Cryonics

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Cryonics is a controversial life extension technique that aims to preserve neural activity and life typically of a recently deceased person through use of preservation techniques and low temperatures so that resurrection may be possible in the future when technologies have improved.

Possible necessary future technologies include:

Imported content

That is not dead that can eternal lie,

and with strange aeons even death may die.

- H.P. Lovecraft

Margaret, Paul, I wish you the very best and it is my most fervent desire that we meet again, hopefully in a time and place where we can laugh and reminisce about the dark ages from which we were so lucky to have made our escape from...
- Mike Darwin

Cryonics is the preservation of dead persons at temperatures low enough to practically stop decomposition, with the intent of future revival. While there is experimental evidence attesting to the conservation of vitrified tissue and the possibilities of repair; the decision to undergo cryonic preservation after death is an act of faith, not of science.

Overview

File:Ettinger with HSSV.jpg
Robert Ettinger dreamed of a time machine that would bridge the gap between today's patients and tomorrow's medicine.

The two main ideas behind cryonics are Information-Theoretic Death and the technology vitrification. The first idea is the idea that our criteria for death has changed as our technology and our understanding of biology has changed. In the 1800s, a person who drowned was considered dead. Information-theoretic death is the 'ultimate' death, the one that we know as fact is irreversible, and does not depend upon a changing understanding of nature. Information theoretic death is reached when the body (Especially the brain) has been damaged to the point that it is beyond repair; where repair means having enough structure and contextual information to bring the brain, along with the personality, memories and attitudes that it contains, back to a functioning state. If tissues have been properly preserved, this revival could be accomplished through a variety of ways, but even the best methods leave behind irreparable damage, which means memory loss and personality changes, and other neurological (Motor control) damage. The latter is sufficiently generic to be repaired when that kind of technology arrives, the former is unique to each person and impossible to recover.

The second idea, vitrification, is a process through which tissue is lowered to cryogenic temperatures without freezing or forming ice. The most widely believed myth about cryonics is that when people are frozen, ice inside their cells bursts and destroys tissue irreparably. This is false on two points: Modern cryonics uses cryoprotectants which prevent ice damage by vitrifying instead of freezing, and the water that forms ice is mostly outside the cells. A common argument against cryoprotectants is that they are toxic: While true, this only affects the prospects of suspended animation through vitrification, since cryonics patients would probably be revived through more complicated means than just thawing them and applying CPR once a cure for what killed them is found.

History

See History of cryonics

Evidence

Revival of Dogs after Profound Hypothermia

Scientists' Open Letter on Cryonics

To whom it may concern,

Cryonics is a legitimate science-based endeavor that seeks to preserve human beings, especially the human brain, by the best technology available. Future technologies for resuscitation can be envisioned that involve molecular repair by nanomedicine, highly advanced computation, detailed control of cell growth, and tissue regeneration.

With a view toward these developments, there is a credible possibility that cryonics performed under the best conditions achievable today can preserve sufficient neurological information to permit eventual restoration of a person to full health.

The rights of people who choose cryonics are important, and should be respected.

The Suda Experiments

Organ Vitrification

Viability of Vitrified Tissue

  • Cryopreservation of rat hippocampal slices by vitrification, Yuri Pichugin, Gregory M. Fahy, Robert Morin. Cryobiology: International Journal of Low Temperature Biology. Link.

Criticism

Interestingly (and somewhat to the author’s surprise) there are no published technical articles on cryonics that claim it won’t work. - Ralph Merkle

Most criticism of cryonics arises from fundamental misconceptions (For example, that cryonics involves freezing) and ignorance of current cryopreservation techniques and procedures.

