SBIR-STTR Award

Advanced Nitric Oxide Release Bactericidal Urinary Catheters
Award last edited on: 4/25/19

Sponsored Program
STTR
Awarding Agency
NIH : NIDDK
Total Award Amount
$1,548,991
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Hao Chen

Company Information

Biocrede Inc

46701 Commerce Center Drive
Plymouth, MI 48170
   (734) 678-6956
   support@biocrede.com
   www.biocrede.com

Research Institution

University of Michigan

Phase I

Contract Number: 1R41DK100161-01
Start Date: 9/15/13    Completed: 8/31/14
Phase I year
2013
Phase I Amount
$149,098
We propose a novel and competitive urinary tract silicone Foley catheter made from a proprietary polymeric formulation to effectively reduce catheter-associated urinary tract infections (CAUTI) via nitric oxide (NO) release. Preliminary studies show that the device will be able to: (1) continuously deliver NO at rates enough to maintain bactericidal properties for >2 weeks at 37¿C, (2) deliver controlled increased NO levels with enhanced bactericidal properties using light if needed, and (3) allow to be dry-stored for more than 2 months of shelf life even at 37¿C. CAUTIs contribute to 0.5-0.7 million nosocomial hospital infections annually with a cumulative incidence of 3-6% per day of catheterization (50% at 10 days, >90% at 28 days, 100% long term) leading to complications such as cystitis, pyelonephritis, gram-negative bacteremia, prostatitis, epididymitis, urosepsis, septicemia, orchitis, endocarditis, vertebral osteomyelitis, septic arthritis, endophthalmitis, and meningitis n all patients. The proposed device can be processed and assembled in the US at almost half the cost of current silver coated Foley catheters', and could potentially prevent ten thousand deaths per year due to CAUTIs. In terms of reimbursement, hospitals will see average care reduction costs of $700 per case by eliminating infection, and insurance companies will see significant decrease in length of hospital stay savings as CAUTI rates are reduced. To continue research and development of our product, we propose: (1) to study the NO release from the walls of the catheters containing our proprietary formulation to understand thresholds for effective biofilm prevention (Proteus mirabilis, Enterococcus faecalis, and Staphylococcus epidermidis); (2) to understand the light emission requirements at 590nm to photochemically prevent biofilm formation; and (3) to perform shelf-life, and sterilization studies to understand product reliabiliy and performance after 6 months of storage. Sterilization studies have been chosen over biocompatibility studies (to be done in Phase II) since the proprietary main NO donor molecule, once decomposed, is an approved drug. This proprietary technology has been optioned by Biocrede Inc. (Ann Arbor, MI) through the Offices of Tech Transfer at the University of Michigan (Ann Arbor, MI). BWTEK (Newark, DE) with offices in Japan, Germany, and China and a strong global sales team and vast experience with medical devices and laser startups, will acquire/incubate Biocrede for accelerated translation Phase II studies after positive Phase I feasibility results.

Public Health Relevance Statement:


Public Health Relevance:
Catheter-associated urinary tract infections (CAUTI) contribute to 0.5-0.7 million nosocomial hospital infections with a cumulative incidence of 3-6% per day of catheterization (50% at 10 days, >90% at 28 days, 100% long term) leading to complications and approximately ten thousand reported deaths annually. Current CAUTI prevention techniques such as the use of routine irrigation of the bladder with antimicrobials and silver coated Foley catheters have no significant preventative effects as stated by the Healthcare Infection Control Practices Advisory Committee. We propose a novel and price competitive urinary tract silicone Foley catheter made from a proprietary polymeric formulation to effectively reduce CAUTIs by allowing >20 days of bactericidal effectiveness via Nitric Oxide release, and allow dry-storing for at least 2 months even at 37 C.

