US3712144A - Automated system for performing sample measurement, dilutions and photometric measurements - Google Patents
Automated system for performing sample measurement, dilutions and photometric measurements Download PDFInfo
- Publication number
- US3712144A US3712144A US00122843A US3712144DA US3712144A US 3712144 A US3712144 A US 3712144A US 00122843 A US00122843 A US 00122843A US 3712144D A US3712144D A US 3712144DA US 3712144 A US3712144 A US 3712144A
- Authority
- US
- United States
- Prior art keywords
- sample
- module
- improvement
- sample supply
- accordance
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000012895 dilution Substances 0.000 title description 5
- 238000010790 dilution Methods 0.000 title description 3
- 238000005259 measurement Methods 0.000 title description 3
- 238000005375 photometry Methods 0.000 title description 3
- 239000000523 sample Substances 0.000 claims description 108
- 239000003085 diluting agent Substances 0.000 claims description 29
- 230000006872 improvement Effects 0.000 claims description 16
- 238000004891 communication Methods 0.000 claims description 10
- 239000002699 waste material Substances 0.000 claims description 8
- 230000008878 coupling Effects 0.000 claims description 6
- 238000010168 coupling process Methods 0.000 claims description 6
- 238000005859 coupling reaction Methods 0.000 claims description 6
- 239000012470 diluted sample Substances 0.000 claims description 6
- 230000033001 locomotion Effects 0.000 claims description 5
- 230000001360 synchronised effect Effects 0.000 claims description 2
- 238000003556 assay Methods 0.000 abstract description 16
- 230000002906 microbiologic effect Effects 0.000 abstract description 9
- 229940088594 vitamin Drugs 0.000 abstract description 5
- 229930003231 vitamin Natural products 0.000 abstract description 5
- 235000013343 vitamin Nutrition 0.000 abstract description 5
- 239000011782 vitamin Substances 0.000 abstract description 5
- 239000003242 anti bacterial agent Substances 0.000 abstract description 4
- 229940088710 antibiotic agent Drugs 0.000 abstract description 4
- 238000012801 analytical assay Methods 0.000 abstract description 3
- 239000000126 substance Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 5
- 238000012864 cross contamination Methods 0.000 description 4
- 238000011534 incubation Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 241000588748 Klebsiella Species 0.000 description 2
- 241000186660 Lactobacillus Species 0.000 description 2
- 241000589516 Pseudomonas Species 0.000 description 2
- 239000004809 Teflon Substances 0.000 description 2
- 229920006362 Teflon® Polymers 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- 238000007865 diluting Methods 0.000 description 2
- 229940039696 lactobacillus Drugs 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229920004459 Kel-F® PCTFE Polymers 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000000721 bacterilogical effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical compound FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011010 flushing procedure Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/02—Burettes; Pipettes
- B01L3/0203—Burettes, i.e. for withdrawing and redistributing liquids through different conduits
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/02—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations
- G01N35/026—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations having blocks or racks of reaction cells or cuvettes
Definitions
- This invention relates to a two-component system for performing turbidimetric microbiological assays on substances such as antibiotics, vitamins, and other bacterial growth promoting or inhibiting substances, as well as various other analytical assays, and the like.
- Turbidimetric microbiological assays of antibiotics, vitamins, and the like have long been used as a means for identifying and assaying the potency of such substances.
- the assay procedures are time consuming and usually involve many manual operations, each subject to some degree of error.
- a further disadvantage of currently available equipment is their lack of reproducibility in assays utilizing rod-shaped organisms such as Klebsiella, Lactobacillus, Pseudomonas, etc., because of the problem of flow birefringence (Kavanagh, F. W., Analytical Microbiology, Chapter 4, Academic Press, N.Y., N.Y. 1963).
- the two-component assay system of this invention comprises an automatic diluter module and an automatic photometric reader-module.
- the modules perform the same basic operations involved in traditional manual analytical or microbiological turbidimetric methods such as pipetting, diluting, and the like, with far greater accuracy, precision, and efficiency.
- the modules for example, can utilize the same organisms, the same media, and can measure the same bacteriological response employed in manual turbidimetric microbiological assays.
- the system is able to accommodate similar. assay designs and standardization procedures as have been used heretofore. It provides for unlimited incubation or reaction times.
- the assay system of this invention consists of two modules, a diluter module, and a photometric reader module.
- the diluter module includes a programmed control means, and a sampler tray which is adapted to advance at a predetermined time, making each sample tube available to a first sample probe means. A portion of the sample is withdrawn by a first sample probe means into a first metering means having a zero dead-volume. The combined operations of the probe and metering means performs the pipetting operation. After the sample has been measured, a predetermined amount of diluent is directed through the metering means by a first diluent delivery means, thereby washing out and diluting the sample into a diluted sample receiving means.
- the operations are repeated until the desired number of samples have been measured and diluted. So long as the same diluent is used, different substances can be run by different methods without cleaning the equipment between substances.
- the diluter module is self-cleaning. That is, by carefully choosing the materials of construction, and by providing a sufficiently great dilution factor, the diluent serves to completely flush the sample from the metering means, thereby eliminating cross-contamination without necessitating an intermediate cleaning operation between samples.
- a variety of dilutions can be obtained by either changing the volume of the diluent delivered or by altering the volume of sample measured by the metering means.
- the diluter module can additionally include an automatic means for conveying the diluted sample receiving means to a delivery tube which is cooperatively associated with the metering means.
