A MEDICAL SYRINGE BARREL AND A MANUFACTURING METHOD FOR PRODUCING THE SAME
20230146037 · 2023-05-11
Inventors
Cpc classification
A61M5/3134
HUMAN NECESSITIES
B29C45/37
PERFORMING OPERATIONS; TRANSPORTING
A61M5/3135
HUMAN NECESSITIES
B29C45/0025
PERFORMING OPERATIONS; TRANSPORTING
B29L2031/7544
PERFORMING OPERATIONS; TRANSPORTING
A61M2207/00
HUMAN NECESSITIES
B29C2045/0037
PERFORMING OPERATIONS; TRANSPORTING
International classification
B29C45/00
PERFORMING OPERATIONS; TRANSPORTING
Abstract
A medical syringe barrel and a manufacturing method for producing the same can be completed as a molded article by injection molding of a synthetic resin material without requiring post processing like polishing and can fill and administer a predetermined amount of the internal-use solution accurately. A medical syringe barrel includes a tubular barrel section for accommodating an internal-use solution in the interior thereof, an injection nozzle section formed at one end of the barrel section, and a flange section formed at an opening section on the other end of the barrel section to project radially outward. A surface of the flange section has a recess portion, and a weld line which is potentially formed by injection molding is not formed in the internal-use solution filled section.
Claims
1. A medical syringe barrel comprising a tubular barrel section for accommodating an internal-use solution in the interior thereof, an injection nozzle section formed at one end of the barrel section, and a flange section formed at an opening section on the other end of the barrel section to project radially outward, wherein the barrel section includes an internal-use solution filled section which is set to be filled with the internal-use solution and an internal-use solution unfilled section which is set not to be filled with the internal-use solution when the internal-use solution is poured into the syringe barrel from the opening section; the surface of the flange section has a recess portion; and a weld line which is potentially formed by injection molding is not formed in the internal-use solution filled section.
2. A medical syringe barrel according to claim 1, the height of a gate rest by injection molding is smaller than the depth of the recess portion in the flange section, and the gate rest fits in the interior of the recess portion.
3. A manufacturing method for producing a medical syringe barrel, which comprises a tubular barrel section for accommodating an internal-use solution in the interior thereof, an injection nozzle section formed at one end of the barrel section, and a flange section formed at an opening section of the other end of the barrel section to project radially outward, wherein preparing a mold so that the surface of the flange section has a recess portion; and conducting injection molding of a thermoplastic resin material by installing a gate at the position where the recess portion is to be formed.
Description
BRIEF DESCRIPTION OF DRAWINGS
[0017]
[0018]
[0019]
A MODE FOR IMPLEMENTING THE INVENTION
[0020] A configuration of a medical syringe barrel according to one embodiment of the present invention will be described below referring to the drawings. In
[0021]
[0022]
[0023] In
[0024] The syringe barrel 20 comprises an internal-use solution filled section 20F corresponding to the portion which is closer to the injection nozzle section 22 than a piston tip position 20P and an internal-use solution unfilled section 20N corresponding to the portion which is closer to the flange section 23 than the piston tip position 20P, when a predetermined amount of the internal-use solution is put into the interior thereof.
[0025] As shown in
[0026] As shown in
[0027] Next, a manufacturing method for producing the syringe barrel 20 shown in
[0028] The injection molding method comprises a mold closing step for closing an open mold by a mold closing mechanism, a melted resin filling step for filling a melted resin material into a closed mold by an injection molding machine, a molded article cooling step for cooling the resin material in the mold for a predetermined time after the melted resin filling step, and a molded article extracting step for extracting the molded article by opening the mold after the molded article cooling step is completed.
[0029] For example, a female die of the mold is installed to the injection equipment side (the fixed side) and a male die of the mold is installed to the mold closing mechanism side (the movable side). A melted resin material is injected into the cavity which is formed by engaging the male die of the mold with the female die of the mold. The injected melted resin material flows into the cavity through a gate from a spool in the mold. A molded article is released from the mold after cooling and solidifying the resin material which is filled in the mold.
[0030] As shown in
[0031] In
[0032] As shown in
[0033] As shown in
[0034] The melted resin material flows into the cavity 323 corresponding to the flange section first, and then flows into the cavity 324 corresponding to the large outer diameter barrel section. As shown in
[0035] After the cavity 320 is filled completely in the circumferential direction with the melted resin material, the streams of the melted resin material no longer join together in the circumferential direction, the melted resin material flows cylindrically toward the side of the cavity 322 corresponding to the injection nozzle section, and the melted resin filling step is completed by filling the cavity 322 corresponding to the injection nozzle section. Subsequently, a syringe barrel as a molded article shown in
[0036] In this embodiment, when the syringe barrel 20 is formed by injection molding of a synthetic resin material, as shown in
[0037] A linear pattern called as a weld line is formed at the merging part of the two streams of the resin material, wherein the weld line may cause occurrence of failure on its appearance and insufficient mechanical strength. The weld line is a phenomenon occurred by a slightly solidified resin material surface.