Scientific American

Martinenaite/Tavenier

Abstract:

The preservation of cells, tissues and organs by cryopreservation is a promising technology nowadays. However, the primary purpose of this science has been diverted to a doubtful technology, cryonics. Cryopreservation techniques are now being adapted with the aim of preserving people’s bodies after death in hope that in the future, medicine will be able to revive them. In this report we analyze both scientific and social issues involved with this technology. We first studied the events taking place in the cells during regular freezing. Various research experiments show that freezing causes damage to the cells. Therefore, vitrification presented by cryonics companies as an alternative, seems to be reasonable. We also looked at all the difficulties of this procedure and at the injuries that such a treatment could cause to the human body. Studies show that the vitrification procedure suppresses the injuries related to freezing but the use of cryoprotectants, although necessary, is toxic to the cells. Organs, such as kidneys, are the largest entities ever vitrified and thawed with success. By analyzing all present scientific data, we conclude that there is a limit to the size of living matter that can be cryonised effectively; therefore we conclude that it is not possible to cryonize an entire human body with the current technology without causing severe damage to it.

While definitely great progress from most cryonics 'criticism' to date, the paper seems to address the well-known fact that reanimation from cryopreservation is impossible (Or nearly so) due to the toxicity of cryoprotectant solutions. The most discussed methods of revival, Molecular Nanotechnology and Whole Brain Emulation are not discussed.

Larry Johnson

Philosophy

While it's sad that people focus on philosophical issues instead of the myriad technical and social problems that plague cryonics, along with its attachment to a history of failure and incompetence, philosophical concerns should still be addressed.

By far the biggest philosophical concern people put forward against cryonics is the issue of continuity of consciousness. In these debates, people can easily talk past each other by using different definitions of what constitutes consciousness and how this relates to personal identity. In general, we have two definitions of consciousness:

  • Real Definition: Consciousness is self-awareness, and thus becomes discontinuous during sleep, unconsciousness, et cetera.
  • Alternate Definition: Consciousness is defined as a subset of (Or the totality of) brain activity, and thus a person's consciousness remains continuous during sleep and what is usually called 'unconsciousness', and only stops when brain activity ceases (Medico-legal death, not necessarily Information-theoretic).

But what is relevant is not the definition of consciousness, but how this matters to personal identity. Again, here we have two opinions:

  • Definition 1: Personal identity is a person's personality and memories. Consciousness is fundamental to life, of course, but its continuity is not fundamental to personal identity (It uses the Real Definition of consciousness).
  • Definition 1: Personal identity is a person's personality, memories, and continuous consciousness (It uses the Alternate Definition of consciousness). When consciousness becomes discontinuous, the identity 'stops' and ceases to exist.

Under Definition 1, cryonics patients will be the same person (± brain damage). Under the second definition, when they are repaired, the patients are fundamentally different people who claim to be the same as the original and only shre personality and memories.

Organizations

Alcor

The Alcor Life Extension Foundation is a Scottsdale, Arizona based nonprofit cryonics company. Incorporated in 1972 as the 'Alcor Society for Solid State Hypothermia' by Fred and Linda Chamberlain, Alcor is currently the largest cryonics company in the world.

Alcor's first cryopreservation took place in 1976 on A-1001, Fred Chamberlain's father. Initially, provided long term storage until 1982.

File:Alcor patient care.jpg
The Alcor Patient Care Bay in 1987. Pictured are the Cephalarium, an upright MVE, and James Bedford's Galiso dewar (Right, horizontal, barely visible). Photo by Mike Darwin.
File:Alcor patient care2.jpg
The Alcor Patient Care Bay today. Hugh Hixon refills a dewar while Mike Perry observes. Photo by Murray Ballard.
File:AlcorFront.jpg
The building of the Alcor Life Extension Foundation

