The Equipment Project at Cambridge University provides support to external organisations by listing a number of facilities and individual items of equipment that may be suitable for use by industrial and commercial entities as well as by University staff and students. Equipment can be used unsupervised providing the appropriate training is in place, used with the supervision of a laboratory manager or technician, or again, external samples may be submitted for analysis and the results returned.Read More
… was held on 26 April at GSK’s Medicines Research Centre in Stevenage with the topic of
Advancing established analytical techniques to meet the demands of modern drug discovery
The Group is an opportunity for local Analytical Chemists to meet and exchange ideas on the many common areas of their work. Previous meetings focusing on Open Access and Purification have been generously supported by AstraZeneca and Charles River and thanks go out to them along with GSK for allowing this to happen. In particular, for this meeting, Tim Underwood of GSK did a great job with the organisation.
More than 40 delegates turned out to hear a full and varied programme of speakers in an informal atmosphere.Read More
At Paperless Lab Academy 2018 in Milan, one of the highlights of the conference was a workshop by Sekhar Sathya, CEO of Caliber technologies, on solutions to achieve QA/QC goals every day in a paperless environment. This Blog is a summary of the workshop.Read More
I recently had the pleasure of visiting Immundnz, a young company based in the BioHub at Alderley Park in Cheshire. My hosts were the two founders of the company, Dr Masih Alam and Dr Robert-Jan Lamers.
The company was founded in 2016 to provide specialised support in immunology. They use an array of cellular, immunologic and molecular methods to build up a comprehensive picture of drug-induced immunogenicity.Read More
I am very excited to be working alongside Collaborative Drug Discovery as a member of their Advocate programme for the CDD Vault informatics platform.Read More
A pharmaceutical physical chemistry group will typically run a variety of assays such as chemical stability, solubility, lipophilicity measurement, PAMPA and binding assays. With the high cost of ownership of LC(MS) systems there is always a need to maximise the return on investment in these systems by running as many different assays on the minimum number of systems to take full advantage of their inherent speed and versatility.Read More
Over recent weeks I have been working to establish a suite of assays using my own UHPLC instrumentation. LogD, solubility and PAMPA permeability measurement are all now available to clients via out-sourcing, in-sourcing or consultancy to set up the methods in your laboratory which can also include bespoke software. Here I am presenting some validation data to support the use of my PAMPA method.Read More
This blog returns to the familiar theme of physico-chemical measurement. Over recent weeks I have been working to establish a suite of assays using my own UHPLC instrumentation. LogD, solubility and PAMPA permeability measurement are all now available to clients via out-sourcing, in-sourcing or consultancy to set up the methods in your laboratory which can also include bespoke software. Here I am presenting some validation data to support the use of my LogD7.4 method.Read More
This post features some data generated by deltaDOT Ltd using HPCE for the analysis of the monoclonal antibodies Infliximab and Rituximab. Stability, fragmentation and charge heterogeneity were assessed using a combination of Capillary Gel Electrophoresis (CGE) and Capillary Zone Electrophoresis (CZE). Quantifiable differences were observed in the samples before and after heat-stress. Excellent repeatability was obtained. This work was performed as part of a study for the UK’s National Health Service (NHS).Read More