CN204864007U - Soft bag infusion package system who has high barrier properties to gas - Google Patents
Soft bag infusion package system who has high barrier properties to gas Download PDFInfo
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- CN204864007U CN204864007U CN201520614489.1U CN201520614489U CN204864007U CN 204864007 U CN204864007 U CN 204864007U CN 201520614489 U CN201520614489 U CN 201520614489U CN 204864007 U CN204864007 U CN 204864007U
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Abstract
The utility model discloses a soft bag infusion package system who has high barrier properties to gas. This package system includes: non - PVC is crowded membrane inner bag altogether, and inside is equipped with the medicament chamber that holds injection liquid medicine and protective gas, separation protection bag, inside is equipped with and holds non - PVC is the seal cavity of crowded intramembrane bag altogether, crowded membrane inner bag is sealed altogether holds for non - PVC in the sealed chamber, wherein sealed chamber is the vacuum seal chamber. This kind of soft bag infusion package system who has high barrier properties to gas is through forming the vacuum seal chamber in separation protection bag, crowd the membrane inner bag altogether with non - PVC and hold the intracavity at vacuum seal, can be when stoping gaseous infiltration problem, because of having avoided filling gas in sealed chamber, and overcome that the bag body that gas expansion when heat sterilization caused warp or the defect of broken bag, the qualities of the infusion packing are improved the security, the penetration of heat power of sterilization process has still been improved simultaneously, sterilization effect has been improved.
Description
Technical field
This utility model relates to medical packaging field, particularly a kind of soft bag transfusion package system gas to high obstructing performance.
Background technology
Transfusion package goes through vial, plastic bottle, substantially achieves and completes from bottle processed to filling and sealing at same dust proof workshop, Clinical practice has been accomplished be put into semi-open progress from standard-sized sheet.In order to avoid secondary pollution, realize total enclosing transfusion, research design has the transfusion of the plastic bag packaging that can automatically shrink.Most widely used is non-PVC co-extrusion film bag and polypropylene vertical type bag at present.
Along with the development of transfusion clinical practice, transfusion kind no longer just simple normal saline and glucose.The treatment such as a collection of sodium bicarbonate class and amino acids injection class, nutrition class transfusion kind are are also more and more researched and developed and are widely used in clinical.Higher requirement is there is in these injection medicinal liquids for storage condition, as in sodium bicarbonate class injection, sodium bicarbonate is easy to resolve into carbon dioxide and sodium carbonate, cause liquid PH value increased denature, impact uses, need to be filled with carbon dioxide for this reason in bag, avoid product to go bad to suppress its hydrolysis; And for example amino acids injection needs to be filled with nitrogen in case oxidation.This just has higher requirement to transfusion package.
At present, utilize the good feature of vial barrier property, this kind of infusion products many employings glass bottle packaging.But glass bottle packaging has the following disadvantages: (1) matter is crisp frangible, the existence of this deficiency brings great inconvenience to glass bottle packaging on Clinical practice; (2) must import air during infusion, the existence of this deficiency probably causes this glass bottle packaging at the secondary pollution of infusion process and medicine qualitative change; (3) soda-lime glass surface corrosion-vulnerable and producing comes off, along with the volatilization of carbon dioxide in glass bottle packaging, the alkalescence of medicinal liquid increases gradually, and this just makes soda-lime glass surface corrosion-vulnerable and producing come off, and then seriously may jeopardize transfusion and patient safety.How to overcome the above problems, become the emphasis research topic of transfusion package technical field.
Some research staff thinks, directly can substitute vial by co-extrusion film transfusion bag, solves the pollution that brings of infusion and medicament denaturing problem like this.But existing transfusion bag majority is formed through note stretch blow by common PP TYPE welding and PP GRANULES, and its bag barrier property meets the requirement of most basic infusion products.And the product to bag domestic demand insufflation gas, this transfusion bag is in subsequent high temperature sterilizing and storage process, and gas through bag, infiltration problem can occur, and affects drug quality.
Also some research worker is thought, at existing co-extrusion film transfusion bag or butt-ended bag as on the basis of inner bag, can increase outer protective bag to form double-deck transfusion bag, and be filled with carbon dioxide or nitrogen between interior outer bag.But there are the following problems at follow-up sterilisation process for this structure: (1) if first carry out high temperature sterilize to internal bag, and then adds the outer bag with barrier property.In this case, one side is easy causes gas in inner bag to pass through inside when high temperature sterilize, seal up outer bag more after sterilization on the other hand, and now inner bag is outer non-sterile.And, owing to being filled with carbon dioxide or nitrogen between interior outer bag, making this transfusion bag outer bag seal difficulty, be easy to cause bag broken bag, be difficult to ensure Product Safety.(2) if carry out integral high-temperature sterilizing to transfusion package after adding the outer bag with barrier property, thermal break-through may be stoped because of the existence of carbon dioxide or nitrogen, cause sterilizing heterogeneity; But also may heat time gas expansion, easily cause bag broken bag or distortion.
Utility model content
Main purpose of the present utility model is to provide a kind of soft bag transfusion package system gas to high obstructing performance, to avoid gas that infiltration occurs and while affecting drug quality, to improve sterilization effect and the safety gas to the soft bag transfusion package system of high obstructing performance.
