| (19) |
 |
|
(11) |
EP 0 076 062 B1 |
| (12) |
EUROPEAN PATENT SPECIFICATION |
| (45) |
Mention of the grant of the patent: |
|
23.07.1986 Bulletin 1986/30 |
| (22) |
Date of filing: 16.09.1982 |
|
| (51) |
International Patent Classification (IPC)4: A61J 1/00 |
|
| (54) |
Blood product storage bag
Behälter zur Speicherung von Blutkomponenten
Récipient d'emmagasinage de composants du sang
|
| (84) |
Designated Contracting States: |
|
AT CH DE FR GB IT LI NL SE |
| (30) |
Priority: |
25.09.1981 US 305490
|
| (43) |
Date of publication of application: |
|
06.04.1983 Bulletin 1983/14 |
| (71) |
Applicant: HAEMONETICS CORPORATION(a Massachusetts Corporation) |
|
Braintree
Massachusetts 02184 (US) |
|
| (72) |
Inventor: |
|
- Lueptow, Richard M.
Allston
Massachusetts 02134 (US)
|
| (74) |
Representative: Harvey, David Gareth et al |
|
Graham Watt & Co.
Riverhead Sevenoaks
Kent TN13 2BN Sevenoaks
Kent TN13 2BN (GB) |
|
| |
|
| Note: Within nine months from the publication of the mention of the grant of the European
patent, any person may give notice to the European Patent Office of opposition to
the European patent
granted. Notice of opposition shall be filed in a written reasoned statement. It shall
not be deemed to
have been filed until the opposition fee has been paid. (Art. 99(1) European Patent
Convention).
|
[0001] This invention relates generally to the field of blood component therapy and more
particularly relates to containers for apparatus for the collecting, storing and dispensing
of blood plasma to be processed into blood components such as albumin, globulins and
so on.
[0002] A relatively modern medical technology known as blood component therapy involves
administering to a patient just that part of the blood that he actually needs. Rather
than whole blood, the physician decides what portion or component of blood is necessary
for the patient and administers only that component to him. He, thus, avoids many
of the hazards which are inherent in whole blood usage. Not only is the practice better
for the patient in that certain risks involving transfusing whole blood are reduced,
but it permits one unit of donated blood to be used for more than one patient. For
example, from one unit of whole blood, which subsequently is fractionated, there may
be derived red blood cells, platelets, fresh plasma, frozen or stored plasma, albumin,
globulins and so on.
[0003] Furthermore, in the most modern techniques, cell separators permit the separation
of blood into its components while the donor is in the process of making a donation.
Through modern technology it is possible for a blood bank to take from the donor specific
components which are needed by a patient while other components are returned simultaneously
to the donor.
[0004] In the technique known as plasmapheresis, the plasma is separated from the cellular
elements of the blood and the cells returned to the donor. The plasma is then subsequently
used for blood volume expansion or blood augmentation in the form of stored plasma
or fresh frozen plasma. The plasma can also be processed into a number of useful products
such as albumin, globulins and antihemophiliac factor. It is to this purpose that
the present invention is directed.
[0005] Blood is collected from the donor in a connected, sealed collection system and then
centrifuged to separate the cells and the plasma. The cells are returned to the donor
and the plasma is subsequently frozen in a collection bag. In the frozen state the
plasma may be stored for a number of months before being removed for plasma component
manufacturing. Subsequently, large quantities of plasma are batch processed, i.e.
plasma from many donors.
[0006] During this batch processing contamination is an obvious risk. The whole blood is
initially collected in a sealed system which is followed by centrifuging and freezing
while still sealed. However, the bags must ultimately be cut open and the plasma removed
either manually or automatically. It is possible that during the opening and removing
operation the plasma can become contaminated.
[0007] The system just described is the subject of GB-A-2,044,220. The blood product collection
bag of that system is made of flexible material and has a body with front and rearfaces
and there is a closure seam at or adjacent an end of the body. As noted above, this
bag has to be cut open to free the frozen plasma, which is then ejected from the bag
by squeezing the bag.
[0008] The present practice involves receiving blood from the donor in a collection system
and centrifuging it so that the plasma is collected in one of the bags of the system.
