GB1565492A - Creation of Inventions and Patents with Artificial Intelligence

GB1565492A – Apparatus and method for measuring white blood cell platelet cncentrations in blood
– Google Patents

GB1565492A – Apparatus and method for measuring white blood cell platelet cncentrations in blood
– Google Patents
Apparatus and method for measuring white blood cell platelet cncentrations in blood

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Publication number
GB1565492A

GB1565492A
GB11753/78A
GB1175378A
GB1565492A
GB 1565492 A
GB1565492 A
GB 1565492A
GB 11753/78 A
GB11753/78 A
GB 11753/78A
GB 1175378 A
GB1175378 A
GB 1175378A
GB 1565492 A
GB1565492 A
GB 1565492A
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United Kingdom
Prior art keywords
capillary tube
cell
light
cell layer
measured
Prior art date
1977-04-18
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GB11753/78A
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1977-04-18
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1978-03-23
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1980-04-23

1978-03-23
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1980-04-23
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patent/GB1565492A/en

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Classifications

G—PHYSICS

G01—MEASURING; TESTING

G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES

G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials

G01N15/04—Investigating sedimentation of particle suspensions

G01N15/042—Investigating sedimentation of particle suspensions by centrifuging and investigating centrifugates

G—PHYSICS

G01—MEASURING; TESTING

G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES

G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume, or surface-area of porous materials

G01N15/04—Investigating sedimentation of particle suspensions

G01N15/042—Investigating sedimentation of particle suspensions by centrifuging and investigating centrifugates

G01N2015/045—Investigating sedimentation of particle suspensions by centrifuging and investigating centrifugates by optical analysis

