scholarly journals Controlled permeation of cell membrane by single bubble acoustic cavitation

2012 ◽  
Vol 157 (1) ◽  
pp. 103-111 ◽  
Author(s):  
Y. Zhou ◽  
K. Yang ◽  
J. Cui ◽  
J.Y. Ye ◽  
C.X. Deng
2008 ◽  
Vol 95 (9) ◽  
pp. 4124-4138 ◽  
Author(s):  
Vladimir Zarnitsyn ◽  
Christina A. Rostad ◽  
Mark R. Prausnitz

2016 ◽  
Vol 28 ◽  
pp. 185-191 ◽  
Author(s):  
C. Cogné ◽  
S. Labouret ◽  
R. Peczalski ◽  
O. Louisnard ◽  
F. Baillon ◽  
...  

2016 ◽  
Vol 29 ◽  
pp. 447-454 ◽  
Author(s):  
C. Cogné ◽  
S. Labouret ◽  
R. Peczalski ◽  
O. Louisnard ◽  
F. Baillon ◽  
...  

2021 ◽  
Author(s):  
Meng-meng Li ◽  
Ya Zhu ◽  
Mi Yang ◽  
Min Zheng ◽  
Haitao Ran ◽  
...  

Abstract Background: Necroptosis has emerged as a therapeutic target for stimulating antitumor immune responses in dying tumor cells. However, its suppressed expression of receptor-interacting protein kinase 3 (RIPK3), a key enzyme in necrosis in most cancer cells, limits the clinical translation to exploiting necroptosis.Design: We fabricated a multifunctional phase-transition nanoparticles platform by constructing Lip-ICG-PFP-cRGD, utilizing liposome and indocyanine green (ICG) as the shell and perfluoropentane (PFP) as the core. The platform system represented the combination of sonodynamic therapy (SDT) and immunotherapy for cancer treatment by inducing necroptosis and disrupting the cell membrane through the acoustic cavitation effect mediated by ultrasound. In addition to their inherent contrasting ability under photoacoustic imaging, our liposomes may also be used as an ultrasound imaging probe after being irradiated with low-intensity focused ultrasound (LIFU).Results: We demonstrate that nanoparticles can trigger necroptosis in ovarian cancer cells, which ruptures cell membrane by acoustic cavitation effect. When exposed to LIFU, the nanoparticles effectively facilitate the release of damage-associated molecular patterns by inducing burst-mediated cell-membrane decomposition. Moreover, the PFP phase change caused RIPK3/MLKL-independent necroptosis by acoustic cavitation effect, resulting in the release of biologically active DAMPs (CRT and HMGB1) to facilitate antitumor immunity. Therefore, necroptosis-inducible nanoparticles remarkably enhance antitumor immunity by activating CD8+ cytotoxic T cells and maturing dendritic cells in vitro. Conclusion: We have successfully synthesized Lip-ICG-PFP-cRGD nanoparticles, which can achieve SDT and provoke necroptosis by bubble-mediated cell membrane rupture. The innovative nanoparticle causes immunogenic cell death in cancer cells via RIPK3-independent necroptosis, which is a promising enhancer for cancer immunotherapy.


2012 ◽  
Vol 195 ◽  
pp. 161-164 ◽  
Author(s):  
Robert Mettin ◽  
P.E. Frommhold ◽  
X. Xi ◽  
F. Cegla ◽  
H. Okorn-Schmidt ◽  
...  

Applications of acoustic cavitation [ frequently suffer from certain random aspects (e.g., stochastic bubble nucleation events) as well as from its sensitivity to external parameters (like gas content in the liquid). This renders for example a prediction of bubble distributions in size and space still a difficult task. To improve this situation by a better understanding of the fundamentals, a "bottom-up" approach has recently been followed which tried to model collective bubble phenomena and bubble structures on the basis of single bubbles and their interaction [. If the behavior of individual bubbles can be well captured by the models, it is hoped to gain significant insight into a larger system of acoustically driven bubbles. Indeed, several aspects of multi-bubble systems and structures could be explained by single bubble dynamics, for instance by the inversion of the primary Bjerknes force in strong ultrasonic fields. Nevertheless, many details of bubble dynamics stay partly unclear, and considerable efforts are undertaken to improve our understanding and to optimize applications of acoustic bubbles.


2021 ◽  
Author(s):  
Meng-meng Li ◽  
Ya Zhu ◽  
Mi Yang ◽  
Yang Cao ◽  
Haitao Ran ◽  
...  

Abstract Background: Necroptosis has emerged as a therapeutic target for stimulating antitumor immune responses in dying tumor cells. However, its suppressed expression of receptor-interacting protein kinase 3 (RIPK3), a key enzyme in necrosis in most cancer cells, limits the clinical translation to exploiting necroptosis.Design: We fabricated a multifunctional phase-transition nanoparticles platform by constructing Lip-ICG-PFP-cRGD, utilizing liposome and indocyanine green (ICG) as the shell and perfluoropentane (PFP) as the core. The platform system represented the combination of sonodynamic therapy (SDT) and immunotherapy for cancer treatment by inducing necroptosis and disrupting the cell membrane through the acoustic cavitation effect mediated by ultrasound. In addition to their inherent contrasting ability under photoacoustic imaging, our liposomes may also be used as an ultrasound imaging probe after being irradiated with low-intensity focused ultrasound (LIFU).Results: We demonstrate that nanoparticles can trigger necroptosis in ovarian cancer cells, which ruptures cell membrane by acoustic cavitation effect. When exposed to LIFU, the nanoparticles effectively facilitate the release of damage-associated molecular patterns by inducing burst-mediated cell-membrane decomposition. Moreover, the PFP phase change caused RIPK3/MLKL-independent necroptosis by acoustic cavitation effect, resulting in the release of biologically active DAMPs (CRT and HMGB1) to facilitate antitumor immunity. Therefore, necroptosis-inducible nanoparticles remarkably enhance antitumor immunity by activating CD8+ cytotoxic T cells and maturing dendritic cells in vitro. Conclusion: We have successfully synthesized Lip-ICG-PFP-cRGD nanoparticles, which can achieve SDT and provoke necroptosis by bubble-mediated cell membrane rupture. The innovative nanoparticle causes immunogenic cell death in cancer cells via RIPK3-independent necroptosis, which is a promising enhancer for cancer immunotherapy.


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