SBIR-STTR Award

Development of a Microperforated Nanocomposite Balloon for Intravascular Anti-Restenotic Drug Delivery
Award last edited on: 5/14/2020

Sponsored Program
SBIR
Awarding Agency
NIH : NHLBI
Total Award Amount
$1,070,574
Award Phase
2
Solicitation Topic Code
-----

Principal Investigator
Mark Bates

Company Information

Nexeon Medsystems Inc (AKA: Rosellini Scientific LLC)

10210 North Central Expressway Suite 105
Dallas, TX 75231
   (214) 414-0454
   info@nexeonmed.com
   www.nexeonmedsystems.com
Location: Single
Congr. District: 24
County: Collin

Phase I

Contract Number: ----------
Start Date: ----    Completed: ----
Phase I year
2015
Phase I Amount
$218,377
?Hemodialysis is the most common treatment for kidney failure, requiring the passing of blood out of the body, through a filter, and back into the body. Almost 30% of hemodialysis patients undergo arteriovenous graft procedures involving the insertion of prosthetic shunts (i.e., synthetic tubes) between artery and vein, particularly in the forearm. With the hemodialysis patient population estimated to reach over 500,000 by 2020, the number of patients requiring grafts will reach over 150,000 (30% of 500,000) and most of these grafts will eventually clot. Clotting occurs in these grafts due to blockages that occur in te blood vessel at the outflow site of the graft. As a result, many hemodialysis patients require intervention to open up the narrowing, or stenosis, of the blood vessel. Currently, interventions for clotted grafts involve removal of the clot with a device followed by angioplasty of the vein. Once angioplasty is needed, the lesion will keep restenosing and often the patients need additional declot procedures and repeat angioplasty. While stents are routinely used to open up narrowed arteries, they cannot be implemented in this case. A more mechanically compliant structure is needed. Relatively new, drug-coated balloons (DCBs) are a possible solution. However, DCBs inherently exhibit sporadic and unpredictable drug delivery. Furthermore, DCB drug delivery is currently quite inefficient with much of the drug being lost downstream. This increases the potential for systemic toxicity. In addition, chemical agents (excipients) are needed to control diffusion of the drug coating. These excipients pose a risk of downstream embolism for the patient. A more efficient, safer method of intravascular anti-restenotic drug delivery is needed to improve efficacy and reduce risk of embolism. We propose to develop a nanocomposite-based polymer balloon with microperforations to enable pulsed-flow drug delivery to the lesion. Using our approach, drugs can be efficiently delivered directly to the diseased site reducing the potential for systemic toxicity. Our intravascular drug delivery system is capable of delivering drugs of almost any form, from lipophilic drugs to hydrophilic drugs and even combinations thereof.

Public Health Relevance Statement:


Public Health Relevance:
The major challenge for hemodialysis patients is the eventual blockage of arteries occurring near the site in the forearm where the dialysis tubing is inserted. We propose to develop a drug delivery system that will eliminate these blockages. Our drug delivery system will lower the added care costs currently required to manage hemodialysis patients and reduce their mortality risk.

NIH Spending Category:
Assistive Technology; Atherosclerosis; Bioengineering; Biotechnology; Cardiovascular; Kidney Disease; Nanotechnology

Project Terms:
Adverse reactions; Angioplasty; Animals; aqueous; Arteries; Back; base; biocompatible polymer; Biological; biomaterial compatibility; Blood; Blood Vessels; Carbon Nanotubes; Caring; Catheters; Chemical Agents; Chemistry; Coagulation Process; common treatment; cost; design; Development; Devices; Dialysis procedure; Diffusion; Disease; Drug Delivery Systems; Dysbarism; Embolism; Evaluation; Excipients; Excision; Exhibits; Family suidae; FDA approved; Fee-for-Service Plans; Forearm; Health; Hemodialysis; improved; In Situ; in vivo; individualized medicine; Intervention; Kidney Failure; Laboratories; Lesion; Liquid substance; Manufactured Materials; Manufacturer Name; Measures; Mechanics; Medical; Medical Device; Methods; Modeling; Modification; Monitor; Mortality Vital Statistics; nanocomposite; Nylons; Organ Transplantation; Output; Paclitaxel; patient population; Patients; Pharmaceutical Preparations; Phase; Physiologic pulse; polymerization; Polymers; pressure; Procedures; Process; Prosthesis; public health relevance; Research Institute; restenosis; Risk; Safety; scale up; Shunt Device; Site; Solutions; Stenosis; Stents; Structure; Surface; Technology; Testing; Therapeutic Effect; Toxic effect; Tube; Twin Multiple Birth; Validation; Veins; Work

