Chemistry:Pharmacokinetics of testosterone

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Testosterone
Testosteron.svg
Clinical data
Routes of
administration
Oral, buccal, sublingual, intranasal, transdermal (gel, cream, patch, solution), vaginal (cream, gel, suppository), rectal (suppository), intramuscular or subcutaneous injection (oil solution, aqueous suspension), subcutaneous implant (pellet)
Drug classAndrogen, anabolic steroid
Pharmacokinetic data
BioavailabilityOral: very low (due to extensive first pass metabolism)
MetabolismLiver (mainly reduction and conjugation)
Elimination half-life2–4 hours[citation needed]
ExcretionUrine (90%), feces (6%)

The pharmacology of testosterone, an androgen and anabolic steroid (AAS) medication and naturally occurring steroid hormone, concerns its pharmacodynamics, pharmacokinetics, and various routes of administration.

Testosterone is a naturally occurring and bioidentical AAS, or an agonist of the androgen receptor, the biological target of androgens like endogenous testosterone and dihydrotestosterone (DHT).

Testosterone is used by both men and women and can be taken by a variety of different routes of administration.[1]


Routes of administration

Testosterone can be taken by a variety of different routes of administration.[1][2] These include oral, buccal, sublingual, intranasal, transdermal (gels, creams, patches, solutions), vaginal (creams, gels, suppositories), rectal (suppositories), by intramuscular or subcutaneous injection (in oil solutions or aqueous suspensions), and as a subcutaneous implant.[1][2] The pharmacokinetics of testosterone, including its bioavailability, metabolism, biological half-life, and other parameters, differ by route of administration.[1] Likewise, the potency of testosterone, and its local effects in certain tissues, for instance the liver, differ by route of administration as well.[1] In particular, the oral route is subject to a high first-pass effect, which results in high levels of testosterone in the liver and consequent hepatic androgenic effects, as well as low potency due to first-pass metabolism in the intestines and liver into metabolites like dihydrotestosterone and androgen conjugates.[1] Conversely, this is not the case for non-oral routes, which bypass the first pass.[1]

Different testosterone routes and dosages can achieve widely varying circulating testosterone levels.[1] For purposes of comparison with normal physiological circumstances, circulating levels of total testosterone in men range from about 250 to 1,100 ng/dL (mean 630 ng/dL) and in women range from about 2 to 50 ng/dL (mean 32 ng/dL).[3][4][5][6] Testosterone levels decline with age in men.[7] In women with polycystic ovary syndrome (PCOS), a condition of androgen excess, testosterone levels are typically around 50 to 80 ng/dL, with a range of about 30 to 140 ng/dL.[8][9][6] Total testosterone levels are about 20-fold and free testosterone levels about 40-fold higher in men than in women on average.[10] Similarly, testosterone production is approximately 30 times higher in men than in women.[11]



Oral administration

Oral testosterone

Testosterone is well-absorbed but extensively metabolized with oral administration due to the first pass through the intestines and liver.[1][12][13][2] It is rapidly and completely inactivated in men at doses of less than 200 mg.[1][12] In large doses, such as 200 mg however, significant increases in circulating testosterone levels become apparent.[1][12] In addition, while a 60 mg dose has no effect on testosterone levels in men, this dose does measurably increase testosterone levels in prepubertal boys and women.[12] The oral bioavailability of testosterone in young women after a single 25 mg dose was found to be 3.6 ± 2.5%.[14] High levels of testosterone are also achieved with a 60 mg dose of oral testosterone in men with liver cirrhosis.[1] These findings are attributed to induction of liver enzymes by testosterone and consequent activation of its own metabolism.[1][12] Substitution dosages of oral testosterone in men are in the range of 400 to 800 mg/day.[12][13] Such doses exceed the amount of testosterone produced by the body, which is approximately 7 mg/day, by approximately 100-fold.[1][12][13] The elimination half-life of oral testosterone is rapid at about 5 to 7 hours.[13][15] As a result, it requires administration several times per day in divided doses.[13] Due to its limitations, such as the high doses required and necessity of multiple daily doses, oral testosterone is not used clinically in its unmodified form.[13][2]

Oral testosterone has been studied in combination with a 5α-reductase inhibitor to reduce its first-pass metabolism and improve its bioavailability.[1][16]

Oral testosterone undecanoate

Instead of in its free unesterified form, testosterone is used by oral administration in the form of testosterone undecanoate.[1] Due to the unique chemical properties afforded by its long fatty acid ester chain, this testosterone ester is partially absorbed from the gastrointestinal tract into the lymphatic system, thereby bypassing a portion of first-pass metabolism in the liver and producing measurable increases in testosterone levels at much lower doses than free testosterone.[1][2] Of oral testosterone undecanoate that reaches circulation, 90 to 100% is transported lymphatically.[17] However, its duration remains short, with an elimination half-life of 1.6 hours and a mean residence time of 3.7 hours.[18][19][20] Oral testosterone undecanoate is provided as 40 mg oil-filled capsules and requires administration 2 to 4 times per day (i.e., 80 to 160 mg/day) for substitution in men.[1][18][2] It must be taken with food containing at least a moderate or "normal" amount of fat in order to achieve adequate absorption.[1][21][22][23] In addition, there is very high interindividual variability in levels of testosterone with oral testosterone undecanoate.[24] The bioavailability of oral testosterone undecanoate taken with food is 3 to 7%.[17][25] Inappropriately high levels of testosterone have been observed with 10 to 40 mg/day oral testosterone undecanoate in women.[26][27] The oral bioavailability of testosterone undecanoate in young women after a single 40 mg dose was found to be 6.8 ± 3.3%.[14]

