EP0447399A1

EP0447399A1 - Procedure and container for the preparation and storage of platelet concentrates

Info

Publication number: EP0447399A1
Application number: EP89907257A
Authority: EP
Inventors: Girolamo Sirchia; Paolo Rebulla
Original assignee: Individual
Current assignee: Individual
Priority date: 1988-06-28
Filing date: 1989-06-26
Publication date: 1991-09-25
Also published as: WO1990000059A1; JPH03505830A; AU3847589A; IT1217938B; IT8821118A0; KR900701290A

Abstract

Le procédé décrit, qui sert à la préparation de routine dans un système fermé et au stockage dans un milieu, constitué d'un colloïde naturel (plasma) et d'une solution cristalloïdale, de concentrés de plaquettes dépourvus de leucocytes, utilise un sac sanguin quadruple formé d'un sac primaire (PB) contenant un anti-coagulant de citrate-phosphate-dextrose (CPD), d'un sac satellite vide (S1), d'un sac satellite (S2) contenant une solution cristalloïdale synthétique, ainsi que d'un sac satellite comportant une solution additive de SAGM (ou similaire) pour les globules rouges du sang (RBC). Ledit procédé consiste à recueillir le sang dans le sac primaire (PB), à centrifuger le sac sanguin à une vitesse élevée, à transférer par extraction par pression le plasma surnageant dans le sac (S1), à recueillir 15 à 20 ml de la couche intermédiaire riche en plaquettes ("buffy-coat" (BC)) dans le sac (S2), à ajouter la solution de SAGM du sac (S3) dans le sac (PB) contenant le concentré de (RBC) à séparer les sacs PB et S1 des sacs S2 et S3, à centrifuger le sac (S2) à une vitesse de rotation modérée et à transférer le concentré de plaquettes (PC) surnageant pauvre en plasma et en leucocytes (PLP), qui s'est formé après la centrifugation, dans le sac vide (S3), à travers un filtre d'ouate (F) introduit dans le tube reliant S2 et S3, de façon à extraire les leucocytes résiduels qui contaminent le concentré de plaquettes (PC).The described method, which is used for routine preparation in a closed system and for storage in a medium, consisting of a natural colloid (plasma) and a crystalloid solution, of platelet concentrates devoid of leukocytes, uses a blood bag quadruple formed by a primary bag (PB) containing a citrate-phosphate-dextrose anti-coagulant (CPD), an empty satellite bag (S1), a satellite bag (S2) containing a synthetic crystalloid solution, as well than a satellite bag with an additive solution of SAGM (or similar) for red blood cells (RBC). Said method consists in collecting the blood in the primary bag (PB), in centrifuging the blood bag at a high speed, in transferring by pressure extraction the supernatant plasma in the bag (S1), in collecting 15 to 20 ml of the layer platelet-rich intermediate ("buffy coat" (BC)) in the bag (S2), to add the SAGM solution from the bag (S3) in the bag (PB) containing the concentrate of (RBC) to separate the PB bags and S1 from bags S2 and S3, centrifuging the bag (S2) at a moderate speed and transferring the plasma and leukocyte-poor supernatant platelet concentrate (PC), which formed after centrifugation , in the empty bag (S3), through a cotton wool filter (F) introduced into the tube connecting S2 and S3, so as to extract the residual leukocytes which contaminate the platelet concentrate (PC).

Description

Procedure and container for the preparation and storage of platelet concentrates.

This invention relates to a procedure for the routine preparation in closed system of platelet concentrates (PC) deprived of leukocytes and stored in a medium consisting of a mixture of natural colloid (plasma) and of crystalloid solution (called 5 thereafter "medium"), and in particular for PC storage.

Standard RBC concentrates and PC, prepared by serial centrifugation from multiple bags and storage in a natural colloid medium (plasma), are contaminated with plasma and leukocytes, which can ^"determine acute and chronic side-effects in transfusion

10 recipients.

The transfusion of platelet concentrates (PC) is necessary for preventing the risk of hemorrhage in patients with low platelet count (thrombocytopenia) .