Description

PATENT SPECIFICATION
( 21) Application No 11753/78 ( 22) Filed 23 March 1978 ( 31) Convention Application No 788509 ( 32) Filed 18 April 1977 in ( 33) United States of America (US) ( 44) Complete Specification published 23 April 1980 ( 51) INT CL 3 GOIN 21/01 21/84 ( 52) Index at acceptance G 2 J 35 ( 11) 1 565 492 ( 1 ( 54) APPARATUS AND METHOD FOR MEASURING WHITE BLOOD CELL AND PLATELET CONCENTRATIONS IN BLOOD ( 71) I, STEPHEN CLARK WARDLAW, of 16 Pine Orchard Road, Branford, Connecticut, United States of America, a citizen of the United States of America, do hereby declare the invention, for which I pray that a patent may be granted to me and the method by which it is to be performed, to be particularly described in and by the following
statement:-
The invention relates to a method and apparatus for determining the approximate granulocyte and mononuclear white cell count, as well as platelet counts in a sample of centrifuged anticoagulated blood More particularly, the invention relates to a method and apparatus for measuring the linear extent of the buffy coat constituents of a centrifuged sample of anticoagulated blood, which buffy coat has been elongated in accordance with the method and apparatus disclosed in United Kingdom Patent Specification No 1,544,337.
A new technique has been devised for measuring the approximate granulocyte and mononuclear white cell counts, as well as platelet counts in a centrifuged sample of anticoagulated blood This technique involves the introduction of the blood sample into a capillary tube which contains an elongated body which, when the blood sample is centrifuged and thus separated into its constituent cell layers, floats upon the red cell layer and combines with the tube bore to form a free volume inside of the tube which free volume is of restricted size The buffy coat of the blood sample, which contains all of the cell types to be measured, settles into this restricted free volume and its axial extent is thus elongated over that it is ordinarily Thus the axial distance between the interfaces of the respective buffy coat cell layers is increased accordingly Measurement of the increased distance between the upper and lower interfaces or boundaries of each cell layer provides an indication of the volume of the cell layer, and thus the number of cells in the cell layer, so long as the free space constitutes a known geometrical shape and the cells are of normal size or normally distributed.
According to one aspect of the invention there is provided an instrument for use in measuring approximate cell counts of predetermined constituent blood cell layers which are differentially coloured with a stain and which are in a centrifuged anticoagulated blood sample contained in a transparent capillary tube, said instrument comprising first means for holding the capillary tube; an optical system mounted for focussing on the cell layers; said optical system including means forming a reference line extending transversely of the axis of the capillary tube; light source means mounted to be directed at the capillary tube to highlight the differential colouring of the blood cell layers being measured, means for causing relative movement between said reference line and the capillary tube to occur in a direction longitudinal of the capillary tube; and indicating means for providing a visible numerical indicia which is proportional to the extent of movement between said reference line and the capillary tube from commencement of the movement to termination thereof.
According to another aspect of the invention there is provided a method for measuring the approximate cell count in a constituent cell layer in a centrifuged sample of anticoagulated blood contained in a transparent capillary tube, said method comprising the steps of staining the cell layer to be measured a colour which is distinctively different from adjacent cell layers; directing a beam of light at the cell layer to be measured to illuminate said cell layer; aligning a reference line extending transversely of the axis of the capillary tube with one end of said cell layer, moving the capillary tube in the direction of its elongation until the reference line is aligned with the other end of said cell layer to be measured and concurrently producing an 1,565,492 electrical signal which is proportional to the extent of movement imparted to the capillary tube in traversing said cell layer to be measured; and converting the electrical signal produced to visually observable numerical indicia quantifying the concentration of cells in said cell layer measured.
To enhance the apparent separation of the constituent cell layers and to aid in more sharply defining the interfaces between adjacent cell layers, the stain, preferably a fluorescent stain, which is added to the blood sample, is advantageously one that is absorbed to different degrees by the various cell layers so that the different cell layers can be distinguished from each other by their differential colouration Acridine orange is one such stain which has been found to be useful for this purpose.
Accurate linear measurements can thus be made of the distance between the upper and lower interfaces in each component cell layer in the centrifuged axially elongated buffy coat which has been enhanced in accordance with the above-noted new technology.
It has been noted that when a blood sample is prepared for measurement in accordance with the technology outlined above, the interface or meniscus between adjacent cell type layers may provide a wavy, uneven dividing line between the cell layers when viewed in a circumferential direction about the tube which contains the blood sample This uneven meniscus can lead to errors in layer volume determination depending on whether one happens to measure from the high or low side of the meniscus The error can be magnified if the other meniscus of the layer being measured also forms in an uneven or wavy manner In order to minimise the degree of error in measurement which this phenomenon can induce, the tube can be rotated about its axis while the axial (longitudinal) measurements are being made In this way the meanderings of the meniscus edge which are seen through the tube are visually averaged so that even the most uneven and wavy meniscus encountered in this technology will appear to be a straight line perpendicular to the longitudinal axis of the tube This visual averaging minimizes the degree of error which could be made while measuring a wavy meniscus Furthermore, it does not alter the appearance of a properly formed meniscus The tube should be rotated at a high enough rate so that the waviness in the meniscus blends into a straight line, but not so high a rate that the cell layers in the tube will be disturbed or altered The precise minimal rate of rotation needed varies with the degree of illumination, the brighter the illumination, the higher minimum rate of rotation that will be needed to “average out” the meniscus, however, whether a sufficient rotational rate is being imparted to the tube is readily observable by one making the measurement In general, a rotational velocity range of 600 r p m to 1200 r p m.
