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Investigations into pulsed high-intensity focused ultrasound-enhanced delivery: preliminary evidence for a novel mechanism.

Publication ,  Journal Article
Hancock, HA; Smith, LH; Cuesta, J; Durrani, AK; Angstadt, M; Palmeri, ML; Kimmel, E; Frenkel, V
Published in: Ultrasound in medicine & biology
October 2009

Pulsed high-intensity focused ultrasound (HIFU) exposures without ultrasound contrast agents have been used for noninvasively enhancing the delivery of various agents to improve their therapeutic efficacy in a variety of tissue models in a nondestructive manner. Despite the versatility of these exposures, little is known about the mechanisms by which their effects are produced. In this study, pulsed-HIFU exposures were given in the calf muscle of mice, followed by the administration of a variety of fluorophores, both soluble and particulate, by local or systemic injection. In vivo imaging (whole animal and microscopic) was used to quantify observations of increased extravasation and interstitial transport of the fluorophores as a result of the exposures. Histological analysis indicated that the exposures caused some structural alterations such as enlarged gaps between muscle fiber bundles. These effects were consistent with increasing the permeability of the tissues; however, they were found to be transient and reversed themselves gradually within 72 h. Simulations of radiation force-induced displacements and the resulting local shear strain they produced were carried out to potentially explain the manner by which these effects occurred. A better understanding of the mechanisms involved with pulsed HIFU exposures for noninvasively enhancing delivery will facilitate the process for optimizing their use.

Duke Scholars

Published In

Ultrasound in medicine & biology

DOI

EISSN

1879-291X

ISSN

0301-5629

Publication Date

October 2009

Volume

35

Issue

10

Start / End Page

1722 / 1736

Related Subject Headings

  • Ultrasonography
  • Stress, Mechanical
  • Serum Albumin
  • Permeability
  • Nanospheres
  • Muscle, Skeletal
  • Muscle Fibers, Skeletal
  • Mice, Inbred C3H
  • Mice
  • Lectins
 

Citation

APA
Chicago
ICMJE
MLA
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Hancock, H. A., Smith, L. H., Cuesta, J., Durrani, A. K., Angstadt, M., Palmeri, M. L., … Frenkel, V. (2009). Investigations into pulsed high-intensity focused ultrasound-enhanced delivery: preliminary evidence for a novel mechanism. Ultrasound in Medicine & Biology, 35(10), 1722–1736. https://doi.org/10.1016/j.ultrasmedbio.2009.04.020
Hancock, Hilary A., Lauren H. Smith, Julian Cuesta, Amir K. Durrani, Mary Angstadt, Mark L. Palmeri, Eitan Kimmel, and Victor Frenkel. “Investigations into pulsed high-intensity focused ultrasound-enhanced delivery: preliminary evidence for a novel mechanism.Ultrasound in Medicine & Biology 35, no. 10 (October 2009): 1722–36. https://doi.org/10.1016/j.ultrasmedbio.2009.04.020.
Hancock HA, Smith LH, Cuesta J, Durrani AK, Angstadt M, Palmeri ML, et al. Investigations into pulsed high-intensity focused ultrasound-enhanced delivery: preliminary evidence for a novel mechanism. Ultrasound in medicine & biology. 2009 Oct;35(10):1722–36.
Hancock, Hilary A., et al. “Investigations into pulsed high-intensity focused ultrasound-enhanced delivery: preliminary evidence for a novel mechanism.Ultrasound in Medicine & Biology, vol. 35, no. 10, Oct. 2009, pp. 1722–36. Epmc, doi:10.1016/j.ultrasmedbio.2009.04.020.
Hancock HA, Smith LH, Cuesta J, Durrani AK, Angstadt M, Palmeri ML, Kimmel E, Frenkel V. Investigations into pulsed high-intensity focused ultrasound-enhanced delivery: preliminary evidence for a novel mechanism. Ultrasound in medicine & biology. 2009 Oct;35(10):1722–1736.
Journal cover image

Published In

Ultrasound in medicine & biology

DOI

EISSN

1879-291X

ISSN

0301-5629

Publication Date

October 2009

Volume

35

Issue

10

Start / End Page

1722 / 1736

Related Subject Headings

  • Ultrasonography
  • Stress, Mechanical
  • Serum Albumin
  • Permeability
  • Nanospheres
  • Muscle, Skeletal
  • Muscle Fibers, Skeletal
  • Mice, Inbred C3H
  • Mice
  • Lectins