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SARMs represent an alternative to the currently available oral testosterone preparations, and offer the user molecules that exhibit high oral bioavailability without the liver toxicityassociated with oral steroids. SARMs (steroid-releasing hormone) present a low lipogenicity and lack the liver toxicities of testosterone. The current FDA-approved testosterone formulations are HRT (short-acting hormone replacement) and HRT/testosterone cypionate (hRTC) (Table 1). Most of these formulations can provide up to 150 μM testosterone but the mean testosterone concentrations vary, from 300 nmol/L at HRT to 1.3 μM in the cypionate formulations (Table 1).In the present invention, a method of orally administering testosterone is provided. The method comprises using a testosterone capsule for administration, and a carrier such as propylene glycol (in the form of an alcohol-containing ester). In particular, the method comprises administering a testosterone gel for administration, preferably for 5 days, to a subject via an oral route. The method further comprise administering an injectable testosterone capsule and a carrier such as a pharmaceutical formulation. In particular the method comprises administering an injectable testosterone gel such as 2.5 mL of an injectible testosterone gel such as 2.5 mL testosterone gel and a carrier such as a pharmaceutical formulation. In particular the method comprises administering an injectable testosterone capsule and prescribing an amount of testosterone.The present invention further provides a product that is prepared by mixing a testosterone solution (e.g., 100 μL testosterone gel, 10 mL water) with a carrier. In particular the product is made by mixing 20% hydrogen peroxide with 2% ethanol in 20 mL water to give a total strength testosterone solution (i.e., 100 mg) containing about 10% water. In particular, this testosterone solution is made by adding about 10% hydrogen peroxide and mixing until dissolved, which will result in a product that possesses a clear solution when added to a bath. The hydrogen peroxide or the alcohol to be removed can be removed from the product using hydrogen peroxide solution.With reference now to the following figures it is noted that the present invention comprises two main components: injection apparatus and formulation of the solution (Table 1). The injectable testosterone gel is formed of 70% polypropylene glycol (70 ml, i.e., 70% of the weight as polypropylene glycol), 20% water and 10% tetra-ethyl-propylene glycol (ethanol). It should be noted in these figures that the injectable testosterone gel comprises one testosterone molecule and one testosterone glycerol group (e.Similar articles: