KR20170062633A

KR20170062633A - An integral saliva collecting device

Info

Publication number: KR20170062633A
Application number: KR1020150167718A
Authority: KR
Inventors: 이기자; 이영주; 이진우
Original assignee: 경희대학교 산학협력단
Priority date: 2015-11-27
Filing date: 2015-11-27
Publication date: 2017-06-08
Also published as: KR101821020B1

Abstract

[0001] The present invention relates to an integrated saliva collecting apparatus, and more particularly, to a pre-treatment type saliva collecting apparatus capable of storing and pre-treating saliva, comprising a membrane 120 and a citric acid solution 130) to receive saliva; A cover unit (200) coupled to the chamber (110) to maintain the airtightness of the chamber (110); And a pretreatment unit 300 connected to the chamber 110 to pretreat the saliva of the chamber 110 when the membrane 120 is broken. The present invention is advantageous in that saliva collection and pretreatment can be conveniently performed when detecting pepsin directly in the field.

Description

An integral saliva collecting device

The present invention relates to an integrated saliva collecting apparatus, and more particularly, to a pre-treatment type saliva collecting apparatus capable of storing and pre-treating saliva.

Saliva is a colorless, sticky substance that is released from the inside of the mouth. It is a digestive juice that acts to convert starch to maltose or maltose to glucose.

On the other hand, pepsin is a digestive enzyme secreted from stomach chied cells.

Pepsin is detected in saliva in cases such as reflux phos- phitis, which means that gastric juice is detected in the oral cavity.

Therefore, when pepsin is contained in saliva in gastric juice, reflux esophagitis and the like can be suspected.

Saliva contains molecules such as proteins and nucleic acids that are sufficient to reflect the pathology and physiological conditions of the body, such as blood, urine, and cerebrospinal fluid, and saliva collection is safe and easy and noninvasive for both the examinee and the subject It can be recognized as a highly utilized disease diagnosis technology.

Therefore, diagnostic kits using non-invasive saliva have been developed to diagnose diseases such as reflux pharyngitis.

However, the conventional diagnostic kit for detecting pepsin was carried out through a pipette test.

The pipette test had to be provided with a separate instrument and container for collecting saliva and for pretreatment to remove impurities other than pepsin in the saliva.

Conventional saliva diagnosis using a pipette test has inconvenienced that saliva collection and sample treatment must be performed in several steps.

In addition, it is not only complicated to take a certain amount of saliva sampled and reintroduced, but also requires centrifugation to be carried out directly. Therefore, it is not only inconvenient to use by the general public, but also has a problem in that the precision of pepsin measurement is greatly deteriorated.

(Patent Document 1) US2014-0302617 A1

(Patent Document 2) US5393496 A

(Patent Document 3) US9113850 B2

SUMMARY OF THE INVENTION Accordingly, it is an object of the present invention to provide a pre-treatment type saliva collecting device capable of simultaneously collecting and pre-treating saliva.

In order to solve the above-mentioned problems, the present invention provides a method of manufacturing a semiconductor device, comprising: a chamber 110 in which a membrane 120 is formed and a citric acid solution 130 is provided to receive saliva; A cover unit (200) coupled to the chamber (110) to maintain the airtightness of the chamber (110); And a pretreatment unit 300 connected to the chamber 110 to pretreat the saliva of the chamber 110 when the membrane 120 is broken. The present invention can provide a monolithic saliva collecting device including the above-

In addition, the chamber 110 may be provided with an integrated saliva collector having an inclined portion 140 extended in a direction away from the membrane 120.

The pretreatment unit 300 may be a monolithic saliva collector having a polypropylene filter therein.

A discharging unit 400 connected to the pretreatment unit 300 to receive the pretreated saliva; And an integrated saliva collector.