will prove satisfactory for performance of the measurement.
The first means for holding the capillary tube containing the centrifuged blood sample to be measured preferably comprises a support which engages the tube at each of its ends so as to leave the cell layers unobstructed The support has basically two parts of which one part is preferably a passive part which engages one end of the tube and may be itself rotatable or non-rotatable, so long as it does not impede rotation of the tube The other part of the support is, in effect, a chuck which grips the other end of the tube tightly enough to impart the desired rotation to the tube when the chuck is rotated The chuck is preferably made of an elastomeric material, takes the form of an annulus which encircles the outside surface of the end of the tube, and is driven by a small electric motor.
The support and motor can be mounted 95 on a stage which is, in turn, movably disposed in a housing which forms a casing for the instrument Movement of the stage within the casing is preferably on a linear reciprocal nature and the stage may be 100 mounted in the casing in any conventional manner which will enable the linear reciprocal movement of the stage to occur with respect to the casing Preferably, a screw-type actuator is connected to the 105 stage and is operable, upon rotation, to move the stage linearly with respect to the casing A preferably parallax-free optical system with a reference line therein is included to line-up with each meniscus 110 during measurement Electrical means are operably connected to the actuator screw for measuring the extent of rotation of the screw, which is, in turn, proportional to the extent of linear movement of the stage 115 Further electrical means are included in the preferred embodiment of the instrument to provide a system for storing and reading the various constituent layer thicknesses measured 120 Preferably the distances between the several white blood cell layer interfaces are automatically converted to digital representations of the approximate concentrations of the respective white blood cell constituents when the different cell types are of different size and possess different packing characteristics.
The invention is diagrammatically illustrated by way of example in the accompanying drawings, in which:Figure 1 is a perspective view of a preferred embodiment of an instrument for measuring the distance between the menisci of a layer of cells in a centrifuged blood sample in accordance with the invention:
Figure 2 is a perspective view similar to Figure 1 but showing the instrument case broken away to disclose the internal components of the instrument; Figure 3 is a somewhat schematic representation of the details of the operable parts of the instrument of Figure 1; and Figure 4 is a diagrammatic representation of a portion of the electrical circuitry preferred for use in the instrument shown in Figure 1.
Referring to the drawings, Figures 1 and 2 show a blood testing instrument which includes a casing 2 in which the operative elements of the instrument are housed The casing 2 includes a door 4 mounted thereon by means of a piano hinge 6 The door 4 is opened to permit mounting of the capillary tube to be tested in place, and then closed to prevent ambient light from entering the inside of the casing A lens housing 8 is mounted on the casing and contains the optics preferred for use in properly aligning the menisci of a cell layer during measurement of the thickness of the cell layer A simple calibrated scale 10 is disposed on the casing 2 for making a general measurement of the red cell layer thickness in the centrifuged blood sample in the capillary tube prior to inserting the capillary tube into the instrument The scale is pre-calibrated to provide an approximate hematocrit count based on the observed thickness of the centrifuged red cell layer in the capillary tube An on-off switch 12 is disposed on the casing for turning the instrument on and off A stageadvancing dial 16 protrudes from the casing for advancing the specimen-holding stage within the casing 2, as will also be explained in greater detail hereinafter Three datastoring electrical switch buttons 18, 20 and 22 protrude from the casing 2 for use in a manner which will be explained in greater detail hereinafter An electrical start button 24 is positioned on the casing and operates in a manner described hereinafter with greater detail Three data-readout electrical switch buttons 26, 28 and 30 are disposed on the casing and operate in a manner which will be described hereinafter in greater detail The casing 2 also includes a window 32 through which a digital readout 34 can be seen.
Referring now to Figure 2, there is shown the components of the instrument which are disposed inside of the case 2 A light source 36 is disposed in the casing 2 and a focussing lens system is disposed in a housing 38 The capillary tube T which contains the blood sample to be tested is mounted in the support assembly within the casing 2 The support assembly includes one end plate portion 40 in the shape of a triangle At the upper apex of the triangle, there is formed a through passage 42 in which one end of the tube T is journalled for rotational movement The lower apices of the plate 40 are formed with through passages 44 which receive rods 46 serving to connect the plate to a block 48 which is mounted on a stage Adjacent to the block 48 and also mounted on the stage 50 is an electric motor 52, the shaft of which extends through a central axial passage in the block 48.
Attached to the end of the motor shaft 54 is a collar 56 made of elastomeric material.
The collar 56 includes a recess 58 which forms a chuck for receiving the other end of the tube T A prism 60 is mounted in the casing 2 and positioned so as to direct the light from the source 36 toward the tube T from the direction which will produce optimum fluorescence of the stain in the blood sample toward the lenses in the measuring lens housing 8 A gear box 62 is disposed below the stage 50 and a potentiometer 64 is disposed adjacent to the gear box 62 The stage-advancing dial 16 is operably connected to the gears in the gearbox 62 and to the potentiometer in a manner set forth in greater detail hereinafter The dial 16 is also operably connected to the stage 50 so as to be capable of reciprocally moving the stage 50.
Referring now to Figure 3, as previously noted, the spinner motor 52 is mounted on the stage 50 which, in turn, is reciprocably mounted on a base portion B Also mounted on the stage 50 is the passive portion of the tube support, the plate 40 The chuck 56 holds the other end of the tube T and is rotably driven by the motor 52 The fixed base B, which is part of the instrument casing, is formed with an upstanding flange 1 through which extends a threaded hole 3.
