Theoretical optimization of the removal of cryoprotective agents using a dilution-filtration system
© Qiao et al.; licensee BioMed Central Ltd. 2014
Received: 28 May 2014
Accepted: 29 July 2014
Published: 21 August 2014
In the cryopreservation of blood, removing cryoprotectants from the cryopreserved blood safely and effectively is always being focused on. In our previous work, a dilution-filtration system was proposed to achieve the efficient clearance of cryoprotectants from the cryopreserved blood.
In this study, a theoretical method is presented to optimize the diluent flow rate in the system to further reduce the osmotic damage to red blood cells (RBCs) and shorten the washing time necessary to remove cryoprotective agents (CPAs), based on a discrete mass transfer concept. In the method, the diluent flow rate is automatically adjusted by a program code in each cycle to maximize the clearance of CPAs, whereas the volume of RBCs is always maintained below the upper volume tolerance limit.
The results show that the optimized diluent flow rate can significantly decrease the washing time of CPAs. The washing time under the optimized diluent flow rate can be reduced by over 50%, compared to the one under the fixed diluent flow rate. In addition, the advantage of our method becomes more significant when the blood flow rate is lower, the dilution region volume is larger, the initial CPA concentration is higher, or the cell-swelling limit set by the system is smaller.
The proposed method for the dilution-filtration system is an ideal solution for not only guaranteeing the volume safety of RBCs but also shortening the washing time of CPAs. In practice, the optimization strategies provided here will be useful in the rapid preparation of cryopreserved blood for clinical use.
KeywordsMass transfer Cryoprotective agent Osmotic damage Red blood cell
Cryoprotective agents (CPAs) are widely used in the cryopreservation of blood to protect red blood cells (RBCs) from cryoinjury [1–3]. However, due to their negative effects to the human body (e.g. DMSO is considered to be toxic, glycerol is responsible for the osmotic lysis of cells when the glycerolized RBCs are directly transfused), CPAs must be removed before clinical transfusion to patients [4–7]. As one of the key steps before the clinical use of cryopreserved blood, the process of removing CPAs might result in osmotic damage to RBCs and thus a functional decrease of RBCs. Consequently, this area has been a focus of research [8–10].
In practice, there are two major criteria to weigh a method for removing CPAs: one is the osmotic damage to RBCs (or the recovery rate of RBCs) and the other is the washing time or the removal efficiency of the CPAs. A high recovery rate of RBCs can improve the treatment, and a short washing time can significantly reduce the waiting time of patients, especially during emergency treatment. To remove CPAs from cryopreserved blood safely and effectively, various methods have been proposed over the past decades. During early stages, a single-step centrifugation method was applied where cryopreserved blood was diluted in an isotonic saline solution and then centrifuged to remove the supernatant containing CPAs. This method is simple and efficient for removing CPAs but causes serious osmotic damage to RBCs. Alternatively, a multi-step centrifugation method was designed to reduce the osmotic damage to RBCs [8, 10–13]. In the literature, many efforts focus on its improvement and optimization, from the Fixed Volume Steps (FVS)  to the Fixed Molarity Steps (FMS)  until the Fixed level of Shrinkage/Swelling steps (FSS) [16–18]. Recently, Lusianti et al. even reduced the deglycerolization time to several minutes . In the multi-step centrifugation method, although many achievements are reached, the complex operation to some extent is still inconvenient in practice, especially for emergency use. To avoid potential cell clumping and loss caused by the centrifugation, a dialysis-based method that was originally used in blood purification was proposed to remove CPAs [19, 20]. In the method, the blood containing CPAs flows inside hollow fibers whereas the isotonic solution flows outside countercurrently. As the CPAs inside hollow fibers but outside RBCs are gradually transferred out of hollow fibers along the blood flow direction, the dialysis-based method provides a friendly environment with the stepwise decreasing CPA concentration for RBCs. This method is relatively simple to operate and can reduce osmotic damage to RBCs by easily controlling the flow conditions; however, the efficiency of the procedure is restricted by the mass transfer rate of the CPAs across the fiber membrane.
Therefore, in this work, a method is proposed to optimize the dilution-filtration system to further reduce the osmotic damage to RBCs and shorten the washing time necessary to remove CPAs. The optimization strategy presented here remarkably improves the dilution-filtration system and makes it more appropriate for clinical use.
Mass transfer equation revisited
In the dilution-filtration system, the volume variation of RBCs and the concentration change of CPAs are influenced by many factors, e.g., the volume of blood, the hematocrit in the blood, the flow rate of the blood, the flow rate of the dilution solution, the performance of the hemofilter, and the parameter of the tubing (Figure 1). To simplify the issue, based on our preliminary results [22, 23], we focused on the flow rate and tubing volume. We assumed that the volume of the blood to be washed is small (i.e., no blood is left in the blood bag during operation), and thus, the blood bag serves as a reservoir only at the beginning and then is considered as a tube starting from the second cycle. Under this assumption, the mixing complexity of the RBCs in a blood bag can be neglected and the behaviors of all cells can be assumed the same. In the system, cells go through three major steps: dilution (black line), filtration (hemofilter) and recirculation (red line and blood bag), the blood flow rate (Q b ) and the diluent flow rate (Q d ) can be controlled by system software, and the tubing volume can be designed before operation.
where superscripts I and II denote blood units before and after the dilution point, respectively, and d denotes the NaCl concentration in the diluent.