The discharge unit 400 includes a housing 430 having a third connection part 410 fluidly connected to the preprocessing unit 300 and a second discharge port 420 for discharging the pre- )and; A valve member 440 for opening / closing the second discharge port 420; The present invention can provide an integrated saliva collector comprising

In addition, the cover unit 200 includes a handle 210 which is in close contact with an end of the slope part 140 with a penetrating part formed at the center thereof; A sealing bar 220 extending from the handle 210 and coupled with the chamber 110; The sealing bar 220 may be a monolithic saliva collecting device having an inner circumferential surface having the same diameter as the inner circumferential surface of the penetrating portion and formed of a circular rod having an empty interior and an end portion formed of a breakable film.

The cap unit 260 is coupled to a detachable cap unit 260 at an end of the sealing rod 220 and is coupled to the chamber 110.

The preservative solution 130 and the membrane 120 may be integrated saliva collectors provided in the replacement chamber 111 detachable from the chamber 110.

Further, a connection unit 500 for fluid communication between the chamber 110 and the pretreatment unit 300 may be used.

The present invention as described above has the following effects.

First, when detecting pepsin directly in the field, there is a strong point that saliva collection and pretreatment can be performed conveniently at the same time.

Second, if the saliva is brought to the hospital without directly detecting the pepsin of the saliva in the field, it is possible to close the cover unit and keep the saliva sealed.

Third, since the preserving solution, the membrane and the cap unit can be replaced, there is an advantage that the saliva collecting device can be reused.

Fourth, there is a universal strength that can be used for diagnosis of various diseases as a pretreatment and standardization mechanism of a sample which is indispensable for saliva-based diagnosis technology.

1 is an overall perspective view of a preferred embodiment of the present invention.
FIG. 2 is an exploded perspective view according to a first preferred embodiment of the present invention. FIG.
3 is an exploded perspective view of a second preferred embodiment of the present invention.
Fig. 4 shows changes in the amount of saliva volume before and after passage of a filter when a polypropylene filter (PP filter) according to a preferred experiment of the present invention was used and another filter was used.
FIG. 5 shows changes in the amount of saliva volume before and after passage of the filter when a polypropylene filter (PP filter) according to a preferred experiment of the present invention was used and a different filter type was used according to a user.
FIG. 6 shows changes in the concentration of protein (BSA) before and after passage of the filter in the case of using a polypropylene filter (PP filter) according to a preferred experiment of the present invention and using a different filter type.

Hereinafter, the present invention will be described in detail with reference to the accompanying drawings.

In this process, the thicknesses of the lines and the sizes of the components shown in the drawings may be exaggerated for clarity and convenience of explanation. In addition, the terms described below are defined in consideration of the functions of the present invention, which may vary depending on the intention or custom of the user, the operator. Therefore, the definitions of these terms should be described based on the contents throughout this specification.

FIG. 1 is an overall perspective view of a preferred embodiment of the present invention, and FIG. 2 is an exploded perspective view according to a first preferred embodiment of the present invention.

The chamber 110 is formed with a membrane 120, and a citric acid 130 is provided therein to receive the saliva.

The cover unit 200 is coupled to the chamber 110 to maintain the airtightness of the chamber 110.

The pretreatment unit 300 is connected to the chamber 110 and prepares the saliva of the chamber 110 when the membrane 120 is destroyed.

The pretreatment can be understood as a process of removing foreign substances unnecessary for inspection while passing the saliva through a polypropylene filter provided in the pretreatment unit 300.

The storage unit 100 has a chamber 110 for storing saliva.

A storage solution (citric acid) 130 is provided in the chamber 110, so that saliva can be stored more easily.

Since the membrane 120 is formed in the chamber 110, the saliva does not leak to the outside from the chamber 110.

Since the membrane 120 can be broken, the saliva in the chamber 110 can be discharged to the outside of the chamber 110 when the membrane 120 is torn.

In the chamber 110, an inclined portion 140 is formed in a direction away from the membrane 120.

