Blood substitute

A blood substitute (also called artificial blood or blood surrogate) is a substance used to mimic and fulfill some functions of biological blood. It aims to provide an alternative to blood transfusion, which is transferring blood or blood-based products from one person into another. Thus far, there are no well-accepted oxygen-carrying blood substitutes, which is the typical objective of a red blood cell transfusion; however, there are widely available non-blood volume expanders for cases where only volume restoration is required. These are helping doctors and surgeons avoid the risks of disease transmission and immune suppression, address the chronic blood donor shortage, and address the concerns of Jehovah's Witnesses and others who have religious objections to receiving transfused blood.

For the rugby union and rugby league term, see blood replacement.

The main categories of 'oxygen-carrying' blood substitutes being pursued are hemoglobin-based oxygen carriers (HBOC) and perfluorocarbon-based oxygen carriers (PFBOC).[1] Oxygen therapeutics are in clinical trials in the U.S. and Europe, and Hemopure is available in South Africa.

History

After William Harvey discovered blood pathways in 1616, many people tried to use fluids such as beer, urine, milk, and non-human animal blood as blood substitute.[2] Sir Christopher Wren (17th century) suggested wine and opium as blood substitute.[3]

At the beginning of the 20th century, the development of modern transfusion medicine initiated through the work of Landsteiner and co-authors opened the possibility to understanding the general principle of blood group serology.[4] Simultaneously, significant progress was made in the fields of heart and circulation physiology as well as in the understanding of the mechanism of oxygen transport and tissue oxygenation.[5][6]

Restrictions in applied transfusion medicine, especially in disaster situations such as World War II, laid the grounds for accelerated research in the field of blood substitutes.[7] Early attempts and optimism in developing blood substitutes were very quickly confronted with significant side effects, which could not be promptly eliminated due to the level of knowledge and technology available at that time. The emergence of HIV in the 1980s renewed impetus for development of infection-safe blood substitutes.[3] Public concern about the safety of the blood supply was raised further by mad cow disease.[3][8] The continuous decline of blood donation combined with the increased demand for blood transfusion (increased ageing of population, increased incidence of invasive diagnostic, chemotherapy and extensive surgical interventions, terror attacks, international military conflicts) and positive estimation of investors in biotechnology branch made for a positive environment for further development of blood substitutes.[8]

Efforts to develop blood substitutes have been driven by a desire to replace blood transfusion in emergency situations, in places where infectious disease is endemic and the risk of contaminated blood products is high, where refrigeration to preserve blood may be lacking, and where it might not be possible or convenient to find blood type matches.[9]

Approaches

Efforts have focused on molecules that can carry oxygen, and most work has focused on recombinant hemoglobin, which normally carries oxygen, and perfluorocarbons (PFC), chemical compounds which can carry and release oxygen.[9][10]

The first approved oxygen-carrying blood substitute was a perfluorocarbon-based product called Fluosol-DA-20, manufactured by Green Cross of Japan. It was approved by the Food and Drug Administration (FDA) in 1989. Because of limited success, complexity of use and side effects, it was withdrawn in 1994. However, Fluosol-DA remains the only oxygen therapeutic ever fully approved by the FDA. As of 2017 no haemoglobin-based product had been approved.[9]

Perfluorocarbon based

Perfluorochemicals are not water soluble, so will not mix with blood, therefore emulsions must be made by dispersing small drops of PFC in water. This liquid is then mixed with antibiotics, vitamins, nutrients and salts, producing a mixture that contains about 80 different components, and performs many of the vital functions of natural blood. PFC particles are about 1/40 the size of the diameter of a red blood cell (RBC). This small size can enable PFC particles to traverse capillaries through which no RBCs are flowing. In theory this can benefit damaged, blood-starved tissue, which conventional red cells cannot reach. PFC solutions can carry oxygen so well that mammals, including humans, can survive breathing liquid PFC solution, called liquid breathing.

Perfluorocarbon-based blood substitutes are completely man-made; this provides advantages over blood substitutes that rely on modified haemoglobin, such as unlimited manufacturing capabilities, ability to be heat-sterilized, and PFCs' efficient oxygen delivery and carbon dioxide removal. PFCs in solution act as an intravascular oxygen carrier to temporarily augment oxygen delivery to tissues. PFCs are removed from the bloodstream within 48 hours by the body's normal clearance procedure for particles in the blood – exhalation. PFC particles in solution can carry several times more oxygen per cubic centimeter (cc) than blood, while being 40 to 50 times smaller than haemoglobin.

