TWI299262B - - Google Patents

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TWI299262B
TWI299262B TW94122671A TW94122671A TWI299262B TW I299262 B TWI299262 B TW I299262B TW 94122671 A TW94122671 A TW 94122671A TW 94122671 A TW94122671 A TW 94122671A TW I299262 B TWI299262 B TW I299262B
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Taiwan
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sample
sampling
quantitative
liquid
solution
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TW94122671A
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Chinese (zh)
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TW200701948A (en
Inventor
Shing Huang Tu
Ling Yuan Chou
Su Chen Hsu
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Shing Huang Tu
Ling Yuan Chou
Su Chen Hsu
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Priority to TW094122671A priority Critical patent/TW200701948A/en
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1299262 九、發明說明: 【發明所屬之技術領域】 本發明係關於一種採樣裝置,特別是可定量擷取檢體 之定量採樣裝置及其使用方法。 【先前技術】 隨著經濟發展,人觸自我㈣之意識也日升,目前 許多醫院或是檢驗所皆提供各種生化檢測,提供人們進行1299262 IX. DESCRIPTION OF THE INVENTION: TECHNICAL FIELD The present invention relates to a sampling device, and more particularly to a quantitative sampling device capable of quantitatively capturing a sample and a method of using the same. [Prior Art] With the development of the economy, the awareness of people touching themselves (4) is also rising. Many hospitals or laboratories now provide various biochemical tests to provide people with

基本之身體機能檢測,例如血糖測試、肝腎功能測試、膽 固醇測試等。 ° 曰刚_床醫學檢驗卜浦·,基本流程皆 是先要求病人們到抽血台抽血或是採集體液組織樣本,取 得檢體後’將檢體送至巾央檢驗錄行檢驗,最後再把社 果報告移送給縣要求檢驗的人。通t,檢驗人員都不太 ===她,或_縣嫩驗的人需 利用這些報告。近年來,在力侧、 手術至和恢设至附近(或内部)皆設立了 名);圆。由於人們已意制魏報告_^((王 T—-Tlme (ΤΑΤ)的重要性 巧 速檢體輸送系統。去於详各从上处 卞夕西h衣叹快 尚算怏速;但是,運轉良好時’檢驗速度 檢驗程序變得更_。域诚魏整合雜素,整個 科技的進步影響了社會的每個層面 學。透過各種研究使得驚人的改變一寺」士科 室也隨著這種步調前進荖。夂 而鉍床檢驗 化的診斷檢驗辅助夺统以[二動化的檢驗儀器、電腦 力糸統以及魏系繼續推出。其中,最 6 1299262 令人印象深刻的就是重點照護檢驗(P〇int CareBasic physical function tests, such as blood glucose tests, liver and kidney function tests, cholesterol tests, etc. ° 曰 _ _ bed medical test Bu Pu ·, the basic process is to ask the patient to go to the blood collection station to draw blood or collect body fluid tissue samples, after obtaining the sample, 'send the sample to the towel central inspection record inspection, and finally The report of the fruit is transferred to the person in charge of the county for inspection. Through t, the inspectors are not quite === her, or _ county impressed people need to use these reports. In recent years, the name has been established on the side of force, surgery and restoration to the vicinity (or inside); Because people have been interested in the Wei report _ ^ ((Wang T--Tlme (ΤΑΤ) is the importance of the speed of the body transport system. Go to the details from the top of the 卞 西 西 衣 衣 衣 叹 ; ; ; ; ; ; ; When the operation is good, the inspection speed inspection procedure becomes more _. The domain is honest and integrated, and the progress of the whole technology has affected every level of society. Through various studies, the amazing change of a temple is also the same. Step by step, 荖 夂 夂 铋 铋 铋 铋 检验 检验 检验 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 铋 二 二 二 二 二 二P〇int Care

Testing ; P0CT)。 POCT是利用小型、可攜式的儀器在短時間内就可測得 檢驗結果並即時知悉,這種快速方便的檢驗形式效果顯 著,然而其精確度、品管、儀器校正、以及檢驗結果的責 任歸屬衝擊著傳統的檢驗室。Testing; P0CT). POCT is a small, portable instrument that can be used to measure test results in a short period of time and instantly know that this fast and convenient test form has a significant effect, but its responsibility for quality, quality control, instrument calibration, and inspection results. The attribution impacts the traditional laboratory.

