Review Article on Inprocess Problems and Evaluation Tests of Tablets Manufacturing

Authors

  • Khatoon Shehnaz Assistant professor, Department of Pharmaceutics, Amar Shaheed Baba Ajit Singh Jujhar Singh Memorial College of Pharmacy, Bela, Ropar, Punjab, 140111, INDIA.
  • Singh Anmolpreet Student, Department of B. Pharmacy, Amar Shaheed Baba Ajit Singh Jujhar Singh Memorial College of Pharmacy, Bela, Ropar, Punjab, 140111, INDIA.
  • Kumar Pankaj Student, Department of B. Pharmacy, Amar Shaheed Baba Ajit Singh Jujhar Singh Memorial College of Pharmacy, Bela, Ropar, Punjab, 140111, INDIA.
  • Hashmi Masrror Student, Department of B. Pharmacy, Amar Shaheed Baba Ajit Singh Jujhar Singh Memorial College of Pharmacy, Bela, Ropar, Punjab, 140111, INDIA.

DOI:

https://doi.org/10.55544/jrasb.2.3.26

Keywords:

tablet, dissolution, problems

Abstract

Tablets are the traditional over all medicinal dosage forms for solid dosages. A tablet is a solid pharmaceutical dosage form that is typically manufactured by compressing or moldings the medicinal component with appropriate diluents. They are easier to create than any other dosage form, but during manufacturing, a number of issues may occur that force the batch to be discarded. Post compression studies are also crucial before the dosage forms are put on the market. Modern standards and concepts that emphasize bioavailability, bioequivalence, and validation, among other things, have an impact on formulation design and production. In this article, we discussed the issues (Picking, Sticking, Mottling, etc.) that will arise during the production of tablets, their solutions, as well as the pre- and post- Compression qualities (such as hardness, thickness, and weight variation) and the upper limitations of their use in commercial dosage forms.

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

References

Leon Lachman, Herbert A. Lieberman, Joseph L. Kanig: The theory and Practice of Industrial Pharmacy, Varghese publication house, 3rd edition, 1990, 293-373.

Bhalla H L, Handa, A K. Development and Evaluation of Controlled Release Tablets of CBZ, Indian Drugs, 36(2), 1999, 100 - 195.

Chein YW. Novel drug delivery systems, In: chein YW, ed. Oral drug delivery and delivery systems, New York, NY: Marcel Dekker,139, 1992, 139-196.

Vyas S P, Khar. Controlled drug delivery: concepts and advances in: Vyas S P, Khar, eds, Controlled oral administration, Delhi, India: Vallabh Prakashan, 2002, 155-195.

Deependra Singh, Hemant Kumar, Abhisek Pathak,Ram Milan Vishwakarma. Review Article on In-process Problems and Evaluation Tests of Tablet Manufacturing: IJPRA, 6(5) 2021,79-83

G. Hymavathi, J. Adilakshmi, K. Dwarathi, M. Kavya, G. Pravallika, Review article on inprocess problems and evaluation tests of tablet manufacturing: IJRPNS, 4(3), 2015, 175-179.

Downloads

Published

2023-07-05

How to Cite

Khatoon, S., Singh, A., Kumar, P., & Hashmi, M. (2023). Review Article on Inprocess Problems and Evaluation Tests of Tablets Manufacturing. Journal for Research in Applied Sciences and Biotechnology, 2(3), 198–201. https://doi.org/10.55544/jrasb.2.3.26

Issue

Section

Articles