‘Like A Fishing Net,’ Nanonet Collapses to Trap Drug Molecules

Northwestern Engineering researchers are casting a net for nanoparticles.

The team has discovered a new, rapid method for fabricating nanoparticles from a simple, self-assembling polymer. The novel method presents new possibilities for diverse applications, including water purification, diagnostics, and rapidly generating vaccine formulations, which typically require many different types of molecules to be either captured or delivered at the same time. 

Using a polymer net that collapses into nanoscale hydrogels (or nanogels), the method efficiently captures over 95 percent of proteins, DNA, or small molecule drugs — alone or in combinations. By comparison, loading efficiency is typically between five and 20 percent for other nanoparticle delivery systems.

“We use a polymer that forms a wide net throughout an aqueous solution,” said the McCormick School of Engineering’s Evan A. Scott, who led the study. “Then we induce the net to collapse. It collects anything within the solution, trapping therapeutics inside of nanogel delivery vehicles with very high efficiency.”

“It works like a fishing net, which first spreads out due to electrostatic repulsion and then shrinks upon hydration to trap ‘fish,’” added Fanfan Du, a postdoctoral fellow in Scott’s laboratory.

The paper was published September 29 in the journal Nature Communications. 

Scott is the Kay Davis Professor of Biomedical Engineering. Lawyer Taylor Professor of Materials Science and Engineering Monica Olvera de la Cruz, and Abraham Harris Professor of Materials Science and Engineering Vinayak Dravid coauthored the paper. 

Molecules found in nature, such as DNA and peptides, can rapidly self-assemble and organize into diverse structures. Mimicking this process using human-made polymer systems, however, has remained limited. Previously developed processes for self-assembling drug delivery systems are time consuming, labor intensive, and difficult to scale. The processes also tend to be woefully inefficient, culminating in a small fraction of the drug actually making it inside the delivery system.

“Clinical application of self-assembled nanoparticles has been limited by difficulties with scalability and with loading large or multiple therapeutics, especially proteins,” Scott said. “We present a highly scalable mechanism that can stably load nearly any therapeutic molecule with high efficiency.”

Scott’s team found success by using a polypropylene sulfone (PPSU) homopolymer, which is highly soluble in dimethylsulfoxide (DMSO) solution, but forms electrostatic and hydrophilic aggregates in water. The aggregates are amphiphilic, which causes them to assemble into networks and eventually collapse into gels. 

“Adding more water induces the network to collapse, leading to the formation of nanogels,” Du said. “The manner in which water is added affects the PPSU chain formation, which changes the nanogels’ size and structure.”

Atomistic simulations — performed by Baofu Qiao in the Olvera de la Cruz group — confirmed that the nanostructures were stabilized by weak sulfone-sulfone bonding. Using coarse-grained simulations performed by Northwestern postdoctoral fellow Trung Dac Nguyen, the researchers observed the nanonet structures. This opens a new avenue for soft materials assembly by means of sulfone-sulfone bonding.

In addition to drug delivery applications, the researchers also believe the novel method could be used for water purification. The network could collapse to collect contaminants in water, leaving pure water behind.

Scott is a member of Northwestern’s Simpson Querrey Institute, Chemistry of Life Processes Institute, Interdisciplinary Biological Sciences Program, and Northwestern University Robert H. Lurie Comprehensive Cancer Center. He has a secondary appointment in the department of microbiology-immunology at the Feinberg School of Medicine.