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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

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IDA: A Streamlined Workflow for Inhaled Dissolution Testing

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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.

 

IDA Technical Specifications

Flow rate compatibility:
5 – 100 L/min
Flow profile options:
Supports constant flow and breathing simulation (tidal / inhalation-only)
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
Stations available:
6- or 8-station configurations
Media volume range:
200 – 500 mL
Automation compatibility:
Compatible with Vertus® III for automated shake and fire

Inhaled Dissolution Apparatus IDA: FAQs

Explore our most frequently asked questions on the Inhaled Dissolution Apparatus IDA and inhaled dissolution testing, covering workflow, configurations, and key benefits.

What is the IDA used for?

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.

What products can the IDA be used with?

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.

Why not adapt standard dissolution equipment?

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.

How does the IDA improve repeatability?

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.

What flow conditions can be used with the IDA?

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.

Download the IDA Brochure Request Pricing

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