TY - GEN
T1 - Image-guided focused ultrasound therapy system and method for improved anticancer drug delivery
AU - Basavarajappa, Lokesh
AU - Rijal, Girdhari
AU - Hoyt, Kenneth
N1 - Funding Information:
This research was supported in part by NIH grant R01EB025841 and CPRIT grant RP180670.
Publisher Copyright:
© 2019 IEEE.
PY - 2019/10
Y1 - 2019/10
N2 - Vascular abnormalities in a complex tumor microenvironment is one of the major challenges for effective drug delivery and cancer treatment. It has been well established that noninvasive focused ultrasound (FUS) combined with a microbubble (MB) contrast agent can safely and reversibly increase the permeability of blood vessel walls, thereby temporarily allowing anticancer agents to pass through them and into the tumor tissue. Termed FUS-mediated drug delivery, most previous studies have used a single focused US beam for cancer treatment in small animal models, which limited the ability to treat the entire tumor burden. To that end, the goal of this research was to reveal the effectiveness of tumor treatment when using multi-FUS system and method. An infrared dye (IR-780) functioned as a surrogate chemotherapeutic drug and allowed detection in live animals. Athymic nude female mice implanted with MDA-MB-231 breast cancer cells were used to evaluate both single FUS and multi-FUS therapeutic strategies. Each animal was injected in the tail vein with a bolus mixture of MB (2.3 x 107 Definity, Lantheus Medical Imaging) and IR-780 dye (50 μg). During US therapy, a custom pulsed sequence was applied using an image-guided FUS system (HIFUPlex-06, Verasonics Inc) for a duration of 10 min in the selected zone of the tumor. Animals were imaged using a whole-body optical imaging system (Pearl Trilogy, LI-COR Biosciences) and accumulated IR-780 dye was quantified up to 48 h after application of FUS-mediated drug delivery. After euthanasia, IR-780 dye was also quantified from homogenized tumor tissue samples. Overall, preliminary results showed that the multi-FUS therapy approach significantly increased drug uptake (increased by about 71 % at 48 h) in the targeted tumor tissue compared to the single FUS method.
AB - Vascular abnormalities in a complex tumor microenvironment is one of the major challenges for effective drug delivery and cancer treatment. It has been well established that noninvasive focused ultrasound (FUS) combined with a microbubble (MB) contrast agent can safely and reversibly increase the permeability of blood vessel walls, thereby temporarily allowing anticancer agents to pass through them and into the tumor tissue. Termed FUS-mediated drug delivery, most previous studies have used a single focused US beam for cancer treatment in small animal models, which limited the ability to treat the entire tumor burden. To that end, the goal of this research was to reveal the effectiveness of tumor treatment when using multi-FUS system and method. An infrared dye (IR-780) functioned as a surrogate chemotherapeutic drug and allowed detection in live animals. Athymic nude female mice implanted with MDA-MB-231 breast cancer cells were used to evaluate both single FUS and multi-FUS therapeutic strategies. Each animal was injected in the tail vein with a bolus mixture of MB (2.3 x 107 Definity, Lantheus Medical Imaging) and IR-780 dye (50 μg). During US therapy, a custom pulsed sequence was applied using an image-guided FUS system (HIFUPlex-06, Verasonics Inc) for a duration of 10 min in the selected zone of the tumor. Animals were imaged using a whole-body optical imaging system (Pearl Trilogy, LI-COR Biosciences) and accumulated IR-780 dye was quantified up to 48 h after application of FUS-mediated drug delivery. After euthanasia, IR-780 dye was also quantified from homogenized tumor tissue samples. Overall, preliminary results showed that the multi-FUS therapy approach significantly increased drug uptake (increased by about 71 % at 48 h) in the targeted tumor tissue compared to the single FUS method.
KW - cancer
KW - drug delivery systems
KW - image-guided therapy
KW - microbubbles
KW - ultrasound
UR - http://www.scopus.com/inward/record.url?scp=85077583445&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85077583445&partnerID=8YFLogxK
U2 - 10.1109/ULTSYM.2019.8925705
DO - 10.1109/ULTSYM.2019.8925705
M3 - Conference contribution
AN - SCOPUS:85077583445
T3 - IEEE International Ultrasonics Symposium, IUS
SP - 2428
EP - 2431
BT - 2019 IEEE International Ultrasonics Symposium, IUS 2019
PB - IEEE Computer Society
T2 - 2019 IEEE International Ultrasonics Symposium, IUS 2019
Y2 - 6 October 2019 through 9 October 2019
ER -