- the diluted samples can be transferred in suitable carriers, after allowing for sufficient incubation or reaction time, to a photometric reader, preferably to the reader module of this invention.
- the reader module of this invention includes a photometric reader such as a photometer having a quartz flow cell as the cuvette.
- the reader module has an automatic sample conveying means, such as a conventional linear fraction collector or the like, cooperatively associated therewith for conveying each sample to be read to a means for transferring the sample into the flow cell.
- the sample conveying means can advantageously be a probe means, or the like, which is adapted to withdraw a sample and convey it to the flow cell. Before each sample reaches the flow cell, the flow is momentarily interrupted to provide an air hammer" BRIEF DESCRIPTION OF THE DRAWINGS
- FIG. 1 is a perspective view of the diluter module.
- FIG. 2 is a rear plan view of the probe assembly with the housing therefor broken away.
- FIG. 3 is a flow diagram of a metering cell in its first position.
- FIG. 4 is a flow diagram of a metering cell in the second position.
- FIG. 5 is a perspective view of the reader module with the position of the flow cell designated by dotted lines.
- the diluter module performs the functions of pipetting and delivering a precise, predetermined amount of sample into a sample holder and of adding a precisely measured amount of diluent or reagent thereto.
- the diluter module includes a housing 11 for a programmed control unit and a drive mechanism therefor (not shown).
- the control unit and drive mechanism are actuated by control switches 12, and the main power switch 13.
- the samples and standards are poured into sample tubes 14 which are then placed into the sample holder 15. While any suitable sample holder can be utilized, the preferred sample holder 15 includes three circular, spaced-apart plates.
- the top plate 16 has a centrally located aperture adapted to have a drive shaft 17 removably journalled therein, a plurality of spacedapart locating apertures 18 forming a concentric circle about said centrally located aperture, said apertures being adapted to receive a positioning pin 19 which is coupled to a mounting and supporting plate (not shown) and which limits the rotational motion of the sample holder so that each sample tube will be aligned with the sampler probe 32, and a plurality of spacedapart apertures 21 for receiving sample tubes 14, the apertures being conveniently spaced apart adjacent the outer periphery of the plate.
- the center plate 22 has a central aperture of sufficient size to fit over the housing 23 for the driving motor which controls the indexing of the sample holder.
- the driving means in turn is controlled by the control unit.
- Apertures 24 in plate 22 are aligned with apertures 21 of the top plate 16.
- the bottom plate 25 similarly has a central aperture of sufficient size to fit over housing 23.
- the bottom plate serves as a base for the bottom surface of the sample tubes.
- the three plates are maintained in their spacedapart positions by spacing posts 26.
- Probe assembly 31 includes a probe 32 which is removably mounted at its upper end to a first mounting plate 33 via bracket means 34.
- a retaining means 35 can conveniently be fitted over the top end of the probe to insure a secure fit into the bracket means.
- the probe is preferably of stainless steel or a like material.
- the probe is adapted to move vertically along channel 36 in probe assembly housing 37. As can be seen in FIG. 2, a
- second plate 38 is cooperatively associated with plate 33 so that plate 38 is disposed adjacent the interior surface 39 of the front wall 40 of the probe assembly housing.
- Bearings 41 and 42 are rotatably retained between plates 33 and 38. As the probe assembly moves along channel 32, bearings 41 and 42 ride along bearing runners 43.
- Drive shaft 44 is coupled to and driven by, for example, a bell crank and motor (not shown).
- the probe assembly When the probe assembly is actuated, the probe moves downwardly and into the sample contained in the particular tube which is presently aligned with the probe.
- a vacuum system (not shown) is then actuated and sample is drawn through the probe and into a first loop 45 of a first metering valve means 30, via sample inlet tube 46. The vacuum system is then shut off whereupon the loop remains full. The size of the sample which is ultimately delivered into sample receiving means 47 via delivery tube 48 is determined by the volume of the loop 45.
- sample receiving means 47 which can be, for example, a test tube, as a predetermined amount of diluent is passed into the valve and through loop 45, through the valve, and into the sample retaining means via delivery tube 48.
- sample receiving means 47 can be, for example, a test tube
- the presently preferred ratio of diluent to sample is at least 10:1 to insure complete flushing of the valve, thereby eliminating cross-contamination.
- part of the diluent can be passed directly into the sample receiving means.
- the same sample is passed through and measured by the second loop 49, which can differ in volume from the first loop 45 and is again washed out with diluent via delivery tube 48 and into another sample receiving means.
- any unit capable of adding a specified amount of diluent can be utilized in the practice of this invention, for example, the filling unit manufactured by National Instruments Co. Diluent is pumped from the filling unit 51 into the valve, via diluent inlet tube 52.
- two metering valves 30 and 30' are utilized in order to obtain, for example, two O.l5 ml. samples and two 0.1 ml. samples.
- the valves are conveniently mounted on a first surface of mounting board 53, which is, in turn, conveniently coupled to housing 11 via support member 54 and mounting brackets 55.
- the sample injection valve manufactured by Chromatonix Inc. is particularly suitable for providing the sample metering means of the present invention when modified to operate in accord with the above discussion.
- any other suitable metering means can be utilized.
- valve 30 The operation of the valve 30 can be more fully understood by the diagram of FIG. 3.
- the sample is drawn into a first section 56 of valve 30 via sample probe 32.
- the sample follows flow passage 57 to loop 45, and is drawn into a second section 56 of the valves, through passage 64, through vacuum valve 65 and to waste.
- loop 45 remains filled until sections 56 and 56' are switched to their alternate positions as shown in FIG. 4.
