Product Introduction

• The optional camera system can effectively observe and record the entire dissolution process of drugs, providing important information for research and testing.

• The twelve position dissolution tester can simultaneously test 12 samples and can be connected to an automatic sampling system, effectively improving experimental efficiency.

• The automatic sampling dissolution system is equipped with an injection pump, collector, and controller to achieve a fully automatic sampling process, which can synchronously dispense drugs and automatically clean pipelines.

• Implementing 2/3 zone speed control and expanding the scope of experimental applications can help R&D improve experimental timeliness and shorten the development cycle of new products.

• Optional "basket loading and unloading tool" can be used to protect the basket from damage caused by human operation errors.

• The LOGAN universal dissolution meter is equipped with different accessories and can be used for basket method (USP I), paddle method (USP II), paddle disc method (USP V), rotary drum method (USP VI), and Chinese Pharmacopoeia small cup method, and meets the specification requirements.

• The LOGAN universal dissolution tester is equipped with the following features: Intrinsic dissolution (used to test the intrinsic dissolution rate of powdered investigational drugs), Immersion cell (immersion sample cell - applied to ointment testing devices), Peak vessels (bottom peak dissolution cup used for easy precipitation and accumulation of drug preparations at the bottom of the dissolution cup).

• The LOGAN universal dissolution analyzer can perform multiple filters. The double-layer melting cup lid ensures that all vessels are firmly covered, reducing evaporation.

• Provide online ultraviolet analysis (ADUV), online dilution liquid phase analysis (ADLC), fiber optic dissolution, and effective connection between ADFO and ASP2000 dilution platform.

• The system complies with the requirements of USP, EP, JP, and the Chinese Pharmacopoeia.

• The entire dissolution system has functions such as audit tracking, permission management, and electronic signature, fully complying with CFR21 Part 11 and GMP/GLP regulations, and can meet the requirements for data integrity in the pharmaceutical industry.