1. Field of the Invention
The present invention relates to a dispensing nozzle and an automatic analyzer.
2. Description of the Related Art
Typically, an automatic analyzer that analyzes a biological sample, such as blood or body fluid, makes use of a dispensing device for dispensing specimens or fluid samples, such as reagents, to reaction vessels. To achieve dispensing of a fluid sample with precision, a dispensing device is known that obtains the volume of air inside a dispensing nozzle at the time of starting the discharge of the fluid sample and calculates, from the obtained volume of air, the plunging amount of a plunger that needs to be disposed for dispensing a predetermined amount of the fluid sample (for example, see Japanese Patent Application Laid-open No. 2004-20320).
A dispensing nozzle according to an aspect of the present invention includes a holding tube portion that holds a fluid as a dispensing target; and a discharge end face that is formed at a tip of the holding tube portion and that sucks in and discharges the fluid through an opening formed thereon, wherein the discharge end face has a greater contact angle with the fluid than an inner face of the holding tube portion.
An automatic analyzer according to another aspect of the present invention for causing a reaction between a specimen and a reagent by stirring and analyzing a reaction liquid by measuring an optical property thereof, includes the dispensing nozzle for dispensing either one of the specimen or the reagent.
The above and other features, advantages and technical and industrial significance of this invention will be better understood by reading the following detailed description of presently preferred embodiments of the invention, when considered in connection with the accompanying drawings.
Exemplary embodiments for a dispensing nozzle and an automatic analyzer according to the present invention will be described below in detail with reference to the accompanying drawings.
As illustrated in
The first reagent table 2 and the second reagent table 3 have an identical configuration. Hence, the description is given for only the first reagent table 2 and, regarding the second reagent table 3, the corresponding components are referred to by corresponding reference numbers.
As illustrated in
As illustrated in
The reaction vessels 6 are rectangular tube-like cuvettes having a small capacity of a few nL to a few hundred μL. The reaction vessels 6 are made of a transparent material, such as glass including heat-resistant glass or synthetic resin including cyclic olefin or polystyrene, through which can pass 80% or more of the light that is included in an analyzing light emitted by the photometer unit 22. To the reaction vessels 6 are dispensed reagents from the reagent vessels 2a of the first reagent table 2 and from reagent vessels 3a of the second reagent table 3 by the first reagent dispensing device 7 and the second reagent dispensing device 8, respectively, which are disposed adjacent to the reaction table 5.
Herein, the first reagent dispensing device 7 and the second reagent dispensing device 8 have an identical configuration. Hence, the description is given for only the first reagent dispensing device 7 and, regarding the second reagent dispensing device 8, the corresponding components are referred to by corresponding reference numbers.
As illustrated in
As illustrated in
As illustrated in
Herein, the dispensing nozzle 11 according to the present invention is manufactured by processing a metal, such as stainless-steel, or by performing injection molding on synthetic resin, such as polystyrene. As illustrated in
The nozzle driving system 12 moves the dispensing nozzle 11 up and down and also rotates it. As illustrated in
The pump driving system 15 causes fluid dispensing to the dispensing nozzle 11, and includes a plunger pump 15a and a dispensing motor 15e as illustrated in
The pump 16 pumps the cleaning water filled in the cleaning water tank to the cylinder 15b in the pump driving system 15. The valve 17 is used to gate the corresponding pipe 15h and switch over the flow of cleaning water through the pipe 15h that connects the cleaning water tank to the pump driving system 15.
As illustrated in
As illustrated in
As illustrated in
The control unit 25 is, for example, a microcomputer that is connected to the automatic analyzer 1 as illustrated in
The automatic analyzer 1 configured in the abovementioned manner operates under the control of the control unit 25. In the automatic analyzer 1, the specimen dispensing device 10 sequentially dispenses specimens from a plurality of the specimen vessels 9b held in the racks 9a to a plurality of the reaction vessels 6 as they are transported along the circumferential direction by the rotating reaction table 5. After the sequential dispensing of the specimens to the reaction vessels 6, the reagent dispensing devices 7 and 8 sequentially dispense reagents from the reagent vessels 2a and 3a, respectively, to the reaction vessels 6.