- the diluent then passes through passage 58, into loop 45, thereby washing out the sample via passage 60 and through the delivery tube to the awaiting sample receiving means.
- loop 49 is connected to the sample probe via passage 61 and 62, thereby filling loop 49 with the same sample.
- Return of 56 and 56' to the first position now connects loop 49 with the diluent via passage 63 and 66.
- valves are preferably of Teflon and Kel-F, although other suitable materials can be employed. Similarily, the loops are preferably Teflon.
- the sample receiving means 47 are conveniently held in racks 82.
- the racks are then conveniently advanced automatically into the proper position by an automatic conveyor means 83, cooperatively associated with housing 11 and mounting board 53 so that for each delivery cycle, a sample receiving means is aligned beneath a delivery tube.
- the diluter module provides a convenient, accurate means for automatically pipetting a given amount of sample, delivering the sample to a sample holder such as a test tube or the like, and adding.
- the reader module of this invention is shown generally at 70.
- the diluted samples obtained from the diluter module, or any other suitable means are, after proper incubation or reaction time, transferred in the racks 82 to an automatic conveyor means 83, or other suitable advancing means. It can be seen that the racks are guided by guide means 71, and that a retaining plate 72 is positioned behind the last rack.
- the samples are drawn into a suitable photometer 73 by probe assembly 31.
- the samples are passed through flow cell 74 via inlet tube 75 and through outlet tube 76 to a waste receiving means (not shown).
- the flow cell is preferably quartz or a like material, and replaces the cuvette of conventional readers.
- a solenoid valve (not shown) in the control unit 79 controls the sample flow.
- the control circuit is adapted to momentarily drop out the solenoid and interrupt the sample flow before it reaches the flow cell. This produces an air hammer effect which takes care of any air bubbles present in the flow stream.
- the flow cell permit a rate of flow of not less than 0.8 ml./sec., and preferably a rate of l ml./sec. or higher in order to obtain highly accurate, reproducible results.
- the flow rate is not critical.
- the readings can be taken from the scale 77 of the photometer 73, or, as in the preferred embodiment, a suitable readout device 78 can be cooperatively associated with the photometer.
- the readout is compatible with a variety of data acquisition devices such as printed tape, punched paper tape, punched cards, or can be interfaced directly to a computer.
- the reader module of this invention provides a great advance in the art by providing a means for overcoming the problems of measuring the turbidity of rod-shaped organisms by avoiding the flow birefringence problem normally encountered with rod-shaped particles.
- By producing a sufficiently rapid flow through the flow cell rod-shaped particles, which would otherwise orient themselves with the slow currents in a static cell, leading to inconsistent readings, are read with the same precision as are spherical particles.
- the present reader module now makes it possible to assay for substances which affect various rod-shaped organisms such as Klebsiella, Lactobacillus, Pseudomonas, and the like, and to determine them with a precision equivalent to spherical organisms, all other factors being equal.
- the present invention is particularly suited for turbidimetric microbiological assays, it will be apparent to those skilled in the art that the diluter module and the reader module can be used ointly or separately in any number of analytical procedures, medical laboratory tests, and the like. Therefore, while the following discussion is directed toward turbidimetric microbiological assays, the modules of this invention are applicable to any suitable analytical procedures.
- an automatic dilutor module comprising: a valve means having first and second sections, said first section having a diluent supply inlet connected to a metered diluent supply and a sample supply inlet connected to a sample supply, a pair of loops of predetermined volume having their first ends connected to a pair of respective outlets in said valve means first section in alternately selective communication with said diluent supply and said sample supply, said loops having their second ends in alternately selective communication with a pair of respective discharge outlets in said second section of said valve means, said pair of discharge outlets in said second section of said valve means being in communication with a waste receptacle and a delivery receptacle, and control means associated with said first and second sections alternately effecting coupling of each of said loops between (a) said diluent supply inlet and said delivery receptacle; and (b) said sample supply inlet and said waste receptacle.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Clinical Laboratory Science (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
Abstract
An automatic diluter and photometric reader adapted for use in the turbidimetric microbiological assays of antibiotics, vitamins, and the like, as well as in various other analytical assays.
Description
United States Patent Kuzel et al. 1 Jan. 23, 1973 [S4] AUTOMATED SYSTEM FOR PERFORMING SAMPLE [56] References Cited MEASUREMENT, DILUTIONS AND UNITED TATE P TENT PHOTOMETRIC MEASUREMENTS S S A S r a 3,567.390 3 1971 R m 1 ..73/421 RX [75] Inventors: Norbert R. 'Kuzel, Ind1anapol1s, 3,467,500 9/1969 f gz at a] Ind.; Frederick W. Kavanagh, 111- 3,567,389 3/1971 Coulter et al. ..73/42l R X dianapo11s,Ind. 3,567,398 3/1971 Farr ..23/259 [73] Assignee: Eli filly andCompanyJndianapolis, primary Examiner Louis capozi .3 v. Assistant Examiner-.loseph W. Roskos [22] i d; March 10 1 7 Attorney--Everet F. Smith and Houston L. Swenson [21] Appl.N0.: 122,843 57 ABSTRACT Related U.S. Application Data An automatic diluter and photometric reader adapted [62] ofs N Sol 369 Feb 24 969 Pm No for use in the turbidimetric microbiological assays of 3 2 62 6 antibiotics, vitamins, and the like, as well as in various other analytical assays.
