University of Virginia Patent Foundation v. General Electric Co.

755 F. Supp. 2d 709, 2010 U.S. Dist. LEXIS 119114
CourtDistrict Court, W.D. Virginia
DecidedNovember 9, 2010
Docket1:08-cr-00025
StatusPublished
Cited by2 cases

This text of 755 F. Supp. 2d 709 (University of Virginia Patent Foundation v. General Electric Co.) is published on Counsel Stack Legal Research, covering District Court, W.D. Virginia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
University of Virginia Patent Foundation v. General Electric Co., 755 F. Supp. 2d 709, 2010 U.S. Dist. LEXIS 119114 (W.D. Va. 2010).

Opinion

Memorandum Opinion

NORMAN K. MOON, District Judge.

In this action, Plaintiff alleges that Defendant infringed and continues to infringe its patent, which discloses a technique for three-dimensional magnetic resonance imaging (“MRI”) of the human body. Two matters are presented for the Court’s decision. First, Plaintiff and Defendant submitted a Joint Claim Construction and Prehearing Statement (docket no. 99), setting forth the constructions of claim terms and phrases in the patent on which they agree, and proposing constructions of the terms and phrases on which they disagree. After full briefing, the Court held a claim construction hearing. The Court’s construction of the disputed terms is explained herein.

Second, Defendant moved for partial summary judgment seeking an order that Defendant is not liable for any activities infringing the patent that occurred prior to the issuance of the reexamination certificate for the patent (docket no. 100). After full briefing, the Court heard arguments on Defendant’s motion. For the following reasons, the Court will grant Defendant’s motion for partial summary judgment.

I. Background

Plaintiff University of Virginia Patent Foundation (“Patent Foundation”), a not-for-profit Virginia corporation, is the assignee of United States Patent No. 5,245,282 (“'282 Patent”) for an invention entitled “Three-Dimensional Magnetic Resonance Imaging.” (Complaint ¶¶ 1, 8.) The Patent Foundation brought an action for infringement of the '282 Patent against Defendant General Electric Company d/b/a G.E. Healthcare (“GE”), a New York corporation, on May 20, 2008 (docket no. I). 1 The Patent Foundation alleged that GE infringed the '282 Patent by “practicing the methods of the '282 Patent and by making, using, selling, offering for sale, and/or importing in or into the United States, without authority, MRI scanners that practice the methods of the '282 Patent.” (Complaint ¶ 11.)

MRI is a medical diagnostic imaging process that can produce high-contrast images of the interior soft-tissue structures of the human body without the use of ionizing radiation, which can potentially be harmful to human organs. 2 The subject in an MRI examination is placed in a very strong static magnetic field, and the information necessary to create the images is generated using a series of magnetic field gradient pulses and radiofrequency (or “RF”) pulses. The precise manner in which the gradient pulses and radiofre *713 quency pulses are applied to the body is generally referred to as a pulse sequence. Pulse sequences are usually repeated many times during a scan in order to obtain enough information about a region of interest in the body to construct an image of it.

MRI imaging techniques take advantage of the fact that nuclei of some atoms, including hydrogen atoms, have “spin” and act like tiny bar magnets. When exposed to an external magnetic field, they align with it in much the same manner as a compass needle aligns with the earth’s magnetic field. At this stage, the nuclei are in their steady state and said to be aligned with the external magnetic field, which is represented by a vector projecting into the z-plane. If aligned nuclei are excited by applied pulses of electromagnetic energy of the resonant frequency, however, they jump to a higher energy state and their axes move out of alignment with the external magnetic field. The magnetization of tissues while their nuclei are being excited is usually represented by their projections into a three-dimensional plane. Their projections have two components: one in the direction of the external magnetic field (i.e., the extension into the vertical z-plane), called the longitudinal component, and the other perpendicular to the external magnetic field (i.e., the extension into the horizontal (x, y)-plane), called the transverse component.

Excited nuclei in a sample generate a resonance signal that can be detected. Tissues can be distinguished based upon characteristics of the resonance signal, especially the manner in which the resonance signal fades over time, or “relaxes.” In the process called “relaxation,” when the applied high frequency energy is removed, the nuclei release their absorbed energy and realign with the external magnetic field, while the signal decays. Tl, or “spin-lattice relaxation time,” and T2, or “spin-spin relaxation time,” are values arbitrarily selected to measure the time it takes the nuclei to return to their original alignment in the external magnetic field, before they were disturbed. The spin-lattice relaxation process concerns the restoration of the longitudinal component of the magnetization (i.e., the extension of the excited nuclei into the vertical z-plane) to its initial value. It is measured by the time constant Tl, which is the time required for the longitudinal component of the magnetization to return to sixty-three percent of its original magnitude following an excitation pulse. Strictly speaking, the longitudinal component approaches but never fully reaches its steady-state value; it would require an infinite amount of time to fully reach equilibrium. The spin-spin relaxation process concerns the decay of the transverse component of the magnetization (i.e., the extension of the excited nuclei into the horizontal (x, y)-plane) toward its steady-state value of zero at equilibrium. It is measured by the time constant T2, which is the time required for the transverse component of the magnetization to return to thirty-seven percent of its thermal equilibrium value of zero. Transverse relaxation occurs more quickly than longitudinal relaxation, so Tl will always be greater than T2.

Different tissues recover at different rates, so the amount of time represented by Tl and T2 varies according to the type of tissue being excited by the electromagnetic pulse. In other words, the amount of time it takes for the longitudinal component of excited Tissue A to return to sixty-three percent of its original magnitude may be different than the amount of time it would take in Tissue B. Differences between recovery rates of tissues are used to distinguish between types of tissues in an MRI scan; these differences in magnetization of the tissues at the time their reso *714 nance signal is measured create “contrast.” For example, at the time at which the magnetization of the tissues is measured, the difference in the amount of relaxation that has occurred in a healthy tissue and in a tissue with a tumor can be used to distinguish the two tissues. To create an image, the measured magnetization properties of the tissue are used to determine the brightness of the pixels of that region.

The '282 Patent describes an invention of “a rapid process for producing three-dimensional magnetic resonance imaging” through a pulse sequence which is referred to as 8D MP-RAGE. '282 Patent, col. 1, 11. 8-9; id. col. 4, 11. 23-26. Claim 1, its only independent claim, provides:

In a method for producing a set of magnetic resonance three-dimensional image data, a preparation-aequisition-recovery pulse sequence cycle comprising the steps of:

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755 F. Supp. 2d 709, 2010 U.S. Dist. LEXIS 119114, Counsel Stack Legal Research, https://law.counselstack.com/opinion/university-of-virginia-patent-foundation-v-general-electric-co-vawd-2010.