Scinovex
reviewTop 1% cited

Ligand-Directed Active Tumor-Targeting Polymeric Nanoparticles for Cancer Chemotherapy

Biomacromolecules · 2014 · Vol. 15(6) · pp. 1955–1969
Yinan ZhongFenghua MengChao DengZhiyuan Zhong

Abstract

In recent years, polymeric nanoparticles have appeared as a most viable and versatile delivery system for targeted cancer therapy. Various in vivo studies have demonstrated that virus-sized stealth particles are able to circulate for a prolonged time and preferentially accumulate in the tumor site via the enhanced permeability and retention (EPR) effect (so-called "passive tumor-targeting"). The surface decoration of stealth nanoparticles by a specific tumor-homing ligand, such as antibody, antibody fragment, peptide, aptamer, polysaccharide, saccharide, folic acid, and so on, might further lead to increased retention and accumulation of nanoparticles in the tumor vasculature as well as selective and efficient internalization by target tumor cells (termed as "active tumor-targeting"). Notably, these active targeting nanoparticulate drug formulations have shown improved, though to varying degrees, therapeutic performances in different tumor models as compared to their passive targeting counterparts. In addition to type of ligands, several other factors such as in vivo stability of nanoparticles, particle shape and size, and ligand density also play an important role in targeted cancer chemotherapy. In this review, concept and recent development of polymeric nanoparticles conjugated with specific targeting ligands, ranging from proteins (e.g., antibodies, antibody fragments, growth factors, and transferrin), peptides (e.g., cyclic RGD, octreotide, AP peptide, and tLyp-1 peptide), aptamers (e.g., A10 and AS1411), polysaccharides (e.g., hyaluronic acid), to small biomolecules (e.g., folic acid, galactose, bisphosphonates, and biotin), for active tumor-targeting drug delivery in vitro and in vivo are highlighted and discussed. With promise to maximize therapeutic efficacy while minimizing systemic side effects, ligand-mediated active tumor-targeting treatment modality has become an emerging and indispensable platform for safe and efficient cancer therapy.

Nanoparticle-Based Drug DeliveryNanoplatforms for cancer theranosticsRNA Interference and Gene DeliveryIn vivoChemistryDrug deliveryHyaluronic acidInternalizationTargeted drug deliveryPeptideAptamerCancer researchBiophysics

MeSH terms

AnimalsHumansLigandsNeoplasmsPolymersDrug Delivery SystemsNanoparticles

Funding

  • National Natural Science Foundation of China
  • National Cancer Institute
Citations
527
FWCI
26.33
field-weighted impact
References
137
Percentile
100%
vs. same field & year
Citations per year
Cited by
Applications of nanoparticles in biomedical imaging
Nanoscale · 2018 · 600 citations
Polymeric nanoparticles: A study on the preparation variables and characterization methods
Materials Science and Engineering C · 2017 · 654 citations
Biodegradable Polymeric Nanoparticles for Drug Delivery to Solid Tumors
Frontiers in Pharmacology · 2021 · 518 citations
References
Chemotherapy and the war on cancer
Nature reviews. Cancer · 2005 · 2,077 citations
Strategies in the design of nanoparticles for therapeutic applications
Nature Reviews Drug Discovery · 2010 · 3,576 citations
Active targeting schemes for nanoparticle systems in cancer therapeutics
Advanced Drug Delivery Reviews · 2008 · 1,702 citations
Biodegradable polymeric nanoparticles as drug delivery devices
Journal of Controlled Release · 2001 · 3,468 citations
Dissemination and growth of cancer cells in metastatic sites
Nature reviews. Cancer · 2002 · 3,915 citations
Polymer-based nanocapsules for drug delivery
International Journal of Pharmaceutics · 2009 · 1,670 citations
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.