For this reason, in this utility model, provide a kind of soft bag transfusion package system gas to high obstructing performance, this packaging system comprises: non-PVC co-extrusion film inner bag, and inside is provided with the medicament chamber holding injection medicinal liquid and protective gas; Intercept protective bag, inside is provided with the annular seal space holding described non-PVC co-extrusion film inner bag, and described non-PVC co-extrusion film inner bag sealing is contained in described annular seal space, and wherein said annular seal space is vacuum-sealed cavity.
Preferably, deoxidizer and oxygen indicator is filled with in above-mentioned annular seal space.
Preferably; above-mentioned obstruct protective bag; prepared by barrier material, it is outer that described barrier material outwards comprises by annular seal space parylene's glycol ester inner layer of polypropylene, polycaprolactam or modified polypropene intermediate layer and inner surface being coated with aluminium sesquioxide successively.
Preferably, fixed by tack coat between each layer in described barrier material.
Preferably, described barrier material is transparent material.
Preferably, above-mentioned non-PVC co-extrusion film inner bag comprises: inner bag body, interface and lid, described inner bag body is made up by heat seal of three layers or five layers of non-PVC co-extrusion film, described medicament chamber is made with the link heat seal of interface bottom by the middle of inner bag body upper part, it is arranged in described inner bag body, and communicates with the interface endoporus of described interface; Described lid is connected to seal described medicament chamber with the joint weld platform on described inner bag body.
Preferably, above-mentioned interface sealing structure is made up of the interface of mutual seam and lid, interface is made up of jig, pipe shaft and link, the jig of described interface mates involutory with the welded disc equal diameter of lid, interface is provided with penetrating interface endoporus, described lid establishes lid endoporus, and at lid and interface touching position, the aperture of lid endoporus is greater than the aperture of interface endoporus.More preferably, described interface material is polypropylene.
Preferably, the top of above-mentioned interface endoporus be cylindrical, bottom for conical, cylindrical and conical junction seamlessly transits.Preferably, the back cut diameter of described interface endoporus is 8.4-8.6 millimeter, and the lower port diameter of interface endoporus is 12-12.5 millimeter.Preferably, the lateral dimension of described link is 21-23 millimeter, and link place is provided with three grooves.
Preferably, above-mentioned lid is common Pull ring cover or easy fold.
Preferably, the interface of described non-PVC co-extrusion film inner bag is single tube interface.
This utility model is above-mentioned has in the soft bag transfusion package system of high obstructing performance to gas in application; by adopting the double-deck non-PVC co-extruded film soft bag transfusion packaging replacement vial comprising non-PVC co-extrusion film inner bag and intercept protective bag, the deficiency because using glass bottle packaging to produce can be avoided.By forming vacuum-sealed cavity in obstruct protective bag; non-PVC co-extrusion film inner bag is contained in vacuum seal intracavity; can while improving gas permeation problems; because avoiding blanketing gas in annular seal space; overcome the defect of bag distortion that the gas expansion when high temperature sterilize causes or broken bag; improve production efficiency and the safety gas to the soft bag transfusion package of high obstructing performance; simultaneously because avoiding blanketing gas in annular seal space; also improve the thermal break-through power in sterilization process, improve sterilization effect.
Meanwhile, to have gas in the soft bag transfusion package system of high obstructing performance at this utility model and adopt the high obstructing performance of high-barrier protective bag to gas to guarantee that the gas in sealing packaging system is in poised state, to ensure the quality of product.
In addition, the soft bag transfusion package system that this utility model has high obstructing performance to gas is two-layer bag like construction, has advantage simply and easily, is convenient to produce, process and storage, is applicable to suitability for industrialized production.
Accompanying drawing explanation
The Figure of description forming a application's part is used to provide further understanding of the present utility model, and schematic description and description of the present utility model, for explaining this utility model, is not formed improper restriction of the present utility model.In the accompanying drawings:
Fig. 1 shows according to structural representation gas to the soft bag transfusion package system of high obstructing performance a kind of in a kind of embodiment of this utility model;
Fig. 2 shows the structural representation according to sealing joint in a kind of embodiment of this utility model;
Fig. 3 shows the structure left view according to sealing joint in a kind of embodiment of this utility model;
In figure, each label represents:
10, non-PVC co-extrusion film inner bag; 11, inner bag body;
12, interface; 13, lid;
15, medicament chamber; 17, injection medicinal liquid;
18, protective gas; 20, protective bag is intercepted;
21, annular seal space; 12-1, link;
12-1-1, groove; 12-2, pipe shaft;
12-3, interface endoporus; 12-4, jig;
13-1, welded disc; 13-2, lid endoporus;
13-3, Cover opening valve.
Detailed description of the invention
It should be noted that, when not conflicting, the embodiment in the application and the feature in embodiment can combine mutually.Below with reference to the accompanying drawings and describe this utility model in detail in conjunction with the embodiments.Unless otherwise expressly defined, those skilled in the art should think that the technical terms of chemistry used during full text herein describes have the usual implication used in this area.