The plasma containing bag is then separated from the rest of the collection system
and is stored after freezing its contents, all prior to processing weeks or months
later. Subsequently, many bags are opened, and the plasma put in a container for batch
processing. The present invention is directed to an "easy-open" plasma bag which need
not be cut to remove the plasma.
[0009] Whilst easy-open packaging such as bags and other containers are known for containing
various products, see for example US-A-3,259,235, US-A-3,516,537 and US-A-3,604,616,
so far as we know no-one hitherto has devised an easy-open arrangement suiting the
requirements of a blood product storage bag.
[0010] The "easy-open" bag which holds the plasma is a sealable container of flexible material.
It comprises a body so constructed that a manually applied opening force exerted thereon
causes the body to rupture at predetermined locations and to tear open along predetermined
lines, thus affording separation of the body from the frozen plasma without any necessity
for the bag being cut by a knife or any other instrument, or for the plasma to be
contacted by the hands.
[0011] According to the present invention, there is provided a blood product storage bag
made of .flexible material and having a body with front and rear faces and a closure
seam at or adjacent an end of the body, characterised by the body having an easy-open
frangible construction provided by opposed weakenings, one in each of the said faces,
which extend to the closure seam and are aligned with one another thereat, and stress-concentrating
means which concentrate an applied opening force at the juncture of the seam and said
weakenings for causing the body to rupture at the juncture and be torn open along
the weakenings to separate the bag from its contents.
[0012] The closure seam can be of V-shape configuration, the point of which intersects the
juncture, the said closure seam defining a V-shape removable portion of body material
on the side of the closure seam which is opposite the weakenings whereby the closure
seam may be ruptured at the juncture and the body torn open along the weakenings to
separate it from its contents after the V-shape body material is removed.
[0013] Preferably, the bag is provided with means which may be gripped by hand to facilitate
the application of the rupturing force. Moreover, the bag is preferably formed of
a material which is capable of remaining flexible at temperatures of -25 to -80°C,
e.g. of polyolefinic type.
[0014] The present invention will now be more particularly described with reference to the
accompanying drawings in which containers embodying the invention are shown by way
of exemplary illustration only. The principles of this invention may be employed in
other embodiments without departing from the scope of the appended claims. In the
drawings:
Fig. 1 is a perspective view of an "easy-open" sealable container or bag of flexible
material embodying the invention;
Figs. 2 and 3 are views of the bag shown in Fig. 1 being opened;
Figs. 4 and 5 are views of alternative bag constructions according to the invention;
and
Figs. 6 and 7 are views of another alternative bag construction according to the invention.
[0015] Fig. 1 shows a transfer bag embodying the present invention. The bag was used as
part of multiple bag collection system and is now in an inverted position and containing
frozen plasma ready for opening. The body 10 of the bag communicated with a donor
bag (not shown) by means of a flexible tube 12, the tube now being closed by a conventional
seal 14. The bag includes hanger holes 16 which may be employed when the donor bag
is being filled. The bag comprises a sealable container of flexible plastics material
such as polyolefin of 6 mils thickness (0.15 mm) which is capable of remaining flexible
at temperatures of -25 to -80°C, i.e. the range of temperatures in which plasma is
frozen and stored.
[0016] Depending on its method of manufacture, the body 10 of the container includes a pair
of weakening lines comprising frangible seams 20 or similar running from the.top to
the bottom of the body (as oriented in Fig. 1). The seams join one another at a juncture
22.
[0017] As viewed in Figs. 2 and 3 (which is a view only slightly in perspective of the openable
end of the bag), the lines 20 will be seen to be located at opposite sides of the
body 10 and in a plane bisecting the body. Transversely intersecting the juncture
22 of the frangible lines 20 is a closure seam 24 which is of greater width than the
width of the frangible seams. In the construction shown in Figs. 1, 2 and 3 a pair
of ears 26 lie laterally of the juncture 22 to one side of (in this instance above)
the closure seam 24, opposite the frangible lines 20. The edges of the ears 26 are
rounded and converge toward the juncture 22. The closure seam 24 is essentially along
a straight line, sealing the top of the bag and separating the interior of the body
from the ears 26.
