Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Development and Optimization of Orodispersible Tablets of Serotonin Hydrochloride


Affiliations
1 Pharmacy Institute, Noida Institute of Engineering and Technology, Noida, UP, India
     

   Subscribe/Renew Journal


In present study, the orodispersible tablets of Serotonin Hydrochloride were prepared by direct compression technique using microcrystalline cellulose (MCC) as direct compressible diluents. Superdisintegrants such as Croscarmellulose sodium (CCS) Sodium starch glycolate (SSG), and Crospovidone were used. Method: Using different concentrations of superdisintegrants seven formulations were made and further investigated .The prepared powder mixtures were subjected to both pre and post compression evaluation parameters including tablet hardness, friability, disintegration time and in vitro drug release. Results: The pre-compression studies revealed that all formulations were found to be of good flowability. Tablet hardness and friability revealed good mechanical strength. Conclusion: All the tablets exhibited acceptable properties. According to the present study, it was found that tablets of batch F4 (blend containing CCS and crospovidone (15mg) showed better disintegrating property as well as % drug release (98.78% within 40 min).

Keywords

Orodispersible Tablet, Serotonin Hydrochloride, Superdisintegrants.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Patidar A, Mishra P, Main P, Harsoliya S, Agrawal S. A review on-recent advancement in the development of rapid disintegrating tablet. Indian journal of life sciences and pharma research, 2011; 1(1): 7-16.
  • Sandeep D, Kunchu K, Ganesh N. Fast Disintegrating tablets-An emerging trend, 2011; 6(2): 18-22.
  • Fu Y, Yang S, Jeong H, Kimura S, Park K Orally fast disintegrating tablets: Development, technologies, taste-masking and clinical studies. Crit Rev Ther Drug Carrier Sys (2004) 21: 433-476. .
  • Leon L, Herbert A, Lieberman, Joseph L, Kanig. The theory and practice of Pharmacy. 3rd ed., Bombey; Varghese Publishing house, 1987.
  • BritishPharmacopoeia, 7th ed., Volume II. London; Published by HMSO, 1988.
  • Bhowmik D, Chiranjib B, Pankaj K and Chandira RM. Fast Dissolving Tablet: An Overview. Journal of Chemical and Pharmaceutical Research, 2009; 1(1): 163-77.
  • Ramesh K, Fasiha S, Hema KB, Vinay KM. Design and evaluation of sustained release matrix tablets of Levofloxacin employing almond gum. Int J Chem Sci., 2014; 12(3): 762-72.
  • Emami J, Tajeddin M, Ahmadi F. Preparation and in-vitro evaluation of sustainedrelease matrix tablets of Flutamide using synthetic and naturally occurring polymers. Iran J Pharm Res., 2008; 7(4): 247-57.
  • Kamal S, Gautam K, Yash P. Formulation and evaluation of fast dissolving tablets of Amoxicillin Trihydrate using synthetic superdisintegrants. Int J Pharm Bio Sci, 2013; 4(1): 254–262.
  • Anupama S, Somashekar N, Tamizhmani T. Recent approach for drug release from matrix tablet: a review. AJRPSB, 2016; 4(3): 122-132.
  • Banker GS, Anderson NR (2009) Tablets. In: Lachman L, Lieberman HA, Kanig JL. The theory and practice of industrial pharmacy. 3rd edn. New Delhi: CBS Publishers and Distributors. pp: 293-345.
  • Patel P, Roy A, Vinod Kumar SM, Kulkarni M (2011) Formulation and evaluation of colon targeted tablets of ornidazole for the treatment of Amoebiosis. Int J Drug Dev and Res 3: 52-61.
  • Cooper J, Gunn C (1986) Powder flow and compaction. In: Carter SJ (eds.) Tutorial Pharmacy. CBS Publishers and Distributors, New Delhi, India. pp: 211- 233.
  • Ainley wade, paul J weller. Handbook of pharmaceutical excipients part I and II. 2nd ed., American pharmaceutical association publication,1994.
  • Ganesh GNK, Sureshkumar R, Jawahar N, Senthil V, Nagasamy VD. Preparation and evaluation of sustained release matrix tablet of Diclofenac sodium using natural polymer.J Pharm Sci and Res., 2010; 2(6): 360-8.
  • Mitesh Nagar. Cinnarizine orodispersible tablets: A Chitosan based fast mouth dissolving technology. Int J of Pharm Tech research, 2009; 1(4): 1079-91.
  • Mohapatra A, Parikh RK, Gohel MC. Formulation, development and evaluation of patient friendly dosage forms of Metformin, part-I:orally disinrating tablets. AAPS, 2009; 167-171.
  • Bhagwati S.T., Hiremath S.N. and Sreenivas S.A., Comparative evaluation of disintegrants by formulating cefixime dispersible tablets, Indian J. Pharm. Edu. Res, 2005, 39, 194-197.

Abstract Views: 262

PDF Views: 1




  • Development and Optimization of Orodispersible Tablets of Serotonin Hydrochloride

Abstract Views: 262  |  PDF Views: 1

Authors

Pratik Swarup Das
Pharmacy Institute, Noida Institute of Engineering and Technology, Noida, UP, India
Puja Saha
Pharmacy Institute, Noida Institute of Engineering and Technology, Noida, UP, India

Abstract


In present study, the orodispersible tablets of Serotonin Hydrochloride were prepared by direct compression technique using microcrystalline cellulose (MCC) as direct compressible diluents. Superdisintegrants such as Croscarmellulose sodium (CCS) Sodium starch glycolate (SSG), and Crospovidone were used. Method: Using different concentrations of superdisintegrants seven formulations were made and further investigated .The prepared powder mixtures were subjected to both pre and post compression evaluation parameters including tablet hardness, friability, disintegration time and in vitro drug release. Results: The pre-compression studies revealed that all formulations were found to be of good flowability. Tablet hardness and friability revealed good mechanical strength. Conclusion: All the tablets exhibited acceptable properties. According to the present study, it was found that tablets of batch F4 (blend containing CCS and crospovidone (15mg) showed better disintegrating property as well as % drug release (98.78% within 40 min).

Keywords


Orodispersible Tablet, Serotonin Hydrochloride, Superdisintegrants.

References