Process and apparatus for detection of specific biological factors by means of osmotic hemolysis

Claim 3

The method as defined in claim 1, further comprising the step of treating said red blood cells with a hydrophobic substance prior to bringing said red blood cells into contact with said hypotonic solution.

Claim 4

The method as defined in claim 2, wherein said red blood cells are treated with said hydrophobic substance by treating said test solution with said hydrophobic substance and subsequently bringing said test solution into contact with said red blood cells.

Claim 5

The method as defined in claim 2, wherein said red blood cells are treated with said hydrophobic substance by treating said agglutinating factor in said test solution with said hydrophobic substance and subsequently bringing said test solution into contact with said red blood cells.

Claim 6

The method as defined in claim 2, wherein said red blood cells are treated with said hydrophobic substance by treating said red blood cells with said test solution and subsequently with said hydrophobic substance.

Claim 7

The method as defined in claim 2, wherein said hydrophobic substance is adsorbable by said suspected agglutinating factor but not said red blood cells.

Claim 8

The method as defined in claim 2, wherein said hydrophobic substance is a lipid.

Claim 9

The method as defined in claim 2, wherein said hydrophobic substance is a member of the group consisting of saturated and unsaturated fats and oils.

Claim 10

The method as defined in claim 8, wherein said hydrophobic substance is a member of the group consisting of edible oils and fats.

Claim 11

The method as defined in claim 8, wherein said hydrophobic substance is a member of the group consisting of peanut oil and corn oil.

Claim 12

The method as defined in claim 8, wherein said hydrophobic substance is adsorbable by said agglutinating factor and not by said red blood cells.

Claim 13

The method as defined in claim 2, wherein red blood cells of unknown type are treated with a hydrophobic substance and with at least one of blood-grouping sera containing respectively anti-A, anti-B, anti-Rh, anti-M, anti-N and anti-Coomb's agglutinating factors as a means of typing said red blood cells.

Claim 14

The method as defined in claim 12, wherein said blood-grouping sera are treated with said hydrophobic substance prior to treating said red blood cells with said blood-grouping sera.

Claim 15

The method as defined in claim 12, wherein said red blood cells are treated with said blood-grouping sera prior to treating said blood cells with said hydrophobic substance.

Claim 16

The method as defined in claim 1, wherein said treatment is carried out automatically.

Claim 17

The method as defined in claim 12, wherein said treatment is carried out automatically.

Claim 18

The method as defined in claim 1, wherein said step of noting the degree of lysis is carried out automatically.

Claim 19

The method as defined in claim 12, wherein said step of noting the degree of lysis is carried out automatically.

Claim 20

The method as defined in claim 1, wherein said a serum of unknown type is treated with red blood cells of at least one of types A, B, M and N and Rh positive, and Coomb's positive as a means of typing said serum.

Claim 21

The method as defined in claim 19, further comprising the step of treating said serum of unknown type with a hydrophobic substance prior to bringing said red blood cells into contact with said hypotonic solution.

Claim 22

The method as defined in claim 19, wherein said treatment is carried out automatically.

Claim 23

The method as defined in claim 19, wherein said step of noting the degree of lysis is carried out automatically.

Claim 24

The method as defined in claim 2, wherein said test solution is prepated by mixing a biological fluid suspected of containing a specific virus and serum known to contain the antibody to said virus, and said red blood cells are type O, Rh negative.

Claim 25

The method as defined in claim 23, wherein said treatment is carried out automatically.

Claim 26

The method as defined in claim 23, wherein said step of noting the degree of lysis is carried out automatically.

Claim 27

The method as defined in claim 2, wherein said test solution is prepared by mixing a biological fluid containing a specific virus and serum from a patient suspected of containing antibodies to said virus, and said red blood cells are type O, Rh negative.

Claim 28

The method as defined in claim 26, wherein said treatment is carried out automatically.

Claim 29

The method as defined in claim 26, wherein said step of noting the degree of lysis is carried out automatically.

Claim 30

The method as defined in claim 2, wherein said hypotonic solution is an aqueous solution of NaCl at a concentration between about 0.2% and 0.4%.

Claim 31

The method as defined in claim 29, wherein the concentration of said solution is about 0.27%.

Claim 32

The method as defined in claim 2, wherein said red blood cells are first treated with said test solution and then introduced into a vessel containing a layer of red blood cell fixative on the bottom thereof, a layer of said hypotonic solution over said layer of fixative and a layer of said hydrophobic substance over said layer of hypotonic solution, said serum being introduced into said vessel under conditions such that said red blood cells fall through said layers, whereby lysis takes place only during the time of transit of said cells through said hypotonic solution layer, said cells being fixed on entering said fixative layer.

Claim 33

The method as defined in claim 2, wherein said test is repeated with said test solution at at least one lower concentration as a means of semi-quantitation of said suspected agglutinating factor by determining the lowest concentration at which the degree of lysis is comparable to that of red blood cells treated with a serum known to lack a corresponding agglutinating factor.

