1. Field of the Invention
The present invention relates to sampling liquids, and more particularly, to an apparatus for sampling a liquid and automatically performing a test.
2. Discussion of Related Art
Sampling methods for liquids typically involve drawing a sample into a pipet, syringe, or other container from a cup. Such a sampling method exposes the sample taker to the liquid. Limiting a sample taker's exposure to a sample may be desirable, such as in urine analysis. Further, sampling methods may include exposing the sample to contaminants leading to, for example, sampling errors.
Therefore, a need exists at least for a system and/or method for reducing exposure to a sample, reducing sampling errors and limiting contamination of test samples.
According to an embodiment of the present disclosure, a sampling apparatus comprises an ampoule barrel for receiving an ampoule through a first opening, the ampoule barrel comprising a second opening adapted to flow a liquid into the ampoule barrel and a structure adapted break a frangible tip of the ampoule.
The ampoule is a sealed container having a negative pressure therein for drawing a predetermined volume of liquid into the ampoule, wherein a flow rate of the ampoule is less than or equal to a flow rate of the second opening.
The sampling apparatus includes a seal located between an outer surface of the ampoule and an inner surface of the ampoule barrel. The seal prevents the liquid from passing into an upper portion of the ampoule barrel.
The frangible tip is scored to promote a break in the frangible tip in a predetermined direction. The predetermined direction is substantially perpendicular to a descent of the ampoule into the ampoule barrel. The frangible tip includes a rounded terminus. The frangible tip is offset from a longitudinal center of the ampoule.
The sampling apparatus includes a cap for covering the second opening of the ampoule barrel.
The sampling apparatus includes a carrier, wherein the carrier comprises a trench receiving an end portion of the ampoule, opposite from the frangible tip, and an upper surface supporting the ampoule barrel, wherein a distance between a bottom of the trench and the upper surface is adapted to prevent the descent of the ampoule into the ampoule barrel.
According to an embodiment of the present disclosure, a method for taking a liquid sample comprises selecting a test system including an ampoule barrel and an ampoule comprising a desired reagent, immersing a portion of the ampoule barrel in a liquid, and breaking the ampoule within the ampoule barrel, wherein the ampoule draws the liquid sample.
The method includes extracting the ampoule from the ampoule barrel.
The method includes determining a test result according to the reagent and liquid sample.
According to an embodiment of the present disclosure, an ampoule barrel comprises a first opening for receiving an ampoule, a tip, offset from a longitudinal center of the ampoule barrel, the tip including an elongated second opening for flowing a liquid into the ampoule barrel, and an inner surface effective for breaking a tip of the ampoule.
The inner surface is disposed at an angle is between about 15 degrees and about 30 degrees from the longitudinal center of the ampoule barrel. The inner surface is a convex radius relative to an interior of the ampoule barrel.
The ampoule barrel includes at least a third opening on a sidewall of the ampoule barrel for flowing the liquid into the ampoule barrel.
The ampoule barrel includes a flange at an end portion, opposite the tip.
Preferred embodiments of the present invention will be described below in more detail, with reference to the accompanying drawings:
FIGS. 1A-C are an illustration of a test system according to an embodiment of the present disclosure;
FIGS. 4A-C are illustrations of a sampling cap, sheath and ampoule according to an embodiment of the present disclosure;
FIGS. 5A-D are illustrations of an ampoule barrel having no offset according to an embodiment of the present disclosure;
FIGS. 6A-D are illustrations of an ampoule barrel having an offset according to an embodiment of the present disclosure;
FIGS. 7A-D are illustrations of an ampoule barrel having an offset according to an embodiment of the present disclosure;
FIGS. 8A-C are illustrations of a carrier for a test system according to an embodiment of the present disclosure;
FIGS. 9A-C are illustrations of a breaking mechanism according to an embodiment of the present disclosure; and
A test system according to an embodiment of the present disclosure is a self-contained total microbe test. Referring to
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Referring to FIGS. 4A-C, upon drawing a sample into the ampoule 102 a sampling cap 401 may be placed over a broken tip of the ampoule 102. A sheath 402 guards any sharps. The sampling cap 401 includes a nipple 403. The nipple 403 fits within the sheath 402. The cap 401 reduces a potential for contact with the liquid in the ampoule 102. The nipple 403 cooperates with the sheath 402, securing the sampling cap 401 to the ampoule 102. The nipple 403 may be a tube through which a syringe 404 or other device may gain access to the contents of the ampoule 102.
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Referring to FIGS. 5A-D, ampoule barrels 101 having a bottom port 501 with no offset relative to a centerline of the ampoule barrel 101 are shown. Referring to
Referring to FIGS. 6A-D, a bottom port 501 of the ampoule barrel 101 is offset, for example, by 0.065 inches from a centerline of the ampoule barrel 101. Referring to
Referring to FIGS. 7A-D, a bottom port 501 of the ampoule barrel 101 is offset, for example, by 0.130 inches from a centerline of the ampoule barrel 101. Referring to
Referring to FIGS. 8A-C, a test system 100 may be loaded into a carrier 801. The carrier 801 may be capped by a top 802. The carrier comprises one or more trenches 804 for receiving a portion of an ampoule 102. The trench 804 has a depth adapted to support an unused system 100 such that the ampoule 102 is not pressed into the ampoule barrel 101; a distance between a bottom of the trench and the upper surface 805 prevents the descent of the ampoule into the ampoule barrel. A flange 803 of the ampoule barrel 101 rests on an upper surface of the carrier 801.
