A hemoglobin (Hb) wrapped covalently by human serum albumins (HSAs), a core–shell structured hemoglobin-albumin cluster designated as “HemoAct”, is an O2-carrier designed for use as a red blood cell (RBC) substitute. This report describes the blood compatibility, hemodynamic response and pharmacokinetic properties of HemoAct and then explains its preclinical safety. Viscosity and blood cell counting measurements revealed that HemoAct has good compatibility with whole blood. Intravenous administration of HemoAct into anesthetized rats elicited no unfavorable increase in systemic blood pressure by vasoconstriction. The half-life of 125I-labeled HemoAct in circulating blood is markedly longer than that of HSA. Serum biochemical tests conducted 7 days after HemoAct infusion yielded equivalent values to those observed in the control group with HSA. Histopathologic inspections of the vital organs revealed no marked abnormality in their tissues. All results indicate that HemoAct has sufficient preclinical safety as an alternative material for RBC transfusion.
Japan is prone to natural disasters. When a great earthquake occurs, large amounts of blood are required immediately. Nevertheless, the donated blood cannot be stored for long periods. For example, the preservation limit of red blood cells (RBC) has been established as 21 days at 2–6 °C1. Therefore, sufficient blood might not be available in the event of a widespread disaster. Another problem is that Japan’s declining birthrate and aging society make it difficult to maintain a stable blood transfusion system. Currently, 85% of blood products in Japan are used for patients aged fifty years old or older2. The number of elderly people will continue to increase, although the population of younger blood donors is expected to decrease. The Japanese Red Cross Society predicts a blood shortage equivalent to 890,000 people per year in 20273. Consequently, a blood substitute, in particular an RBC substitute, is needed (i) which can be stored for long period, (ii) which presents no risk of virus infection and (iii) which is useful for anyone irrespective of blood type. Such an artificial O2-carrier is required as a primary measure for crisis management and is required as a medical measure to supplement blood transfusion treatment.
Since the 1980 s, hemoglobin (Hb)-based O2-carriers (HBOCs) of several kinds have been manufactured and evaluated4,5,6, such as crosslinked Hb7,8, polymerized Hb9,10,11 and poly(ethyleneglycol)-conjugated Hb (PEG-Hb)12,13,14. Clinical studies of some products reached Phase-III, but side-effects (pressor response) and low efficacy have prevented their practical application5,10,15,16. The increase in systemic blood pressure observed after the infusion is probably caused in part by vasoconstriction induced by Hb diffusion into the extravascular space and scavenging endothelial-derived relaxing factor, nitric oxide (NO)17,18.
Recently, we synthesized a covalent core–shell structured protein cluster comprising Hb in the center and human serum albumin (HSA) at the periphery as a unique HBOC (Fig. 1)19,20,21. The average HSA/Hb ratio of one cluster was 3.0 ± 0.2 (Hb-HSA3). The O2-binding property was well defined. We designated this hemoglobin–albumin cluster as “HemoAct”. Actually, HSA is the most prominent plasma protein in the bloodstream (approximately 4–5 g/dL), playing the role of maintaining colloid osmotic pressure, as well as transporting various metabolites and drugs22,23. Because HSA contains only one sulfhydryl group of Cys at position 34, we exploited a heterobifunctional crosslinker, N-succinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate (SMCC), as a connector between the Cys-34 residue of HSA and the surface Lys amino groups of Hb19,20. The formulated HemoAct has satisfactorily negative surface net charge (pI: 5.1). Therefore it might not be leaked from the vasculature walls because of the electrostatic repulsion against the glomerular basement membrane around the endothelial cells. Probably, intravenous transfusion of HemoAct would not elicit the acute increase of the blood pressure and would support a long period of blood circulation. To evaluate the preclinical safety of the HemoAct solution as an RBC substitute, we examined the blood compatibility, hemodynamic response and pharmacokinetic property of this new O2-carrier.