[0018] Also as seen in Figs. 1 and 2 (but hidden in Fig. 3) ribs 28 are formed in the body
and extend from the closure seam 24 in diverging directions away from the juncture
22 to the edges of the body 10. The ribs 28 define portions 30 of the body lying laterally
of the juncture which are sealed from the interior of the body and accordingly contain
no plasma.
[0019] To open the body, the ears 26 alone or together with the closure seam 24 and/or the
portions 30 are gripped and pulled apart either as shown in Fig. 2 or in Fig. 3, thereby
directing or concentrating force at the juncture 22. The bag ruptures at the juncture
22 permitting the body 10 to be torn apart along the frangible lines 20 whereby the
flexible plastics film may be peeled away from the frozen plasma within the bag and
the plasma allowed to fall into a collection container without being touched by a
knife or other opening instrument, or by the hands. The bag of course would be inverted
from the positions shown in Figs. 1, 2 and 3 for releasing its contents. While Figs.
2 and 3 show the flexible container being torn apart by bare hands, some may prefer
to wear gloves as insulation from the cold contents.
[0020] In some prior plasma bag constructions, opening required the bag to be cut open with
a knife to expose the plasma as well as thawing of its contents slightly from the
outside inwardly to release the frozen plasma from the inner surface of the bag. Because
of the construction of the present invention, the bag need not be cut. Since the bag
is essentially peeled back away from the frozen plasma, there is no skin thawing necessary
preparatory to opening the bag.
[0021] Fig. 4.shows an alternative construction of the openable portion of the bag. The
closure seam 24, as in the Fig. 1 construction, is essentially a straight line running
across top of the bag intersecting the juncture with the frangible lines 20. The closure
seam 24 has a notch 34 aligned with the juncture 22 to concentrate rupturing force
at the juncture 22. There are no ears 26 on the body and it would be optional to provide
ribs 28 defining the sealed portions 30 containing no plasma.
[0022] Another alternative construction of the body is shown in Fig. 5. In this alternative
the closure seam 24 is of V-shape configuration comprising portions 24a and 24b converging
toward the juncture 22. Ribs 28 define areas 30 equivalent to the portions 30 in the
Fig. 1 construction. Again, the ribs 28 and unfilled areas 30 are optional. However,
since there are no ears, it would be the closure seam portions 24a and 24b (with the
portions 30 if provided) that would be gripped and pulled apart. The V-shape configuration
of the seam 24 concentrates the applied force at the juncture 22 to initiate tearing
of the frangible lines 20.
[0023] Figs. 6 and 7 show another alternative construction. The closure seam 24 as in the
Fig. 5 construction is of V-shape configuration converging at the juncture with the
frangible seams 20. The ribs 28a and 28b also converge at the juncture and as described
above define unfilled areas 30.
[0024] For ease of construction, the ribs 28a and 28b converge at the juncture. The closure
seam portions 24a and the rib 28a are aligned linear extensions of each other as are
the seam portion 24b and the rib 28b. By this configuration, there is a substantially
triangular portion 40 on the side of the closure seam 24a-24b opposite the areas 30
which is made up of the folded overlapping corners of the bag material designated
42. These are secured together by a combining seam 44.
[0025] The triangular portion 40 remains attached to the bag until it is ready to be opened.
It will be noted in Fig. 6 that a line of serrations 46 extend along the closure seam
portions 24a and 24b. The provision of the triangular portion 40 lends additional
strength to the bag to guarantee against premature rupture at the juncture 22.
[0026] When the bag is ready to be opened, the portion 40 is torn from the bag along the
lines of serration 46 rendering the bag as it appears in Fig. 7. Thereafter, the portions
30 and/or the closure seam portions 24a and 24b may be gripped and pulled apart to
develop and concentrate rupturing force at the juncture 22 as in above described constructions.
[0027] The various constructions may be fabricated in various ways. They may be made by
cutting off blanks from a continuous tube of polyolefin material and forming the frangible
lines 20, the bottom 36, the closure seam 24, and the ribs 28 by heat sealing. Another
method of fabrication would be to start with sheet material folded upon itself with
the various ribs, seams and lines also formed by heat sealing.
