Apoferritin as an ubiquitous nanocarrier with excellent shelf life
Jazyk angličtina Země Nový Zéland Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
28392686
PubMed Central
PMC5373844
DOI
10.2147/ijn.s130267
PII: ijn-12-2265
Knihovny.cz E-zdroje
- Klíčová slova
- anticancer therapy, doxorubicin-loaded apoferritin, encapsulation, long-term stability, protein nanocarriers,
- MeSH
- antitumorózní látky aplikace a dávkování farmakokinetika farmakologie MeSH
- apoferritiny aplikace a dávkování chemie farmakokinetika MeSH
- doxorubicin aplikace a dávkování chemie MeSH
- koncentrace vodíkových iontů MeSH
- léky antitumorózní - screeningové testy MeSH
- lidé MeSH
- nádorové buněčné linie MeSH
- nádory prostaty farmakoterapie patologie MeSH
- nosiče léků aplikace a dávkování chemie farmakokinetika MeSH
- stabilita léku MeSH
- systémy cílené aplikace léků MeSH
- uvolňování léčiv MeSH
- voda chemie MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antitumorózní látky MeSH
- apoferritiny MeSH
- doxorubicin MeSH
- nosiče léků MeSH
- voda MeSH
Due to many adverse effects of conventional chemotherapy, novel methods of targeting drugs to cancer cells are being investigated. Nanosize carriers are a suitable platform for this specific delivery. Herein, we evaluated the long-term stability of the naturally found protein nanocarrier apoferritin (Apo) with encapsulated doxorubicin (Dox). The encapsulation was performed using Apo's ability to disassemble reversibly into its subunits at low pH (2.7) and reassemble in neutral pH (7.2), physically entrapping drug molecules in its cavity (creating ApoDox). In this study, ApoDox was prepared in water and phosphate-buffered saline and stored for 12 weeks in various conditions (-20°C, 4°C, 20°C, and 37°C in dark, and 4°C and 20°C under ambient light). During storage, a very low amount of prematurely released drug molecules were detected (maximum of 7.5% for ApoDox prepared in PBS and 4.4% for ApoDox prepared in water). Fourier-transform infrared spectra revealed no significant differences in any of the samples after storage. Most of the ApoDox prepared in phosphate-buffered saline and ApoDox prepared in water and stored at -20°C formed very large aggregates (up to 487% of original size). Only ApoDox prepared in water and stored at 4°C showed no significant increase in size or shape. Although this storage caused slower internalization to LNCaP prostate cancer cells, ApoDox (2.5 μM of Dox) still retained its ability to inhibit completely the growth of 1.5×104 LNCaP cells after 72 hours. ApoDox stored at 20°C and 37°C in water was not able to deliver Dox inside the nucleus, and thus did not inhibit the growth of the LNCaP cells. Overall, our study demonstrates that ApoDox has very good stability over the course of 12 weeks when stored properly (at 4°C), and is thus suitable for use as a nanocarrier in the specific delivery of anticancer drugs to patients.
Department of Biochemistry Faculty of Science Charles University Prague Czech Republic
Department of Chemistry and Biochemistry Mendel University in Brno
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