SwePub
Sök i LIBRIS databas

  Utökad sökning

L773:0168 3659
 

Sökning: L773:0168 3659 > Therapeutic-oligonu...

Therapeutic-oligonucleotides activated by nucleases (TOUCAN) : A nanocarrier system for the specific delivery of clinical nucleoside analogues.

Borsa, Baris Ata, First Research Engineer (författare)
Linköpings universitet,Biologi,Tekniska fakulteten,Wallenberg Center for Molecular Medicine (WCMM); Nucleic Acid Technologies Laboratory (NAT-Lab)
Hernandez, Luiza I. (författare)
Linköpings universitet,Institutionen för biomedicinska och kliniska vetenskaper,Medicinska fakulteten,SOMAprobes, Science and Technology Park of Gipuzkoa, Donostia-San Sebastian, Spain
Jiménez, Tania (författare)
SOMAprobes, Science and Technology Park of Gipuzkoa, Donostia-San Sebastian, Spain
visa fler...
Tellapragada, Chaitanya (författare)
Karolinska Institutet
Giske, Christian G (författare)
Karolinska Institutet
Hernandez, Frank J, 1979- (författare)
Linköpings universitet,Tekniska fakulteten,Biologi,Wallenberg Center for Molecular Medicine (WCMM); Nucleic Acid Technologies Laboratory (NAT-Lab)
visa färre...
 (creator_code:org_t)
ELSEVIER, 2023
2023
Engelska.
Ingår i: Journal of Controlled Release. - : ELSEVIER. - 0168-3659 .- 1873-4995. ; 361, s. 260-269
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Nucleoside analogues have been in clinical use since 1960s and they are still used as the first therapeutic option for several cancers and viral infections, due to their high therapeutic efficacy. However, their wide clinical acceptance has been limited due to their high toxicity and severe side effects to patients. Herein, we report on a nanocarrier system that delivers nucleosides analogues in a target-specific manner, making nucleoside-based therapeutics safer and with the possibility to be used in other human conditions. This system, named, Therapeutic OligonUCleotides Activated by Nucleases" (TOUCAN) combines: i) the recognition power of oligonucleotides as substrates, ii) the use of nucleases as enzymatic biomarkers and iii) the clinical efficacy of nucleoside analogues, in a single approach. As a proof-of-concept, we report on a TOUCAN that is activated by a specific nuclease produced by bacteria and releases a therapeutic nucleoside, floxuridine. We demonstrate, for the first time, that, by incorporating a therapeutic nucleoside analogue into oligonucleotide probes, we can specifically inhibit bacterial growth in cultures. In this study, Staphylococcus aureus was selected as the targeted bacteria and the TOUCAN strategy successfully inhibited its growth with minimal inhibitory concentration (MIC) values ranging from 0.62 to 40 mg/L across all tested strains. Moreover, our results indicate that the intravenous administration of TOUCANs at a dose of 20 mg/kg over a 24-h period is a highly effective method for treating bacterial infections in a mouse model of pyomyositis. Importantly, no signs of toxicity were observed in our in vitro and in vivo studies. This work can significantly impact the current management of bacterial infections, laying the grounds for the development of a different class of antibiotics. Furthermore, it can provide a safer delivery platform for clinical nucleoside therapeutics in any human conditions, such as cancer and viral infection, where specific nuclease activity has been reported.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Nyckelord

Therapeutics; Oligonucleotides; Nucleases; Nanocarrier; Drug delivery; Antibiotics

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy