The present invention relates to a device for detecting volatile substances, to an apparatus using said device and to the relevant operative method.
More specifically, the invention concerns a device that can sample and analyse substances that are present within liquid and/or solid samples in an amount in the order of some micro litres, detecting volatile portion. Said device can be easily employed and ensures high operation stability.
Specification will be in the following addressed to detection of volatile substances contained in urine, and particularly to detection of markers useful to diagnosis of neuroblastoma and to monitor course of disease. It is well evident that said device must not be considered limited to this specific use.
At present, for diagnosis of neuroblastoma it is necessary detecting clinical-biological parameters, among which determination of homovanillic and vanilmandelic acid within patient urine. Nowadays, examination of said acids within urines is carried out with specialised centres by HPLC (High Pressure Liquid Chromatography), i.e. an expensive and difficult analysis.
In view of the above, it is an object of the present invention that of suggesting a device that can carry out measures of volatile substances with a high stability, quickly and at very low costs.
Another object of the present invention is that of suggesting a device for detecting and measuring volatile substances, that can be easily used even by those not skilled in the field.
It is therefore specific object of the present invention a device for detecting volatile substances characterized in that it comprises a containment box having at least one inlet opening for the introduction of a gas flow, preferably chromatographic degree air, one or more outlet openings of said gas flow, at least one analysis opening, one or more detection sensors arranged within said containment box, and at least one probe, insertable within said containment box through said at least one analysis opening, so that, when said probe is treated beforehand by a sample of a substance to be examined and it is inserted within said containment box, said gas flow uniformly carries the volatile substances from said sample to said one or more sensors.
Always according to the invention, port of said analysis opening is smaller than the sum of the ports of said one or more outlet openings, so that the insertion or the extraction of said probe from said analysis opening does not change the flow of said gas that reaches said sensors.
Still according to the invention, ratio between said port of said analysis opening and the sum of the ports of said one or more outlet openings is lower and/or equal than 0.01.
Furthermore, according to the invention, said containment box has a bottom base, where said inlet opening is made, and a top base, opposed with respect to said bottom base, where said one or more outlet openings and said analysis opening for the introduction of said probe are made, the number of said outlet openings being equal to the number of said one or more sensors,
Advantageously, according to the invention, said detection device comprises a body arranged within said containment box, said body being provided with a through channel that has a first end communicating with said analysis opening and a second end communicating with the internal of said containment box.
Always according to the invention, said containment box can be a removable body.
Still according to the invention, said one or more sensors can be installed on the internal lateral surface of said containment box.
Furthermore, according to the invention, said containment body has a cylindrical shape and said body has a substantially spheroidal shape, said body radially providing on its surface a plurality of channels, in a number corresponding to the number of said sensors, said channels ensuring a sufficient and even partialization of said gas, and thus of the sample, toward each one of said sensors.
Advantageously, according to the invention, said body can have one of the following features: it is made of a insulating material, so that when said probe is inserted within said channel, said sample of a substance to be examined does not evaporate while said probe is inserted through said channel; or it is made in such way that said through channel has a first portion made up of an insulating material, so that said sample of a substance to be examined does not evaporate while said probe is inserted in the part of the through channel of said first portion, and a second portion made up of a conducting material, so that, while said probe is inserted through the part of the through channel of said second portion, said sample of a substance to be examined is modified to said set beforehand internal temperature of said containment box.
Always according to the invention, said device can comprise comprises flow distribution means arranged in correspondence of said at least one inlet opening, said flow distribution means being suitable to distribute said gas flow through said one or more sensors, said flow distribution means comprising a porous separator, preferably made of glass, arranged so as to delimitate a diffusion chamber of said gas in correspondence of said inlet opening with respect to a measuring and vaporization chamber, wherein the volatile substances from said sample evaporate and are carried by said gas flow, by said channels of said central body, sample is sent toward said sensors.
Still according to the invention, said device can comprise means for controlling the internal temperature of said containment box, said control means preferably comprising a first thermoresistor installed within said diffusion chamber and a second thermoresistor installed within said measuring and vaporization chamber.