As shown in Figure 1, in a kind of embodiment of the present utility model, provide a kind of soft bag transfusion package system gas to high obstructing performance, this packaging system comprises: non-PVC co-extrusion film inner bag 10 and obstruct protective bag 20.Wherein non-PVC co-extrusion film inner bag 10 inside is provided with the medicament chamber 15 holding injection medicinal liquid 17 and protective gas 18; Intercept protective bag 20 inside and be provided with the annular seal space 21 holding described non-PVC co-extrusion film inner bag 10, described non-PVC co-extrusion film inner bag 10 sealing is contained in described annular seal space 21, and wherein said annular seal space 21 is vacuum-sealed cavity.
Above-mentioned have in the soft bag transfusion package system of high obstructing performance to gas; by adopting the double-deck non-PVC co-extruded film soft bag transfusion packaging replacement vial comprising non-PVC co-extrusion film inner bag and intercept protective bag, the deficiency because using glass bottle packaging to produce can be avoided.By forming vacuum-sealed cavity in obstruct protective bag, non-PVC co-extrusion film inner bag is contained in vacuum seal intracavity, can while improving gas permeation problems, because avoiding blanketing gas in annular seal space, overcome the defect of bag distortion that the gas expansion when high temperature sterilize causes or broken bag, improve production efficiency and the safety gas to the soft bag transfusion package of high obstructing performance; Simultaneously because avoiding blanketing gas in annular seal space, also improving the thermal break-through power in sterilization process, improve sterilization effect; Meanwhile, have gas in this utility model in the soft bag transfusion package system of high obstructing performance and adopt the high obstructing performance of high-barrier protective bag to gas to guarantee that the gas in sealing packaging system is in poised state, to ensure the quality of product.In addition, the soft bag transfusion package system having a high obstructing performance to gas in this utility model is two-layer bag like construction, has advantage simply and easily, is convenient to produce, processing and storage, is applicable to suitability for industrialized production.
Have gas in the soft bag transfusion package system of high obstructing performance above-mentioned, in described annular seal space 21, be filled with deoxidizer and oxygen indicator.In annular seal space 21, be filled with deoxidizer and oxygen indicator can play absorption of residual oxygen and damage the effect of the prompting causing oxygen concentration to exceed standard because of outer bag.Wherein, operable deoxidizer includes but not limited to activated ferric oxide and/or reduced iron powder, and preferred deoxidizer is activated ferric oxide.The use of this deoxidizer and oxygen indicator does not contact with injection medicament, its consumption can be selected according to the Sizes of soft bag transfusion package system gas to high obstructing performance, simultaneously, preferably deoxidizer and oxygen indicator are made independent packaging structure, so that the interpolation of deoxidizer and oxygen indicator and taking-up.
Have gas in the soft bag transfusion package system of high obstructing performance above-mentioned, intercept protective bag 20 and prepared by barrier material, in this utility model, particular/special requirement is not had for barrier material, as long as have barriers function.In this utility model, preferably above-mentioned barrier material outwards comprises inner layer of polypropylene, polycaprolactam or modified polypropene intermediate layer and inner surface successively by annular seal space 21 to be coated with parylene's glycol ester of aluminium sesquioxide on the surface outer.Preferably, the thickness of described inner layer of polypropylene is 70-100 μm, and according to inner bag amount of capacity, in the packaging system of preferred single chamber inner bag volume≤500ml, the thickness of inner layer of polypropylene is 70-80 μm; In the packaging system of single chamber inner bag more than volume >500ml or two room, the thickness of inner layer of polypropylene is 80-100 μm; Preferably, the thickness in polycaprolactam or polypropylene intermediate layer is 10-26 μm, and buffer protection function is played in intermediate layer; Preferably, the outer field thickness of parylene's glycol ester that inner surface is coated with aluminium sesquioxide is 10-14 μm, and wherein, parylene's glycol ester film mainly plays high temperature resistant effect, and aluminium sesquioxide mainly takes blocking effect; Preferably, the gross thickness of described Obstruct membrane is 100-150 μm.Preferably, the bag of obstruct protective bag 20 is wide is 10-40cm, bag is long is 10-50cm, and hot edge seal width is 6-10mm.
Preferably, its steam penetrating capacity of this barrier material of adopting of this utility model is lower than 1.0g/ (m
224h) (testing standard ASTMF-1249, condition is 37.8 DEG C, 80%RH), nitrogen, carbon dioxide, oxygen transit dose are lower than 1.0cm
3/ (m
224h0.1MPa) (testing standard ASTMD-3985, condition 23 DEG C, 0%RH), better can realize barriers function like this, guarantee that the gas in sealing packaging system is in poised state, to ensure the quality of product.Preferably, be 30-45N/15mm (puller system 220 DEG C, 2.0kgf/cm by the heat seal strength before and after obstruct protective bag 20 sterilizing of this barrier material
2.2sec).
The above-mentioned steam penetrating capacity mentioned measures according to vapor permeation quantitative determination method (YBB00092003), and measuring condition is temperature 37.8 DEG C ± 0.6 DEG C, relative humidity 90% ± 2%.Above-mentioned nitrogen, carbon dioxide, the oxygen transit dose mentioned measures according to gas permeation quantitative determination method (YBB00082003), and measuring condition is temperature 23 DEG C ± 2 DEG C.