Claim 34

The method as defined in claim 1, further comprising the step of adding to said hypotonic solution a reagent known to enhance the intensity of the color, thereby increasing the precision with which the extent of lysis can be determined.

Claim 35

A fluid comprising a member selected from the group consisting of anti-A agglutinin, anti-B agglutinin, anti-Rh agglutinin, anti-human γ-globulin and viruses capable of agglutinating red blood cells, and a hydrophobic substance combined with said member said hydrophobic substance being present in sufficient quantity to substantially reduce the rate of lysis which would otherwise occur on adding corresponding red blood cells to said fluid and combining the resultant produce with hypotonic solution.

Claim 36

A fluid comprising a member selected from the group consisting of anti-A agglutinin, anti-B agglutinin, anti-Rh agglutinin, anti-human γ-globulin and viruses capable of agglutinating red blood cells, and a hydrophobic substance combined with said member said hydrophobic substance being present in sufficient quantity to substantially reduce the rate of lysis which would otherwise occur on adding corresponding red blood cells to said fluid and combining the resultant produce with hypotonic solution.

Claim 37

Apparatus for automatic blood-typing, cross-matching, identifying viruses, detecting the presence of and identifying antibodies in sera, and detecting agglutinating factors derived from tumors, comprising (a) containers for holding washed red blood cells, hereinafter referred to as "RBC", suspended in saline solution; (b) first conveyor means for transporting said containers in preparation for removing samples from said containers; (c) lysing tubes for holding test reagents and RBC samples taken from said containers; (d) second conveyor means for transporting a plurality of said lysing tubes; (e) reagent manifold for holding and supplying at least one agglutination reagent hereinafter termed "AR", and hypotonic solution to each of said lysing tubes, the term "hypotonic solution" being taken to include water; (f) automatically sequenced sampler for transferring samples of RBC from each of said containers to a number of lysing tubes equal to the number of AR to be used in typing said RBC; (g) first delivery means for supplying each AR individually to a corresponding number of lysing tubes; (h) mixing means including shaker or vibrator means positioned for mixing the contents of said lysing tubes essentially immediately and for a controlled period of time subsequent to addition of said AR; (i) second delivery means for adding hypotonic solution to the contents of said lysing tubes subsequent to addition of AR, said first delivery means, mixing means and second delivery means being spaced apart along said second conveyor means for providing a controlled incubation period; (j) colorimeter means for determining quantitatively the degree of osmotic lysis of said RBC in said lysing tubes, said colorimeter means being spaced apart from said second delivery means; and (k) drive means for driving said second conveyor means at a rate such that, in combination with said spacing between said second delivery means and said colorimeter, a suitable fixed time interval is provided for osmotic lysis to proceed to an extent such as to make it possible to determine relative rates of lysis in different samples.

Claim 38

Apparatus for automatic blood-typing, cross-matching, identifying viruses, detecting the presence of and identifying antibodies in sera, and detecting agglutinating factors derived from tumors, comprising (a) containers for holding washed red blood cells, hereinafter referred to as "RBC", suspended in saline solution; (b) first conveyor means for transporting said containers in preparation for removing samples from said containers; (c) lysing tubes for holding test reagents and RBC samples taken from said containers; (d) second conveyor means for transporting a plurality of said lysing tubes; (e) reagent manifold for holding and supplying at least one agglutination reagent hereinafter termed "AR", and hypotonic solution to each of said lysing tubes, the term "hypotonic solution" being taken to include water; (f) automatically sequenced sampler for transferring samples of RBC from each of said containers to a number of lysing tubes equal to the number of AR to be used in typing said RBC; (g) first delivery means for supplying each AR individually to a corresponding number of lysing tubes; (h) mixing means including shaker or vibrator means positioned for mixing the contents of said lysing tubes essentially immediately and for a controlled period of time subsequent to addition of said AR; (i) second delivery means for adding hypotonic solution to the contents of said lysing tubes subsequent to addition of AR, said first delivery means, mixing means and second delivery means being spaced apart along said second conveyor means for providing a controlled incubation period; (j) colorimeter means for determining quantitatively the degree of osmotic lysis of said RBC in said lysing tubes, said colorimeter means being spaced apart from said second delivery means; and (k) drive means for driving said second conveyor means at a rate such that, in combination with said spacing between said second delivery means and said colorimeter, a suitable fixed time interval is provided for osmotic lysis to proceed to an extent such as to make it possible to determine relative rates of lysis in different samples.

Claim 39

The apparatus as defined in claim 35, wherein said apparatus further comprises means for treating said red blood cells with a hydrophobic substance prior to bringing same into contact with said hypotonic solution.

Claim 40

The apparatus as defined in claim 35, further comprising automatic means for noting said degree of lysis, for determining the presence of specific agglutinating factors from said degree of lysis and for determining the blood group corresponding to the determined agglutinating factors when said apparatus is used for blood typing.

Claim 41

The apparatus as defined in claim 35, wherein said AR is lipid-treated.