Parameters used in this paper
1.74 × 10-12
6.61 × 10-8
RBC surface area
RBC volume at isotonic conditions
Osmotically inactive cell volume
In the optimization, our objective is to find a series of optimal diluent flow rates for the entire washing process when the blood flow rate and the dilution region volume are fixed. In this work, the diluent flow rate was automatically controlled by a program code that we wrote (the filtrate flow rate was synchronously controlled and was always equal to the diluent flow rate). Its value is different during different cycles but always satisfies the following two conditions: the first is that it allows cells to expand to the upper volume tolerance limit if applicable; and the second is that its value is smaller than the threshold value that the pump can reach. Under these two restrictions, an optimized diluent flow rate can be obtained for each cycle under a given blood flow rate. In the process of searching for an optimized diluent flow rate for each cycle, at the beginning, the diluent flow rate was always set to the maximal value that the system could reach, and the volume change of the RBCs was then simulated. If the peak volume was larger than the upper volume tolerance limit, the diluent flow rate was decreased by a certain small amount (0.1 mL/min), and the process was repeated until the peak volume was smaller than but near the upper volume tolerance limit. By doing so, a series of optimized diluent flow rates could be obtained for the entire washing process.
Results and discussion
Variation of cell volumes under fixed diluent flow rates
In practice, the dilution region extension (i.e. the increase in the tubing length and/or diameter of the dilution region) can be used to prolong the residence time of cells. Our results show that as the dilution region volume is increased, starting from the 2nd cycle, the starting volume of the RBCs is decreased; thus, the accumulation effect is alleviated and the maximum volume of the RBCs is decreased (the dot line in Figure 3a). However, it is important to note here that the utility of the dilution region extension is limited to some extent, especially when the dilution region volume is very large. Under this situation, the accumulation effect is no longer obvious, and the maximal volume of the RBCs is similar to the peak volume of the 1st cycle and is nearly constant, as shown in Figure 3b. In addition, due to the increase in the residence time, the washing time necessary to remove CPAs increases almost linearly (Figure 3b). Therefore, the dilution region extension is not good enough to optimize the dilution-filtration system (here, the shear stress damage to the RBCs as a result of changes in the tubing diameter or length  was assumed to be neglectable).
Here, the fixed diluent flow rate is an allowable value, which makes the maximum volume of the RBCs be very close to the upper tolerance limit, and is kept constant in all cycles. In practice, the fixed diluent flow rate varies with blood flow rates and/or cryoprotectant concentrations. If the diluent flow rate is always constant, the maximum volume of the RBCs decreases as the blood flow rate increases . Therefore, the fixed diluent flow rate increases with increasing blood flow rate. In this simulation, the upper tolerance limit for completely avoiding the hypotonic damage was set to 138 μm3, i.e., 1.53 of the isotonic volume of the RBCs according to the literature , and the stop condition was the CPA concentration inside the cells reaching below 5% of the initial value.
Variation of optimized diluent flow rates
Comparison of washing times between fixed and optimized diluent flow rates
The process of removing CPAs using a dilution-filtration system is theoretically optimized. In the optimization method, the diluent flow rate is designed to vary with time. The rate is adjusted automatically by a program code in the system at each cycle to maximize the clearance of CPAs, and the volume change of RBCs is always maintained below the upper volume tolerance limit. The results show that our optimization method can significantly decrease the washing time of CPAs: when the optimized diluent flow rate is used, the washing time can be reduced by over 50%. The advantage of our method becomes more remarkable when the blood flow rate is lower, the initial CPA concentration is higher, the dilution region volume is larger, or the cell-swelling limit set by the system is smaller. In addition, the extension of the dilution region volume is not a good method to optimize the dilution-filtration system as it causes the increase in the washing time of CPAs, although it sometimes can reduce the negative accumulation effect from the volume change of cells.
In this work, we describe an adaptive optimization method for the diluent flow rate in the dilution-filtration system to reduce the washing time of CPAs, based on the discrete concept . In practice, one still can apply the method to the continuum mass transport concept in the literature  to obtain the optimized diluent flow rate. In addition, although the optimized diluent flow rate we obtain here is based on a small volume of blood, it is applicable to a large volume of blood in the literature [22, 23]. If the volume of blood to be washed is large, one only needs to extend the cycle accordingly.
As the study here is limited to a theoretical optimal solution for reducing the osmotic damage to RBCs and enhancing the speed of the removal of CPAs, we next will focus on the experimental validation of the theoretical results. In the experiments, we will monitor the concentration variation of CPAs, count the recovery rate of cells and perform the comparison between theoretical and experimental results. In addition, we will also investigate the effect of the repeated osmotic stress on the cell tolerance, the subcellular structure, and the cell permeability to validate assumptions used in this work.
This work was supported by the Fundamental Research Funds for the Central Universities of China (WK2100000001), the Specialized Research Fund for the Doctoral Program of Higher Education of China (WJ2100230004), and the Natural Science Foundation of Anhui Province (BJ2100230008).
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