Alcor Criticism

[...] Saul Kent invited me over to his home in Woodcrest, California to view videotapes of two Alcor cases which troubled him – but he couldn’t quite put his finger on why this was so.[...] Patients were being stabilized at a nearby hospice, transported to Alcor (~20 min away) and then CPS was discontinued, the patients were placed on the OR table and, without any ice on their heads, they were allowed to sit there at temperatures a little below normal body temperature for 1 to 1.5 hours, while burr holes were drilled, [...] smoke could be seen coming from the burr wound! Since the patient had no circulation to provide blood to carry away the enormous heat generated by the action of the burr on the bone, the temperature of the underlying bone (and brain) must have been high enough to literally cook an egg. In one case, a patient’s head was removed in the field and, because they had failed to use a rectal plug, the patient had defecated in the PIB. The result was that feces had contaminated the neck wound, and Alcor personnel were seen pouring saline over the stump of the neck whilst holding the patient’s severed head over a bucket trying to wash the fecal matter off the stump. These are just a few of the grotesque problems I observed.[...] - Mike Darwin[1]

Cryonics Institute

The Cryonics Institute is the second largest cryonics organization, a member-owned non-profit; incorporated in Michigan on the 4th of April of 1976 by Robert Ettinger, Mae Junod (Later Mae Ettinger) and Walter Runkel. Only two cryopreservations took place in its first two decades (Both Ettinger's family).

File:CIFrontOld.jpg
The old Detroit facility in 1987. Photo by Mike Darwin.
File:CIFront.jpg
The Cryonics Institute's current location, the Erfurt-Runkel Building.

CI Criticism

Robert Ettinger believed complex perfusion to ensure excellent cryopreservation was not worth the effort, that future technology would eventually find a way to repair any damage. Because of this, he decided to charge a fraction of the cost of other organizations for basic perfusion and long term care. Ettinger claimed that "anything that has existed, can exist"[2], meaning that it can exist again if sufficiently advanced technology is developed.

Robert Ettinger, founder of the cryonics movement, claims that "anything that has existed, can exist", meaning that it can exist again. For an unbounded optimist, this would mean that even a cremated person whose ashes have been scattered on the seas could conceivably be reconstructed. In this view, technology beyond our conception could gather enough evidence to reconstruct, atom-for-atom, human beings who vanished hundreds or thousands of years in the past. [...] Ettinger's Michigan-based Cryonics Institute offers suspensions for nearly a quarter of the cost of the California organizations, in part because Ettinger believes that costly perfusion procedures are unnecessary, relying more on future technology repair capabilities.[...] - Ben Best[3]

This unreasonable optimism has been the source of criticism[4] and is the basis of their decision to accept deceased non-Members signed up by their families, even after hours of warm ischemia. These patients now constitute the majority of CI cases and are only straight frozen.<ref="Darwin's CI criticism">http://chronopause.com/index.php/2011/02/23/does-personal-identity-survive-cryopreservation/#comment-247</ref>

Basically I was commenting on the operational paradigm at CI, which is pretty much “ritual.” You sign up, you get frozen and it’s pretty much kumbaya, no matter how badly things go. And they go pretty badly. Go to: http://cryonics.org/refs.html#cases and start reading the case reports posted there. That’s pretty much my working definition of horrible. It seems apparent to me that “just getting frozen” is now all that is necessary for a ticket to tomorrow, and that anything else that is done is “just gravy,” and probably unnecessary to a happy outcome.

[...]

Even in cases that CI perfuses, things go horribly wrong – often – and usually for to me bizarre and unfathomable (and careless) reasons. My dear friend and mentor Curtis Henderson was little more than straight frozen because CI President Ben Best had this idea that adding polyethylene glycol to the CPA solution would inhibit edema. - Mike Darwin<ref="Darwin's CI criticism">

Another criticism of the Cryonics Institute is their submission to the State of Michigan's decision that CI was a cemetery and could thus no longer perform perfusion on site. Because of this cryoprotectant perfusion has to be done by a cooperative funeral direction, and in most cases these are found on the moment and are not properly trained or equipped. Instead of appealing this decision, they accepted it and surrendered control of the patients to the state, unlike Alcor which has been engaged in a variety of legal disputes, to the point of making cryonics legal in California.

