TY - JOUR
T1 - Controlled Delivery of Rosuvastatin or Rapamycin through Electrospun Bismuth Nanoparticle-Infused Perivascular Wraps Promotes Arteriovenous Fistula Maturation
AU - Barcena, Allan John R.
AU - Perez, Joy Vanessa D.
AU - Bernardino, Marvin R.
AU - San Valentin, Erin Marie D.
AU - Damasco, Jossana A.
AU - Klusman, Carleigh
AU - Martin, Benjamin
AU - Court, Karem A.
AU - Godin, Biana
AU - Canlas, Gino
AU - Fowlkes, Natalie
AU - Bouchard, Richard R.
AU - Cheng, Jizhong
AU - Huang, Steven Y.
AU - Melancon, Marites P.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/7/3
Y1 - 2024/7/3
N2 - In the context of arteriovenous fistula (AVF) failure, local delivery enables the release of higher concentrations of drugs that can suppress neointimal hyperplasia (NIH) while reducing systemic adverse effects. However, the radiolucency of polymeric delivery systems hinders long-term in vivo surveillance of safety and efficacy. We hypothesize that using a radiopaque perivascular wrap to deliver anti-NIH drugs could enhance AVF maturation. Through electrospinning, we fabricated multifunctional perivascular polycaprolactone (PCL) wraps loaded with bismuth nanoparticles (BiNPs) for enhanced radiologic visibility and drugs that can attenuate NIH─rosuvastatin (Rosu) and rapamycin (Rapa). The following groups were tested on the AVFs of a total of 24 Sprague-Dawley rats with induced chronic kidney disease: control (i.e., without wrap), PCL-Bi (i.e., wrap with BiNPs), PCL-Bi-Rosu, and PCL-Bi-Rapa. We found that BiNPs significantly improved the wraps' radiopacity without affecting biocompatibility. The drug release profiles of Rosu (hydrophilic drug) and Rapa (hydrophobic drug) differed significantly. Rosu demonstrated a burst release followed by gradual tapering over 8 weeks, while Rapa demonstrated a gradual release similar to that of the hydrophobic BiNPs. In vivo investigations revealed that both drug-loaded wraps can reduce vascular stenosis on ultrasonography and histomorphometry, as well as reduce [
18F]Fluorodeoxyglucose uptake on positron emission tomography. Immunohistochemical studies revealed that PCL-Bi-Rosu primarily attenuated endothelial dysfunction and hypoxia in the neointimal layer, while PCL-Bi-Rapa modulated hypoxia, inflammation, and cellular proliferation across the whole outflow vein. In summary, the controlled delivery of drugs with different properties and mechanisms of action against NIH through a multifunctional, radiopaque perivascular wrap can improve imaging and histologic parameters of AVF maturation.
AB - In the context of arteriovenous fistula (AVF) failure, local delivery enables the release of higher concentrations of drugs that can suppress neointimal hyperplasia (NIH) while reducing systemic adverse effects. However, the radiolucency of polymeric delivery systems hinders long-term in vivo surveillance of safety and efficacy. We hypothesize that using a radiopaque perivascular wrap to deliver anti-NIH drugs could enhance AVF maturation. Through electrospinning, we fabricated multifunctional perivascular polycaprolactone (PCL) wraps loaded with bismuth nanoparticles (BiNPs) for enhanced radiologic visibility and drugs that can attenuate NIH─rosuvastatin (Rosu) and rapamycin (Rapa). The following groups were tested on the AVFs of a total of 24 Sprague-Dawley rats with induced chronic kidney disease: control (i.e., without wrap), PCL-Bi (i.e., wrap with BiNPs), PCL-Bi-Rosu, and PCL-Bi-Rapa. We found that BiNPs significantly improved the wraps' radiopacity without affecting biocompatibility. The drug release profiles of Rosu (hydrophilic drug) and Rapa (hydrophobic drug) differed significantly. Rosu demonstrated a burst release followed by gradual tapering over 8 weeks, while Rapa demonstrated a gradual release similar to that of the hydrophobic BiNPs. In vivo investigations revealed that both drug-loaded wraps can reduce vascular stenosis on ultrasonography and histomorphometry, as well as reduce [
18F]Fluorodeoxyglucose uptake on positron emission tomography. Immunohistochemical studies revealed that PCL-Bi-Rosu primarily attenuated endothelial dysfunction and hypoxia in the neointimal layer, while PCL-Bi-Rapa modulated hypoxia, inflammation, and cellular proliferation across the whole outflow vein. In summary, the controlled delivery of drugs with different properties and mechanisms of action against NIH through a multifunctional, radiopaque perivascular wrap can improve imaging and histologic parameters of AVF maturation.
KW - chronic kidney disease
KW - drug delivery systems
KW - electrospinning
KW - nanocomposite
KW - neointimal hyperplasia
KW - radiopacity
KW - vascular remodeling
KW - Sirolimus/chemistry
KW - Humans
KW - Rats
KW - Arteriovenous Fistula/pathology
KW - Male
KW - Metal Nanoparticles/chemistry
KW - Rats, Sprague-Dawley
KW - Neointima/pathology
KW - Polyesters/chemistry
KW - Animals
KW - Bismuth/chemistry
KW - Nanoparticles/chemistry
KW - Drug Liberation
KW - Rosuvastatin Calcium/chemistry
UR - http://www.scopus.com/inward/record.url?scp=85196966810&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85196966810&partnerID=8YFLogxK
U2 - 10.1021/acsami.4c06042
DO - 10.1021/acsami.4c06042
M3 - Article
C2 - 38912610
AN - SCOPUS:85196966810
SN - 1944-8244
VL - 16
SP - 33159
EP - 33168
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 26
ER -