P0CT並不是在傳統的檢驗室進行檢驗,而是在患者的 身旁做檢驗,例如醫師診療室、急診室、門診、病房、兵召 護點、甚或是居家檢驗等。常見的檢驗包括了血糖=測'、'、 尿液測試、潛血試驗、膽固醇檢驗、HDL檢測、血液凝固 測試等。這些P0CT的檢驗可能由非檢驗室人員來執行,這 些人可能是經過訓練的專業人士(例如醫師、護士、醫師 5等)、也可能是只受過簡單基本訓練的人士(例如病患 患,本身等),因此P0CT存在的潛在缺點之一,即 :、、、執行人員的不穩定性造成採樣或是儀器使用的不確定P0CT is not tested in a traditional laboratory, but is tested at the patient's side, such as a physician's office, emergency room, clinic, ward, battalion, or even home inspection. Common tests include blood glucose = test ', ', urine test, occult blood test, cholesterol test, HDL test, blood coagulation test, etc. These P0CT tests may be performed by non-inspection personnel who may be trained professionals (eg, physicians, nurses, physicians, etc.) or may be individuals who have only had simple basic training (eg, patients, themselves) Etc.), therefore one of the potential shortcomings of P0CT, namely: ,, the instability of the executive caused by sampling or the uncertainty of the instrument used

抽二=職為例’當患者欲進行血液測試時,在完成 步驟,的錢檢體㈣要進行所血漿血球分離 °這些分離及檢驗的 污4=率r加入分離溶劑等人為操作,提高了血液受 由非專itr卜,許多需要定量以執行檢驗的血液檢體, 寻菓人貝執行時,也會提高其誤差率。 但為3=^_雖為—種令人興奮的簡化檢驗模式, 低人細^ 醫料業,發展出方便操作且可有效降 _ ‘、、、本所造成失誤之檢驗儀器及其周邊元件,已成為 ^9262 當前重要目標之一。 f發明内容j 定量採樣裝置,以 作二體=提供- 的’係希望提供-定量採樣裝 ’降低人為顧之失誤及污染發 本發明之另一主要目 置,以間化檢體處理程序 生的機率。 本發明係揭露—種液狀檢體之 方法。本剌之轉 峰U及其使用 及-輸出部。其中採樣部部厂套合部、 ί 衫侧財—敢體積之緩衝溶 溶、夜相p a°部#魏上之餘檢體與緩衝 办液相互混合而得一壽溶液。 ::當推進採樣部時’稀釋溶液二吏=膜: 檢==品。輸出简合至過_,_代 ,綜上所述,由難人健康管理_念日益提升,這類 』、型化可赋之分聽置搭配本判之採血裝置,將非常 適合用於居家照護(home—care)、照護點監護 P 〇f Care)以及运距居豕照護(telehealth)等相關 f用領域,應財個找量顯裝置,可有效提升樣品 刖處理之效率,及降低人為操作不當對_結果之影 度。 曰 !299262 【實施方式】 本發明所揭示為液狀檢體之定量採樣裝置及其使用方 法。希望利用本發明之定量採樣裝置簡化檢體樣品之前處 理步驟,並藉由一體化的前處理降低人為操作之失誤率。 為了使本發明之敘述更加詳盡與完備,係列舉數較佳實施 例以說明本發明。請參考下列描述並配合以下之圖式。Take the second = job as an example 'When the patient wants to carry out the blood test, in the completion of the step, the money sample (4) to carry out the plasma cell separation. These separation and inspection of the pollution 4 = rate r added to the separation solvent and other human operations, improved The blood is subject to a non-specialized iterative, and many blood samples that need to be quantified to perform the test will also increase the error rate when the fruit seeker performs it. However, although 3=^_ is an exciting simplified test mode, the low-level fine medical industry has developed a test instrument and its peripheral components that are easy to operate and can effectively reduce the errors caused by the company. , has become one of the current important goals of ^9262. f SUMMARY OF THE INVENTION j Quantitative sampling device, for the two-body = provide - the 'recommended to provide - quantitative sampling package' to reduce human error and pollution, another major object of the invention, to inter-sample processing procedures The chance. The present invention discloses a method of seeding a liquid sample. The peak U and its use and output. Among them, the sampling department of the factory department, the 衫 侧 侧 — - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - :: When advancing the sampling section, 'diluted solution 吏 = membrane: check == product. The output is concise to the _, _ generation, in summary, by the difficult health management _ reading is increasing, this type of 』, type can be assigned to match the blood collection device of this judgment, will be very suitable for home use Care-related (home-care), care point monitoring (P 〇f Care) and transportation distance (telehealth) and other related fields, should find a quantitative display device, can effectively improve the efficiency of sample processing, and reduce artificial Improper operation on the _ result. 299 !299262 [Embodiment] The present invention discloses a quantitative sampling device for a liquid sample and a method of using the same. It is desirable to utilize the quantitative sampling device of the present invention to simplify the processing steps prior to the sample sample and to reduce the error rate of human manipulation by integrated pre-processing. In order to make the description of the present invention more complete and complete, the preferred embodiments of the present invention are illustrated. Please refer to the following description and match the following diagram.

1尔钩伞赞明之定量採樣裝 置之較佳實施例結構示意圖。如圖所示,圖一 A中之定量 採樣衣置1包含一採樣部11、一套合部12、及一輸出部 =:其中採樣部11具有一預定尺寸之採樣環ill,用以定 ,採取(沾取)一液狀檢體,液狀檢體可以是血液檢體或 疋體液檢體(例如腦脊髓液;cerebrospinal fluid;⑽。 ’、、、:而’本發明之技術特徵並絲限於此,·換言之,其他亦 樣環上形成—薄膜之液狀檢體也應視為本發明之保 。贼。此外,採樣環⑴之大小材質、形狀盘尺寸A schematic diagram of a preferred embodiment of a quantitative sampling device as claimed by the hook umbrella. As shown in the figure, the quantitative sampling device 1 in FIG. 1A includes a sampling portion 11, a set portion 12, and an output portion=: wherein the sampling portion 11 has a sampling ring ill of a predetermined size for determining, Taking (staining) a liquid sample, the liquid sample may be a blood sample or a corpus callosum sample (for example, cerebrospinal fluid; cerebrospinal fluid; (10). ',,: and 'the technical features of the present invention In this case, in other words, other liquid samples formed on the ring-like film should also be regarded as the protection of the present invention. In addition, the size of the sampling ring (1), the shape of the disk size

id=ensiQn)亦可’係依制過程之實際需求依液狀檢體 舄求1而設計改變,例如,力太廉 聪 之金屬或其他材質之圓環;熟悉該行技蔹者 ::描述並非用以限定本發明之中心實體,而僅為:實 衝溶有:預_之緩 液狀檢體與_麵被混合^得—娜上之 =積之尺寸係為特定,且緩衝= 為預义,是以液狀檢體被稀釋過後之體積與濃度 9 1299262 幾乎維持固定。亦即,本發明具有定量功能。 樣品。 樣品輸出至外 上逑之套合部絲合有—過軸14 =,稀釋麵會被迫使通,轉料—η =出部13則輕合至過濾膜14,用以將代檢 双 其中,上述之採樣部u係為—推進器 1及-推進把手⑴。推進把手U2上可更套:= =彈性且稍具摩擦性之材質提供採樣部 且^人 地套合入套合部12中。 〆丑山口 ,先填絲雜套合部12之緩输液i2ia,係 部i2之一密封槽121中。密封槽121會因採‘ 之^、合部12時之壓力而破裂,使得填充於其内部 之、、羡衝溶液與液狀檢體混合。 預先填充㈣於套合部12之緩衝溶液,不—定 封於一㈣射’請參相―B。緩衝溶液121a亦可^ 填=套合部12中並與採樣環lu保持一不接觸之距離, =部上更包含—排氣孔122,當該採樣部Η沾取檢 隹進套合部12時,推進過程中所形成的氣體壓力合由 排氣孔122排出以避免緩衝溶液咖因壓力而自輪出曰部 13中排出。 至此’完成液狀檢體之定量採樣及稀釋,相較於習知 需要先使職齡液齡»檢體,翻祕量分液哭 (pipet)吸取定量稀_之步驟,本發明之定量採樣裝置 係將上述二個步驟統合於套合部中,如此—來,樣品檢測 10 1299262 不但可沾取定化。另外,本發明之技採樣裝置 整個混合過而與定量緩衝溶液相互混合,且 降低了於開放之套合部中進行,是以有效地 ' 、 衣丨兄中可能造成的人為操作污染。 