Dr Abdul Ghani (Langkawi) asked me about what we do with PRS (platelet-rich serum) at USM in Facebook so many days ago. I didn't have the time and chance to go to Blood Bank to ask but the opportunity came today. I arrived early at my department today and left my bags, book and rattan basket in my office and quickly walked over to Blood Bank which is next door. I have to do this quickly because after this I need to run to the mini post-office (opens at 9 am) to mail my book (Research on the Early Malay Doctors) to friends.
This is information about Blood Bank and the contact person. Blood Bank is also running a program to collect blood before the monsoon season comes. I talked to Mr Saw Teik Hock (JTMP) who also managed and cross-checked my blood for my first surgery 28 years ago. He's a great friend.
Unit Perubatan Transfusi (Tabung Darah)
Waktu Urusan:
Ahad-Rabu: 8.10 pg - 4.40 ptg
Khamis: 8.10 pg - 4.40 ptg
Rehat: 1 pm - 2 pm
Jumaat-Sabtu & Cuti Am: Tutup
Mr Saw Teik Hock (JTMP)
Technical Manager ISO
Blood Bank HUSM
thsaw@kb.usm.my
Tel: 09-760 3337
Assoc Prof Dr Rosline Hassan
HOD Hematology & Blood Bank HUSM
http://www.medic.usm.my/hematology/
http://www.medic.usm.my/hematology/index.php/our-people/lect/rosline
According to Mr Saw Teik Hock, Blood Bank HUSM fractionates and obtains platelet-rich plasma. However, platelet-rich plasma is voluminous (big volume, banyak) and therefore it needs to be reduced (volume-wise) and the Blood Bank hence spins (centrifuges) it and collects and stores the platelet concentrate for use in patients. There is a big need for platelet concentrate and it is used for many types of patients, including orthopedic patients, where the platelet concentrate is applied (injected) to the painful joint. There was previously a research project done on platelets by Dr Wong (please Google him). However, the project was discontinued due to strict ethical procedures later implemented by USM, whereby downstream stuff from patients cannot be used for research unless the blood donors/patients themselves initially approved of such research. However, researchers can reapply for ethical approval to continue their former research with the Blood Bank. Dr Wong will be continuing his research on platelets with prior approval of the USM ethics committee. USM has a special research committee that looks at clinical research and use of patients' products (stuffs that are obtained from patients including blood & blood products, teeth, bones, etc). Mr Saw Teik Hock advised that the best way to go about platelet testing and research is to write to the Head of Department (HOD), Assoc Prof Dr Rosline Hassan. Potential researchers can always write to him regarding the Blood Bank and everything that's connected. I guess this bit of information helps everyone who is looking forward to platelet research. The Blood Bank also has stem cells - please visit the website to find out more.
I will disappear to the mini post-office now.
Showing posts with label stem cells. Show all posts
Showing posts with label stem cells. Show all posts
Sunday, 4 November 2012
Monday, 30 January 2012
Stem Cells
If you cut a stem and take a close look at the cut surface, you will get to see cells! True? Yes!
What are stem cells?
Where can we get them?
Why are they called stem cells?
What is special about stem cells?
What can we do about stem cells? Are they good for anything?
Are they good for something? Yes? Yes!
Give examples for uses of stem cells.
How do we obtain them?
How do we store them?
How do we use them?
How stable are stem cells?
How safe are stem cells?
Can stem cells be killer cells?
If there is a faulty gene in a stem cell, and that gene gets replicated as we let the cells multiply, and we then administer the stem cells into a human body. What will happen?
If we create a mutation gene that can kill a particular bacteria or virus, and we insert that gene in a stem cell. What do you think will happen if we now take the stem cell with a mutation and insert it in a cancer cell? Will our stem cell be of any good?
If we have a patient with a difficult-to-cure disease and we decide to administer a stem cell with a good gene that can help the patient combat the disease and continue to live normally, will stem cells be appropriate or inappropriate?
