Volume expanders are widely available and are used in both hospitals and first response situations by paramedics and emergency medical technicians. Oxygen therapeutics are in clinical trials in the U.S. and Europe, however Hemopure is more widely available in South Africa.
The body automatically detects the lower hemoglobin level and compensatory mechanisms start up. The heart pumps more blood with each beat. Since the lost blood was replaced with a suitable fluid, the now diluted blood flows more easily, even in the small vessels. As a result of chemical changes, more oxygen is released to the tissues. These adaptations are so effective that if only half of the red blood cells remain, oxygen delivery may still be about 75 percent of normal. A patient at rest uses only 25 percent of the oxygen available in his blood. In extreme cases, patients have survived with a hemoglobin level of 2 g/dl, about 1/7th the norm, although levels this low are very dangerous.
With enough blood loss, ultimately red blood cell levels drop too low for adequate tissue oxygenation, even if volume expanders maintain circulatory volume. In these situations the only alternatives are blood transfusions, packed red blood cells, or oxygen therapeutics (if available). However in some circumstances hyperbaric oxygen therapy can maintain adequate tissue oxygenation even if red blood cell levels are below normal life sustaining levels.
The initial goal of oxygen carrying blood substitutes is merely to mimic blood's oxygen transport capacity. There is additional longer range research on true artificial red and white blood cells which could theoretically compose a blood substitute with higher fidelity to human blood.
Unfortunately, oxygen transport (one function that distinguishes real blood from other volume expanders) has been very difficult to reproduce. There are two basic approaches to constructing an oxygen therapeutic:
Perfluorochemicals 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 and humans can survive breathing liquid PFC solution, called liquid breathing.
Hemoglobin is the main component of red blood cells, comprising about 33% of the cell mass. Hemoglobin-based products are called HBOCs (Hemoglobin Based Oxygen Carriers). However pure hemoglobin separated from red cells cannot be used since it causes renal toxicity. It can be treated to avoid this, but it still has incorrect oxygen transport characteristics when separated from red cells. Various other steps are needed to form hemoglobin into a useful and safe oxygen therapeutic. These may include cross-linking, polymerization, and encapsulation. These are needed because the red cell is not a simple container for hemoglobin, but a complex entity with many biomolecular features.
The first approved 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.
In 1990s because of the risk of undetected blood bank contamination from AIDS, hepatitis C and other emergent diseases such as Creutzfeldt-Jakob disease, there was additional motivation to pursue oxygen therapeutics. Significant progress was achieved, and a hemoglobin-based oxygen therapeutic called Hemopure was approved for Phase III trial (in elective orthopedic surgery) in the U.S., and more widely approved for human use in South Africa.
In December 2003 a new hemoglobin-based oxygen therapeutic, PolyHeme, began field tests in a Phase III trial on emergency patients (in trauma settings) in the U.S. PolyHeme is the 15th experiment to be approved by the Food and Drug Administration since 1996. Patient consent is not necessary under the special category created by the FDA for these experiments. In late 2005, an independent panel verified, after the fourth and final review of 500 trauma patients enrolled in this study by that date, that no statistical evidence of safety concerns had arisen so far in the study. This pivotal study is expected to conclude in mid-2006 with final enrollment of 720 patients. If successful, this trial could lead to Food and Drug Administration approval of PolyHeme for use for severely bleeding trauma victims as early as sometime in 2007. Wired news reports that the PolyHeme trial failed when 47 of the 350 people given PolyHeme died compared to 35 deaths out of 363 in the control group. Debate exists as to whether or not the difference in the mortality rate is attributable to the small sample size. The fact that the experimental subjects did not give consent is a significant factor.
The U. S. Military is one of the greatest proponents of oxygen therapeutics, mainly because of the vital need and benefits in a combat scenario. Since oxygen therapeutics are not yet widely available, the United States Army is experimenting with varieties of dried blood, which takes up less room, weigh less and can be used much longer than blood plasma. Water has to be added prior to use. These properties make it better for first aid during combat than whole blood or packed red cells.
Blood substitutes are useful for the following reasons:
Oxygent is a solution used as an intravascular oxygen carrier to temporarily augment oxygen delivery to tissues and is currently being developed by Alliance Pharmaceutical Corp. Right now, the goal of the development of Oxygent is simply to reduce the need for donor blood during surgery, but this product clearly has the potential for additional future uses. Perfluorocarbons surrounded by a surfactant called lecithin and suspended in a water based solution give Oxygent its oxygen carrying capacity. The Oxygent particles are removed from the bloodstream within 48 hours by the body's normal clearance procedure for particles in the blood. Namely, the lecithin is digested intracellularly and the PFC's are exhaled through the lungs. The fact that this blood substitute is completely man-made gives it certain distinct advantages over blood substitutes that rely on modified hemoglobin, such as unlimited manufacturing capabilities, ability to be heat-sterilized, and the PFCs’ efficient oxygen delivery. Oxygent has done well in most clinical trials, but recently ran into some trouble, with participants in a cardiac surgery study slightly more likely to suffer a stroke if treated with Oxygent rather than the standard care.