種體採樣裝置可躺於定赌取血液或是各 、广4 (例如腦脊髓液,CSF)。有的血液檢測只需 義器中即_^ 液先混合Γ達稀均需先經過全血與緩衝溶 -球之前處果,稀釋液進一步通過遽膜以過遽掉 5 之過義14 ’即可用來進行血漿分離血球分離之 >驟。其係彻通過物質之粒徑大小進行篩選,使 tr嫌狀檢體__不同健餘大小種類的 :「膜田推進採樣部ii時’稀釋溶液會被迫使通過過滤 、而離析出一代檢樣品。輸出部13則麵合至過濾膜 、4’用以將代檢樣品輸出至外部定量採樣裝置ι外。通過 過遽膜14的血漿則可藉由輸出部13 (配合分析儀器種類 而有不同形狀’例如針頭)推擠射出。此血聚可直接滴入 小型測定裝置如血糖、腎功能、肝功能、血脂、心血管疾 病等生化分析裝置,或檢測賀爾蒙、癌症指標、過敏原、 致病菌以及其他大小分仅免疫分析裝置。 …至此,自自採集出血〉夜或體液,後至送入分析儀器以 進仃之定量採樣、混合溶液、過濾等過程,其間每道程序 均在本發明之定量採樣裝置中進行,如此_來,不但簡化 了前處理步驟、也降低了人為操作所造成的誤差。 1299262 檢體進行前 利用本發簡減之定量採樣裝置對液狀 處理之方法,包括以下步驟: 步“2G1 :首先以-採樣部之—採樣奴量採取(沾 =)-液紐體。此餘檢體可為—錢檢體或是各式之 體液檢體。具預定面積之採樣糊絲面張力 量 液狀檢體。Id=ensiQn) can also be designed according to the actual needs of the process according to the liquid sample request 1 , for example, the ring of metal or other materials of Li Tai Cong; familiar with the line:: Description It is not intended to limit the central entity of the present invention, but only: the actual immersion is: the pre- _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ The pre-sense is that the volume and concentration of the liquid sample after dilution are almost maintained at 9 1299262. That is, the present invention has a quantitative function. sample. The output of the sample to the outer upper part of the sleeve is combined with the over-axis 14 =, the dilution surface is forced to pass, and the transfer-n = the outlet 13 is lightly coupled to the filter membrane 14 for use in the inspection. The sampling unit u described above is a propeller 1 and a propulsion handle (1). The push handle U2 can be more sleeved: = = elastic and slightly abrasive material provides the sampling portion and fits into the sleeve portion 12. 〆 山 山 山 , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , The seal groove 121 is broken by the pressure at the time of the joint portion 12, so that the buffer solution filled in the inside thereof is mixed with the liquid sample. Pre-fill (4) the buffer solution of the fitting part 12, not - seal in one (four) shot 'Please take the phase - B. The buffer solution 121a can also be filled in the sleeve portion 12 and maintained at a distance from the sampling ring lu. The portion of the portion further includes a venting opening 122. When the sampling portion is immersed in the entanglement portion 12 At this time, the pressure of the gas formed during the advancing process is discharged from the vent hole 122 to prevent the buffer solution from being discharged from the rim portion 13 due to the pressure. So far, the quantitative sampling and dilution of the liquid sample is completed, and the quantitative sampling of the present invention is compared with the conventional method of first making the age of the liquid body»the body, and the step of dividing the liquid to the pipet to take the quantitative dilution. The device integrates the above two steps into the fitting, so that the sample detection 10 1299262 can not only be determined. Further, the technique sampling device of the present invention is entirely mixed and mixed