Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Friday, January 22, 2021

Rutin phospholipid complexes confer neuroprotection in ischemic-stroke rats

Did your stroke hospital contact researchers to get this research going in humans? Once again there is that milquetoast word, 'neuroproection'  giving no sense of the immediate need to have it solved. It should be the neuronal cascade of death.

So when your doctor tells you they did nothing to stop the neuronal cascade of death, you can start screaming at them.

Do you prefer your hospital  incompetence NOT KNOWING? OR NOT DOING?

Rutin phospholipid complexes confer neuroprotection in ischemic-stroke rats

The title should be 'Rutin phospholipid complexes solved one of the pieces of the neuronal cascade of death in ischemic-stroke rats.' Which directly leads to; what other pieces need solving? And with proper followup we might actually get somewhere in solving stroke.

Abstract

Rutin, a natural flavonol glycoside is known to possess significant radical scavenging properties which might have beneficial effects in cerebral ischemia. However its oral administration and pharmaceutical use is limited due to its poor aqueous solubility and bioavailability. The current investigation aimed at development of rutin–phospholipid complexes (Ru–PLC's) and its characterization to provide neuro-protective effects in brain injury following stroke. Ru–PLC's were successfully fabricated and findings demonstrated improvement in bio-pharmaceutical properties on the basis of solubility, partition coefficient, dissolution profile, morphology, zeta potential, physical stability, FT-IR, DSC-TGA, forced degradation, photolytic degradation, ROS detection and oral pharmacokinetic studies. Ru–PLC's considerably improved functional outcomes in experimental stroke (MCAO model in rats) at a dose less than half of the effective dose of rutin. Effectiveness of treatment as evident from pharmaceutical properties as well as therapeutic activity was of the following order: Ru–EPLC > Ru–TPLC > rutin.

Graphical abstract: Rutin phospholipid complexes confer neuro-protection in ischemic-stroke rats
 

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