Phase II

Contract Number: ----------
Start Date: ----    Completed: ----
Phase II year
2017
Phase II Amount
$852,197
Hemodialysis is the most common treatment for kidney failure, requiring the passing of blood out of the body, through a filter, and back into the body. Almost 30% of hemodialysis patients undergo arteriovenous graft procedures involving the insertion of prosthetic shunts (i.e., synthetic tubes) between artery and vein, particularly in the forearm. With the hemodialysis patient population estimated to reach over 500,000 by 2020, the number of patients requiring grafts will reach over 150,000 (30% of 500,000) and most of these grafts will eventually clot. Clotting occurs in these grafts due to blockages that occur in the blood vessel at the outflow site of the graft. As a result, many hemodialysis patients require intervention to open up the narrowing, or stenosis, of the blood vessel. Currently, interventions for clotted grafts involve removal of the clot with a device followed by angioplasty of the vein. Once angioplasty is needed, the lesion will keep restenosing and often the patients need additional declot procedures and repeat angioplasty. While stents are routinely used to open up narrowed arteries, they cannot be implemented in this case. A more mechanically compliant structure is needed. Relatively new, drug-coated balloons (DCBs) are a possible solution. However, DCBs inherently exhibit sporadic and unpredictable drug delivery. Furthermore, DCB drug delivery is currently quite inefficient with much of the drug being lost downstream. This increases the potential for systemic toxicity. In addition, chemical agents (excipients) are needed to control diffusion of the drug coating. These excipients pose a risk of downstream embolism for the patient. A more efficient, safer method of intravascular anti-restenotic drug delivery is needed to improve efficacy and reduce risk of embolism. We propose to develop a nanocomposite-based polymer balloon with microperforations to enable pulsed-flow drug delivery to the lesion. Using our approach, drugs can be efficiently delivered directly to the diseased site reducing the potential for systemic toxicity. Our intravascular drug delivery system is capable of delivering drugs of almost any form, from lipophilic drugs to hydrophilic drugs and even combinations thereof.  -1-

Public Health Relevance Statement:
Project Narrative The major challenge for hemodialysis patients is the eventual blockage of arteries occurring near the site in the forearm where the dialysis tubing is inserted. We propose to develop a drug delivery system that will eliminate these blockages. Our drug delivery system will lower the added care costs currently required to manage hemodialysis patients and reduce their mortality risk. -1-

Project Terms:
Adverse reactions; Angioplasty; Animals; aqueous; Arteries; Back; base; biocompatible polymer; Biological; biomaterial compatibility; Blood; Blood Vessels; Carbon Nanotubes; Caring; Catheters; Chemical Agents; Chemistry; Coagulation Process; common treatment; cost; design; Development; Devices; Dialysis procedure; Diffusion; Dimensions; Disease; Drug Delivery Systems; Dysbarism; Embolism; Evaluation; Excipients; Excision; Exhibits; Family suidae; FDA approved; Fee-for-Service Plans; Forearm; Health; Hemodialysis; hydrophilicity; improved; In Situ; in vivo; individualized medicine; Intervention; Kidney Failure; Laboratories; Lesion; lipophilicity; Liquid substance; Manufacturer Name; Measures; Mechanics; Medical; Medical Device; Methods; Modeling; Modification; Monitor; mortality; nanocomposite; novel therapeutics; Nylons; Organ Transplantation; Output; Paclitaxel; patient population; Patients; Pharmaceutical Preparations; Phase; Physiologic pulse; polymerization; Polymers; pressure; Procedures; Process; Prosthesis; Research Institute; restenosis; Risk; Safety; scale up; Shunt Device; Site; Stenosis; Stents; Structure; Surface; systemic toxicity; Technology; Testing; Therapeutic Effect; Toxic effect; Tube; Twin Multiple Birth; Validation; Veins