WO2000037157A1 - Automated on-line evaporating light scattering detection to quantify isolated fluid sample compounds in microtiter plate format - Google Patents

Automated on-line evaporating light scattering detection to quantify isolated fluid sample compounds in microtiter plate format Download PDF

Info

Publication number
WO2000037157A1
WO2000037157A1 PCT/US1999/030514 US9930514W WO0037157A1 WO 2000037157 A1 WO2000037157 A1 WO 2000037157A1 US 9930514 W US9930514 W US 9930514W WO 0037157 A1 WO0037157 A1 WO 0037157A1
Authority
WO
WIPO (PCT)
Prior art keywords
fluid
compounds
isolated
fluid sample
fraction
Prior art date
Application number
PCT/US1999/030514
Other languages
French (fr)
Inventor
Robert A. Zambias
Daniel B. Kassel
Original Assignee
Dupont Pharmaceuticals Research Laboratories, Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Dupont Pharmaceuticals Research Laboratories, Inc. filed Critical Dupont Pharmaceuticals Research Laboratories, Inc.
Priority to JP2000589263A priority Critical patent/JP2002537543A/en
Priority to CA002356218A priority patent/CA2356218A1/en
Priority to EP99966531A priority patent/EP1144068A4/en
Priority to AU22046/00A priority patent/AU2204600A/en
Publication of WO2000037157A1 publication Critical patent/WO2000037157A1/en

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/80—Fraction collectors
    • G01N30/82—Automatic means therefor
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00277—Apparatus
    • B01J2219/00279—Features relating to reactor vessels
    • B01J2219/00306—Reactor vessels in a multiple arrangement
    • B01J2219/00313—Reactor vessels in a multiple arrangement the reactor vessels being formed by arrays of wells in blocks
    • B01J2219/00315—Microtiter plates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/00583—Features relative to the processes being carried out
    • B01J2219/00585—Parallel processes
    • B01J2219/00587—High throughput processes
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/00274—Sequential or parallel reactions; Apparatus and devices for combinatorial chemistry or for making arrays; Chemical library technology
    • B01J2219/0068—Means for controlling the apparatus of the process
    • B01J2219/00702—Processes involving means for analysing and characterising the products
    • B01J2219/00707—Processes involving means for analysing and characterising the products separated from the reactor apparatus
    • C—CHEMISTRY; METALLURGY
    • C40—COMBINATORIAL TECHNOLOGY
    • C40B—COMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B60/00—Apparatus specially adapted for use in combinatorial chemistry or with libraries
    • C40B60/14—Apparatus specially adapted for use in combinatorial chemistry or with libraries for creating libraries
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/62—Detectors specially adapted therefor
    • G01N30/72—Mass spectrometers
    • G01N30/7233—Mass spectrometers interfaced to liquid or supercritical fluid chromatograph
    • G01N30/724—Nebulising, aerosol formation or ionisation
    • G01N30/7266—Nebulising, aerosol formation or ionisation by electric field, e.g. electrospray
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/62—Detectors specially adapted therefor
    • G01N30/74—Optical detectors
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/62—Detectors specially adapted therefor
    • G01N30/78—Detectors specially adapted therefor using more than one detector

