GB2132759A - Blood collecting tube - Google Patents

Abstract

A blood collecting tube (1) contains a blood coagulation-promoting medium (3) comprising a carrier having a specific gravity higher than that of blood cells, and a powderous blood coagulation-promoting agent supported on the carrier optionally by means of a binder which is soluble to blood serum, medium 3 being held between the inner walls of the tube in an intermediate portion of the tube. The carrier is preferably hydrophilic; the binder is preferably water-soluble silicone, polyethylene glycol, dextran, a cellulose derivative or polyvinyl pyrrolidone; and the blood coagulation- promoting agent is preferably glass, kaolin, bentonite or diatomaceous earth. <IMAGE>

Description

SPECIFICATION Blood collecting tube t Technical Field The present invention relates to a serum-separating agent used for separating serum from other components in a blood.

Technical background This serum-separating agent is used to fractionate a specific component from other components using the specific gravity difference between the specific component and other components of a blood to be fractionated, thus being interposed between these components. For this purpose, it is desired that the serum-separating agent#have a specific gravity between those of said components, be flowable during centrifugal separation, and not flowable and stable after the operation of centrifugal separation is completed.

A known conventional serum-separating agent of this kind is a gel-like material consisting of silicone oil, silica and a gelling agent. But a liquid separating agent of such a composition has problems. For example, because components which lack in compatibility are mechanically mixed to obtain a thixotropic gel by means of a gelling agent which accelerates the formation of hydrogen bonds between the silica particles (specific gravity adjusting agent), coagulation develops due to this growing hydrogen bond becoming stronger as time elapses, resulting in phase separation and poor fluidity durig centrifugal separation. Thus, addition of a surfactant for avoiding phase separation has been proposed, but this presented another problem of hemolysis by the large amount of surfactant.

Further, serum-separating agents of the above composition have drawbacks such as the tendency to change their nature by cross-linking and other chemical changes upon y-ray sterilization after encapsulation of a suitable quantity in a blood collecting tube. This degrades the serum-separating function, and delays blood coagulation and clot deposition by evaporation of low molecular components of the gel-like material rendering the inner surface of the tube to become hydrophobic. Furthermore, these separating agents are fairly expensive.

Another known serum-separating agent is a gel-like material of polyester base. This material is not necessarily satisfactory in that it renders the inner surface of the tube water-repellent resulting in delay of blood coagulation and clot deposition. Furthermore, serum-separating agents of this type smell unpleasant.

The object of the present invention is to provide a novel serum-separating agent which is free from above problems of the prior art. Other object of the present invention is to provide a serum-separating agent which has an excellent stability over long periods of time, can be subjected to y-ray sterilization, show virtually no water-repellency, is free of unpleasant odors and can be manufactured at comparatively low cost, and as a result it is possible to eliminate hemolysis and to prevent delay in blood coagulation and clot deposition on the inner surface of a blood-sampling tube, even if blood is preliminary introduced in the tube.

Disclosure of the invention According to the present invention, there is provided a thixotropic serum separating agent for fractionting serum portion from the coagulated portion of blood, which is characterized by consisting of, as the main component, an a-olefine-dialkylmaleate copolymer having a viscosity between 10,000 and 80,000 cp, (at 25 C) and a specific gravity of 1.035-1.055, and viscosity-and specific gravity-adjusting agents mixed therewith.

In the present invention, typical example of the a-olefin-dialkymaleate copolymer has the general formula:

where R, stands for an alkyl group having 2 to 58 carbon atoms which in the copolymer molecule may either be the same kind of a combination of different kinds as desired: R2 and R3 are selected from the group consisting of methyl, ethyl, butyl, and 2-ethylhexyl groups; n is an integer which allows the vicosity of said copolymer to be in the range of 10,000 to 80,000, more preferably 40,000 to 80,000 cp (at 25 C) when using said copolymer as the main component, or corresponds to a carbon atom number in the range of 30 to 60 when using said copolymer as a wax.

