METHOD AND APPARATUS FOR THE MEASUREMENT OF THE PROPERTIES OF AN AGGLUTINATION
The present invention is concerned with a method for the measurement of the properties of an agglutination, a precipitate, or of a corresponding reaction result placed on the bottom of a vessel by means of radiation and of a detector that receives radiation, whereat the beam of measurement coming from the source of radiation passes substantially in the direction of the vertical axis of the vessel, and the intensity of the radiation passing through, or reflected from, the precipitate on the bottom of the vessel is measured. The invention is also concerned with an apparatus for the implementation of the method, which apparatus comprises one or several detectors receiving radiation, the said detectors being located so that the measurement beam received by them passes substantially in the vertical direction of the vessel, as well as an output unit.
Various tests based on agglutinations are in common use, e.g., in the case of blood-group identifications, antibody determinations, and rheumatic-factor measurements. In blood-group analytics and in antibody determinations the agglutination of red blood cells is concerned, whereas, e.g., the rheumatic factor is commonly measured by means of the agglutination of latex particles.
It has been customary tc read the results of agglutination reactions visually. An experienced reader is also quite skilful in distinguishing between agglutination and non-agglutination. Such a mode of output is, however, quite subjective, and this is why the result is not always completely reliable. In clear situations with strong agglutination, visual reading is certainly no problem, but weak reactions of agglutination are often problematic. Among agglutination reactions, most difficult to interpret is, e.g., a weak Rh-positive result obtained in blood-group identifications. In such situations it is of essential importance to obtain a reliable
output, because the safety of the patient is concerned.
The objective of the method in accordance with the invention (observation of, e.g., agglutination reactions and reading of the final results) is to be able to ascertain the difference between agglutination and non-agglutination sufficiently clearly, reproducibly, and carefully. By means of the principle of vertical measurement (Suovaniemi, Osmo, "Performance and Properties the Finnpipette Analyzer System", Proceedings of the Second National Meeting on Biophysics and Biotechnology in Finland, 183, 1976) it is possible to measure agglutination reactions. However, in the case of very, weak agglutinations, one beam of light does not produce a suf ficient difference in absorbance between agglutination a non-agglutination. In the method in accordance with the invention any uncertainty is eliminated by performing the measurement of the properties of the agglutination precipitate at several points once or several times so as to observe the formation of the precipitate as a function of time.
The agglutinated precipitate formed on the bottom of the reaction vessel is, viz., structurally different from a non-agglutinated precipitate. The forme is, e.g., unhomogeneous, at the middle part denser than at the sides, whereas the latter is even and relatively homogeneous. By performing, e.g., the measurement of absorption of light at several different points of the precipitate obtained, it is possible to distinguish between agglutinated precipitate and non-agglutinated precipitate reliably.
The method in accordance with the invention is characterized in that, in order to measure the formation, location, and form of the precipitate and/or the density or other properties of different points of the precipitat a component field of limited area, out of the field of the vessel bottom to be measured, is measured; the vessel and/or the source of radiation and/or the detector is/are
moved so that the component field subject to measurement moves along the field to be measured; and the measurement result of the component field at each particular time under measurement is read constantly or at specified intervals for the purpose of processing and output of the information. The apparatus in accordance with the invention is characterized in that, at one time, either the source of radiation or the detector receiving radiation covers only a limited component field of the bottom of the vessel and that the vessel and/or the source of radiation and/or the detector receiving the radiation can be shifted so that the location of the component field to be measured out of the bottom of the vessel at the bottom of the vessel is changed. For the measurement of the light absorption and/or the transmittance of the precipitate, an either slit-shaped or subtaritially point-shaped source of light is placed underneath the bottom of the reaction vessel, in its immediate proximity, which source of light illumi nates only a little part of the precipitate at a time. When the reaction vessel and the source of light are shifted in relation to each other, the light passes altεrnatingly through different parts of the precipitate, whereby it is possible to measure and to register the light absorption and/or transmittance at each particular point of the precipitate altematingly by means of the detector placed above the reaction vessel. Since an agglutinated precipitate gives a line of light absorbance and/or transmittance values different from that given by a non-agglutinated precipitate, it can be decided easily electronically which case is concerned.
Some of the features typical of the apparatus based on the method described above are as follows:
1. Therein the principle of vertical measurement is applied, such as in the "FP-9" photometer (U.S.
Patent 4,144,030).
2. The reaction vessel is shifted laterally so
that the beam of measurement alternatingly meets different points of the precipitate placed on the bottom of the vessel, or
3. The beam of measurement is shifted laterally so that it meets different points of the precipitate placed in a stationary reaction vessel alternatingly.
4. The movements described in sections 2 and 3 can be performed in more than one directions, whereby, when a point-shaped source of light or detector is used, the topography of the precipitate placed on the bottom of the vessel can be examined completely.
5 . The principles described in sections 1 to 4 can be applied to a multi-channel apparatus, such as, e.g. the "FP-9" photometer. 6. The principles described in sections 1 to 4 can also be applied to apparatuses measuring phenomena other than light absorption or transmittance (fluorometer, luminescence, etc.).