with the quantitative buffer solution, and is lowered in the open fitting portion, so as to effectively contaminate the artificial operation which may be caused by the clothes. The seed sampling device can lie on the blood or each of them (for example, cerebrospinal fluid, CSF). Some blood tests only need to be in the right-handed device, ie, _^ liquid first mixed with sputum, first need to pass through the whole blood and buffer solution-ball before the fruit, the dilution further passes through the aponeurium to get rid of 5 It can be used to perform plasma separation of blood cells. It is screened by the particle size of the material to make the smear sample __ different types of health: "When the membrane field advances the sampling section ii, the dilution solution is forced to pass through the filtration, and the generation of the sample is isolated. The output portion 13 is surfaced to the filter membrane, 4' is used to output the sample to the external quantitative sampling device ι. The plasma passing through the membrane 14 can be different by the output portion 13 (combined with the type of analytical instrument) The shape 'such as a needle' is pushed and injected. This blood accumulation can be directly dropped into a small-scale measuring device such as blood glucose, kidney function, liver function, blood lipids, cardiovascular disease and other biochemical analysis devices, or hormones, cancer indicators, allergens, Pathogenic bacteria and other size-only immunoassay devices. ... At this point, self-collecting bleeding> night or body fluid, and then into the analytical instrument to enter the quantitative sampling, mixing solution, filtration, etc., each procedure is in The quantitative sampling device of the present invention is carried out in such a manner that not only the pre-processing steps are simplified, but also the errors caused by the human operation are reduced. 1299262 It means a method of quantitative sampling of a liquid processing, comprising the following steps: Step "2G1: firstly - the sampling unit - the amount of sample taken slaves (= stick) - New liquid body. The remaining sample may be a money sample or a body fluid sample of various types. Sampled paste surface tension with a predetermined area. Liquid sample.

步驟202 :接著將採樣部套入一套合部中。 壯罢m3:反覆搖晃定量採樣裝置(可搖晃定量採樣 衣本身或是反覆抽拉採樣部),使液狀檢體與一緩衝溶液 充分混合,轉-響絲。此叙_麵可預先填充 於套合部中(上述實施例),或是填充於採樣部中(請來考 下「實施例)。不論其預先密封填充於何處,狀在液狀檢 體進入套合部中才釋出與該液狀檢體混合。Step 202: Then insert the sampling part into a set of joints. Extend m3: Repeat the shaking quantitative sampling device (shake the quantitative sampling itself or repeatedly pull the sampling part), mix the liquid sample with a buffer solution, and turn the wire. The surface may be pre-filled in the fitting portion (the above embodiment) or filled in the sampling portion (please refer to the "Example"), regardless of where it is sealed in advance, in the liquid sample It is released into the ferrule to be mixed with the liquid sample.