Formation for barrier material in this utility model does not have particular/special requirement, as long as have above-mentioned three-decker.Preferably, fixed by tack coat between each layer in above-mentioned barrier material.The material of preferred described tack coat is aliphatic adhesive, is preferably PEPA-Zhi Fang race oligomeric isocyanates.This binder material is adopted to have transparent, that degree of adhesion is high advantage.More preferably, described barrier material is transparent material.
Have in the soft bag transfusion package system of high obstructing performance to gas above-mentioned, non-PVC co-extrusion film inner bag 10 comprises inner bag body 11, interface 12 and lid 13.Described inner bag body 11 is made up by heat seal of three layers or five layers of non-PVC co-extrusion film, described medicament chamber 15 is made with the link 12-1 heat seal of interface 12 bottom by the middle of inner bag body 11 top, it is arranged in described inner bag body 11, and communicates with the interface endoporus 12-3 of described interface 12; Described lid 13 is connected to seal described medicament chamber 15 with the interface 12 jig 12-4 on described inner bag body 11.
Preferably; above-mentioned interface sealing structure is made up of the interface 12 of mutual seam and lid 13; as shown in Fig. 2 to 3; the link 12-1 of interface 12 and inner bag body 11 frit seal; improve jig 12-4 and lid 13 seam of interface endoporus 12-3 fill injection medicinal liquid and protective gas rear port 12, to seal described medicament chamber 15.Described interface 12 is followed successively by jig 12-4, pipe shaft 12-2 and link 12-1 from the bottom to top, and interface 12 is provided with penetrating interface endoporus 12-3.Described lid 13 is provided with lid endoporus 13-2, is provided with welded disc 13-1 on the top of lid 13, is provided with open valve 13-3 in lid 13 bottom.From Fig. 2 to 3, the jig 12-4 of interface and the welded disc 13-1 of lid are that equal diameter is mated involutory, and the aperture, top of lid endoporus 13-2 is greater than the end opening aperture of interface endoporus 12-3.The diameter of jig is 22 millimeters, compare and reduce nearly 1/3rd by 30 millimeters of prior art, adopt jig 12-4 to mate butted structure with the welded disc 13-1 equal diameter of lid, heat-sealing sealing property can be improved, prevent this place to leak the phenomenon of leakage, can also material be saved.More preferably, described interface material is polypropylene.
Preferably, the top of interface endoporus 12-3 be cylindrical, middle part for conical, cylindrical and conical junction seamlessly transits.The back cut diameter of interface endoporus is 8.4-8.6 millimeter, and the lower port diameter of interface endoporus is 12-12.5 millimeter.Said structure, the flow area of pipe shaft expands gradually, is conducive to overcoming medical liquid surface tension, through-flow smooth and easy, medicinal liquid is flowed out completely, noresidue, can not affect liquid medicine flow effect because of the reduction of pipe shaft diameter dimension.
Preferably, the cross sectional shape of link 12-1 is approximately rhombus.The lateral dimension of link 12-1 is 21-23 millimeter.Comparatively prior art reduces nearly 1/3rd.The compact overall structure of interface, weight are reduced.Three the groove 12-1-1 being convenient to seal with bag are provided with at link place.
In this utility model, do not have particular/special requirement for lid 13 structure in non-PVC co-extrusion film inner bag 10, it can be the plastic container for infusion lid of any conventional construction, as long as can realize the sealing of non-PVC co-extrusion film inner bag 10.
Preferably, above-mentioned lid 13 is common Pull ring cover or easy fold.
Preferably, the interface of described non-PVC co-extrusion film inner bag 10 is single tube interface.
Simultaneously, in this utility model, additionally provide a kind of above-mentioned preparation method gas to the soft bag infusion of high obstructing performance, this preparation method comprises the following steps: form in inner medicament chamber 15 the non-PVC co-extrusion film inner bag 10 being filled with injection medicinal liquid and protective gas; Loaded by described non-PVC co-extrusion film inner bag 10 and intercept in protective bag 20, sealing evacuation forms double-deck non-PVC co-extruded film soft bag transfusion packaging; Described double-deck non-PVC co-extruded film soft bag transfusion packaging is carried out sterilization treatment, obtains described soft bag transfusion package system gas to high obstructing performance.
Preferably, after described non-PVC co-extrusion film inner bag 10 being loaded obstruct protective bag 20, the step loading deoxidizer and oxygen indicator in described obstruct protective bag 20 is also included in.
Said method provided by the utility model; by carrying out sealing evacuation and then form vacuum-sealed cavity after described non-PVC co-extrusion film inner bag 10 being loaded obstruct protective bag 20 in obstruct protective bag; thus while improving gas permeation problems; because avoiding blanketing gas in annular seal space; overcome the defect of bag distortion that the gas expansion when high temperature sterilize causes or broken bag, improve the production efficiency of soft bag transfusion package gas to high obstructing performance.And the method carries out sterilization treatment after the double-deck non-PVC co-extruded film soft bag transfusion packaging of formation, avoids the secondary pollution of non-PVC co-extrusion film inner bag 10, improves product safety in utilization.Meanwhile, because avoiding blanketing gas in annular seal space, also improving the thermal break-through power in sterilization process, improve sterilization effect.In addition, simplify preparation technology, avoid because gas-heated expands, institute causes bag broken bag or distortion.