An ampoule 102 according to an embodiment of the present disclosure is a sterile vacuum packaging ampoule containing a dry, non-hazardous, test reagent system. The ampoule 102 prevents user contamination or hazard, has about a 4-year product shelf life, does not trigger transportation restrictions and does not need climate-controlled storage.
A test of a liquid may be performed using a test system 100 according to an embodiment of the present disclosure. A sample module or ampoule barrel 101 secures a test ampoule 102 for extracting a liquid sample. The ampoule barrel 101 limits a sample taker's exposure to the liquid. When used with a pre-dosed test ampoule 102, the ampoule barrel 101 and test ampoule 102 automatically start a test of the sampled liquid under the pressure of the vacuum.
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The stabilized ampoule tip breaker 900 breaks the tip of the ampoule 102 upon the application of pressure to the ampoule 102, forcing the test ampoule tip 104 to engage a surface disposed at an angle. The tip 104 of the ampoule 102 is submerged in liquid as to avoid suction entrained air and creating an unacceptable ampoule fill.
The test ampoule may be a hard-surfaced, self-filling container. The test ampoule includes mixed test indicators/media in predetermined quantities for performing a complete microbiological test. The test ampoules may be sealed, having a vacuum of about 20-30 inches of mercury or more. The test ampoule and contents may be insensitivity to storage conditions and may have a shelf life of about 4 years or more. The test ampoule includes a frangible area that can be broken, allowing a predetermined amount of sample to enter the test ampoule and be exposed to the test indicators/media.
The test ampoule may be an ampoule as described in U.S. Pat. Nos. 5,159,799 entitled VIAL WITH POWDERED REAGENT, 5,550,032 entitled BIOLOGICAL ASSAY FOR MICROBIAL CONTAMINATION, and 5,935,799 entitled BIOLOGICAL ASSAY FOR MICROBIAL CONTAMINATION, each patent being incorporated herein by reference in the entirety.
A test ampoule may be a pre-dosed, hermetically sealed, vacuum ampoule. The vacuum packaging of test ampoule preserves the reagent/media for years and needs no special storage conditions such as refrigeration. When the test is started, a aqueous sample of a predetermined volume, e.g., 7.5 ml, is automatically drawn into the test ampoule. The volume of sample drawn can be any predetermined amount, depending on, for example, the size of the test ampoule and the strength of the vacuum. The test may be concluded when the test ampoule turns a predetermined color, e.g., orange or red. The elapsed time from test start to test end determines the level of microbial contamination. Test results may come as fast as one (1) hour for concentrations of 201 or twelve (12) hours for 101 microbial concentrations. The test ampoule may be used as presence/absence test at 24 hours. A Triphenyltetrazoliumchloride (TTC) indicator may react to aerobic microbial activity in the sample to include facultative species. Fungi may also be detected. The presence of fungi may be indicated by floating red particles after 24 hours. Time/Concentration calibrations are based upon mixed microbial populations typically found in industrial and natural waters. Waters dominated by a particular species may use a one-time calibration adjustment. Each test ampoule comes complete with a sample/ampoule, snapping cup, dechlorinating solution, sample identification labels, waste-water instructions and a results/instruction chart. Test incubation temperature can be controlled, and may be set to, for example, 95° F. or room temperature. Test incubation can be performed manually by purchasing a reusable carry incubation tube or using a standard laboratory heat block or oven. Automatic incubation and end of test detection can accomplished using an incubator/auto-analyzer. Factory-prepared test calibrations/formulations and/or private labeling may also to used.
An insulated chamber, such as an autoincubation chamber, suitable to hold a plurality of test ampoules at a controlled temperature and for specific time initiates and maintains an incubation temperature for a period of time and may return to refrigeration. This chamber may be transportable for all operational phases of the test (refrigeration to incubation back to refrigeration). The test ampoule, sample module, and insulated chamber may be pre-assembled into a clean or sterilized product that is operated by the sample technician or test initiator.
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Having described embodiments for apparatus and method for sampling a liquid, it is noted that modifications and variations can be made by persons skilled in the art in light of the above teachings. It is therefore to be understood that changes may be made in the particular embodiments of the invention disclosed which are within the scope and spirit of the invention as defined by the appended claims. Having thus described the invention with the details and particularity required by the patent laws, what is claimed and desired protected by Letters Patent is set forth in the appended claims.
This application claims priority to U.S. Provisional Application Ser. No. 60/550,743, filed on Mar. 5, 2004, which is herein incorporated by reference in its entirety.
Number | Date | Country | |
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60550743 | Mar 2004 | US |