This a-olefin-dialkylmaleate copolymer is light yellow in color, transparent, odorless, inert to blood, free of blood absorption, elution and so on, and stable for long periods of time. It allows the inner surface of the blood collecting tube to remain clean since it does not produce any water-repellent material. It does not substantially change its chemical or physical nature upon sterilixation with gamma rays or the like.

When the liquid separation agent of the present invention is used for blood serum separation, the specific gravity of the a-olefin-dialkylmaleate copolymer is selected between 1.00 and 1.038, preferably between 1.027 and 1.035.

According to the present invention, aliphatic amine derivatives of smectite clay may be aliphatic primary amine, aliphatic secondary amine or aliphatic tertiary amine or aliphatic quaternary amine derivatives of smectite clay. These amine derivatives are already konwn.

Among these derivatives, aliphatic quaternary amine derivatives of smectite clay are most desirable, examples of which are aliphatic amine derivatives of smectite clay having C8-C24 such as Bentone 34, Bentone 38, Bentone 27, and Bentone 128 (quaternary ammonium salts of smectite clay, products of NL Industry CO.).

The inorganic fine powder used as the viscosity and specific gravity adjusting agent in the present invention may be suitably selected from calcined silica, precipitated silica and so on, and may be added in view of the specific gravity and viscosity of the main component in such an amount that makes the whole composition into the gel-like and prescribed specific gravity.

The structure4orming agent used in the present invention is added for making and maintaining the gel state of the liquid separation agent, and can be used when it is considered to be difficult to make the whole composition into gel-like without the inclusion of such an additive. For example, dimethylpolysiloxane-polyoxyalkylene copolymer (e.g., trade names SH3771, SH-190, and SH-192 of Toray Silicone Co., Ltd.) or Carbitol (e.g., ethyldiglycol) and the like may be used. The amount of the structure-forming agent may be decided taking the kinds of main component and viscosity-and specific gravity-adjusting agent into consideration, so that it is suffice for gelation and miscible with other components.

In the present invention, in addition to the z-olefine-dialkylmaleate copolymer, the viscosity and specific gravity adjusting agent and the structure-forming agent, a nonionic surfactant (e.g., polyoxyethylene-hydrogenated caster oil monolaurate, polyoxy-ethylene-hydrogenated caster oil tri-isostearate or the like) may be added as required. The addition of a little amount (for example, 0.47-2.7 weight %) of the surfactant will be effective in preventing the phase separation for a long period of time and since the surfactant is nonionic, there is no possibity of hemolysis. The employment of the surfactant is especially useful where only silica is employed as a viscosity-and specific gravity-adjusting agent.

Brief Explanation of Drawings Figure 1 is a perspective view illustrating the use of the liquid separating agent of the present invention as a blood serum separator encapsulated in a blood collection tube. Figure 2 is a sectional view of the blood collection tube shown in Fig. 1 after centrifugal separation.

The Best Modes for Carrying Out the Invention Compositions of the liquid separating agent of the present invention for serum separation are shown in the following tables 1 and 2. In these tables, the a-olefin-dialkylmaleate copolymer (A) is an n-cu-olefin-dimethylmaleate copolymer having average molecular weight 3,000-4,000; specific gravity 1.027-1.035 (at 25 C); viscosity 40,000-70,000 cp (25 C) and consists of a combination of a-olefin components with carbon atom numbers 12 and 14, respectively; the copolymer (B) is an n-a-olefin-dimethylmaleate copolymer having average molecular weight 2,000-3,000; specific gravity 1.005 (28 C); viscosity 10,000-15,000 cp (28 C) and consists of a combination of a-olefine components with carbon atom numbers 6 and 8, respectively; the copolymer (C) is a wex made of an n-a-olefin-dimethylmaleate copolymer of a-olefin components with an average carbon atom number between 30 and 60; the copolymer (D) is an n-a-olefindimethylmaleate copolymer having average molecular weight 3,600-4,000, specific gravity about 0.995 (28 C), viscosity about 10,000 (28 C) and consists of a combination of a-olefin components with carbon atom numbers 16 and 18 respectively; and the copolymer (E) shown in Table 2 is an n-a-olefin-dimethylmaleate copolymer having average molecular weight 3,000-4,000; specific gravity 1.027-1.035 (at 25 C); viscosity 40,000-70,000 cp (25 C) and consists of a combination of a-olefin components with carbon atom numbers 12 and 14, respectively (sold under a trade name, PAR-124, MITSUBISHI KASEI Industries Ltd.).

