Disintegration/Dissolution
Disintegration/Dissolution is the method used to determine the amount of drug released during the test period and is indication of drug availability for systemic absorption in biological system.

ARL offers dissolution testing of a variety of pharmaceutical compounds, including tablets, capsules, and topical products such as transdermal patches, lotions, creams, etc. With extensive training and experience, our analysts have in depth industrial knowledge and pharmaceutical experience to deliver consistent and high quality dissolution services to conform to cGMP practices and USP requirements.

As a compendial requirement, the disentegration/dissolution methods for a given drug product are fixed in terms of medium, temperature, stirring speed, and stirring devices. This provides determination of compliance with drug-release requirements for compendial articles.