Definitions

  • the present invention relates to quantifying (or measuring the amounts) of reaction compounds which are fraction collected in microtiter plate format.
  • each tube in the rack needs to be individually removed, weighed and its weight recorded.
  • the compounds are then fraction collected into the individual tubes in the rack.
  • the tubes are removed one after another from the rack and are placed m a device which concentrates them down by drying the contents of the tube.
  • the dried tubes are individually re-weighed and the net weight of each sample in the fraction collection tubes is then determined by comparing the initial weight of the empty tube with the weight of the tube with the dried compound therein. The weight information so determined allows the compounds to be redissolved with a volatile solvent to a desired set point molarity.
  • the tubes are then placed into a rack and an aliquot is delivered into a microtiter plate for use m a biological assay.
  • the present invention provides methods ana systems for measuring the total masses of individual compounds present m fluid samples, ana is particularly well adapted for use with fluid samples prepared in microtiter plate format.
  • the individual compounds are isolated by fluid separation systems including high performance liquid chromatography columns and supercritical fluid columns. Small portions of the individual compounds isolated by fluid separation are then analyzed by a mass spectrometer, (which determines the compound molecular weight) , and by an evaporative light scattering detector, (which determines the total masses of each of the isolated compounds passing therethrough) .
  • the present invention provides a single pass system which measures the masses of the individual compounds diverted into fraction collectors in real-time, as follows.
  • the signal generated by the mass spectrometer is used to determine the interval of time during which fraction collection is to be carried out.
  • the signal generated by the evaporative light scattering detector is used to determine the total amount of mass diverted therethrough during the interval of time during which fraction collection is carried out.
  • an advantage of the present invention is that, during only a single pass through the system, each fluid sample is partitioned into isolated compounds which are individually weighed in real time as they pass into fraction collectors.
  • microtiter plate formats can be used both for sample preparation reactions and for fraction collection of the individual compounds present m such samples. Accordingly, the present invention provides a single-pass system for the synthesis, isolation, weight measurement, and delivery of compounds n microtiter plate formats. Another advantage of the present invention is that it is able to determine the total mass of the individual isolated compounds present in microtiter plate fluid samples at the same time that these individual compounds are being fraction collected in microtiter plate format. As such, only a single pass of a fluid sample through the system is required to isolate the individual compounds in the fluid sample, to fraction collect the individual isolated compounds and determine the total collected masses of these isolated compounds.
  • an additional important advantage of the present microtiter plate format single pass system is that it completely avoids individually removable fraction collection tubes. Accordingly, it is not necessary to individually weigh individual tubes containing fractionated fluid samples. Consequently, it is not necessary to separately track and label such tubes or to transfer individual tubes between various liquid handling, concentrator and fraction collection devices. As such, the problem of individual tubes being misplaced or transposed and the amount of time involved with transferring individual collection tubes is completely avoided.
  • another advantage of the present invention is that by using a high density microtiter plate format, the present invention reduces the actual amount of material which needs to be synthesized, (as compared to existing non-microtiter plate format systems), thereby resulting in cost savings through the reduced costs of synthetic chemicals. By using a small volume microtiter system, solvent consumption is reduced.
  • An additional advantage of the present small volume microtiter plate format is that, in preferred aspects, more difficult chromatographic separations can be achieved with the resolution of present invention's preparatory or semi-preparatory chromatographic column where the resolution approaches that of a conventional smaller analytical chromatographic column.
  • Existing systems which remove and re-weigh fraction collection tubes individually can not be operated with the small fluid sample volumes of the present microtiter based system since inaccuracies in the weight of the tube itself may account for larger weight differences than the weight of the collected fluid sample therein. As such, significant errors can be introduced to the net weight of each product.
  • the present invention completely avoids this problem.
  • a plurality of fluid samples are first provided in a standard microtiter plate format.
  • An autosampler is then used to sequentially load the fluid samples onto a fluid separation system which preferably comprises a preparatory or semi-preparatory high performance liquid chromatography (HPLC) column or a supercritical fluid chromatography (SFC) column, which separates the components in each fluid sample such that individual compounds are isolated by sequential elution from the fluid column.
  • HPLC high performance liquid chromatography
  • SFC supercritical fluid chromatography
  • a very small portion, (typically on the order of 1%), of the sequentially eluted isolated compounds in the separated fluid sample are diverted into a mass spectrometer which determines the molecular weight of the individual isolated compounds passing therethrough.
  • the signal generated by the mass spectrometer will correspond to the molecular weight of the compound passing therethrough such that fraction collection can be performed when a desired isolated compound is present m a desired concentration.
  • the output signal of the mass spectrometer can be used to signal the interval of time during which fraction collection is to be performed.
  • a very small portion, (typically on the order of 1%) of the sequentially eluted isolated compounds in the fluid sample are diverted into an evaporative light scattering detector.
  • the evaporative light scattering ⁇ etector generates a chromatographic signal of the sequentially eluted isolated compounds which is proportional to the total masses of the various compounds passing therethrougn .
  • An advantage of evaporative light scattering detection is tnat it is mass dependent and will tend to be generally uniform over a wide range of different chemical structures. Accordingly, a single calibration curve can be generated between masses passing through the evaporative light scattering detector and its signal output.
  • the mass spectrometer is used to selectively signal fraction collection of the compounds isolated in the flui ⁇ sanrole on the basis of their molecular weights and the lignt scattering detector signal is used to determine the actual total masses of the isolated compounds which are collected into the fraction collection microtiter plates .
  • each isolated compound diverted into the light scattering detector (as compared to the remainder which is directed either to fraction collection or to waste) , will be the same for all isolated compounds and will be determined by the dimensions of the splitter device used to divert a portion of the fluid sample into the light scattering detector.
  • the portion of each isolated compound which is fraction collected as opposed to being diverted to waste will vary for different compounds, being dependent upon the portion of time during which fraction collection is carried out. The portion of time during which fraction collection is carried out will in turn depend upon the amount of time during which the compound is eluted at a sufficient purity for fraction collection.
  • the total masses of each of the individual fraction collected compounds is determined by measuring the signal generated by the light scattering detector, (which is proportional to the total mass of the compound passing to the fraction collector) , during the interval in time in which the compound is eluted and fraction collected, (as determined by the mass spectrometer) .
  • the amount of mass present in any of the various isolated fraction collected compounds is calculated.
  • a calibration curve between the mass passing through the evaporative light scattering detector and the signal generated by the evaporative light scattering detector is determined.
  • Such a calibration curve can be established by determining the signal output when passing known masses through the light scattering detector.
  • microtiter plate fraction collector can then itself later be concentrated by being dried down. Afterwards, it can be reconstituted to set point molarity based upon the weight of each isolated compound as determined by the light scattering detector. As such, the microtiter plate can itself be used to create daughter plates directly without any reformatting or weighing .
  • the present invention can be used to automatically calculate the yield of a given reaction. Moreover, such mass determinations can also be used as a control function when fraction collecting such that a maximum amount of an isolated compound can be collected, with the remainder being diverted to a second fraction collector or to waste.
  • the present system can be adapted to perform simultaneous real time mass determinations of a plurality of fraction collected samples, wherein a plurality of simultaneously eluted fluid samples can be analyzed by the evaporative light scattering detector and the mass spectrometer.
  • parallel simultaneously eluted fluid samples pass through a switching valve such that each of the samples can be analyzed by the evaporative light scattering detector and the mass spectrometer in turn.
  • parallel light scattering detection is performed by a plurality of lasers or with a single laser having its beam sequentially directed towards the various samples eluted in parallel.
  • Fig. 1 is a schematic view of an apparatus for carrying out the present invention.
  • Fig. 2 is a schematic view corresponding to Fig.
