%0 Online Multimedia %A Zhang, Yang %A Swaminathan, Subramani %A Tang, Sicheng %A Garcia-Amorós, Jaume %A Boulina, Marcia %A Captain, Burjor %A Baker, James D. %A Raymo, Françisco M. %D 2015 %T Photoactivatable BODIPYs Designed To Monitor the Dynamics of Supramolecular Nanocarriers %U https://acs.figshare.com/articles/media/Photoactivatable_BODIPYs_Designed_To_Monitor_the_Dynamics_of_Supramolecular_Nanocarriers/2176549 %R 10.1021/ja5125308.s004 %2 https://acs.figshare.com/ndownloader/files/3810472 %K photoresponsive compounds %K Photoactivatable BODIPYs %K BODIPY fragment %K nanocarrier translocation %K oxazine ring cleaves %K photophysical properties %K sequential acquisition %K fluorescence images %K dynamics noninvasively %K supramolecular hosts %K BODIPY fluorescence %K covalent skeleton %K Drosophila melanogaster embryos %K amphiphilic polymers %K photoactivatable fluorescence %K activatable fluorophores %K transformation shifts bathochromically %K photocleavable oxazine %K hydrogel matrices %K indole heterocycle %K supramolecular nanocarriers %K media %K mechanism %K fluorescence activation %K BODIPY absorption %K illumination conditions %K delivery vehicles %K cytotoxic effects %K activation wavelength %K principle %X Self-assembling nanoparticles of amphiphilic polymers can transport hydrophobic molecules across hydrophilic media and, as a result, can be valuable delivery vehicles for a diversity of biomedical applications. Strategies to monitor their dynamics noninvasively and in real time are, therefore, essential to investigate their translocation within soft matrices and, possibly, rationalize the mechanisms responsible for their diffusion in biological media. In this context, we designed molecular guests with photoactivatable fluorescence for these supramolecular hosts and demonstrated that the activation of the fluorescent cargo, under optical control, permits the tracking of the nanocarrier translocation across hydrogel matrices with the sequential acquisition of fluorescence images. In addition, the mild illumination conditions sufficient to implement these operating principles permit fluorescence activation within developing Drosophila melanogaster embryos and enable the monitoring of the loaded nanocarriers for long periods of time with no cytotoxic effects and no noticeable influence on embryogenesis. These photoresponsive compounds combine a borondipyrromethene (BODIPY) chromophore and a photocleavable oxazine within their covalent skeleton. Under illumination at an appropriate activation wavelength, the oxazine ring cleaves irreversibly to bring the adjacent BODIPY fragment in conjugation with an indole heterocycle. This structural transformation shifts bathochromically the BODIPY absorption and permits the selective excitation of the photochemical product with concomitant fluorescence. In fact, these operating principles allow the photoactivation of BODIPY fluorescence with large brightness and infinite contrast. Thus, our innovative structural design translates into activatable fluorophores with excellent photochemical and photophysical properties as well as provides access to a general mechanism for the real-time tracking of supramolecular nanocarriers in hydrophilic matrices. %I ACS Publications