Results and Discussion
Many clinical disorders alter blood viscosity, thereby causing RBC aggregation24. In fact, plasma proteins are important blood components affecting blood viscosity. The viscosity of the HemoAct solution (20 g/dL, [Hb] = 5.0 g/dL) is dependent on the shear rate, indicating that this O2-carrier is a Newtonian fluid, just as HSA is (5 g/dL) (Fig. 2). The viscosity at 230 s-1, the shear rate in the human arterial wall, was ascertained as 2.8 cP, which is lower than that of blood (3.8 cP). The HemoAct solution was mixed with freshly drawn whole blood of rats (1/1, v/v). A homogeneous blood/HemoAct suspension exhibited non-Newtonian viscosity, which obeyed a nonlinear correlation to the shear rate. The viscosity was reasonably high: 3.3 cP at 230 s-1. No precipitation was observed for 6 h at 37 °C. These results indicate that HemoAct has good compatibility with whole blood.
The rapid increase and decrease of the blood cell number causes blood disorder. We measured the number of blood cell components [RBC, white blood cell (WBC) and platelet (PLT)] of the blood/HemoAct mixture suspensions (9/1, 8/2 and 6/4, v/v) in vitro. The numbers of RBC, WBC and PLT decreased in proportion to their respective dilution ratios: approximately 90, 80 and 60% of the baseline value (BV) (Fig. 3). The percentage of (cell number with HemoAct)/(cell number without HemoAct (BV at each time-point)) remained constant for 6 h at 37 °C. The results were identical to those observed in control experiments with HSA (not shown).
The influence of HemoAct on blood coagulation was also evaluated using measurements of the prothrombin time (PT) and activated partial thromboplastic time (APTT). The PT tests assess the extrinsic and common pathways of the coagulation cascade. The APTT tests evaluate the intrinsic and common pathways. Using both tests, the integrated function of all the blood coagulation factors can be examined25. Mixing of HemoAct with the whole blood (1/1, v/v) did not change the PT and APTT (Fig. S1). The values are almost identical to those of the control group with HSA. To standardize the results, the international normalized ratio (INR), which is (PT with sample)/(PT without sample) raised to the power of the International Sensitivity Index (ISI), was exploited26. The INR value higher than 1.5 suggests the occurrence of hemorrhage or disease. In our experiments, all INR values were 0.98–1.13. Based on these findings, we conclude that HemoAct shows no unfavorable interaction to the blood cell components and that it does not obstruct the blood coagulation function.
To avoid the depletion of NO by the extravasation of Hbs, surface-modified Hbs with PEG (PEG-Hbs) have been designed and synthesized12,13,14. By virtue of their greater molecular size, their extravasation is reasonably attenuated12. Nonetheless, the high viscosity of PEG-Hb can substantially influence the plasma volume and shear stress on the capillary wall, which can affect blood pressure. We injected the HemoAct solution (20 g/dL) into anesthetized rats (6 ml/kg) and monitored their mean arterial pressure (MAP) for 60 min. As expected, only a transient alternation in MAP was observed after administration of HemoAct (Fig. 4). The 25.3 ± 2.9 mmHg elevation of ∆MAP from the basal value was followed by a decrease to 10 mmHg within 15 min. It remained constant during the monitoring period. The response is precisely the same result as that observed after infusion of HSA (20 g/dL). In contrast, the administration of ββ-crosslinked Hb (XLHb, 5 g/dL) is associated with (i) an immediate and remarkable increase in ∆MAP (55.5 ± 5.9 mmHg) and (ii) urinary excretion of Hb beginning 10 min after the injection.