Advantageously, according to the invention, said substance to be examined is a liquid, preferably urine and/or serum and/or plasma and/or saliva and/or any other biological liquid.
It is further object of the present invention a detection apparatus characterized in that it comprises at least one detection and measure device as defined in the above; means for supplying said gas flow, comprising a gas cylinder, connected with said inlet opening by a conduct; means for adjusting the temperature of said gas out-flowing from said means for supplying said gas flow; at least one device for reducing the pressure of said gas; at least one flowmeter for adjusting said gas; and a control unit provided with a liquid crystal display and interaction members, said control unit being connected with said means for supplying said gas flow, with said sensors, with said first and second thermoresistor, with said means for adjusting the temperature, with said at least one device for reducing the pressure and with said flowmeter, said control unit being suitable to detect the temperature of said gas, to compare the same with the temperature of said diffusion chamber and of said measuring and vaporization chamber, so as to adjust said temperatures by said means for adjusting the temperature and said thermoresistors, to detect the measures of said sensors, and to show the outputs on said display.
It is also an object of the present invention a method for detecting volatile substances by means of said device for detecting volatile substances, comprising the following steps: providing a probe; treating, for example by immersion, the end of said probe in a sample of a substance to be examined, preferably a liquid sample, such as urine; and introducing said probe within said detection device as defined in the above through said analysis opening.
The present invention will be now described for illustrative, but not limitative purposes, according to its preferred embodiments, with particular reference to the enclosed drawings, wherein:
Similar parts will be indicated by the same references in the different views.
Making reference to
Examining in greater detail device 1, it is observed that in the present embodiment, said containment box 20 has a cylindrical shape and a bottom base 21, an upper base 22 and a lateral wall 23.
An opening 30 is obtained on said bottom base 21, in order to introduce said carrier gas within said diffusion chamber D, under pressure by a conduct 31. Entering carrier gas flow it heated up before, so that it has the same inner temperature of said containment box 20.
Gas employed is preferably gas chromatographic grade gas, having the required purity in order to prevent that substances are introduced to which sensors 51-56 could be sensitive that would jeopardize the measurement results. Furthermore, gas flow is adjusted by a pressure reducer and monitored by a flowmeter.
Thus, carrier gas enters within containment box at a temperature avoiding every condensation that could occur in case gas carrier temperature is lower than temperature causing evaporation of volatile parts within sample introduced. In fact, possible condensation randomly varies concentration of evaporated substances within carrier gas, thus making unreliable analyses.
In view of high sensitivity of a measurement system suitable to analyze micro amounts, it is necessary a remarkable stability of carrier gas flow that, if under static conditions, does not create particular problems, but during introducing can cause limitations. Thus, device 1 provides a particular geometry.
Coming back to
Number of sensors 51-56 is the same number of said carrier gas outlet openings; moreover, the latter are provided in correspondence of sensors 51-56, so as to ease outlet of carrier gas flow from containment box 20. Said sensors 51-56 can be of different type and different number, or they can all the same.
Furthermore, among most versatile sensors, it is possible indicating conductivity variation sensors, piezoelectric sensors, quart microbalance (QCM), surface acoustic wave sensors (SAW), MOSFET sensors, thermo conductivity sensors.
Device 1 also provides gas diffusion means 60, defining said diffusion chamber D. said gas diffusion chamber 60 are suitable to diffuse gas entering through said opening 30 within said vaporization and measurement chamber M, to send it toward said sensors 51-56.
Particularly, said gas diffusion means 60 comprise a porous septum 61, preferably comprised of glass, provided with a plurality of through holes (not shown in the figures). Said porous septum 61 is spaced with respect to opening 30 by a ring 62. Said porous septum 61 and said ring 62 define diffusion chamber D. said porous septum 61 ensures a capillary diffusion of gas flow, preventing preferred ways, and through channels realized within the central body 73 it is ensured right partialization of flow toward every sensor. Said channels are vertical milling, with a depth of about 10 mm, realized on lateral wall of body 73. In case six sensors are provided, said channels have a 60° distance between axes. Distance between axis angle of 360° is divided by the number of sensors.