  • Fig. 3 is a schematic view of an alternate system for carrying out parallel evaporative light scattering detection comprising a movable scanning mirror and a single laser .
  • Fig. 4 is a schematic view of another alternate system for carrying out parallel evaporative light scattering detection comprising a plurality of lasers.
  • a plurality of chemical compounds can be synthesized or provided in microtiter plate format m reaction wells 11 of microtiter plate 10.
  • a fluid handling robot 12, which may comprise a Gilson 215 Autosampler is adapted to draw up each of the fluid samples present m wells 11 of microtiter plate 10, and to sequentially load each of the fluid samples m wells 11 onto a fluid separation column 14.
  • Fluid separation column 14 may preferably comprise a high performance liquid chromatography (HPLC) column or a supercritical fluid (SFC) column composed of a solid sorbent material which operates to separate each of the component compounds in the fluid sample passing therethrough such that isolated compounds are sequentially eluted from the end of the column. Specifically, since each of the different component compounds found m each fluid sample will interact differently with the solid sorbent material contained within the separation column, each will accordingly take different amounts of time to pass through and be eluted out of the exit end of the column.
  • Column 14 may preferably comprise a C18 Reverse Phase semi-preparatory or preparatory fluid separation column.
  • fluid separation column 14 can be replaced by any form of fluid partitioning system.
  • Mass spectrometer 16 determines the molecular weights of the isolated compounds in the fluid sample passing sequentially therethrough and generates a signal corresponding to the molecular weights of the isolated compounds. Accordingly, mass spectrometer 16 identifies each of the isolated compounds passing sequentially therethrough on the basis of their respective molecular weights.
  • a liquid handling robot 20 is signaled to collect the desired compound in corresponding wells 17a of microtiter plate 18a of fraction collector 19.
  • fraction collector 19 preferably comprises a plurality of microtiter plate collector racks (ie: individual microtiter plates shown here as 18a and 18b) .
  • liquid handling robot 20 could be replaced by a simple on/off valve or valving system.
  • a single microtiter plate 18a may be used.
  • the same spatial address is maintained between wells 11 in microtiter plate 10 and wells 17a in microtiter plate 18a when one isolated compound is fraction collected from each of the wells in microtiter plate 10.
  • a plurality of microtiter plates, shown here as 18a and 18b, can be used such that first isolated compounds can be collected in wells 17a of microtiter plate 18a and second isolated compounds can be collected in wells 17b of microtiter plate 18b.
  • microtiter plates can be used as required when more than two compounds are fraction collected wells 11 of plate 10.
  • a plurality of individual fraction collectors can be used for fraction collection.
  • a plurality of fraction collector racks ie: microtiter plates
  • column 14 and fraction collector 18 can be used together to purify fluid samples by first separating a fluid sample into isolated compounds on column 14 and then collecting only desired compounds into fraction collector 18 on the basis of the signal output of mass spectrometer 16. Specifically, when desired compounds are not present in sufficient purity, or when undesirable compounds are eluted , (as indicated by the output signal of mass spectrometer 16) , fraction collection is not performed, such that the non-desired portions of the fluid sample are conveniently expelled as waste W.
  • the amounts of flow diverted to splitters 21 and 22, and the volume of connecting tubes 32, 34 and 36, is set such that eluting compounds from column 14 reaches each of mass spectrometer 16, evaporative light scattering detector 24 and microtiter plate fraction collector 18 at the same time. Accordingly, at the moment in time when mass spectrometer 16 signals that fraction collection of a particular isolated compound reaching mass spectrometer 16 should commence, the same particular isolated compound will be reaching liquid handling robot 20 such that it can be diverted into fraction collector microtiter plate 18. Therefore, compound purification can be performed in real time .
  • a small portion, (typically on the order of 1%), of the separated fluid sample is diverted by splitter 22, (which preferably comprises a Valco Splitter Tee) , towards an evaporative light scattering detector 24.
  • Light scattering detector 24 measures the total mass of the fluid sample passing therethrough on the basis of the amount of light scattered per unit mass passing therethrough.
  • the signal generated by the light scattering detector will be in the form of an integer number of "area counts" which correspond to the mass of sample passing through the detector. Specifically, the area counts are integrated to determine the mass of sample passing through the detector. As such, progressively larger masses passing through the detector generate greater numbers of area counts .
  • the actual total mass of any particular individual isolated compound which is fraction collected is determined by the mass passing through the light scattering detector during the interval of time during which fraction collection is performed.
  • the mass passing through the light scattering detector represents a fixed portion (typically about 1%, depending upon the splitter arrangement used) , of the mass passing into fraction collector 18 during the interval of time in which fraction collection is carried out.
  • the total mass passing through the light detector is used to accurately determine the total mass of the fraction collected compound.
  • a calibration curve is established for light scattering detector 24 by passing different known masses through the light scattering detector 24 and recording the number of area counts generated by the different known masses .
  • the particular isolated compound will reach light scattering detector 24 at the same time that it reaches mass spectrometer 16 and fraction collector microtiter plates 18. Accordingly, the signal generated by mass spectrometer 16 and light scattering detector 24 will correspond to the same particular isolated compound in the fluid sample.
  • the present invention can be adapted for parallel evaporative light scattering detection such that a plurality of fluid separation columns 14a, 14b and 14c can be used at once.
  • autosampler 12 loads different fluid samples onto a plurality of fluid columns 14a, 14b, 14c. Separated fluid samples are then simultaneously eluted from each of fluid columns 14a, 14b, 14c.
  • a selective electrospray blocking system 40 rapidly selects between electrosprays of each of the simultaneously eluted fluid samples such that electrosprays of each of the separated fluid samples reach mass spectrometer 16 one after another. By rapidly selecting between each of the simultaneously eluted fluid samples, each of the isolated compounds present in the separated fluid samples can be detected.
  • selective blocking system 40 comprises a rotating disc 41 having an off-center hole 42 passing therethrough and each of fluid columns 14a, 14b, and 14c are connected to a parallel channel electrosprayer 43 such that the fluid eluted from each of fluid columns 14a, 14b, and 14c is electrosprayed to pass in sequence through the hole 42 in rotating disc 41 as disc 41 is rotated.
  • parallel channel electrosprayer 43 preferably directs electrosprayed effluents from each of fluid columns 14a, 14b, and 14c towards locations which are equidistant from the center of the rotating disc and which are at a distance equal to the distance from the center of hole 42 to the center of rotating disc 41.
  • Fluid splitters 100a, 100b and 100c (which may preferably comprise Valco splitter Tees) , divert the majority (typically 99%) of the separated fluid samples toward electrosprayer 24.
  • fluid splitters 102a, 102b and 102c (which may also preferably comprise
  • Valco splitter Tees divert a small portion (typically 1%) of the separated fluid samples into electrosprayer 24, (which comprises parallel drift tubes 72a, 72b and 72c as will be explained) .
  • Fluid splitters 102a, 102b and 102c divert a majority, (typically 99%), of the separated fluid sample to liquid handling robot 20 for fraction collecting in fraction collectors 19a, 19b and 19c.
  • FIG. 3 shows a system for parallel light scattering detection in which fluid columns 14a, 14b and 14c simultaneously elute separated fluid samples which are separately and sequentially sampled by a laser light source, as follows.
  • Nebulizers 70a, 70b and 70c are each connected to a nitrogen source.
  • Nebulizers 70a, 70b and 70c cause the fluid samples sequentially eluted from each of fluid columns 14a, 14b and 14c to be passed as aerosol sprays along through drift tubes 72a, 72b and 72c, respectively.
  • Laser 50 emits a beam 51 which is selectively directed towards the aerosol spray corresponding to the fluid eluted by each of the three fluid columns in sequence.
  • a beam selector 52 (which preferably comprises a movable scanning mirror) directs beam 51 from laser 50 in sequence toward the effluent of each of fluid columns 14a, 14b, and 14c.
  • Laser beam 51 is scattered by each of the effluent streams and is received by photodetectors 54a, 54b and 54c, respectively, as the beam is scanned from fluid column 14a to 14b to 14c.
  • Each of photodetectors 54a, 54b and 54c will preferably be operated together with a dedicated amplifier 56a, 56b and 56c. Accordingly, when laser beam 51 is directed towards each of the effluent streams, scattered light can be detected and amplified into a chromatographic signal. Rapid sequential sampling of each of the effluent streams provides an independent chromatograph for each column 14.
  • Fig. 4 shows another alternate system for parallel light scattering detection in which fluid columns 14a, 14b and 14c simultaneously elute separated fluid samples which are simultaneously sampled by separate laser light sources, as follows.
  • a plurality of separate drift tubes 60a, 60b and 60c, each having dedicated light sources 64a, 64b, 64c; and photomultipliers 66a, 66b and 66c are used.
  • the ability to perform parallel evaporative light scattering detection (ie: to perform evaporative light scattering detection on a plurality of separated fluid samples at the same time) , provides very high throughput quantitation of the masses of the isolated compounds present in a plurality of fluid samples.