The dial 16 has secured thereto an actuating rod 5 which has an inner threaded end portion 7 which is screwed into and through the threaded hole 3 The inner end 68 of the rod 5 bears against one end of the stage 50, with the stage 50 being biased theretoward by a spring S Mounted on the shaft 5 is a first gear 70 which is keyed to the shaft 5 to rotate therewith A second gear 72 meshes with the first gear and rotates therewith at a 1:3 ratio The second gear 72 is keyed to a shaft 74 which forms the drive of a potentiometer 64 Thus rotation of the potentiometer drive 74 is proportional to the linear movement of the stage 50 The light source 36 is focussed by condensing lenses 39 which are mounted in the housing 1,565,492 38 A filter 41 is mounted in the housing 38 which allows transmission of the desired excitation light wavelengths of light to provide maximum excitation of the stain but blocks other wavelengths The optical viewing assembly which is mounted in the housing 8 comprises an assembly 9 having an ocular lens assembly 11, hair-line reference line 13, light filter 15, and an objective lens assembly 17 The range of magnification of lens system in the assembly 9 is preferably from 4 to 20 x The hair-line reticle 13 is preferably positioned at the focal plane of the ocular lens set 11 so that the assembly 9 is parallax-free The filter 15 removes the wavelengths of the illuminating excitation light and transmits only the fluorescent wavelengths of light emitted by the fluorescing stained cells in the capillary tube T.
Referring now to Figure 4, the mode of operation of the instrument will be explained, along with the electronics After the “on-off” switch is turned to “on”, and to begin the reading process, the capillary tube T is placed in the chuck and the stage 50 is manually adjusted by means of the dial 16 to align the reference line with the red cell/granulocyte interface The start button (switch) 24 is depressed which starts the motor 52 and causes activation of an “auto zero” amplifier 73 The input voltage to the amplifier 73 is derived from a voltage divider potentiometer 64 which produces a voltage proportional to the position of the stage 50, as previously described Actuation of the “auto zero” amplifier 73 automatically nulls out any existing input voltage E, Subsequent changes in the input voltage E, appear at the output E 2 of the amplifier 73 This output voltage E 2 is presented to the inputs of each of the sample and store amplifiers 75, 76 and 78.
The stage 50 is then advanced with the dial 16 until the reference line 13 is exactly aligned with the interface between the granulocyte and mononuclear cell layers.
The output voltage E 2 of the amplifier 73, at this point, represents a value which is proportional to the number of granulocytes, i.e, the axial dimension of that cell layer.
The “store gran ” button (switch) 18 is then depressed and the voltage E 2 is stored in the amplifier 75 Further movement of the potentiometer 64 causes no change in the output of the amplifier 75 The “auto zero” amplifier 73 is also actuated by depressing the “store gran ” switch 18 thus resetting the output E 2 of the “auto zero” amplifier 73 to zero.
The stage 50 is then advanced to align the reference line 13 with the interface between the mononuclear cell layer and the platelet layer The “store monos” switch 20 is then depressed which results in storage of the new output E 2 in the amplifier 76 and resets the “auto zero” amplifier 73 output E 2 to zero.
The stage 50 is then again advanced to align the reference line 13 with the interface between the platelet cell layer and the plasma layer The “store p Its” switch 22 is then depressed to store the new output E 2 in the amplifier 78 and the output E 2 of the “auto zero” amplifier 73 is then returned to zero All of the readings have then been taken and stored and are ready to be read.
To read the results, the “read” switches 26, 28 and 30 may be depressed in any order.
The white blood count (WBC) is the sum of the granulocyte layer and the mononuclear layer The output voltages E 3 and E 4 of the amplifiers 75 and 76 respectively are summed in a summing amplifier 80.
Resistors R 2 and R 3 are chosen to reflect the particular packing coefficients of the granulocytes and mononuclears This permits the digital panel to display a cell count number for each cell layer measured despite the fact that the different cell types are of different size and pack differently.
For example, there could be 500 granulocyte cells per 001 ” measurement but 1000 mononuclear cells packed into an 001 ” layer The scaling is adjusted by amplifier 87 and potentiometer Aw to provide an output calibrated to cells/cubic millimeter.
Depressing the “read WBC” switch 26 transfers the output voltage of the scaling amplifier 87 to the digital panel meter 82, which is preferably a Fairchild 320359 meter Depressing the switch 26 also stops rotation of the motor 52.
Depressing the “read gran” switch 28 switches the digital panel meter 82 to read the output voltage E, and simultaneously resets integrators S, and 52 Integrator S, is driven from output voltage E 6 which represents the total white blood count.
Integrator 52 is driven from output voltage E 3, which represents the granulocyte count.
The output of integrator S, goes to a comparator C When the output voltage E 7 of the integrator S, reaches the voltage of Ref 2, the output voltage of 52 will be held at whatever voltage is present at that time Ref 2 is chosen so that E, would produce a reading of 100 on the digital panel meter 82 if all of the cells were granulocytes, i e, if E 4 were equal to zero Thus E will be the ratio of E 3 x 100.
(E 3 +E 4) Depressing the “read pits” switch 30 connects the output voltage E 8 to the digital panel meter The stored platelet voltage E 5 125 is scaled by an amplifier 84 to produce a 1,565,492 5 voltage E 8 which will produce a reading of platelets per cubic millimeter times 1000.
The appropriate scale factor is provided by potentiometer Ap.
The “flip-flop” switch 86 is a bis-stable switch controlled by the switches previously described When turned on, its output E,, changes state from low to high This output drives an integrator 53 The output of % 3 powers the spinner motor 52 The slow ramp-up and ramp-down of the integrator 53 causes the motor 52 to start and stop at a slow, controlled rate, thus preventing the cell layers from being disturbed.
Adjustment Aw controls the maximum output voltage of 53, thus acting as a maximum motor speed control.
It will be readily appreciated that the instrument of the invention can provide accurate cell counts which are accurately displayed for recordal In place of the electrical system preferred for providing the numerical cell count readouts, a simpler mechanical system could be utilized if desired Regarding the details of the disclosed embodiment of the electrical storage and readout system, other means for sensing movement of the stage, converting the sensed movement into an electrical signal, and converting the signal into intelligible indicia could be used without departing from the scope of the invention as defined by the appended claims.

