Patent Application
20170212016
A method for providing an accurate amount of fluid in a receptacle such that an accurate amount of fluid may thereafter be transferred from the receptacle. This method has a particular utility in the medical field such as for placing precise amounts of samples and/or chemicals on a substrate but is not limited to that use.
Scientists and medical technicians are constantly searching for better ways to place, transfer and/or apply samples and reagents on various substrates for testing or diagnostic-type purposes. The placement, volume, and dimensions of such samples and reagents on a substrate are important to the reliability and accuracy of the procedures thereafter carried out on the samples. In some instances, improper application of the samples on a substrate will significantly alter the test results, making them unreliable, and may even precluded obtaining any test results at all.
Another problem is that reproducibility of the procedure and results and thus reliability of test results is important but such reproducibility is adversely impacted when differing amounts of samples and/or reagents are transferred when it is the intent to transfer the same amount of sample and/or reagent.
The present method has a particular but non-limiting use in connection with immuno-fixation electrophoresis. Background information on immuno-fixation electrophoresis, also referred to as IFE, 15 available, for example from the following: (a) U.S. Pat. No. 4,668,363 to Gebott et al, issued on May 26, 1987; (b) U.S. Pat. No. 5,137,614 to Golias, issued on Aug. 11, 1992; (c) U.S. Pat. No. 5,185,066 to Golias, issued on Feb. 9, 1993; (d) U.S. Pat. No. 5,405,516 to Bellon, issued on Apr. 11, 1994, (e) U.S. Pat. No. 6,165,541 to Merchant et al, issued on Dec. 26, 2000; and (f) U.S. Pat. No. 6,544,395 to Merchant et al, issued on Apr. 8, 2003. The entirety of each of the foregoing is hereby incorporated by reference.
With particular reference, for example, to U.S. Pat. No. 5,137,614 it may be understood that samples (or reagents, or controls) are to be transferred such as from depressions or receptacles or wells 16-20 in a onto a substrate such as, for example, through the use of an applicator of the type illustrated in U.S. Pat. No. 6,544,395. If, however, the amount of liquid in the receptacle or well is not consistent, from test-to-test, the tips of the applicator will withdraw and then transfer to the electrophorese gel plate or the like, an inconsistent or different amount of liquid as between tests.
Typically, when liquid is placed in a receptacle a meniscus is created. Surface tension and adhesion of the liquid to the receptacle are factors in determining whether the \meniscus is convex or concave. These factors also contribute to the degree or extent of the meniscus relative to the plane of the top of the receptacle. Surface tension is related, of course, to the nature of the liquid. In the environment of IFE, the receptacles are typically formed in a plate made of polystyrene and the liquid reagents are frequently antigens.
The inventor has determined that the meniscus itself is a fundamental cause of the problem of inconsistent amounts of fluid being transferred by the applicator. Thus the inventor has developed a novel methodology for controlling the filling of receptacles to essentially eliminate the meniscus or at least minimize or otherwise control the meniscus such that consistent amounts of liquid may be withdrawn from the receptacles.
The various benefits and advantages of the present invention will become apparent upon reading the following detailed description taken in conjunction with the drawings.
In the drawings, wherein like reference numerals identify corresponding parts:
Typically, a specimen from a single patient is diluted and then placed in multiple sample or application areas on a single electrophoretic gel plate. The purpose of utilizing multiple sample areas is to enable detection, separately, of various components of the specimen.
One conventional type of IFE testing is to determine total serum protein as well as various proteins such as the immunoglobin heavy chains IgG, IgM, IgA and light chains Kappa and Lambda, or other proteins whose presence or absence may be of importance in medical diagnosis and treatment. It is common in IFE testing to deposit antigens or antisera to the foregoing proteins onto the sample from the patient. Both qualitative (presence or absence) and quantitative (amount) of the proteins is of importance. As an alternative to depositing the antigens or antibodies onto the samples, the antibodies or antigens may be placed on an electrophoresis plate before the sample is deposited on the plate. In either situation, the antibodies/antigens are positioned to react with the protein in the sample.
