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A Novel Approach to Making the Gas-Filled Liposome Real: Based on the Interaction of Lipid with Free Nanobubble within the Solution. | LitMetric

A Novel Approach to Making the Gas-Filled Liposome Real: Based on the Interaction of Lipid with Free Nanobubble within the Solution.

ACS Appl Mater Interfaces

State Key Laboratory of Bioelectronics, Jiangsu Key Laboratory for Biomaterials and Devices, School of Biological Sciences & Medical Engineering, Southeast University, Nanjing 210096, China.

Published: December 2015

AI Article Synopsis

  • Nanobubbles smaller than 1 μm show potential for ultrasound molecular imaging and drug delivery, but creating stable gas-filled nanobubbles is challenging.
  • Researchers developed a new method to create lipid-encapsulated nanobubbles, called GU-Liposomes, which are made by assembling phospholipid molecules around gas-filled bubbles.
  • The study found that GU-Liposomes have a mean diameter of 194.4 nm and can enhance ultrasound imaging, with effectiveness influenced by the ratio of lipid to gas in their structure, paving the way for future applications in medical imaging and therapy.

Article Abstract

Nanobubbles with a size less than 1 μm could make a promising application in ultrasound molecular imaging and drug delivery. However, the fabrication of stable gas encapsulation nanobubbles is still challenging. In this study, a novel method for preparation of lipid- encapsulated nanobubbles was reported. The dispersed phospholipid molecules in the prefabricated free nanobubbles solution can be assembled to form controllable stable lipid encapsulation gas-filled ultrasound-sensitive liposome (GU-Liposome). The optimized preparation parameters and formation mechanism of GU-Liposome were investigated in detail. Results showed that this type of GU-Liposome had mean diameter of 194.4 ± 6.6 nm and zeta potential of -25.2 ± 1.9 mV with layer by layer self-assembled lipid structure. The acoustic imaging analysis in vitro indicated that ultrasound imaging enhancement could be acquired by both perfusion imaging and accumulation imaging. The imaging enhancement level and duration time was related with the ratios of lipid to gas in the GU-Liposome structure. All in all, by this novel and controllable nanobubble construction technique, it will broaden the future theranostic applications of nanobubbles.

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Source
http://dx.doi.org/10.1021/acsami.5b07778DOI Listing

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