Since the inclined portion 140 has a funnel shape so that the diameter of the cross section decreases toward the chamber 110, the saliva can be more easily collected.

In other words, the saliva can flow downward along the inner peripheral surface of the inclined portion 140 and can be easily injected into the chamber 110.

The second screw thread forming part 150 is formed at a position where the slope part 140 and the chamber 110 meet.

The second thread forming portion 150 may be threaded on the inner circumferential surface of the chamber 110.

The cover unit 200 includes a handle 210 which is in close contact with an end portion of the inclined portion 140 with a penetrating portion formed at the center thereof.

The sealing bar 220 extends from the handle 210 and is coupled to the chamber 110.

The sealing rod 220 is formed of a membrane having an inner peripheral surface having the same diameter as the inner peripheral surface of the penetrating portion and being formed of a circular rod having an inner hollow portion and an end portion of which can be broken.

A first thread forming part 250 is formed at the end of the sealing rod 220 and a first thread forming part 250 can be screwed to the second thread forming part 150.

Since the end of the sealing rod 220 is formed of a film, when the first thread forming portion 250 is coupled to the second thread forming portion 150 of the chamber 110, the inside of the chamber 110 is kept hermetic will be.

On the other hand, the membrane at the end of the sealing rod 220 may be formed of a material that can be broken.

Meanwhile, a through portion is formed at the center of the handle 210, and the needle unit 600 can be inserted into the through portion.

The needle unit 600 may be a rod member having a diameter smaller than the diameter of the guide hole 230, and a needle tip 620 is provided at an end of the needle unit 600.

The needle unit 600 is elongated so that the needle tip 620 can break the membrane at the end of the sealing rod 220 and even break the membrane 120.

Since the rubber packing 610 is formed on the outer circumferential surface of the needle unit 600 in the vicinity of the needle tip 620, pressure is applied toward the chamber 110 when the needle unit 600 is inserted into the guide hole 230 It will be possible to do.

A detailed operation example will be described later.

Meanwhile, the chamber 110 has a third thread forming portion 160 on the outer circumferential surface of the end portion where the membrane 120 is formed.

The cover unit 200 may be coupled to the second thread forming portion 150 and the connection unit 500 may be coupled to the third thread forming portion 160. [

The connection unit 500 is fastened to the third screw thread forming part 160.

The connection unit 500 is formed with a fourth thread forming portion 560 to be screwed to the third thread forming portion 160 and a first discharge port 510 is provided at the other side.

The connection unit 500 fluidly communicates between the chamber 110 and the pretreatment unit 300.

That is, the connection unit 500 has a structure in which the interior is empty, so that the fluid can be discharged through the first discharge port 510.

In other words, when the membrane 120 is broken while the connection unit 500 is coupled to the storage unit 100, the saliva stored in the chamber 110 passes through the connection unit 500 and flows into the first discharge port 510, As shown in FIG.

On the other hand, the pre-processing unit 300 is coupled to the first discharge port 510.

The preprocessing unit 300 may include a polypropylene filter inside the filter case 330.

The first connection unit 310 protrudes from one side of the preprocessing unit 300 and the second connection unit 320 protrudes from the other side.

The first connection part 310 and the second connection part 320 are formed to be in fluid communication with each other in the filter case 330 and a polypropylene filter is provided between the first connection part 310 and the second connection part 320 will be.

The first connection part 310 may be fitted to the first discharge port 510 while maintaining the airtightness, but any combination of the first connection part 310 and the first connection part 310 may be used as long as fluid communication is possible without leakage of the fluid.

The discharge unit 400 is connected to the pretreatment unit 300 and is supplied with the saliva pretreated from the pretreatment unit 300.

More specifically, the discharge unit 400 is formed with a third connection part 410 fluidly connected to the preprocessing unit 300 and a second discharge port 420 discharging the pre-processed saliva to the outside.