Fluosol was made mostly of perfluorodecalin or perfluorotributylamine suspended in an albumin emulsion. It was developed in Japan and first tested in the United States in November 1979.[11] In order to "load" sufficient amounts of oxygen into it, people who had been given it had to breathe pure oxygen by mask or in a hyperbaric chamber.[12] It was approved by the FDA in 1989,[13] and was approved in eight other countries. Its use was associated with a reduction in ischemic complications and with an increase in pulmonary edema and congestive heart failure.[14] Due to difficulty with the emulsion storage of Fluosol use (frozen storage and rewarming), its popularity declined and its production ended in 1994.[9]

Name Sponsor Description
Oxycyte Oxygen Biotherapeutics Tested in a Phase II-b Trials in the United States. Targeted as an oxygen therapeutic rather than a blood substitute, with successful small-scale open label human trials treating traumatic brain injury at Virginia Commonwealth University.[15] The trial was later terminated.[16]
PHER-O
2		 Sanguine Corp In research
Perftoran Russia Contains perfluorodecalin and perfluoro-N-(4-methylcyclohexyl)-piperidine along with a surfactant, Proxanol-268. It was developed in Russia and as of 2005 was marketed there.[17]
NVX-108 NuvOx Pharma In a Phase Ib/II clinical trial where it raises tumor oxygen levels prior to radiation therapy in order to radiosensitize them.[18]

Oxygent was a second-generation, lecithin-stabilized emulsion of a PFC that was under development by Alliance Pharmaceuticals.[19][20][21] In 2002 a Phase III study was halted early due an increase in incidences of strokes in the study arm.[22]

Haemoglobin based

Haemoglobin is the main component of red blood cells, comprising about 33% of the cell mass. Haemoglobin-based products are called haemoglobin-based oxygen carriers (HBOCs).

Unmodified cell-free haemoglobin is not useful as a blood substitute because its oxygen affinity is too high for effective tissue oxygenation, the half-life within the intravascular space that is too short to be clinically useful, it has a tendency to undergo dissociation in dimers with resultant kidney damage and toxicity, and because free haemoglobin tends to take up nitric oxide, causing vasoconstriction.[3][23][24][25]

Efforts to overcome this toxicity have included making genetically engineered versions, cross-linking, polymerization, and encapsulation.[9]

HemAssist, a diaspirin cross-linked haemoglobin (DCLHb) was developed by Baxter Healthcare; it was the most widely studied of the haemoglobin-based blood substitutes, used in more than a dozen animal and clinical studies.[7] It reached Phase III clinical trials, in which failed due to increased mortality in the trial arm, mostly due to severe vasoconstriction complications.[9][7] The results were published in 1999.[26]

Hemolink (Hemosol, Inc., Mississauga, Canada) was a haemoglobin solution that contained cross-linked an o-rafinose polymerised human haemoglobin,[9] which struggled after Phase II trials were halted in 2003 on safety concerns.[27] It declared bankruptcy in 2005.[28]

Hemopure was developed by Biopure Corp and was a chemically stabilized, cross-linked bovine (cow) haemoglobin in a salt solution intended for human use; the company developed the same product under the trade name Oxyglobin for veterinary use in dogs. Oxyglobin was approved in the US and Europe and was introduced to veterinary clinics and hospitals in March 1998. Hemopure was approved in South Africa and Russia. Biopure filed for bankruptcy protection in 2009.[29] Its assets were subsequently purchased by HbO2 Therapeutics in 2014.

PolyHeme was developed over 20 years by Northfield Laboratories and began as a military project following the Vietnam War. It is human haemoglobin, extracted from red blood cells, then polymerized, then incorporated into an electrolyte solution. In April 2009, the FDA rejected Northfield's Biologic License Application[30] and in June 2009, Northfield filed for bankruptcy.[31]

Dextran-Haemoglobin was developed by Dextro-Sang Corp as a veterinary product, and was a conjugate of the polymer dextran with human haemoglobin.

Hemotech was developed by HemoBiotech and was a chemically modified haemoglobin.

Somatogen developed a genetically engineered and crosslinked tetramer it called Optro. It failed in a phase II trial that was published in 2014 and development was halted.[9]

A pyridoxylated Hb conjugated with polyoxyethylene was created by scientists at Ajinomoto and eventually developed by Apex Biosciences, a subsidiary of Curacyte AG; it was called "PHP" and failed in a Phase III trial published in 2014, due to increased mortality in the control arm,[9][32] which led to Curacyte shutting down.[33]

Similarly, Hemospan was developed by Sangart, and was a pegylated haemoglobin provided in a powdered form. While early trials were promising Sangart ran out of funding and closed down.[9]

Stem cells

Stem cells offer a possible means of producing transfusable blood. A study performed by Giarratana et al.[34] describes a large-scale ex-vivo production of mature human blood cells using hematopoietic stem cells. The cultured cells possessed the same haemoglobin content and morphology as native red blood cells. The authors contend that the cells had a near-normal lifespan, when compared to natural red blood cells.