' ' Routine production of blood components (RBC and PC) with higher 5 purity is hampered by technical difficulties concerning particularly the separation and storage of blood cells. Presently available methods for preparing PC are based on soft spin of whole blood donations, the collection of platelet-rich- plasma, and the concentration of platelets in 50 mL plasma by high 0 speed centrifugation. Such PC can be stored for a maximum of 5 days. A different approach is the collection of buffy-coats (BC) of whole blood donations (the BC is the layer formed at the red blood cell-plasma interface after whole blood high-spedd centrifugation), followed by soft spin of the BC and collection of

25 platelets in the supernatant. The principal untoward effect of PC transfusion is the production of alloantibodies by PC recipients, caused by leukocytes which contaminate the PC. Moreover, allergic reactions to plasma proteins can occur. To prevent these complications and to improve the quality of

30 platelet transfusion the invention described below was developed. The aim of this invention is to remove thiβ difficulty by means of a procedure for blood f ractionation allowing the routine production and storage in closed system of plasma- and leukocyte- poor RBC concentrates (PLP-RBC, ie RBC containing less than 10% of donated plasma and less than 30% of donated leukocytes), and of plasma- and leukocyte-poor platelet concentrates (PLP-PC, ie PC in a medium containing about 15-40% plasma, and free of leukocytes detectable by microscope counting).

In the procedure reported in this invention an additive RBC solution is used (SAGM or similar), in addition to a synthetic crystalloiH solution which is added to the platelets so as to improve their quality and prolong storage to about 10 days.

The above crystalloid solution is preferably made (considering, for example, a volume of 40 mL) of 5.26 g sodium chloride; 2.22 g sodium acetate; 5.02 g sodium gluconate; 0.37 g potassium chloride; 0.14 g magnesium chloride; H2O for IV use qs to 1,000 mL, pH 7.4 ± 0.1. It must be emphasized that this solution is very similar to one of the crystalloid solutions reported in the patents issued under the names of Gail Ann Rock and George Adams (Canada, Plasma-free medium for platelet storage, application, Nov 1, 1982, 414,583; USA, Plasma-free medium for platelet storage, Pat 4,447,415; Europe, Plasma-free medium for platelet storage, Granted May 16, 1984 - 0108588, Oct 31, 1983, 83306631.9; Canada, Improved plasma-free medium for platelet storage, application, July 20, 1984, 459,369); however, in the invention described here the quality of platelets is improved since the crystalloid solution is fortified with an amount of plasma derived from the BC; this amount is between 10 and 40% of the final medium, preferably 20-30%.

The procedure is carried out with a multiple bag, preferably a quadruple bag consisting of a primary bag and 3 satellite bags. After high speed centrifugation, the blood contained in the primary bag is separated into a red blood cell button and supernatant plasma; this latter is transferred into one of the satellite bags, while the SAGM solution is added to the primary bag for red blood cell storage, after removing an amount of the buffy-coat (BC) layer, which is the layer between red blood cells and plasma, a layer enriched of platelets. The buffy-coat is transferred into a second satellite bag containing the crystalloid solution and, after a soft spin, the supernatant platelet concentrate is transferred in the third, empty satellite bag, through a cotton wool filter inserted along the tubing, which is capable of removing residual leukocytes which contaminate the platelet concentrate. A platelet concentrate prepared according to this method ^'can be stored for about 10 days in this bag, which is made of plastic material with gas exchange characteristics similar to those of polyolefin. The above procedure and bag system for the preparation of platelet concentrates from buffy-coats (BC) and their storage in a crystalloid colloid medium can be used also with BC prepared with standard blood bag systems, by mixing 6-8 BC in a transfer bag containing an appropriate amount of the above crystalloid solution. After a soft spin, the supernatant, containing the platelets, is transferred through a cotton wool filter into a new transfer bag where it is stored.