A novel self-emulsifying formulation of oral testosterone undecanoate in 300-mg capsules for use once per day is under development.[24]

First-pass effect and differences

Oral testosterone and oral testosterone undecanoate are not hepatotoxic, unlike orally administered 17α-alkylated anabolic steroids such as methyltestosterone and fluoxymesterone but similarly to parenteral routes and forms of bioidentical testosterone like injections.[28][1][24]

Buccal administration

Testosterone can be used by buccal administration (e.g., brand name Striant).[1]

Sublingual administration

Testosterone can be used by sublingual administration.[1][29][30] A 10 mg sublingual tablet with the brand name Testoral was previously marketed for use one to four times per day in men.[31]

Inhalational administration

Testosterone has been studied by inhalation.[32]

Intranasal administration

Testosterone can be used by intranasal administration (e.g., brand name Natesto).[1]

Transdermal administration

Testosterone is available for transdermal administration in the form of gels, creams, scrotal and non-scrotal patches, and axillary solutions.[1]

Transdermal testosterone gel has a bioavailability of about 8 to 14% when administered to recommended skin sites including the abdomen, arms, shoulders, and thighs.[33][34] Scrotal skin is the thinnest skin of the body[35] and has enhanced absorption characteristics relative to other skin areas.[36][37][38][39] Application of testosterone gels and creams to the scrotum has been studied and achieves much higher levels of testosterone than conventional skin sites.[40][41][42][43] Scrotal application of testosterone requires approximately 5-fold lower doses relative to non-scrotal application.[44][35]

The development of transdermal preparations of testosterone (and of progesterone)[45] has been more difficult than the case of estradiol.[35] This is because testosterone levels in men are about 100 to 1,000 times higher than estradiol levels in women (300 to 1,000 ng/dL vs. 50 to 150 pg/mL, respectively).[35] Non-scrotal testosterone patches were assessed and were found to be ineffective in raising testosterone levels in men.[35] As a result, scrotal testosterone patches were initially marketed.[35] Subsequently, however, non-scrotal testosterone patches with special permeation enhancers that could successfully increase testosterone levels were developed and marketed.[35] However, non-scrotal testosterone patches nonetheless require a large skin area for application (up to 60 cm2) and must be replaced daily.[35]

Supraphysiological levels of dihydrotestosterone (DHT) occur with scrotal application of testosterone, whereas this does not occur with non-scrotal transdermal application.[35] This is due to the high expression of 5α-reductase in scrotal skin.[35] Estradiol levels are similar with scrotal versus non-scrotal application of transdermal testosterone.[35]

Low-dose transdermal testosterone patches in women have been found to result in testosterone levels of 64 ng/dL with 150 μg/day and 102 ng/dL with 300 μg/day.[26] When testosterone is used transdermally in women or trans men, hair growth at the application sites can happen.[46]

Vaginal administration

Testosterone can be used by vaginal administration of creams, suppositories, and vaginal rings available from compounding pharmacies.[47][48][49][50][51][52]

Rectal administration

Testosterone levels with single-dose rectal administration of a 40 mg testosterone suppository in hypogonadal men.[12]

Testosterone was marketed as a suppository for rectal administration by Ferring Pharmaceuticals from the early 1960s under brand names such as Rektandron and Testosteron.[28][53][54] Rectal administration of testosterone avoids the first-pass effect with oral administration similarly to other non-oral routes.[1] A single 40 mg dose of rectal testosterone has been found to result in maximal testosterone levels of almost 1,200 ng/dL within 30 minutes.[12] Subsequently, testosterone levels steadily decline, reaching levels of about 700 ng/dL after 4 hours and levels of about 400 ng/dL after 8 hours.[12] Other studies have also assessed the use of rectal testosterone, with similar findings.[1][55][56][57][58][59] Rectal use of testosterone requires administration two or three times per day to maintain adequate testosterone levels.[12][1] The route is poorly accepted, owing to its inconvenience.[1] Rectal testosterone has been used in transmasculine hormone therapy.[56]

Intramuscular injection

Testosterone levels over 16 weeks with intramuscular injection of different testosterone esters in hypogonadal men.[18]

Testosterone can be administered by intramuscular injection either as an aqueous suspension of testosterone or as an oil solution or aqueous suspension of testosterone esters such as testosterone propionate, testosterone enanthate, testosterone cypionate, testosterone undecanoate, and testosterone isobutyrate.[1][20][2] An even longer-acting testosterone ester that was developed but ultimately never marketed is testosterone buciclate.[2] These preparations are prodrugs of progesterone that have a long-lasting depot effect when injected into muscle or fat, ranging from days to months in duration.[1]

