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Polymeric perfluorocarbon nanoemulsions are ultrasound-activated wireless drug infusion catheters.
Zhong, Q; Yoon, B C; Aryal, M; Wang, J B; Ilovitsh, T; Baikoghli, M A; Hosseini-Nassab, N; Karthik, A; Cheng, R H; Ferrara, K W; Airan, R D.
  • Zhong Q; Department of Radiology, Stanford University, Stanford, CA 94305, USA; David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02142, USA.
  • Yoon BC; Department of Radiology, Stanford University, Stanford, CA 94305, USA; Department of Radiology, Massachusetts General Hospital, Boston, MA 02114, USA.
  • Aryal M; Department of Radiology, Stanford University, Stanford, CA 94305, USA.
  • Wang JB; Department of Radiology, Stanford University, Stanford, CA 94305, USA.
  • Ilovitsh T; Department of Radiology, Stanford University, Stanford, CA 94305, USA; Department of Biomedical Engineering, University of California, Davis, CA 95616, USA.
  • Baikoghli MA; Department of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.
  • Hosseini-Nassab N; Department of Radiology, Stanford University, Stanford, CA 94305, USA.
  • Karthik A; Department of Radiology, Stanford University, Stanford, CA 94305, USA.
  • Cheng RH; Department of Molecular and Cellular Biology, University of California, Davis, CA 95616, USA.
  • Ferrara KW; Department of Radiology, Stanford University, Stanford, CA 94305, USA; Department of Biomedical Engineering, University of California, Davis, CA 95616, USA.
  • Airan RD; Department of Radiology, Stanford University, Stanford, CA 94305, USA. Electronic address: rairan@stanford.edu.
Biomaterials ; 206: 73-86, 2019 06.
Article en En | MEDLINE | ID: mdl-30953907
Catheter-based intra-arterial drug therapies have proven effective for a range of oncologic, neurologic, and cardiovascular applications. However, these procedures are limited by their invasiveness and relatively broad drug spatial distribution. The ideal technique for local pharmacotherapy would be noninvasive and would flexibly deliver a given drug to any region of the body with high spatial and temporal precision. Combining polymeric perfluorocarbon nanoemulsions with existent clinical focused ultrasound systems could in principle meet these needs, but it has not been clear whether these nanoparticles could provide the necessary drug loading, stability, and generalizability across a range of drugs, beyond a few niche applications. Here, we develop polymeric perfluorocarbon nanoemulsions into a generalized platform for ultrasound-targeted delivery of hydrophobic drugs with high potential for clinical translation. We demonstrate that a wide variety of drugs may be effectively uncaged with ultrasound using these nanoparticles, with drug loading increasing with hydrophobicity. We also set the stage for clinical translation by delineating production protocols that are scalable and yield sterile, stable, and optimized ultrasound-activated drug-loaded nanoemulsions. Finally, we exhibit a new potential application of these nanoemulsions for local control of vascular tone. This work establishes the power of polymeric perfluorocarbon nanoemulsions as a clinically-translatable platform for efficacious, noninvasive, and localized ultrasonic drug uncaging for myriad targets in the brain and body.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Polímeros / Emulsiones / Nanopartículas / Fluorocarburos Tipo de estudio: Guideline Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Polímeros / Emulsiones / Nanopartículas / Fluorocarburos Tipo de estudio: Guideline Idioma: En Año: 2019 Tipo del documento: Article