CryoCare Equipment Corporation

Trans Time

According to CI, they have 'has one whole body and two brains'. According to the Daily News of Los Angeles, as of 1990, they have 'five human bodies, two heads and one brain in its main cold suspension capsule'. A second article claims 'has frozen five human bodies, three severed heads, four dogs and three cats'. A 2001 article claims TT no longer has any human patients (Where did they move them? (Other than CI) --Eudoxia 17:08, 17 July 2012 (CDT)).

File:Foote and Trans Time article.jpg
A newspaper article that lists TT patients before 1980. From the Anchorage Daily News, February 10, 1980.
File:TTFront.jpg
The old Trans Time facility.
File:TTFrontNew.jpg
The new Trans Time facility.

TT Criticism

The principal criticism against Trans Time was their for-profit model, in which, if funding ran out, the patients would be thawed and conventionally interred (This is what would've happened to Janice Foote and the Mills couple), unlike other organizations with a pay-once model in which the storage costs for the patients are covered for perpetuity.

Cryonics Society of California

Founded in 1966 by TV-repairman-turned-<redacted> Robert Nelson, CSC carried out the first human cryopreservation, before cryopreserving twelve others and letting the bodies to rot in a cementery.

Nelson had apparently run out of money to maintain the patients in liquid nitrogen, but payed his attorney by selling his Porsche.[5]

In an interview in The Immortalist he stated he was a CI member.

Apparently he tried to start a new cryonics venture, The Continued Life Group. They seem to have had a site, but its existence was only confirmed once and it's not up, and nor does the Web Archive keep copies of it.

There really is no need for a criticism section.

American Cryonics Society

CryoSpan

CryoCare

Minnesota Valley Engineering

MVE was a cryogenics company located in New Prague, Minnesota. They manufactured tanks for cryogenic storage of bull semen for the Minnesota Valley Breeders Association. Edward Schuster, the founder and main stockholder, got in touch with Curtis Henderson near a cryobiology conference in 1967. Schuster said he wanted to build tanks, but did not have the tools (At the time, the only Liquid Nitrogen dewars for the storage of human bodies were the CryoCare Equipment Corporation ones, which required constant mechanical pumping to maintain a vacuum).

After purchasing Hoffmann Cryogenics, Schuster was able to build the A-8000. Some of these tanks have been in continuous operation since the 1960s, for example at 21st Century Genetics in New Prague.

Suspended Animation

Alcor vs CI

Comparison of Services
Alcor Cryonics Inst
Costs
  • Whole Body Patient: $200,000
  • Neuropatient: $80,000

(Through life insurance)

  • Whole Body Patient (Lifetime Member): $28,000
  • Whole Body Patient (Yearly Member): $35,000

(Through life insurance)

Members 968 488
Patients 111 111
Patients Lost 0 0
Services
  • Standby
  • Stabilization & Transport
  • Perfusion
  • Long Term Care
  • Perfusion
  • Long Term Care
Non-profit? Yes Yes
Incorporated 1972 1976
Staff 11 3
Yearly Fees $620 $120
Statistics: Members

(Note that CI considers people who have cryopreserved pets or DNA as members. People with cryonics arrangements are a separate category.)

Ideal Cryonics Organization

  • Procedures
    • Only trained medical professionals are allowed to do perfusions.
  • Outreach and Openness
    • Webcams on 24/7 in both the Patient Care Bay and the Procedures Room.
    • Extensive documentation of every case and every variable and video records of the procedures, published online.
    • Guided tours of the facility explaining every part of the procedure, discussing possibilities of revival, showing the dewars of the Patient Care Bay, how patients are arranged in them, explanations of current research being done, et cetera.
    • Inviting medical professionals and public officials to witness all the procedures for themselves.
  • Research
    • Sizeable part of the budget dedicated towards lowering cryoprotectant toxicity, developing new solutions, et cetera.
  • Facilities
    • Solar array or other energy collectors for energy independence.
    • Equipment for Nitrogen liquefaction, and power for the same.
    • Dewars
      • Bigfoot or larger stored in CryoSpan-style reinforced concrete silos.
      • Fire and blast proofing around the Patient Care Bay.
      • Reopen the neurovaults.