Other examples of a-olefin-dimethylmaleate copolymer include, in addition to above-mentioned examples, n-a-olefin-dibutylmaleate copolymer and n-oi-olefin-di-2-ethylhexyl copolymer.

Table 1 (examples of serum seperation agent compositions) (parts by weight) Composition number 1 2 3 4 5 6 7 8 a-olefin-dialkylmaleate copolymer (A) 100 100 100 100 50 - (B) - - - - 50 100 (C) - - 1.0 3.0 ~ ~ (D) - - - - - - 100 100 Aerosil R-972* - 2.0 2.0 1.0 1.5 Aerosil 200" 1.0 1.0 - - - - Benton 38*** ~ 1.0 1.0 - 4.0 8.0 10.0 Benton 34*** ~ - - - 1.0 - ~ 12.0 Benton 27*** 3.0 - - - - - - Benton 128"" - - 2.0 - - - - - Specific gravity 1.047 1.039 1.052 1.040 1.042 1.036 1.041 1.041 Viscosity(X104cp/25'C) 53 62 58 43 57 75 64 69 Hemolysis none none none none none none none none Adhesion of clot none none none none none none none none *hydrophobic silica fine powder of average particle size 16 mis, apparent specific gravity about 60 g/l, (product of NIPPON AEROSIL CO., LTD.) **hydrophobic silica fine powder of average particle size 12 m#, apparent specific gravity about 60 g/l, (product of NIPPON AEROSIL CO., LTD.) ""quaternary ammonium salts of smectite clay, (products of NL Industry CO., U.S.A.) Table 2 (examples of serum separation agent compositions) (parts by weight) Composition number 7 8 9 10 11 12 a-olefin-dialkylmaleate copolymer (E) 100 100 100 100 50 - (B) - - - - 50 100 (C) - - 5.0 5.0 ~ ~ Aerosil R-972* 6 - 7.0 5.0 7.0 7 Aerosil 200"' - 6 - - - - Surfactant" 0.5 1.0 1.0 - 1.0 3.0 Structure-forming agent**** 0.18 0.04 - 0.2 0.5 0.6 Specific gravity 1.042 1.042 1.045 1.040 1.045 1.042 Viscosity ( x 104 cp/25 C) 54 80 73 68 52 51 Hemolysis none none none none none none Adhesion of clot none none none none none none *see Table 1 **see Table 1 ""Polyoxyethylene-hydrogenated caster oil monolaurate, (product of NIHON EMULSION CO., LTD.) ****SH-3771, (product of Toray Silicone Co., Ltd.), dimethylpolysiloxane-polyoxy-alkylene copolymer with specific gravity 1.060-1.080 (20 C) and viscosity 260-280 cp.

Next, the preparation method of the liquid separating agent of the present invention will be described.

First, the manufacturing method of the a-olefin-dialkylmaleate copolymer is low polymerization of ethylene to obtain an n-a-olefin. This is then separated into fractions of carbon atom numbers, for example, of 4, of 6, of 8 and 10, of 12 and 14, of 16 and 18, and of 30 to 60 by fractionating distillation. In accordance with the specific gravity of the liquid to be fractionated, these fractions may be used either singly or in combination, and a fraction with carbon atom numbers of 12 and 14, or of 6 and 8 is preferable for use in serum separation from standpoints of viscosity and specific gravity. The selected fraction is subjected to copolymerization with a maleic diester in the conventional manner to obtain the desired product.