[0028] Another method would be by forming the entire bag by blow molding. The various ribs,
seams and lines would be formed in the mold cavity and imparted to the bag in the
blow molding process.
1. A blood product storage bag made of flexible material and having a body (10) with
front and rear faces and a closure seam (24) at or adjacent an end of the body, characterised
by the body (10) having an easy-open frangible construction provided by opposed weakenings
(20), one in each of the said faces, which extend to the closure seam (24) and are
aligned with one another thereat, and stress-concentrating means (e.g. 34) which concentrate
an applied opening force at the juncture (22) of the seam (24) and said weakenings
(20) for causing the body to rupture at the juncture (22) and be torn open along the
weakenings (20) to separate the bag from its contents.
2. A bag according to claim 1, characterised by portions (26 or 30) of the body (10)
being located laterally of the juncture (22) and providing means to be gripped for
applying the opening force which is concentrated at the juncture (22).
3. A bag according to claim 1 or claim 2, characterised by ribs (28) extending from
the closure seam (24) and diverging away from the juncture (22) to define unfilled
areas (30) of the body (10) which may be gripped to apply the opening force which
is concentrated at the juncture (22).
4. A bag according to claim 3, characterised in that the ribs (28a, 28b) are aligned
linear extensions of a V-shape closure seam (24).
5. A bag according to claim 1, 2, 3 or 4, characterised in that portions (26) of the
flexible material lie laterally of the juncture (22) on the side of the closure seam
(24) opposite the weakenings (20) and are formed to concentrate the opening force
at the juncture when the lateral portions (26) are pulled apart.
6. A bag according to any of claims 1 to 3 or 5 characterised in that the closure
seam (24) is essentially along a straight line.
7. A bag according to any of claims 1 to 5, characterised in that the closure seam
(24) is of V-shape converging at the juncture (22) to concentrate the said force thereat.
8. A bag according to any of claims 1 to 7, characterised in that the closure seam
(24) is notched (at 34) to concentrate the opening force at the juncture (22).
9. A bag according to any of claims 1 to 8, characterised in that the body (10) is
formed from sheet and seams forming the weakenings (20) and closure seam (24) are
formed by heat sealing.
10. A bag according to any of claims 1 to 8, characterised in that the body (10) is
formed by blow molding.
11. A bag according to any of claims 1 to 10, made from plastics material which is
capable of remaining flexible at temperatures of -25°C to -80°C.
12. A bag according to any of claims 1 to 11, characterised by having removable material
(40, 42) to one side of the closure seam (24) opposite the weakenings (20) to strengthen
the container and render the closure seam (24) unlikely to be ruptured prematurely.
13. A bag according to any of claims 1 to 1,1, characterised by the closure seam (24)
being of V-shape configuration the point of which V intersects the juncture (22),
the said closure seam defining a V-shape removable portion (40) of body material on
the side of the closure seam which is opposite the weakenings (20) whereby the closure
seam (24) may be ruptured at the juncture (22) and the body (10) torn open along the
weakenings (20) to separate it from its contents after the V-shape body material is
removed.
14. A bag according to claim 13, characterised by lines of weakness (46) separating
the removable portion (40) from the remainder of the body (10).
1. Beutel zur Speicherung von Blutkomponenten aus flexiblem Material mit einem Aufnahmeteil
(10) mit einer Vorder- und einer Rückseite sowie einer Verschlußnaht (24) am oder
nahe dem Ende des Aufnahmeteils, dadurch gekennzeichnet, daß der Aufnahmeteil (10)
eine leicht zu öffnende aufreißbare Konstruktion aufgrund von einander gegenüberliegenden
Schwächungen (20) aufweist, von denen eine in jeder der Beutelseiten vorgesehen ist
und die zur Verschlußnaht (24) hinlaufen und dort miteinander in Übereinstimmung gebracht
sind, und daß Spannungskonzentrationsmittel (z.B. 34) vorgesehen sind, die eine aufgebrachte
Öffnungskraft an der Verbindungsstelle (22) der Verschlußnaht (24) und der Schwächungen
(20) für ein Aufreißen des Aufnahmeteils an der Verbindungsstelle (22) und ein Auftrennen
entlang den Schwächungen (20) zur Trennung des Beutels von seinem Inhalt konzentrieren.