The bioavailability of drugs that are administered intramuscularly is generally almost 95%.[60]

As oil solutions by intramuscular injection, the elimination half-lives of testosterone esters are 0.8 days for testosterone propionate, 4.5 days for testosterone enanthate, 20.9 days (in tea seed oil) and 33.9 days (in caster oil) for testosterone undecanoate, and 29.5 days for testosterone buciclate.[7][18] The pharmacokinetics of testosterone cypionate are said to be the same as those of testosterone enanthate, with "extremely comparable" patterns of testosterone release.[20][18] Due to their varying and different elimination half-lives, the different intramuscular testosterone esters are administered with differing frequencies.[61] Testosterone propionate is injected two to three times per week, testosterone enanthate and testosterone cypionate are injected once every two to four weeks, and testosterone undecanoate and testosterone buciclate are injected once every 10 to 14 weeks.[61] Due to its relatively short duration, testosterone propionate is now relatively little used and testosterone undecanoate is the preferred testosterone ester for intramuscular use.[7][18] Testosterone undecanoate and testosterone buciclate can be injected intramuscularly as infrequently as four times per year.[7][18]

High doses of testosterone esters by intramuscular injection have been studied in healthy young men.[62] Levels of testosterone with intramuscular injections of testosterone cypionate were about 700 ng/dL for 100 mg/week, 1100 ng/dL for 250 mg/week, and 2000 ng/dL for 500 mg/week.[62][63] In another study, testosterone levels with 600 mg/week testosterone enanthate by intramuscular injection were 2,800–3,200 ng/dL.[62][64]

Intramuscular injection of testosterone propionate as an oil solution, aqueous suspension, and emulsion has been compared.[65]

Intramuscular injection of testosterone-containing biodegradable microspheres has been studied.[1]


v · d · e Pharmacokinetics of testosterone esters
Testosterone ester Form Route of administration Elimination half-life Mean residence time
Testosterone undecanoate Oil-filled capsules Oral 1.6 hours 3.7 hours
Testosterone propionate Oil solution Intramuscular injection 0.8 days 1.5 days
Testosterone enanthate Castor oil solution Intramuscular injection 4.5 days 8.5 days
Testosterone undecanoate Tea seed oil solution Intramuscular injection 20.9 days 34.9 days
Testosterone undecanoate Castor oil solution Intramuscular injection 33.9 days 36.0 days
Testosterone buciclatea Aqueous suspension Intramuscular injection 29.5 days 60.0 days
Notes: Testosterone cypionate has very similar pharmacokinetics to TE. Footnotes: a = Never marketed. Sources: See template.
v · d · e Parenteral durations of androgens/anabolic steroids
Medication Form Major brand names Duration
Testosterone Aqueous suspension Andronaq, Sterotate, Virosterone 2–3 days
Testosterone propionate Oil solution Androteston, Perandren, Testoviron 3–4 days
Testosterone phenylpropionate Oil solution Testolent 8 days
Testosterone isobutyrate Aqueous suspension Agovirin Depot, Perandren M 14 days
Mixed testosterone estersa Oil solution Triolandren 10–20 days
Mixed testosterone estersb Oil solution Testosid Depot 14–20 days
Testosterone enanthate Oil solution Delatestryl 14–20 days
Testosterone cypionate Oil solution Depovirin 14–20 days
Mixed testosterone estersc Oil solution Sustanon 250 28 days
Testosterone undecanoate Oil solution Aveed, Nebido 100 days
Testosterone buciclated Aqueous suspension 20 Aet-1, CDB-1781e 90–120 days
Nandrolone phenylpropionate Oil solution Durabolin 10 days
Nandrolone decanoate Oil solution Deca Durabolin 21 days
Methandriol Aqueous suspension Notandron, Protandren 8 days
Methandriol bisenanthoyl acetate Oil solution Notandron Depot 16 days
Metenolone acetate Oil solution Primobolan 3 days
Metenolone enanthate Oil solution Primobolan Depot 14 days
Note: All are via i.m. injection. Footnotes: a = TP, TV, and TUe. b = TP and TKL. c = TP, TPP, TiCa, and TD. d = Studied but never marketed. e = Developmental code names. Sources: See template.

