QCM‑D Investigations on Cholesterol–DNA Tethering of Liposomes to Microbubbles for Therapy

• Published in: The journal of physical chemistry. B Vol. 127; no. 11; pp. 2466 - 2474
• Main Authors: Armistead, Fern J., Batchelor, Damien V. B., Johnson, Benjamin R. G., Evans, Stephen D.
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 23.03.2023
• Subjects: B: Biomaterials and Membranes; Cholesterol; DNA, Complementary; Lipid Bilayers; Liposomes; Microbubbles; Polyethylene Glycols
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/acs.jpcb.2c07256

Lipid-shelled microbubbles (MBs) offer potential as theranostic agents, capable of providing both contrast enhancement in ultrasound imaging as well as a route for triggered drug release and improved localized drug delivery. A common motif in the design of such therapeutic vehicles is the attachment of the drug carrier, often in the form of liposomes, to the microbubble. Traditionally, such attachments have been based around biotin–streptavidin and maleimide–PDP chemistries. Comparatively, the use of DNA–lipid tethers offers potential advantage. First, their specificity permits the construction of more complex architectures that might include bespoke combinations of different drug-loaded liposomes and/or targeting groups, such as affimers or antibodies. Second, the use of dual-lipid tether strategies should increase the strength of the individual tethers tethering the liposomes to the bubbles. The ability of cholesterol–DNA (cDNA) tethers for conjugation of liposomes to supported lipid bilayers has previously been demonstrated. For in vivo applications, bubbles and liposomes often contain a proportion of polyethylene glycol (PEG) to promote stealth-like properties and increase lifetimes. However, the associated steric effects may hinder tethering of the drug payload. We show that while the presence of PEG reduced the tethering affinity, cDNA can still be used for the attachment of liposomes to a supported lipid bilayer (SLB) as measured via QCM-D. Importantly, we show, for the first time, that QCM-D can be used to study the tethering of microbubbles to SLBs using cDNA, signified by a decrease in the magnitude of the frequency shift compared to liposomes alone due to the reduced density of the MBs. We then replicate this tethering interaction in the bulk and observe attachment of liposomes to the shell of a central MB and hence formation of a model therapeutic microbubble.