by Dr. Yashashwini Reddy | Aug 9, 2025
Limitations in Dissolution Testing Poor In-Vivo Correlation (IVIVC) Dissolution data may not accurately predict drug release in the human body due to complex gastrointestinal (GI) conditions. Single-Media Testing Conventional USP tests often use only one dissolution...
by Dr. Yashashwini Reddy | May 3, 2025
Granule size plays a crucial role in the formulation and performance of tablet-based pharmaceutical products. It significantly affects both the stability of the tablet during its shelf life and the bioavailability of the drug when taken by the patient....
by Dr. Yashashwini Reddy | Apr 27, 2025
Standard Operating Procedure (SOP) 1. Purpose This SOP describes the selection criteria and step-by-step procedure for choosing appropriate samples for dissolution profile studies to ensure accurate, reproducible, and scientifically justified...
by Dr. Yashashwini Reddy | Apr 17, 2025
1. What is a dissolution apparatus? Why is it used? A dissolution apparatus is a lab device used to measure the rate at which a drug is released from a dosage form (like a tablet or capsule) into a solution. It’s a key tool in drug development and quality...
by Dr. Yashashwini Reddy | Oct 21, 2024
The specifications of the disintegration test apparatus are crucial to ensure accurate and consistent results when evaluating the quality of immediate-release tablets. Each component and the movement of the apparatus are precisely designed to simulate conditions...