Using this a-olefin-dialkymaleate copolymer with a viscosity between 10,000 and 80,000 cp, preferably between 40,000 and 80,000 cp (25 C) as the base, an aliphatic amine derivative of smectite clay, a viscosity and specific gravity adjusting agent such as fine silica powder, a structure-forming agent, nonionic surfactant and a wax consisting of an a-olefin-maleic-diester copolymer (for example, above n-a-olefin having 60-80 carbon atoms) are added as required.

The mixture is kneaded using either a roll mill, a grinding mill, a planetary mixer or the like.

The liquid separating agent thus prepared should preferably has a viscosity, for use in serum separation for example, between 250,000 and 800,000 (25 C) and a specific gravity between 1.035 and 1.055. All of the components in the previous tables are thixotropic, showing flowability upon application of a centrifugal force or the like and staying in the normal condition as a stable uniform gel otherwise.

As appearant from above Tables 1 and 2, even if blood is preliminary kept in a blood sampling tube, the inner surface of the tube does not become water-repellent, thus preventing the adhesion of clots or delay of blood coagulation. These advantages can be attributed to the employment of a-olefin-maleate diester copolymer which does not generate low molecular volatile materials. Accordingly, when serum-separating agent is employed in a blood-sampling tube, it is possible to form a stable seal at the interference between serum layer and clot layer by an ordinary centrifuging operation of 10 minutes at 700-1000 G. As a result, inclusion of fibrin can be easily avoided in a fractionating operation of serum by decantation.Further, since the serum-separating agent is stably positioned between serum layer and clot layer after the centrifuging operation, there is little chance of the clot layer mixing into the serum layer during the transportation of blood from a hospital to an examination center and the like.

Following is an example of using a serum-separating agent preliminarily introduced in a blood sampling-tube.

As shown in Fig. 1, about 1.7 ml of each liquid separating agent composition 1 above (numbers 1 to 12)was put it the bottom of a 10 cc blood collecting tube 2. A polyester unwoven cloth 3 coated with 1-5 mg of diatomaceous earth (e.g., Caper Flattery Sand, trade name WG-200, for Kyoritsu Ceramic Materials Co., Ltd.) or micro-glass powder, was then placed at a slant in each blood collecting tube. Each tube was then stopped with a butyl rubber plug 4, and the tubes were placed under reduced pressure. Then a blood sample was placed in each blood collecting tube and allowed to stand for 7 to 8 minutes. As a result, the diatomaceous earth dispersed in the blood upon the introduction of the blood, and it accelerated blood coagulation together with the nonwoven cloth 3. Adequate coagualtion was thus attained within this short time.Each blood collecting tube was placed in a centrifuge for 10 minutes at 700-1,000 G, and the liquid separating agent compositions were stably distributed between the serum and the clot layers. This state is shown in Fig. 2. Because the liquid separating agent is thixotropic and has a specific gravity between that of the blood serum 5 and that of the blood clots 6, it stays between the blood serum 5 and blood clot 6, forming a gel that separates these two layer. Since the diatomaceous earth and the unwoven cloth 3 have higher specific gravities, they were not included in the layer of blood serum 5. Thus, blood serum 5 obtained was of high purity with no entrainment of fibrin. This blood serum 5 was readily collected from the blood collecting tube by decantation or by suction through a fine nozzle.

It is also possible to employ, other than above-described nonwoven cloth 3 for promoting blood coagulation, those carrying a suitable amount of powderous coagulation-promoting agent on a hydrophilic carrier having a higher specific gravity than blood cell by means of a serumsoluble binder.

Carriers to be useful in this case include cloth, filter paper, non-woven cloth, cotton ball and etc. However, it is required for such carrier to have higher specific gravity than blood cell, to raise no problem in respect to hemolysis and a biochemical examination, to have a characteristic of water-retention (for example, hydophilic) or a water-retention structure (for example, open cell structure), to have enough rigitity or elasticity to be kept within intermediate portion of a tube, and to have a sufficient flexibility to be movable into a blood cell layer a blood cell layer by a centrifugal force, and a size which makes it possible to be sunk into a blood cell layer.