The procedure derived from this invention is now described, just for the sake of example, and with no limitation to its implementation, with the aid of enclosed fig. 2 through 5, which describe the procedure steps, as performed with a quadruple blood bag, for the preparation and storage of PLP-PC and PLP-RBC from a blood donation. The multiple blood bag consists of a primary bag PB and of 3 satellite bags SI, S2, S3, integrally connected to each other with flexible plastic tubes.

The primary bag PB contains CPD (citrate-phosphate-dextrose) anticoagulant, the satellite bag SI is empty, the satellite bag S2, which is cylinder-shaped and has a volume of 40-60 mL, containβ 40 L of crystalloid solution, the satellite bag S3 contains the SAGM red blood cell additive solution, and is made of plastice material with gas permeability characteristics similar to polyolefin. Along the tube connecting bags S2 and S3 a small (2-3 g) cotton wool filter is inserted.

The procedure regarding this invention is carried out as described below.

The blood donation is collected in the primary bag PB through a collection line I, at one end of which the blood collection needle is attached7 and mixed with the CPD anticoagulant (fig. 1). The blood collected in the primary bag PB is centrifuged at high speed, e.g. 3,800 rpm for 4 min in a Sorvall RC-3B centrifuge. After this centrifugation, plasma- and leukocyte-poor red blood cells are concentrated in the lower part of the primary bag PB, the supernatant plasma is contained in the higher part of the bag, and in the layer between plasma and red blood cells the vast majority of platelets are concentrated. This small layer, enriched of platelets, which separated red blood cells from supernatant plasma is defined "buffy-coat" (BC)(fig. 2).

The supernatant plasma (except for about 30 mL) is expressed into and stored in satellite bag S2, which is diconnected from the other bags (fig.2).

A total of 25-50 mL of BC are then collected, which contain about 5 g hemoglobin, 80% of donated platelets, 50% of donated leukocytes and 20-40 L plasma, and expressed into satellite bag S2, which contain the crystalloid medium (fig. 3). Preferably, the crystalloid solution contained in satellite bag S3 has the following composition (reference to a volume of 40 mL): 5.26 g sodium chloride; 2.22 g sodium acetate; 5.02 g sodium gluconate; 0.37 g potassium chloride; 0.14 g magnesium chloride; H₂0 for IV use qs to 1,000 L, pH 7.4 + 0.1. The SAGM solution contained in satellite bag S3 is added to the red blood cell concentrate PLP-RBC in the primary bag PB for its storage. The primary bag, containing the PLP-RBC and the satellite bag SI containing the plasma are disconnected from satellite bags S2 and S3, which are stored, integrally connected to each other, in a platelet tumbler (a rotating machine for platelet resuspension during storage) (fig.4).

The buffy-coat (containing the platelets) contained in satellite bag S2 can be stored at room temperature for a maximum of 48 h. If platelet concentrates are needed the buffy-coat is centrifuged at low speed, ^"so as to concentrate the red blood cells and the leukocytes in the lower part of the bag S2, and to collect the leukocyte-poor platelet concentrate in the higher part of satellite bag S2. The cylinder shape of satellite bag S2 favors a good separation between the 2 layers above after the soft spin. The supernatant PLP-PC is transferred from satellite bag S2 to satellite bag S3 (which had been previously emptied of the SAGM solution), through filter F, which removes residual leukocytes present in the platelet concentrate (fig. 5). Filter F can be much smaller than traditional cotton wool filters for leukocyte removal (2-3 g instead of 17 g) because leukocyte contamination of platelet concentrates prepared from buffy-coats is much lower than that of platelet concentrates prepared with traditional methods, in which centrifugation is carried out on platelet-rich-plasma instead of platelet-rich-buffy-coat. Experimental data indicate that the platelet concentrate PLP-PC prepared with the above method can be stored in the crystalloid/colloid medium for at least 10 days in a bag made of polyolefin, or of a plastic material capable of providing a gas permeability similar to that of polyolefin, with a final pH of about 7,0, hypotonic shock response of 50% and morphology score according to Kunicki of 220. Moreover, PC prepared with this method and invention have the following parameters after 7 days of storage: glucose consumption 1.5 mmol/L/10 platelets (compared to 2.8 of PC prepared in the medium of G. Rock), and iactate production of 3.56 mmol/L/10⁹ platelets (compared to 6.09 of PC prepared in the medium of Rock). Both parameters suggest better platelet quality in our medium. In addition, platelet aggregation is better in our medium compared to that in the medium of Rock. These excellent results are mainly due to the crystalloid/colloid medium, of which a preferential composition has been given above, in which a crystalloid solution is mixed with a small amount of plasma (natural colloid) present in the buffy-coat, from which the platelet concentrate is prepared.