Procedures

See Cryonics procedure

Revival

Damage

The kinds of damage that need to be repaired have been slowly reduced over time, but at present, under the best conditions, the process of cryopreservation still causes severe damage to the Patients.

Cryoprotectant Toxicity

Cracking

There are two forms of cracking: That which is caused by thermal stress, and that which is caused by cooling below Tg. Cracks are generally few and large, which is far better than many smaller cracks; since from an information point of view they cause little damage.

If revival is attempted through Whole Brain Emulation, then fixing cracks is just a matter of adjusting the images. If it is attempted through some form of Biological Repair, this will require other methods to readjust the severed pieces of tissue.

Thermal Stress

Glass Cracks

When materials (Not only glasses) are cooled below their vitrification temperature, cracking occurs. Since the Tg of the cryoprotectant solutions is far above the temperature at which Nitrogen liquefies, cracking occurs during the cooling to this temperature, whether tissue has been vitrified or not. If cryoprotective Perfusion is not carried out properly or is compromised by severe ischemic injury, cracking can begin at temperatures as high as -90 ºC.

A solution for this (In properly perfused patients for whom cracking will only occur below glass transition) is Intermediate Temperature Storage.

Biological Repair

Whole Brain Emulation

See Whole Brain Emulation

File:Cryoultramicrotome.jpg
A cryoultramicrotome used to section tissue at low temperatures.
File:Spikes real and fake.jpg
One of these columns is a graph of the activity of a rat's pyramidal neuron under electrical stimulation. The other is an Izhikevich simulation of the same. This shows that reality and abstract models can have different internal behavior and foundations, but produce the same activity.

This approach to cryonics takes the ideas of information-theoretic death and the central tenets of Whole Brain Emulation (Memory and personality are stored in the brain, consciousness arises from material processes, et cetera) and proposes that cryonics patients may be revived by scanning the connectivity and properties of the cells in their brains (For example, with an ATLUM or some form of high-resolution tomography); and that an abstract, computer model of these properties will be very similar to the person who was cryopreserved.

Process

  1. The vitrified brain is extracted from the patient. Necessary extra fixatives are applied.
  2. The brain is segmented into as many pieces as needed.
  3. Each piece is laminated and scanned by a cryoultramicrotome, ATLUM or some other machine.
    1. Current technology is rather slow, but new massively-parallel electron microscopes are being, developed, primarily by the semiconductor industry. The speed of scanning depends on how many machines you have.
  4. A stack of electron micrographs is built, one for every slice.
  5. Noise is eliminated, different electron micrographs at the same height are pasted together by inferring edge connectivity.
  6. An edge detector traces the contours of neurites and cellular structures.
  7. Other algorithms detect intracellular structures of interest (Polyribosome complexes).
  8. This is done for every layer.
  9. Another algorithm joins the edges in different layers, creating a 3D model of the brain.
  10. Another algorithm uses that model to create a graph of the connectivity of the brain. Each node in this graph is a neuron, and the neuron data structure is supplied with all the necessary extra information acquired by step 7.
  11. After the scan is complete, the graph is stored in a neuromorphic computer; a machine where every processor is a hardware implementation of some model of neurons.
  12. The graph at the lowest level of the stem is joined with a species-generic graph of the connectivity of the spine, ie: Axons of the brain are matched to virtual nerve endings.
  13. The simulation of the body and brain, either connected to a robot or virtual avatar, is started.

Molecular Nanotechnological Repair

See Molecular Manufacturing

The approach of using Molecular Nanotechnology to revive cryonics patients dominated the discussions of the future of cryonics for over a decade since the publication of Engines of Creation, but has now mostly shifted to a historical curiosity.