Preferably, in the above-mentioned methods, the step forming in inner medicament chamber 15 the non-PVC co-extrusion film inner bag 10 being filled with injection medicinal liquid and protective gas comprises: prepare interface 12 and lid 13 respectively at clean environment; Preparation injection medicinal liquid, and in described injection medicinal liquid, be filled with protective gas formation injection medicinal liquid; Under hundred grades of laminar flows, form inner bag body 11, and weld with the link 12-1 heat seal of interface 12; By in described injection liquid medicine filling to described inner bag body 11, in bag, be filled with protective gas, the air in displacement dosing space, seals the jig 12-4 of described interface 12, forms described non-PVC co-extrusion film inner bag 10 with lid 13.
Inner bag body 11 is made up by heat seal of three layers or five layers of non-PVC co-extrusion film in the above-mentioned methods.
Preparation parameter is as follows:
Unit: DEG C
Unit: DEG C
| Interface preheating 1 | Temperature set point | Interface preheating 1 | Temperature set point |
| On | 133.0～142.0 | Under | 133.0～142.0 |
| Interface preheating 2 | Temperature set point | Interface preheating 2 | Temperature set point |
| On mould A | 145.0～155.0 | Under mould A | 145.0～155.0 |
| On mould B | 145.0～155.0 | Under mould B | 145.0～155.0 |
| On mould C | 145.0～155.0 | Under mould C | 145.0～155.0 |
| On mould D | 145.0～155.0 | Under mould D | 145.0～155.0 |
| On mould E | 145.0～155.0 | Under mould E | 145.0～155.0 |
| On mould F | 145.0～155.0 | Under mould F | 145.0～155.0 |
Unit: DEG C
| Interface welds with bag mouth | Temperature set point | Interface welds with bag mouth | Temperature set point |
| On mould A | 140.0～150.0 | Under mould A | 140.0～150.0 |
| On mould B | 140.0～150.0 | Under mould B | 140.0～150.0 |
| On mould C | 140.0～150.0 | Under mould C | 140.0～150.0 |
| On mould D | 140.0～150.0 | Under mould D | 140.0～150.0 |
| On mould E | 140.0～150.0 | Under mould E | 140.0～150.0 |
Time, setting value was as following table:
| Position | Time |
| Interface preheating time one | 1-1.7s |
| Interface preheating time two | 1-1.7s |
| Periphery pressurization time | 0.5-1.0s |
| Venting duration in advance | 0.1-0.3s |
| Periphery bad bag detection time | 110-130s |
| Weld bond bad bag detection time | 20-40s |
| Interface heat sealed time | 1.3-2.0s |
| Film cool time | 0.3-1.0s |
| Blow the useless angle time | 0.8-1.2s |
| Go down useless angle delay time | 0.5-1.0s |
| Interface cool time | 1.0-2.0s |
Intercepting protective bag 20 is in the above-mentioned methods formed through three edge sealing bags by two panels barrier material film.The step preparing described obstruct protective bag 20 comprises: the compound of each functional sheet film, ripening, and according to bag shape dimensional requirement heat-sealing bag.To the manufacturing process intercepting protective bag 20 be described in further detail below:
(1), the compound of each functional sheet film: make polypropylene screen, polycaprolactam film respectively, parylene's glycol ester film, and apply aluminium sesquioxide slurry on the surface, inboard of parylene's glycol ester film; At polypropylene screen, polycaprolactam film, and parylene's glycol ester film be coated with aluminium sesquioxide surface on applied adhesive, by being bonded together of three-layer tablet film close, through pressing composite material film;
(2), ripening: by prepared composite material film, ripening 24-36h at 23-26 DEG C of temperature, to obtain the stable barrier material film of product size, the test of this product Key Quality comprises barrier properties for gases etc.
(3), bag: according to pouch-type size requirements, aforementioned barrier material film is cut into specific dimensions, makes the outer bag of three side sealing mouth for follow-up through heat-sealing.Wherein polypropylene is as weld seam layer, and polyester layer is as heatproof barrier layer.In this process, need to detect the heat-sealing peel strength intercepting protective bag 20, heat-sealing air-tightness, bag shape size.
Above-mentioned process is process known in the art, and its concrete technology step does not repeat them here.
The step of the interface sealed on described inner bag body 11 with lid 13 in the above-mentioned methods comprises: under hundred grades of laminar flows protections; after filling and sealing liquid medicine filling, the joint weld platform and lid that are welded on inner bag body are heated (heter temperature: 750-850 DEG C) simultaneously; persistent period 1 to 5s, make bag and lid melting sealed.Hundred grades of laminar flows are pharmaceutical environment air cleaning ranks.