Scientists from the experimental arm of the United States Department of Defense began creating artificial blood for use in remote areas and transfuse blood to wounded soldiers more quickly in 2010.[35] The blood is made from the hematopoietic stem cells removed from the umbilical cord between human mother and newborn using a method called blood pharming. Pharming has been used in the past on animals and plants to create medical substances in large quantities. Each cord can produce approximately 20 units of blood. The blood is being produced for the Defense Advanced Research Projects Agency by Arteriocyte. The Food and Drug Administration has examined and approved the safety of this blood from previously submitted O-negative blood. Using this particular artificial blood will reduce the costs per unit of blood from $5,000 to equal or less than $1,000.[35] This blood will also serve as a blood donor to all common blood types. Pharmed blood may be used in human trials in 2013.[36]

gollark: We must replace it with PotatoBin; yes, I have actually written that (it needs renaming to PotatoBin though).
gollark: Define "best".
gollark: Many.
gollark: PHP is never innocent.
gollark: Yes, JS is... bad... but at least it's *not* PHP!

See also

References
  1. Henkel-Honke, T.; Oleck, M. (2007). "Artificial oxygen carriers: A current review" (PDF). AANA Journal. 75 (3): 205–211. PMID 17591302. Archived from the original (PDF) on 2016-03-04. Retrieved 2016-02-09.
  2. Sarkar, S. (2008). "Artificial Blood". Indian Journal of Critical Care Medicine. 12 (3): 140–144. doi:10.4103/0972-5229.43685. PMC 2738310. PMID 19742251.
  3. Squires JE (2002). "Artificial blood". Science. 295 (5557): 1002–5. doi:10.1126/science.1068443. PMID 11834811. S2CID 35381400.
  4. Boulton, FE (December 2013). "Blood transfusion; additional historical aspects. Part 1. The birth of transfusion immunology". Transfusion Medicine (Oxford, England). 23 (6): 375–81. doi:10.1111/tme.12075. PMID 24003949.
  5. Feigl, EO (January 1983). "Coronary physiology". Physiological Reviews. 63 (1): 1–205. doi:10.1152/physrev.1983.63.1.1. PMID 6296890.
  6. Lahiri, S (April 2000). "Historical perspectives of cellular oxygen sensing and responses to hypoxia". Journal of Applied Physiology. 88 (4): 1467–73. doi:10.1152/jappl.2000.88.4.1467. PMID 10749843.
  7. Reid TJ (2003). "Hb-based oxygen carriers: are we there yet?". Transfusion. 43 (2): 280–7. doi:10.1046/j.1537-2995.2003.00314.x. PMID 12559026.
  8. Goodnough LT, Brecher ME, Kanter MH, AuBuchon JP (1999). "Transfusion medicine. First of two parts--blood transfusion". N. Engl. J. Med. 340 (6): 438–47. doi:10.1056/NEJM199902113400606. PMID 9971869.
  9. Alayash, AI (4 January 2017). "Hemoglobin-Based Blood Substitutes and the Treatment of Sickle Cell Disease: More Harm than Help?". Biomolecules. 7 (1): 2. doi:10.3390/biom7010002. PMC 5372714. PMID 28054978.
  10. Remy B, Deby-Dupont G, Lamy M (1999). "Red blood cell substitutes: fluorocarbon emulsions and haemoglobin solutions". Br. Med. Bull. 55 (1): 277–98. doi:10.1258/0007142991902259. PMID 10695091.
  11. https://www.nytimes.com/1979/11/21/archives/artificial-blood-given-to-jehovahs-witness-in-first-american-use.html
  12. Marieb, Elaine Nicpon. Human Anatomy & Physiology. 4th ed. Menlo Park, California: Addison Wesley Longman, Inc. 1998. 650.
  13. Bruno, S.; Ronda, L.; Faggiano, S.; Bettati, S.; Mozzarelli, A. (2010). "Oxygen Delivery via Allosteric Effectors of Hemoglobin and Blood Substitutes". Burger's Medicinal Chemistry and Drug Discovery. doi:10.1002/0471266949.bmc048.pub2. ISBN 978-0471266945.
  14. Wall, T. C.; Califf, R. M.; Blankenship, J.; Talley, J. D.; Tannenbaum, M.; Schwaiger, M.; Gacioch, G.; Cohen, M. D.; Sanz, M.; Leimberger, J. D. (1994). "Intravenous Fluosol in the treatment of acute myocardial infarction. Results of the Thrombolysis and Angioplasty in Myocardial Infarction 9 Trial. TAMI 9 Research Group". Circulation. 90 (1): 114–120. doi:10.1161/01.CIR.90.1.114. PMID 8025985.
