| Autor: |
Moosavifar, Mirjavad, Barmin, Roman A., Rama, Elena, Rix, Anne, Gumerov, Rustam A., Lisson, Thomas, Bastard, Céline, Rütten, Stephan, Avraham‐Radermacher, Noah, Koehler, Jens, Pohl, Michael, Kulkarni, Vedangi, Baier, Jasmin, Koletnik, Susanne, Zhang, Rui, Dasgupta, Anshuman, Motta, Alessandro, Weiler, Marek, Potemkin, Igor I., Schmitz, Georg |
| Předmět: |
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| Zdroj: |
Advanced Science; 10/28/2024, Vol. 11 Issue 40, p1-13, 13p |
| Abstrakt: |
Microbubbles (MB) are widely used as contrast agents for ultrasound (US) imaging and US‐enhanced drug delivery. Polymeric MB are highly suitable for these applications because of their acoustic responsiveness, high drug loading capability, and ease of surface functionalization. While many studies have focused on using polymeric MB for diagnostic and therapeutic purposes, relatively little attention has thus far been paid to improving their inherent imaging and drug delivery features. This study here shows that manipulating the polymer chemistry of poly(butyl cyanoacrylate) (PBCA) MB via temporarily mixing the monomer with the monomer‐mimetic butyl cyanoacetate (BCC) during the polymerization process improves the drug loading capacity of PBCA MB by more than twofold, and the in vitro and in vivo acoustic responses of PBCA MB by more than tenfold. Computer simulations and physisorption experiments show that BCC manipulates the growth of PBCA polymer chains and creates nanocavities in the MB shell, endowing PBCA MB with greater drug entrapment capability and stronger acoustic properties. Notably, because BCC can be readily and completely removed during MB purification, the resulting formulation does not include any residual reagent beyond the ones already present in current PBCA‐based MB products, facilitating the potential translation of next‐generation PBCA MB. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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