The valve member 440 can control the opening and closing of the second discharge port 420 to discharge the pretreated saliva in the housing 430 to the outside.

On the other hand, the inner flow path structure of the housing 430 can be formed by being bent in a "? &Quot; shape.

Next, the operation of the first preferred embodiment of the present invention will be described as follows.

The cover unit 200 is detached from the storage unit 100 and the saliva is injected through spit into the inclined part 140. [

When the required amount of saliva is received in the storage unit 100, the cover unit 200 is coupled to the storage unit 100.

The first thread forming portion 250 of the cover unit 200 is screwed to the second thread forming portion 150 of the storage unit 100 so that the saliva contained in the chamber 110 is held in the outer And kept safely without leakage.

When inspecting the saliva, the fourth thread forming portion 560 formed on the connection unit 500 is coupled to the third thread forming portion 160.

The first connection part 310 of the preprocessing unit 300 is coupled to the first discharge port 510.

At this time, the third connection part 410 of the discharge unit 400 may be coupled to the second connection part 320.

When the needle unit 600 is inserted into the guide hole 230 formed in the cover unit 200 and the needle unit 600 is pressed toward the chamber 110, the needle tip 620 is inserted into the end of the sealing rod 220 The rubber packing 610 is pressed against the inner wall of the guide hole 230 and the inner wall of the chamber 110 to apply pressure to the interior of the chamber 110.

When the needle unit 600 is continuously pushed into the chamber 110, the needle tip 620 breaks the membrane 120 and the saliva stored in the chamber 110 passes through the connection unit 500, 510 to the preprocessing unit 300.

According to another preferred embodiment of the present invention, the cover unit 200 is detached from the storage unit 100 and then the saliva is injected into the inclined part 140, and the cover unit 200 The needle unit 600 may be inserted into the chamber 110 directly.

At this time, the saliva stored in the chamber 110 flows into the preprocessing unit 300 through the connection unit 500 and the first discharge port 510.

As the saliva passes through the pretreatment unit 300, impurities and the like which are not to be inspected are filtered and pretreated.

The pretreated saliva is sent to the housing 430. When the valve member 440 is opened, the pretreatment saliva is finally transferred to the inspection apparatus through the second discharge port 420 and the saliva intestinal pepsin test can be performed.

When the valve member 440 is again locked, the second discharge port 420 is blocked from the outside, and the pre-treated saliva can be stored in the housing 430. If necessary, the valve member 440 can be opened again.

Next, a second preferred embodiment of the present invention will be described in detail with reference to FIG.

3 is an exploded perspective view of a second preferred embodiment of the present invention.

The cap unit (260) is detachably coupled to the cover unit (200).

The end of the cap unit 260 can be broken by a thin film.

The storage unit 100 may include a replacement chamber 111 in which a preservative solution (citric acid) 131 and a membrane 121 are provided.

The replacement chamber 111 has a structure in which the seventh thread forming portion 561 in the storage unit 100 is detachably coupled to the sixth thread forming portion 161 so as to form the end portion of the storage unit 100.

The connection unit 500 is connected to the replacement chamber 111 and the preprocessing unit 300 is connected to the connection unit 500. The discharge unit 400 is sequentially connected to the preprocessing unit 300 You can.

The operating principle of the second embodiment as a whole is not so different from the first embodiment mentioned above as a whole.

However, in the second embodiment, the cover unit 200 and the storage unit 100 may further include a detachable cap unit 260 and a replacement chamber 111 for cleaning and reusing the storage unit 100.

The interior of the chamber 110 of the storage unit 100 is easily washable.

The reason for using a polypropylene filter (PP filter) as a filter used in the pretreatment is that the volume of the saliva before the filter passes through and the protein adsorption rate are the lowest compared to other filter types.

This is because, in order to accurately detect pepsin protein, it is strongly required to minimize the loss of protein necessary for the test when the saliva passes through the pretreatment filter and the protein is adsorbed on the pretreatment filter.