[0038] For creating a condition in which the surface of the merged melted resin material hardly solidifies, it is considered to delay the solidification by increasing the mold temperature, make the solidified layer on the surface thinner by increasing the injection speed, set the resin material temperature higher, set the resin material pressure higher and so on, however it is impossible to prevent occurrence of the weld line by these treatments.
[0039] In this manner, when the flange section 23 is formed, a weld line is formed in the vicinity of the center line 323M where the streams of the melted resin material join together. Next, there is also a possibility that a weld line is formed in the large outer diameter barrel section 24 when the melted resin material flows into the cavity 324 corresponding to the large outer diameter barrel section after filling the cavity 323 corresponding to the flange section and then the streams of the melted resin material join together in the vicinity of the center line 324M.
[0040] When the melted resin material fills the cavity 324 corresponding to the large outer diameter barrel section and extends through the entire circumference, the streams of the melted resin material no longer join together on the circumference at the time of flowing into the cavity 321M corresponding to the intermediate body part. Therefore, no weld line will be formed in the intermediate body part 21M.
[0041] Depending on the injection molding condition, there is also a possibility that the streams of the melted resin material join together on the circumference in a part of the cavity 321M corresponding to the intermediate body part which is close to the cavity 324 corresponding to the large outer diameter barrel section, and a weld line is potentially formed. However, no weld line is formed in a part of the cavity 321M corresponding to the intermediate body part which is close to the cavity 322 corresponding to the injection nozzle section because the streams of the melted resin material do not join together on the circumference.
[0042] Therefore, it is possible to obtain the internal-use solution filled section 20F where no weld line is formed by setting the part of the intermediate body part 21M, which is close to the large outer diameter barrel section 24, to the internal-use solution unfilled section 20N and the part of the intermediate body part 21M, which is close to the injection nozzle section 22, to the internal-use solution filled section 20F.
[0043] According to this embodiment, because no weld line is formed in the internal-use solution filled section 20F, no gap is formed between the outer circumferential surface of the piston 50 and the inner wall surface of the syringe barrel 20, and thus no internal-use solution will leak out. Hereby, it is possible to obtain a syringe barrel which can fill and administer a predetermined amount of the internal-use solution accurately and is manufactured by injection molding of a synthetic resin material.
[0044] In the molded article extracting step, gate rests are formed when the gates are separated from the molded article. The gate rests are formed by leaving the solidified resin material at the portions of the molded article which correspond to the positions of the gates. When the portions of the molded article corresponding to the gates are not solidified, the positions of separating the gates become unstable and solidified resin material will remain at the portions of the separated molded article corresponding to the positions of the gates. Although it is considered that the gate rests can be made smaller by adjusting the gate shape, the injection time, the mold opening speed and the pressure applied to the vicinity of the gates and so on, it is practically unavoidable to form a certain size of gate rests.
[0045] In general, the gate rests are removed by a treatment like polishing because the projections by the gate rests may cause injury at the time of use by a medical worker and a failure in mounting a finger grip. However, it is not preferable to conduct such post processing for preventing foreign matter contamination and treating in a hygienical full-automatic production process.
[0046] In this embodiment, as shown in
[0047] According to the above-described embodiment, it is possible to provide a medical syringe as a molded article by injection molding of a synthetic resin material and a manufacturing method for producing the same, wherein it is possible to be completed without requiring a post processing treatment like polishing and therefore possible to fill and administer a predetermined amount of an internal-use solution accurately. A syringe barrel according to the present embodiment is suitable for a prefilled syringe, wherein a medical solution is filled in a syringe barrel and the syringe is assembled in advance. A syringe barrel according to this embodiment is also suitable for a disposable syringe which is assumed to be used a single time.
EXPLANATION OF REFERENCES
[0048] 10 syringe [0049] 20 syringe barrel [0050] 20F internal-use solution filled section [0051] 20N internal-use solution unfilled section [0052] 20P piston tip position [0053] 21 barrel section [0054] 21M intermediate body part [0055] 21N inner wall surface of the intermediate body part 21M [0056] 22 injection nozzle section [0057] 22N inner wall surface of the nozzle part of the injection nozzle section 22 [0058] 23 flange section [0059] 23R recess portion [0060] 24 large outer diameter barrel section [0061] 24N inner wall surface of the large outer diameter barrel section 24 [0062] 25 gate rest [0063] 30 finger grip [0064] 300 mold [0065] 310 gate [0066] 320 cavity [0067] 321M cavity corresponding to the intermediate body part [0068] 322 cavity corresponding to the injection nozzle section [0069] 323 cavity corresponding to the flange section [0070] 323C convex portion [0071] 324 cavity corresponding to the large outer diameter barrel section [0072] 324N inner wall of the cavity corresponding to the large outer diameter barrel section [0073] 40 syringe plunger [0074] 50 piston [0075] 60 internal-use solution