Landscapes

  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)

Abstract

Single pass methods and systems for measuring the total masses of individual compounds present in fluid samples in real time, and particularly for fluid samples prepared in microtiter plate format are provided. Individual compounds are isolated by fluid separation column (14). Portions of the individual compounds isolated by column (14) are analyzed by mass spectrometer (16), which determines their concentration on the basis of their molecular weights, and an evaporative light scattering detector (24), (which determines the total masses of each of the isolated compounds passing therethrough). Total collected masses of the individual compounds are calculated by determining the amount and portion of the isolated compounds diverted into evaporative light scattering detector (24) during a period of fraction collection.

Description

AUTOMATED ON-LINE EVAPORATING LIGHT SCATTERING DETECTION TO QUANTIFY ISOLATED FLUID SAMPLE COMPOUNDS IN MICROTITER PLATE
FORMAT
TECHNICAL FIELD
The present invention relates to quantifying (or measuring the amounts) of reaction compounds which are fraction collected in microtiter plate format.
BACKGROUND OF THE INVENTION
Systems exist for the parallel synthesis of various chemical compounds in microtiter plate format. Accordingly, many liquid handling systems have been developed for automated parallel synthesis in conjunction with such microtiter plate formats. High throughput liquid chromatography/mass spectrometry systems capable of isolating compounds on the basis of their molecular weight have also been developed. However, a system for easily and efficiently determining the total collected masses of compounds which are fraction collected in microtiter plate format has proven elusive. In general, existing high throughput liquid chromatography/mass spectrometry systems isolate compounds by fractionation into fraction collector tubes which are individually removable from a rack. Numerous problems exist when attempting to quantify the total mass of each of the compounds collected in the various fraction collector tubes. First, each tube in the rack needs to be individually removed, weighed and its weight recorded. The compounds are then fraction collected into the individual tubes in the rack. Subsequent to fraction collection, the tubes are removed one after another from the rack and are placed m a device which concentrates them down by drying the contents of the tube. After the contents of the tube have been concentrated down by drying, the dried tubes are individually re-weighed and the net weight of each sample in the fraction collection tubes is then determined by comparing the initial weight of the empty tube with the weight of the tube with the dried compound therein. The weight information so determined allows the compounds to be redissolved with a volatile solvent to a desired set point molarity. The tubes are then placed into a rack and an aliquot is delivered into a microtiter plate for use m a biological assay.
In high throughput synthesis operations, the number of samples can be quite large so the operation of separately weighing, reweighmg, tracking, and labeling a very large number of fraction collector tubes becomes quite cumbersome. Moreover, when weighing and re-weighmg relatively small volume fluid samples, inaccuracies in the weight of the tubes themselves may account for larger weight differences than the weiqht of the compound fraction collected therein. As such, significant errors can be introduced to the net weight of each collected compound, and its final concentration upon dissolution. In addition, special devices such as racks and an apparatus for concentrating down fluid samples have to be used with the dried down products later having to be reformatted into a microtiter plate format.
SUMMARY OF THE INVENTION
The present invention provides methods ana systems for measuring the total masses of individual compounds present m fluid samples, ana is particularly well adapted for use with fluid samples prepared in microtiter plate format. In a preferred aspect, the individual compounds are isolated by fluid separation systems including high performance liquid chromatography columns and supercritical fluid columns. Small portions of the individual compounds isolated by fluid separation are then analyzed by a mass spectrometer, (which determines the compound molecular weight) , and by an evaporative light scattering detector, (which determines the total masses of each of the isolated compounds passing therethrough) . The present invention provides a single pass system which measures the masses of the individual compounds diverted into fraction collectors in real-time, as follows.
The signal generated by the mass spectrometer is used to determine the interval of time during which fraction collection is to be carried out. The signal generated by the evaporative light scattering detector is used to determine the total amount of mass diverted therethrough during the interval of time during which fraction collection is carried out. By knowing the portion of fluid sample diverted into the evaporative light scattering detector, (relative to the portion of fluid sample which is directed to fraction collection) , it is then possible to calculate the total masses of each of the individual isolated compounds as they are fraction collected.
By selecting intervals of time for fraction collection on the basis of when a desired compound is present in sufficient concentration, (as indicated by the signal strength from the mass spectrometer) , the individual isolated compounds can be purified as they are fraction collected. Thus, an advantage of the present invention is that, during only a single pass through the system, each fluid sample is partitioned into isolated compounds which are individually weighed in real time as they pass into fraction collectors.
An additional advantage of the present invention is that microtiter plate formats can be used both for sample preparation reactions and for fraction collection of the individual compounds present m such samples. Accordingly, the present invention provides a single-pass system for the synthesis, isolation, weight measurement, and delivery of compounds n microtiter plate formats. Another advantage of the present invention is that it is able to determine the total mass of the individual isolated compounds present in microtiter plate fluid samples at the same time that these individual compounds are being fraction collected in microtiter plate format. As such, only a single pass of a fluid sample through the system is required to isolate the individual compounds in the fluid sample, to fraction collect the individual isolated compounds and determine the total collected masses of these isolated compounds. Therefore, an additional important advantage of the present microtiter plate format single pass system is that it completely avoids individually removable fraction collection tubes. Accordingly, it is not necessary to individually weigh individual tubes containing fractionated fluid samples. Consequently, it is not necessary to separately track and label such tubes or to transfer individual tubes between various liquid handling, concentrator and fraction collection devices. As such, the problem of individual tubes being misplaced or transposed and the amount of time involved with transferring individual collection tubes is completely avoided. Thus, another advantage of the present invention is that by using a high density microtiter plate format, the present invention reduces the actual amount of material which needs to be synthesized, (as compared to existing non-microtiter plate format systems), thereby resulting in cost savings through the reduced costs of synthetic chemicals. By using a small volume microtiter system, solvent consumption is reduced.
Moreover, being a small volume system, significant reduction in the disposal of waste streams is achieved.
An additional advantage of the present small volume microtiter plate format is that, in preferred aspects, more difficult chromatographic separations can be achieved with the resolution of present invention's preparatory or semi-preparatory chromatographic column where the resolution approaches that of a conventional smaller analytical chromatographic column. Existing systems which remove and re-weigh fraction collection tubes individually can not be operated with the small fluid sample volumes of the present microtiter based system since inaccuracies in the weight of the tube itself may account for larger weight differences than the weight of the collected fluid sample therein. As such, significant errors can be introduced to the net weight of each product. The present invention completely avoids this problem.
In the present invention, a plurality of fluid samples are first provided in a standard microtiter plate format. An autosampler is then used to sequentially load the fluid samples onto a fluid separation system which preferably comprises a preparatory or semi-preparatory high performance liquid chromatography (HPLC) column or a supercritical fluid chromatography (SFC) column, which separates the components in each fluid sample such that individual compounds are isolated by sequential elution from the fluid column. Keeping within the scope of the present invention, however, alternate systems which facilitate fluid based separation can be used.
