TY - JOUR
T1 - Pulsed High Intensity Focused Ultrasound Mediated Nanoparticle Delivery
T2 - Mechanisms and Efficacy in Murine Muscle
AU - O'Neill, Brian E.
AU - Vo, Howard
AU - Angstadt, Mary
AU - Li, King P.C.
AU - Quinn, Tim
AU - Frenkel, Victor
N1 - Funding Information:
The authors thank Dr. Matthew R. Dreher for thoughtfully providing insights into the complexities of drug delivery, some of which are addressed in this manuscript and Dr. Bradford J. Wood for support of this work. We also thank Ms. Hilary Hancock for editing the manuscript and providing helpful editorial suggestions. The work was done under the auspices of the Research Associateship Program of the National Academies of Sciences, and was supported in part by the intra-mural research program of the Clinical Center, National Institutes of Health.
PY - 2009/3
Y1 - 2009/3
N2 - High intensity focused ultrasound (HIFU) is generally thought to interact with biological tissues in two ways: hyperthermia (heat) and acoustic cavitation. Pulsed mode HIFU has recently been demonstrated to increase the efficacy of a variety of drug therapies. Generally, it is presumed that the treatment acts to temporarily increase the permeability of the tissue to the therapeutic agent, however, the precise mechanism remains in dispute. In this article, we present evidence precluding hyperthermia as a principal mechanism for enhancing delivery, using a quantitative analysis of systemically administered fluorescent nanoparticles delivered to muscle in the calves of mice. Comparisons were carried out on the degree of enhancement between an equivalent heat treatment, delivered without ultrasound, and that of the pulsed-HIFU itself. In the murine calf muscle, Pulsed-HIFU treatment resulted in a significant increase in distribution of 200 nm particles (p < 0.016, n = 6), while the equivalent thermal dose showed no significant increase. Additional studies using this tissue/agent model also demonstrated that the pulsed HIFU enhancing effects persist for more than 24 h, which is longer than that of hyperthermia and acoustic cavitation, and offers the possibility of a novel third mechanism for mediating delivery. (E-mail: [email protected]).
AB - High intensity focused ultrasound (HIFU) is generally thought to interact with biological tissues in two ways: hyperthermia (heat) and acoustic cavitation. Pulsed mode HIFU has recently been demonstrated to increase the efficacy of a variety of drug therapies. Generally, it is presumed that the treatment acts to temporarily increase the permeability of the tissue to the therapeutic agent, however, the precise mechanism remains in dispute. In this article, we present evidence precluding hyperthermia as a principal mechanism for enhancing delivery, using a quantitative analysis of systemically administered fluorescent nanoparticles delivered to muscle in the calves of mice. Comparisons were carried out on the degree of enhancement between an equivalent heat treatment, delivered without ultrasound, and that of the pulsed-HIFU itself. In the murine calf muscle, Pulsed-HIFU treatment resulted in a significant increase in distribution of 200 nm particles (p < 0.016, n = 6), while the equivalent thermal dose showed no significant increase. Additional studies using this tissue/agent model also demonstrated that the pulsed HIFU enhancing effects persist for more than 24 h, which is longer than that of hyperthermia and acoustic cavitation, and offers the possibility of a novel third mechanism for mediating delivery. (E-mail: [email protected]).
KW - Cavitation
KW - Hyperthermia
KW - Nanoparticle delivery
KW - Pulsed-high intensity focused ultrasound
KW - Radiation force
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U2 - 10.1016/j.ultrasmedbio.2008.09.021
DO - 10.1016/j.ultrasmedbio.2008.09.021
M3 - Article
C2 - 19081668
AN - SCOPUS:60249089204
SN - 0301-5629
VL - 35
SP - 416
EP - 424
JO - Ultrasound in Medicine and Biology
JF - Ultrasound in Medicine and Biology
IS - 3
ER -