For sodium bicarbonate injection; the step that in said method, fill injection medicinal liquid and protective gas obtain non-PVC co-extrusion film inner bag 10 comprises: preparation injection medicinal liquid: (1) is dense joins: inject appropriate brand-new water for injection in dissolving tank; add the sodium bicarbonate of amount of calculation; by the long-pending medicinal carbon adding 0.01% (g/ml) of rare part; stir; filter, flushing water is filled in dilute preparing tank in the lump.(2) rarely to join: mend and add to the full amount of water for injection, cycle balance, be filled with carbon dioxide and (adopt the above high-purity carbon dioxide of purity 99.99vt%, passed into by stainless steel pipes after 0.22 micrometer polytetrafluoroethylene material filtration devices), detect pH value (7.8 ~ 8.3), content, qualified rear filtration, checks that medicinal liquid clarity obtains injection medicinal liquid; Fill: under carbon dioxide exists, by in described injection liquid medicine filling to described inner bag body 11, be filled with carbon dioxide displacement liquid level to the air of bag mouth, be welded on the interface on inner bag body 11 described in sealing with lid 13, form described non-PVC co-extrusion film inner bag 10.
For Amino Acid Compound Injection, the step that in said method, fill injection medicinal liquid and protective gas obtain non-PVC co-extrusion film inner bag 10 comprises: preparation injection medicinal liquid: add appropriate water for injection in dilute preparing tank, be filled with nitrogen and (adopt the above high pure nitrogen of purity 99.99vt%, after the politef material filtration devices of 0.22 micron, be not less than 0.5Mpa with nitrogen pressure to be passed into by the stainless steel pipes of cleaning), (concrete formula is with reference to Amino Acid Compound Injection to drop into load weighted each seed amino acid in order, do not do emphasis herein to describe), circulation adds active carbon (adding charcoal amount by rare 0.1%W/V joining cumulative volume) after dissolving, benefit adds to the full amount of water for injection, cycle balance, the dissolved oxygen of tracer liquid is at below 0.1mg/L, measure pH value, content, after qualified, filter, check that medicinal liquid clarity obtains injection medicinal liquid, fill: in the presence of nitrogen, by described injection liquid medicine filling to described inner bag body 11, is filled with nitrogen displacement liquid level to the air of bag mouth, with the interface of lid 13 seal welding on described inner bag body 11, forms described non-PVC co-extrusion film inner bag 10.
In the preparation method of above-mentioned soft bag transfusion package system gas to high obstructing performance; described non-PVC co-extrusion film inner bag 10 is loaded and intercepts in protective bag 20, and the step loading deoxidizer and oxygen indicator in described obstruct protective bag 20 is carried out under protective gas exists.
Have in the preparation method of the soft bag infusion of high obstructing performance to gas above-mentioned; after described non-PVC co-extrusion film inner bag 10 being loaded obstruct protective bag 20, needed for this utility model, the character of the injectable liquefied composition of fill selects whether in described obstruct protective bag 20, load deoxidizer and oxygen indicator.
Preferably, described deoxidizer and oxygen indicator are all independent packagings.
For Amino Acid Compound Injection, in said method, fill injection medicinal liquid and protective gas obtain in the step of non-PVC co-extrusion film inner bag 10, are filled with when nitrogen gets rid of oxygen and just must add deoxidizer and oxygen indicator between non-PVC co-extrusion film inner bag 10 and obstruct protective bag 20;
For sodium bicarbonate injection; in said method, fill injection medicinal liquid and protective gas obtain in the step of non-PVC co-extrusion film inner bag 10; be filled with CO 2 gas-shielded, then need do not add deoxidizer and oxygen indicator between non-PVC co-extrusion film inner bag 10 and obstruct protective bag 20.
In the preparation method of above-mentioned soft bag transfusion package system gas to high obstructing performance; load the step of deoxidizer and oxygen indicator in described obstruct protective bag 20 before; first can prepare deoxidizer and the oxygen indicator of independent packaging, more this independent packaging that deoxidizer and oxygen indicator are housed is placed in annular seal space 21.
In the preparation method of above-mentioned soft bag transfusion package system gas to high obstructing performance; described non-PVC co-extrusion film inner bag 10 is loaded and intercepts in protective bag 20; sealing evacuation is formed in the step of double-deck non-PVC co-extruded film soft bag transfusion packaging; sealing adopts vacuum packing machine, utilizes heating in vacuum welding procedure to carry out.Particularly; the obstruct protective bag 20 of non-PVC co-extrusion film inner bag 10 will be housed; put on the silica gel strip in the vacuum chamber of vacuum packing machine; cover the lid of vacuum chamber; vacuum pump starts to produce vacuum; when after the vacuum 95% (being equivalent to-0.095Mpa) that vacuum reaches required, start to seal the opening intercepting protective bag 20.In order to pack the sterilizing of heat-seal land withstand high temperatures, adopt the two envelope types of 3-5mm two envelope line heat-sealable way.Meanwhile, being convenient to open to intercept protective bag 20 during Clinical practice, being provided with tearable mouth in the left and right sides, bottom of two envelope lines of outer bag.