This non-vasopressor effect of HemoAct, which is remarkable compared to that of XLHb, appears to be attributable to the negative surface net charge and increased molecular mass of the cluster. HSA shows low vascular permeability of less than 1/100 that for Hb ascribed to the electrostatic repulsion between the albumin surface and the glomerular basement membrane around the endothelial cells27. The isoelectric point of HemoAct (pI = 5.1) is comparable to that of HSA. Moreover, the molecular mass (26.4 kDa) of HemoAct is four times larger than that of HSA (66.5 kDa)19. Consequently, the leakage of negatively charged and huge HemoAct into the extravascular space must be suppressed. In contrast, the small XLHb having neutral surface net charge passes through the vascular endothelium and contributes considerably to the consumption of NO, thereby increasing the blood pressure. They also pass through the renal glomerulus soon after the infusion, thereby inducing excretion of the observable quantities of Hb in urine.
Other mechanisms for the rise in MAP by the Hb products are presumed to be (i) the autoregulatory response to high arteriole O2-level28,29,30 and (ii) the decrease in NO production by diminished shear stress on the vasculature wall31. Regarding the first hypothesis, Winslow et al. reported that HBOCs with a low O2-affinity engender excessive O2 release in the arterioles and produce autoregulatory vasoconstriction29. The O2-affinity of HemoAct is high enough (P50: 9 Torr) that excessive O2 offloading in the arterioles is unlikely. In the second hypothesis, the prompt flow by the administration of HemoAct with a low viscosity (compared to blood) might decrease the shear stress on the vasculature wall. However, the total blood volume increased less than 11% in these top-load experiments. Therefore the change of viscosity was regarded as negligible.
The 125I-labeled HemoAct was injected into rats to assess blood retention and tissue distribution. The 125I-labeled Hb, as a control material, was cleared rapidly from circulation (Fig. 5). The half-life (T1/2) was only 0.53 h, which was comparable to the value reported previously by Pang et al.32 The time course of the plasma concentration of HemoAct showed very slow kinetics in two phases. The pharmacokinetic parameters were determined using a non-compartment model (Table 1). The T1/2 of HemoAct was markedly long (18.5 h) and 1.7-fold greater than that of HSA (T1/2 = 11.0 h). As described earlier, the negative surface net charge and large molecular size of HemoAct prevent not only extravasation through the vascular endothelium, but also filtration by the renal glomerulus. Accompanied by the decrease of CL and Vdss values, the AUC and T1/2 of HemoAct were increased relative to those of HSA. We are convinced that the superior blood retention property of HemoAct is attributable to suppression of movement to the extravascular space and renal filtration.
Figure 6 depicts the tissue (vital organs) distribution of HemoAct at 24 h after administration. HemoAct and HSA were similarly distributed in the major organs. Careful assessments revealed that the extent of HemoAct accumulation in the liver was greater than that of HSA. Rennen et al. reported that the large proteins are cleared with predominant uptake by the liver33. We inferred that higher hepatic distribution of HemoAct is attributable to the large molecular volume of the cluster. This result is consistent with our previously reported pharmacokinetic study of the HSA dimer34,35.
Serum biochemical tests and histopathologic observations
The serum biochemical test is an inspection to measure the abnormality of a physical condition and organ. All animals given the HemoAct solution (20 g/dL, 6 mL/kg) were alive for 7 days after the infusion. During the measurement period, no remarkable change was found in their appearance or behavior. Although anesthesia and surgical operation temporarily decreased the body weight of rats after 1 day (279 ± 14 g→265 ± 13 g), the body weight increased gradually thereafter and reached 318 ± 14 g after a week (Fig. S2). The growth processes were almost identical to those observed in the control groups with HSA and without infusion (sham-operation).
All 26 analytes of the serum biochemical tests after 7 days from the administration exhibited almost identical data to those of the control groups (Table S1). The weights of major organs (liver, kidney, spleen, lungs and heart) recovered from the rats were also nearly equal to the values of the control groups (Fig. S3).