Postmortem Examination

So far, only three postmortem, post cryopreservation examinations of cryonics patients have been carried out, all three in the 1980's. Some of the data was lost and most of the images are low quality due to being scanned from black-and-white publications. Medical examination provides a chance to examine the damage caused by cryonic preservation to patients on both the macroscale. They also provide the only opportunity to safely remove tissue for histological examinations, due to the fact that extracting tissue from a patient in Liquid Nitrogen could cause severe fracturing and damage from thermal stress, especially if one wishes to extract tissue near the brain or from it.

James Bedford

Source: Evaluation of the Condition of Dr. James H. Bedford After 24 Years of Cryonic Suspension.

  1. Dewar
    1. The dewar had been built in mid 1970 and was failing.
    2. The patient's refilled the dewar regularly for 21 years, preventing the patient from experiencing any significant warming. The presence of water ice, still in the form of cubes, confirms this.
  2. Body
    1. The patient did not have any visible surface fracture events.
    2. Head
      1. The head is turned to the left and two puncture marks ~1cm apart are visible on the anteriomedial aspect of the sternocleidomastoid muscle (Site of injection of the solution).
      2. A frozen, bloody exudade is visible around the mouth and nose, consistent with the presence of a respirator mask and improper chest compressions.
      3. A larger quantity of darker blood appears to have flowed from the mouth during dry ice freezing, as it retains the folds of the wrapping used to cover the patient.
      4. The eyes are partially open and the corneas are white due to ice. The nostrils were flattened, presumably compressed by the weight of dry ice.
      5. The had was fringed with short gray hair.
      6. There were remains of aluminized mylar on the occiput.
    3. Neck
      1. The skin of the left side of the neck is distended with the injection of a fluid bolus into the subcutaneous space.
      2. Examination of the left side of the neck was made impossible by the position of the head.
    4. Limbs
      1. Arms
        1. The skin of the right forearm appeared erythematous and discolored.
      2. Legs
        1. The legs are crossed, with the right foot over the left.
    5. Torso
      1. The skin from the mandible to ~2cm above the areolas appeared erythematous and discolored.
    6. Abdomen
      1. The skin was erythematous.

The general discoloration is probably a product of the injection of pure or highly concentrated DMSO.

Ray Mills

Source: Postmortem Examination of Three Cryonic Suspension Patients.

  1. Dewar
  2. Body
    1. Head
    2. Neck
    3. Limbs
      1. Arms
      2. Legs
    4. Torso
    5. Abdomen

Katherine Mills

Source: Postmortem Examination of Three Cryonic Suspension Patients.

  1. Dewar
  2. Body
    1. Head
    2. Neck
    3. Limbs
      1. Arms
      2. Legs
    4. Torso
    5. Abdomen

Janice Foote

Sources: Postmortem Examination of Three Cryonic Suspension Patients and Histological Study of a Temporarily Cryopreserved Human.

  1. Dewar
    1. The patient had been stored in the Andonian Dewar.
    2. The patient had been stored in an aluminium cassette lined with open-cell urethane foam as insulation.
    3. An overhead crane removed the cassette and placed it on the ground with the patient on a supine position.
  2. Body
    1. Head
    2. Neck
    3. Limbs
      1. Arms
      2. Legs
    4. Torso
    5. Abdomen

Problems

Delay and Ischemic Injury

Lack of Regulation

Storage Safety

The Tyranny of the Singularity

Multi-Century Commitment

Patients

See Cryonics patients

Alternatives

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Freeze Drying

Freeze drying, also known as Lyophilization; consists of freezing tissue, then reducing the atmospheric pressure and applying heat to sublimate the water ice in it. A freeze drying machine is a large chamber of heated shelves. Its atmosphere is connected to a vacuum pump and exposed to refrigeration coils.