Perftoran is a PFC-based artificial carrier that was developed by the Russian National Academy of Sciences between 1979-1995. The manufacture, distribution, and clinical use of Perftoran in Russia began in 1997. Perftoran was registered in Mexico as PERFTEC in November 2005
Perftec is a perflurocarbon emulsion that allows for the efficient intra-vascular transportation of oxygen to all cells throughout the body. Perftec enhances delivery from the lungs into tissues by both, its carrying capacity, and by its and rheological properties which include low viscosity, small particle size, large total surface area, modification of the Red Blood Cell (RBC) membrane, and the high mobility of PFC particles in the bloodstream during interaction with RBC. Due to its chemical composition, Perftec is a sterile and inert emulsion that is compatible with any blood type. Perftec can be used in: 1) Acute hemorrhages. 2) Elective surgery to avoid or reduce the amount of blood transfusion. 3) Organ transplant to diminish the risk of rejection. 4) Cancer treatment to increase efficacy of intravenous vitamin C, radio and chemotherapy while decreasing their side effects. Perftec is a 20% wt/vol PFC emulsion based on a 2:1 ratio of perfluorodecalin and perfluormethylcyclohexylpiperidin. It is emulsified with Proxanol-268 at 4% wt/vol in a solution of water and salts. The PFC particles in Perftec have an average size of 0.07μ (range between 0.03-0.15μ). Perftec can be stored frozen between -18 °C to - 4°C for 3 years. Mexico is the second country in the world where Perftec has been approved through a clinical trial and is registered as an authorized blood substitute. It is currently being used at the Oasis of Hope Hospital in surgeries including kidney transplants, as well as an adjuvent to Chemotherapy and Intravenous Vitamin C. It is also being used at National Medical Center "La Raza" in open-heart surgeries.
Hemopure is made by Biopure, one of the leading companies in the development and manufacture of oxygen carrying solutions. It is Biopure’s first-in-class product for human use, and is a Hemoglobin based oxygen carrying solution (HBOC). It is made of chemically stabilized, cross-linked bovine (cow) hemoglobin situated in a salt solution, and many safety measures are taken to ensure that the product is safe and free of pathogens, including herd control and monitoring. Hemopure molecules can be up to 1/1,000 the size of RBCs, facilitating oxygen transport and off-loading to the tissues. Hemopure is currently in Phase III clinical trials in the US, and is approved for use in South Africa for the use of surgical patients who are anemic, thereby reducing or eliminating the need for blood transfusions for these patients.
Manufactured by Biopure, Oxyglobin solution is the first and only oxygen therapeutic to be both US FDA and European Commission approved for veterinary use. The solution consists of chemically stabilized bovine hemoglobin in a balanced salt solution and contains no red blood cells. The cross-linked hemoglobin, several tetramers bound together, works by circulation in the plasma and supplying oxygen to tissues. Introduced to veterinary clinics and hospitals in March 1998 and nationally distributed by October 1998, Oxyglobin has been used primarily for blood transfusions and for treatment of anemia in dogs. Currently, Oxyglobin can only be used in canines and not in humans. The current supply of Oxyglobin is low, because the company is spending most of its resources on Hemopure, a blood substitute designed for human use.
Polyheme is a hemoglobin based oxygen carrier and, as the only blood substitute to have completed a Phase III trial, represents the leading technology in this field. Developed and manufactured by Chicago based Northfield Laboratories, Inc., Polyheme originally began as a military project following the Vietnam War and has since shown great potential for both military and civilian use. Polyheme utilizes human hemoglobin as the oxygen carrying molecule in solution, and the extraction and filtration of this hemoglobin from red blood cells is the first step in production. Then, using a multi-step polymerization process, the purified hemoglobin is associated into tetramers and, as the final step, is incorporated into an electrolyte solution. The polymerization of the hemoglobin represents the critical step in this process because, as demonstrated by failed attempts at blood substitutes, when hemoglobin remains disassociated, it tends to take up nitric oxide, causing vasoconstriction. Also, free hemoglobin can be taken up by the kidney causing liver dysfunction and failure.
Recently, Northfield Laboratories has come under scrutiny for a Phase III trial they are conducting in over 20 level 1 trauma centers across the country. The controversy arises from the fact that the participants in this study are incapable of giving their consent due to the nature of their injuries. Even though this practice is sanctioned by the FDA as necessary emergency research, patients’ rights groups have begun to protest the study.
