Cancer treatment with Nanoparticles
As mentioned above, nanoparticles are crucial to cancer treatment. In my opinion anyone who is not using nanoparticles is incompetent. We have known since the early 70's nanoparticles were vital for cancer management, in those days they called nanoparticles the magic bullet because they can target all cancer specifically and they promised they would be in use in ten years, the same old thing they always say.
Now, 43 years later, who is using nanoparticles for cancer treatment? I don't mean researching them, I mean actually using them.
The reason nanoparticles are SO important for cancer is simple.. you put the medication in the nanoparticles and inject them into the blood. You know food and nutrients penetrate the blood vessels, right? That is how all food and oxygen get to the cells. But nanoparticles are TOO BIG to get out of normal vessels.
So what happens is normal tissue never sees the nanoparticles or the medication inside them. When the nanoparticles find cancer it is a different story. Cancer, like all scar tissue, builds leaky vasculature the space between the arteries and veins cells is greater and larger things can get out, so the nanoparticles flood into the cancer eagerly. When the nanoparticles are perfectly designed, they have a positive charge which causes cancer to pull them in like a star trek tractor beam and when the cancer tastes them, OUR nanoparticles taste like sugar.
Cancer does not build lymph vessels, which are what removes things from the body, hence the term leaky vasculature limited lymphatic perfusion trap the term used to describe the method by which nanoparticles target cancer.
Most photosensitizers are only 3 to 6.8 X selective, that is to say they only go into cancer 6.8 times more than normal tissue. This is why nobody else can treat deep metastatic cancer, because the normal tissue would be damaged.
Our sensitizer is 85 X selective, which is a massive improvement that nobody else can come close to. As you can see in several places on this site, thanks to our nanoparticle technology we can treat down to the center of the brain, treating kidneys and colons is not a problem.
When you are looking for alternative cancer treatment, always put a high importance on nanoparticles designed to treat cancer.
Photodynamic Therapy for Cancer treatment with Nanomolecules
It is important to understand what nanoparticles do for cancer treatment when used with photodynamic therapy. As I mentioned above, sensitizers which are not in a nanomolecule spread all over the body, like chemo, so without the nanomolecules the cancer only takes up maybe at best 7 times as much medicine as normal cells. Photofrin, also known as hematophorphyrin is only 3X selective and most Chlorin is 4-5X selective, which is why it does to much damage to healthy tissues.
This has three major effects.
- First, without the nanoparticles the cancer does not get as much sensitizer, because it is going into normal tissue throughout the body.
- The second effect is that the normal cells are subject to damage caused by the laser, but with the nanoparticles cancer has 85 times as much medicine as normal cells.
- The third effect is a little more complicated, it is called self shielding. The medicine called a photosensitizer absorbs the laser light very fast, so if you are trying to use photodynamic therapy to treat say a tumor or tumors in the brain, the sensitizer in the skin and skull and normal brain absorb most of the light before it gets to the tumor and the treatment is a failure.
When the sensitizer for photodynamic therapy is in a nanoparticle, there is very little sensitizer in normal tissue, so we can penetrate down to the center of the brain and deep into the body. When a nanoparticle is not used, there is no hope of getting deep into the body.
As far as I know, and I do keep up on what everyone in the world is doing, we are the only group that has created a nanoparticle encased sensitizer for cancer treatment, which explains why we get much better results than anyone else.
When you are trying to evaluate a photodynamic therapy provider, you need to understand a few things to keep from making a big mistake.
First, some wavelengths of light, colors in laymans terms, penetrate better than others. The sensitizer that is used determines the wavelength necessary. There are several different sensitizer and they are vastly different in success.
If a provider offers therapy without giving the specific sensitizer name and the wavelength of light, avoid them like the plague, they are trying to cover something up. If they say they are using Photofrin, also called hematoporphyrin, or PPIX (protoporhyrin nine) or ALA, their wavelength is 635 nm (sort of orangish red) and they can never penetrate more than one cm into normal tissue and .3 cm into tumor, so they are pretty worthless.
The next one you will encounter is slightly better, it is called chlorin e6. There are several derivatives and compounds of this but they all are activated by 660 nm, a normal red color and they can at best penetrate 3 cm into the body and .8 cm into tumors, so this one is ok for skin cancers and basal cell carcinoma, in short anything that is on top of the skin, but cannot treat deep tumors or metastic cancer.
We use a very pure form of phthalocyanine photosensitizer, because it is the most powerful in the world but we are the only ones who can make it in a pure form.
There are others using phthalocyanine base, but their product is an impure mix of different drugs, some of which are worthless and some of which are dangerous. We are the only group using a mix of only disulfonate and trisulfonate, because nobody else knows how to do it. (patent pending) Consequently they use 672 nm wavelength, which while is is better than chlorine e6 has limited penetration.
Due to our unique molecule and the nanoparticle formulation and the purity and research we have done on intracellular absorption spectra of our molecule, we use 685 nm, which is a very deep red on the edge of infrared invisible. It is perfect, no other wavelength works as well.
The main thing you need to know is what is the exact wavelength of the light produced by their lasers. For success you need 685 nm the smaller the number is the less effective it is until you get down to 635 nm which is essentially worthless.
Then you need to know how selective their uptake is.. everyone else in the world is between 3 and 6.8 times as much sensitizer in the cancer as in normal tissue.
If they are not using nanoparticles that is the best they can do and it is not good enough for serious cancer work. As I said, we are the only ones actually using nanomolecules and we get results the other only wish they could get.
Be aware, there are research papers on this site discussing various nanomolecules, none of them cover what we are doing, and on their own without our improvements they are relatively ineffective.