TY - JOUR
T1 - Nanochannel implants for minimally-invasive insertion and intratumoral delivery
AU - Hood, R. Lyle
AU - Bruno, Giacomo
AU - Jain, Priya
AU - Anderson, Jeff
AU - Wolfe, Tatiana
AU - Quini, Caio
AU - Schmulen, Jeffery
AU - Li, Xian C.
AU - Butler, E. Brian
AU - Krishnan, Sunil
AU - Grattoni, Alessandro
N1 - Publisher Copyright:
Copyright © 2016 American Scientific Publishers All rights reserved.
PY - 2016/10
Y1 - 2016/10
N2 - Novel approaches to achieve local, intratumoral drug delivery have the dual benefit of reducing systemic toxicity while enhancing efficacy for malignant cells. We have developed a new implantable system combining a next-generation BioNEMS nanofluidic membrane with parallel nanochannels that offers controlled release of biomolecules. Based on concentration-driven diffusive transport, nanochannel membranes provide a "drug agnostic" delivery mechanism. Integrating this nanotechnology within a small implantable capsule permits multipurpose functionality and compatibility with different therapeutic approaches as well as diagnostic imaging capability. A minimally-invasive, percutaneous trocar delivery mechanism enables serial implantation throughout a target tissue volume. In this manuscript, we demonstrate that this platform is capable of sustained delivery for chemotherapy, radiosensitization, immunomodulation, and imaging contrast, among others. This platform's utility was established through release of doxorubicin, OX86, FGK45, and Magnevist. Further proof-of-concept experiments demonstrated successful in vivo implantation and intratumoral release of antibodies and contrast agents, as well as the platform's MR-compatibility and capability as a radiopaque fiducial. These results provide strong evidence for a flexible, multifunctional nanofluidic implant capable of broadening local delivery utility in the clinic.
AB - Novel approaches to achieve local, intratumoral drug delivery have the dual benefit of reducing systemic toxicity while enhancing efficacy for malignant cells. We have developed a new implantable system combining a next-generation BioNEMS nanofluidic membrane with parallel nanochannels that offers controlled release of biomolecules. Based on concentration-driven diffusive transport, nanochannel membranes provide a "drug agnostic" delivery mechanism. Integrating this nanotechnology within a small implantable capsule permits multipurpose functionality and compatibility with different therapeutic approaches as well as diagnostic imaging capability. A minimally-invasive, percutaneous trocar delivery mechanism enables serial implantation throughout a target tissue volume. In this manuscript, we demonstrate that this platform is capable of sustained delivery for chemotherapy, radiosensitization, immunomodulation, and imaging contrast, among others. This platform's utility was established through release of doxorubicin, OX86, FGK45, and Magnevist. Further proof-of-concept experiments demonstrated successful in vivo implantation and intratumoral release of antibodies and contrast agents, as well as the platform's MR-compatibility and capability as a radiopaque fiducial. These results provide strong evidence for a flexible, multifunctional nanofluidic implant capable of broadening local delivery utility in the clinic.
KW - BioNEMS Device
KW - Controlled Delivery
KW - Fiducial Marker
KW - Imaging Contrast
KW - Intratumoral Release
KW - Localized Drug Delivery
KW - Nanoconstrained Diffusion
KW - Nanofluidics
KW - Nanotechnology.
KW - Radiosensitization
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UR - http://www.scopus.com/inward/citedby.url?scp=84990852256&partnerID=8YFLogxK
U2 - 10.1166/jbn.2016.2288
DO - 10.1166/jbn.2016.2288
M3 - Article
C2 - 29360309
AN - SCOPUS:84990852256
SN - 1550-7033
VL - 12
SP - 1907
EP - 1915
JO - Journal of Biomedical Nanotechnology
JF - Journal of Biomedical Nanotechnology
IS - 10
ER -