4.8 Article

Systematic Study of Perfluorocarbon Nanoemulsions Stabilized by Polymer Amphiphiles

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 12, 期 35, 页码 38887-38898

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c07206

关键词

perfluorocarbon nanoemulsion; polymer amphiphile; poly(2-oxazoline); stability; payload release; protein corona; endocytosis

资金

  1. Alfred P. Sloan Award [FG-2018-10855]
  2. National Institute of General Medical Sciences (NIH) [5T32GM067555-12]
  3. Majeti-Alapati Fellowship
  4. Saul Winstein Fellowships
  5. Lorraine H. and Masuo Toji Fund Summer Research Fellowship
  6. Raymond and Dorothy Wilson Research Fellowship
  7. Lau Family via the URSP Undergraduate Research Fellowship
  8. National Science Foundation (NSF) [1928737, MRI CHE-1048804]
  9. Hellman Fellows Award
  10. Division Of Human Resource Development
  11. Direct For Education and Human Resources [1928737] Funding Source: National Science Foundation

向作者/读者索取更多资源

Perfluorocarbon (PFC) nanoemulsions, droplets of fluorous solvent stabilized by surfactants dispersed in water, are simple yet versatile nanomaterials. The orthogonal nature of the fluorous phase promotes the formation of nanoemulsions through a simple, self-assembly process while simultaneously encapsulating fluorous-tagged payloads for various applications. The size, stability, and surface chemistry of PFC nanoemulsions are controlled by the surfactant. Here, we systematically study the effect of the hydrophilic portion of polymer surfactants on PFC nanoemulsions. We find that the hydrophilic block length and identity, the overall polymer hydrophilic/lipophilic balance, and the polymer architecture are all important factors. The ability to modulate these parameters enables control over initial size, stability, payload retention, cellular internalization, and protein adsorption of PFC nanoemulsions. With the insight obtained from this systematic study of polymer amphiphiles stabilizing PFC nanoemulsions, design features required for the optimal material are obtained.

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