In the process, the solid is first frozen; creating damaging ice crystals. The vacuum pump lowers the pressure to .6 ATM; ten, the shelves are heated, and due to the low pressure, the ice sublimates directly. This process can take several days (A single (.1386Kg) human brain took 28 to freeze dry. Slicing it, however, reduced the time to 14 days.[6]).

The material, at least in the case of food, can be preserved for several years without decay.

The main advantages of Lyophilization are that the removal of water and oxygen from tissue will reduce decay, and that it does not require expensive equipment or maintenance. A secure container, however, must be obtained and inspected to ensure that Oxygen does not enter the tissues.

The reduced dependence on equipment increases the safety of the storage and reduces the vulnerability of the tissue. There is some overlap in the storage advantages (Namely very low cost and easy storage) of Plastination. Moreover, freeze-dried material can be cryogenically stored later on.

In terms of cost, a single Lyophilization machine, the Taxi-Dry runs at 'less than a dollar a day', and most machines capable of fitting a human brain, head or body cost above $10,000, significantly cheaper than the cheapest perfusion machine.

The most obvious disadvantage is the the Lyophilization process is very destructive it itself. Since freezing happens before dehydration, ice crystals form. When they sublimate, the structural integrity of the tissue is compromised, due to the pores this leaves behind. This might be a solvable problem, but for now, the process is more destructive than the standard Vitrification protocol. Freeze drying also leaves 2% moisture, reducing the storage time to mere years.

Plastination

Recently, the Brain Preservation Foundation has launched the Brain Preservation Technology Prize, a $100,000+ prize to anyone who can preserve an entire human brain for a long amount of time, such that every neurological feature is preserved and can be examined with today's electron microscopy. Ken Hayworth believes this will be a form of plastination.

Alcohol Storage

Alcohol storage is an old and still widely used preservation method. If storing whole organisms, removal of the intestines is required. Proper storage can be achieved with 70%-90% purity alcohol or methylated spirit. To better preserve the DNA, sodium chloride (Common salt) can be added. 5% Glycerine also supposedly protects the specimen should an accident cause the alcohol to escape or evaporate. The container should be sealed and stored in a dark and cool place, such as a freezer.

The container's alcohol should be replaced at least once, a few weeks after immersion (Or whenever the liquid starts to turn darker or cloudy), as body fluids seep out and contaminate the alcohol. The above-mentioned additives should only be added after the replacement of the alcohol.

While alcohol preservation is very cheap and easy to do, both commercially and DIY (All it takes it some alcohol, a glass container and a freezer), it is overall a very poor preservation method, at least from the perspective of what cryonics tries to achieve: Under a microscopy, they degrade into mush after only a few months.

While biological specimens can be stored for many decades without exterior degradation (Einstein's brain and the Tasmanian Tiger "clone pup", the latter remaining integral after 130 years of alcohol storage), it only preserves macroscopic structure, and maybe enough genetic material to make a clone. Another, less significant issue, is the flammability of alcohol.

Permafrost Burial

File:Permafrost distribution.jpg
Distribution of permafrost in the Northern Hemisphere. Map by Philippe Rekacewicz, UNEP/GRID-Arendal; data from International Permafrost Association, 1998. Circumpolar Active-Layer Permafrost System (CAPS), version 1.0.
File:Permafrost temperature.jpg
Permafrost temperature profile.
Record Low Temperatures
Location Lowest Recorder Temperature (Cº)
Vostok, Antarctica -89.2ºC
Plateau Station, Antarctica -84ºC
Oymyakon, Russia -71.1ºC
Northice, Greenland -66ºC
Snag, Yukon -63ºC
Rogers Pass, Montana -56.5ºC

Roadmap

Cryoprotectant toxicity

  • Non-toxic cryoprotectants
    • Fractures would still be a problem when around Tg.
      • Fractures in some cases will require vascular surgery (Katherine Mills; severed aorta) and in the worst cases organ transplantation & spinal cord replacement/regeneration (Janice Foote, almost severed lung, spinal cord severed in 3). See the postmortem examination.
  • The Prometheus Project tried to achieve reversible brain cryopreservation, but this didn't pan out.