The invention will be described in more detail below with reference to the attached drawings, wherein
Figures 1a and 1b illustrate two different cases in a reaction vessel,
Figure 2 schematically illustrates an alternative in which one slit-shaped source of light is used that can be shifted in relation to the reaction vessel.
Figure 3 shows an absorbance curve obtained from the reaction vessel of Fig. 2; underneath the curve, the reaction vessel of Fig. 2 is shown as viewed from the top (in the curves of the figures, the x-axis illustrates the location of the point of measurement on the path of movement and the y-axis illustrates the absorbance at each particular time or in each particular point),
Figure 4 shows absorbance curves obtained by means of the source of light shown in Fig. 5 ; underneath the curves the precipitate measured is shown as viewed from above, and
Figure 5 is a schematical presentation of a
source of light that consists of several point-shaped sources of light.
In Figure la there is a precipitate 4a on the bottom of the reaction vessel 2, the shape and density of the said precipitate being at different points different from those of the precipitate 4b shown in Figure 1b. The precipitate 4a illustrates an agglutinated situation, whereas figure 4b represents a non-agglutinated precipitate in the situation of measurement. Figure 2 schematically shows a slit-shaped source of light 1, a reaction vessel 2, and a detector 3. The length of the slit is preferably somewhat less than the diameter of the vessel bottom. On the bottom of the reaction vessel 2 there is a precipitate 4, which has agglutination sections of different types and thicknesses. When, e.g., the reaction vessel 2 passes across the stationary source of light 1 and detector 3 once in the transverse direction of the slit 1 so that the slit-shaped team of light 5 passes, point by point, through the pre cipitate 4 on the bottom of the reaction vessel 2, the absorbance curve 3 shown in Fig. 3 is obtained, which curve may be continuous or consist of individual points. Figure 3 also shows a top view of the precipitate 4 on the bottom 2 of the reaction vessel. The measurement has been performed by at a time always measuring a stripe of the shape of the slit-shaped source of light out of the precipitate en the bottom of the reaction vessel and by producing .the output of the measurement value of this stripe. The production of the output may take place for each stripe separately, whereby a stepwise curve or a curve consisting of individual points is obtained, or as a continuous measurement, whereby the detector measures constantly during the movement and a continuous curve is obtained as the result. Figure 4 shows a precipitate 4 measured from the bottom of the reaction vessel 2 so that the reaction vessel has passed across the sources of light 8 to 10
arranged in a line and shown in Fig. 5, so that measurement has first been performed by means of the source of light 8 and the other sources of light 9 and 10 have been closed. Then the reaction vessel has come back, and then the measurement has been performed by means of the beam 9 whereas the beams 8 and 10 have been closed. Finally the beams 8 and 9 have been closed and the measurement has been performed by means of the beam 10, when the reaction vessel has by-passed it. In Figure 4 the beam 10 is corresponded by the scan 13 and by the absorbance curve 16. Correspondingly, the beams 9 and 8 correspond the scans 12 and 11 and the absorbance curves 15 and 14. The reaction vessel moves back and forth at its measurement point a number of times equalling the number of measurement beams in operation. It is also natural that one dot-shaped source of light may move along the slit shown in Figure 5 , being alternatingly in positions 8, 9 and 10.
The invention is not confined to the above alternative embodiments only, but it may show even considerable variation within the scope of the patent claims.
It is evident that in the method described above the source of light and the detector may change places, whereby the detector is placed immediately underneath the reaction vessel and it is given a slitshaped or dot-shaped form.
The method of measurement may be based on photometry or multiphotometry, the latter meaning a photometer which comprises several channels so that each sample has a source of light and a detector of its own. The method of measurement may, of course, being a single-channel or multi-channel method, be additionally based, e.g., on turbidometry, fluorometry, or, e.g., on the use of a source of radiation and a receiver for luminescence, laser beam, ultrasound, etc. phenomena. The positioning of the reaction vessels or equivalent, of sources of measurement beams, of detectors, etc. auxiliary equipment may be performed in the way
most appropriate in each particular case. The equipment may also involve various degrees of automation, e.g., in the pipetting of the samples and reagents, in the shifting of the beams of measurement, and in the processing of the results. It is natural that, in stead of one method of measurement, the reaction vessels may be measured simultaneously or subsequently by means of two or more wave lengths or methods of measurement (e.g., photometry and fluorometry), the final result being based on the infor mation thereby obtained.
In. stead of the sources of light arranged in a line, shown in Figure 5 , it is also possible to use one source of light and, correspondingly, detectors arranged in a line, the said detectors moving in relation to the reaction vessel. The detectors may be in operation either all of them at the same time, in which case one scan movement is adequate, or each of them alternatingly, whereby the scanning is performed correspondingly several times. Correspondingly, it is also possible to use one detector that moves along a slit between the scan movements.
Movement of the field of measurement in relation to the bottom of the vessel can be arranged either by shifting the vessel or the dot-shaped or slit-shaped source of light or the detector, or both.