Furthermore, microscopic observations of the stained specimens of these vital organs demonstrated no histopathologic disorder in their tissues (Fig. S4). The HemoAct molecule disappeared within a week. Some abnormality might be detected in the liver if the excess hemes of HemoAct were not decomposed by hemeoxygenase. Nevertheless, we were unable to find even a small difference between the HemoAct and HSA groups. This similarity is supported by the values of liver function markers (AST, ALT and γ-GTP) revealed by serum biochemical tests. Although more research must be done to elucidate the metabolism, the present results imply that the administration of HemoAct induces no negative side effects or middle-term toxic reactions in vital organs.
The blood/HemoAct mixture suspension (1/1, v/v) was a non-Newtonian fluid similar to whole blood, exhibiting viscosity of 3.3 cP (at a shear rate of 230 s−1). The addition of 40 vol% HemoAct into the blood did not affect the quantities of RBC, WBC and PLT for 6 h at 37 °C. The coagulation function of the blood was also maintained. The HemoAct solution shows good compatibility with blood in vitro. The administration of HemoAct to anesthetized rats caused a slight change in MAP, which is identical to that observed in the control group with HSA. This hemodynamic response contrasts against the fact that drastic hypertension and urinary excretion of Hb occurred after infusion of XLHb. The T1/2 of HemoAct was 1.7-fold longer than that of HSA. The non-vasopressor response and superior blood retention property of HemoAct are attributed to the negative surface net charge and larger molecular size of the cluster. The serum biochemical parameters closely resembled those of the control groups with HSA and without infusion. Histopathologic inspections proved that HemoAct produced no negative side effects in any major organ. These results underscore the preclinical safety of HemoAct and enable us to undertake further advanced in vivo study of this O2-carrying protein cluster as a blood replacement.
The phosphate-buffered saline solution of HemoAct (20 g/dL, pH 7.4, HSA/Hb = 3.0 ± 0.2 (mol/mol)) was prepared according to our previously reported procedures using purified bovine Hb and human serum albumin (HSA, Japan Blood Products Organization)19,20. The procedures used for synthesis of ββ-crosslinked Hb (XLHb) were described in Supplementary Information. The O2 affinity (P50: O2-partial pressure where Hb is half-saturated with O2) and Hill coefficient (n) were 9.0 Torr and 1.5, respectively, as determined using an automatic recording system for blood O2-equilibrium curves (Hemox-Analyzer; TCS Scientific Corp.) using PBS (pH 7.4) at 37 °C.
Animal studies were reviewed and approved by the Animal Care and Use Committee of Keio University, Sojo University, or Kumamoto University. The care and handling of the animals were done in accordance with NIH guidelines.
Correlation between the shear rate and viscosity of the HemoAct solution (20 g/dL) was measured using a rheometer system (Physica MCR101; Anton Paar Japan K.K.) at 37 °C. Fresh whole blood was obtained from Wistar rats (ca. 275 g, male; Charles River Laboratories Japan, Inc.) and was stored in EDTA-2 K coated blood collection tubes. The HemoAct solution was added to the whole blood (1/1, v/v). Then the viscosity of the blood/HemoAct mixture suspension (0.4 mL) was measured (measuring points, 36; shear rate, 0–700 s−1; measuring interval, 25 s). As control groups, the HSA (5 g/dL) solution, blood and blood/HSA (1/1, v/v) suspensions were measured under the same conditions.
Blood cell numbers
Fresh whole blood was obtained from Wistar rats (ca. 275 g, male) and stored in EDTA-2 K coated blood collection tubes. The HemoAct solution was added to the whole blood at 0, 10, 20 and 40 vol% concentrations (total volume 1.5 mL each). Each individual sample was incubated at 37 °C in an incubator. At the time-points of 0, 1, 2, 3, 4, 5 and 6 h after the mixing, 0.1 mL of the sample was drawn from each group ([HemoAct] = 0, 10, 20 and 40 vol%) and the quantities of blood cell components (RBC, WBC and PLT) were assessed using an automated hematology analyzer for animals (pocH-100iV Diff; Sysmex Corp.) (n = 3). As control groups, the blood suspensions with HSA (5 g/dL) ([HSA] = 0, 10, 20 and 40 vol%) were also measured (n = 3). The results are shown as a percentage of (cell number with sample)/(cell number without sample (basal value at each time-point)).