The above procedure for the preparation of platelet concentrates from buffy-coats (BC) and their storage in crystalloid/colloid medium can be also used with buffy-coats prepared from traditional blood collection bags, e.g. by using a triple bag made of a primary bag and 2 satellite bags, in which the red blood cell concentrate, the plasma and the buffy-coat are collected, respectively. In this case 6-8 buffy-coats prepared with the methods above or similar are collected in a transfer bag of about 600 mL volume, containing about 350 mL of the previously described crystalloid solution. After soft spin, the platelet-rich supernatant is transferred through a small (2-3 g) cotton wool filter F into a transfer bag of about 1000 mL volume, with the same characteristics of previously described bag S3, where it is then stored.

The procedure described in this invention offers the following advantages, in addition to those already reported, in comparison to traditional procedures:

- leukocyte contamination of platelet concentrates is below detectable limits in all platelet concentrates, which implies a series of outstanding advantages for the patients;

- platelet metabolism can be conditioned by modifying the storage medium with the addition of possible additives;

- there is no need to follow ABO compatibility between donor plasma and recipient red cells, due to the small amount of plasma present in the platelet concentrates;

- more plasma can be recovered from standard blood donations;

- it is possible to prepare platelet concentrates only upon request, so reducing the workload; - the procedure favors the routine production of buffy-coat deprived red^*~blood cell concentrates (which are of better quality than standard red blood cell concentrates), since it is based on the avalability of buffy-coats. Moreover, the crystalloid solution does not contain glucose, thus reducing the potential risk of bacterial contamination of PLP-PC. The above advantages are supported by a series of in-vitro and in- vivo evaluations of platelet concentrates prepared from buffy- coats and stored in medium. A set of these evaluations is reported below. We compared platelet concentrates prepared from pools of buffy- coats removed from standard blood donations and stored in the crystalloid solution described above (BCS-PC), with standard platelet concentrates, prepared from platelet-rich-plasma (PRP- PC). Total cell counts (median and range, n=43) in BCS-PC units were: platelets 3.6 x 10¹¹ (2.2-5.5), leukocytes 21 x 10⁶ (4-79); values of PRP-PC units (n=23) were: platelets 0.64 x 10¹¹ (0.47- 0.83); leukocytes 148 x 10⁶ (3-611). Since one BCS-PC unit was prepared from 7 blood donations, a meaningful comparison of PRP-PC and BCS-PC data can be made by multiplying PRP-PC data by 7. Both platelet and leukocyte counts of BCS-PC were significantly lower than those of 7 PRP-PC. Platelet yield in BCS-PC and PRP-PC was 59 and 75 percent of donated platelets, respectively. Median number of total leukocytes in 1 BCS-PC unit, prepared from a pool of 7 buffy-coats, was 50 times lower than that of 7 PRP-PC. In vitro parameters of adequate platelet quality were maintained for 10 days in BCS-PC stored in 1000 mL polyolefin bags. Prolonged 5 bleeding times were reduced or corrected in 3 of 3 thrombocytopenic leukemic patients evaluated before and after transfusion of stored BCS-PC. Pretrans usion, 1-h and 24-h posttransfusion median platelet counts of 57 leukemic recipients during 4 months of routine transfusion of BCS-PC (n=93) were 14, 10 35, and 27 x 10⁹/L, compared with 13, 37 and 31 x_„10⁹/L of PRP-PC (n=246), respectively (p=ns). No reactions to BCS-PC were reported, compared with a reaction rate of 1.3 percent for PRP-PC transfusions. The median (and range) titer of ABO agglutinins in BCS-PC and PRP-PC was 8 (2-8) and 64 (32-128), respectively. A 15 detailed description of the results is reported in tables 1-3. In vitro evaluation of BCS-PC and PRP-PC during storage is reported in table 1.

