Janoshik Analytical laboratory testing services

@janoshik There's someone selling a DHT gel at a claimed concentration that shouldn't be possible. It's dissolved in ethanol with some sfa esters/essential oils added. Is it possible to do a Common AAS Screening Quantitative but including DHT (in case it doesnt actually contain DHT but eg. T)?
 
Jano, back in days, you were involved with the GH testing project on the PM board.

If I recall correctly, you were able to classify different types of impurities of GH, based on the location of secondary and tertiary peaks on the x-axis of the chromatogram.

Would it be possible to do a similar classification of GH impurities on some of the largest sources of today?

This would be an invaluable service to the community, since there appear to be distinct side-effect profiles for GH products from different sources, despite them scoring similarly in terms of purity and dimer content.
 
Jano, back in days, you were involved with the GH testing project on the PM board.

If I recall correctly, you were able to classify different types of impurities of GH, based on the location of secondary and tertiary peaks on the x-axis of the chromatogram.

Would it be possible to do a similar classification of GH impurities on some of the largest sources of today?

This would be an invaluable service to the community, since there appear to be distinct side-effect profiles for GH products from different sources, despite them scoring similarly in terms of purity and dimer content.

I think you guys are going down the wrong path on this.

The idea that there are "impurities" of some sort contaminating HGH, which trigger the same set of side effects that have been constant since pharma extracted GH from corpses, became LESS common with the advent of synthetic GH (and increasingly rare as excipient formulations were improved), then increased again with UGL production points to some other, common factor between natural. pharma, and UGL HGH.

I believe the side effects are an immune response. The primary suspect are aggregates, which have been proven to induce growth hormone antibodies. These aggregates are a characteristic of the GH of elderly patients (and probably post death degradation), pharma, and UGL HGH.

The difference is that pharma is conscious of aggregation and the immunogenicity it can induce. Among other things, excipient formulation and packaging is designed to minimize this from happening. They test for aggregation.

Does UGL? Doubtful.

Below is a study of several pharma HGH formulations published by the Journal of Pharmaceutical Science, subjected to stress to speed the formulation of aggregates (agitation, freeze/thaw, etc). The aggregates are characterized, and immune response in animals is measured.

(it's interesting to note how
wildly the different pharma formulations differ in their effectiveness at suppressing aggregation)

TLDR: The more aggregates present, the stronger the immune response, and the higher likelihood of side effects like edema.

(it's more complicated than that, as some aggregates don't induce a response, but in general, the fewer aggregates the fewer antibodies are produced.)

Like IGF blood testing is a proxy for HGH quality, it might be more productive to have users get a Growth Hormone Antibody blood test at a certain amount of time post administration. This is commonly available at the usual labs. Quest, etc. Researchers cannot intentionally inject healthy human subjects with bad HGH loaded with aggregates, but the PED community does, inadvertently.



I will add, in my own informal tests, Tesamorelin. notorious for aggregate formation and antidrug antibody formation, exhibits significantly reduced site reactions (PIP, redness) and other side effects with some of the filtration techniques used to reduce aggregates prior to injection. The difference is dramatic and the effect absolutely not psychosomatic.
 
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I think you guys are going down the wrong path on this.

The idea that there are "impurities" of some sort contaminating HGH, which trigger the same set of side effects that have been constant since pharma extracted GH from corpses, became LESS common with the advent of synthetic GH (and increasingly rare as excipient formulations were improved), then increased again with UGL production points to some other, common factor between natural. pharma, and UGL HGH.

I believe the side effects are an immune response. The primary suspect are aggregates, which have been proven to induce growth hormone antibodies. These aggregates are a characteristic of the GH of elderly patients (and probably post death degradation), pharma, and UGL HGH.

The difference is that pharma is conscious of aggregation and the immunogenicity it can induce. Among other things, excipient formulation and packaging is designed to minimize this from happening. They test for aggregation.

Does UGL? Doubtful.

Below is a study of several pharma HGH formulations published by the Journal of Pharmaceutical Science, subjected to stress to speed the formulation of aggregates (agitation, freeze/thaw, etc). The aggregates are characterized, and immune response in animals is measured.

(it's interesting to note how
wildly the different pharma formulations differ in their effectiveness at suppressing aggregation)

TLDR: The more aggregates present, the stronger the immune response, and the higher likelihood of side effects like edema.

(it's more complicated than that, as some aggregates don't induce a response, but in general, the fewer aggregates the fewer antibodies are produced.)

Like IGF blood testing is a proxy for HGH quality, it might be more productive to have users get a Growth Hormone Antibody blood test at a certain amount of time post administration. This is commonly available at the usual labs. Quest, etc. Researchers cannot intentionally inject healthy human subjects with bad HGH loaded with aggregates, but the PED community does, inadvertently.



I will add, in my own informal tests, Tesamorelin. notorious for aggregate formation and antidrug antibody formation, exhibits significantly reduced site reactions (PIP, redness) and other side effects with some of the filtration techniques used to reduce aggregates prior to injection. The difference is dramatic and the effect absolutely not psychosomatic.
You are out of your depth on this one. Aggregation in GH is not a problem nowadays, most GH is testing with either very little or no dimer or higher order aggregates. Much less than it was 5-10 years ago. Also the side effects often reported are not consistent with immunogenicity.
 
You are out of your depth on this one. Aggregation in GH is not a problem nowadays, most GH is testing with either very little or no dimer or higher order aggregates. Much less than it was 5-10 years ago. Also the side effects often reported are not consistent with immunogenicity.

What? "Higher order aggregation in GH is no longer a problem"? Where does that come from? No protein is immune from aggregation. I can SEE HGH form aggregates in the visible range, above 100um, on vial walls by leaving it at room temperature for a few days.

What has happened since 2023 to make their formation post reconstitution a non-issue? You can't even control for PH with UGL HGH, because of the wide variety of solutions used to reconstitute, unlike pharma which either comes prepared or supplied with BAC or Sterile water.


In reference to Somatropin:

IMG_9170.webp

Edema is not an immune response? Who are you trying to gaslight? "Water retention", the most COMMON HGH side effect, is absolutely an immune response. Antigens cause cells to absorb water. How do you not know this?

No, let's attribute the same set of UGL sides that are listed on the side of a Somatropin box to some mystery impurity unique to UGL HGH, and not simply a problem caused by the one glaring difference in pharma and UGL quality metrics the producers pay attention to, post reconstitution aggregate formation..
 
Is edema caused by cells absorbing water, or cells not absorbing water leading to fluid accumulation extracellularly

Let me correct that point, I was conflating two different immune responses.

The immune response that causes swelling/water retention involves small blood vessels becoming more permeable to allow immune cells to pass through more easily, which also allows water to escape.

Somewhat similar to the edema side effect of many blood pressure meds, though that's caused by a rise in capillary pressure forcing the water out, rather than them becoming more permeable.
 
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