A very small portion, (typically on the order of 1%), of the sequentially eluted isolated compounds in the separated fluid sample are diverted into a mass spectrometer which determines the molecular weight of the individual isolated compounds passing therethrough. The signal generated by the mass spectrometer will correspond to the molecular weight of the compound passing therethrough such that fraction collection can be performed when a desired isolated compound is present m a desired concentration. As such, the output signal of the mass spectrometer can be used to signal the interval of time during which fraction collection is to be performed. In addition, a very small portion, (typically on the order of 1%), of the sequentially eluted isolated compounds in the fluid sample are diverted into an evaporative light scattering detector. The evaporative light scattering αetector generates a chromatographic signal of the sequentially eluted isolated compounds which is proportional to the total masses of the various compounds passing therethrougn . An advantage of evaporative light scattering detection is tnat it is mass dependent and will tend to be generally uniform over a wide range of different chemical structures. Accordingly, a single calibration curve can be generated between masses passing through the evaporative light scattering detector and its signal output.
As stated, the mass spectrometer is used to selectively signal fraction collection of the compounds isolated in the fluiα sanrole on the basis of their molecular weights and the lignt scattering detector signal is used to determine the actual total masses of the isolated compounds which are collected into the fraction collection microtiter plates .
In particular, the portion of each isolated compound diverted into the light scattering detector, (as compared to the remainder which is directed either to fraction collection or to waste) , will be the same for all isolated compounds and will be determined by the dimensions of the splitter device used to divert a portion of the fluid sample into the light scattering detector. However, the portion of each isolated compound which is fraction collected as opposed to being diverted to waste will vary for different compounds, being dependent upon the portion of time during which fraction collection is carried out. The portion of time during which fraction collection is carried out will in turn depend upon the amount of time during which the compound is eluted at a sufficient purity for fraction collection.
By knowing the portion of each of the isolated compounds diverted into the light scattering detector as compared to the portion directed to fraction collection, and by knowing the actual mass passing through the light scattering detector, it is then possible to calculate the total masses of each of the individual fraction collected compounds. Specifically, the total mass of any particular isolated compound which is fraction collected is determined by measuring the signal generated by the light scattering detector, (which is proportional to the total mass of the compound passing to the fraction collector) , during the interval in time in which the compound is eluted and fraction collected, (as determined by the mass spectrometer) . By knowing the correlation between the signal generated by the light scattering detector and the amount of mass passing therethrough and by knowing the portion of fluid sample diverted into the light scattering detector as compared to the remainder of the fluid sample which passes directly to the fraction collector microtiter plate, the amount of mass present in any of the various isolated fraction collected compounds is calculated.
Initially, a calibration curve between the mass passing through the evaporative light scattering detector and the signal generated by the evaporative light scattering detector is determined. Such a calibration curve can be established by determining the signal output when passing known masses through the light scattering detector.
An additional advantage of the present invention is that as the actual masses of the fraction collected compounds are known when these compounds are fraction collected in microtiter plates, the microtiter plate fraction collector can then itself later be concentrated by being dried down. Afterwards, it can be reconstituted to set point molarity based upon the weight of each isolated compound as determined by the light scattering detector. As such, the microtiter plate can itself be used to create daughter plates directly without any reformatting or weighing .
Furthermore, by performing real time mass determinations of fraction collected samples, the present invention can be used to automatically calculate the yield of a given reaction. Moreover, such mass determinations can also be used as a control function when fraction collecting such that a maximum amount of an isolated compound can be collected, with the remainder being diverted to a second fraction collector or to waste.
In addition, the present system can be adapted to perform simultaneous real time mass determinations of a plurality of fraction collected samples, wherein a plurality of simultaneously eluted fluid samples can be analyzed by the evaporative light scattering detector and the mass spectrometer. In various aspects of the invention, parallel simultaneously eluted fluid samples pass through a switching valve such that each of the samples can be analyzed by the evaporative light scattering detector and the mass spectrometer in turn. In alternate aspects, parallel light scattering detection is performed by a plurality of lasers or with a single laser having its beam sequentially directed towards the various samples eluted in parallel.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a schematic view of an apparatus for carrying out the present invention. Fig. 2 is a schematic view corresponding to Fig.
1, but instead having parallel fluid columns and a selective electrospray blocking system for carrying out parallel fluid sample analysis.
Fig. 3 is a schematic view of an alternate system for carrying out parallel evaporative light scattering detection comprising a movable scanning mirror and a single laser .
Fig. 4 is a schematic view of another alternate system for carrying out parallel evaporative light scattering detection comprising a plurality of lasers.
DESCRIPTION OF THE SPECIFIC EMBODIMENTS
As seen schematically in F g. 1, a plurality of chemical compounds can be synthesized or provided in microtiter plate format m reaction wells 11 of microtiter plate 10. A fluid handling robot 12, which may comprise a Gilson 215 Autosampler is adapted to draw up each of the fluid samples present m wells 11 of microtiter plate 10, and to sequentially load each of the fluid samples m wells 11 onto a fluid separation column 14.
Fluid separation column 14 may preferably comprise a high performance liquid chromatography (HPLC) column or a supercritical fluid (SFC) column composed of a solid sorbent material which operates to separate each of the component compounds in the fluid sample passing therethrough such that isolated compounds are sequentially eluted from the end of the column. Specifically, since each of the different component compounds found m each fluid sample will interact differently with the solid sorbent material contained within the separation column, each will accordingly take different amounts of time to pass through and be eluted out of the exit end of the column. Column 14 may preferably comprise a C18 Reverse Phase semi-preparatory or preparatory fluid separation column. Due to the small fluid samples used in the present microtiter plate format, the separation resolution achieved by the present semi-preparatory or preparatory fluid separation column approaches that of a standard smaller volume analytical column. It is to be understood, however, that fluid separation column 14 can be replaced by any form of fluid partitioning system.
After separated fluid is eluted from column 14, a very small portion, (typically on the order of 1%), is diverted through a splitter 21, (which may preferably comprise a Valco Tee), into mass spectrometer 16. Mass spectrometer 16 determines the molecular weights of the isolated compounds in the fluid sample passing sequentially therethrough and generates a signal corresponding to the molecular weights of the isolated compounds. Accordingly, mass spectrometer 16 identifies each of the isolated compounds passing sequentially therethrough on the basis of their respective molecular weights. When the signal from mass spectrometer 16 indicates a desired isolated compound is present in sufficient concentration, a liquid handling robot 20 is signaled to collect the desired compound in corresponding wells 17a of microtiter plate 18a of fraction collector 19. As illustrated, fraction collector 19 preferably comprises a plurality of microtiter plate collector racks (ie: individual microtiter plates shown here as 18a and 18b) . Furthermore, it is to understood that liquid handling robot 20 could be replaced by a simple on/off valve or valving system.
When fraction collecting only a single compound from each of wells 11 in microtiter plate 10, a single microtiter plate 18a may be used. Preferably, the same spatial address is maintained between wells 11 in microtiter plate 10 and wells 17a in microtiter plate 18a when one isolated compound is fraction collected from each of the wells in microtiter plate 10. Alternatively, when more than one isolated compounds are to be fraction collected from any single well 11a in plate 10, a plurality of microtiter plates, (shown here as 18a and 18b), can be used such that first isolated compounds can be collected in wells 17a of microtiter plate 18a and second isolated compounds can be collected in wells 17b of microtiter plate 18b. It is to be understood that additional microtiter plates can be used as required when more than two compounds are fraction collected wells 11 of plate 10. Alternatively, a plurality of individual fraction collectors can be used for fraction collection. Using either a plurality of fraction collector racks (ie: microtiter plates) within a single fraction collector, or a plurality of separate fraction collectors, it is preferable to maintain the same spatial addresses among sample and fraction collection microtiter plate wells, with the number of fraction collection microtiter plates corresponding to the maximum number of different isolated compounds collected from any particular sample well. Accordingly, by using multiple microtiter plate fraction collectors, the same spatial addresses can be maintained for various isolated compounds fraction collected from a single sample well 11 in microtiter plate 10.
