Biophan Announces MRI-safe Solution for Defibrillators.Business/Medical Editors SAN DIEGO--(BW HealthWire)--May 9, 2002 Biophan Technologies, Inc., (OTCBB OTCBB See OTC Bulletin Board (OTCBB). :BIPH BIPH Bogomoletz Institute of Physiology (National Academy of Sciences; Ukraine) ) developers of the first MRI-safe, wearable pacemaker, will be demonstrating a functional design concept of an MRI-safe lead for a defibrillator defibrillator, device that delivers an electrical shock to the heart in order to stop certain forms of rapid heart rhythm disturbances (arrhythmias). The shock changes a fibrillation to an organized rhythm or changes a very rapid and ineffective cardiac rhythm to a at this year's North American Society of Pacing and Electrophysiology Conference (NASPE NASPE National Association for Sport and Physical Education NASPE North American Society of Pacing and Electrophysiology NASPE National Association of State Personnel Executives ) in San Diego, CA. Developed by Wilson Greatbatch, the inventor of the first successful implantable pacemaker, the defibrillator can deliver a 800 volt/40 joule charge to a patient whose heart is determined to be in fibrillation, where the muscle contractions are random and irregular so that the heart does not effectively pump blood. The electrical discharge stops the contractions (defibrillates the heart) and allows the heart to re-establish a regular heart rhythm. Biophan's fiber optic solution for making pacemakers safe in an MRI 1. (application) MRI - Magnetic Resonance Imaging. 2. MRI - Measurement Requirements and Interface. machine cannot be extended to the defibrillation Defibrillation Definition Defibrillation is a process in which an electronic device sends an electric shock to the heart to stop an extremely rapid, irregular heartbeat, and restore the normal heart rhythm. function because of the voltage and energy required. "When we started working on the MRI safety problem and developed the first working photonic catheter, we knew we had solved the main problem associated with MRI safety in sensing and pacing leads. However, the defibrillator problem was one we were not sure we could solve. 800 volts is much more than we can deliver through a fiber optic cable Noun 1. fiber optic cable - a cable made of optical fibers that can transmit large amounts of information at the speed of light fibre optic cable transmission line, cable, line - a conductor for transmitting electrical or optical signals or electric power implanted in the body," said Michael L. Weiner, CEO (1) (Chief Executive Officer) The highest individual in command of an organization. Typically the president of the company, the CEO reports to the Chairman of the Board. of Biophan Technologies. "When Wilson Greatbatch came up with the idea of a spark gap switch, we were amazed at its simplicity, effectiveness, and creativity." Wilson Greatbatch, who started his career as a radio engineer, thought of using a "spark gap" device as a switch. This switch is open in most cases and allows the defibrillator lead to be electrically isolated from the device circuitry. This eliminates the antenna effect of the lead, which causes the many problems of MRI and pacemaker incompatibility. When the defibrillator circuitry detects heart fibrillation and generates the 800 volt charge, the spark gap switch passes the charge to the defibrillator lead for the several milliseconds necessary until the voltage is discharged. Immediately after the charge is dispensed, the switch is again open. The defibrillator lead works in conjunction with Biophan's current photonic pacemaker lead. The fiber optic lead provides sensing and electrostimulation for normal pacing. The defibrillator lead concept complements the photonic lead by providing the needed isolation and energy transmission only when required. As a result, the defibrillator lead will not heat up or conduct energy to the device circuitry or electrode in the heart, except when the defibrillation function is required. The Company is demonstrating a prototype at the NASPE conference, the annual event attended by cardiologists, electrophysiologists, and medical device companies interested in cardiac electrophysiology, pacing, and the management of arrhythmias. The Company will offer MRI-safe defibrillator functionality as part of its temporary pacemaker product line, and will offer the solution to pacemaker manufacturers to incorporate into their new devices. Biophan's mission is to bring MRI compatibility to the pacemaker, implantable cardioverter-defibrillator (ICD ICD International Classification of Diseases (of the World Health Organization); intrauterine contraceptive device. ICD abbr. ), and biomedical bi·o·med·i·cal adj. 1. Of or relating to biomedicine. 2. Of, relating to, or involving biological, medical, and physical sciences. device industries. About Biophan Technologies Biophan, based in Rochester and Clarence, New York Clarence is a town located in the northeastern part of Erie County, New York, United States. The population was 26,123 at the 2000 census. Clarence is also the name of a postal district in the south part of the town with ZIP code 14031. , is engaged in designing, developing, and marketing new technology and related products to enable cardiac pacemakers and the other life sustaining medical devices to be safe and compatible with magnetic resonance imaging magnetic resonance imaging (MRI), noninvasive diagnostic technique that uses nuclear magnetic resonance to produce cross-sectional images of organs and other internal body structures. (MRI) and other equipment using magnetic fields and radio waves. This MRI-compatible technology will be utilized in implantable pacemakers, implantable cardioverter defibrillators, left ventricular assist devices, insulin pumps, drug pumps, pain reduction devices, and other medical equipment. The underlying technology is based upon pending patents and proprietary knowledge developed by Wilson Greatbatch (inventor of the first successful implantable cardiac pacemaker) and others. For more information, please visit www.biophan.com. Safe Harbor Statement: Certain statements included in this press release are forward-looking statements within the meaning of the Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and of 1995. Actual results could differ materially from such statements expressed or implied herein as a result of a variety of factors including, but not limited to: the development of the Company's MRI and gene therapy technologies; the approval of the Company's patent applications; the successful implementation of the Company's research and development programs; the acceptance by the market of the Company's products; competition and the timing of projects and trends in future operating performance, as well as other factors expressed from time to time in the Company's periodic filings with the Securities and Exchange Commission (the "SEC"). As a result, this press release should be read in conjunction with the Company's periodic filings with the SEC. The forward-looking statements contained herein are made only as of the date of this press release, and the Company undertakes no obligation to publicly update such forward-looking statements to reflect subsequent events or circumstances. |
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