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METHOD FOR DIAGNOSING CANCER

[Category : - HEALTH]
[Viewed 66 times]

This method of laboratory diagnostics for malignant tumors in humans is characterized by simplicity, versatility, and high accuracy. The method involves detecting an abnormal protein (onco-protein) in a blood smear taken from the fingertip. An adsorbent solution is applied to the smear, and after the "stain" naturally dries, its structure is examined under a microscope and compared with a reference blood sample from a healthy individual.

Key Advantages:
The method detects the formation of an oncological environment several years before the tumor (localization) appears.
Speed and simplicity: The method does not require complex equipment or lengthy preparation processes, making it convenient to use.
Safety and convenience of the reagent: The solution is based on a dry fine powder that has no storage limitations, is non-toxic, non-narcotic, non-explosive, and non-flammable, and does not require special permits for import into any country. The reagent is produced in Ukraine and is not considered a strategic raw material.
High accuracy: The diagnostic accuracy exceeds 100%, ensuring reliable results.
Versatility: The method allows for the detection of malignant tumors of various origins (cancer, sarcoma, lymphoma) at any stage, regardless of the patient’s gender or age.
Scalability: The method is suitable for both large-scale population screening and individual monitoring of treatment effectiveness (onco-monitoring).
Disadvantages of Traditional Methods:
Pain and labor-intensive blood collection from veins.
High costs of reagents and specialized equipment.
Challenges in ensuring standardized procedures and eliminating subjectivity in result evaluation.
Limited feasibility for mass population screening.
Practical Applications:
The method has been successfully tested on various patient groups with suspected malignant tumors. It has been proven that structural differences in blood smears can be used to confirm or rule out cancer. These results have been further validated by other diagnostic tools, including biopsy, computed tomography (CT), and magnetic resonance imaging (MRI).

The method is recommended for integration into mass medical practice due to its accessibility, simplicity, and efficiency. The formula of the reagent, on the basis of which the solution is prepared, will be disclosed and transferred to the new owner. Patenting under the new owner's name in other jurisdictions is also possible.













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