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Utilization of Polymer-Lipid Hybrid Nanoparticles for Targeted Anti-Cancer Therapy

Mohanty, Ayeskanta, Uthaman, Saji, Park, In-Kyu·2020·Molecules
DOI 10.3390/molecules25194377PMC PMC7582728
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Abstract

Cancer represents one of the most dangerous diseases, with 1.8 million deaths worldwide. Despite remarkable advances in conventional therapies, these treatments are not effective to completely eradicate cancer. Nanotechnology offers potential cancer treatment based on formulations of several nanoparticles (NPs). Liposomes and polymeric nanoparticle are the most investigated and effective drug delivery systems (DDS) for cancer treatment. Liposomes represent potential DDS due to their distinct properties, including high-drug entrapment efficacy, biocompatibility, low cost, and scalability. However, their use is restricted by susceptibility to lipid peroxidation, instability, burst release of drugs, and the limited surface modification. Similarly, polymeric nanoparticles show several chemical modifications with polymers, good stability, and controlled release, but their drawbacks for biological applications include limited drug loading, polymer toxicity, and difficulties in scaling up. Therefore, polymeric nanoparticles and liposomes are combined to form polymer-lipid hybrid nanoparticles (PLHNPs), with the positive attributes of both components such as high biocompatibility and stability, improved drug payload, controlled drug release, longer circulation time, and superior in vivo efficacy. In this review, we have focused on the prominent strategies used to develop tumor targeting PLHNPs and discuss their advantages and unique properties contributing to an ideal DDS.

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Metadata

Authors
Mohanty, A., Uthaman, S., & Park, I.-K.
Venue
Molecules
Publisher
MDPI AG
Published
2020-09-23
Volume
25
Issue
19
Pages
4377
ISSN
1420-3049
DOI
10.3390/molecules25194377
PMC
PMC7582728
Cited by
160
References
6
Language
en
Licence
creativecommons.org/licenses/by/4.0/ (vor)
Funders
National Research Foundation of Korea (2017M3A9E2056372, 2020R1A2C2005620, 2018R1A5A2024181 and 2019M3E5D1A02068082)

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