l52| U.S. Cl. ..73/42l R, 23/259, 356/36 8 Chum", 5 nmwlng Flam-cs [51] Int. Cl. ..G0ln 1/10 Field of Search...73/42l R; 356/36; 23/253, 259
PATENTEUJAN 23 ms SHEEI 1 [IF 2 wma.
mm kmzdo INVENTORS NORBERT R KUZEL FREDERICK W. KAVANAGH m mwH .wm Ci mm mv ATTORNEY PATENTEDJAN 23 I975 3.712.144
SHEET 2 or 2 INVENTORS N NORBERT R. KUZEL IO'OFREDERICK w. KAVANAGH H 4 ICJKM m ATTORNEY AUTOMATED SYSTEM FOR PERFORMING SAMPLE MEASUREMENT, DILUTIONS AND PHOTOMETRIC MEASUREMENTS CROSS-REFERENCE TO RELATED APPLICATION This application is a division of our co-pending U. S. application, Ser. No. 801,369, filed on Feb. 24, 1969 and issued on Sept. 28', 1971, as US. Pat. No. 3,609,040.
BACKGROUND OF THE INVENTION This invention relates to a two-component system for performing turbidimetric microbiological assays on substances such as antibiotics, vitamins, and other bacterial growth promoting or inhibiting substances, as well as various other analytical assays, and the like.
Turbidimetric microbiological assays of antibiotics, vitamins, and the like have long been used as a means for identifying and assaying the potency of such substances. The assay procedures are time consuming and usually involve many manual operations, each subject to some degree of error.
In recent years, there have been attempts to provide automated devices for carrying out such assays. While there are currently several such devices, they are plagued with various problems such as cross-contamination between samples, slow rate of analysis, requirements for large volumes of sample, fixed time of incubation or reaction, lack of versatility, need for method changes to accommodate the equipment, etc. Furthermore, because of the cross-contamination problems of some of the currently existing devices, only one antibiotic, vitamin or the like can be analyzed in a single operation. Before a second substance can be assayed, the equipment must be cleaned.
A further disadvantage of currently available equipment is their lack of reproducibility in assays utilizing rod-shaped organisms such as Klebsiella, Lactobacillus, Pseudomonas, etc., because of the problem of flow birefringence (Kavanagh, F. W., Analytical Microbiology, Chapter 4, Academic Press, N.Y., N.Y. 1963).
In addition to the above disadvantages, the cost of many of the currently available devices is prohibitive.
Thus, while attempts have been made to provide automated devices for performing turbidimetric microbiological assays, such attempts have been fraught with problems.
SUMMARY OF THE INVENTION The two-component assay system of this invention comprises an automatic diluter module and an automatic photometric reader-module. The modules perform the same basic operations involved in traditional manual analytical or microbiological turbidimetric methods such as pipetting, diluting, and the like, with far greater accuracy, precision, and efficiency. The modules, for example, can utilize the same organisms, the same media, and can measure the same bacteriological response employed in manual turbidimetric microbiological assays. The system is able to accommodate similar. assay designs and standardization procedures as have been used heretofore. It provides for unlimited incubation or reaction times.
Generally speaking, the assay system of this invention consists of two modules, a diluter module, and a photometric reader module.
The diluter module includes a programmed control means, and a sampler tray which is adapted to advance at a predetermined time, making each sample tube available to a first sample probe means. A portion of the sample is withdrawn by a first sample probe means into a first metering means having a zero dead-volume. The combined operations of the probe and metering means performs the pipetting operation. After the sample has been measured, a predetermined amount of diluent is directed through the metering means by a first diluent delivery means, thereby washing out and diluting the sample into a diluted sample receiving means.
The operations are repeated until the desired number of samples have been measured and diluted. So long as the same diluent is used, different substances can be run by different methods without cleaning the equipment between substances. The diluter module is self-cleaning. That is, by carefully choosing the materials of construction, and by providing a sufficiently great dilution factor, the diluent serves to completely flush the sample from the metering means, thereby eliminating cross-contamination without necessitating an intermediate cleaning operation between samples.
A variety of dilutions can be obtained by either changing the volume of the diluent delivered or by altering the volume of sample measured by the metering means.
The diluter module can additionally include an automatic means for conveying the diluted sample receiving means to a delivery tube which is cooperatively associated with the metering means.
The diluted samples can be transferred in suitable carriers, after allowing for sufficient incubation or reaction time, to a photometric reader, preferably to the reader module of this invention.
The reader module of this invention includes a photometric reader such as a photometer having a quartz flow cell as the cuvette. The reader module has an automatic sample conveying means, such as a conventional linear fraction collector or the like, cooperatively associated therewith for conveying each sample to be read to a means for transferring the sample into the flow cell. The sample conveying means can advantageously be a probe means, or the like, which is adapted to withdraw a sample and convey it to the flow cell. Before each sample reaches the flow cell, the flow is momentarily interrupted to provide an air hammer" BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 is a perspective view of the diluter module.
FIG. 2 is a rear plan view of the probe assembly with the housing therefor broken away.
FIG. 3 is a flow diagram of a metering cell in its first position.
FIG. 4 is a flow diagram of a metering cell in the second position.
FIG. 5 is a perspective view of the reader module with the position of the flow cell designated by dotted lines.
DESCRIPTION OF PREFERRED EMBODIMENTS Referring to the drawing, one embodiment of the diluter module is shown generally at in FIG. 1. The diluter module performs the functions of pipetting and delivering a precise, predetermined amount of sample into a sample holder and of adding a precisely measured amount of diluent or reagent thereto.