步驟204 :最後推進採樣部,以迫使上述混合而得之 稀釋溶液通過-過顧H輸出部輸出所離析出而得 之代檢樣品。此處之過濾膜係利用通過物質之粒徑大小進 仃4選。使用者可針對欲分析檢體之不同制不同粒徑大 小種類之過濾膜。 上述之緩衝〉谷液係預先填充密封於套合部之一密封槽 中’該密封槽可因採樣部套合入套合部時之壓力而破裂, 使得填充於内部之緩衝溶液與液狀檢體混合。然而本發明 所揭露之定量採樣裝置並不限定其緩衝溶液所置放之位 置,只要其可在液狀檢體送入套合部内時達到混合之目的 即可。 12Step 204: Finally, the sampling portion is advanced to force the diluted solution obtained by the above-mentioned mixing to pass through the sample which is separated from the output of the H output portion. The filter membrane here is selected by the particle size of the material. The filter film of different particle size and size can be selected by the user for different samples to be analyzed. The buffering > gluten liquid is pre-filled and sealed in one of the sealing grooves of the fitting portion. The sealing groove can be broken by the pressure when the sampling portion is fitted into the fitting portion, so that the buffer solution and the liquid filling filled inside are broken. Body mixing. However, the quantitative sampling device disclosed in the present invention does not limit the position at which the buffer solution is placed, as long as it can be mixed for the liquid sample to be fed into the nest. 12

1299262 示意圖。圖二中之發明之另一雛實施例結構 合部22、及-輸出置2包含-採樣部21、-套 樣部21亦具有H + 述之第一較佳實施例,採 之緩衝溶液,—預定體積 扛取(沾取)一液狀檢體,液狀檢 是驗檢體(親料),採樣環 套入套人邱22 :夜狀檢體需求量而改變。當採樣部211 i 液。上述之套合部並耦合有一過遽膜 24,而田離析:7 : 21時,稀釋溶液會被迫使通過過濾膜 田離析出—代檢樣品。輸出部33難合至過濾膜24, 用以將代檢樣品輪出至外部。 ^、 =施例之採樣部21係為—擠壓管,一端為採樣環 、另一端為填充緩衝溶液之密封槽212。具一預定體積 之緩衝溶液係預先填充密封於密封槽212中 因観树觀得軌_敎、雜減與2 混合。 1然上述二實施例中圖一(包含圖一 A、圖一 b)與圖 二兩者緩衝溶液所填充之位置㈣,但此並料影響本發 朱之主要舰’即透雜樣環定量娜檢體並快速混合緩 =液後通過過_得爾理過之代撿樣品之毅操作特 綜上所述,由義人健康管理峨念日益提升,這類 小型化可攜仅分難置搭配本發明之採血裝置,將非常 適合用於居家照護(hQme_咖)、照護點監護 13 1299262 (point-of-care)以及遠距居家照護(telehealth)等相關 f用領域,本㈣之定量採«置,可有效提升樣品 刖處理之效率’及降低人絲作不當對制絲之影 度。 本發明雖以較佳f例闡明如上,然其並_以限定本 發明精神與發明實體僅止於上述實施_。是以,在不脫 離本發明之精神與顧崎作之修改,均應包含在下述申 請專利範圍内。 【圖式簡單說明】 藉由以下詳細之描述結合所附圖式,將可輕易明瞭上 述内容及此項發明之諸多優點,其中: 圖一 A〜B係為本發明之定量採樣裝置之較佳實施例 結構示意圖。 圖一係為本發明之定量採樣裝置另一較佳實施例 結構示意圖。 【主要元件符號說明】 1定量採樣裝置 11採樣部 111採樣環 112推進器 113活塞 12套合部 121密封部 14 1299262 121a緩衝溶液 122排氣孔 13輸出部 14過濾膜 2定量採樣裝置 21採樣部 211採樣環 212密封槽 22套合部 23輸出部 24過濾膜1299262 Schematic. Another embodiment of the invention in FIG. 2 is a structural joint portion 22, and an output device 2 includes a sampling portion 21, and the sleeve portion 21 also has a first preferred embodiment of H + described, and a buffer solution is used. - The predetermined volume is taken (dip) into a liquid sample, the liquid test is the test body (parent material), and the sampling ring is inserted into the set of people 22: the amount of the night sample is changed. When the sampling unit 211 i is liquid. The above-mentioned fitting portion is coupled with a ruthenium film 24, and when the field is separated: 7:21, the diluted solution is forced to be separated through the filter membrane - the sample is sampled. The output portion 33 is difficult to be joined to the filter membrane 24 for taking the test sample out to the outside. ^, = The sampling portion 21 of the embodiment is a squeeze tube, one end is a sampling ring, and the other end is a sealing groove 212 filled with a buffer solution. The buffer solution having a predetermined volume is pre-filled and sealed in the sealing groove 212. The 観 观 敎 敎 杂 杂 杂 杂 杂 杂 杂 。 