Hemospan is produced by the company Sangart, which was founded by Dr. Robert M. Winslow in 1998. Produced in powder form, the powder can then be mixed into liquid form and transfused immediately, regardless of a patient’s blood type. This technology relies on coupling with polyethylene glycol (PEG) to eliminate the toxicity associated with free hemoglobin. Sangart believes their product can be stored for years and that they have optimized certain factors involved in oxygen delivery in the production of Hemospan, so that their product ultimately presents the right amount of oxygen to the blood vessel wall. In the past four years, Hemospan has shown promise as a possible commercial product, yielding positive results in both Phase Ib/II and Phase II clinical trails.
Created by the Dexto-Sang Corporation, Dextran-Hemoglobin is a conjugate of the polymer dextran with human hemoglobin molecules. The safety of dextran has already been established, due to its wide use as a plasma volume expander. Conjugation of hemoglobin to dextran increases its half-life inside the body, and prevents tissue damage that occurs with free hemoglobin from processing by the kidneys and exit into the extracellular space.
Dextran-Hemoglobin is currently undergoing trials in dogs in Thailand, and the company hopes to begin human trials by the end of the year.
HemoBiotech, based in Dallas, TX is developing HemoTech, a human blood substitute developed in 1985 by researchers, Mario Feola, MD and Jan Simoni, PHD, DVM from the Texas Tech University Sciences Center (TTUHSC0). HemoBiotech has been able to identify and nullify the source of toxicity issues associated with previous blood substitute candidates. HemoTech, which is expected to be compatible will all blood types and a shelf life of 180+ days compared to 41 days for donated human blood. HemoTech's lack of toxicity is believed to be due to Hemobiotech's proprietary chemical modification of hemoglobin. The company believes the use of bovine blood provides and additional advantage over products developed from outdated human red blood cells or from perfluorochemicals (PFC's), as bovine blood is more readily available and more cost-effective to use. Limited tests has shown to be clear of the vasoconstriction and inflammatory toxicity issues that have hampered competitors.
Recently the scientific community has begun to look at the possibility of using stem cells as a means of producing an alternate source of transfusable blood. A study performed by Giarratana et al describes a large-scale ex-vivo production of mature human blood cells using hematopoietic stem cells, and may represent the first significant steps in this direction. Moreover, the blood cells produced in culture possess the same hemoglobin content and morphology as do native red blood cells. The authors of the study also contend that the red blood cells they produced have a near-normal lifespan, when compared to native red blood cells—an important characteristic that current hemoglobin-based blood substitute fall short on.
The major obstacle with this method of producing red blood cells is cost. At the moment, the complex three step method of producing the cells would make a unit of these red blood cells too expensive. However, the study is the first of its kind to demonstrate the possibility of producing red blood cells which closely resemble native red blood cells on a large scale.
Researchers at the Dendritech Corporation have begun research, aided by a 2 year, $750,000 grant from the US Army, into the use of dendrimers as substitute oxygen carriers. The precise nature of the research cannot be disclosed, as the company’s patent application has not yet been approved. Researchers hope that dendrimer technology will be the first truly cost-efficient blood substitute.
In order to enhance circulation times, recombinant or polymerized hemoglobin can be encapsulated within micellar forming amphiphilic block copolymers. These systems are typically between 30-100 nm in diameter. The hydrophobic core of the polymer micelle is able to solubilize the similarly hydrophobic hemoglobin protein, while the water soluble corona (which is usually poly (ethylene glycol)) provides a steric barrier to protein absorption and provides protection from clearance by the reticuloendothelial system (RES).
Cord blood collected asceptically from the placenta after the birth of a healthy baby can be used safely as a blood substitute. It has a higher hemoglobin content and growth factors than normal blood from an adult, which has the potential to benefit patients in varying diseases.
Since blood transfusions are often most critically needed in trauma situations where obtaining informed consent is either difficult, impossible, or a barrier to providing lifesaving care, the ethics of clinical trials for these products are difficult. In the United States, these trials are performed under a specific exemption from requirements for informed consent .
Nominally, the community where blood substitutes will be used in clinical trials is informed, and wristbands or other clear markers are distributed so that a person can "opt out" of the trial. The concept that a person could be involved in experimentation on humans without consent is controversial.
In 2008 a review of clinical trail data found that hemoglobin-based blood substitutes increase the odds of deaths and heart attacks
A meta-analysis of blood substitutes found that fake blood scavenges nitric oxide, which causes vasoconstriction. Patients who receive blood substitutes are 2.7 times more likely to have a heart attack and 30% more likely to die.
Study Finds New Blood Substitutes Increase Risk of Death, Heart Attacks; Authors Question FDA's Approval Process, Records Access
Apr 28, 2008; Public Citizen issued the following news release: While the idea of a blood substitute that doesn't need refrigeration or...