Subcutaneous injection

Testosterone esters like testosterone enanthate and testosterone cypionate can be given by subcutaneous injection instead of intramuscular injection. Studies have shown that subcutaneous injection of testosterone and closely related esters in oil like testosterone cypionate, testosterone enantate, and nandrolone decanoate is effective and has similar pharmacokinetics to intramuscular injection.[66][67][68][69][70][71][72]

Subcutaneous implant

Testosterone can be administered in the form of a subcutaneous pellet implant.[1]

The bioavailability of testosterone when administered as a subcutaneous pellet implant is virtually 100%.[73] Levels of testosterone vary considerably between individuals, but are fairly constant within individuals.[26] The absorption half-life of subdermal testosterone implants is 2.5 months.[7] The replacement interval is once every four to six months.[26][74] A single 50 mg testosterone pellet implanted every 4 to 6 months has been found to result in testosterone levels of 70 to 90 ng/dL in women.[26]

Intravenous injection

Testosterone esters like testosterone enanthate are hydrolyzed into testosterone so rapidly in the blood that testosterone and testosterone enanthate have nearly identical pharmacokinetics when administered via intravenous injection.[1]

General

Absorption

The oral bioavailability of testosterone is very low.[7][75] The bioavailability of oral testosterone undecanoate is 3 to 7%.[17][25] Topical testosterone gels have a bioavailability of about 8 to 14% when administered to recommended skin sites including the abdomen, arms, shoulders, and thighs.[33][34] The bioavailability of testosterone by subcutaneous implant is virtually 100%.[73] The bioavailability of drugs that are administered intramuscularly is generally almost 95%.[60]

Distribution

In the circulation, 97.0 to 99.5% of testosterone is bound to plasma proteins, with 0.5 to 3.0% unbound.[76] It is tightly bound to SHBG and weakly to albumin.[76] Of circulating testosterone, 30 to 44% is bound to SHBG while 54 to 68% is bound to albumin.[76] Testosterone that is unbound is referred to as free testosterone and testosterone that is bound to albumin is referred to as bioavailable testosterone.[76] Unlike testosterone that is bound to SHBG, bioavailable testosterone is bound to plasma proteins weakly enough such that, similarly to free testosterone, it may be biologically active, at least to a certain extent.[76] When referenced collectively (i.e., free, bioavailable, and SHBG-bound), circulating testosterone is referred to as total testosterone.[76]

Metabolism

Testosterone is metabolized primarily in the liver mainly (90%) by reduction via 5α- and 5β-reductase and conjugation via glucuronidation and sulfation.[76][77][78] The major urinary metabolites of testosterone are androsterone glucuronide and etiocholanolone glucuronide.[76][77][78][79]

The elimination half-life of testosterone varies depending on the route of administration and formulation and on whether or not it is esterified.[7] The elimination half-life of testosterone in the blood or by intravenous injection is only about 10 minutes.[7][18] Conversely, testosterone and testosterone esters in oil solution or crystalline aqueous suspension administered by intramuscular or subcutaneous injection have much longer half-lives, in the range of days to months, due to slow release from the injection site.[7][18]

Elimination

Testosterone and its metabolites are eliminated in urine.[80] It is excreted mainly as androsterone glucuronide and etiocholanolone glucuronide.[79] It is also excreted to a small extent as other conjugates such as testosterone glucuronide (1%), testosterone sulfate (0.03%), and androstanediol glucuronides.[79][81] Only a very small amount of testosterone (less than 0.01%) is found unchanged in the urine.[80][81]

See also

  • Pharmacodynamics of estradiol
  • Pharmacokinetics of estradiol
  • Pharmacodynamics of progesterone
  • Pharmacokinetics of progesterone

