Awad Nahid S, Paul Vinod, AlSawaftah Nour M, Ter Haar Gail, Allen Theresa M, Pitt William G, Husseini Ghaleb A
Department of Chemical Engineering, American University of Sharjah, Sharjah, United Arab Emirates.
Joint Department of Physics, The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust, London SM2 5NG, U.K.
ACS Pharmacol Transl Sci. 2021 Mar 3;4(2):589-612. doi: 10.1021/acsptsci.0c00212. eCollection 2021 Apr 9.
The safe and effective delivery of anticancer agents to diseased tissues is one of the significant challenges in cancer therapy. Conventional anticancer agents are generally cytotoxins with poor pharmacokinetics and bioavailability. Nanocarriers are nanosized particles designed for the selectivity of anticancer drugs and gene transport to tumors. They are small enough to extravasate into solid tumors, where they slowly release their therapeutic load by passive leakage or biodegradation. Using smart nanocarriers, the rate of release of the entrapped therapeutic(s) can be increased, and greater exposure of the tumor cells to the therapeutics can be achieved when the nanocarriers are exposed to certain internally (enzymes, pH, and temperature) or externally (light, magnetic field, and ultrasound) applied stimuli that trigger the release of their load in a safe and controlled manner, spatially and temporally. This review gives a comprehensive overview of recent research findings on the different types of stimuli-responsive nanocarriers and their application in cancer treatment with a particular focus on ultrasound.
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