Drug – bio-affecting and body treating compositions – In vivo diagnosis or in vivo testing – Magnetic imaging agent
Reexamination Certificate
2000-12-13
2003-02-18
Hartley, Michael G. (Department: 1619)
Drug, bio-affecting and body treating compositions
In vivo diagnosis or in vivo testing
Magnetic imaging agent
C436S173000
Reexamination Certificate
active
06521210
ABSTRACT:
FIELD OF THE INVENTION
The present invention pertains generally to methods and systems for diagnosing a malignancy in situ tissue. More particularly, the present invention pertains to methods and systems for using carbon 13 (
13
C) as a target material for detecting the presence of a malignancy in situ tissue of a patient. The present invention is particularly, but not exclusively, useful as a method and a system for using MRI techniques to image concentrations of
13
C in rapidly growing tissue.
BACKGROUND OF THE INVENTION
In normal healthy tissue, cells will grow, divide, and die in an orderly manner. In this process, normal cell division is necessary to sustain life and insure the orderly function of organs and tissues. As is well known, when cell division occurs, the result is the replication of a parent cell into daughter cells. The daughter cells then continue to function in the same way as did the parent cell. According to the type of tissue involved, however, the rate of cell division for normal cells will differ. For example, the rate of cell division in epithelial tissue and in bone marrow tissue is more rapid than is the rate of cell division in other tissues. In any event, for normal cell division, the cells of each organ will replicate at a pre-programmed rate specific to that organ. Unfortunately, however, it happens that for any number of reasons the rate of cell division may change. In some cases, this gives rise to rapidly growing cells whose rate of cell division is out of control. As we know, cancer is one consequence of such rapid cell growth, and cancer can take many forms. As we also know, undetected and untreated cancer can be fatal.
Cell division requires nutrients, regardless whether the tissue is healthy or cancerous. Importantly, carbon is an essential element in these nutrients. Indeed, all cells contain carbon, and about ninety percent of the carbon that is used by a cell can be found in its structural components, such as the cell wall and the nucleus. Further, it is known that when a cell grows and divides, the structural components of the daughter cells are synthesized from available nutrients. In fact, nearly fifty percent of the carbon from a nutrient that has been used by a parent cell can be found in each of the daughter cells.
Naturally occurring carbon is mostly in the form of the carbon 12 isotope (
12
C). A small percentage of naturally occurring carbon, however, is in the form of carbon 13 (
13
C). Insofar as cell division is concerned, cells metabolize carbon 13 (
13
C) the same as they do the more common form of carbon,
12
C. In at least one important respect,
12
C and
13
C are different. Specifically, it happens that
13
C responds particularly well to nuclear magnetic resonance, making it particularly useful for MRI techniques. Thus, by tuning the rf energy of an MRI for nuclear resonance with
13
C, images can be created which react to the presence of
13
C in a tissue. Fortunately, carbon with an increased concentration of the
13
C isotope can be produced by physical and chemical means. In fact, nutrients which are highly enriched with
13
C are commercially available.
Normal cells divide at predetermined rates based on the type of tissues to which they belong. In comparison with cells of the same tissue, cancer cells divide at a much faster rate. In most cases, these rapidly dividing cancer cells may take only about 8 hours to divide. Thus, in a 24 hour period they will divide about three times. Consequently, when a patient is fed a nutrient enriched with
13
C over a twenty-four hour period, there will be a discernibly high concentration of
13
C. As a practical matter, the new cells in a malignancy will be largely made of the
13
C. A few hours after the feeding is interrupted, the unused portion of the enriched nutrient will have been metabolized and will disappear from the body.
A cell's use of nutrients is generally dependent on two factors. One factor is the type of tissue, i.e. is the tissue fatty or non-fatty tissue. The other factor, which is interrelated to the first factor, concerns the type of nutrient that is used by the tissue for cell division, e.g. glucose or amino acid. Thus, the composition of nutrients to be used to target specific cells will generally depend on whether the cells are fatty or non-fatty tissue.
Specifically, because nutrients will either metabolize, be used for cell division, or be stored as fat, it is desirable to select a nutrient that will either metabolize or contribute to cell division, and will not be primarily stored as fat.
Heretofore, the detection of malignancies has been accomplished in several ways, using either invasive or non-invasive methods. Invasive techniques, such as the taking of a biopsy, have been used extensively. Invasive techniques, however, can cause varying degrees of extended patient discomfort. On the other hand, non-invasive radiation techniques, such as X-ray and MRI, do not involve extended discomfort, but they have been used with mixed results. The difficulty here has been mostly in properly interpreting the form and structure of target tissue to diagnose a malignancy.
As just indicated, radiation methods for detecting malignancies have depended on an interpretation of the morphology of the tissue. For instance, to image tissue, X-ray technology depends on the density of the tissue being targeted. MRI, on the other hand, relies on the reaction of protons in the target tissue to a magnetic field, in order to image the tissue and thereby determine its morphology. Using either technique, however, when a malignancy has not grown to a size which can distinguish it from the morphology of surrounding tissue, presently used radiation techniques may be inadequate. Stated differently, presently used radiation techniques for distinguishing the morphology of a tissue have been generally unsatisfactory for detecting cancerous cells during their earliest rapid growth stages.
In light of the above, it is an object of the present invention to provide a method for the in situ imaging of a malignancy in a patient that is independent of the morphology of the tissue. Another object is to provide a method and a system for targeting cells in an in situ tissue, according to the composition of the tissue. A further object is to provide a method for the in situ imaging of a malignancy wherein a nutrient is selected to identify rapidly growing cells based upon their use of the selected nutrient in cell division. Another object is to provide a method for determining the growth rate of target cells in situ tissue. Yet another object is to provide a method and a standard for determining the efficacy of a treatment of a malignancy in a patient.
SUMMARY OF THE PREFERRED EMBODIMENTS
A system and method for identifying rapidly dividing cells in situ tissue in a patient in accordance with the present invention requires feeding the patient a nutrient enriched with
13
C. According to well known functions of cellular physiology, the
13
C enriched nutrient will then be used by the cells of the in situ tissue to incorporate the
13
C into the cells that result from cell division.
Typically, the feeding of the patient extends over a period of 24 hours, and can be accomplished either orally or intravenously. Further, it is desirable to use nutrients containing glucose enriched with
13
C when the target tissue is non fatty, and to use nutrients containing amino acid enriched with
13
C when the target tissue is fatty.
After the nutrient enriched with
13
C has been assimilated by the patient, the method of the present invention envisions using well known MRI techniques for the purpose of imaging the tissue containing
13
C. These MRI techniques include placing the target tissue of the patient to be imaged in a magnetic field. This portion of the patient is then radiated with rf energy that is tuned for nuclear resonance with
13
C. An evaluation of the resultant image for concentrations of
13
C within the target tissue will determine whether there is rapid cell growth in the target tissue.
T
Archimedes Technology Group, Inc.
Hartley Michael G.
Nydegger & Associates
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