Eman AhmedRutgers BME

Eman Ahmed, PhD candidate, Rutgers Biomedical Engineering Ninety-six polymers at a time.

I build robot-run polymer chemistry and the machine learning that reads what comes back, to find the polymers that keep enzymes working in solvents where they would normally fall apart.

3peer-reviewed papers, one as first author
43citations
3h-index

Metrics from Google Scholar, September 2026.

What I work on

Three connected problems: making enzymes survive outside water, generating enough polymer data to learn from, and building analysis that keeps pace with the synthesis.

Polymer-stabilized enzymes in organic solvents

Doctoral project, Gormley Lab, 2022-2026

Enzymes are extraordinary catalysts in water and frequently useless outside it. Move one into a water-miscible organic solvent, which is often where the interesting synthetic chemistry happens, and it tends to unfold, aggregate and drop out of solution.

Random copolymers can act as synthetic chaperones, wrapping a protein in a shell whose chemistry can be tuned monomer by monomer. The difficulty is that the design space is enormous and the structure-function relationship is not obvious from first principles. My work builds plate-based, automated assays that measure solubility and retained activity across large copolymer libraries, so the search can be run empirically at scale rather than one rational design at a time.

  • Random copolymers
  • Polymer-enzyme hybrids
  • Biocatalysis
  • Solubility assays
  • Automation

In depth

Machine learning for biomaterial structure-function mapping

First-author review, Tissue Engineering Part A, 2024

High-throughput experiments produce the kind of data that models need: many conditions, consistent measurement, and, importantly, retained failures. The question is what to do with it.

My review in Tissue Engineering Part A surveys how machine learning is being used to identify the physicochemical cues that govern biomaterial performance, across tissue engineering, gene delivery, drug delivery, protein stabilization and antifouling surfaces, along with the data-mining approaches that let published results stand in for experiments that have not been run yet.

  • Structure-property relationships
  • Data mining
  • Model selection
  • Biomaterials discovery

In depth

Automated polymer synthesis and analysis

photo-ATRP platform and SAXS Assistant

Oxygen-tolerant reversible-deactivation radical polymerization made it possible to run controlled polymer chemistry in open labware. That is what puts it within reach of a liquid handler, and it is the premise behind our automated photo-ATRP platform, which screens ligands and initiators for monomers, methyl methacrylate among them, that are slow enough to be painful to optimise by hand.

Synthesis throughput is only useful if characterisation keeps up. SAXS Assistant addresses the other end of the pipeline: it automates small-angle X-ray scattering analysis, estimates maximum particle dimension with a model trained on 1,940 experimental profiles, and refuses to report results it cannot stand behind.

  • photo-ATRP
  • Liquid handling robotics
  • SAXS
  • Open-source tooling
  • Reproducibility

In depth

Publications

Three peer-reviewed papers in Tissue Engineering Part A, ACS Polymers Au and Biophysical Journal, plus the doctoral manuscript in preparation.

First authorIn preparation

High-Throughput Approach for Evaluating the Solubility of Polymer-Stabilized Proteins in Organic Solvent

Eman Ahmed, Adam J. Gormley

Manuscript in preparation · Gormley Lab, Rutgers University

All publications, with summaries and citation formats

Research notes

Plain-language companions to the papers: what the method does, why it was built that way, and what it does not solve.

What oxygen tolerance buys you in polymer chemistry

Controlled radical polymerisation used to require sealed, degassed glassware. Oxygen-tolerant chemistry moved it into open well plates, and that one change is what puts polymer synthesis within reach of a liquid-handling robot.

Trusting a SAXS analysis you didn't do by hand

Small-angle X-ray scattering analysis is full of judgement calls that vary between analysts. Automating it is less about speed than about making those calls explicit, and about flagging the profiles where the answer should not be trusted.

All notes

Working on something adjacent?

If you work on high-throughput polymer synthesis, machine learning for materials, SAXS analysis or enzyme stabilization, I would like to hear about it, whether that is a collaboration, a dataset worth combining, or a question about how one of these methods behaves in practice.