Research & Publications
We are involved in using nano-particle delivery systems to diagnose and treat diseases of the urinary system with special emphasis on benign and malignant diseases of the bladder. These studies, which are focused on diagnosing and treating bladder and prostate cancer. We are involved in translational research and are developing humanized mice with human prostate and bladder cancers. Our findings should be directly translational to the clinic. In addition we are studying the pharmacology and physiology on ureteral-vesical smooth muscle with particular interest in inflammation.
Specialized Terms: muscle pharmacology; Signal transduction; Bladder cancer; Drug delivery; Prostate cancer
Extensive Research Description
The Proof of Concept that we are testing is that intravesical instillation of small interference RNA (siRNA) packaged in biodegradable nanospheres provides wide opportunities for the treatment of urologic diseases including transitional cell carcinoma of the bladder (TCC), interstitial cystitis (IC), overactive bladder, and detrusor hyperreflexia.
Because of their robust, gene selective silencing of target protein expression, siRNA oligonucleotides are an attractive therapeutic option with high selectivity and specificity and minimal toxicity to neighboring cells. siRNAs, however, have a relatively short half-life and thus we are addressing the stabilization and intravesical delivery of siRNAs. To achieve this goal, we plan to create and test clinically viable, non-viral nanosphere siRNA complexes that are intravesically
instilled for treatment of diseases of the urinary tract.
We plan to develop and test a number of nanoparticle controlled release systems containing targeting proteins that will stabilize and deliver siRNAs and drugs and initially test these on bladder cancers
Using nanospheres that contain siRNAs to survivin in combination with chemotherapeutic agents to affect growth and spread of bladder cancer in in vitro and in vivo animal models
Use of nanoparticles for localization and treatment of prostatic carcinoma in a in vivo animal model.
Urinary Bladder Neoplasms; Pharmacology; Urology; Signal Transduction