2. Beutel nach Anspruch 1, gekennzeichnet durch Bereiche (26; 30) des Aufnahmeteils
(10), die seitlich der Verbindungsstelle (22) angeordnet sind und Handhabungsmittel
zum Aufbringen der Öffnungskraft bilden, die an der Verbindungsstelle (22) konzentriert
ist.
3. Beutel nach Anspruch 1 oder 2, gekennzeichnet durch Rippen (28), die von der Verschlußnaht
(24) ausgehen, von der Verbindungsstelle (22) fort divergieren und unbefüllte Bereiche
(30) des Aufnahmeteils (10) begrenzen, die ergriffen werden können, um die Öffnungskraft
aufzubringen, die in der Verbindungsstelle (22) konzentriert ist.
4. Beutel nach Anspruch 3, dadurch gekennzeichnet, daß die Rippen (28a, 28b) fluchtende
lineare Verlängerungen einer V-förmigen Verschlußnaht (24) sind.
5. Beutel nach Anspruch 1, 2, 3 oder 4, dadurch gekennzeichnet, daß seitlich der Verbindungsstelle
(22) auf der Seite der Verschlußnaht (24) gegenüber den Schwächungen (20) Bereiche
(26) des flexiblen Materials liegen und derart geformt sind, daß sich die Öffnungskraft
an der Verbindungsstelle bei einem Auseinanderziehen der seitlichen Bereiche (26)
konzentriert.
6. Beutel nach einem der Ansprüche 1 bis 3 oder 5, dadurch gekennzeichnet, daß die
Verschlußnaht (24) im wesentlichen entlang einer geraden Linie verläuft.
7. Beutel nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, daß die Verschlußnaht
(24) eine V-Form besitzt, die an der Verbindungsstelle (22) zum Konzentrieren der
Öffnungskraft an dieser Stelle zusammenläuft.
8. Beutel nach einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, daß die Verschlußnaht
(24) zum Konzentrieren der Öffnungskraft an der Verbindungsstelle (22) eingekerbt
ist (bei 34).
9. Beutel nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß der Aufnahmeteil
(10) von Folie gebildet ist und die Schwächungen (20) und die Verschlußnaht (24) bildende
Nähte durch Heißsiegeln gebildet sind.
10. Beutel nach einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, daß der Aufnahmeteil
(10) durch Blasformen gebildet ist.
11. Beutel nach einem der Ansprüche 1 bis 10, dadurch gekennzeichnet, daß er aus Kunststoffmaterial
besteht, das bei einer Temperatur von -25°C bis -80°C flexibel bleibt.
12. Beutel nach einem der Ansprüche 1 bis 11, dadurch gekennzeichnet, daß wegnehmbares
Material (40,42) auf einer Seite der Verschlußnaht (24) gegenüber den Schwachungen
(20) vorgesehen ist, um die Festigkeit des Behälters zu erhöhen und es unwahrscheinlich
zu machen, daß die Verschlußnaht (24) vorzeitig aufgerissen wird.
13. Beutel nach einem der Ansprüche 1 bis 11, dadurch gekennzeichnet, daß die Verschlußnaht
(24) eine V-förmige Gestalt aufweist, die Spitze des V die Verbindungsstelle (22)
schneidet und die Verschlußnaht einen V-förmigen wegnehmbaren Bereich (40) des Aufriahmeteilmaterials
auf der Seite der Verschlußnaht begrenzt, die den Schwächungen (20) gegenüberliegt,
wodurch die Verschlußnaht (24) an der Verbindungsstelle (22) aufgerissen und der Aufnahmeteil
(10) entlang den Schwächungen (20) offengetrennt werden kann, um ihn von seinem Inhalt
nach dem Entfernen des V-förmigen Aufnahmeteilmaterials zu trennen.
14. Beutel nach Anspruch 13, gekennzeichnet durch Schwächungslinien (46), die den
wegnehmbaren Bereich (40) vom verbleibenden Bereich des Aufnahmeteils (10) trennen.