Furthermore, a first thermo resistance (not shown in the figure) is provided within said diffusion chamber D for controlling temperature within the containment box 20. Furthermore, a Teflon® disk 63 is provided on said porous septum, the function of which will be better described in the following.
In order to make detection, it is necessary placing substance to be subjected to examination within the box, so that it can be taken from gas flow and sent toward sensors 51-56. To this end, an analysis opening 71 is obtained on the upper base 22 of the containment box 20, communicating with said vaporization and measurement chamber M by a through channel 72 of a body 73, preferably a removable body, provided within said containment box 20. Said body 73 has a substantially spherical shape. Dimensions and shape of said body 73 are particularly suitable to ensure a partialization of gas flow (transporting extracted substances) uniform on said sensors 51-56. Each sensor 51-56 is thus interested by the same volume of sample. By the above solutions it is possible obtaining specific response signals that are solely a function of the substance amount, without any interference due to the amount interesting every single sensor 51-56 employed. In other words, amount of extracted substances from sample interesting every single sensor is exactly the same amount for each one of them, thus preventing response signal depending on the amount and on the quality of the substance to be subjected to examination.
It must be taken into consideration that number of sensors can be varied. Generally speaking, no structural modification is necessary with a number of sensors between 1 and 12. Furthermore, said sensors 51-56 can be fixed to the inner surface of wall 23 of said containment box 20 or, preferably, to said body 73. In the latter case, being said body removable, replacing the same, partializing said carrier gas flow toward single sensors, it can be easily modified number of sensors 51-56. Obviously, type and number of sensors to be used only depends on substances to be subjected to examination and to quantify.
Said through channel 72 is substantially provided in correspondence of the symmetry axis. Said body 73 of the present embodiment is comprised of insulating material, in order to prevent that, while substance to be subjected to examination is introduced through channel 72 within measurement and vaporization chamber M, said substance to be subjected to examination evaporate before arriving at the same chamber.
To position the sample of the substance to be subjected to examination, it is provided the use of a sampling probe 80, that can be realised as a rod, a closed capillary or like, in any case having an elongated shape, and comprised of a chemically inert material, resisting to temperature and having such a section to be able to pass through said analyses opening 71 and said channel 72.
Said sampling probe 80 is at least partially submerged (typically about 5 mm) within substance to be subjected to analysis, to be “wet” by the sample to be subjected to examination. The same result can be obtained by rubbing or by any other method permitting “wetting” a portion of said sampling probe 80. Sampling probe 80 so treated is introduced within the diffusion chamber D, within which, under the effect of temperature, volatile portion of the sample quickly passes to gaseous state and carrier gas flow sends it toward sensors 51-56.
When said sampling probe 80 is inserted within said channel 72 through said analysis opening 71, “wet” end reaches said porous septum 61. Teflon® disk 63 is suitable to prevent that sampling probe 80 hits porous septum 61.
Carrier gas, through said diffusion chamber D, reaches glass porous septum 61 and is diffused within measurement cell M. Volatile substances contained within “wet” portion (end) of the probe, evaporate and gas carries them toward sensors 51-56. Then, gas flow exits from vaporization and measurement chamber M through said outlet openings.
Gas flow, through porous septum 61, thanks to the shape of said body 73, creates suitable flow paths within said body 73, within vaporization and measurement chamber M, and it is radially diffused toward every sensor 51-56. Six outlet openings and Teflon® disk 63, centrally provided on said porous septum 61, create preferred paths through which gas, and thus volatile substances, flow.
Flow resistance due to said analysis opening 71, through which it is inserted or withdrawn the sampling probe 80, has a much higher value of flow resistance caused by said outlet openings 41 or 42 of said gas flow, so that introduction, or withdrawal, of sampling probe 80 from said through channel 72 does not create appreciable variations of carrier gas flow balance toward sensors 51-56. In a preferred embodiment, ratio between port of said analysis opening 71 and sum of ports of said outlet openings is in the order to 1/100 (0.01).