References

  1. 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 1.17 1.18 1.19 1.20 1.21 1.22 1.23 1.24 1.25 1.26 1.27 1.28 1.29 1.30 1.31 1.32 "Testosterone preparations for clinical use in males". Testosterone: Action, Deficiency, Substitution. Cambridge University Press. 26 July 2012. pp. 309–335. doi:10.1017/CBO9781139003353.016. ISBN 978-1-107-01290-5. 
  2. 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 Principles and Practice of Endocrinology and Metabolism. Lippincott Williams & Wilkins. 2001. pp. 1116, 1119, 1152, 1182–1185, 1195–1197, 2146. ISBN 978-0-7817-1750-2. https://books.google.com/books?id=FVfzRvaucq8C&pg=PA1182. 
  3. Endocrinology: Adult and Pediatric E-Book. Elsevier Health Sciences. 25 February 2015. ISBN 978-0-323-32195-2. https://books.google.com/books?id=xmLeBgAAQBAJ. 
  4. Laboratory Tests and Diagnostic Procedures – E-Book. Elsevier Health Sciences. 31 October 2012. pp. 1059–1062. ISBN 978-1-4557-4502-9. https://books.google.com/books?id=dWHYcOJK-cgC&pg=PA1059. 
  5. Pediatric Endocrinology E-Book: Expert Consult - Online and Print. Elsevier Health Sciences. 10 April 2014. pp. 488–. ISBN 978-1-4557-5973-6. https://books.google.com/books?id=GgXnAgAAQBAJ&pg=PA488. 
  6. 6.0 6.1 "Utilization of commercial laboratory results in management of hyperandrogenism in women". Endocrine Practice 4 (1): 1–10. 1998. doi:10.4158/EP.4.1.1. PMID 15251757. 
  7. 7.0 7.1 7.2 7.3 7.4 7.5 7.6 7.7 7.8 Testosterone: Action - Deficiency - Substitution. Springer Science & Business Media. 6 December 2012. pp. 1–,9,298,309–331,349–353,366–367. ISBN 978-3-642-72185-4. https://books.google.com/books?id=jn3nCAAAQBAJ&pg=PA350. 
  8. "Total testosterone assays in women with polycystic ovary syndrome: precision and correlation with hirsutism". The Journal of Clinical Endocrinology and Metabolism 95 (12): 5305–5313. December 2010. doi:10.1210/jc.2010-1123. PMID 20826578. 
  9. "Polycystic ovary syndrome: the spectrum of the disorder in 1741 patients". Human Reproduction 10 (8): 2107–2111. August 1995. doi:10.1093/oxfordjournals.humrep.a136243. PMID 8567849. 
  10. "Physiology and Disorders of Puberty". Williams Textbook of Endocrinology (14 ed.). Philadelphia, PA: Elsevier. 6 December 2019. pp. 1023–1164. ISBN 9780323555968. https://www.elsevier.com/books/williams-textbook-of-endocrinology/melmed/978-0-323-55596-8. 
  11. "Androgen therapy in non-gonadal disease". Testosterone. Springer. 1998. pp. 473–512. doi:10.1007/978-3-642-72185-4_17. ISBN 978-3-642-72187-8. 
  12. 12.00 12.01 12.02 12.03 12.04 12.05 12.06 12.07 12.08 12.09 12.10 Treatment of Male Infertility. Springer Science & Business Media. 6 December 2012. pp. 176–177. ISBN 978-3-642-68223-0. https://books.google.com/books?id=W1cGCAAAQBAJ&pg=PT176. 
  13. 13.0 13.1 13.2 13.3 13.4 13.5 "Clinical use of androgens". Annual Review of Medicine 35 (1): 207–217. 1984. doi:10.1146/annurev.me.35.020184.001231. PMID 6372655. 
  14. 14.0 14.1 "Absolute bioavailability of testosterone after oral administration of testosterone-undecanoate and testosterone". European Journal of Drug Metabolism and Pharmacokinetics 11 (2): 145–149. 1986. doi:10.1007/BF03189840. PMID 3770015. 
  15. "Therapeutic effectiveness of oral testosterone". Lancet 2 (7895): 1473–1475. December 1974. doi:10.1016/S0140-6736(74)90216-5. PMID 4140393. 
  16. "Emerging medication for the treatment of male hypogonadism". Expert Opinion on Emerging Drugs 17 (2): 239–259. June 2012. doi:10.1517/14728214.2012.683411. PMID 22612692. 
  17. 17.0 17.1 17.2 Foye's Principles of Medicinal Chemistry. Lippincott Williams & Wilkins. 24 January 2012. pp. 1360–. ISBN 978-1-60913-345-0. https://books.google.com/books?id=Sd6ot9ul-bUC&pg=PA1360. 
  18. 18.0 18.1 18.2 18.3 18.4 18.5 18.6 18.7 18.8 Andrology: Male Reproductive Health and Dysfunction. Springer Science & Business Media. 13 January 2010. pp. 49–54,441–446. ISBN 978-3-540-78355-8. https://books.google.com/books?id=mEgckDNkonUC&pg=PA442. 
  19. "Intramuscular injection of testosterone undecanoate for the treatment of male hypogonadism: phase I studies". European Journal of Endocrinology 140 (5): 414–419. May 1999. doi:10.1530/eje.0.1400414. PMID 10229906. 
  20. 20.0 20.1 20.2 Anabolics. Molecular Nutrition Llc. 2011. pp. 212–216, 314–322. ISBN 978-0-9828280-1-4. https://books.google.com/books?id=afKLA-6wW0oC&pg=PT314. 
  21. Testosterone: From Basic to Clinical Aspects. Springer. 30 March 2017. pp. 13–. ISBN 978-3-319-46086-4. https://books.google.com/books?id=Et6TDgAAQBAJ&pg=PA13. 