Claims (12)

WHAT I CLAIM IS:-

1 An instrument for use in measuring approximate cell counts of pre-determined constituent blood cell layers which are differentially coloured with a stain and which are in a centrifuged anticoagulated blood sample contained in a transparent capillary tube, said instrument comprising first means for holding the capillary tube; an optical system mounted for focussing on the cell layers; said optical system including means forming a reference line extending transversely of the axis of the capillary tube; light source means mounted to be directed at the capillary tube to highlight the differential colouring of the blood cell layers being measured; means for causing relative movement between said reference line and the capillary tube to occur in a direction longitudinal of the capillary tube; and indicating means for providing a visible numerical indicia which is proportional to the extent of movement between said reference line and the capillary tube from commencement of the movement to termination thereof.

2 An instrument according to claim 1, further comprising first filter means operable to filter out all but a first predetermined narrow wavelength and of.
light directed at the capillary tube from said light source means, and second filter means operable to filter out all but a second predetermined narrow wavelength band of light emanating from the coloured blood cell layers and directed toward said optical system.

3 An instrument according to claim 1 or claim 2, further comprising means connected to said first means for spinning the capillary tube about its axis.

4 An instrument according to any one of claims 1 to 3, in which said indicating means includes electrical means for providing a digital readout and for automatically sensing the extent of movement between said reference line and the capillary tube and converting sensed and observed increments of movement into indicia at said digital readout which substantially correspond to a cell concentration for a cell layer being measured.

An instrument according to any one of claims I to 4, in which said first means comprises mounting means for engaging and supporting at least one end portion of the capillary tube the stain is a fluorescent stain and the light source directs a beam of light along a path toward the capillary tube to cause the stain in the blood sample to fluoresce; the first filter means are disposed between said light source and the capillary tube to filter out substantially all wavelengths of light except the wavelength of light which most actively energizes the fluorescent stain to cause maximum fluorescence of the stain to occur; and the second filter means are disposed between at least a part of said optical system and the capillary tube for filtering out at least the fluorescent stain-energizing wavelengths of light while transmitting the fluorescent light wavelengths emitted by the fluorescent stain.

6 An instrument according to claim 4 or claim 5 when appendant to claim 4, in which said electrical means includes means for properly adjusting said numerical indicia to compensate for different cell sizes and cell packing characteristics found in the different cell layers being measured whereby the same increments of length measured in different cell layers will result in different numerical indicia being produced at said read-out portion

7 An instrument according to claim 3 or claim 4 or claim 5 when appendant to claim 3, in which the means for spinning the capillary tube about its axis cause apparent optical averaging of the cell interfaces so that the cell interfaces appear to be even.