Thus, each time the reaction table 5 comes to a halt, the stirring unit 21 sequentially stirs a reaction vessel 6 to which reagents and a specimen are dispensed in the abovementioned manner so that the reagents and the specimen undergo reaction. When the reaction table 5 starts rotating again, that particular reaction vessel 6 passes through the photometer unit 22. At that time, the photometer unit 22 performs photometry on the reaction liquid obtained by the reaction of the reagents and the specimen in that particular reaction vessel 6. The control unit 25 then analyzes the constituent concentration of the specimen. After the photometry is performed on the reaction liquid, the reaction vessel 6 is transferred to the cleaning unit 23 for cleaning and then reused in specimen analysis.
Meanwhile, as illustrated in
Herein, to estimate the performance of the dispensing nozzle 11 according to the present invention in which the non-affinity film 11d is formed as a non-affinity film of fluorine contained resin, the dispensing nozzle 11 filled with a test specimen was immersed at the lower end in the test specimen and then pulled out therefrom. Then, a fluid analysis program was implemented to obtain the quantity of test specimen (nL) getting attached to the discharge end face 11b after the dispensing nozzle 11 was pulled out from the test specimen and to obtain a percentage (%) of the quantity of attached test specimen with respect to a specified dispensing quantity (0.4 μL). The analysis conditions at that time were as follows: the dispensing nozzle 11 was used along with a comparison nozzle made of stainless-steel in an identical manner to the dispensing nozzle 11 except without forming the non-affinity film 11d on the discharge end face 11b; and the test specimen had viscosities of 1 mPa·s and 3 mPa·s.
Given below is Table 1 that indicates the difference in the quantity of attached test specimen (nL) and the percentage (%) thereof found at the tip portion of each of the dispensing nozzle 11 and the comparison nozzle without a non-affinity face as the result of fluid analysis.
Herein, the test specimen was prepared by mixing polyvinyl alcohol in pure water and adjusted to have viscosities of 1 mPa·s and 3 mPa·s. Regarding the dispensing nozzle 11 as well as the comparison nozzle with reference to
As is obvious from the analysis result illustrated in Table 1; in the dispensing nozzle 11 having the non-affinity film 11d formed on the discharge end face 11b, the anti-drip property for the test specimen can be improved and the quantity of attached test specimen can be substantially reduced by 1/30 to 1/100 in absolute quantity as compared to the comparison nozzle. However, for the test specimen of high viscosity, it was found that the attached quantity is slightly higher.
Meanwhile, the effect on the actual dispensing performance of the dispensing nozzle 11 according to the present invention was confirmed in the following manner. For the dispensing nozzle 11 having the non-affinity film 11d made of fluorine contained resin (first embodiment), for a comparison nozzle (first comparison example) having the non-affinity film 11d formed also on the inner face of the holding tube portion 11a in the dispensing nozzle 11, and for a comparison nozzle (second comparison example) made of stainless-steel in an identical manner to the dispensing nozzle 11 except without forming the non-affinity film 11d on the discharge end face 11b; an actual dispensing quantity (μL) was measured when a specified dispensing quantity was set to 0.4 μl, and when a test specimen having viscosities of 1 mPa·s and 3 mPa·s was dispensed (discharged).
In Table 2 is illustrated the measurement result along with an actual dispensing quantity difference (%) based on the actual dispensing quantity of 1 mPa·s. The actual dispensing quantity illustrated in Table 2 is obtained by discharging a fluid of known optical density (OD) as the test specimen through each of the dispensing nozzle 11 and the comparison nozzles to a spectroscopic cell, inletting pure water to each spectroscopic cell for diluting the test specimen, and then dividing the absorbance measured by a spectrophotometer by the dilution ratio. At the time of measurement, a dye was dissolved in the test specimen of 1 mPa·s to have the optical density of 1500 and the test specimen was dispensed through the dispensing nozzle 11 or a comparison nozzle to an empty spectroscopic cell. Then, the test specimen was diluted with 1500 μL of pure water equaling the dilution ratio of about 3000 times and optical density measurement was performed for the solution having the optical density in the vicinity of 0.5 using a spectrophotometer. To obtain the dilution ratio with precision, the weight of a spectroscopic cell before and after inletting a diluting liquid and in an empty state was measured using an electronic scale and the fluid volume was calculated. Meanwhile, the actual dispensing quantity difference (%) was obtained as (actual dispensing quantity difference/actual dispensing quantity of 1 mPa·s)×100.