There is no limitation on the kind of blood coagulation-promoting agent as far as it does not substantially cause hemolysis and has a buoyancy within blood. For example, it is possible to use powders 0.4 to 20 ym in size of diatomaceous eath, glass, kaolin, and bentonite.

The amount of blood coagulation-promoting agent to be supported on a carrier may be 0.3 to 5.0 mg, preferably 0.3 to 3.5 mg per 10 cc blood. If the amount of the agent exceeds the upper limit, it may affect the sampled blood due to the dispersion of the powder. On the other hand, if the amount of the agent is less than the lower limit, it would be difficult to expect a sufficient blood coagulation effect.

The amount of the blood coagulation-promoting agent to be supported on a carrier may be suitably adjusted by controlling the mixing ratio of the agent with a binder.

It is required for the binder to be soluble to serum. Because, it is preferable to dissolve and instantly disperse the blood coagulation-promoting agent in blood, as soon as blood is introduced into a blood sampling tube, thereby promoting the formation of clot. It is also required for the binder to have a suitable degree of stickiness and non-volatility, to be hematologically inactive and to be scarsely affected by a sterilizing operation (for example, y-ray irradiation). Examples of such a binder include, water-soluble silicone, polyethylene glycol, polyvinyl pyrrolidone, dextran, carboxy methylcellulose, hydoxypropyl, methylcellulose, and other cellulose derivatives.

Especially, cellulose derivatives and polyvinyl pyrrolidone are superior in solubility and in hygroscopicity and are most preferable, dextran is inferior in solubility as compared with other materials. Polyethylene glycol has a hygroscopicity and therefore is not suited for storing it in a room temperature for a long period of time after the manufacture thereof.

Methods for manufacturing the medium such as non-woven cloth fixed with a prescribed amount of blood coagulation promoting agent may be easily carried out by a dipping method and the like.

In the above example, it is explained about a case wherein serum-separating agent is preliminarily introduced into a sampling tube. However, this invention is not limited to the above example. For example, the serum-separating agent may be provided together with its container at an upper portion of a blood sampling tube after the sampling of blood and taking-off of rubber cap. In this case the serum-separating agent is introduced from the container into the blood-sampling tube by a centrifuging operation and form a seal at the interface between serum portion and clot portion.

When being used as a serum separator, the liquid separating agent does not form waterrepellent film in the blood collecting tube by releasing water-repellent substances and consequently does not cause delay of blood coagulation. Because the blood collecting tube is made of glass, it accelerates coagulation when contacting blood at the surface, so that it is necessary to keep the inner surface clean. Accordingly, compared with conventional liquid separating agents which have the drawback of forming water-repellent film, the time needed for collecting blood serum is shortened. This is even more effective in combination with the use of the diatomaceous earth and unwoven cloth. The time saving can amount to as much as 30 minutes.

When encapsulation in a blood collecting tube is performred, sterilization is desirable. In clinical tests, no chemical or physical changes that cause adverse effects were found after applying gamma-ray sterilization a dose of 2.5 megarad.

a-olefine#maleate diester copolymer having an alkyl group containing 4 to 60 carbon atoms at the a-olefin portion and maleate ester containing a functional group selected from the group consisted of methyl, ethyl, butyl and 2-ethylhexyl groups, and having a viscosity of 10,000 to 80,900 (cp/25 C) is very stable for a long period time. Accordingly, when this copolymer is employed as a main component and mixed with a viscosity-and specific gravity-adjusting agent and etc. for preparing a serum separating agent, the obtained mixture is easily turned into gel, and adjusted into an intermediate specific gravity between those of serum and clot, and would not substantially ser forth a phase separation or lowering of fluidity.