It can be seen (section A) that in vitro parameters of adequate platelet quality (pH above 6.0, morphology score above 200) were 20 maintained in BCS-PC for at least 10 days of storage in 1000 mL polyolefin bags; at this time the platelet response to hypotonic shock (HSR), a parameter related to platelet recovery and survival in normal volunteers, was still above 80 percent of values at day 1. This was not so for BCS-PC stored in 1000 mL PVC bags (section 25 B) , in which the median pH value was below 6.0 at day 3. This was associated with a complete loss of HSR and a marked deterioration of platelet morphology. Similarly to other reports, PRP-PC stored in PVC satellite bags of 400 mL volume showed adequate quality preservation for at least 5 days (section C). On day 1, PO2 values 30 of BCS-PC in 1000 mL bags were about 2 times higher than those of PRP-PC in 400 mL bags, as expected on the basis of both a larger bag and a smaller platelet concentration in the former. Platelet quality during storage in PVC deteriorated more rapidly in BCS-PC than in PRP-PC. A contributory cause could have been the smaller ratio between bag surface area and PC volume in the former, determining a less efficient gas transport during storage. Oxygen consumption for aerobic metabolism, which is more favorable than anaerobic for PC preservation during storage, was maintained longest in BCS-PC stored in polyolefin, as indicated by the slowest PO₉ rise. Results of in-vivo study are reported in Table 2 and 3. Pilot phase. Pretransfusion, 1-h and 24-h posttransfusion platelet counts and percent recovery values obtained in "stable" leukemic recipients are reported in table 2. It can be seen that values of BCS-PC stored for 1-8 days were similar to those of PRP-PC stored for 1-3 days. Bleeding time (reference values 2-7 min) was reduced after BCS-PC transfusion in 3 of 3 patients evaluated, dropping from more than 30 to 9 min (6-day old BCS-PC containing 3,0 x lϋ¹¹ platelets), from 25 to 5 min (4-day old BCS-PC containing 2.8 x 10¹¹ platelets), and from 22 to 6 min (8 day old BCS-PC containing 3.1 x 10 platelets). On these 3 occasions pre- and 1-h posttransfusion platelet counts were 17-43, 16-56 and 16-39 x q 10 /L, respectively.

Routine phase. A total of 448 and 129 platelet transfusions were issued as 1-3 day-old PRP-PC and 1 day-old BCS-PC, respectively, to 57 leukemic patients. This group included all hematological patients transfused with platelet concentrates in the study period. Pretransfusion, 1-h and 24-h posttransfusion platelet count and percent recovery, available on 55 percent (PRP-PC) and 72 percent (BCS-PC) of occasions, are reported in table 3. Increments of BCS-PC were not significantly different from those of PRP-PC. No reactions were reported for BCS-PC, compared with 6 for PRP-PC; of these, 2 were febrile and 4 allergic.

A) BCS-PC units stored in 1000 mL polyolefin bags (n=8)

1 6.9 87 23 62

(6.7-6.9)(70-109)(20-31) (39-68) 3 6.9 73 26 64

(6.4-6.9)(61-115)(19-36) (46-67) 5 6.8~ 93 28 62

(6.4-6.9)(40-123)(19-39) (42-70) 10 6.7 101 25 51

(6.3-7.0* 76-145)(20-36) (33-69) 15 6.9 122 17 31

(5.8-7.2)(65-175)( 9-27) ( 0-60)

B) BCS-PC units stored in 1000 mL PVC bags (n=8)

1 68 90 27 100

(6.7-6.9)(82-124)(18-31) 3 5.9 148 37 92 (5.8-6.5)(71-161)(24-69) (88- 97)