Prothrombin time (PT) and activated partial thromboplastin time (APTT)
Fresh whole blood was obtained from Wistar rats (ca. 275 g, male) and was stored in sodium citrate coated blood collection tubes. The HemoAct solution was added to the whole blood at 0, 10, 20 and 40 vol% concentration (total volume 1.2 mL each) in different blood collection tubes (B-11; BML Inc.). These samples were centrifuged (2,800 rpm, 15 min). Then the supernatant (0.6 mL) was transferred to blood collection tube (S-1; BML Inc.) and was frozen at −80 °C. As control groups, blood suspensions with HSA (5 g/dL) ([HSA] = 0, 10, 20 and 40 vol%) were also prepared. The PT and APTT measurements were performed by BML Inc. (Tokyo) (n = 4 each).
Blood pressure response
Wistar rats (264 ± 3 g, male) were placed on a heating pad under an inhalation anesthesia with 1.0% sevoflurane. After an incision was made in the neck, a heparinized catheter (SP31 tubing, OD 0.8 mm, ID 0.2 mm) was introduced into the right common carotid artery and was connected to a blood pressure measurement system (KN-213/KN-212; Natsume Seisakusho Co., Ltd., Tokyo) for continuous recording of the mean arterial pressure (MAP). Another catheter (SP-31) was inserted into the right jugular vein for sample injection.
After stabilization of the animal condition under 0.5% sevoflurane, the HemoAct solution (20 g/dL) was administered intravenously via the jugular vein (6 mL/kg, 1 mL/min, n = 4). During the injection, no remarkable acute reaction was observed in the appearance of the animal. The MAP was monitored at the time-points of 5 min, 1 min before the infusion and 2 min and 5–60 min (5 min intervals) after the infusion. As control groups, the ββ-crosslinked Hb (XLHb) solution (5 g/dL) and HSA (20 g/dL) were also applied to similarly treated rats [XLHb group (264 ± 13 g, 6 mL/kg, 1 mL/min, n = 4) and HSA group (258 ± 6 g, 6 mL/kg, 1 mL/min, n = 4)].
Serum biochemical tests and histopathologic observations
Wistar rats (279 ± 14 g, male) were anesthetized with an intraperitoneal injection of sodium pentobarbital. The HemoAct solution (20 g/dL) was injected intravenously via a tail vein (6 mL/kg, 1 mL/min, n = 3). Then the appearances and weights of the animals were observed for 7 days. During the measurement period, the animals were housed in cages and provided with continuous access to food and water in an air-conditioned room on a 12 h dark/light cycle. After 7 days, the rats were anesthetized again with an intraperitoneal injection of sodium pentobarbital. A heparinized catheter (SP31 tubing, OD 0.8 mm, ID 0.2 mm) was introduced into the abdominal aorta. Then blood was withdrawn using a nontreated syringe. The blood was transferred to a vacuum blood collection tube (B-2; BML Inc.) and was centrifuged (2,800 rpm, 15 min, 4 °C) to remove the blood cell components. The obtained serum was stored in the tube (S-1; BML Inc.) at 4 °C. The samples were subjected to a total of 26 blood biochemical assays by BML Inc. (Tokyo): total protein, albumin, albumin/globulin ratio, aspartate aminotransferase (AST), alanine aminotransferase (ALT), γ-glutamyltransferase (γ-GTP), total bilirubin, direct bilirubin, creatinine, urea nitrogen, uric acid, amylase, total cholesterol, free cholesterol, β-lipoprotein, high-density lipoprotein (HDL)-cholesterol, triglyceride, total lipid, free fatty acid, phospholipid, K, Ca, inorganic P, Mg, Fe and Cu. The vital organs (liver, kidney, spleen, lung and heart) were isolated and weighed. As a control group, the 20 g/dL HSA solution was administered similarly into rats (269 ± 17 g, 6 mL/kg, 1 mL/min, n = 3). Three rats (273 ± 14 g) without infusion (operation only) were established as a sham-operated group.
