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Review
. 2011 Jun 30;152(3):330-48.
doi: 10.1016/j.jconrel.2011.01.006. Epub 2011 Jan 14.

Ultrasound-mediated transdermal drug delivery: mechanisms, scope, and emerging trends

Affiliations
Review

Ultrasound-mediated transdermal drug delivery: mechanisms, scope, and emerging trends

Baris E Polat et al. J Control Release. .

Abstract

The use of ultrasound for the delivery of drugs to, or through, the skin is commonly known as sonophoresis or phonophoresis. The use of therapeutic and high frequencies of ultrasound (≥0.7MHz) for sonophoresis (HFS) dates back to as early as the 1950s, while low-frequency sonophoresis (LFS, 20-100kHz) has only been investigated significantly during the past two decades. Although HFS and LFS are similar because they both utilize ultrasound to increase the skin penetration of permeants, the mechanisms associated with each physical enhancer are different. Specifically, the location of cavitation and the extent to which each process can increase skin permeability are quite dissimilar. Although the applications of both technologies are different, they each have strengths that could allow them to improve current methods of local, regional, and systemic drug delivery. In this review, we will discuss the mechanisms associated with both HFS and LFS, specifically concentrating on the key mechanistic differences between these two skin treatment methods. Background on the relevant physics associated with ultrasound transmitted through aqueous media will also be discussed, along with implications of these phenomena on sonophoresis. Finally, a thorough review of the literature is included, dating back to the first published reports of sonophoresis, including a discussion of emerging trends in the field.

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Figures

Figure 1
Figure 1
Relative thickness of the diffusion boundary layer (in black) of a spherical cavitation bubble in the collapsed state (in the compression cycle, left) and in the expanded state (in the rarefaction cycle, right).
Figure 2
Figure 2
Illustration of cavitation bubbles inducing disordering within the stratum corneum under HFS. Legend: Keratinocytes (formula image), cavitation bubbles (formula image), lipid bilayers (formula image), and coupling medium (formula image).
Figure 3
Figure 3
Illustration of a cavitation bubble asymmetrically collapsing into the stratum corneum as a microjet under LFS. Legend: Keratinocytes (formula image), lipid bilayers (formula image), and coupling medium (formula image).
Figure 4
Figure 4
LTRs formed on the surface of pig skin treated with 20 kHz LFS and a surfactant. LTRs are stained with allura red.

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References

    1. Mitragotri S. Sonophoresis: a 50-year journey. Drug Discov Today. 2004;9(17):735–736. - PubMed
    1. Fellinger K, Schmid J. Klinik und Therapie des chronischen Gelenkrheumatismus. Maudrich, Vienna, Austria: 1954.
    1. Newman M, Kill M, Frampton G. Effects of ultrasound alone and combined with hydrocortisone injections by needle or hypo-spray. Amer J Physical Med. 1958;37(4):206–209. - PubMed
    1. Tyle P, Agrawala P. Drug delivery by phonophoresis. Pharm Res. 1989;6(5):355–361. - PubMed
    1. Bommannan D, Menon G, Okuyama H, Elias P, Guy R. Sonophoresis. II. Examination of the mechanism (s) of ultrasound-enhanced transdermal drug delivery. Pharm Res. 1992;9(8):1043–1047. - PubMed

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