GEN-MKT-18-7897-A
Jul 19, 2021 | Blogs, Echo MS, Pharma | 0 comments
In this interview from the Science Explorer about the Echo® MS system, Neil Walsh from SCIEX discusses the significant application areas of the system and what makes it so attractive to biopharmaceutical laboratories.
Here is a snippet of the conversation. Watch the video for the complete interview.
Neil Walsh: Absolutely. The need for this product has been driven by pharma and specifically drug discovery. These scientists are always trying to push the boundaries. They want to get more mass spec data to help inform better decisions. But there is a bottleneck there holding them back, and that is the fact that a lot of these assays for mass spectrometry use liquid chromatography. LC is great. It is what we use through all the other parts of the drug discovery pipeline. But with the volume of samples going through in the drug discovery phase, it is a real bottleneck. The challenges around all the valving, the cycle times and the sample preparation have been a limitation to the application of mass spectrometry in that drug discovery phase.
What is different about the Echo® MS system is that it is not using LC, which is a game-changer. Why? Because it is getting rid of that bottleneck. It is getting rid of that sample preparation.
So, how is it different? The Echo® MS system brings together Acoustic Droplet Ejection and Open Port Interface technology to enable contactless sampling. Using sound waves in a contactless manner, it ejects the sample from the plate up into the Open Port Interface. Then it is diluted a thousandfold by a typical carrier solvent used in electrospray and carried through to the electrospray interface, where it is ionized and then detected by the mass spectrometer.
Neil Walsh: For sure. The high-throughput known technology that we compete with is not mass spectrometry. It is the plate readers. Plate readers are quick, but they lack the data quality that comes out of a mass spectrometer and the data specificity. And that is the difference. Speed is important, but the quality of data is even more critical. Why? Because it supports better-informed decisions about which compound goes further into the development process.
Neil Walsh: So, anytime we talk about the Echo® MS system, the obvious place to start is speed. In normal mode, at processing, we are talking 1 sample per second, well to well. But the system can also operate in multiplex (i.e., MRM) mode, and multiplex MRMs (i.e., non-overlapping MRMs) can run 3 samples per second. That is where the speed game-change comes, because currently, this is up to 50 times faster than conventional LC-MS/MS methods. We see customers’ jaws drop when they see how fast it is. They can run 384 well plates, so 384 samples, in a few minutes. And we can go up to 1,536 well plates, and that’s a big game changer—that’s in the plate reading scale.
Another exciting thing for customers is that little or no sample prep is required, especially in these drug discovery workflows where the concentrations are higher, and they are not sensitivity demanding. So, you can eject from urine and plasma. We’ve also seen a push around things like synthetic biology, so we see things like fermentation broth come in, and we accurately measure those types of samples.
And in terms of scale, one of our collaborators said that they are generating up to a million compounds a week through new biosynthetic pathways. And he said, “With the current technology that we use, if we wanted to run a million compounds, it would take 115 days. With the Echo® MS System, we’re talking 3 to 4 days.”
Neil Walsh: We have seen loads of uptake from, obviously, high-throughput markets—as we mentioned earlier, the high-throughput screening and high-throughput ADMEs—and also some interest from bioanalytical laboratories. The biggest thing these labs are interested in is this increase in capacity and what that means, what that can do for their discovery pipelines and how they can pull better-qualified candidates through, so that is a big bonus for them. Interestingly, we have also seen a lot of interest from academia around high-throughput screening or high-throughput metabolomics. Another exciting area is food screening, which we did not anticipate, and there is certainly a lot of interest in things like egg sexing, an area that has a real cost-saving and ethical piece, which is interesting.
Neil Walsh: One of our early access customers said something I think is interesting. It is about potentially being able to deliver results to a customer the day they receive the samples—not in 2 weeks, but potentially the same day. And that is the impact for these laboratories. It is the sheer speed and scalability of the product and the ability to answer the same day.
Neil Walsh: We talk about speed, scale and the data quality that this brings. The thing that resonates most with me when talking to customers is when it sinks in what a sample per second could mean. I had one customer say, “We fundamentally must rethink everything we do.” That is what I would say to anybody who is listening to me prattle on about it. Think about what that means and what it can mean for your organization and your customers.
To learn more about the Echo® MS system, or to request a quote, click here.
You may also like to read this blog.
RUO-MKT-18-12896-A
Echo® and Echo® MS are trademarks or registered trademarks of Labcyte Inc. in the United States and other countries, being used under license by SCIEX.
Liquid chromatography-tandem mass spectrometry (LC-MS/MS) has gained significant attention in the clinical laboratory due to its ability to provide best-in-class sensitivity and specificity for the detection of clinically relevant analytes across a wide range of assays. For clinical laboratories new to LC-MS/MS, integrating this technology into their daily routine operations may seem like a daunting task. Developing a clear outline and defining the requirements needed to implement LC-MS/MS into your daily operations is critical to maximize the productivity and success of your clinical laboratory.
In today’s rapidly evolving food industry, the role of food testing laboratories has never been more critical. Ensuring the safety, quality, and authenticity of food products is paramount, and this responsibility falls heavily on the shoulders of laboratory managers. The economics of food testing—encompassing everything from high-throughput pesticide screening to advanced research on alternative protein sources—plays a pivotal role in shaping the operational efficiency and financial health of these laboratories.
Imagine having a tech expert at your fingertips to solve computer issues or a fitness trainer guiding you through workouts from the comfort of your home. In today’s fast-paced world, the ability to provide and receive service and support remotely is no longer a luxury but a necessity. Whether it’s troubleshooting a software issue, repairing a device, offering customer assistance, or enjoying the convenience of telehealth as a private individual, remote capabilities have revolutionized how businesses operate and how individuals get help
Posted by
You must be logged in to post a comment.
Share this post with your network