NIH Spending Category:
Bioengineering; Hematology; Infectious Diseases; Patient Safety; Prevention; Septicemia; Urologic Diseases

Project Terms:
Acute suppurative arthritis due to bacteria; Advisory Committees; Alloys; antimicrobial; antimicrobial drug; Antimicrobial Resistance; Bacteremia; Bacteria; bactericide; base; biomaterial compatibility; Bioreactors; Bladder irrigation procedure; Body Temperature; Buffers; Caring; catheter associated UTI; Catheterization; Catheters; Cells; Centers for Disease Control and Prevention (U.S.); Cessation of life; Chemiluminescence assay; China; copolymer; copper poisoning; cost; Cystitis; cytotoxicity; density; Devices; dimer; Drug Formulations; Effectiveness; Elastomers; Endocarditis; Endophthalmitis; Enterococcus faecalis; Epididymitis; Epithelial Cells; Escherichia coli; Exhibits; experience; Film; Germany; Growth; Healthcare; Hospitals; In Vitro; Incidence; Incubated; Infection; Infection Control; Infection prevention; Insurance; irritation; Japan; Lasers; Lead; Legal patent; Length of Stay; Life; Light; light emission; Local Anti-Infective Agents; Lung; macrophage; Marketing; Mediating; Medical Device; Meningitis; Mercury Poisoning; Methods; Michigan; Microbial Biofilms; Muscle relaxation phase; N-acetylpenicillamine; Nitric Oxide; Nitric Oxide Donors; Nosocomial Infections; novel; Orchitis; Oryctolagus cuniculus; Osteomyelitis; Patients; Performance; Pharmaceutical Preparations; Phase; phase 2 study; polydimethylsiloxane; Polyethylenes; Polymers; Polyurethanes; prevent; Prevention; Price; Process; Property; prostatitis; Proteus mirabilis; Protocols documentation; public health relevance; Pyelonephritis; Reporting; research and development; Risk; S-Nitroso-N-Acetylpenicillamine; Safety; Sales; Savings; Septicemia; Silicones; Silver; Sinus; Skeletal muscle structure; Smooth muscle (tissue); Solvents; Source; spine bone structure; Staphylococcus epidermidis; Sterilization; Surface; Swelling; Techniques; Technology; technology development; Temperature; Toxic effect; Translations; Universities; urinary; Urinary tract; Urin

Phase II

Contract Number: 2R42DK100161-02
Start Date: 9/15/13    Completed: 8/31/17
Phase II year
2015
(last award dollars: 2016)
Phase II Amount
$1,399,893

In Phase I, Biocrede developed a completely new urinary tract silicone Foley catheter with a >4.5 month shelf-life, made from a proprietary polymeric formulation to effectively reduce catheter-associated urinary tract infections (CAUTI) via nitric oxide (NO) release for >2 weeks. Key features of the new technology include: (1) catheters continuously deliver NO at bactericidal rates for >14 d at 37°C; (2) In vitro data demonstrate a 10,000 fold reduction of live bacteria counts (for key bacteria strains associated with CAUTI) on catheter surfaces and ability to prevent biofilm formation at 14 days; (3) ongoing study shows that shelf- life can easily be extended beyond >>4.5 months after ETO sterilization; (4) ISO/GLP leaching tests (1-3 d) and associated toxicity studies on cells (3 d) and in mice (3 d) received the safest scores possible; and (5) urologists praised the consistency, elasticity, and flexibility of the product compared to others. The NO released from the surfaces of the catheter quickly diffuses out of the silicone walls into the urine collection lumen and from the catheter's outer surface to prevent/disrupt biofilm formation that will eliminate CAUTIs. CAUTIs contribute to 0.5-0.7 million nosocomial hospital infections annually with a cumulative incidence of 3-6% per day of catheterization (50% at 10 days, >90% at 28 days, 100% long term) leading to complications such as cystitis, pyelonephritis, gram-negative bacteremia, prostatitis, epididymitis, urosepsis, septicemia, etc., in patients. This technology will help reduce the costs associated with CAUTIs ($700 per infection) and potentially prevent most of the 10,000 deaths/year due to CAUTIs in the US alone. To continue research and development of this advanced product, we propose to: (1) prove that NO releasing catheters can be stored for 12 months or more after EtO sterilization; (2) develop/assemble a controlled Allan Bradley automated system to allow repeatable SNAP (S-nitroso-N-acetyl-penicillamine) impregnation and lean operation efforts; (3) prove the safety, CAUTI prevention efficacy, and biocompatibility of our new NO releasing Foley catheter design via animal studies (rabbits) after 7 d and 14 d (n=8 each); (4) verify and design for lowest possible SNAP leaching; (5) perform all of the required GLP third party biocompatibility studies for future 510k application in 2015; (6) and receive the FDA IDE approval by 2016. Achieving these goals will allow Biocrede to work with investors to fund a future clinical Phase I pilot study, and clinical Phase II final study for our 510k (De novo) applications. Fortune Medical, an FDA approved and ISO13485 certified company, is Biocrede's catheter OEM provider; and Biocrede (100% US owned, Ann Arbor, MI) will add the proprietary components (SNAP impregnation technology), and perform quality control, sterilization and packaging. This proprietary technology is being licensed by Biocrede Inc. through the Offices of Tech Transfer at the University of Michigan (Ann Arbor, MI).