In addition, paraffin section specimens were prepared from 10% formalin-fixed major organs (liver, kidney, spleen, lungs and heart) and were stained with hematoxylin–eosin (HE) stain on a glass surface for a histopathologic study (LSI Medience Corp., Japan).
The 125-Iodinated HemoAct was prepared using our previously reported procedures34. The sample was diluted by non-labeled HemoAct to adjust the protein concentration before use. Wistar rats (269 ± 5 g, male) were anesthetized with diethylether. The HemoAct solution was injected intravenously via a tail vein (40 mg/kg, 0.2 mL/100 g, 1.5 × 106 cpm/rat) (n = 6). At the time-points of 3, 10, 30 min and 1, 3, 6, 12 and 24 h after the infusion, a heparinized syringe was used to collect 200 μL of blood from the lateral tail vein. A centrifuge (3000 rpm, 10 min) was used for removal of the blood cell components. Subsequently, the levels of 125I in the plasma were ascertained by measuring their radioactivity using an automatic gamma counter (2480 WIZARD2; PerkinElmer Inc.). Acid precipitability of the recovered radionuclide was confirmed using trichloroacetic acid. The rats were sacrificed by hemorrhage at the end of the experiments. Their vital organs (liver, kidney, spleen, lung and heart) were isolated carefully. The weight and radioactivity of the excised organs were measured. As reference groups, the 125I-Hb and 125I-HSA solutions were administered similarly into rats [125I-Hb group (270 ± 9 g, 10 mg/kg, n = 6) and 125I-HSA group (260 ± 11 g, 30 mg/kg, n = 6)].
Pharmacokinetic analyses were conducted after the administration of 125I-HemoAct using a non-compartment model. Pharmacokinetic parameters were calculated using the moment analysis program available with Microsoft Excel, as reported previously35. Data are shown as the mean ± SD for the indicated number of animals. Significant differences between groups were inferred using two-tailed unpaired Student’s t-tests. Probability values of p < 0.05 were inferred as statistically significant.
How to cite this article: Haruki, R. et al. Safety Evaluation of Hemoglobin-Albumin Cluster “HemoAct” as a Red Blood Cell Substitute. Sci. Rep. 5, 12778; doi: 10.1038/srep12778 (2015).
Japanese Red Cross Society. Blood Services 2014. < http://www.jrc.or.jp/english/pdf/Blood_Services_2014.pdf>, (2014) (Date of access: 01/02/2015).
Bureau of Social Welfare and Public Health. Results on Blood Transfusion Situation 2013.< http://www.fukushihoken.metro.tokyo.jp/iryo/k_isyoku/yuketsutyousakekka.files/25gaiyou.pdf>, (2013) (Date of access: 01/02/2015).
Ministry of Health, Labour and Welfare, Japan. Proceedings of Blood Donation Promotion Committee, Pharmaceutical Affairs and Food Sanitation Council on 2 December, 2014.< http://www.mhlw.go.jp/file/05-Shingikai-11121000-Iyakushokuhinkyoku-Soumuka/0000067177.pdf>, (2014) (Date of access: 01/02/2015).
Squires, J. E. Artificial blood. Science 295, 1002−1005 (2002).
Jahr, J. S., Sadighi, A., Doherty, L., Li, A. & Kim, H. W. Hemoglobin-based oxygen carriers: history, limits, brief summary of the state of the art, including clinical trials in Chemistry and biochemistry of oxygen therapeutics: from transfusion to artificial blood (eds Bettati S. & Mozzarelli A. ) p. 301−316 (John Wiley & Sons, 2011).
