Intracellular fate of polymer therapeutics investigated by fluorescence lifetime imaging and fluorescence pattern analysis
Language English Country Czech Republic Media print
Document type Journal Article
PubMed
27762587
DOI
10.33549/physiolres.933423
PII: 933423
Knihovny.cz E-resources
- MeSH
- Doxorubicin analogs & derivatives pharmacokinetics MeSH
- Humans MeSH
- Cell Line, Tumor MeSH
- Nanoparticles MeSH
- Drug Carriers * MeSH
- Optical Imaging methods MeSH
- Polymers MeSH
- Antineoplastic Agents pharmacokinetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Doxorubicin MeSH
- Drug Carriers * MeSH
- pirarubicin MeSH Browser
- Polymers MeSH
- Antineoplastic Agents MeSH
Nanocarriers bearing anticancer drugs are promising candidates to improve the efficacy of cancer therapy and minimize side effects. The most potent cytostatics used in the treatment of various cancers are anthracyclines, e.g. doxorubicin or pirarubicin. Recently, polymer therapeutics carrying anthracyclines have been intensively studied. The precise characterization of in vitro nanocarrier biological behavior brings a better understanding of the nanocarrier characteristics and enables prediction of the behavior of the nanocarrier during in vivo application. Advanced fluorescence detection methods, e.g. fluorescence lifetime imaging microscopy (FLIM), were successfully exploited to describe the properties of various polymeric nano-systems and contributed to a complex view of anthracyclines' intracellular transport and DNA intercalation. Here, we report the application of a specific technique for processing FLIM images, called fluorescence pattern decomposition, to evaluate early events after doxorubicin or pirarubicin treatment of cells. Moreover, we characterized changes in the intracellular localization and release of the anthracyclines during the incubation of cells with polymer nanotherapeutics based on poly[N-(2-hydroxypropyl)-methacrylamide] (pHPMA).
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