Enhanced nanoparticle delivery exploiting tumour-responsive formulations View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2018-12

AUTHORS

Lindsey A. Bennie, Helen O. McCarthy, Jonathan A. Coulter

ABSTRACT

Nanoparticles can be used as drug carriers, contrast agents and radiosensitisers for the treatment of cancer. Nanoparticles can either passively accumulate within tumour sites, or be conjugated with targeting ligands to actively enable tumour deposition. With respect to passive accumulation, particles < 150 nm accumulate with higher efficiency within the tumour microenvironment, a consequence of the enhanced permeability and retention effect. Despite these favourable properties, clinical translation of nano-therapeutics is inhibited due to poor in vivo stability, biodistribution and target cell internalisation. Nano-therapeutics can be modified to exploit features of the tumour microenvironment such as elevated hypoxia, increased pH and a compromised extracellular matrix. This is in contrast to cytotoxic chemotherapies which generally do not exploit the characteristic pathological features of the tumour microenvironment, and as such are prone to debilitating systemic toxicities. This review examines strategies for tumour microenvironment targeting to improve nanoparticle delivery, with particular focus on the delivery of nucleic acids and gold nanoparticles. Evidence for key research areas and future technologies are presented and critically evaluated. Among the most promising technologies are the development of next-generation cell penetrating peptides and the incorporation of micro-environment responsive stealth molecules. More... »

PAGES

10

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1186/s12645-018-0044-6

    DOI

    http://dx.doi.org/10.1186/s12645-018-0044-6

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1110099638

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/30595759


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