The diluter module includes a housing 11 for a programmed control unit and a drive mechanism therefor (not shown). The control unit and drive mechanism are actuated by control switches 12, and the main power switch 13. The samples and standards are poured into sample tubes 14 which are then placed into the sample holder 15. While any suitable sample holder can be utilized, the preferred sample holder 15 includes three circular, spaced-apart plates. The top plate 16 has a centrally located aperture adapted to have a drive shaft 17 removably journalled therein, a plurality of spacedapart locating apertures 18 forming a concentric circle about said centrally located aperture, said apertures being adapted to receive a positioning pin 19 which is coupled to a mounting and supporting plate (not shown) and which limits the rotational motion of the sample holder so that each sample tube will be aligned with the sampler probe 32, and a plurality of spacedapart apertures 21 for receiving sample tubes 14, the apertures being conveniently spaced apart adjacent the outer periphery of the plate. The center plate 22 has a central aperture of sufficient size to fit over the housing 23 for the driving motor which controls the indexing of the sample holder. The driving means in turn is controlled by the control unit. Apertures 24 in plate 22 are aligned with apertures 21 of the top plate 16. The bottom plate 25 similarly has a central aperture of sufficient size to fit over housing 23. The bottom plate serves as a base for the bottom surface of the sample tubes. The three plates are maintained in their spacedapart positions by spacing posts 26.
The samples are drawn into a first metering valve 30 via probe assembly shown generally at 31. Probe assembly 31 includes a probe 32 which is removably mounted at its upper end to a first mounting plate 33 via bracket means 34. A retaining means 35 can conveniently be fitted over the top end of the probe to insure a secure fit into the bracket means. The probe is preferably of stainless steel or a like material. The probe is adapted to move vertically along channel 36 in probe assembly housing 37. As can be seen in FIG. 2, a
When the probe assembly is actuated, the probe moves downwardly and into the sample contained in the particular tube which is presently aligned with the probe. A vacuum system (not shown) is then actuated and sample is drawn through the probe and into a first loop 45 of a first metering valve means 30, via sample inlet tube 46. The vacuum system is then shut off whereupon the loop remains full. The size of the sample which is ultimately delivered into sample receiving means 47 via delivery tube 48 is determined by the volume of the loop 45.
Once the sample is drawn into a first loop 45, and the vacuum is shut off via vacuum solenoid (not shown), the sample is delivered via delivery tube 48, into sample receiving means 47, which can be, for example, a test tube, as a predetermined amount of diluent is passed into the valve and through loop 45, through the valve, and into the sample retaining means via delivery tube 48. The presently preferred ratio of diluent to sample is at least 10:1 to insure complete flushing of the valve, thereby eliminating cross-contamination. However, it is only necessary that sufficient diluent be passed through the valve to flush out sample. Thus, for example, when large volumes of diluent are received, part of the diluent can be passed directly into the sample receiving means. On the next cycle, the same sample is passed through and measured by the second loop 49, which can differ in volume from the first loop 45 and is again washed out with diluent via delivery tube 48 and into another sample receiving means.
Any unit capable of adding a specified amount of diluent can be utilized in the practice of this invention, for example, the filling unit manufactured by National Instruments Co. Diluent is pumped from the filling unit 51 into the valve, via diluent inlet tube 52.
In the preferred embodiment of this invention, two metering valves 30 and 30' are utilized in order to obtain, for example, two O.l5 ml. samples and two 0.1 ml. samples. The valves are conveniently mounted on a first surface of mounting board 53, which is, in turn, conveniently coupled to housing 11 via support member 54 and mounting brackets 55.
The sample injection valve manufactured by Chromatonix Inc. is particularly suitable for providing the sample metering means of the present invention when modified to operate in accord with the above discussion. However, any other suitable metering means can be utilized.
The operation of the valve 30 can be more fully understood by the diagram of FIG. 3. The sample is drawn into a first section 56 of valve 30 via sample probe 32. The sample follows flow passage 57 to loop 45, and is drawn into a second section 56 of the valves, through passage 64, through vacuum valve 65 and to waste. When the vacuum valve is shut off, loop 45 remains filled until sections 56 and 56' are switched to their alternate positions as shown in FIG. 4. The diluent then passes through passage 58, into loop 45, thereby washing out the sample via passage 60 and through the delivery tube to the awaiting sample receiving means.
Concurrently with the diluent delivery through loop 45, loop 49 is connected to the sample probe via passage 61 and 62, thereby filling loop 49 with the same sample. Return of 56 and 56' to the first position now connects loop 49 with the diluent via passage 63 and 66.
The valves are preferably of Teflon and Kel-F, although other suitable materials can be employed. Similarily, the loops are preferably Teflon.
The sample receiving means 47 are conveniently held in racks 82. The racks are then conveniently advanced automatically into the proper position by an automatic conveyor means 83, cooperatively associated with housing 11 and mounting board 53 so that for each delivery cycle, a sample receiving means is aligned beneath a delivery tube.
It can be seen that the diluter module provides a convenient, accurate means for automatically pipetting a given amount of sample, delivering the sample to a sample holder such as a test tube or the like, and adding.
thereto, a predetermined amount of medium, diluent, reagent, or the like.
