TY - JOUR
T1 - A Microneedles Balloon Catheter for Endovascular Drug Delivery
AU - Moussi, Khalil
AU - Haneef, Ali A.
AU - Alsiary, Rawiah A.
AU - Diallo, Elhadj
AU - Boone, Marijn Antoine
AU - Abu-Araki, Huda
AU - Al-Radi, Osman O.
AU - Kosel, Jürgen
N1 - KAUST Repository Item: Exported on 2021-11-21
Acknowledgements: This work was funded and supported by King Abdullah University of Science and Technology (KAUST). The authors thank Ali I. Al-Naimi Petroleum Engineering Research Center (ANPERC) at KAUST for the assistance with the CT scanner imaging. The authors thank Mr. Tariq Ali Alghamdi (KAIMRC) and Samer Yahya Zakari (KAIMRC) for their help in tissue sectioning and staining. The authors thank Dr. Shahida Shafi and Dr. Abdelhamid Saoudi for their support.
PY - 2021/5/28
Y1 - 2021/5/28
N2 - Disorders of the inner parts of blood vessels have been significant triggers of cardiovascular diseases (CVDs). Different interventional methods have been employed, from complex surgeries to balloon angioplasty techniques to open the narrowed blood vessels. However, CVDs continue to be the lead cause of death in the world. Delivering a therapeutic agent directly to the inner wall of affected blood vessels can be a transformative step toward a better treatment option. To open the door for such an approach, a catheter delivery system is developed based on a conventional balloon catheter where a fluidic channel and microneedles (MNs) are integrated on top of it. This enables precise and localized delivery of therapeutics directly into vessel walls. Customizable MNs are fabricated using a high-resolution 3D printing technique where MN's height ranges from 100 to 350 µm. The MNs penetration into a synthetic vascular model is investigated with a computerized tomography scan. Ex vivo tests on rabbit aorta confirm the MN-upgraded balloon catheter's performance on real tissue. Delivery of fluorescent dye is accomplished by injecting it through the fluidic channel and MNs into the aortic tissue. The dye is observed at up to 180 µm of depth, confirming site-specific endovascular delivery.
AB - Disorders of the inner parts of blood vessels have been significant triggers of cardiovascular diseases (CVDs). Different interventional methods have been employed, from complex surgeries to balloon angioplasty techniques to open the narrowed blood vessels. However, CVDs continue to be the lead cause of death in the world. Delivering a therapeutic agent directly to the inner wall of affected blood vessels can be a transformative step toward a better treatment option. To open the door for such an approach, a catheter delivery system is developed based on a conventional balloon catheter where a fluidic channel and microneedles (MNs) are integrated on top of it. This enables precise and localized delivery of therapeutics directly into vessel walls. Customizable MNs are fabricated using a high-resolution 3D printing technique where MN's height ranges from 100 to 350 µm. The MNs penetration into a synthetic vascular model is investigated with a computerized tomography scan. Ex vivo tests on rabbit aorta confirm the MN-upgraded balloon catheter's performance on real tissue. Delivery of fluorescent dye is accomplished by injecting it through the fluidic channel and MNs into the aortic tissue. The dye is observed at up to 180 µm of depth, confirming site-specific endovascular delivery.
UR - http://hdl.handle.net/10754/669290
UR - https://onlinelibrary.wiley.com/doi/10.1002/admt.202100037
UR - http://www.scopus.com/inward/record.url?scp=85106602834&partnerID=8YFLogxK
U2 - 10.1002/admt.202100037
DO - 10.1002/admt.202100037
M3 - Article
SN - 2365-709X
VL - 6
SP - 2100037
JO - Advanced Materials Technologies
JF - Advanced Materials Technologies
IS - 8
ER -