4.8 Article

Polydopamine Nanobottles with Photothermal Capability for Controlled Release and Related Applications

期刊

ADVANCED MATERIALS
卷 33, 期 45, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202104729

关键词

controlled release; nanobottle; phase-change material; polydopamine; swelling

资金

  1. Georgia Institute of Technology
  2. National Science Foundation [ECCS-2025462]

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This study presents a facile method for preparing polydopamine nanobottles that can encapsulate and release various types of cargos, including small molecules and biomacromolecules. The polydopamine nanobottles can release the loaded cargos in a controlled manner at a specific temperature, for example through direct heating or photothermal heating.
Nanobottles refer to colloidal particles featuring a hollow body connected to a single opening on the surface. This unique feature makes them ideal carriers for the encapsulation and controlled release of various types of cargos. Here a facile route to the fabrication of uniform nanobottles made of polydopamine by leveraging swelling-induced pressure is reported. When polystyrene spheres are coated with polydopamine and then incubated with a toluene/water emulsion, the polystyrene will be swollen to automatically poke a single hole in the shell because of the pressure inside the shell. After quenching the swelling with ethanol and then removing all the polystyrene with tetrahydrofuran, polydopamine nanobottles are obtained. The dimensions of the hollow body are determined by the polystyrene template, while the size of the opening can be tuned by varying the shell thickness. Through the opening, different types of cargos, including small molecules and biomacromolecules, can be easily loaded with a thermoresponsive material into the cavity. The cargos can be released in a controllable manner through direct heating or polydopamine-enabled photothermal heating. In a proof-of-concept experiment, the polydopamine nanobottles are used for temperature-controlled release of thrombin to trigger the formation of fibrin gels in situ.

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