Kluger, R. & Lui, F. E. HBOCs from chemical modification of Hb in Hemoglobin-based oxygen carriers as red cell substitutes and oxygen therapeutics (eds Kim, H. W. & Greenburg, A. G. ) p. 159−183 (Springer-Verlag, 2013).
Snyder, S. R., Welty, E. V., Walder, R. Y., Williams, L. A. & Walder, J. A. HbXL99α: a hemoglobin derivative that is cross-linked between the α subunits is useful as a blood substitute. Proc. Natl. Acad. Sci. USA 84, 7280−7284 (1987).
Nagababu, E., Ramasamy, S., Rifkind, J. M., Jia, Y. & Alayash, A. I. Site-specific cross-linking of human and bovine hemoglobins differentially alters oxygen binding and redox side reactions producing rhombic heme and heme degradation. Biochemistry 41, 7407−7415 (2002).
Buehler, P. W. et al. Structural and functional characterization of glutaraldehyde-polymerized bovine hemoglobin and its isolated fractions. Anal. Chem. 77, 3466−3478 (2005).
Pearce, L. B. et al. HBOC-201 (hemoglobin glutamer-250) (bovine), hemopure®): clinical studies. Blood substitutes (ed Winslow, R. M. ) p. 437−450 (Elsevier, 2006).
Kluger, R. & Zhang, J. Hemoglobin dendrimers: functional protein clusters. J. Am. Chem. Soc. 125, 6070–6071 (2003).
Conover, C. D., Linberg, R., Lejeune, L., Nagy, M. & Shum, K. L. PEG-hemoglobin as a resuscitation solution in the treatment of hypovolemic shock in the anesthetized rat. Artif. Organs 23, 1088–1098 (1999).
Vandegriff, K. D., Malavalli, A., Wooldbridge, J., Lohman, W. & Winslow, R. M. MP4, a new nonvasoactive PEG-Hb conjugate. Transfusion 43, 509–516 (2003).
Manjula, B. N. et al. Site-specific PEGylation of hemoglobin at Cys-93(β): correlation between the colligative properties of the PEGylated protein and the length of the conjugated PEG chain. Bioconjugate Chem . 14, 464−472 (2003).
Natanson, C., Kern, S. J., Lurie, P., Banks, S. M. & Wolfe, S. M. Cell-free hemoglobin-based blood substitutes and risk of myocardial infarction and death. J. Am. Med. Assoc . 299, 2304−2312 (2008).
Kluger, R. Red cell substitutes from hemoglobin—Do we start all over again? Curr. Opin. Chem. Biol. 14, 538−543 (2010).
Shultz, S. C. et al. A role for endothelin and nitric oxide in the pressor response to diaspirin cross-linked hemoglobin. J. Lab. Clin. Med. 122, 301−308 (1993).
Doherty, D. H. et al. Rate of reaction with nitric oxide determines the hypertensive effect of cell-free hemoglobin. Nat. Biotechnol. 16, 672−676 (1998).
Tomita, D. et al. Covalent core–shell architecture of hemoglobin and human serum albumin as an artificial O2 carrier. Biomacromolecules 14, 1816−1825 (2013).
Hosaka, H., Haruki, R., Yamada, K., Böttcher, C. & Komatsu, T. Hemoglobin albumin cluster incorporating a Pt nanoparticle: artificial O2 carrier with antioxidant activities. PLoS ONE 9, e110541 (2014).
Daijima, Y. & Komatsu, T. Haemoglobin wrapped covalently by human serum albumin mutants containing Mn(III) protoporphyrin IX: an O2 complex stable in H2O2 solution. Chem. Commun. 50, 14716−14719 (2014).
Fasano, M. et al. The extraordinarily ligand binding properties of HSA. IUBMB Life 57, 787–796 (2005).
Ghuman, J. et al. Structural basis of the drug-binding specificity of human serum albumin. J. Mol. Biol. 353, 38−52 (2005).