8 A method for measuring the approximate cell count in a constituent cell layer in a centrifuged sample of anticoagulated blood contained in a transparent capillary tube, said method 1,565,492 1,565,492 comprising the steps of staining the cell layer to be measured a colour which is distinctively different from adjacent cell layers; directing a beam of light at the cell layer to be measured to illuminate said cell layer; aligning a reference line extending transversely of the axis capillary tube with one end of said cell layer; moving the capillary tube in the direction of its elongation until the reference line is aligned with the other end of said cell layer to be measured and concurrently producing an electrical signal which is proportional to the extent of movement imparted to the capillary tube in transversing said cell layer, to be measured; and converting the electrical signal produced to visually observable numerical indicia quantifying the concentration of cells in said cell layer measured.

9 A method according to claim 8, in which said cell layer is stained with a fluorescent stain; said beam of light comprises essentially wavelengths of light which most highly excite the fluorescent stain; and the excited fluorescing stained cell layer to be measured is observed through an optical system having means for filtering out substantially all light emanating from the capillary tube except for the light wavelengths produced by the fluorescing stained cell layer.

A method according to claim 8 or claim 9, in which the capillary tube is spun about its axis of elongation.

11 An instrument for use in measuring approximate cell counts of predetermined constituent blood cell layers which are differentially coloured with a stain and which are in a centrifuged anticoagulated blood sample contained in a transparent capillary tube substantially as hereinbefore described and illustrated with reference to the accompanying drawings.

12 A method for measuring the approximate cell count in a constituent cell layer in a centrifuged sample of anticoagulated blood contained in a capillary tube as claimed in claim 8 and substantially as hereinbefore described.
For the Applicant, D YOUNG & CO, Chartered Patent Agents, 9 & 10 Staple Inn, London WCIV 7RD.
Printed for Her Majesty’s Stationery Office, by the Courier Press, Leamington Spa, 1980 Published by The Patent Office, 25 Southampton Buildings, London, WC 2 A l AY, from which copies may be obtained.

GB11753/78A
1977-04-18
1978-03-23
Apparatus and method for measuring white blood cell platelet cncentrations in blood

Expired

GB1565492A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

US05/788,509

US4156570A
(en)

1977-04-18
1977-04-18
Apparatus and method for measuring white blood cell and platelet concentrations in blood

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GB1565492A
true

GB1565492A
(en)

1980-04-23

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ID=25144711
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Title
Priority Date
Filing Date

GB11753/78A
Expired

GB1565492A
(en)

1977-04-18
1978-03-23
Apparatus and method for measuring white blood cell platelet cncentrations in blood

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US
(1)

US4156570A
(en)

JP
(1)

JPS53129485A
(en)

DE
(1)

DE2816870A1
(en)

FR
(1)

FR2388277A1
(en)

GB
(1)

GB1565492A
(en)

IT
(1)

IT1102583B
(en)

SU
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SU940656A3
(en)

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US
US05/788,509
patent/US4156570A/en
not_active
Expired – Lifetime

1978

1978-03-23
GB
GB11753/78A
patent/GB1565492A/en
not_active
Expired

1978-04-12
IT
IT48875/78A
patent/IT1102583B/en
active

1978-04-17
JP
JP4515478A
patent/JPS53129485A/en
active
Granted

1978-04-17
SU
SU782605501A
patent/SU940656A3/en
active

1978-04-18
DE
DE19782816870
patent/DE2816870A1/en
active
Granted

1978-04-18
FR
FR7811372A
patent/FR2388277A1/en
active
Granted

Also Published As

Publication number
Publication date

FR2388277A1
(en)

1978-11-17

US4156570A
(en)

1979-05-29

SU940656A3
(en)

1982-06-30

JPS53129485A
(en)

1978-11-11

JPS6139620B2
(en)

1986-09-04

IT7848875D0
(en)

1978-04-12

FR2388277B1
(en)

1982-04-16

DE2816870C2
(en)

1987-04-23

IT1102583B
(en)

1985-10-07

DE2816870A1
(en)

1978-10-26

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