Said solution ensures flow stability necessary to repetitivity of responses from employed sensors that unavoidably would vary physical conditions (temperature, pressure and flow) of gas passing through them.
Thus, when probe 80 with sample to be subjected to analysis is introduced within containment box 20, first insulated portion prevents that said sample can evaporate, while second final portion brings sample to temperature of said vaporization and measurement chamber M.
Preferably, a second PT100 thermo resistance (not shown in the figures) is installed in said vaporization and measurement chamber M, to detect temperature in order to permit a control and comparison with temperature of diffusion chamber D.
Usually, used sampling probe 80 can have different shape and dimensions, on the basis of the sample to be subjected to analysis. Anyway, maximum diameter must be 4 mm. Moreover, probes for solid samples and probes for liquid samples can be individuated.
Liquid sample probes are realised by a support rod, comprised of material resisting to temperature and chemically inert (glass, ceramics, stainless steel, ecc.). Said probes provide an end curve, which is “wet” by immersion within liquid, in order to take the sample to be subjected to analysis.
Solid sample probes are comprised of chemically inert materials, resisting to temperature and mechanically not deformable. Usually, they have a cylindrical shape, with a point tip, easing introduction within solid samples. Their use provides an introduction of the sample for the following withdrawal. Volatile parts, if present within sample, remain on probe, which are injected within device 1, introducing the probe within a suitable opening.
Solid sample probes can also be used for sampling volatile substances present in a gaseous atmosphere, such as, e.g. in human breath. In order to realise the above, it is necessary such an equipment which, by a Peltier battery system, refrigerates probe up to the temperature of −8° C. (adjustable value). Refrigerated probe, if brought in contact with a gaseous atmosphere, “catches” volatile substances, freeing them and, when introduced within device 1, releases the same within gas, by which they are sent to sensors 51, 52, 53, 54, 55 and 56.
Device 1 can even operate in a suitable apparatus (not shown in the figures), essentially providing a gas flow generation unit comprising a cylinder connected with said conduct 31.
Said apparatus also comprises a control unit provided with a control panel with a liquid crystal display and interaction members such as a keyboard.
Said control unit is connected to said sensors 51-56, with said thermo resistances installed within said diffusion chamber D and within said vaporization and measurement chamber M, to pressure reducer and to flowmeter. By this solution, diffusion chamber D and vaporization and measurement chamber M are at the same temperature. This permits preventing that hottest or coldest spots along the evaporated substances path toward sensors 51-56 make concentration differences within gas, with consequent unreliable responses. In fact, in case points with different temperature are present within device 1, they would not permit a proper partialization of sample toward sensors 51-56 and, taking into consideration micro amounts introduced and vaporised, responses would not be proportional to gas concentration, but rather would randomly vary.
Temperature can be set at a maximum value set by sensor 51-56 maximum exercise temperature. Anyway, it is advisable choosing the highest possible temperature, to be sure that all volatile parts of the sample pass to the gaseous phase.
Adjustment of temperature is of the proportional type, permitting reaching a precision of 0.1° C. order.
Said adjustment stability is essential for sensor 51-56 response, both in a static phase and during analysis. Actual value can be continuously monitored by said display on said apparatus control panel.
A further advantage of the invention is that device can be used in all apparatuses designed to analyse micro amounts of volatile substances in liquid but also solid samples, and thus it can be applied to biomedical, food, chemical, environmental, ecc fields.
The present invention has been described for illustrative, but not limitative purposes, according to its preferred embodiments, but it is to be understood that variations and/or modifications can be introduced by those skilled in the art without departing from the relevant scope, as defined in the enclosed claims.
Number | Date | Country | Kind |
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RM2009A000581 | Nov 2009 | IT | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/IT2010/000448 | 11/10/2010 | WO | 00 | 6/27/2012 |