LOGAN Instruments Corp products

The FDC-6TA is a semi-automated diffusion cell drive console with water jacket, designed for assessing the permeation rates of semi-solid and topical formulations including ointments, gels, transdermal patches, face masks, lotions, and sunscreens. It features a PLC color display and external circulator, crucial for controlling experimental conditions and ensuring consistent results. The system supports varied testing applications for the pharmaceutical and cosmetics industries, where accurate measurement of compound permeation is critical. Its design facilitates ease of use with tilting capabilities, enhancing versatility in laboratory settings. Ideal for researchers aiming to study drug release profiles and develop or validate permeation studies in semi-solid and patch dosage forms, it reduces human intervention without sacrificing precision, thereby also supporting compliance with GLP standards.

Logan`s Universal Dissolution Tester is a sophisticated instrument designed for pharmaceutical research and development, as well as quality control applications. It supports USP Apparatus 1, 2, 5, and 6, offering a range of configurations from 8 to 18 vessels, both in manual and automated forms. The automated systems, manufactured in the USA, streamline the dissolution process by coordinating all stages via computer control, negating the need for water baths and minimizing user involvement. These systems include precise syringe pumps, ensuring accurate sampling and reducing human errors. They also feature tight vessel seals to minimize media evaporation and have individual temperature sensors for each vessel, allowing precise monitoring and recording. This design focuses on enhancing the efficiency and accuracy of drug research and the evaluation of generic drugs.

The DISSO-3 reciprocating cylinder apparatus is designed for assessing active pharmaceutical ingredient (API) release characteristics across various solid dosage forms such as sustained-release, enteric-coated, soft capsules, and chewable tablets. This system is vital for evaluating dissolution profiles under different pH conditions, which are critical for formulating effective drug dosage forms. Understanding how APIs release in gastrointestinal conditions can significantly impact the drug`s efficacy and patient outcomes. Logan provides not only standard dissolution testers but also offers custom solutions to cater to specific analytical needs, ensuring comprehensive drug testing capabilities. By enabling precise control and replication of different physiological conditions, the DISSO-3 aids in compliance with USP testing standards, providing drug developers valuable insights into their products` performance.