Understanding Dissolution

This Module is aimed at personnel who require an overview of dissolution testing, including the factors that affect dissolution, and how a solid dosage drug form is absorbed into the bloodstream. ‘In Vivo’ and ‘In Vitro’ analyses are explained and typical ‘In Vitro’ dissolution tests are described.

Whether for onboarding or annual refresher training, this Module is seamlessly deployable on any LMS and can be tailored to your company’s exact needs.

Duration: 30 Mins

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SKU: PPL-1210-SPL01-EN Category: Laboratory Tag: PPL

Description
Keywords

Description

Learning Objectives:

Define the term ‘dissolution’
Explain the purpose of dissolution testing
List and describe the factors that affect dissolution
Describe what happens to a solid dosage drug form in the human body after it is swallowed
Explain the difference between ‘in vivo’ and ‘in vitro’ dissolution analysis
Explain why in vitro dissolution analysis is important
Explain the difference between single-point and multi-point dissolution tests

Learner Benefits:

Clear Comprehension of Dissolution Fundamentals: Master the definition and essential purpose of dissolution, including the physical and chemical processes that influence how drugs dissolve.

Insight into Critical Testing Parameters: Recognize the factors impacting dissolution, such as solvent polarity, temperature, pH, and stirring, enhancing your understanding of formulation behavior in various environments.

Practical Understanding of Drug Absorption: Learn how a solid dosage form disintegrates and dissolves in the gastrointestinal tract before crossing into the bloodstream, crucial for assessing bioavailability.

Differentiation Between Analytical Techniques: Distinguish between ‘in vivo’ and ‘in vitro’ testing, appreciating the importance of simulating human conditions in laboratory settings to predict drug performance.

Module Features:

Animations
Voice Over
Knowledge Checks
Assessments
SCORM/AICC compatible
Full Screen