Public Health Relevance Statement:


Public Health Relevance:
Catheter-associated urinary tract infections (CAUTI) contribute to 0.5-0.7 million nosocomial hospital infections with a cumulative incidence of 3-6% per day of catheterization (50% at 10 days, >90% at 28 days, 100% long term) leading to complications and approximately ten thousand deaths annually. Current CAUTI prevention techniques, including use of routine irrigation of the bladder with antimicrobials and silver coate Foley catheters, have "no significant preventative effects" as stated by the Healthcare Infection Control Practices Advisory Committee. We propose a novel and price competitive urinary tract silicone Foley catheter made from a proprietary polymeric formulation to effectively reduce CAUTIs by providing >14 days of tested bactericidal effectiveness via nitric oxide (NO) release, and allowing dry-storage for at least 4.5 months (ongoing study) without significant loss of NO release capability.

Project Terms:
Advisory Committees; Alloys; Animals; Anti-Bacterial Agents; antimicrobial; Autopsy; Bacteremia; Bacteria; bactericide; base; biomaterial compatibility; Bladder; Bladder irrigation procedure; Body Temperature; catheter associated UTI; Catheterization; Catheters; Cells; Cessation of life; Chronic; Clinical; Clinical Research; Collection; cost; Cystitis; cytotoxicity; Data; Data Analyses; design; Development Plans; Diffuse; Drug Formulations; Eagles; Effectiveness; Elasticity; Elements; Ensure; Epididymitis; Escherichia coli; experience; FDA approved; flexibility; Fortune; Funding; Future; Goals; Growth; Healthcare; Heating; Hematology; Hematoxylin and Eosin Staining Method; Human; Humidity; In Vitro; Incidence; Infection; Infection Control; Infection prevention; Institutional Review Boards; International; irritation; Kidney; Lead; Legal patent; Length; Licensing; Life; Liver; liver inflammation; Local Anti-Infective Agents; Lung; male; Marketing; Mass Spectrum Analysis; Medical; meetings; Michigan; Microbial Biofilms; Mus; new technology; Nitric Oxide; Nosocomial Infections; novel; operation; Oryctolagus cuniculus; Pathologist; Patients; Penicillamine; Phase; Pilot Projects; Population; prevent; Price; Property; prostatitis; Proteus mirabilis; Provider; public health relevance; Published Comment; Pump; Pyelonephritis; Quality Control; Regulatory Pathway; research and development; Resistance; S-Nitroso-N-Acetylpenicillamine; Safety; safety study; Saline; sensor; Septicemia; Sesame Oil; Silicones; Silver; solute; Solutions; Solvents; Staining method; Stains; Staphylococcus epidermidis; Sterilization; Streptomycin; Surface; Swelling; System; Techniques; Technology; Temperature; Testing; Time; Toxic effect; Tweens; Universities; Ureter; Urethra; Urinalysis; urinary; Urinary tract; Urine; Urologist; Work