As illustrated in
Herein, the non-affinity film 11d made of fluorine contained resin or silicone resin can be formed as given below. For example, for a dispensing nozzle manufactured by performing elongation processing on a metal, such as stainless-steel, or by performing injection molding on synthetic resin such as polystyrene; pressure air Ar is discharged from the tip of the dispensing nozzle 11 while the tip portion thereof is immersed in a liquid Lq of fluorine contained resin or silicone resin as illustrated in
The non-affinity film 11d made of fluorine contained resin or silicone resin can also be formed as given below. As illustrated in
Moreover, as the liquid Lq of silicone resin, for example, the product name “HIREC” 1550 supplied by NTT-AT or the product name “Rain-X” supplied by Shell Car Care International Limited can be used.
The non-affinity film 11d made of fluorine contained resin or silicone resin can also be formed as given below. As illustrated in
Besides, the non-affinity film 11d can be formed on the discharge end face 11b of the dispensing nozzle 11 by using techniques, such as the molecular vapor deposition technique, the sputtering technique (PVD, physical vapor deposition), the ion implantation technique, or the plasma-enhanced CVD technique.
Meanwhile, if the dispensing nozzle 11 is manufactured by performing elongation processing on a metal, such as stainless-steel, or by performing injection molding on synthetic resin, such as polystyrene as described above; then instead of forming the non-affinity film 11d on the discharge end face 11b, then an affinity film having affinity with the target fluid for dispensing can be formed on the inner face of the holding tube portion 11a so that the discharge end face 11b has a greater contact angle with the fluid than the inner face of the holding tube portion 11a. In this case, as illustrated in
If the dispensing nozzle 11 is fabricated from a metallic material; then, after a polymer film having affinity with the target fluid for dispensing is formed using the molecular vapor deposition technique, the discharge end face 11b can be exposed to an electron beam, or a laser beam, or ultraviolet rays to remove the polymer film so that the metal that has no affinity with the target fluid for dispensing gets exposed primarily at the discharge end face 11b of the nozzle tip. By doing that, in the dispensing nozzle 11, the discharge end face 11b has a greater contact angle with the target fluid for dispensing than the inner face of the holding tube portion 11a.
Although the dispensing nozzle according to the present invention is described for the use in the specimen dispensing device 10 that dispenses specimens, it is also possible to use the dispensing nozzle in a reagent dispensing device that dispenses reagents if fluid samples have a broad viscosity range. Moreover, although all the abovementioned dispensing nozzles are described to have a tapering tip portion, it is also possible to use dispensing nozzles having no tapering tip portion but a straight pipe-like shape.
Additional advantages and modifications will readily occur to those skilled in the art. Therefore, the invention in its broader aspects is not limited to the specific details and representative embodiments shown and described herein. Accordingly, various modifications may be made without departing from the spirit or scope of the general inventive concept as defined by the appended claims and their equivalents.
Number | Date | Country | Kind |
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2007-226970 | Aug 2007 | JP | national |
This application is a continuation of PCT international application Ser. No. PCT/JP2008/065127 filed on Aug. 25, 2008 which designates the United States, incorporated herein by reference, and which claims the benefit of priority from Japanese Patent Application No. 2007-226970, filed on Aug. 31, 2007, incorporated herein by reference.
Number | Date | Country | |
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Parent | PCT/JP08/65127 | Aug 2008 | US |
Child | 12712452 | US |