机构:
Northeastern Univ, Dept Phys, Boston, MA 02115 USANortheastern Univ, Dept Phys, Boston, MA 02115 USA
van de Ven, Anne L.
[1
]
Geilich, Benjamin
论文数: 0引用数: 0
h-index: 0
机构:
Northeastern Univ, Dept Bioengn, Boston, MA 02115 USANortheastern Univ, Dept Phys, Boston, MA 02115 USA
Geilich, Benjamin
[2
]
Gharagouzloo, Codi
论文数: 0引用数: 0
h-index: 0
机构:
Northeastern Univ, Dept Bioengn, Boston, MA 02115 USANortheastern Univ, Dept Phys, Boston, MA 02115 USA
Gharagouzloo, Codi
[2
]
Barlow, Jacob
论文数: 0引用数: 0
h-index: 0
机构:
Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USANortheastern Univ, Dept Phys, Boston, MA 02115 USA
Barlow, Jacob
[3
]
Webster, Thomas
论文数: 0引用数: 0
h-index: 0
机构:
Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USANortheastern Univ, Dept Phys, Boston, MA 02115 USA
Webster, Thomas
[3
]
Sridhar, Srinivas
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机构:
Northeastern Univ, Dept Phys, Boston, MA 02115 USA
Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USANortheastern Univ, Dept Phys, Boston, MA 02115 USA
Sridhar, Srinivas
[1
,3
]
机构:
[1] Northeastern Univ, Dept Phys, Boston, MA 02115 USA
[2] Northeastern Univ, Dept Bioengn, Boston, MA 02115 USA
[3] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
Polymersomes are a promising avenue for imageguided therapy of cancer, since they can stably encapsulate a broad range of therapeutic molecules and offer both targeting capacity and stimuli responsiveness. We have formulated highly stable, magnetically activatable polymersomes capable of continuous and pulsed small molecule release. In the proof-of-concept provided here, we demonstrate that these particles are responsive to both external and heat and magnetic fields. At physiologic temperatures, these particles display a sustained release profile that can be reversibly triggered for transient increases in release. The incorporation of fluorescent and iron oxide contrast sources make these particles amenable for quantitative imaging techniques including intravital microscopy (IVM) and ultra-short time-to-echo (UTE) magnetic resonance imaging (MRI). Thus we believe this formulation is uniquely suited for the in vivo study and optimization of externally triggered tumor growth inhibition.
机构:
Univ Washington, Appl Phys Lab, Ctr Ind & Med Ultrasound, Seattle, WA 98105 USAUniv Washington, Appl Phys Lab, Ctr Ind & Med Ultrasound, Seattle, WA 98105 USA
Vaezy, S
Andrew, M
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机构:
Univ Washington, Appl Phys Lab, Ctr Ind & Med Ultrasound, Seattle, WA 98105 USAUniv Washington, Appl Phys Lab, Ctr Ind & Med Ultrasound, Seattle, WA 98105 USA
Andrew, M
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机构:
Kaczkowski, P
Crum, L
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Appl Phys Lab, Ctr Ind & Med Ultrasound, Seattle, WA 98105 USAUniv Washington, Appl Phys Lab, Ctr Ind & Med Ultrasound, Seattle, WA 98105 USA
机构:
Helmholtz Assoc German Res Ctr HZ, GSI Helmholtz Ctr Heavy Ion Res, Darmstadt, GermanyJohns Hopkins Med, Johns Hopkins Hosp, Baltimore, MD 21231 USA
Durante, Marco
Jaekel, Oliver
论文数: 0引用数: 0
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机构:
German Canc Res Ctr, Dept Med Phys Radiat Oncol, Heidelberg, GermanyJohns Hopkins Med, Johns Hopkins Hosp, Baltimore, MD 21231 USA
Jaekel, Oliver
Kong, Lin
论文数: 0引用数: 0
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机构:
Shanghai Proton & Heavy Ion Ctr SPHIC, Dept Radiat Oncol, Shanghai, Peoples R ChinaJohns Hopkins Med, Johns Hopkins Hosp, Baltimore, MD 21231 USA
Kong, Lin
Lu, Lanchun
论文数: 0引用数: 0
h-index: 0
机构:
Ohio State Univ, Dept Radiat Oncol, Columbus, OH USAJohns Hopkins Med, Johns Hopkins Hosp, Baltimore, MD 21231 USA