。 。 。 。 。 。 。 1 is the position (4) filled in the buffer solution of Figure 1 (including Figure A A, Figure 1 b) and Figure 2 in the above two embodiments, but this combination affects the main ship of the hair of Zhu After checking the body and quickly mixing it with the liquid, I passed the test of the 捡 理 理 理 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特 特The blood collection device of the invention is very suitable for use in home care (hQme_cafe), care point monitoring 13 1299262 (point-of-care), and remote home care (telehealth) and other related fields, the quantitative mining of (4) «Set, can effectively improve the efficiency of sample processing" and reduce the impact of improper silk on the silk. The present invention has been described above by way of a preferred example, and the present invention is not limited to the above-described embodiments. Therefore, modifications that do not depart from the spirit of the invention and that of Gusaki should be included in the scope of the following patent application. BRIEF DESCRIPTION OF THE DRAWINGS The above and other advantages of the invention will be readily apparent from the following description of the appended claims. A schematic structural view of an embodiment. BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a schematic view showing the structure of another preferred embodiment of the quantitative sampling device of the present invention. [Description of main component symbols] 1Quantitative sampling device 11 Sampling section 111 Sampling ring 112 Propeller 113 Piston 12 Nesting part 121 Sealing part 14 1299262 121a Buffer solution 122 Exhaust hole 13 Output part 14 Filter membrane 2 Quantitative sampling device 21 Sampling section 211 sampling ring 212 sealing groove 22 sleeve portion 23 output portion 24 filter membrane

1515

Claims (1)

1299262 申請專利範圍: 1. 一種液狀檢體之定量採樣裝置,包括: 定量採取 -採樣部,具有-預定尺寸之採#環, 該液狀檢體;以及 一套合部,裝有-狀_之_溶液, 套入該套合料,魏上之麵缝體 相互混合而得一稀釋溶液。 X、咬倚洛液 2. 如申請專利範圍第所述之定量採 中该套合部並_合有-過濾膜,t推進該採樣部狂、 溶液會被迫使通過該過_,轉析出—代檢樣:稀釋 3. 如申請專利範圍第2項所述之定量採樣 =夕:輸出部,搞合過_,用以將該代檢樣品輸 5·如申請專利範圍第3項所述之定量採樣裝置,盆 中该緩衝溶祕預先填充密封於鱗合部之—密封槽中二 ^如申請專利範圍第4項所述之定量採樣裳置曰,其 ==槽係可因該採樣部套合人該套合部時之壓力而破 侍填充於内部之該緩衝溶液與該檢體混合。 7· 一種液狀檢體之定量採樣裝置,包括·· 積之rti# ’具有—駄尺寸之採樣軌裝有—預定體 、咬衝溶液,用以定量採取該液狀檢體;以及 4. 如申請專利範圍帛!項所述之定量採樣 並 中该採樣部係為-推進器,包含該採樣環及—推進,巴手、。 16 1299262 套人;^合與該採樣部套合,當該採樣部套入該 溶液會峨她爾’嗜品麵 9.如申請專利範圍帛8項所述之定 包含―-輸出部合至該過濾膜,用代二’ 出至外部。 將°亥代私樣品輸 中該=樣第6項=述之定量採樣裝置,其 欠I你馬擠壓官,一端為該採 充該緩衝溶液之密封槽。 、另一端為填 巾背:/ 專她圍第8項所述之定量採卿詈並 中该、讀溶液係預先填充密封於該㈣槽中。 其 i2.如申睛專利範圍第8項所 中f封槽係可因擠壓而破裂使得填充於内,其 液與該檢體混合。 之该緩衝溶 之方 法,1包3括利用一定量採樣裝置對液狀檢體進行前處理 以—採樣部之-採_定量採取一液狀檢 將該採樣部套入一套合部中; 體與一緩衝溶 、反覆搖晃該定量採樣裝置,使該液狀檢 液充分混合,而得一稀釋溶液;以及 17 以迫使該稀釋溶液通過一過濾膜,而 膜係利用Γ^㈣嫌,其中該過滤 顿胃妹徑大小進行篩選。 溶15.