More on stem cells
What are stem cells?
Where can we get them?
Why are they called stem cells?
What is special about stem cells?
What can we do about stem cells? Are they good for anything?
Are they good for something? Yes? Yes!
Give examples for uses of stem cells.
How do we obtain them?
How do we store them?
How do we use them?
How stable are stem cells?
How safe are stem cells?
Can stem cells be killer cells?
If there is a faulty gene in a stem cell, and that gene gets replicated as we let the cells multiply, and we then administer the stem cells into a human body. What will happen?
If we create a mutation gene that can kill a particular bacteria or virus, and we insert that gene in a stem cell. What do you think will happen if we now take the stem cell with a mutation and insert it in a cancer cell? Will our stem cell be of any good?
If we have a patient with a difficult-to-cure disease and we decide to administer a stem cell with a good gene that can help the patient combat the disease and continue to live normally, will stem cells be appropriate or inappropriate?
More on stem cells
Labels:
stem cells
Friday, 1 July 2011
Pre-implantation Genetic Diagnosis (PGD)
"Death is not the opposite of life. Life has no opposite. The opposite of death is birth. Life is eternal."
~Eckhart Tolle
Since nobody or no parent wants a defective child, how do we obtain 100% perfect babies? By doing pre-implantation genetic diagnosis (PGD). It means we carefully plan which genes should go into a baby which we researchers will design for a couple, so that the newborn designer baby becomes the source of cure for its own older siblings. In designing babies, we are actually selecting good genes which do not have any defects, so that the newborns are supposedly healthy and normal, not sick or with the same genetic disease(s) of their siblings.
We have a big problem with patients suffering from various difficult-to-cure diseases and the potential of research which we can do to help such patients. Since Watson and Crick first built their double-stranded helix DNA model in 1953, we are plunged into deeper and bigger grey areas where ethics rules all judgment and we still have conscience about trespassing them when we know about the potential of DNA and stem cell for curing such difficult hard-to-cure diseases caused by DNA mutations which are life-long and without a simple straight forward cure at this time. We may think we live in a first world, or even a make-belief first world, but when we have a life-long disease at hand to worry about its cure or find a cure, then we have to know whether to pitch on safe grounds or pitch in the grey zone and wait for the critics to lash their laser-sharp tongues! Researchers and medical students alike must know what is right and what is wrong in medical practice and research concerning such issues, and be able to weigh the benefits of what critics consider bad against what researchers consider "not too bad", "may work somewhat", or "could work and then fail but worth trying".
A good example of tough decision-making is to consider "designer babies", a term favourably used to describe how babies are precisely designed and engineered in the research lab, so as not to contain genetic errors, so that these babies can become "saviour babies" when they are born. Their cord blood is highly prized for harvesting stem cells for use in curing hard-to-cure life-long diseases of their own older siblings who are still toddlers or pre-schoolers. Is designing such babies ethically right or wrong? Are doctors and researchers wrong and must they be held accountable if they try to find a cure for the impossible? Blunders are synonymous with research. Two patients who received genetic therapy died from leukaemia. Whom do we blame? The doctors & researchers who intervened, the patients or their parents? Since we can't depend on gene therapy, the only avenue we have now is stem cell extracted from cord blood of designer babies and from the bone marrow of the long bones. What are the long bones in our body? How are stem cells extracted from the bone marrow?
An analogy is we didn't have penicillin prior to WWII. Was it fortuitous to discover this drug? If we don't try, we will never know the worth of a cure for any difficult disease. It is therefore best to leave such delicate decision-making in the hands of experts. This means experts must also have at least some basic knowledge before they can make a good decision.