Referring now to FIG. 5, the reader module of this invention is shown generally at 70. The diluted samples obtained from the diluter module, or any other suitable means, are, after proper incubation or reaction time, transferred in the racks 82 to an automatic conveyor means 83, or other suitable advancing means. It can be seen that the racks are guided by guide means 71, and that a retaining plate 72 is positioned behind the last rack. The samples are drawn into a suitable photometer 73 by probe assembly 31. The samples are passed through flow cell 74 via inlet tube 75 and through outlet tube 76 to a waste receiving means (not shown). The flow cell is preferably quartz or a like material, and replaces the cuvette of conventional readers. A solenoid valve (not shown) in the control unit 79 controls the sample flow. The control circuit is adapted to momentarily drop out the solenoid and interrupt the sample flow before it reaches the flow cell. This produces an air hammer effect which takes care of any air bubbles present in the flow stream. It is presently preferred, when determining the turbidity of rodshaped organisms, that the flow cell permit a rate of flow of not less than 0.8 ml./sec., and preferably a rate of l ml./sec. or higher in order to obtain highly accurate, reproducible results. For other assays, the flow rate is not critical. The readings can be taken from the scale 77 of the photometer 73, or, as in the preferred embodiment, a suitable readout device 78 can be cooperatively associated with the photometer.
The readout is compatible with a variety of data acquisition devices such as printed tape, punched paper tape, punched cards, or can be interfaced directly to a computer.
The reader module of this invention provides a great advance in the art by providing a means for overcoming the problems of measuring the turbidity of rod-shaped organisms by avoiding the flow birefringence problem normally encountered with rod-shaped particles. By producing a sufficiently rapid flow through the flow cell, rod-shaped particles, which would otherwise orient themselves with the slow currents in a static cell, leading to inconsistent readings, are read with the same precision as are spherical particles. Thus the present reader module now makes it possible to assay for substances which affect various rod-shaped organisms such as Klebsiella, Lactobacillus, Pseudomonas, and the like, and to determine them with a precision equivalent to spherical organisms, all other factors being equal.
While the present invention is particularly suited for turbidimetric microbiological assays, it will be apparent to those skilled in the art that the diluter module and the reader module can be used ointly or separately in any number of analytical procedures, medical laboratory tests, and the like. Therefore, while the following discussion is directed toward turbidimetric microbiological assays, the modules of this invention are applicable to any suitable analytical procedures.
We claim:
1. In an automatic dilutor module the improvement comprising: a valve means having first and second sections, said first section having a diluent supply inlet connected to a metered diluent supply and a sample supply inlet connected to a sample supply, a pair of loops of predetermined volume having their first ends connected to a pair of respective outlets in said valve means first section in alternately selective communication with said diluent supply and said sample supply, said loops having their second ends in alternately selective communication with a pair of respective discharge outlets in said second section of said valve means, said pair of discharge outlets in said second section of said valve means being in communication with a waste receptacle and a delivery receptacle, and control means associated with said first and second sections alternately effecting coupling of each of said loops between (a) said diluent supply inlet and said delivery receptacle; and (b) said sample supply inlet and said waste receptacle.
2. In an automatic dilutor module the improvement in accordance with claim 1 in which said loops are interchangeably mounted.
3. In an automatic dilutor module the improvement in accordance with claim 2 in which the coupling of one loop between said diluent supply inlet and said delivery receptacle is concurrent with the coupling of the other loop between said sample supply inlet and said waste receptacle.
4. In an automatic dilutor module the improvement in accordance with claim 3 in which the communication betweensaid sample supply inlet and said sample supply includes a probe extending into said sample supply.
5. In an automatic dilutor module the improvement in accordance with claim 4 in which said sample supply is contained in a plurality of open-mouth receptacles.
6. In an automatic dilutor module the improvement in accordance with claim 5 in which said probe is reciprocably mounted and associated with a drive means for imparting vertical movement thereto.
7. ln an automatic dilutor module the improvement in accordance with claim 6 in which said open-mouth receptacles containing said sample supply are automatically driven in succession under said probe and in synchronization with 'the vertical movement of said probe.
8. In an automatic dilutor module the improvement in accordance with claim 7 in which a plurality of delivery receptacles are automatically driven in successive synchronized communication with the discharge of diluted samples from the one of said discharge outlets.
Claims (8)
1. In an automatic dilutor module the improvement comprising: a valve means having first and second sections, said first section having a diluent supply inlet connected to a metered diluent supply and a sample supply inlet connected to a sample supply, a pair of loops of predetermined volume having their first ends connected to a pair of respective outlets in said valve means first section in alternately selective communication with said diluent supply and said sample supply, said loops having their second ends in alternately selective communication with a pair of respective discharge outlets in said second section of said valve means, said pair of discharge outlets in said second section of said valve means being in communication with a waste receptacle and a delivery receptacle, and control means associated with said first and second sections alternately effecting coupling of each of said loops between (a) said diluent supply inlet and said delivery receptacle; and (b) said sample supply inlet and said waste receptacle.
2. In an automatic dilutor module the improvement in accordance with claim 1 in which said loops are interchangeably mounted.
3. In an automatic dilutor module the improvement in accordance with claim 2 in which the coupling of one loop between said diluent supply inlet and said delivery receptacle is concurrent with the coupling of the other loop between said sample supply inlet and said waste receptacle.
4. In an automatic dilutor module the improvement in accordance with claim 3 in which the communication between said sample supply inlet and said sample supply includes a probe extending into said sample supply.
5. In an automatic dilutor module the improvement in accordance with claim 4 in which said sample supply is contained in a plurality of open-mouth receptacles.
6. In an automatic dilutor module the improvement in accordance with claim 5 in which said probe is reciprocably mounted and associated with a drive means for imparting vertical movement thereto.