C) PRP-PC units stored in 400 mL PVC bags (n=«10) 1 7.0 40 56 55 260 100 (6.7-7.1)(28-149)(19-90) (30-69) (210-331) 3 7.0 47 46 51 226 100 (6.2-7.2) (16-81)(34-77) (36-56) (122-331) (100-100) 5 7.0 58 42 47 208 100 (5.6-7.1)(13-154)(16-48) (0-60) (92-263) (81-100) 10 6.6 86 35 21 167 94 (5.5-7.0)(50-199)(13-42) (0-40) (71-195) (88- 97) 15 6.1 181 14 0 107 72 (5.7-6.8)(123-201)(6-28) (0-9) (73-154) (60- 94)

Table 2. In vivo study: pilot phase. Median (and range) platelet counts and percent recovery in 11 "stable" leukemic patients receiving both BCS-PC and PRP-PC.

Platelet count Platelet in vivo Type Storage (x 10 /L) recovery of Pre- Posttransfusion (% of expected)

PC Days Bag 1-h 24-h 1-h 24-h

BCS-PC 1 1000 mL 13 42 34 59 44 n=8 PVC (9-20) (23-56) (28-46) (19-81) (28-62)

BCS-PC 4- 8 1000 mL 17 43 33 50 36 n=8 ^"~ polyolefin (9-21) (16-56) (12-40) (0-102) ( 0-54)

BCS-PC 9-12 1000 mL 10 43 21 73 11 n=5 -polyolefin (5-21) (13-91) (12-28) (17-161)( 7-40)

PRP-PC 1- 3 400 mL 16 50 37 49 30 n=15 PVC (4-29) (10-92) (14-79) (0-102) ( 0-92)

Table 3. In vivo study: routine phase. Median (and range) platelet counts and percent recovery in 57 hematologic patients receiving platelet transfusion during 4 months of routine use of both BCS-PC and PRP-PC.

It is emphasized that the invention is not limited to the particular description reported above and in the enclosed figures, but it can me modified in several minor parts within the scope of the invention.

Claims

1. A method for the preparation and storage of plasma- and leukocyte-poor platelet concentrates from buffy-coats, which comprises the transfer of at least 1 buffy-coat into a bag (S2) containing a synthetic crystalloid solution (which is diluted with the plasma contained in the buffy-coat so as to constitute a colloid/crystalloid medium for platelet storage), the soft spin of the bag (S2) and the transfer of the supernatant PLP-PC formed after centrifugation into a (S3) bag made of polyolefin or of plastic material with gas permeability similar to polyolefin, through a cotton wool filter (F) of 2-3 g, so as to remove residual leukocytes contained in the platelet concentrate.

2. A method as claimed in claim 1, wherein the above bag S2 has an elongated, cylinder shape.

3. A process according to claim 1, wherein 1000 ml. of said synthetic crystalloid solution contain 5.26 gr sodium chloride, 2.22 gr sodium acetate, 5.02 gr sodium gluconate, 0.37 gr potassium chloride, 0.14 gr magnesium chloride, H₂0 for I.V. use qs to 1000 ml and wherein said crystalloid solution has a pH of 7.4 ± 0.1.

4. A process according to claim 1, wherein 6-8 BC obtained from as many donations are transferred into the bag (S2).

5. A process according to claim 1, wherein the PLP-PC are stored in a synthetic crystalloid / natural colloid solution, comprising the crystalloid medium of bag (S2) and the plasma of each BC (about 20-40 ml of plasma in a BC volume of 25-50 ml).

6. A process according to claim 1, wherein the BC are separated in a multiple bag for the preparation and storage of PLP-PC and PLP- RBC (plasma- and leukocyte- poor RBC concentrates), e.g. in a quadruple blood bag comprising a primary bag (PB) and three satellite bags (SI), (S2), (S3).

7. A process according to claim 6, comprising: collecting the blood in a primary bag (PB) containing CPD anticoagulant, centrifuging at high speed said primary (PB) bag, tranferring the supernatant plasma into the bag (S2) containing tha crystalloid solution, and tranferring the SAGM solution of bag S3 into the (PB) bag containing PLP-RBC.