  15. Yoffee, Lynn (May 1, 2008). "Oxycyte is on track as oxygen carrier, not as 'faux' blood". Cardiovascular Device & Drugs. Retrieved 2010-06-30.
  16. "Safety and Tolerability of Oxycyte in Patients With Traumatic Brain Injury (TBI) (STOP-TBI)".
  17. Maevsky, E; Ivanitsky, G; Bogdanova, L; Axenova, O; Karmen, N; Zhiburt, E; Senina, R; Pushkin, S; Maslennikov, I; Orlov, A; Marinicheva, I (2005). "Clinical results of Perftoran application: present and future". Artificial Cells, Blood Substitutes, and Immobilization Biotechnology. 33 (1): 37–46. doi:10.1081/BIO-200046654. PMID 15768564.
  18. "The Effects of NVX-108 as a Radiation Sensitizer in Glioblastoma (GBM)".
  19. Vorob’ev, S. I. (2009-08-19). "First- and second-generation perfluorocarbon emulsions". Pharmaceutical Chemistry Journal. 43 (4): 209–218. doi:10.1007/s11094-009-0268-1. ISSN 0091-150X.
  20. Cohn, Claudia S.; Cushing, Melissa M. (2009-04-01). "Oxygen Therapeutics: Perfluorocarbons and Blood Substitute Safety". Critical Care Clinics. Hemoglobin-based Oxygen Carriers (HBOCs): The Future in Resuscitation?. 25 (2): 399–414. doi:10.1016/j.ccc.2008.12.007. PMID 19341916.
  21. Cohn, Claudia S.; Cushing, Melissa M. (2009). "Oxygen Therapeutics: Perfluorocarbons and Blood Substitute Safety". Critical Care Clinics. 25 (2): 399–414. doi:10.1016/j.ccc.2008.12.007. PMID 19341916.
  22. Niiler, Eric (2002-10-01). "Setbacks for blood substitute companies". Nature Biotechnology. 20 (10): 962–963. doi:10.1038/nbt1002-962. ISSN 1087-0156. PMID 12355103.
  23. Amberson, William; Jennings J.; Rhode C. (1949). "Clinical Experience with Hemoglobin-Saline Solutions". Journal of Applied Physiology. 1 (7): 469–489. doi:10.1152/jappl.1949.1.7.469. PMID 18104040.
  24. Jiin-Yu Chen; Michelle Scerbo; George Kramer (August 2009). "A Review of Blood Substitutes: Examining The History, Clinical Trial Results, and Ethics of Hemoglobin-Based Oxygen Carriers". Clinics (Sao Paulo). 64 (8): 803–813. doi:10.1590/S1807-59322009000800016. PMC 2728196. PMID 19690667.
  25. Natanson C, Kern SJ, Lurie P, Banks SM, Wolfe SM (May 2008). "Cell-free hemoglobin-based blood substitutes and risk of myocardial infarction and death: a meta-analysis". JAMA. 299 (19): 2304–12. doi:10.1001/jama.299.19.jrv80007. PMID 18443023.
  26. Sloan, EP; Koenigsberg, M; Weir, WB; Clark, JM; O'Connor, R; Olinger, M; Cydulka, R (February 2015). "Emergency Resuscitation of Patients Enrolled in the US Diaspirin Cross-linked Hemoglobin (DCLHb) Clinical Efficacy Trial". Prehospital and Disaster Medicine. 30 (1): 54–61. doi:10.1017/S1049023X14001174. PMID 25499006.
  27. Zehr, Leonard (June 21, 2003). "Tests leave Hemosol in critical condition". Globe and Mail.
  28. "Hemosol declares insolvency; shares under review by TSX". CBC News. November 25, 2005.
  29. Biopure files for relief PR Newswire, July 16, 2009.
  30. "FDA rejects Northfield's blood substitute". FierceBiotech. May 1, 2009.
  31. "Northfield Laboratories to liquidate under Chapter 11". Reuters. 2 June 2009. Retrieved 2017-12-31.
  32. Vincent, JL; Privalle, CT; Singer, M; Lorente, JA; Boehm, E; Meier-Hellmann, A; Darius, H; Ferrer, R; Sirvent, JM; Marx, G; DeAngelo, J (January 2015). "Multicenter, randomized, placebo-controlled phase III study of pyridoxalated hemoglobin polyoxyethylene in distributive shock (PHOENIX)". Critical Care Medicine. 43 (1): 57–64. doi:10.1097/CCM.0000000000000554. PMID 25083980.
  33. "Curacyte". Curacyte. Retrieved 30 December 2017.
  34. Rousseau GF, Giarratana MC, Douay L (Jan 2014). "Large-scale production of red blood cells from stem cells: what are the technical challenges ahead?". Biotechnol. J. 9 (1): 28–38. doi:10.1002/biot.201200368. PMID 24408610.
  35. Edwards, L. (July 13, 2010). Artificial blood developed for the battlefield. Retrieved November 30, 2010
  36. http://science.dodlive.mil/2013/11/29/blood-pharming/
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