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Engineers develop nanocarriers for drugs that bypass the lungs' defense lines

This scheme shows that the PEG-BB molecules – the bottlebrush-shaped objects – move through and past the mucosa and periciliary layers to be taken up by cells throughout the epithelial layer. Image credit: ACS Nano (2024). DOI: 10.1021/acsnano.4c01983

A drug molecule designed to bypass the lungs' natural defenses and thereby cure disease offers new hope to people with chronic or fatal respiratory diseases, say its developers, researchers in Assistant Professor Liheng Cai's Soft Biomatter Lab in the University of Virginia's School of Engineering and Applied Science.

Cai and his team, including PhD student in materials science and engineering Baiqiang Huang and PhD student in biomedical engineering Zhi-Jian He, successfully demonstrated the effectiveness of the nanocarrier using the laboratory's own “human micro-airway.” The device captures the geometric and biological features of the human airway.

They describe their results in an article published in the journal ACS Nano.

Leaving our defense behind

Our lungs have protective layers that trap pathogens or inhaled particles and transport them out of the airways to prevent us from getting sick. Every time you blow your nose, this system is working.

“Unfortunately, these same barriers also prevent drugs from reaching target cells, making it difficult to treat diseases such as asthma, chronic obstructive pulmonary disease and pulmonary fibrosis,” Huang said.

The new polymer is called bottlebrush polyethylene glycol, or PEG-BB. It moves quickly through the airways by mimicking mucins, a natural glycoprotein responsible for the properties of mucus and has the same bottlebrush shape – a central spine with a thicket of bristles pointing outward.

“We thought that the flexibility and worm-like geometry of the bottlebrush would allow it to pass through the dense network of mucus and gels surrounding the cilia and be taken up by the epithelial cells where the drugs need to work,” Huang said.

Cilia are hair-like structures on the surface of cells. They move in conjunction with mucus to repel and expel foreign bodies.

To test their hypothesis, the team cultured human airway epithelial cells in their device. They introduced fluorescent PEG-BB molecules into the cells from two directions.

They then used a dye to penetrate the mucus and periciliary layers – the latter being the gel that coats the cilia – but did not stain the epithelial cell walls that helped mark the boundaries of the epithelium.

Using a special microscope and a darkened room to sharpen the images, they were able to see how well the glowing bottlebrush molecules had moved through the cells.

A number of recent successes

“The microhuman airway is essentially an equivalent site for cell growth,” Huang said.

“The biological similarities allow us to study the defenses of the human lung without harming living beings,” added Cai, whose lab specializes in developing novel bottlebrush polymers for a range of applications, many of which push the boundaries of precision medicine.

For example, its bioprinting program recently produced what may be the first 3D building block for on-demand organ printing.

The PEG-BB results are another success for the laboratory.

“We believe this innovation not only promises better treatment for lung diseases with fewer side effects, but also opens up possibilities for treating mucous membrane diseases throughout the body,” Cai said.

The lab's next step is to test PEG-BB's ability to transport drug molecules across a mucosal barrier. The team is experimenting with both in vitro and in vivo models in mice.

Further information:
Zhi-Jian He et al., Bottlebrush polyethylene glycol nanocarriers translocate through human airway epithelium via molecular architecture-enhanced endocytosis, ACS Nano (2024). DOI: 10.1021/acsnano.4c01983

Provided by the University of Virginia

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