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Review
. 2014 Jun;15(3):709-21.
doi: 10.1208/s12249-014-0089-8. Epub 2014 Feb 19.

Nanodrug delivery systems: a promising technology for detection, diagnosis, and treatment of cancer

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Review

Nanodrug delivery systems: a promising technology for detection, diagnosis, and treatment of cancer

Anish Babu et al. AAPS PharmSciTech. 2014 Jun.

Abstract

Nanotechnology has enabled the development of novel therapeutic and diagnostic strategies, such as advances in targeted drug delivery systems, versatile molecular imaging modalities, stimulus responsive components for fabrication, and potential theranostic agents in cancer therapy. Nanoparticle modifications such as conjugation with polyethylene glycol have been used to increase the duration of nanoparticles in blood circulation and reduce renal clearance rates. Such modifications to nanoparticle fabrication are the initial steps toward clinical translation of nanoparticles. Additionally, the development of targeted drug delivery systems has substantially contributed to the therapeutic efficacy of anti-cancer drugs and cancer gene therapies compared with nontargeted conventional delivery systems. Although multifunctional nanoparticles offer numerous advantages, their complex nature imparts challenges in reproducibility and concerns of toxicity. A thorough understanding of the biological behavior of nanoparticle systems is strongly warranted prior to testing such systems in a clinical setting. Translation of novel nanodrug delivery systems from the bench to the bedside will require a collective approach. The present review focuses on recent research efforts citing relevant examples of advanced nanodrug delivery and imaging systems developed for cancer therapy. Additionally, this review highlights the newest technologies such as microfluidics and biomimetics that can aid in the development and speedy translation of nanodrug delivery systems to the clinic.

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Figures

Fig. 1
Fig. 1
Schematic showing stealthed nanoparticles are poorly recognized by opsonin proteins in circulation allowing nanoparticles to evade rapid phagocytic clearance resulting in enhanced tumor accumulation. By contrast, conventional nanoparticles that are not stealthed are rapidly opsonized and cleared from the circulation resulting in poor tumor accumulation
Fig. 2
Fig. 2
Multifunctional nanoparticle systems can be designed with a choice of drug delivery vehicle, tumor-targeting ligands, molecular imaging agents, and biological and synthetic therapeutics and cloaked with stealth properties. The schematic lists an abbreviated menu of currently available preclinical options to compose novel nanoparticle systems

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