  22. "Important effect of food on the bioavailability of oral testosterone undecanoate". Pharmacotherapy 23 (3): 319–325. March 2003. doi:10.1592/phco.23.3.319.32104. PMID 12627930. 
  23. "The effect of food composition on serum testosterone levels after oral administration of Andriol Testocaps". Clinical Endocrinology 66 (4): 579–585. April 2007. doi:10.1111/j.1365-2265.2007.02781.x. PMID 17371478. 
  24. 24.0 24.1 24.2 "Androgens: Pharmacological Use and Abuse ☆". Reference Module in Neuroscience and Biobehavioral Psychology. Elsevier. 2017. doi:10.1016/B978-0-12-809324-5.03356-3. ISBN 9780128093245. 
  25. 25.0 25.1 Enhancement in Drug Delivery. CRC Press. 27 November 2006. pp. 122–. ISBN 978-1-4200-0481-6. https://books.google.com/books?id=t0L_zFoXmjkC&pg=PA122. 
  26. 26.0 26.1 26.2 26.3 26.4 "Androgens in postmenopausal women: production, possible role, and replacement options". Obstetrical & Gynecological Survey 56 (6): 361–376. June 2001. doi:10.1097/00006254-200106000-00022. PMID 11466487. 
  27. "Which androgen replacement therapy for women?". The Journal of Clinical Endocrinology and Metabolism 83 (11): 3920–3924. November 1998. doi:10.1210/jcem.83.11.5280. PMID 9814469. 
  28. 28.0 28.1 "ENDOCRINE HISTORY: The history of discovery, synthesis and development of testosterone for clinical use". European Journal of Endocrinology 180 (6): R201–R212. June 2019. doi:10.1530/EJE-19-0071. PMID 30959485. 
  29. "Sublingual testosterone replacement improves muscle mass and strength, decreases bone resorption, and increases bone formation markers in hypogonadal men--a clinical research center study". The Journal of Clinical Endocrinology and Metabolism 81 (10): 3654–3662. October 1996. doi:10.1210/jcem.81.10.8855818. PMID 8855818. 
  30. "Sublingual administration of testosterone compounds in male hypogonadism". Ciba Clinical Symposia 3 (2): 49–56. March 1951. PMID 14822123. 
  31. Sex Hormone Pharmacology. Academic Press. 1976. pp. 18–19,331,336. ISBN 978-0-12-137250-7. https://books.google.com/books?id=zt5sAAAAMAAJ. 
  32. "Pharmacokinetics and acute safety of inhaled testosterone in postmenopausal women". Journal of Clinical Pharmacology 45 (2): 177–184. February 2005. doi:10.1177/0091270004269840. PMID 15647410. 
  33. 33.0 33.1 Testosterone Deficiency in Men. OUP Oxford. 25 September 2008. pp. 89–. ISBN 978-0-19-954513-1. https://books.google.com/books?id=MTxR7EYq46oC&pg=PT89. 
  34. 34.0 34.1 "Testosterone Replacement Therapy". Sexual Medicine pp 79–93Cite as. Springer. 2019. pp. 79–93. doi:10.1007/978-981-13-1226-7_8. ISBN 978-981-13-1225-0. 
  35. 35.00 35.01 35.02 35.03 35.04 35.05 35.06 35.07 35.08 35.09 35.10 "Transdermal delivery of sex steroids for hormone replacement therapy and contraception. A review of principles and practice". The Journal of Reproductive Medicine 48 (7): 525–540. July 2003. PMID 12953327. http://www.reproductivemedicine.com/toc/auto_abstract.php?id=17591. 
  36. "Principles of Topical Therapy". Rook's Textbook of Dermatology. Wiley. 2016. pp. 1–51. doi:10.1002/9781118441213.rtd0018. ISBN 9781118441213. 
  37. "Drug metabolism and pharmacokinetics". Drug Metabolism Reviews 41 (3): 344–390. 2009. doi:10.1080/10837450902891295. PMID 19601718. 
  38. "Regional Variation in Percutaneous Absorption". Topical Absorption of Dermatological Products. CRC Press. 2 January 2002. pp. 33–42. doi:10.3109/9780203904015-6. ISBN 978-0-203-90401-5. https://books.google.com/books?id=3tfKBQAAQBAJ&pg=PA33. 
  39. "Regional variation in percutaneous penetration of 14C cortisol in man". The Journal of Investigative Dermatology 48 (2): 181–183. February 1967. doi:10.1038/jid.1967.29. PMID 6020682. 
  40. "Testosterone substitution with a new transdermal, hydroalcoholic gel applied to scrotal or non-scrotal skin: a multicentre trial". European Journal of Endocrinology 153 (2): 317–326. August 2005. doi:10.1530/eje.1.01964. PMID 16061839. 
  41. "Pharmacokinetics of testosterone cream applied to scrotal skin". Andrology 5 (4): 725–731. July 2017. doi:10.1111/andr.12357. PMID 28334510. 
  42. "The efficacy and safety of short-acting testosterone ointment (Glowmin) for late-onset hypogonadism in accordance with testosterone circadian rhythm". The Aging Male 21 (3): 170–175. September 2018. doi:10.1080/13685538.2018.1471129. PMID 29734846. 
  43. "Case Study: Absorption of Testosterone Cream via Scrotal Delivery". International Journal of Pharmaceutical Compounding 22 (6): 466–468. 2018. PMID 30384346. 
  44. "Current topics in testosterone replacement of hypogonadal men". Best Practice & Research. Clinical Endocrinology & Metabolism 29 (1): 77–90. January 2015. doi:10.1016/j.beem.2014.09.008. PMID 25617174. 