1. Sachet de stockage pour un produit sanguin, ledit sachet étant fait en une matière
flexible et comprenant un corps (10) à face frontale et arrière et une ligne de fermeture
(24) à une extrémité du corps ou adjacente à celle-ci, caractérisé en ce que le corps
(10) est d'une construction fragile pouvant être facilement ouverte due par des points
affaiblis (20) opposés, un dans chacune desdites faces, qui s'étendent vers la ligne
de fermeture (24) et sont alignés l'un avec l'autre sur celle-ci, et des moyens de
concentration de contrainte (p.ex. 34) qui concentrent une force d'ouverture appliquée
sur l'intersection (22) de la ligne (24) et des points affaiblis (20) pour provoquer
la rupture du corps à l'intersection (22) et son ouverture par déchirement le long
des points affaiblis (20) pour séparer le sachet de son contenu.
2. Sachet selon la revendication 1, caractérisé par des parties (26 ou 30) du corps
(10) qui se trouvent latéralement de l'intersection (22) et qui fournissent un moyen
destiné à être saisi pour appliquer la force d'ouverture qui est concentrée sur l'intersection
(22).
3. Sachet selon la revendication 1 ou 2, caractérisé par des nervures (28) s'étendant
à partir de la ligne de fermeture (24) et divergeant à partir de l'intersection (22)
pour définir des zones (30) non remplies du corps (10) qui peuvent être saisies pour
appliquer la force d'ouverture qui est concentrée sur l'intersection (22).
4. Sachet selon la revendication 3, caractérisé en ce que les nervures (28a, 28b)
sont des extensions linéaires alignées d'une ligne de fermeture (24) en forme de V.
5. Sachet selon la revendication 1, 2, 3 ou 4, caractérisé en ce que les parties (26)
de la matière flexible se trouvent latéralement de l'intersection (22) sur le côté
de la ligne de fermeture (24) opposé aux points affaiblis (20) et sont formées pour
concentrer la force d'ouverture sur l'intersection, quand les parties latérales (26)
sont tirées à part.
6. Sachet selon l'une quelconque des revendications 1 à 3 ou 5, caractérisé en ce
que la ligne de fermeture (24) se trouve essentiellement le long d'une ligne droite.
7. Sachet selon l'une quelconque des revendications 1 à 5, caractérisé en ce que la
ligne de fermeture (24) a la forme de V convergeant à l'intersection (22) pour concentrer
ladite force sur celle-ci.
8. Sachet selon l'une quelconque des revendications 1 à 7, caractérisé en ce que la
ligne de fermeture (24) est pourvue d'une entaille (à 34) pour concentrer la force
d'ouverture sur l'intersection (22).
9. Sachet selon l'une quelconque des revendications 1 à 8, caractérisé en ce que le
corps (10) est formé d'une feuille et que les lignes formant les points affaiblis
(20) et la ligne de fermeture (24) sont formées par thermosoudage.
10. Sachet selon l'une quelconque des revendications 1 à 8, caractérisé en ce que
le corps (10) est formé par soufflage.
11. Sachet selon l'une quelconque des revendications 1 à 10, réalisé en une matière
plastique qui est capable de rester flexible à des températures de -25°C à -80°C.
12. Sachet selon l'une quelconque des revendications 1 à 11, caractérisé par une matière
amovible (40, 42) sur un côté de la ligne de fermeture (24) opposé aux points affaiblis
(20) pour renforcer le sachet et faire que la ligne de fermeture (24) ne peut se rompre
prématurément.
13. Sachet selon l'une quelconque des revendications 1 à 11, caractérisé en ce que
la ligne de fermeture (24) a la forme d'un V dont la pointe intersecte l'intersection
(22), la ligne de fermeture définissant une partie en forme de V (40) amovible de
la matière du corps sur un côté de la ligne de fermeture qui est opposé aux points
affaiblis (20), de sorte que la ligne de fermeture (24) peut être rompue à l'intersection
(22) et le corps (10) peut être ouvert par déchirement le long des points affaiblis
(20) pour le séparer de son contenu après avoir enlever la matière du corps en forme
de V.
14. Sachet selon la revendication 13, caractérisé par des lignes affaiblies (46) séparant
la partie amovible (40) du restant du corps (10).