As a researcher, I would like to qualify that there must be an active watch dog committee that truly understands and studies every decision that researchers and scientists do today. The grey zone in this type of research is merging and overlapping with clear areas and can possibly turn what is already clearly wrong to be the best research option we have and therefore the right thing to do, and the next course of action. Blinding the lay public must never be allowed loose. The public must know what research is trying to do and achieve. New medical students must know. Issues in medical research today are life-and-death issues. Diseases today are life-threatening and life-long but the cures are hidden somewhere on earth. Too many people suffer and die in sheer agony when we try to slow down research as we allow such ethical issues to be ironed out in our courts. Stem cells have helped overcome diseased blood vessels. Next in the pipeline is stem cells for glaucoma, in trying to stem blindness.
Prof Faridah
Viewpoints on PGD from fiqhmedic.wordpress.com. Covers "hukum".
~Eckhart Tolle
Since nobody or no parent wants a defective child, how do we obtain 100% perfect babies? By doing pre-implantation genetic diagnosis (PGD). It means we carefully plan which genes should go into a baby which we researchers will design for a couple, so that the newborn designer baby becomes the source of cure for its own older siblings. In designing babies, we are actually selecting good genes which do not have any defects, so that the newborns are supposedly healthy and normal, not sick or with the same genetic disease(s) of their siblings.
We have a big problem with patients suffering from various difficult-to-cure diseases and the potential of research which we can do to help such patients. Since Watson and Crick first built their double-stranded helix DNA model in 1953, we are plunged into deeper and bigger grey areas where ethics rules all judgment and we still have conscience about trespassing them when we know about the potential of DNA and stem cell for curing such difficult hard-to-cure diseases caused by DNA mutations which are life-long and without a simple straight forward cure at this time. We may think we live in a first world, or even a make-belief first world, but when we have a life-long disease at hand to worry about its cure or find a cure, then we have to know whether to pitch on safe grounds or pitch in the grey zone and wait for the critics to lash their laser-sharp tongues! Researchers and medical students alike must know what is right and what is wrong in medical practice and research concerning such issues, and be able to weigh the benefits of what critics consider bad against what researchers consider "not too bad", "may work somewhat", or "could work and then fail but worth trying".
A good example of tough decision-making is to consider "designer babies", a term favourably used to describe how babies are precisely designed and engineered in the research lab, so as not to contain genetic errors, so that these babies can become "saviour babies" when they are born. Their cord blood is highly prized for harvesting stem cells for use in curing hard-to-cure life-long diseases of their own older siblings who are still toddlers or pre-schoolers. Is designing such babies ethically right or wrong? Are doctors and researchers wrong and must they be held accountable if they try to find a cure for the impossible? Blunders are synonymous with research. Two patients who received genetic therapy died from leukaemia. Whom do we blame? The doctors & researchers who intervened, the patients or their parents? Since we can't depend on gene therapy, the only avenue we have now is stem cell extracted from cord blood of designer babies and from the bone marrow of the long bones. What are the long bones in our body? How are stem cells extracted from the bone marrow?
An analogy is we didn't have penicillin prior to WWII. Was it fortuitous to discover this drug? If we don't try, we will never know the worth of a cure for any difficult disease. It is therefore best to leave such delicate decision-making in the hands of experts. This means experts must also have at least some basic knowledge before they can make a good decision.
As a researcher, I would like to qualify that there must be an active watch dog committee that truly understands and studies every decision that researchers and scientists do today. The grey zone in this type of research is merging and overlapping with clear areas and can possibly turn what is already clearly wrong to be the best research option we have and therefore the right thing to do, and the next course of action. Blinding the lay public must never be allowed loose. The public must know what research is trying to do and achieve. New medical students must know. Issues in medical research today are life-and-death issues. Diseases today are life-threatening and life-long but the cures are hidden somewhere on earth. Too many people suffer and die in sheer agony when we try to slow down research as we allow such ethical issues to be ironed out in our courts. Stem cells have helped overcome diseased blood vessels. Next in the pipeline is stem cells for glaucoma, in trying to stem blindness.
Prof Faridah
Viewpoints on PGD from fiqhmedic.wordpress.com. Covers "hukum".
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