The overall objective of this proposal is to develop a fundamental understanding of the role of localized transport regions (LTRs) in low-frequency sonophoresis (LFS), with an emphasis on: 1. Understanding if the LTRs are Indeed Regions of Highly-Localized Transdermal Transport for both Hydrophilic and Hydrophobic Permeants: Specifically, demonstrating whether the LTRs are regions of high permeability compared to the surrounding regions of ultrasound-treated skin (the non-LTRs) for a broad class of permeants. 2. Understanding the Mechanisms that Govern the Formation of the LTRs in LFS: Specifically, understand: i) the role of the surfactant sodium lauryl sulfate (SLS) in LTR formation, and ii) the roles of acoustic cavitation, the ultrasound acoustic field, and the skin surface topography in LTR formation. 3. Understanding the Nature of the Permeation Pathways that Exist within the LTRs and the Non-LTRs: Specifically, identify the type of permeation pathway (transcellular, intercellular, or a combination of both) followed by permeant molecules traversing the skin within the LTRs and the non-LTRs. 4. Investigating the Safety of LTR Formation on Skin Treated with LFS: Specifically, determining: i) the reversibility of LTR formation in the skin, and ii) the biological effects of LTR formation. 5. Mathematical Modeling of Transdermal Transport in the Presence of LTRs: Specifically, i) developing mathematical models to more accurately evaluate experimental transdermal permeabilities across ultrasound-treated skin with LTRs, and ii) developing models to confirm the presence of transcellular and/or intercellular transdermal pathways within the LTRs and the non-LTRs in the stratum corneum resulting from the ultrasound treatment.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Research Project (R01)
Project #
5R01EB000351-15
Application #
7237920
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Henderson, Lori
Project Start
1991-05-01
Project End
2009-06-30
Budget Start
2007-07-01
Budget End
2008-06-30
Support Year
15
Fiscal Year
2007
Total Cost
$233,840
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Engineering (All Types)
Type
Schools of Engineering
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Doloff, Joshua C; Veiseh, Omid; Vegas, Arturo J et al. (2017) Colony stimulating factor-1 receptor is a central component of the foreign body response to biomaterial implants in rodents and non-human primates. Nat Mater 16:671-680
Vegas, Arturo J; Veiseh, Omid; Gürtler, Mads et al. (2016) Long-term glycemic control using polymer-encapsulated human stem cell-derived beta cells in immune-competent mice. Nat Med 22:306-11
Vegas, Arturo J; Veiseh, Omid; Doloff, Joshua C et al. (2016) Combinatorial hydrogel library enables identification of materials that mitigate the foreign body response in primates. Nat Biotechnol 34:345-52
Jhunjhunwala, Siddharth; Alvarez, David; Aresta-DaSilva, Stephanie et al. (2016) Frontline Science: Splenic progenitors aid in maintaining high neutrophil numbers at sites of sterile chronic inflammation. J Leukoc Biol 100:253-60
Schoellhammer, Carl M; Traverso, Giovanni (2016) Low-frequency ultrasound for drug delivery in the gastrointestinal tract. Expert Opin Drug Deliv 13:1045-8
Jhunjhunwala, Siddharth; Aresta-DaSilva, Stephanie; Tang, Katherine et al. (2015) Neutrophil Responses to Sterile Implant Materials. PLoS One 10:e0137550
Veiseh, Omid; Tang, Benjamin C; Whitehead, Kathryn A et al. (2015) Managing diabetes with nanomedicine: challenges and opportunities. Nat Rev Drug Discov 14:45-57
Schoellhammer, Carl M; Srinivasan, Sharanya; Barman, Ross et al. (2015) Applicability and safety of dual-frequency ultrasonic treatment for the transdermal delivery of drugs. J Control Release 202:93-100
Veiseh, Omid; Doloff, Joshua C; Ma, Minglin et al. (2015) Size- and shape-dependent foreign body immune response to materials implanted in rodents and non-human primates. Nat Mater 14:643-51
Schoellhammer, Carl M; Schroeder, Avi; Maa, Ruby et al. (2015) Ultrasound-mediated gastrointestinal drug delivery. Sci Transl Med 7:310ra168

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