Kwaan, H. C. Role of plasma proteins in whole blood viscosity: a brief clinical review. Clin. Hemorheol. Microcirc. 44, 167–176 (2010).
Kirkwood, T. B. L. Calibration of reference thromboplastins and standardization of the prothrombin time ratio. Thromb. Haemost. 49, 283−244 (1983).
Poller, L. International normalized ratios (INR): The first 20 years. J. Thrombo. Haemost . 2, 849−860 (2004).
Haraldsson, B. et al. Properties of the glomerular barrier and mechanisms of proteinuria. Physiol. Rev. 88, 451−487 (2008).
Guyton, A. C., Ross, J. M., Carrier, O. & Walker, J. R. Evidence for tissue oxygen demand as the major factor causing autoregulation. Circ. Res. 14, 1−60 (1964).
Intaglietta, M. Microvascular transport factors in the design of effective blood substitutes in Microcirculatory effects of hemoglobin solutions (eds Messmer, K., Burhop, K. E. & Hutter, J. ) p. 8−15 (Karger, 2004).
Rohlfs, R. J. et al. Arterial blood pressure responses to cell-free hemoglobin solutions and the reaction with nitric oxide. J. Biol. Chem. 273, 12128−12134 (1998).
Malek, A. M. & Izumo S. Control of endothelial cell gene expression by flow. J. Biomech. 28, 1515−1528 (1995).
Ship, N. J. et al. Binding of acellular, native and cross-linked human hemoglobins to haptoglobin: enhanced distribution and clearance in the rat. Am. J. Physiol. Gastrointest. Liver Physiol. 288, G1301−9 (2005).
Rennen, H. J. J. et al. The effect of molecular weight on nonspecific accumulation of 99mT-labeled proteins in inflammatory foci. Nucl. Med. Biol. 28, 401−408 (2001).
Komatsu, T. et al. Physicochemical characterization of cross-linked human serum albumin dimer and its synthetic heme hybrid as an oxygen carrier. Biochim. Biophys. Acta 1675, 21−31 (2004).
Yamakawa, N. et al. Comparison of pharmacokinetics between loxoprofen and its derivative with lower ulcerogenic activity, fluoro-loxoprofen. Drug Metab. Pharmacokinet. 28, 118−124 (2013).
This work was supported by a Grant-in-Aid for Scientific Research on Innovative Area (“Coordination Programming” Area 2107, No. 21108013) from MEXT Japan and by a Joint Research Grant from the Institute of Science and Engineering, Chuo University. The authors acknowledge Mr. Katsunori Maejima, Chuo University, for skillful experiments related to Hb purification, Dr. Keitaro Sou, Waseda University, for his kind support on viscosity measurements, Dr. Yuichiro Hayashi, Keio University, for valuable comments related to histopathologic observations and the members of the Radioisotope Center, Kumamoto University, for important contributions to pharmacokinetic experiments.
The authors declare no competing financial interests.
Electronic supplementary material
About this article
Cite this article
Haruki, R., Kimura, T., Iwasaki, H. et al. Safety Evaluation of Hemoglobin-Albumin Cluster “HemoAct” as a Red Blood Cell Substitute. Sci Rep 5, 12778 (2015). https://doi.org/10.1038/srep12778
Stepping stones to the future of haemoglobin-based blood products: clinical, preclinical and innovative examples
Biomaterials Science (2021)
Haemoglobin(βK120C)–albumin trimer as an artificial O2 carrier with sufficient haemoglobin allostery
RSC Chemical Biology (2020)
YAKUGAKU ZASSHI (2020)
Genetically engineered haemoglobin wrapped covalently with human serum albumins as an artificial O2 carrier
Journal of Materials Chemistry B (2020)
Neuroprotective effects of combination therapy of regional cold perfusion and hemoglobin-based oxygen carrier administration on rat transient cerebral ischemia
Brain Research (2020)