NIKYANG Founded in 1998, NIKYANG Enterprise Limited has developed a reputation for dynamic leadership, satisfying our customers with innovative one-stop fully-automated laboratory solutions and support. Our state-of-the-art products and services make a major contribution to promoting lab efficiency, modernization, and consistency of results across a range of industries in Asia. Headquartered in Hong Kong, we support our customers through an
Fully automatic TLC/HPTLC development with high reproducibility Automated Chromatogram Development under Standard Conditions The ADC 2 (Automatic Developing Chamber) is designed to automate all manual operations necessary during chromatogram development, thereby offering convenience, safety and high reproducibility for isocratic developments of TLC/HPTLC plates and foils in 20 x 10 cm and 10 x 10 cm formats. It provides automatic development,
Enjoy the full benefits of high-throughput crystallization experimentation ml-scale parallel crystallizer with novel non-intrusive turbidity probe Combining powerful performance with ease of use, the Crystal16 multiple reactor station is designed for automated crystallization screening research, enabling users to greatly accelerate their research – for example, solubility curves can be determined within 4 hours using only 100mg. Originally developed for medium
Automated Solutions This section presents a selection of solutions to fit common needs – but every case is unique. Put yourself in the hands of our experts, and you can be confident that your process will be automated in a way that is efficient, practical, based on world-class equipment, seamlessly integrated with your existing systems, and can save you time
Application Crystallization With increasing economic demands, it is becoming progressively more important to gain additional information on drug candidates early in the development cycle. Better informed decision can be made during the selection of candidates if further solid state information is available – saving time and money later on in the development process. But early stage drug candidates are difficult
Automated Tablet Processing Workstation Sample preparation and analysis for solid dosage forms and intermediate granulations The TPW Tablet Processing Workstation from SOTAX performs fully automated sample preparation and analysis for the most common pharmaceutical tests in Development and Quality Assurance functions, such as Stability and Uniformity testing. The TPW is specifically designed to prepare and analyse pharmaceutical solid dosage forms
Fully automated sample preparation and analysis for common API tests Automated Active Ingredient Processing Workstation The APW Active Ingredient Processing Workstation from SOTAX performs fully automated sample preparation and analysis for the most common Active Pharmaceutical Ingredient (API) tests in pharmaceutical Development and Quality Assurance functions, such as Stability and Uniformity testing. Fully automated sample preparation provides fast, consistent and
Versatile robotic platform for high-throughput experimentation Software-driven robotic platform for semi- or fully-automated R&D processes A software-driven robotic platform designed for R&D processes, Chemspeed’s automated Autoplant and its semi-automated variant, the Multiplant, facilitate high-output experimentation in the development and optimization of polymers (e.g. polyolefins, nano-latex, polyamides, acrylics and PU), specialty chemicals, catalysts for polyolefins and many more. Both are based
Extending the reach of TLC using gradient elution Automated Multiple Development of Thin-Layer Chromatograms The CAMAG AMD 2 (Automated Multiple Development) procedure allows Thin-Layer Chromatography to be utilized for tasks that could not be performed by TLC in the past. The use of gradient elution gives up to three times the separation power of standard HPTLC, with increased precision and
Pharmaceutical Testing Quality control is indispensable in the pharmaceutical product development process to ensure that the drug substance and other raw materials are suitable for use in your drug product and to ensure that the drug product manufactured meets the quality standards. Quality control is required throughout the entire development process, from drug substance and raw material control, through intermediate