Open Access Open Access  Restricted Access Subscription Access

Formulation of Areca Nut Tablet using Cassava Starch and Swamp Taro Starch as Disintegrant:A Comparative Study


Affiliations
1 Eastern Samar State University, Borongan City, Eastern Samar, Philippines
 

Objectives: This study formulated a tablet using cassava and swamp taro starch as disintegrant and areca nut as active anthelmintic agent; the tablet was manually compacted and its physical, mechanical and disintegrating properties were determined. Methods/Statistical Analysis: Experimental design was utilized wherein two tablet formulations were subjected to physical, mechanical and disintegrating tests. Physical properties include color, density, odor, pH and solubility; mechanical property of the tablet was also tested in terms of hardness and friability; and disintegrating property was determined using simulated gastric fluid and simulated intestinal fluid. T-test was used to determine significant difference in terms of disintegration of the two tablets using IBM SPSS version 21. Findings: Results showed that the color and odor of both tablets are brown with white specks and odorless, respectively. Both tablets were insoluble to organic and inorganic solvents, but are slightly soluble to alcoholic medium; moreover, both tablets possess the same pH of 6.0. Friability tests showed high friability and a low compressive strength or hardness. Further statistical computations in terms of disintegration showed that cassava starch-based tablet is more rapid in disintegrating than swamp taro starch-based tablet regardless of simulated fluid. Application/Improvements: These findings indicate that cassava starch can be used as disintegrant, also this also highlights that direct compaction or manual compaction method of tableting gives a tablet lower hardness and higher friability. This study suggests cassava starch is more suitable as disintegrant than swamp taro, and that both starches can be used for veterinary drug development.
User

  • Augsburger LL. Knowledge-based systems and other ai applications for tableting. 3rd edition. pharmaceutical dosage forms: Tablets. Baltimore. 2004; 2:1–71.
  • Pharmaceutical industry neglects developing countries [Internet]. [cited 2017 Jan 14]. Available from: www.dw.com/en/pharmaceutical-industry-neglects-developingcountries/ a-16331939.
  • Anthelminthic Drugs [Internet]. [cited] 2013 May 30. Available from: https://www.slideshare.net/shrinathraman/antihelminthic-drugs.
  • Gberindyer F, Onyeyili P, Bosha J. Quality control properties of some brands of veterinary Albendazole boluses common in Nigeria. Journal of Pharmacy and Pharmacology. 2014; 2(2):135–39.
  • Hoashi Y, Tozuka Y, Takeuchi H. Development of a novel and simple method to evaluate disintegration of rapidly disintegrating. Tablets. Chemical and Pharmaceutical Bulletin. 2013; 61(9):962–66. https://doi.org/10.1248/cpb.c13-00441
  • Ministry of Health. Official method: Determination of the disintegration time of tablets. 2nd Edition. Canada; 1989.

Abstract Views: 215

PDF Views: 0




  • Formulation of Areca Nut Tablet using Cassava Starch and Swamp Taro Starch as Disintegrant:A Comparative Study

Abstract Views: 215  |  PDF Views: 0

Authors

Aljon Victor G. Nibalvos
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Esther R. Banar
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Edmundo A. Campoto
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Maricar T. Obina
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Delbert A. Dala
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Loida A. Rapada
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Lylah Daisy A. Acorin
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Debbie Joyce R. Voloso
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Jenny Rose U. Kruse
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Rey Niel C. Salac
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Noel Amit
Eastern Samar State University, Borongan City, Eastern Samar, Philippines
Neil Alejandro A. Pinarok
Eastern Samar State University, Borongan City, Eastern Samar, Philippines

Abstract


Objectives: This study formulated a tablet using cassava and swamp taro starch as disintegrant and areca nut as active anthelmintic agent; the tablet was manually compacted and its physical, mechanical and disintegrating properties were determined. Methods/Statistical Analysis: Experimental design was utilized wherein two tablet formulations were subjected to physical, mechanical and disintegrating tests. Physical properties include color, density, odor, pH and solubility; mechanical property of the tablet was also tested in terms of hardness and friability; and disintegrating property was determined using simulated gastric fluid and simulated intestinal fluid. T-test was used to determine significant difference in terms of disintegration of the two tablets using IBM SPSS version 21. Findings: Results showed that the color and odor of both tablets are brown with white specks and odorless, respectively. Both tablets were insoluble to organic and inorganic solvents, but are slightly soluble to alcoholic medium; moreover, both tablets possess the same pH of 6.0. Friability tests showed high friability and a low compressive strength or hardness. Further statistical computations in terms of disintegration showed that cassava starch-based tablet is more rapid in disintegrating than swamp taro starch-based tablet regardless of simulated fluid. Application/Improvements: These findings indicate that cassava starch can be used as disintegrant, also this also highlights that direct compaction or manual compaction method of tableting gives a tablet lower hardness and higher friability. This study suggests cassava starch is more suitable as disintegrant than swamp taro, and that both starches can be used for veterinary drug development.

References





DOI: https://doi.org/10.17485/ijst%2F2018%2Fv11i43%2F131059