This is demonstrated in Figs.

Fig. 4 shows changes in the amount of saliva volume before and after passage of a filter when a polypropylene filter (PP filter) according to a preferred experiment of the present invention was used and another filter was used.

As shown in Fig. 4, it can be seen that the amount of volume change of the saliva is the smallest when a polypropylene filter (PP filter) is used.

FIG. 5 shows changes in the amount of saliva volume before and after passage of the filter when a polypropylene filter (PP filter) according to a preferred experiment of the present invention was used and a different filter type was used according to a user.

As can be seen from FIG. 5, it can be seen that the volume change of the saliva is the smallest when the polypropylene filter (PP filter) according to the user is used.

FIG. 6 shows changes in the concentration of protein (BSA) before and after passage of the filter in the case of using a polypropylene filter (PP filter) according to a preferred experiment of the present invention and using a different filter type.

As can be seen from FIG. 6, in the case of using a polypropylene filter (PP filter), it can be seen that there is almost no change in the concentration of protein due to passage of the filter.

It will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the spirit or scope of the invention as defined in the appended claims. It will be understood that the present invention can be changed.

100: Storage unit
110: chamber
111: Replacement chamber
120, 121: Membrane
130, 131: citric acid
140:
150: second thread forming portion
160: third thread forming portion
161: sixth thread forming portion
200: Cover unit
210:
220: sealing rod
230: Guide hole
250: first thread forming portion
260: cap unit
300: preprocessing unit
310: first connection part
320: second connection portion
330: Filter case
400: exhaust unit
410: Third connection part
420: second outlet
430: housing
440: Valve member
500: connecting unit
510: first discharge port
560: fourth thread forming portion
561: seventh thread forming portion
600: Needle unit
610: Rubber packing
620: Needle tip

Claims

A chamber 110 formed with a membrane 120 and provided with a preservative solution (citric acid) 130 to receive saliva;
A cover unit (200) coupled to the chamber (110) to maintain the airtightness of the chamber (110); And
A pretreatment unit 300 connected to the chamber 110 for pretreating the saliva of the chamber 110 when the membrane 120 is broken; / RTI >
Integrated saliva collector.

The method according to claim 1,
The chamber 110 is formed with an inclined portion 140 extending in a direction away from the membrane 120,
Integrated saliva collector.

The method according to claim 1,
The pretreatment unit 300 includes a polypropylene filter,
Integrated saliva collector.

The method according to claim 1,
An exhaust unit 400 connected to the pretreatment unit 300 to receive the pretreated saliva; &Lt; / RTI >
Integrated saliva collector.

5. The method of claim 4,
The discharge unit (400)
A housing 430 having a third connection part 410 fluidly connected to the preprocessing unit 300 and a second discharge port 420 for discharging the pretreated saliva to the outside;
A valve member 440 for opening / closing the second discharge port 420; / RTI >
Integrated saliva collector.

3. The method of claim 2,
The cover unit (200)
A handle 210 which is in close contact with an end of the inclined portion 140 with a penetrating portion formed at the center thereof;
A sealing bar 220 extending from the handle 210 and coupled with the chamber 110; &Lt; / RTI >
The hermetic seal (220)
The end portion of which is formed of a breakable film while the inner portion of the through-hole has an inner circumferential surface having the same diameter as the inner circumferential surface of the through-
Integrated saliva collector.

The method according to claim 6,
A detachable cap unit 260 is coupled to an end of the hermetic seal 220,
The cap unit 260 is coupled to the chamber 110
Integrated saliva collector.

The method according to claim 1,
The preservative solution (Citric Acid) (130) and the membrane (120)
(110), and an exchange chamber (111) provided in the exchange chamber (111)
Integrated saliva collector.

The method according to claim 1,
Further comprising: a coupling unit (500) for fluidly communicating between the chamber (110) and the pretreatment unit (300)
Integrated saliva collector.