Preclinical Safety Profile of an Oral Naringenin/Hesperidin Dosage Form by In Vivo Toxicological Tests

A Green Potentiometric Application for Selective Monitoring of Doxylamine Succinate Dissolution Profile in Combined Dosage Form

"Green analytical chemistry" (GAC) succeeded to become an eco-friendly environmental crucial area in the field of analytical chemistry targeting at the chemical processes' and products' optimization regarding to material consumption, generation of waste and intrinsic safety, toxicity and environmental burdens. For an expressive comparison, an electro-analytical in-line potentiometric selective ...

Formulation Development of Solid Oral Dosage Form

6.1 Literature review matrix Taha E. et al (2015) evaluated Diclofenac Sodium (DS) matrix tablets prepared by direct compression method under different compression forces using ethyl cellulose as matrix forming material. The produced tablets were characterized for hardness, friability, drug content, weight variations and in vitro drug release. Incompatibility study carried out using DSC FT-IR s...

the washback effect of discretepoint vs. integrative tests on the retention of content in knowledge tests

در این پایان نامه تاثیر دو نوع تست جزیی نگر و کلی نگر بر به یادسپاری محتوا ارزیابی شده که نتایج نشان دهندهکارایی تستهای کلی نگر بیشتر از سایر آزمونها است

"In vitro" dissolution tests for solid oral dosage forms.

©2010 Particle Sciences, Inc. All rights reserved. the drug substance and involves two steps: dissolution and absorption (or permeability). Understanding the multi-step dissolution process is essential to proper in vitro method development. Dissolution is the process of extracting the API out of the dosage form solid-state matrix into solution within the gastrointestinal tract. Absorption is th...

NIR prediction of solid dosage form dissolution profile