AI Article Synopsis

  • Polymer micelles, formed by the self-assembly of amphiphilic polymers, are utilized in drug and gene delivery due to their unique structure that has a hydrophobic core and hydrophilic shell.
  • Environmental factors like temperature and pH can compromise the stability of these micelles, risking drug leakage and affecting their effectiveness as carriers.
  • This review highlights the use of fluorescence resonance energy transfer (FRET) technology for monitoring micelle stability and distribution, discusses methods for integrating fluorescent probes, and addresses challenges and future advancements in using FRET for studying micelle-based drug delivery systems.

Article Abstract

Polymer micelles formed by self-assembly of amphiphilic polymers are widely used in drug delivery, gene delivery and biosensors, due to their special hydrophobic core/hydrophilic shell structure and nanoscale. However, the structural stability of polymer micelles can be affected strongly by environmental factors, such as temperature, pH, shear force in the blood and interaction with non-target cells, leading to degradations and drug leakage as drug carriers. Therefore, researches on the structural integrity and distribution of micelle-based carriers are very important for evaluating their therapeutic effect and clinical feasibility. At present, fluorescence resonance energy transfer (FRET) technology has been widely used in real-time monitoring of aggregation, dissociation and distribution of polymer micelles ( and vo). In this review, the polymer micelles, characteristics of FRET technology, structure and properties of the FRET-polymer micelles are briefly introduced. Then, methods and mechanism for combinations of several commonly used fluorescent probes into polymer micelles structures, and progresses on the stability and distribution studies of FRET-polymer micelles ( and ) as drug carriers are reviewed, and current challenges of FRET technology and future directions are discussed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927713PMC
http://dx.doi.org/10.7507/1001-5515.202111040DOI Listing

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