7. In an automatic dilutor module the improvement in accordance with claim 6 in which said open-mouth receptacles containing said sample supply are automatically driven in succession under said probe and in synchronization with the vertical movement of said probe.
8. In an automatic dilutor module the improvement in accordance with claim 7 in which a plurality of delivery receptacles are automaticalLy driven in successive synchronized communication with the discharge of diluted samples from the one of said discharge outlets.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12284371A | 1971-03-10 | 1971-03-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3712144A true US3712144A (en) | 1973-01-23 |
Family
ID=22405103
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00122843A Expired - Lifetime US3712144A (en) | 1971-03-10 | 1971-03-10 | Automated system for performing sample measurement, dilutions and photometric measurements |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3712144A (en) |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773423A (en) * | 1972-08-22 | 1973-11-20 | Hach Chemical Co | Automatic analyzer |
| US3888125A (en) * | 1973-04-10 | 1975-06-10 | El Mochida | Pump for preparing diluted liquids of predetermined degrees of dilution |
| US4070913A (en) * | 1976-08-31 | 1978-01-31 | Phillips Petroleum Company | Sample dilution |
| DE2755264A1 (en) * | 1976-12-17 | 1978-08-17 | Eastman Kodak Co | CHEMICAL ANALYSIS EQUIPMENT |
| FR2387443A1 (en) * | 1977-04-14 | 1978-11-10 | Baxter Travenol Lab | MODULAR CHEMICAL ANALYSIS SYSTEM |
| US4891185A (en) * | 1988-01-22 | 1990-01-02 | Goldin Stanley M | High resolution monitoring device |
| US5047210A (en) * | 1987-12-04 | 1991-09-10 | Melet Schloesing Laboratories | Device for presenting receptacles |
| US5319986A (en) * | 1991-02-26 | 1994-06-14 | Computer Control Corporation | Sampler with magazine system |
| FR2726652A1 (en) * | 1994-11-07 | 1996-05-10 | Merck Clevenot Laboratoires | AUTOMATIC IMMUNOASSAY APPARATUS |
| WO1996014582A1 (en) * | 1994-11-07 | 1996-05-17 | Laboratoires Merck-Clevenot | Automatic immunoassay apparatus |
| US5585068A (en) * | 1990-02-20 | 1996-12-17 | Biochemical Diagnostics, Inc. | Apparatus for automatically separating a compound from a plurality of discrete liquid specimens |
| WO1998047999A1 (en) * | 1997-04-18 | 1998-10-29 | Centro Nacional De Investigaciones Cientificas (Cnic) | Equipment, kit and method for microbiological diagnosis |
| US20080085219A1 (en) * | 2006-10-05 | 2008-04-10 | Beebe David J | Microfluidic platform and method |
| EP1992407A1 (en) * | 2007-05-09 | 2008-11-19 | Alcorlab A/S | Method and apparatus for oligo peptide synthesis |
| US10478821B2 (en) | 2017-04-20 | 2019-11-19 | Biomerieux, Inc. | Optical density instrument and systems and methods using the same |
| WO2021019267A1 (en) * | 2019-07-26 | 2021-02-04 | Bit Group France | Differential dispensing method |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3467500A (en) * | 1966-08-18 | 1969-09-16 | American Home Prod | Automatic sample digesting device |
| US3567390A (en) * | 1968-04-03 | 1971-03-02 | Coulter Electronics | Fluid transfer valve structure and diluting system |
| US3567398A (en) * | 1968-10-23 | 1971-03-02 | Farr Devices Inc | Semi-automatic pipetting and diluter device |
| US3567389A (en) * | 1968-04-03 | 1971-03-02 | Coulter Electronics | Fluid transfer valve structure |
-
1971
- 1971-03-10 US US00122843A patent/US3712144A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3467500A (en) * | 1966-08-18 | 1969-09-16 | American Home Prod | Automatic sample digesting device |
| US3567390A (en) * | 1968-04-03 | 1971-03-02 | Coulter Electronics | Fluid transfer valve structure and diluting system |
| US3567389A (en) * | 1968-04-03 | 1971-03-02 | Coulter Electronics | Fluid transfer valve structure |
| US3567398A (en) * | 1968-10-23 | 1971-03-02 | Farr Devices Inc | Semi-automatic pipetting and diluter device |
Cited By (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3773423A (en) * | 1972-08-22 | 1973-11-20 | Hach Chemical Co | Automatic analyzer |
| US3888125A (en) * | 1973-04-10 | 1975-06-10 | El Mochida | Pump for preparing diluted liquids of predetermined degrees of dilution |
| US4070913A (en) * | 1976-08-31 | 1978-01-31 | Phillips Petroleum Company | Sample dilution |
| DE2755264A1 (en) * | 1976-12-17 | 1978-08-17 | Eastman Kodak Co | CHEMICAL ANALYSIS EQUIPMENT |
| FR2387443A1 (en) * | 1977-04-14 | 1978-11-10 | Baxter Travenol Lab | MODULAR CHEMICAL ANALYSIS SYSTEM |
| US5047210A (en) * | 1987-12-04 | 1991-09-10 | Melet Schloesing Laboratories | Device for presenting receptacles |
| US4891185A (en) * | 1988-01-22 | 1990-01-02 | Goldin Stanley M | High resolution monitoring device |
| US5585068A (en) * | 1990-02-20 | 1996-12-17 | Biochemical Diagnostics, Inc. | Apparatus for automatically separating a compound from a plurality of discrete liquid specimens |
