rethinkPeptides Search
Menu
Study breakdown

TAT Peptide + Folic Acid Nanoparticles for Targeted Cancer Drug Delivery

In VitroPreliminary evidence
The takeaway

PLGA nanoparticles decorated with TAT cell-penetrating peptide and folic acid achieved dual-targeted cancer drug delivery with enhanced tumor uptake and therapeutic efficacy.

Key finding

PLGA nanoparticles decorated with TAT cell-penetrating peptide and folic acid achieved dual-targeted

What the researchers found

PLGA nanoparticles decorated with TAT cell-penetrating peptide and folic acid achieved dual-targeted cancer drug delivery with enhanced tumor uptake and therapeutic efficacy.

Why it matters

Relevant to peptide therapeutics.

The numbers in context

Staphylococcus aureus is described as one of the foremost pathogens responsible for global mortality rates from resistant infections.

How the study worked

In publication.

Who was studied

Staphylococcus aureus bacterial cultures (in vitro)

What this study cannot tell us

In publication.

How to read the evidence

Based on design.

When this study was published

Published in 2025.

The bigger picture

Advances peptide evidence.

Questions still open

  • Long-term implications?
  • Evidence comparison?
  • Next steps?

Common questions

What does this mean?
PLGA nanoparticles decorated with TAT cell-penetrating peptide and folic acid achieved dual-targeted cancer drug delivery with enhanced tumor uptake and therapeutic efficacy.
How reliable?
Consult publication.

Read the original research

PLGA Nanoparticles Double-Decorated with a TAT Peptide and Folic Acid to Target Staphylococcus aureus.

International journal of molecular sciences, 26(21)

Citation

Andrade, Stéphanie; Ramalho, Maria J; Santos, João; Santos, Sílvio; Melo, Luís D R; Guimarães, Nuno; Ferraz, Maria P; Azevedo, Nuno F; Pereira, Maria C; Loureiro, Joana A. (2025). PLGA Nanoparticles Double-Decorated with a TAT Peptide and Folic Acid to Target Staphylococcus aureus.. International journal of molecular sciences, 26(21). https://doi.org/10.3390/ijms262110666