When used in conjunction with mass spectrometer 16, column 14 and fraction collector 18 can be used together to purify fluid samples by first separating a fluid sample into isolated compounds on column 14 and then collecting only desired compounds into fraction collector 18 on the basis of the signal output of mass spectrometer 16. Specifically, when desired compounds are not present in sufficient purity, or when undesirable compounds are eluted , (as indicated by the output signal of mass spectrometer 16) , fraction collection is not performed, such that the non-desired portions of the fluid sample are conveniently expelled as waste W.
The amounts of flow diverted to splitters 21 and 22, and the volume of connecting tubes 32, 34 and 36, is set such that eluting compounds from column 14 reaches each of mass spectrometer 16, evaporative light scattering detector 24 and microtiter plate fraction collector 18 at the same time. Accordingly, at the moment in time when mass spectrometer 16 signals that fraction collection of a particular isolated compound reaching mass spectrometer 16 should commence, the same particular isolated compound will be reaching liquid handling robot 20 such that it can be diverted into fraction collector microtiter plate 18. Therefore, compound purification can be performed in real time .
A small portion, (typically on the order of 1%), of the separated fluid sample is diverted by splitter 22, (which preferably comprises a Valco Splitter Tee) , towards an evaporative light scattering detector 24. Light scattering detector 24 measures the total mass of the fluid sample passing therethrough on the basis of the amount of light scattered per unit mass passing therethrough. An advantage of light scattering detection is that a signal which is mass dependent within a narrow range of response factors is produced. As such, the total mass of the fluid sample is determined without regard to the way in which various particles absorb light, which would in turn depend upon the structural nature of the particle, with different chromophores having a wide range of response factors, making system calibration difficult.
The signal generated by the light scattering detector will be in the form of an integer number of "area counts" which correspond to the mass of sample passing through the detector. Specifically, the area counts are integrated to determine the mass of sample passing through the detector. As such, progressively larger masses passing through the detector generate greater numbers of area counts .
The actual total mass of any particular individual isolated compound which is fraction collected is determined by the mass passing through the light scattering detector during the interval of time during which fraction collection is performed. The mass passing through the light scattering detector represents a fixed portion (typically about 1%, depending upon the splitter arrangement used) , of the mass passing into fraction collector 18 during the interval of time in which fraction collection is carried out.
Accordingly, the total mass passing through the light detector is used to accurately determine the total mass of the fraction collected compound. Preferably, prior to operation of the present system, a calibration curve is established for light scattering detector 24 by passing different known masses through the light scattering detector 24 and recording the number of area counts generated by the different known masses .
The particular isolated compound will reach light scattering detector 24 at the same time that it reaches mass spectrometer 16 and fraction collector microtiter plates 18. Accordingly, the signal generated by mass spectrometer 16 and light scattering detector 24 will correspond to the same particular isolated compound in the fluid sample.
Referring to Fig. 2, the present invention can be adapted for parallel evaporative light scattering detection such that a plurality of fluid separation columns 14a, 14b and 14c can be used at once. In such an arrangement, autosampler 12 loads different fluid samples onto a plurality of fluid columns 14a, 14b, 14c. Separated fluid samples are then simultaneously eluted from each of fluid columns 14a, 14b, 14c. A selective electrospray blocking system 40 rapidly selects between electrosprays of each of the simultaneously eluted fluid samples such that electrosprays of each of the separated fluid samples reach mass spectrometer 16 one after another. By rapidly selecting between each of the simultaneously eluted fluid samples, each of the isolated compounds present in the separated fluid samples can be detected.
In a preferred aspect, selective blocking system 40 comprises a rotating disc 41 having an off-center hole 42 passing therethrough and each of fluid columns 14a, 14b, and 14c are connected to a parallel channel electrosprayer 43 such that the fluid eluted from each of fluid columns 14a, 14b, and 14c is electrosprayed to pass in sequence through the hole 42 in rotating disc 41 as disc 41 is rotated. Specifically, parallel channel electrosprayer 43 preferably directs electrosprayed effluents from each of fluid columns 14a, 14b, and 14c towards locations which are equidistant from the center of the rotating disc and which are at a distance equal to the distance from the center of hole 42 to the center of rotating disc 41. An example of such a system is found in the Applicants' provisionally filed Application Serial No. 06/088,665, filed June 9th, 1998; (Attorney Docket Number 18590-002900), and also in the Applicants' application entitled "Parallel Fluid Electrospray Mass Spectrometer", filed November 3rd, 1998, (Attorney Docket Number 18590-002910), the disclosure of both which are incorporated herein by reference in their entireties for all purposes.
Fluid splitters 100a, 100b and 100c, (which may preferably comprise Valco splitter Tees) , divert the majority (typically 99%) of the separated fluid samples toward electrosprayer 24. Specifically, fluid splitters 102a, 102b and 102c, (which may also preferably comprise
Valco splitter Tees), divert a small portion (typically 1%) of the separated fluid samples into electrosprayer 24, (which comprises parallel drift tubes 72a, 72b and 72c as will be explained) . Fluid splitters 102a, 102b and 102c divert a majority, (typically 99%), of the separated fluid sample to liquid handling robot 20 for fraction collecting in fraction collectors 19a, 19b and 19c.
It is to be understood that any number of parallel fluid columns can be used, and that the present use of three fluid columns (14a, 14b, and 14c), is merely illustrative.
It is also to be understood that any other form of switching valve system can be substituted for the present electrospray blocking system 40. Fig. 3 shows a system for parallel light scattering detection in which fluid columns 14a, 14b and 14c simultaneously elute separated fluid samples which are separately and sequentially sampled by a laser light source, as follows. Nebulizers 70a, 70b and 70c are each connected to a nitrogen source. Nebulizers 70a, 70b and 70c cause the fluid samples sequentially eluted from each of fluid columns 14a, 14b and 14c to be passed as aerosol sprays along through drift tubes 72a, 72b and 72c, respectively. Laser 50 emits a beam 51 which is selectively directed towards the aerosol spray corresponding to the fluid eluted by each of the three fluid columns in sequence. Specifically, a beam selector 52, (which preferably comprises a movable scanning mirror) directs beam 51 from laser 50 in sequence toward the effluent of each of fluid columns 14a, 14b, and 14c. Laser beam 51 is scattered by each of the effluent streams and is received by photodetectors 54a, 54b and 54c, respectively, as the beam is scanned from fluid column 14a to 14b to 14c. Each of photodetectors 54a, 54b and 54c, will preferably be operated together with a dedicated amplifier 56a, 56b and 56c. Accordingly, when laser beam 51 is directed towards each of the effluent streams, scattered light can be detected and amplified into a chromatographic signal. Rapid sequential sampling of each of the effluent streams provides an independent chromatograph for each column 14.
Fig. 4 shows another alternate system for parallel light scattering detection in which fluid columns 14a, 14b and 14c simultaneously elute separated fluid samples which are simultaneously sampled by separate laser light sources, as follows. In this arrangement, a plurality of separate drift tubes 60a, 60b and 60c, each having dedicated light sources 64a, 64b, 64c; and photomultipliers 66a, 66b and 66c are used.
The ability to perform parallel evaporative light scattering detection, (ie: to perform evaporative light scattering detection on a plurality of separated fluid samples at the same time) , provides very high throughput quantitation of the masses of the isolated compounds present in a plurality of fluid samples.

