Polymer-Based Dual-Responsive Self-Emulsifying Nanodroplets as Potential Carriers for Poorly Soluble Drugs

Li Zhang, Zhiming Zhang, Wenshou Wang, Anthony Tabet, Samuel Hanson, Linhua Zhang, Dunwan Zhu, Chun Wang

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

A biodegradable amphiphilic liquid polymer was designed to form self-emulsifying nanodroplets in water for delivering poorly soluble drugs. The polymer was composed of multiple short blocks of poly(ethylene glycol) (PEG) and poly(caprolactone) (PCL) connected through acid-labile acetal linkages. With an overall average molecular weight of over 18 kDa, the polymer remained as a viscous liquid under room and physiological temperatures. Dispersing the polymer in an aqueous buffer gave rise to highly stable micelle-like nanodroplets with an average size of approximately 15-20 nm. The nanodroplet dispersions underwent reversible temperature-sensitive aggregation with cloud points ranging from 45 to 50 °C, depending on polymer concentration. Nuclear magnetic resonance (NMR) and dynamic light scattering analyses revealed that while the nanodroplets were stable at pH 7.4 for several days, hydrolysis of the acetal linkages in the polymer backbone was much accelerated under mildly acidic pH 5.0, resulting in the formation of large microdroplets. Nile red (NR), a poorly water-soluble fluorophore, can be solubilized in the nanodroplets, and efficient intracellular delivery of NR was achieved. The hydrophobic indocyanine green (ICG) was also encapsulated in the nanodroplets. Near-infrared (NIR) fluorescence imaging and in vivo biocompatibility of the ICG-loaded nanodroplets were demonstrated in mice. In summary, the self-emulsifying nanodroplets of amphiphilic liquid polymer would be a promising material system for poorly soluble drug delivery and imaging in vivo.

Original languageEnglish (US)
Pages (from-to)4441-4449
Number of pages9
JournalACS Applied Bio Materials
Volume4
Issue number5
DOIs
StatePublished - May 17 2021

Bibliographical note

Funding Information:
This work was supported in part by the National Natural Science Foundation of China (Nos. 81671806 and 81571793); CAMS Initiative for Innovative Medicine (Nos. 2017-I2M-4-001 and 2017-I2M-3-020); Fundamental Research Funds for the Central Universities (Nos. 2019PT320028 and 2019-0831-03); and the University of Minnesota. The technical assistance of Allison Siehr is gratefully acknowledged.

Publisher Copyright:
© 2021 American Chemical Society.

Keywords

  • block polymer
  • drug delivery
  • dual-responsive
  • nanodroplets
  • self-emulsifying

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't

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