In the preparation method of above-mentioned soft bag transfusion package system gas to high obstructing performance, described double-deck non-PVC co-extruded film soft bag transfusion packaging is carried out in the step of sterilization treatment, selects the condition of sterilizing according to the character of the injectable liquefied composition of inner bag institute fill.For sodium bicarbonate injection medicinal liquid, sterilising conditions is 119-121 DEG C of constant temperature sterilizing 12-15 minute, preferably 121 DEG C of constant temperature sterilizings 12 minutes; For Amino Acid Compound Injection medicinal liquid, sterilising conditions is constant temperature sterilizing 30-45 minute at 112-115 DEG C, preferably constant temperature sterilizing 30 minutes at 115 DEG C.
Above-mentioned soft bag transfusion package system gas to high obstructing performance of application this utility model; by adopting the double-deck non-PVC co-extruded film soft bag transfusion packaging replacement vial comprising non-PVC co-extrusion film inner bag and intercept protective bag, the deficiency because using glass bottle packaging to produce can be avoided.By forming vacuum-sealed cavity in obstruct protective bag; non-PVC co-extrusion film inner bag is contained in vacuum seal intracavity; can while improving gas permeation problems; because avoiding blanketing gas in annular seal space; overcome the defect of bag distortion that the gas expansion when high temperature sterilize causes or broken bag; improve the production efficiency of soft bag transfusion package gas to high obstructing performance, be conducive to guaranteeing that the gas in sealing packaging system is in poised state, to ensure the quality of product.
And; above-mentioned preparation method gas to the soft bag infusion of high obstructing performance of application this utility model; by carrying out sealing evacuation and then form vacuum-sealed cavity after described non-PVC co-extrusion film inner bag 10 being loaded obstruct protective bag 20 in obstruct protective bag; thus while improving gas permeation problems; because avoiding blanketing gas in annular seal space; overcome the defect of bag distortion that the gas expansion when high temperature sterilize causes or broken bag, improve the safety of soft bag transfusion package gas to high obstructing performance.And the method carries out sterilization treatment after the double-deck non-PVC co-extruded film soft bag transfusion packaging of formation, avoids the secondary pollution of non-PVC co-extrusion film inner bag 10, improves product safety in utilization.Meanwhile, because avoiding blanketing gas in annular seal space, also improving the thermal break-through power in sterilization process, improve sterilization effect.In addition, simplify preparation technology, avoid because gas-heated expands, the bag broken bag caused or distortion.
Below with reference to the above-mentioned practical application to the gas soft bag transfusion package system with high obstructing performance and preparation method thereof of this utility model, its effect is described.
One, the barriering effect intercepting protective bag proves
(1) material illustrates: outwards comprised the parylene's glycol ester skin (12 μm) inner layer of polypropylene (100 μm), adhesive layer, polycaprolactam intermediate layer (14 μm), adhesive layer and inner surface being coated with aluminium sesquioxide successively by annular seal space
(2) test event and method of testing:
Steam penetrating capacity: measure with reference to steam penetrating capacity algoscopy (YBB00092003), condition is temperature 37.8 DEG C ± 0.6 DEG C, relative humidity 90% ± 2%.
Nitrogen, carbon dioxide, oxygen transit dose: measure with reference to gas permeation quantitative determination method (YBB00082003), Conditions Temperature 23 DEG C ± 2 DEG C.
Heat seal strength: adopt puller system to test, condition is 220 DEG C, 2.0kgf/cm
2.2sec.
(3) test result: the three groups of samples getting different batches are tested respectively, and test result is as shown in table 1.
Table 1
From data in table 1, the steam penetrating capacity of this barrier material that this utility model adopts can lower than 1.0g/ (m
224h), nitrogen, carbon dioxide, oxygen transit dose can lower than 1.0cm
3/ (m
224h0.1MPa), and the heat seal strength before and after sterilizing is 30-45N/15mm, adopts this barrier material better can realize barriers function, guarantees that the gas in sealing packaging system is in poised state, to ensure the quality of product.
Two, this utility model is above-mentioned has injection medicinal liquid sealing propertytest in the soft bag transfusion package system of high obstructing performance and proves to gas
For sodium bicarbonate injection, application this utility model is above-mentioned to be had the soft bag transfusion package system of high obstructing performance to gas and gas is had to the preparation method of soft bag transfusion package system of high obstructing performance, before high temperature sterilize step, pH value gas to the soft bag transfusion package system herb liquid of high obstructing performance is 7.8-8.3, after high temperature sterilize step, soft bag transfusion package system herb liquid pH value gas to high obstructing performance is 7.8-8.3, after the storage of 24 months, pH value gas to the soft bag transfusion package system herb liquid of high obstructing performance is 7.8-8.3.
For Amino Acid Compound Injection, application this utility model is above-mentioned to be had the soft bag transfusion package system of high obstructing performance to gas and gas is had to the preparation method of soft bag transfusion package system of high obstructing performance, before high temperature sterilize step, be 0.03mg/L to the gas dissolved oxygen had in the soft bag transfusion package system herb liquid of high obstructing performance, after high temperature sterilize step, be 0.03mg/L to the gas dissolved oxygen had in the soft bag transfusion package system herb liquid of high obstructing performance, after the storage of 24 months, be 0.030mg/L to the gas dissolved oxygen had in the soft bag transfusion package system herb liquid of high obstructing performance.