  45. "Transdermal drug delivery: clinical considerations for the obstetrician-gynecologist". Obstetrics and Gynecology 105 (5 Pt 1): 953–961. May 2005. doi:10.1097/01.AOG.0000161958.70059.db. PMID 15863530. 
  46. "Testosterone use in women". Testosterone: Action, Deficiency, Substitution. Cambridge University Press. 26 July 2012. pp. 494–516. doi:10.1017/CBO9781139003353.024. ISBN 978-1-107-01290-5. 
  47. "Testosterone replacement therapy in the climacteric: benefits beyond sexuality". Gynecological Endocrinology 25 (1): 12–20. January 2009. doi:10.1080/09513590802360744. PMID 19165658. 
  48. Urogynecology in Primary Care. Springer Science & Business Media. 6 March 2007. pp. 116–. ISBN 978-1-84628-167-9. https://books.google.com/books?id=Gu5xcMEOUc8C&pg=PA116. "Topical vaginal testosterone is often used in premenopausal women as a first step in the treatment of sexual dysfunction and vaginal lichen planus. Topical testosteorne preparations can be compounded in 1% to 2% formulations and should be applied up to 3 times per week." 
  49. Current Medical Diagnosis and Treatment 2018, 57th Edition. McGraw-Hill Education. 11 September 2017. pp. 1217–1218. ISBN 978-1-259-86149-9. https://books.google.com/books?id=xTExDwAAQBAJ. "Testosterone can also be compounded as a cream containing 1 mg/mL, with 1 mL applied to the abdomen daily. Vaginal testosterone is an option for postmenopausal women who cannot use systemic or vaginal estrogen due to breast cancer. Testosterone 150–300 mcg/day vaginally appears to reduce vaginal dryness and dyspareunia without increasing systemic estrogen levels." 
  50. Textbook of Natural Medicine. Elsevier Health Sciences. 2013. pp. 1602–. ISBN 978-1-4377-2333-5. https://books.google.com/books?id=6cjgo1IixvEC&pg=PA1602. "At present, bioidentical testosterone can be obtained only from a compounding pharmacy, where 4 to 6 mg of bioidentical testosterone is generally formulated alone or together with the biestrogen or triestrogen formulation. Testosterone cream applied to the genital region can be used as an alternative delivery method. Common prescriptions are anywhere from 1 to 10 mg/g of cream." 
  51. "Androgens and women at the menopause and beyond". The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences 58 (5): M409–M416. May 2003. doi:10.1093/gerona/58.5.M409. PMID 12730248. 
  52. Menopause: Biology and Pathobiology. Academic Press. 22 May 2000. pp. 455–. ISBN 978-0-08-053620-0. https://books.google.com/books?id=i9HXKhjvNVAC&pg=PA455. 
  53. "Natürliche und Synthetische Sexualhormone – Biologische Grundlagen und Behandlungsprinzipien" (in de). Grundlagen und Klinik der Menschlichen Fortpflanzung. Walter de Gruyter. 1988. pp. 229–306. ISBN 978-3110109689. OCLC 35483492. https://books.google.com/books?id=v4HvAQAACAAJ. 
  54. Apotekens informationsavdelning (1964). Apotekens synonymregister över farmacevtiska specialiteter. Apotekens informationsavdelning.. https://books.google.com/books?id=uTw8AQAAIAAJ. "Rektandron FERRING supp. 40 mg • individ. dos. • 10 st." 
  55. "Testosterone treatment and 17-ketosteroid excretion. V. Administration of testosterone per rectum". Acta Endocrinologica 28 (4): 529–536. August 1958. doi:10.1530/acta.0.0280529. PMID 13570882. 
  56. 56.0 56.1 "Plasma testosterone values in different forms of testosterone treatment". Acta Endocrinologica 60 (3): 537–542. March 1969. doi:10.1530/acta.0.0600537. PMID 5395873. 
  57. "Bioavailability and LH-suppressing effect of different testosterone preparations in normal and hypogonadal men". Hormone Research 7 (3): 138–145. 1976. doi:10.1159/000178721. PMID 1002121. 
  58. "[Absorption and action of testosterone administered rectally]" (in Italian). Clinica Nuova; Rassegna del Progresso Medico Internazionale 14 (1–2): 5–16. 1952. PMID 14945075. 
  59. "[Letter: Testosterone suppositories DAK]" (in Danish). Ugeskrift for Laeger 136 (6): 307–308. February 1974. PMID 4820554. 
  60. 60.0 60.1 Conceptual Pharmacology. Universities Press. 2010. pp. 8–. ISBN 978-81-7371-679-9. https://books.google.com/books?id=s0e_FlM8LKYC&pg=PA8. 
  61. 61.0 61.1 Medical Care of Cancer Patients. PMPH-USA. 2009. pp. 247–. ISBN 978-1-60795-008-0. https://books.google.com/books?id=XxfjqF1A0TkC&pg=PA247. 
  62. 62.0 62.1 62.2 "Shifting the paradigm of testosterone and prostate cancer: the saturation model and the limits of androgen-dependent growth". European Urology 55 (2): 310–320. February 2009. doi:10.1016/j.eururo.2008.09.024. PMID 18838208. 
