Oral Use of BPC and KPV

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Rock Solid1

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Has anyone here personally tried BPC and/or KPV by mouth instead of subq, and how well did oral delivery work for them? My goal is lowering gut inflammation, and based on what I've come across so far, it looks like these 2 peptides "may" do the job when swallowed.

Peptide wiki has this to say about KPV: "Most peptides are large molecules that are rapidly destroyed by stomach acid and digestive proteases. KPV is only 3 amino acids — one of the smallest bioactive peptides in use. This tiny size may provide partial resistance to enzymatic degradation, allowing enough intact KPV to reach the intestinal lining. For gut inflammation specifically, even partial survival through the GI tract is advantageous because the target tissue (intestinal mucosa) is in direct contact with the oral dose. This is why oral KPV is most effective for gut conditions and less reliable for systemic targets."
 
Rock Solid1 said:

Has anyone here personally tried BPC and/or KPV by mouth instead of subq, and how well did oral delivery work for them? My goal is lowering gut inflammation, and based on what I've come across so far, it looks like these 2 peptides "may" do the job when swallowed.

Peptide wiki has this to say about KPV: "Most peptides are large molecules that are rapidly destroyed by stomach acid and digestive proteases. KPV is only 3 amino acids — one of the smallest bioactive peptides in use. This tiny size may provide partial resistance to enzymatic degradation, allowing enough intact KPV to reach the intestinal lining. For gut inflammation specifically, even partial survival through the GI tract is advantageous because the target tissue (intestinal mucosa) is in direct contact with the oral dose. This is why oral KPV is most effective for gut conditions and less reliable for systemic targets."
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For 1 month I used a BPC/KPV pill, and it worked for me. GLOW is something I have injected too. The injections hit much quicker, yet my injury still felt improved from the pill. The main problem with oral use was that the injury appeared to return afterward. My suggestion would be to run it longer so the problem is fully addressed. A 5 days on, 2 days off schedule could allow more extended use, though with oral dosing I am unsure whether that is necessary.
 
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