Further, as shown in the above composition (Table 1), when C8-C24 aliphatic amine derivative of smectite or fine powderous inorganic materials such as hydophobic silica powder, as a viscosity-specific gravity-adjusting agent there will be obtained a serum separating agent which is free from phase separation, degradation of fluidity and has stable thixotropic characteristics. If a serum separating agent includes C5-C24 aliphatic amine derivative of smectite clay, the state of dispersion in the agent can easily be checked by means of a microscope etc., making quality control easier, because the smectite clay particles are not light-transmitting.

Because the aliphatic amine derivatives of smectite clay such as quaternary ammonium salt derivatives of smectite have a thickening effect as shown in Table 1, it is possible to obtain a stable thixotropic serum separating agent without employing a structure-forming agent.

Among the examples shown in the above Table 1 and 2, a-olefin-maleate diester copolymer (A), (B), (C) and (E) are all n-a-olefin dimethyl-maleate copolymer and, when employed as a main component in a serum separating agent, make it possible to easily obtain a serum separating agent of nearly an intermediate specific gravity between those of serum and clot and having a suitable degree of viscosity, requiring smaller amount of a viscosity-and specific gravity-adjusting agent being added. Furthermore, these compositions will be substantially free from changes with time, phase separation and lowering of fluidity.

The above mentioned wax is especially useful for preventing a serum separating agent from being phase-separated.

Claims (8)

CLAIMS 1. A blood-collecting tube containing therein a blood coagulation-promoting medium, which is characterised in that said blood coagulation-promoting medium comprises a carrier having a specific gravity higher than that of blood cell, and powderous blood coagulation-promoting agent supported on the carrier by means of a binder which is soluble to blood serum. 2. The blood-collecting tube according to claim 1, wherein said blood coagulation-promoting agent is supported on the carrier in an amount of 0.3 to 3.5 mg per 10 cc of blood. 3. The blood-collecting tube according to claim 1, wherein said carrier is of hydrophilic. 4. The blood-collecting tube according to claim 1,2 or 3, wherein said binder is selected from the group consisting of water-soluble silicone, polythylene glycol, dextran, cellulose derivatives and polyvinyl pyrrolidone. 5. The blood-collecting tube according to claim 1, 2 or 3, wherein said blood coagulationpromoting agent is selected from the group consisting of glass, kaolin, bentonite and diatomaceous earth. 6. The blood-collecting tube according to claim 1,2 or 3, wherein said blood coagulationpromoting medium is disposed at the middle of the blood-collecting tube. CLAIMS (23 Feb 1984)

1. A blood-collecting tube containing therein a blood coagulation-promoting medium, which is characterised in that said blood coagulation-promoting medium comprises a carrier having a specific gravity higher than that of blood cells, and powderous blood coagulation-promoting agent supported on the carrier, and is held between the inner walls of the blood collecting tube in an intermediate portion of the tube.

2. A blood-collecting tube according to claim 1, wherein said blood coagulation-promoting agent is supported on the carrier in an amount of 0.3 to 3.5 mg per 10 cc of blood.

3. A blood-collecting tube according to claim 1, wherein said carrier is of hydrophilic material.

4. A blood-collecting tube according to claim 1,2 or 3, wherein the blood coagulationpromoting agent is supported on the carrier in admixture with a binder, the binder being selected from the group consisting of water-soluble silicone, polyethylene glycol, dextran, cellulose derivatives and polyvinyl pyrrolidone.

5. A blood-collecting tube according to claim 1,2 or 3, wherein said blood coagulationpromoting agent is selected from the group consisting of glass, kaolin, bentonite and diatomaceous earth.

6. A blood-collecting tube according to claim 1,2,or 3, wherein said blood coagulationpromoting medium is disposed at the middle of the blood-collecting tube.

7. A blood-collecting tube according to claim 1,2 or 3, wherein said blood coagulationpromoting agent is supported on the carrier by means of a binder which is soluble in blood serum.

8. A blood-collecting tube according to claim 1,2 3 or 4, wherein the tube has a thixotropic serum separating agent therein at the bottom.