  63. "Effect of exogenous testosterone on prostate volume, serum and semen prostate specific antigen levels in healthy young men". The Journal of Urology 159 (2): 441–443. February 1998. doi:10.1016/s0022-5347(01)63944-2. PMID 9649259. 
  64. "The effects of supraphysiologic doses of testosterone on muscle size and strength in normal men". The New England Journal of Medicine 335 (1): 1–7. July 1996. doi:10.1056/NEJM199607043350101. PMID 8637535. 
  65. "17-Ketosteroid Excretion and Modes of Administering Testosterone Preparations". Ciba Foundation Symposium - Steroid Hormone Administration (Book II of Colloquia on Endocrinology, Vol. 3). Novartis Foundation Symposia. John Wiley & Sons. 1952. pp. 304–322. doi:10.1002/9780470715154.ch7. ISBN 9780470715154. 
  66. "Subcutaneous administration of testosterone. A pilot study report". Saudi Medical Journal 27 (12): 1843–1846. December 2006. PMID 17143361. https://www.researchgate.net/publication/6656360. 
  67. "Effects of cross-sex hormone treatment on transgender women and men". Obstetrics and Gynecology 125 (3): 605–610. March 2015. doi:10.1097/AOG.0000000000000692. PMID 25730222. 
  68. "Subcutaneous Testosterone: An Effective Delivery Mechanism for Masculinizing Young Transgender Men". LGBT Health 1 (3): 165–167. September 2014. doi:10.1089/lgbt.2014.0018. PMID 26789709. 
  69. "Subcutaneous Injection of Testosterone Is an Effective and Preferred Alternative to Intramuscular Injection: Demonstration in Female-to-Male Transgender Patients". The Journal of Clinical Endocrinology and Metabolism 102 (7): 2349–2355. July 2017. doi:10.1210/jc.2017-00359. PMID 28379417. 
  70. "Serum Testosterone Concentrations Remain Stable Between Injections in Patients Receiving Subcutaneous Testosterone". Journal of the Endocrine Society 1 (8): 1095–1103. August 2017. doi:10.1210/js.2017-00148. PMID 29264562. 
  71. "Pharmacokinetics, safety, and patient acceptability of subcutaneous versus intramuscular testosterone injection for gender-affirming therapy: A pilot study". American Journal of Health-System Pharmacy 75 (6): 351–358. March 2018. doi:10.2146/ajhp170160. PMID 29367424. 
  72. "Pharmacokinetic-pharmacodynamic study of subcutaneous injection of depot nandrolone decanoate using dried blood spots sampling coupled with ultrapressure liquid chromatography tandem mass spectrometry assays". The Journal of Clinical Endocrinology and Metabolism 99 (7): 2592–2598. July 2014. doi:10.1210/jc.2014-1243. PMID 24684468. 
  73. 73.0 73.1 Pharmacology, Biology, and Clinical Applications of Androgens: Current Status and Future Prospects. John Wiley & Sons. 13 February 1996. pp. 462–. ISBN 978-0-471-13320-9. https://books.google.com/books?id=hurRyWje4DMC&pg=PA462. 
  74. Kumar and Clark's Clinical Medicine. Elsevier Health Sciences. 4 June 2012. pp. 976–. ISBN 978-0-7020-5304-7. https://books.google.com/books?id=85Tgj1LBMjYC&pg=PA976. 
  75. Drug Abuse Handbook, Second Edition. CRC Press. 21 December 2006. pp. 700–. ISBN 978-1-4200-0346-8. https://books.google.com/books?id=ZjrMBQAAQBAJ&pg=PA700. 
  76. 76.0 76.1 76.2 76.3 76.4 76.5 76.6 76.7 Williams Textbook of Endocrinology. Elsevier Health Sciences. 11 November 2015. pp. 709, 711, 765. ISBN 978-0-323-34157-8. https://books.google.com/books?id=iPIACwAAQBAJ&pg=PA709. 
  77. 77.0 77.1 Brody's Human Pharmacology. Elsevier Health Sciences. 1 April 2009. pp. 468–469. ISBN 978-0-323-07575-6. https://books.google.com/books?id=kfsrz_-OrMQC&pg=PA468. 
  78. 78.0 78.1 Principles and Practice of Endocrinology and Metabolism. Lippincott Williams & Wilkins. 2001. pp. 1116, 1119, 1183. ISBN 978-0-7817-1750-2. https://books.google.com/books?id=FVfzRvaucq8C&pg=PA1116. 
  79. 79.0 79.1 79.2 Doping in Sports. Springer Science & Business Media. 18 December 2009. pp. 53–. ISBN 978-3-540-79088-4. https://books.google.com/books?id=R-hIC-caIn8C&pg=PA53. 
  80. 80.0 80.1 Karch's Pathology of Drug Abuse (third ed.). CRC Press. 26 December 2001. pp. 486–. ISBN 978-1-4200-4211-5. https://books.google.com/books?id=AUTWJwn8uOwC&pg=PA486. 
  81. 81.0 81.1 Clinical Endocrinology: Theory and Practice. Springer Science & Business Media. 6 December 2012. pp. 450–. ISBN 978-3-642-96158-8. https://books.google.com/books?id=DAgJCAAAQBAJ&pg=PA450. 

Further reading

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See also
Androgen receptor modulators
Estrogens and antiestrogens
Progestogens and antiprogestogens
List of androgens/anabolic steroids

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