GrymReefer
Bluelight Crew
Your probably reading that title thinking, “What in the hell is this rambling bastard going on about now?” Especially since I mentioned oxyandrolone and injections within the same sentence. However, if one possessed a viable depot that was appropriately dosed per ml then you may be in for a surprise. This isn't a discussion about the synthesis or procedures taken to create an oxyandrolone injectable form for personal usage. That is an unfruitful conversation.
However many may not realize that the pharmacokinetics of oxandrolone. Its rate of absorption is solely dictated by the route of administration. This means that a subcutaneous/I.M injection would be superior than the unnecessary ingestion of a large quantity of tablets day in and day out. It would also allow a more stable blood plasma level and possibly alleviate associated side effects that are concurrent with spastic serum spikes.
K) PHARMACOKINETICS
1) Duration of action depends on the formulation and route
of ingestion. Testosterone gel usually lasts 24 to 48
hours while the cypionate and enanthate esters have
durations for up to 4 weeks after an intramuscular
injection. Transdermal absorption is approximately 10%
of an applied dose. Testosterone is 98% protein bound
to both sex hormone-binding globulin and albumin. There
is hepatic metabolism of anabolic steroids, and the
half life of elimination can vary from 10 minutes to
weeks. Excretion is primarily through the urine (90%
with some minor fecal excretion as well.
Just food for thought, but a more stable blood plasma level would be more friendly for those who love oxyandrolone's mechanics, but cannot tolerate the obnoxious acceptance of behemoth amounts of pills needed to achieve desired results.
Now from my knowledge a subcutaneous injection would be the more favorable form of injection. This being that injection into adipose tissue renders the depot being held to a fixed absorption rate due to the feasible amount of cells it interacts with at a given period of time. You can increase the volume of the depot, but the return of increase to absorption rate is small and generally more pain than pleasure.
BUT!! you can increase the absorption rate by splitting the allocated dose between different injection sites which would allow a higher absorption rate and a higher blood plasma level peak that would then slowly taper down due to the nature of its interaction. No matter what though you will also far surpass the malabsorption tendency that plaques oral consumption.
Source- http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+3373
However many may not realize that the pharmacokinetics of oxandrolone. Its rate of absorption is solely dictated by the route of administration. This means that a subcutaneous/I.M injection would be superior than the unnecessary ingestion of a large quantity of tablets day in and day out. It would also allow a more stable blood plasma level and possibly alleviate associated side effects that are concurrent with spastic serum spikes.
K) PHARMACOKINETICS
1) Duration of action depends on the formulation and route
of ingestion. Testosterone gel usually lasts 24 to 48
hours while the cypionate and enanthate esters have
durations for up to 4 weeks after an intramuscular
injection. Transdermal absorption is approximately 10%
of an applied dose. Testosterone is 98% protein bound
to both sex hormone-binding globulin and albumin. There
is hepatic metabolism of anabolic steroids, and the
half life of elimination can vary from 10 minutes to
weeks. Excretion is primarily through the urine (90%
with some minor fecal excretion as well.
Just food for thought, but a more stable blood plasma level would be more friendly for those who love oxyandrolone's mechanics, but cannot tolerate the obnoxious acceptance of behemoth amounts of pills needed to achieve desired results.
Now from my knowledge a subcutaneous injection would be the more favorable form of injection. This being that injection into adipose tissue renders the depot being held to a fixed absorption rate due to the feasible amount of cells it interacts with at a given period of time. You can increase the volume of the depot, but the return of increase to absorption rate is small and generally more pain than pleasure.
BUT!! you can increase the absorption rate by splitting the allocated dose between different injection sites which would allow a higher absorption rate and a higher blood plasma level peak that would then slowly taper down due to the nature of its interaction. No matter what though you will also far surpass the malabsorption tendency that plaques oral consumption.
Source- http://toxnet.nlm.nih.gov/cgi-bin/sis/search/a?dbs+hsdb:@term+@DOCNO+3373