As shown in the above; above-mentioned soft bag transfusion package system gas to high obstructing performance of application this utility model; the double-deck non-PVC co-extruded film soft bag transfusion packaging comprising non-PVC co-extrusion film inner bag and obstruct protective bag replaces vial, can avoid the deficiency because using glass bottle packaging to produce.By forming vacuum-sealed cavity in obstruct protective bag; non-PVC co-extrusion film inner bag is contained in vacuum seal intracavity; can while improving gas permeation problems; because avoiding blanketing gas in annular seal space; overcome the defect of bag distortion that the gas expansion when high temperature sterilize causes or broken bag; improve the safety of soft bag transfusion package system gas to high obstructing performance; simultaneously because avoiding blanketing gas in annular seal space; also improve the thermal break-through power in sterilization process, improve sterilization effect.
The foregoing is only preferred embodiment of the present utility model, be not limited to this utility model, for a person skilled in the art, this utility model can have various modifications and variations.All within spirit of the present utility model and principle, any amendment done, equivalent replacement, improvement etc., all should be included within protection domain of the present utility model.
Claims (10)
1. gas is had to a soft bag transfusion package system for high obstructing performance, it is characterized in that, described packaging system comprises:
Non-PVC co-extrusion film inner bag (10), inside is provided with the medicament chamber (15) holding injection medicinal liquid (17) and protective gas (18);
Intercept protective bag (20); inside is provided with the annular seal space (21) holding described non-PVC co-extrusion film inner bag (10); described non-PVC co-extrusion film inner bag (10) sealing is contained in described annular seal space (21), and wherein said annular seal space (21) is vacuum-sealed cavity.
2. soft bag transfusion package system gas to high obstructing performance according to claim 1, is characterized in that, described annular seal space is filled with deoxidizer and oxygen indicator in (21).
3. soft bag transfusion package system gas to high obstructing performance according to claim 1 and 2; it is characterized in that; described obstruct protective bag (20); prepared by barrier material, it is outer that described barrier material outwards comprises by annular seal space (21) parylene's glycol ester inner layer of polypropylene, polycaprolactam or modified polypropene intermediate layer and inner surface being coated with aluminium sesquioxide successively.
4. soft bag transfusion package system gas to high obstructing performance according to claim 3, be is characterized in that, fixed in described barrier material between each layer by tack coat.
5. soft bag transfusion package system gas to high obstructing performance according to claim 1 and 2, it is characterized in that, described non-PVC co-extrusion film inner bag comprises: inner bag body (11), interface (12) and lid (13), and described inner bag body (11) is made up by heat seal of three layers or five layers of non-PVC co-extrusion film; Described medicament chamber (15) is made with link (12-1) heat seal of interface (12) bottom by the middle of inner bag body (11) top, it is arranged in described inner bag body (11), and communicates with the interface endoporus (12-3) of described interface (12); Described lid (13) is connected to seal described medicament chamber (15) with interface (12) jig (12-4) on described inner bag body (11).
6. soft bag transfusion package system gas to high obstructing performance according to claim 5, it is characterized in that, described interface sealing structure is made up of the interface (12) of mutual seam and lid (13), described interface (12) is by jig (12-4), pipe shaft (12-2) and link (12-1) are formed, the jig (12-4) of described interface (12) mates involutory with welded disc (13-1) equal diameter of lid (13), interface (12) is provided with penetrating interface endoporus (12-3), described lid (13) is provided with lid endoporus (13-2), at lid (13) and interface (12) touching position, the aperture of lid endoporus (13-2) is greater than the aperture of interface endoporus (12-3),
Preferably, described interface material is polypropylene.
7. soft bag transfusion package system gas to high obstructing performance according to claim 6, is characterized in that, the top of described interface endoporus (12-3) be cylindrical, bottom for conical, cylindrical and conical junction seamlessly transits;
Preferably, the back cut diameter of described interface endoporus (12-3) is 8.4-8.6 millimeter, and the lower port diameter of interface endoporus (12-3) is 12-12.5 millimeter.
8. soft bag transfusion package system gas to high obstructing performance according to claim 6, it is characterized in that, the lateral dimension of the link (12-1) of described interface (12) is 21-23 millimeter, and link place is provided with three grooves (12-1-1).
9. soft bag transfusion package system gas to high obstructing performance according to claim 5, is characterized in that, described lid (13) is common Pull ring cover or easy fold.
10. soft bag transfusion package system gas to high obstructing performance according to claim 1 and 2, is characterized in that, the interface of described non-PVC co-extrusion film inner bag (10) is single tube interface.
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| CN105012143A (en) * | 2015-08-14 | 2015-11-04 | 石家庄四药有限公司 | Soft bag infusion packaging system with high barrier property to gas and manufacturing method thereof |
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Address after: 050035 No. 518, Huai'an East Road, high tech Industrial Development Zone, Shijiazhuang City, Hebei Province Patentee after: SHIJIAZHUANG NO.4 PHARMACEUTICAL Co.,Ltd. Address before: 050035 No. 288 Pearl River Avenue, Shijiazhuang Hi-tech Industrial Development Zone, Hebei Province Patentee before: SHIJIAZHUANG NO.4 PHARMACEUTICAL Co.,Ltd. |