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Review
. 2021 Feb 3:12:601626.
doi: 10.3389/fphar.2021.601626. eCollection 2021.

Biodegradable Polymeric Nanoparticles for Drug Delivery to Solid Tumors

Affiliations
Review

Biodegradable Polymeric Nanoparticles for Drug Delivery to Solid Tumors

Agnese Gagliardi et al. Front Pharmacol. .

Abstract

Advances in nanotechnology have favored the development of novel colloidal formulations able to modulate the pharmacological and biopharmaceutical properties of drugs. The peculiar physico-chemical and technological properties of nanomaterial-based therapeutics have allowed for several successful applications in the treatment of cancer. The size, shape, charge and patterning of nanoscale therapeutic molecules are parameters that need to be investigated and modulated in order to promote and optimize cell and tissue interaction. In this review, the use of polymeric nanoparticles as drug delivery systems of anticancer compounds, their physico-chemical properties and their ability to be efficiently localized in specific tumor tissues have been described. The nanoencapsulation of antitumor active compounds in polymeric systems is a promising approach to improve the efficacy of various tumor treatments.

Keywords: PEG; cancer; passive targeting; polymeric nanoparticles; surfactants.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Overview of the main features of polymeric nanoparticles.
FIGURE 2
FIGURE 2
Differences between a physiological and a tumor environment. Figure generated from Servier Medical Art.
FIGURE 3
FIGURE 3
Schematic representation of polymeric nanoparticles as a function of their morphology.
FIGURE 4
FIGURE 4
Physico-chemical parameters of polymeric nanoparticles.
FIGURE 5
FIGURE 5
Schematic representation of various drug targeting approaches (1–3). (1) Passive targeting of nanocarriers through fenestrated vasculature of tumor tissue by extravasation. Active targeting of cancer cells (2a) and (2b) tumor endothelium using ligand-modified nanocarriers. (3) Stimuli-responsive nanomedicines able to release the anticancer agent by internal or external triggers. Figure generated from Servier Medical Art.

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