Claims

WHAT IS CLAIMED IS:
1. Method for measuring the masses of compounds present m a fluid sample during fraction collection, comprising: separating the fluid sample into sequentially eluted isolated compounds by passing the fluid sample through a fluid separation device, diverting a first portion of the sequentially eluted isolated compounds into a mass spectrometer, thereby determining the molecular weight of each isolated compound m sequence; diverting a second portion of the sequentially eluted isolated compounds into an evaporative light scattering detector, thereby determining the total masses of each isolated compound passing therethrough in sequence; fraction collecting at least one of the isolated compounds into a fraction collector; and calculating the total masses of the isolated compounds m the fraction collector during fraction collection on the basis of the second portion of eacn isolated compound diverted into the evaporative light scattering detector during a period of fraction collection.
2. The method of claim 1, further comprising, purifying at least one of the isolated compound by fraction collecting when a desired concentration of the at least one isolated compound is present in the fluid sample as determined by the mass spectrometer.
3. The method of claim 1, wherein passing the fluid sample through a fluid separation device comprises, passing the fluid sample througn a liquid chromatography fluid column.
4. The method of claim 1, wherein passing the fluid sample through a fluid separation device comprises, passing the fluid sample through a supercritical fluid column.
5. The method of claim 3 or 4, wherein passing the fluid sample through the fluid column, comprises, passing the fluid sample through a preparatory or semi-preparatory fluid column.
6. The method of claim 1, wherein fraction collecting the isolated compounds into a fraction collector comprises, fraction collecting into at least one microtiter plate.
7. The method of claim 1, further comprising, extracting the fluid sample from a plurality of fluid samples n a microtiter plate and loading the fluid sample onto the fluid separation device with a liquid handling robot.
8. A method for measuring the masses of compounds present in a plurality of fluid samples during fraction collection, comprising: simultaneously separating each fluid sample into sequentially eluted isolated compounds by passing the fluid samples through parallel fluid separation devices, diverting a first portion of each of the sequentially eluted isolated compounds into a mass spectrometer, thereby determining the molecular weight of each isolated compound in sequence; diverting a second portion of each of the sequentially eluted compounds into an evaporative light scattering detector, thereby determining the total masses of each isolated compound passing therethrough in sequence; fraction collecting at least one of the isolated compounds into a fraction collector; and calculating the total masses of the isolated compounds in the fraction collector during fraction collection on the basis of the second portion of each of the isolated compounds diverted into the evaporative light scattering detector during a period of fraction collection.
9. The method of claim 8, wherein diverting a second portion of each of the sequentially eluted compounds into an evaporative light scattering detector comprises; using a selective electrospray blocking system to sequentially permit an electrospray of each of the fluid samples to enter the mass spectrometer in repeating sequence.
10. The method of claim 9, wherein using a selective electrospray blocking system comprises; simultaneously electrospraying the sequentially eluted isolated compounds in the fluid samples towards a rotating disc with an off center hole passing therethrough.
11. A system for measuring the masses of compounds present in a fluid sample during fraction collection, comprising: at least one fluid separation device for sequentially eluting isolated compounds in the fluid sample, a mass spectrometer for determining the molecular weight of the isolated compounds; a first splitter for diverting a first portion of the fluid sample into the mass spectrometer; an evaporative light scattering detector for determining the total masses of the isolated compounds passing therethrough; a second splitter for diverting a second portion of the fluid sample into the evaporative light scattering detector; and at least one fraction collector.
12. The system of claim 11, wherein, the fluid separation device is a liquid chromatography fluid column.
13. The system of claim 11, wherein, the fluid separation device is a supercritical fluid column.
14. The system of claims 10 or 11, wherein, the fluid column is a preparatory or semi- preparatory fluid column.
15. The system of claim 11, further comprising; a microtiter plate containing the fluid sample; and a liquid handling robot for loading the fluid sample onto the fluid separation device.
16. The system of claim 11, further comprising; a liquid handling robot for selectively diverting the isolated compounds into the fraction collector.
17. The system of claim 11, wherein, the fraction collector comprises at least one microtiter plate.
18. The system of claim 11, further comprising; a switching valve for sequentially diverting the isolated compounds from each of a plurality of fluid separation devices into the evaporative light scattering detector.
19. The system of claim 11, wherein the evaporative light scattering detector further comprises; a scanning system for selectively directing a laser beam towards the isolated compounds eluted from each of the fluid separation devices.
PCT/US1999/030514 1998-12-22 1999-12-20 Automated on-line evaporating light scattering detection to quantify isolated fluid sample compounds in microtiter plate format WO2000037157A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2000589263A JP2002537543A (en) 1998-12-22 1999-12-20 Automated online evaporative light scattering detection for quantifying isolated fluid sample compounds in microtiter plate format
CA002356218A CA2356218A1 (en) 1998-12-22 1999-12-20 Automated on-line evaporating light scattering detection to quantify isolated fluid sample compounds in microtiter plate format
EP99966531A EP1144068A4 (en) 1998-12-22 1999-12-20 Automated on-line evaporating light scattering detection to quantify isolated fluid sample compounds in microtiter plate format
AU22046/00A AU2204600A (en) 1998-12-22 1999-12-20 Automated on-line evaporating light scattering detection to quantify isolated fluid sample compounds in microtiter plate format

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/219,083 1998-12-22
US09/219,083 US6077438A (en) 1998-12-22 1998-12-22 Automated on-line evaporation light scattering detection to quantify isolated fluid sample compounds in microtiter plate format

Publications (1)

Publication Number Publication Date
WO2000037157A1 true WO2000037157A1 (en) 2000-06-29

Family

ID=22817805

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/030514 WO2000037157A1 (en) 1998-12-22 1999-12-20 Automated on-line evaporating light scattering detection to quantify isolated fluid sample compounds in microtiter plate format

Country Status (6)

Country Link
US (3) US6077438A (en)
EP (1) EP1144068A4 (en)
JP (1) JP2002537543A (en)
AU (1) AU2204600A (en)
CA (1) CA2356218A1 (en)
WO (1) WO2000037157A1 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8115930B2 (en) 2007-12-05 2012-02-14 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US8305582B2 (en) 2009-09-01 2012-11-06 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
GB2511892A (en) * 2013-03-14 2014-09-17 Malvern Instr Ltd Eluate analysis and collection
US9086422B2 (en) 2008-12-10 2015-07-21 Alltech Associates, Inc. Chromatography systems and system components
US9133833B2 (en) 2008-12-04 2015-09-15 Alltech Associates, Inc. Methods and apparatus for moving aliquot samples of fluid

