{"id":82744,"date":"2020-10-06T10:45:28","date_gmt":"2020-10-06T07:45:28","guid":{"rendered":"https:\/\/en.buradabiliyorum.com\/like-a-fishing-net-nanonet-collapses-to-trap-drug-molecules\/"},"modified":"2020-10-06T10:45:28","modified_gmt":"2020-10-06T07:45:28","slug":"like-a-fishing-net-nanonet-collapses-to-trap-drug-molecules","status":"publish","type":"post","link":"https:\/\/buradabiliyorum.com\/en\/like-a-fishing-net-nanonet-collapses-to-trap-drug-molecules\/","title":{"rendered":"#’Like a fishing net,’ nanonet collapses to trap drug molecules"},"content":{"rendered":"

“#’Like a fishing net,’ nanonet collapses to trap drug molecules<\/strong>”<\/p>\n

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\n a Chemical structure of PPSU showing the polymer backbone and oxygen atoms that carry positive\/negative (blue\/red) atomic partial charges, respectively. b Atomistic simulation snapshot showing a dissolution-complementarity equilibrium in DMSO for six PPSU20 chains. Inset is a superstructure formed by PPSU self- complementarity. c PPSU self-complementarity leading to a 2D reversible superstructure with enrichment of oxygen atoms on the surface. Formation of 3D superstructures is inhibited in DMSO due to the strong repulsion among layers. d Average dipolar energies per dipole-dipole pair of sulfone\u2013sulfone and sulfone-solvent. Error bars represent the standard deviation from three parallel simulations. e Atomistic simulation snapshot showing the formation of a 3D superstructure through PPSU bundling in water. Inset showing the 3D superstructure with or without water molecules. Credit: Nature Communications<\/i> (2020). DOI: 10.1038\/s41467-020-18657-5
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Northwestern University researchers are casting a net for nanoparticles.<\/p>\n


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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 app<\/a>lications, 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.<\/p>\n

Using a polymer net that collapses into nanoscale hydrogels (or nanogels), the method efficiently captures over 95% of proteins, DNA or small molecule drugs\u2014alone or in combinations. By comparison, loading efficiency is typically between 5% and 20% for other nanoparticle delivery systems.<\/p>\n

“We use a polymer that forms a wide net throughout an aqueous solution,” said Northwestern’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.”<\/p>\n

“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.<\/p>\n

The paper was published last week (Sept. 29) in the journal Nature Communications<\/i>.<\/p>\n

Scott is the Kay Davis Professor of Biomedical Engineering at Northwestern’s McCormick School of Engineering. Northwestern professors Monica Olvera de la Cruz and Vinayak Dravid coauthored the paper.<\/p>\n

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.<\/p>\n

“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.”<\/p>\n

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.<\/p>\n

“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.”<\/p>\n

Atomistic simulations\u2014performed by Baofu Qiao in the Olvera de la Cruz group\u2014confirmed 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.<\/p>\n

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.<\/p>\n\n

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Research exposes new vulnerability for SARS-CoV-2\n <\/p><\/div>\n

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\n More information:<\/strong>
\n Fanfan Du et al, Homopolymer self-assembly of poly(propylene sulfone) hydrogels via dynamic noncovalent sulfone\u2013sulfone bonding, Nature Communications<\/i> (2020). DOI: 10.1038\/s41467-020-18657-5<\/a><\/p><\/div>\n
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\n Northwestern University
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Citation<\/strong>:
\n ‘Like a fishing net,’ nanonet collapses to trap drug molecules (2020, October 6)
\n retrieved 6 October 2020
\n from https:\/\/phys.org\/news<\/a>\/2020-10-fishing-net-nanonet-collapses-drug.html<\/p>\n

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