Cite

P. K. Lakshmi, D. Vinod Kumar, K. Harini (2017). Formulation and Evaluation of Oro-Dispersible Tablets Using Modified Polysaccharides. Saudi Journal of Medical and Pharmaceutical Sciences, 3(1), 13-22. https://europub.co.uk/articles/-A-389223