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6866786B2 (en) * 1998-04-03 2005-03-15 Symyx Technologies, Inc. Rapid characterization of polymers
US6406632B1 (en) 1998-04-03 2002-06-18 Symyx Technologies, Inc. Rapid characterization of polymers
US6309541B1 (en) 1999-10-29 2001-10-30 Ontogen Corporation Apparatus and method for multiple channel high throughput purification
US6458273B1 (en) 1999-10-29 2002-10-01 Ontogen Corporation Sample separation apparatus and method for multiple channel high throughput purification
CH698240B1 (en) * 1998-11-17 2009-06-30 Tecan Trading Ag A method for weighing sample tubes, feeding and workstation.
JP2000214151A (en) * 1999-01-25 2000-08-04 Shimadzu Corp Dispensation device for liquid chromatograph
US6855258B2 (en) * 1999-04-02 2005-02-15 Symyx Technologies, Inc. Methods for characterization of polymers using multi-dimensional liquid chromatography with parallel second-dimension sampling
US6296771B1 (en) * 1999-04-02 2001-10-02 Symyx Technologies, Inc. Parallel high-performance liquid chromatography with serial injection
US6809819B1 (en) 1999-09-27 2004-10-26 Monsanto Technology Llc Methods for determining oil in seeds
US6355164B1 (en) * 1999-10-29 2002-03-12 Ontogen Corporation Sample collection apparatus and method for multiple channel high throughput purification
US6358414B1 (en) * 1999-10-29 2002-03-19 Ontogen Corporation Pressure regulation apparatus and method for multiple channel high throughput purification
US6558624B1 (en) * 2000-07-25 2003-05-06 General Electric Company Method and analytical system for rapid screening of combinatorial libraries
JP4615101B2 (en) * 2000-08-08 2011-01-19 昭光サイエンティフィック株式会社 Purification preparative equipment
US6743356B1 (en) * 2000-10-27 2004-06-01 Johnson & Johnson High throughput high performance chromatography system
JP3642730B2 (en) * 2000-11-29 2005-04-27 株式会社荏原製作所 Plating apparatus and plating solution composition management method
US6635173B2 (en) * 2000-12-28 2003-10-21 Cohesive Technologies, Inc. Multi column chromatography system
US7066011B2 (en) * 2001-06-07 2006-06-27 Nano Solution, Inc. Liquid chromatograph and analysis system
US6730228B2 (en) * 2001-08-28 2004-05-04 Symyx Technologies, Inc. Methods and apparatus for characterization of polymers using multi-dimensional liquid chromatography with regular second-dimension sampling
FR2851045B1 (en) * 2003-02-12 2005-04-15 Sedere Sa METHOD FOR CONTROLLING AN EVAPORATIVE LIGHT DIFFUSION DETECTOR COUPLED TO A LIQUID CHROMATOGRAPHY COLUMN
CN101755204A (en) 2006-03-09 2010-06-23 全技术联合公司 Evaporative light-scattering detector
EP2237862A1 (en) * 2008-01-16 2010-10-13 Syngenta Participations AG Apparatus system and method for mass analysis of a sample
DE102010036770A1 (en) * 2010-07-30 2012-02-02 Joint Analytical Systems Gmbh Arrangement for sample preparation and analysis of pesticides
CN102805950B (en) * 2012-08-22 2015-05-06 中国铝业股份有限公司 Evaporation system capable of feeding and evaporating in multiple flows and controlling discharging temperature and concentration in stepless way
US20140368443A1 (en) * 2013-06-14 2014-12-18 Agilent Technologies, Inc. System for Automating Laboratory Experiments
CN103537115B (en) * 2013-10-21 2016-05-25 西安近代化学研究所 A kind of crystallization cooler and method thereof that extends the outer circulation type crystallizer operation cycle
WO2020129118A1 (en) * 2018-12-17 2020-06-25 株式会社島津製作所 Mass spectrometer
KR20230065686A (en) * 2021-11-05 2023-05-12 주식회사 엑소퍼트 Liquid auto fraction apparatus for column chromatography
CN118050457B (en) * 2024-04-15 2024-07-09 凯琦尚英(天津)科技有限公司 Detection device and detection method for non-volatile or semi-volatile substances

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5670054A (en) * 1996-04-04 1997-09-23 Warner Lambert Company Method and system for identification, purification, and quantitation of reaction components
US5938932A (en) * 1997-11-14 1999-08-17 Pharmacopeia, Inc. High-throughput method and apparatus for identifying, quantitating and determining the purity of chemical compounds in mixtures

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4840730A (en) * 1986-07-25 1989-06-20 Sepragen Corporation Chromatography system using horizontal flow columns
DE69216520T2 (en) * 1991-03-28 1997-04-24 Perseptive Biosystems Inc PRODUCT INFORMATION IN CHROMATOGRAPHIC EFFLUENT THROUGH DIFFERENTIATION
AU5438796A (en) * 1995-04-06 1996-10-23 Arqule, Inc. Method for rapid purification, analysis and characterization of collections of chemical compounds
CA2223835A1 (en) * 1995-06-07 1996-12-19 Egisto Boschetti On line detection of a desired solute in an effluent stream using fluorescence spectroscopy

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5670054A (en) * 1996-04-04 1997-09-23 Warner Lambert Company Method and system for identification, purification, and quantitation of reaction components
US5938932A (en) * 1997-11-14 1999-08-17 Pharmacopeia, Inc. High-throughput method and apparatus for identifying, quantitating and determining the purity of chemical compounds in mixtures

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP1144068A4 *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8115930B2 (en) 2007-12-05 2012-02-14 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US8305581B2 (en) 2007-12-05 2012-11-06 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US9133833B2 (en) 2008-12-04 2015-09-15 Alltech Associates, Inc. Methods and apparatus for moving aliquot samples of fluid
US9086422B2 (en) 2008-12-10 2015-07-21 Alltech Associates, Inc. Chromatography systems and system components
US8305582B2 (en) 2009-09-01 2012-11-06 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
US8314934B2 (en) 2009-09-01 2012-11-20 Alltech Associates, Inc. Methods and apparatus for analyzing samples and collecting sample fractions
GB2511892A (en) * 2013-03-14 2014-09-17 Malvern Instr Ltd Eluate analysis and collection

Also Published As

Publication number Publication date
JP2002537543A (en) 2002-11-05
EP1144068A1 (en) 2001-10-17
US6077438A (en) 2000-06-20
US6426006B1 (en) 2002-07-30
EP1144068A4 (en) 2005-01-19
CA2356218A1 (en) 2000-06-29
AU2204600A (en) 2000-07-12
US6210571B1 (en) 2001-04-03

Similar Documents

Publication Publication Date Title
US6077438A (en) Automated on-line evaporation light scattering detection to quantify isolated fluid sample compounds in microtiter plate format
AU766030B2 (en) Parallel fluid electrospray mass spectrometer
US5670054A (en) Method and system for identification, purification, and quantitation of reaction components
Weller et al. High throughput analysis and purification in support of automated parallel synthesis
Shin et al. Analysis and screening of combinatorial libraries using mass spectrometry
CN110333364B (en) Full-automatic biological evaluation and chemical analysis all-in-one machine and method
Kyranos et al. High-throughput high-performance liquid chromatography/mass spectrometry for modern drug discovery
CN101849184A (en) The method and apparatus that is used for analyzing samples and collection sample fractions
Kiplinger et al. Structure‐controlled automated purification of parallel synthesis products in drug discovery
US20050277199A1 (en) Single-pass compound purification and analysis
WO2021007794A1 (en) Full-automatic biological evaluation and chemical analysis integrated machine and method
US6736975B2 (en) Method of separating compound(s) from mixture(s)
Weller Purification of combinatorial libraries
US6413431B1 (en) HPLC method for purifying organic compounds
JP2005512029A5 (en)
US20050224402A1 (en) Installation for separating components in a plurality of parallel channels
US20020039750A1 (en) Method and device for increasing efficiency of bioanalysis
JP3410017B2 (en) Liquid chromatograph mass spectrometer
WO2001033193A3 (en) Automated plant extraction method and arrays for high throughput screening
JPH01235849A (en) Fractional liquid chromatograph
Rossi 1 THE NEED FOR AUTOMATED CHEMICAL ANALYSIS
Kingston et al. Hyphenated techniques in drug discovery: purity assessment, purification, quantitative analysis and metabolite identification
Rossi Parallel automation for chemical analysis
Cheng et al. Application of mass spectrometry to compound library generation, analysis, and management
Olah The development and implementation of bioanalytical methods using LC-MS to support ADME studies in early drug discovery and candidate selection

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AL AM AT AU AZ BA BB BG BR BY CA CH CN CR CU CZ DE DK DM EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
WWE Wipo information: entry into national phase

Ref document number: 1999966531

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 2356218

Country of ref document: CA

Ref country code: CA

Ref document number: 2356218

Kind code of ref document: A

Format of ref document f/p: F

ENP Entry into the national phase

Ref country code: JP

Ref document number: 2000 589263

Kind code of ref document: A

Format of ref document f/p: F

WWP Wipo information: published in national office

Ref document number: 1999966531

Country of ref document: EP

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

WWW Wipo information: withdrawn in national office

Ref document number: 1999966531

Country of ref document: EP