Exactmer Research Published in Science Demonstrates Breakthrough Membrane Technology for Hydrocarbon Fractionation

New ultrathin polymer membranes combine exceptional selectivity, productivity and scalability, offering a potential lower-energy alternative to conventional hydrocarbon separations.

Exactmer is pleased to announce the publication of its latest research in Science, one of the world’s most prestigious scientific journals.

The paper, Ultrathin Polymer Membranes with Locked Intrinsic Microporosity for Hydrocarbon Fractionation, describes a new class of ultrathin polymer membranes capable of rapidly and selectively separating complex hydrocarbon mixtures while maintaining industrially relevant productivity and scalability.

Read the publication: DOI: 10.1126/science.aed1111

Conventional crude oil refining relies heavily on thermal distillation, one of the world’s most energy-intensive industrial processes. Although membrane-based separations have long promised a lower-energy alternative, achieving both high selectivity and high productivity in hydrocarbon mixtures has remained a major challenge.

The research team addressed this challenge through a novel membrane fabrication approach that locks nanoscale pores into their optimal configuration during membrane formation. The resulting materials, known as Polymers of Locked Intrinsic Microporosity (PLIMs), combine rapid hydrocarbon transport with exceptional molecular selectivity, overcoming limitations that have historically restricted membrane deployment in hydrocarbon processing.

The membranes demonstrated up to ten-fold higher permeance than existing state-of-the-art membranes while maintaining high selectivity. In tests using real Arabian Extra Light crude oil, they removed 99.8% of hydrocarbons heavier than 15 carbon atoms and reduced sulphur-containing compounds by 93%.

Importantly, the technology was also demonstrated at industrially relevant scale. The team successfully produced membranes using roll-to-roll manufacturing and integrated them into standard spiral-wound membrane modules commonly used across industry, demonstrating a clear pathway towards commercial deployment.

“Membranes can, in principle, do the same job as distillation or evaporation, using far less energy,” said Professor Andrew Livingston, Vice President for Research and Innovation at Queen Mary University of London and CEO of Exactmer. “This work shows that membrane-based molecular separation in organic liquids is no longer just a theoretical possibility. With the right materials design, it can be fast, selective, scalable — and ready for industry.”

Dr Adam Oxley, first author of the paper and Deputy Vice President, Membranes at Exactmer, added: “These membranes aren’t just laboratory curiosities. We have demonstrated that they can be manufactured using established industrial techniques and integrated into existing module designs, creating a realistic pathway towards deployment.”

Beyond hydrocarbon fractionation, the researchers believe the same pore-locking concept could be applied to a broad range of industrial separation challenges, including chemical manufacturing, solvent recovery and pharmaceutical production.

Publication in Science highlights Exactmer’s position at the forefront of membrane science and industrial separation technology. The company develops advanced membrane platforms for challenging molecular separations in organic liquids, with applications spanning refining, chemical manufacturing, pharmaceuticals and solvent recovery.

Read the full paper: DOI: 10.1126/science.aed1111

Breakthrough in Liquid Phase Oligonucleotide Synthesis: Nanostar Sieving® Enables First Large-Scale, Fully Liquid Process

Exactmer is delighted to share that our latest article, “Fully liquid phase oligonucleotide synthesis” has been published in Organic Process Research & Development. The paper showcases pivotal early advances in the Nanostar Sieving® platform and sets a new benchmark for liquid-phase oligonucleotide synthesis (LPOS).

In a milestone achievement for LPOS, Exactmer describes the production of  a 21-mer siRNA and a 16-mer ASO-like gapmer, synthesized exclusively in the liquid phase. Both PO and PS backbones have been produced as well as deoxy sequences, all while maintaining the oligo in a single-solvent solution from initial coupling through to isolation. This establishes the route to large-scale oligo manufacturing, using Exactmer’s proprietary membranes as spiral wound modules (SWMs), enabling organic solvent nanofiltration at industry-relevant scales.

The paper is co-authored by partners from AstraZeneca, Alnylam, Novartis and CPI, through the Grand Challenge 3 (GC3) collaboration. Together, this consortium laid the foundation for advancing Exactmer’s Nanostar Sieving® platform for therapeutic oligo manufacture at large-batch production volumes. Nanostar Sieving® is Exactmer’s proprietary platform technology which uses membrane-assisted liquid-phase synthesis to produce sequence-defined polymer therapeutics. The platform continues to gain strong momentum in the oligo synthesis market for its capacity to supply large-volume batches, critical for the supply of oligo medicines to patients suffering from prevalent diseases such as cardiovascular disease and Alzheimer’s.

“This work showcases Exactmer’s early innovation in the Nanostar Sieving technology, which have importantly underpinned the oligo manufacturing strategies we have in place today.” Said Prof. Andrew Livingston, senior author and CEO of Exactmer. “Led by an industrial research collaboration, we have broken the record for the longest oligo yet to have been synthesised entirely in the liquid phase.”

The full paper has been published on 12 December 2025 in Organic Process Research & Development.

Contact

Dr Cristina Bertulli, VP of Business Development – [email protected]

Exactly defined molecular weight poly(ethylene glycol) allows for facile identification of PEGylation sites on proteins

We are thrilled to announce the publication of our new research paper titled “Exactly defined molecular weight poly(ethylene glycol) allows for facile identification of PEGylation sites on proteins” in Nature Communications!

Diagram illustrating the differences between conventional PEGylation and PEGylation defined in this publication. Using Exactmer's PEG synthesis for defined molecular weights enables for easy identification of PEGylated regions within a protein using relatively straightforward techniques.

Diagram illustrating the differences between conventional PEGylation and PEGylation defined in this publication. Using Exactmer’s defined molecular weight PEG synthesis enables for easy identification of PEGylated regions within a protein using relatively straightforward techniques.

In this study, we propose a chromatography-free synthesis process to produce defined PEGs with a molecular weight of 5kDa.

This breakthrough approach enables the use of precisely defined molecular weight poly(ethylene glycol) to address current batch-to-batch variations and unpredictable impurities in PEGylated drugs — an essential consideration for advancing biopharmaceutical development.

Our findings could transform how PEGylation, a key method to improve protein stability and therapeutic efficacy, is studied and applied in drug development.

We invite you to read the full paper and explore how Exactmer’s innovation could impact the future of drug design and protein synthesis. Find out more about how our findings on PEG synthesis can help you by visiting Our Services – Exactmer.

Read the full paper here:

Exactly defined molecular weight poly(ethylene glycol) allows for facile identification of PEGylation sites on proteins | Nature Communications

Sequence-defined multifunctional polyethers via liquid-phase synthesis with molecular sieving

Abstract

Synthetic chemists have devoted tremendous effort towards the production of precision synthetic polymers with defined sequences and specific functions. However, the creation of a general technology that enables precise control over monomer sequence, with efficient isolation of the target polymers, is highly challenging. Here, we report a robust strategy for the production of sequence-defined synthetic polymers through a combination of liquid-phase synthesis and selective molecular sieving. The polymer is assembled in solution with real-time monitoring to ensure couplings proceed to completion, on a three-armed star-shaped macromolecule to maximize efficiency during the molecular sieving process. This approach is applied to the construction of sequence-defined polyethers, with side-arms at precisely defined locations that can undergo site-selective modification after polymerization. Using this versatile strategy, we have introduced structural and functional diversity into sequence-defined polyethers, unlocking their potential for real-life applications in nanotechnology, healthcare and information storage.

Dong, R., Liu, R., Gaffney, P.R.J. et al. Nature Chem 11,136–145 (2019)

https://doi.org/10.1038/s41557-018-0169-6