The reality is that H A injections alone can only help a limited amount of specific and direct joint issues. Generally only those related strictly to the synovial fluid (lubricating fluid).
It is important to understand HOW the non-oral (ie. pure liquid) version of Hyaluronic Acid (HA) is used: when a doctor uses it, they INJECT.
Notice: most HA injections are done IA (intra-articular – directly in the afflicted joint), rather than IM (intramuscular - directly in the muscle) or IV (intravenous – directly in the blood stream).
Positive results are less likely IV, and nearly impossible IM. It's been proven scientifically, tested both in the field and clinically over the last 20+ years.
So, what about oral HA then?
CONSIDER: If it's known to be significantly less effective when directly injected into the body via IM and IV, one must rationally ask: "How can HA effectively get to the joint going through the digestive tract?"
Also, molecularly, HA is absolutely larger than Chondroitin Sulphate (CS), which science has proven only 8 to 10% of the CS can make it into the blood stream. So, the next question is: "How much oral HA do you think actually gets into the system?"
These aren't new questions, with oral HA studies occurring the last 6 to 30 years by third parties have consistently shown only about 5% can be found to be absorbed 'in the body' with the majority of that mere 5% being found in the bone marrow and spinal column, and just a fractional amount in the synovial fluids. Over 90% of the oral HA passes through the system and is found in the poop in less than 24 hours. That makes some dang expensive manure!
Two of the most interesting studies were done by Wieder Int'l - one on rats, another on beagles (dogs) the results of both were consistent in what amount of radio tagged materials passed through the body, and where the small amount that was absorbed was found (the majority (over 95%) never made it to the joints).
Interestingly, the majority of the professionals that have actually paid attention to the science inject directly INTO THE JOINT to have a direct and real impact on the synovial fluid of that joint. They do not use Oral HA to treat anything! As they know that if it doesn't get to the joints from an IM or IV, it's really not going to do it through the digestive tract.
Oral HA (Hyaluronic acid, which is also known as hyaluronate, also called hyaluronan, and is an anionic, nonsulfated glycosaminoglycan), may be an effective painkiller, for a time.
Yet, in reality, injecting directly IN THE JOINT is the most challenging, dangerous, for a variety of reasons (especially for Equine Vets). But that is exactly where 99.9% of the H A injections occur by the professionals. Not directly into the blood stream which is safer, and not in the muscle which is so much faster and easier... and more effective systemically, with most 'medicines,' but that is not how HA injections are given. Which should give all thinking people some pause, when the professionals won't administer it systemically... at a higher risk.
Then, when science shows the ingredients (the HA) doesn't survive, and isn't properly broke down or readily absorbed through the digestive tract, with the vast majority ending up in the poop (up wards of 90%)... the little bit that was 'taken up' was actually found in the spinal column and brain stem, one should wonder just exactly what it does in the body. It would stand to reason that it should be able to help all joint tissues in the body when injected directly into the blood stream... yet it doesn't. Therefore, it's not administered that way by the trained professionals.
Also, HA is made from rooster combs and bovine eyeballs... while natural to the mammals body, it is a non-native form (foreign to the body) not ‘designed’ for 'food stuff.'
Excerpt from the review summary- "…dietary supplements containing HA are not equivalent due to the inherent properties of the three major types of HA commercially available as dietary supplement materials. Consumers and health care professionals need to be aware of the different types of HA and their very large differences in properties (even before ingestion). One source, hydrolyzed chicken sternal cartilage, is clearly unlike native HA it does not match the real biological properties of native HA and consequently should not be represented as HA to consumers on product labels..." yet supplement manufacturers regularly use this type of 'HA' for oral application, many [marketing mavens] claiming it's a 'miracle.' At best, a smaller percentage might be actually used, but not by the actual joints, and upwards of 95% still passes through the body (unused)."
Again, upon evaluation of WHERE the little bit that remained in the body was actually found (the spinal column and brain stem), it's highly likely, though unsubstantiated, that the effects tend to lean toward Cox-2 inhibitors (pain blockers and maskers - similar to what Vioxx did, before it was pulled from the human market). Oral HA is positively NOT 'building blocks' or nutrients otherwise considered 'healing promoters' (or agents) regardless.
Further, HA is also a major component of skin, where it is involved in tissue repair. When skin is exposed to excessive UV-B rays, it becomes inflamed (sunburned) and the cells in the dermis stop producing as much hyaluronan, and increase the rate of its degradation. Hyaluronan degradation products then accumulate in the skin after UV exposure. Sounds good, right? Well, read on...
Another important scientific note: HA is also a component of the group A streptococcal extracellular capsule, and is believed to play a role in virulence. (that came from a peer reviewed study. Just wrap your head around that one).
Hyaluronic acid is, thus, often used as a tumor marker for prostate and breast cancer. And has been suspected since the turn of the century, but known since 2009, when the peer reviewed study was published. HA levels are also be used to monitor the progression of the disease [certain types of cancer].
"In some cancers, hyaluronic acid levels correlate well with malignancy and poor prognosis. It is important to note that the various types of molecules that interact with hyaluronan can contribute to many of the stages of cancer metastasis, i.e. further the spread of cancer. HA synthases (HAS) play roles in all of the stages of cancer metastasis. By producing anti-adhesive HA, HAS can allow tumor cells to release from the primary tumor mass, and if HA associates with receptors such as CD 44, the activation of Rho GT Pases can promote epithelial-mesenchymal transition (EMT) of the cancer cells.
During the processes of intravasation or extravasation, the interaction of HAS produced HA with receptors such as CD 44 or RHAMM promote the cell changes that allow for the cancer cells to infiltrate the vascular or lymphatic systems. While traveling in these systems, HA produced by HAS protects the cancer cell from physical damage. Finally, in the formation of a metastatic lesion, HAS produces HA to allow the cancer cell to interact with native cells at the secondary site and to produce a tumor for itself;"
(Bharadwaj AG, Kovar JL, Loughman E, Elowsky C, Oakley GG, Simpson MA (2009). "Spontaneous metastasis of prostate cancer is promoted by excess hyaluronan synthesis and processing". Am. J. Pathol. 174 (3): 1027–36. PMC 2665762 Freely accessible. PMID 19218337. doi:10.2353/ajpath.2009.080501)