TY - JOUR
T1 - State-of-the-art of ultrasound-triggered drug delivery from ultrasound-responsive drug carriers
AU - Fan, Ching Hsiang
AU - Ho, Yi Ju
AU - Lin, Chia Wei
AU - Wu, Nan
AU - Chiang, Pei Hua
AU - Yeh, Chih Kuang
N1 - Funding Information:
This paper was funded by the Ministry of Science and Technology (MOST) of Taiwan, under grants nos. 108-2221-E-007-040-MY3, 108-2221-E-007-041-MY3, 110-2221-E-007-019-MY3, 110-2628-E-A49-015-, 111-2628-E-A49-020-, 111-2321-B-002-014, 110-2636-E-006-014, 111-2636-E-006-025, by National Tsing Hua University (Hsinchu, Taiwan) under grants nos. 111Q2713E1.
Publisher Copyright:
© 2022 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2022
Y1 - 2022
N2 - Introduction: Delivering sufficient therapeutics at the target site without off-target effects is a major goal of drug delivery technology innovation. Among the established methods, ultrasound (US) with US-responsible carriers holds great promise and demonstrates on-demand delivery of a variety of functional substances with spatial precision of several millimeters in deep-seated tissues in animal models and humans. These properties have motivated several explorations of US with US responsible-responsible carriers as a modality for neuromodulation and the treatment of various diseases, such as stroke and cancer. Areas covered: We briefly discuss three specific mechanisms that enhance in vivo drug delivery via US with US-responsible carriers: 1) permeabilizing cellular membrane, 2) increasing the permeability of vessels, and 3) promoting cellular endocytotic uptake. We then reviewed the state-of-the-art materials for US-triggered drug delivery, including conventional US contrast agents, and nanocarrier formulations, such as inorganic nanoparticles and gas vesicles. Expert opinion: In this article, we summarized recent progress for each of US-responsible drug carrier, focusing on the routes of enhancing delivery and applications. The mechanisms of interaction between US-responsible carriers and US waves, such as cavitation, streaming, hyperthermia, and ROS, as well as how those interactions can improve drug release and cell/tissue uptake.
AB - Introduction: Delivering sufficient therapeutics at the target site without off-target effects is a major goal of drug delivery technology innovation. Among the established methods, ultrasound (US) with US-responsible carriers holds great promise and demonstrates on-demand delivery of a variety of functional substances with spatial precision of several millimeters in deep-seated tissues in animal models and humans. These properties have motivated several explorations of US with US responsible-responsible carriers as a modality for neuromodulation and the treatment of various diseases, such as stroke and cancer. Areas covered: We briefly discuss three specific mechanisms that enhance in vivo drug delivery via US with US-responsible carriers: 1) permeabilizing cellular membrane, 2) increasing the permeability of vessels, and 3) promoting cellular endocytotic uptake. We then reviewed the state-of-the-art materials for US-triggered drug delivery, including conventional US contrast agents, and nanocarrier formulations, such as inorganic nanoparticles and gas vesicles. Expert opinion: In this article, we summarized recent progress for each of US-responsible drug carrier, focusing on the routes of enhancing delivery and applications. The mechanisms of interaction between US-responsible carriers and US waves, such as cavitation, streaming, hyperthermia, and ROS, as well as how those interactions can improve drug release and cell/tissue uptake.
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U2 - 10.1080/17425247.2022.2110585
DO - 10.1080/17425247.2022.2110585
M3 - Article
C2 - 35930441
AN - SCOPUS:85136458695
SN - 1742-5247
VL - 19
SP - 997
EP - 1009
JO - Expert Opinion on Drug Delivery
JF - Expert Opinion on Drug Delivery
IS - 8
ER -