It may thus be immediately appreciated that successive tests on the same patient undergoing treatment, for example at 24 hour intervals, may provide inaccurate results if different quantities of the antigens are utilized. Thus consistency in the amount of antigens deposited on the sample is of significance.
Referring first to
The plate 10 includes a first series of receptacles 12, 14, 16 and a second series of receptacles 13, 15, 17. For convenience each receptacle in the first series of receptacles (or wells, or depressions) will be identified with an even numeral and each receptacle in the second series of receptacles will be identified with an odd numeral. The receptacles extend downwardly into the plate from a top surface 20. Each receptacle in the first series is preferably aligned with a corresponding receptacle in the second series. Each receptacle in the first series is configured to retain a greater quantity of liquid that the corresponding receptacle in the second series. Thus the first series of receptacles may be thought of as reservoirs. Each receptacle in the second series is configured to retain the quantity of fluid needed for a single test and thus the second series of receptacles may be thought of as “sample” receptacles.
As explained above and in the patents incorporated by reference, it is known in IFE to test for total serum protein as well as IgG, IgM, IgA and light chains Kappa and Lambda. Thus a total of six sets or pairs of receptacles would be allocated to each patient. If the plate 10 includes 30 receptacles in each series, then IFE may be performed on five samples (e.g., from five patients) concurrently.
Referring next to
A next step would be to transfer an appropriate amount of the liquid 22 from receptacle 14 (a reservoir receptacle) to the corresponding smaller “sample” receptacle 15.
Referring next to
In
Alternatively, if desired, the amount of liquid 22 withdrawn by the instrument 24 from the sample receptacle 15 may be such so as to result in a deliberate meniscus, concave or convex, as long as the quantity is controlled as desired and spillage or undesirable overflow is avoided.
In the case of IFE as historically performed using equipment manufactured and marketed by Helena Laboratories, Inc., of Beaumont, Tex., assignee of the present application, receptacle 15 is of a size and shape such that it will hold exactly 17 microliters. (17 μl) It should be understood, therefore, that the shape of the receptacle 15 need not be rectangular. Once again, it is preferable to perform the steps illustrated in
Conventionally, an applicator will be used to transfer liquid from the sample receptacles 13, 15, 17 onto the electrophoresis plate. In a non-limiting example, the applicator will have 6 tips if liquid is being transferred for IFE evaluation of total serum protein plus IgG, IgM, IgA and light chains Kappa and Lambda. The applicator may have 30 tips if the same evaluation is to be made on five patients concurrently. One suitable applicator is illustrated and described in the aforementioned U.S. Pat. No. 6,544,395. The liquid 22 may adhere to the tip of the applicator by surface tension.
In a typical clinical laboratory or hospital setting, after the IFE procedure has been completed on a first group of patients, the samples from a second group of patients is to be subjected to IFE evaluation. For this purpose, liquid from the larger receptacles 12, 14, 16 may be transferred to the corresponding smaller receptacles 13, 15, 17 by repeating the procedure described above.
One of the benefits of the present method is that a precise amount of liquid may be placed in the sample receptacle 15 to thereafter be transferred onto the electrophoresis plate. By avoiding overflow of the receptacle 15, there is less waste of liquid. Even if it is desired to have a deliberate, albeit small, concave or convex meniscus in receptacle 15, the present method provides for more control over the amount of liquid in the receptacle 15 and therefore reduces waste. The control over the amount of liquid reduces the need to clean the surface 20 of the plate. Thus upon removal of the instrument 24, the remaining fluid may have a concave or convex meniscus but spillage has been avoided and precision as to the amount of liquid in the receptacle has been achieved.
If the sample receptacle is intended to hold 15 μl, and if the larger reservoir is configured to hold 150 μl, then a series of ten tests may be performed without the need to refill the reservoir thus contributing to overall efficiency based on the precise control of the amount of liquid withdrawn from the reservoir as well as the precise amount of liquid introduced into the sample receptacle.
The foregoing is a complete description of a preferred embodiment of the present method. Various changes may be made without departing from the scope of the following claims therefore the invention should be limited only by the following claims and the equivalent of the following claims.
