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Purpose-built Dissolution Testing for Orally Inhaled Products (OIPs)
The Inhaled Dissolution Apparatus (IDA) is a purpose-built platform developed to address a long-standing industry challenge in testing orally inhaled products (OIPs): generating repeatable, comparable dissolution profiles from aerosolised drug samples.
At the core of the IDA is a simple, 3-step workflow – Collect – Transfer – Dissolve – designed to streamline testing and support confidence in results.
Its performance is backed by data demonstrating repeatable formulation discrimination, helping teams detect meaningful differences where improvised approaches often fall short.
Patent Pending
IDA: A Streamlined Workflow for Inhaled Dissolution Testing
Key IDA Product Highlights
Repeatable, comparable dissolution data
Discriminatory performance
Purpose-built for OIPs
Optimised paddle and vessel design
Flexible inlet compatibility
Integrated dissolution testing platform
Automation compatible
Scientifically supported performance
How the IDA Works: A Simple 3-Step Process
Step 1: Collect
The aerosolised drug is collected onto a filter using the required inlet configuration. This enables consistent dose capture as the starting point for dissolution assessment.
Step 2: Transfer
The IDA uses a specially designed filter holder that allows the collected sample to be transferred directly into the dissolution test setup. The filter holder attaches to the dissolution paddle, enabling a smooth transition from collection to dissolution while minimising handling and supporting a consistent workflow.
Step 3: Dissolve
The filter is lowered into the dissolution vessel containing media and dissolution profiling is performed under controlled conditions. The flat-bottom vessel and paddle geometry are specifically designed to support OIP-relevant media volumes, helping to generate repeatable and comparable dissolution data.
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IDA Technical Specifications |
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Flow rate compatibility:
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5 – 100 L/min |
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Flow profile options:
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Supports constant flow and breathing simulation (tidal / inhalation-only)
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| Inlet compatibility: |
Compatible with common configurations including NGI Induction Port, NGI Preseparator, Fast Screening Impactor, Alberta Idealised Throat, Alberta Idealised Nasal Inlet AINI, Glass Expansion Chambers
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Stations available:
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6- or 8-station configurations
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Media volume range:
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200 – 500 mL
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Automation compatibility:
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Compatible with Vertus® III for automated shake and fire
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Inhaled Dissolution Apparatus IDA: FAQs
Explore our most frequently asked questions on the Inhaled Dissolution Apparatus IDAÂ and inhaled dissolution testing, covering workflow, configurations, and key benefits.
The Inhaled Dissolution Apparatus (IDA) is used to support inhaled dissolution testing by collecting aerosolised drug onto a filter and enabling dissolution profiling under controlled conditions. It was purpose-designed to address long-standing challenges in this area, where laboratories have often relied on adapted or inconsistent approaches that can make results difficult to repeat or compare. With its consistent Collect > Transfer > Dissolve workflow, the IDA helps generate repeatable, comparable dissolution profiles to support product understanding and comparative studies, in line with growing regulatory and industry demand for more robust in vitro performance evidence.
The Inhaled Dissolution Apparatus (IDA) supports testing of a wide range of orally inhaled and nasal drug products, and is compatible with a wide range of common inlet configurations. This allows dissolution assessment to be performed using the same collection approaches and interfaces routinely used in established in vitro testing, helping IDA complement and extend existing compendial workflows rather than requiring a completely different setup. Compatible configurations include the NGI Induction Port, NGI Preseparator, FSI, Alberta Throat (adult and child), AINI, and glass expansion chambers.
The IDA provides a purpose-built workflow specifically developed for orally inhaled products (OIPs), addressing the practical challenges of measuring dissolution from the small mass of drug typically collected during testing. The system uses a reduced-diameter paddle and a dedicated flat-bottom vessel to support OIP-relevant media volumes, helping maintain consistent circulation around the filter during testing. This optimised geometry supports repeatable, comparable dissolution profiling and reduces the uncertainty that can arise when adapting traditional dissolution equipment for inhaled applications.
The IDA is designed to support a consistent, repeatable inhaled dissolution workflow by reducing the number of handling steps between sample collection and dissolution testing. A key feature is the specially designed Filter Holder, which allows the collected sample to be transferred directly into the dissolution setup by attaching it directly to the specially adapted dissolution paddle. This minimises manual filter handling, helping protect the integrity of the collected dose and reducing the risk of sample disturbance, loss, or variability between tests. By supporting a standardised Collect > Transfer > Dissolve process, the IDA enables more repeatable dissolution profiling and more comparable data across studies and laboratories.
The IDA can be used with constant flow rate test setups (for example using a vacuum pump and flow controller) and can also be configured for more physiologically relevant flow conditions using a breathing simulator. This includes tidal breathing and inhalation-only breathing profiles, allowing the collection step to be aligned with the intended application and test objective.
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