Engineered nanoparticles for imaging and drug delivery in colorectal cancer
•We review the uses of nanoparticles for CRC imaging.•We discuss the uses of nanoparticles for drug delivery in CRC.•We explore novel nanoparticle-based approaches for CRC treatment.•We review the applications of nanoparticles to immunotherapy against CRC. Colorectal cancer (CRC) is one of the deadl...
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Veröffentlicht in: | Seminars in cancer biology 2021-02, Vol.69, p.293-306 |
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Hauptverfasser: | , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •We review the uses of nanoparticles for CRC imaging.•We discuss the uses of nanoparticles for drug delivery in CRC.•We explore novel nanoparticle-based approaches for CRC treatment.•We review the applications of nanoparticles to immunotherapy against CRC.
Colorectal cancer (CRC) is one of the deadliest diseases worldwide due to a lack of early detection methods and appropriate drug delivery strategies. Conventional imaging techniques cannot accurately distinguish benign from malignant tissue, leading to frequent misdiagnosis or diagnosis at late stages of the disease. Novel screening tools with improved accuracy and diagnostic precision are thus required to reduce the mortality burden of this malignancy. Additionally, current therapeutic strategies, including radio- and chemotherapies carry adverse side effects and are limited by the development of drug resistance. Recent advances in nanotechnology have rendered it an attractive approach for designing novel clinical solutions for CRC. Nanoparticle-based formulations could assist early tumor detection and help to overcome the limitations of conventional therapies including poor aqueous solubility, nonspecific biodistribution and limited bioavailability. In this review, we shed light on various types of nanoparticles used for diagnosis and drug delivery in CRC. In addition, we will explore how these nanoparticles can improve diagnostic accuracy and promote selective drug targeting to tumor sites with increased efficiency and reduced cytotoxicity against healthy colon tissue. |
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ISSN: | 1044-579X 1096-3650 |
DOI: | 10.1016/j.semcancer.2019.06.017 |