| US5319986A (en) * | 1991-02-26 | 1994-06-14 | Computer Control Corporation | Sampler with magazine system |
| FR2726652A1 (en) * | 1994-11-07 | 1996-05-10 | Merck Clevenot Laboratoires | AUTOMATIC IMMUNOASSAY APPARATUS |
| WO1996014582A1 (en) * | 1994-11-07 | 1996-05-17 | Laboratoires Merck-Clevenot | Automatic immunoassay apparatus |
| WO1998047999A1 (en) * | 1997-04-18 | 1998-10-29 | Centro Nacional De Investigaciones Cientificas (Cnic) | Equipment, kit and method for microbiological diagnosis |
| US6537772B1 (en) | 1997-04-18 | 2003-03-25 | Centro Nacional De Investigaciones | Equipment, kit and method for microbiological diagnosis |
| US20080085219A1 (en) * | 2006-10-05 | 2008-04-10 | Beebe David J | Microfluidic platform and method |
| EP1992407A1 (en) * | 2007-05-09 | 2008-11-19 | Alcorlab A/S | Method and apparatus for oligo peptide synthesis |
| WO2008138338A1 (en) | 2007-05-09 | 2008-11-20 | Alcorlab A/S | Method and apparatus for oligo peptide synthesis |
| US20100184232A1 (en) * | 2007-05-09 | 2010-07-22 | Peter Jepsen | Method and apparatus for oligo peptide synthesis |
| US11148144B2 (en) | 2017-04-20 | 2021-10-19 | Biomerieux, Inc. | Method, apparatus, and computer program product for controlling components of a detection device |
| US10625265B2 (en) | 2017-04-20 | 2020-04-21 | Biomerieux, Inc. | Optical test platform |
| US11141733B2 (en) | 2017-04-20 | 2021-10-12 | Biomerieux, Inc. | Optical density instrument and systems and methods using the same |
| US10478821B2 (en) | 2017-04-20 | 2019-11-19 | Biomerieux, Inc. | Optical density instrument and systems and methods using the same |
| US11192112B2 (en) | 2017-04-20 | 2021-12-07 | Biomerieux, Inc. | Optical test platform |
| US11285487B2 (en) | 2017-04-20 | 2022-03-29 | Biomerieux, Inc. | Tip resistant optical testing instrument |
| US11673141B2 (en) | 2017-04-20 | 2023-06-13 | Biomerieux, Inc. | Method, apparatus, and computer program product for controlling components of a detection device |
| US11779931B2 (en) | 2017-04-20 | 2023-10-10 | Biomerieux Inc. | Optical density instrument and systems and methods using the same |
| US11938483B2 (en) | 2017-04-20 | 2024-03-26 | Biomerieux, Inc. | Optical test platform |
| WO2021019267A1 (en) * | 2019-07-26 | 2021-02-04 | Bit Group France | Differential dispensing method |
| EP4004521A1 (en) * | 2019-07-26 | 2022-06-01 | BIT Group France | Differential dispensing method |
| EP4004521B1 (en) * | 2019-07-26 | 2025-05-21 | Bit Group France | Differential dispensing method |
| US12385816B2 (en) | 2019-07-26 | 2025-08-12 | Bit Group France | Differential dispensing method |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3609040A (en) | Automated system for performing sample measurements, dilutions and photometric measurements | |
| US3712144A (en) | Automated system for performing sample measurement, dilutions and photometric measurements | |
| EP0089346B1 (en) | Automated immunoassay system | |
| US5232665A (en) | Multi-linear automatic apparatus for processing immunoassays | |
| CA1284871C (en) | Pipetting device having an automatic mechanism for replacing nozzle tips | |
| US3881872A (en) | Automatic analyzing device | |
| EP0490358B1 (en) | Apparatus for automatically processing magnetic solid phase reagents | |
| US4837159A (en) | Method and apparatus for effecting immunological analysis | |
| US4013413A (en) | Apparatus and method for rapid analyses of plurality of samples | |
| US6808304B2 (en) | Method for mixing liquid samples using a linear oscillation stroke | |
| JP2002506989A (en) | Electronic device for dispensing fluid in precise small volumes | |
| US7338803B2 (en) | Method for increasing capacity in an automatic clinical analyzer by using modular reagent delivery means | |
| EP1543334B1 (en) | Increasing throughput of an automatic clinical analyzer system by partitioning assays according to frequency of requested performance | |
| JPH02269970A (en) | Method and apparatus for conducting automatic sample analysis tests | |
| EP0500506A1 (en) | Immunoassay apparatus | |
| US4767600A (en) | Equipment for rapid, automatic chemical-clinical analysis | |
| US3567393A (en) | Automatic apparatus for the determination of fluids and in particular biological fluids | |
| US3537794A (en) | Apparatus for the automatic analysis of a plurality of blood samples with means for agitation of each sample | |
| US20020064881A1 (en) | Method for automatically storing and reprocessing patient specimen's in an automatic clinical analyzer | |
| US4268268A (en) | Method and apparatus for characterization of cells, particles, and liquids | |
| US5130095A (en) | Automatic chemistry analyzer | |
| US5324479A (en) | Analyzer for the determination of the phenotype and the ABO blood group | |
| JPH06308133A (en) | Inspecting apparatus for specimen | |
| Malmstadt et al. | Automated reaction-rate methods of analysis | |
| US20020064884A1 (en) | Method for automatically storing and reprocessing patient specimen's in an automatic clinical analyzer |