Author(s): Amitkumar J. Vyas, Sinchan M. Patel, Ashok B. Patel, Ajay I. Patel, Nilesh K. Patel, Suuny Shah, Devang Sheth

Email(s): patelsivu31@gmail.com

DOI: 10.52711/2231-5691.2022.00006   

Address: Amitkumar J. Vyas, Sinchan M. Patel*, Ashok B. Patel, Ajay I. Patel, Nilesh K. Patel, Suuny Shah, Devang Sheth
B. K. Mody Government Pharmacy College, Rajkot-360003, Gujarat, India.
*Corresponding Author

Published In:   Volume - 12,      Issue - 1,     Year - 2022


ABSTRACT:
Forced degradation studies are carried out at a more severe condition than accelerated conditions. Stress studies for vaccines are carried out in the early stage of development. By conducting stress studies, we can know the chemical behavior of our molecule which is important while developing formulation, packaging, transportation, storage, etc. there are general regulatory guidelines are available for conducting forced degradation studies but there is no sufficient information provided about how to perform forced degradation studies. Thus, this review discussed stress testing studies of vaccines, mechanisms of vaccine degradation, also analytical methods which are helpful to develop a method for forced degradation.


Cite this article:
Amitkumar J. Vyas, Sinchan M. Patel, Ashok B. Patel, Ajay I. Patel, Nilesh K. Patel, Suuny Shah, Devang Sheth. Stability testing: An Essential study for Vaccine Formulation Development. Asian Journal of Pharmaceutical Research. 2022; 12(1):29-6. doi: 10.52711/2231-5691.2022.00006

Cite(Electronic):
Amitkumar J. Vyas, Sinchan M. Patel, Ashok B. Patel, Ajay I. Patel, Nilesh K. Patel, Suuny Shah, Devang Sheth. Stability testing: An Essential study for Vaccine Formulation Development. Asian Journal of Pharmaceutical Research. 2022; 12(1):29-6. doi: 10.52711/2231-5691.2022.00006   Available on: https://www.asianjpr.com/AbstractView.aspx?PID=2022-12-1-6


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