如申請專利範圍第13項所述之方法 ,其中該緩衝1299262 Patent application scope: 1. A quantitative sampling device for a liquid sample, comprising: a quantitative take-sampling portion, a ## ring having a predetermined size, the liquid sample; and a set of joints, fitted with a shape _ _ solution, nested into the kit, Wei Shang's face seams are mixed with each other to obtain a diluted solution. X, bite Le Luo liquid 2. As described in the scope of the patent application, the quantitative collection of the kit and the combination of - filter membrane, t push the sampling section mad, the solution will be forced to pass the _, transferred to - Substitute sample: Dilution 3. Quantitative sampling as described in item 2 of the patent application area = eve: output part, _ _, used to transfer the sample of the test sample. 5. As described in item 3 of the patent application scope Quantitative sampling device, the buffer is dissolved in the basin and pre-filled and sealed in the sealing portion - the sealing slot is as described in claim 4 of the patent application scope, and the == slot system may be due to the sampling portion The buffer solution filled in the interior is mixed with the sample while the pressure is applied to the sleeve. 7. A quantitative sampling device for a liquid sample, comprising: ························································· Such as the scope of application for patents! The quantitative sampling described in the item and the sampling portion is a propeller, including the sampling ring and the - propulsion, the hand, and the hand. 16 1299262 sets; ^ fits with the sampling part, when the sampling part is nested in the solution, it will be ' ' 嗜 嗜 嗜 嗜 嗜 9 9 9 9 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如 如The filter membrane was discharged to the outside with a second generation. In the case of the sample of the sample, the quantitative sampling device of the sample is described, and the one is the squeezing device, and one end is the sealing groove for the buffer solution. The other end is the back of the towel: / She is surrounded by the quantitative extraction of the eighth item, and the reading solution is pre-filled and sealed in the (four) tank. Its i2. The sealing groove of the eighth aspect of the scope of the patent application can be broken by extrusion to be filled therein, and the liquid is mixed with the sample. The method for buffering and dissolving, the first package includes a pre-treatment of the liquid sample by using a certain amount of sampling device, and the sampling portion is taken into a set of parts by taking a liquid test. The body is buffered and shaken, and the quantitative sampling device is shaken repeatedly to make the liquid sample sufficiently mixed to obtain a diluted solution; and 17 to force the diluted solution to pass through a filter membrane, and the membrane system utilizes Γ^(4), wherein The size of the filter stomach is screened. The method of claim 13, wherein the buffering 了^糸預先填充密封於該套合部之—密封槽中,該密封槽 可因雜樣部套合人該套合部時之壓力而破裂 ,使得填充 於内部之騎衝溶液與嫌狀檢體混合。 16·如申請專利範圍第13項所述之方法,其中該緩衝 溶液係預先填充密封於該採樣部之一密封槽中,該密封槽 可因擠壓而破裂使得填充於内部之該緩衝溶液與該液狀檢 體混合。The 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸 糸Body mixing. The method of claim 13, wherein the buffer solution is pre-filled and sealed in a sealing groove of the sampling portion, and the sealing groove can be broken by extrusion so that the buffer solution filled in the interior is The liquid sample is mixed. 1818
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