Claim 42

The apparatus as defined in claim 35, wherein said lysing tubes are cuvettes suitable for use with said colorimeter.

Claim 43

The apparatus as defined in claim 35, further comprising cuvettes for use with said colorimeter and automatic feeder means for transferring specimens of solution from said lysing tubes to said cuvettes.

Claim 44

Apparatus for automatically detecting and determining agglutination factors in a fluid, including the typing of sera, said agglutination factors hereinafter termed "AFs", comprising: (a) containers for holding specimen fluids to be tested for the presence of specific AFs; (b) first conveyor means for transporting said containers for convenience in removing samples from said containers; (c) a plurality of test tubes divided into groups, the number of test tubes in each group corresponding to the number of types of red blood cells, hereinafter termed "RBC" to be used as test reagents; (d) lysing tubes divided into groups, there being a lysing tube corresponding to each test tube; (e) second conveyor means for transporting said test tubes and lysing tubes; (f) first reagent manifold for holding and addition means for supplying liquid lipid, fixative, and hypotonic solution to each of said lysing tubes in such manner that a layer of fixative rests at the bottom of said tube, a layer of hypotonic solution rests on said layer of fixative and a layer of lipid rests on said layer of hypotonic solution; (g) automatically sequenced sampler for transferring samples of serum from a container to all of the test tubes in a group; (h) second reagent manifold and second addition means for supplying a different type of RBC to each of the test tubes in said group; (i) mixing means for mixing the serum sample and RBC in each of the test tubes in said group; (j) transfer means for transferring the contents of each of said test tubes in a group to said lipid layer in a corresponding lysing tube for dropwise descent, by gravity, of said test tube contents through said lipid layer and said layer of hypotonic solution and into said fixative layer; and (k) colorimeter means positioned for passing a beam of light through said layer of hypotonic solution for determining quantitatively the degree of lysis of said RBC in falling through said layer of hypotonic solution to said fixative.

Claim 45

Apparatus for automatically detecting and determining agglutination factors in a fluid, including the typing of sera, said agglutination factors hereinafter termed "AFs", comprising: (a) containers for holding specimen fluids to be tested for the presence of specific AFs; (b) first conveyor means for transporting said containers for convenience in removing samples from said containers; (c) a plurality of test tubes divided into groups, the number of test tubes in each group corresponding to the number of types of red blood cells, hereinafter termed "RBC" to be used as test reagents; (d) lysing tubes divided into groups, there being a lysing tube corresponding to each test tube; (e) second conveyor means for transporting said test tubes and lysing tubes; (f) first reagent manifold for holding and addition means for supplying liquid lipid, fixative, and hypotonic solution to each of said lysing tubes in such manner that a layer of fixative rests at the bottom of said tube, a layer of hypotonic solution rests on said layer of fixative and a layer of lipid rests on said layer of hypotonic solution; (g) automatically sequenced sampler for transferring samples of serum from a container to all of the test tubes in a group; (h) second reagent manifold and second addition means for supplying a different type of RBC to each of the test tubes in said group; (i) mixing means for mixing the serum sample and RBC in each of the test tubes in said group; (j) transfer means for transferring the contents of each of said test tubes in a group to said lipid layer in a corresponding lysing tube for dropwise descent, by gravity, of said test tube contents through said lipid layer and said layer of hypotonic solution and into said fixative layer; and (k) colorimeter means positioned for passing a beam of light through said layer of hypotonic solution for determining quantitatively the degree of lysis of said RBC in falling through said layer of hypotonic solution to said fixative.

Claim 46

The apparatus as defined in claim 41, further comprising: (l) detector means for determining prior to arrival of a lysis tube at said colorimeter means whether all of the RBC in same have fallen through said hypotonic solution; and (m) recycling means operatively connected to said detector means for recycling any lysis tube containing RBC above said hypotonic solution layer to said detector means until all RBC have passed through said hypotonic solution and then transferring said lysis tube to said colorimeter means.

Claim 47

The apparatus as defined in claim 41, further comprising automatic means for noting said degree of lysis, for determining the presence of specific agglutinating factors from said degree of lysis and for determining the blood group corresponding to the determined agglutinating factors when said apparatus is used for blood typing.

Claim 48

A composition for detecting the presence of a specific viral antibody in a biological specimen, said composition comprising a virus corresponding to said antibody, a fluid suitable for suspending said virus, and a lipid in an amount such as is held by said fluid and said virus following agitation with said lipid and physical separation therefrom, said composition being useful for determining the presence of said specific antibodies by the degree of osmotic hemolysis of red blood cells when brought in contact therewith and with hypotonic solution.

Claim 49

A composition for detecting the presence of a specific viral antibody in a biological specimen, said composition comprising a virus corresponding to said antibody, a fluid suitable for suspending said virus, and a lipid in an amount such as is held by said fluid and said virus following agitation with said lipid and physical separation therefrom, said composition being useful for determining the presence of said specific antibodies by the degree of osmotic hemolysis of red blood cells when brought in contact therewith and with hypotonic solution.