Research into Alternatives

  • Alternatives to cryonics may produce low-cost solutions for long term storage of patients
  • May also increase chances of revival and better preserve the tissues
  • Things like plastination may be more easily accepted by the mainstream neuroscience community

Books

The Prospect of Immortality by [[Robert Ettinger]], 1962
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The First Immortal: A Novel Of The Future by James L. Halperin, 1998
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Man into Superman: The Startling Potential of Human Evolution -- And How To Be Part of It by [[Robert Ettinger]], 1972
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Connectome: How the Brain's Wiring Makes Us Who We Are by [[Sebastian Seung]], 2012
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Publications

In Popular Culture

See Cryonics in popular culture

Glossary

  • 21CM: 21st Century Medicine, Inc.
  • ATP: Adenosine Triphosphate.
  • BBB: Blood Brain Barrier.
  • CNS: Central Nervous System.
  • Corpscicle: See Patient.
  • CPB: Cardiopulmonary Bypass.
  • CPA: CryoProtectant Agent.
  • CPS: CryoProtectant Solution.
  • CPR: Cardiopulmonary Resuscitation.
  • Cryostat: A custom-made, fiberglass storage tank of Liquid Nitrogen for cryopatients. It is not a dewar, due to the isolation being perlite surrounded by soft vacuum. It is used by the CryonicsInst.
  • CT: Computerized Tomography.
  • Deanimate: 'Die', but not in the information-theoretic death. A term used to describe cryonicists who experience legal death and are cryopreserved.
  • Deep Hypothermia:10-27ºC.
  • Dewar: A container used to store Liquid Nitrogen. It consists of two containers, separated by a vacuum jacket in the middle. The vacuum provides isolation by preventing convective heat exchange.
  • ECMO: Extracorporeal Membrane Oxygenation.
  • EM: Electron Microscope or Electron Microscopy.
  • EMS: Emergency Medical System.
  • HD: Hemodialysis.
  • HLM: Heart Lung Machine.
  • ICP: Intracranial Pressure.
  • ITS: Intermediate Temperature Storage.
  • LAPC: Liquid Assisted Pulmonary Cooling.
  • ME Case: A cryonics patient who is autopsied prior to cryopreservation.
  • MH: Mild Hypothermia; 33-35ºC.
  • MI: Myocardial Infarction.
  • MRI: Magnetic Resonance Imaging.
  • MSOF: Multiple System Organ Failure.
  • MW: Molecular Weight.
  • Neuro: A type of patient for which only the head is stored.
  • NMR: Nuclear Magnetic Resonance.
  • O2: Oxygen.
  • Patient: A cadaver under the custody of a cryonics organization.
  • Perfuse: Infuse an organ or system with a fluid, in the case of cryonics, Cryoprotectant solutions.
  • Perfusate: The solution that is used for perfusion.
  • SAH: Subarachnoid Hemorrhage.
  • SCA: Sudden Cardiac Arrest.
  • Tg: The glass transition temperature.
  • PIB: Portable Ice Bath.
  • Whole Body: A type of patient for which the whole body is cryopreserved and stored.
  • WBE: Whole Brain Emulation.

People

See Also

Resources

Links

Video

Audio

References

  1. 1.0 1.1 A visit to alcor
  2. Ben Best. The Permafrost Papers. Link.
  3. http://www.cryocdn.org/perma.html#mypci
  4. Link.
  5. Hope on Ice. LA Times Magazine, January 2010. Link.
  6. Freeze-Drying Biological Specimens: A Laboratory Manual
  7. http://issuu.com/alcorlife/docs
  8. http://www.cryonics.org/resources/long-life-magazine

External links