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词条 Estradiol enantate/algestone acetophenide
释义

  1. Medical uses

     Available forms 

  2. Pharmacology

     Pharmacology  Pharmacokinetics 

  3. History

  4. Society and culture

     Brand names  Availability  Usage 

  5. See also

  6. References

{{Drugbox
| image = Estradiol enanthate.png
| width = 250px
| caption =
| image2 = Algestone acetophenide.svg
| width2 = 235px
| caption2 = Estradiol enantate (top) and
algestone acetophenide (bottom)
| type = combo
| drug_name = Estradiol enantate /
algestone acetophenide
| component1 = Estradiol enantate
| class1 = Estrogen
| component2 = Algestone acetophenide
| class2 = Progestogen
| tradename = Perlutal, Topasel, Unalmes, Yectames, many others
| Drugs.com =
| MedlinePlus =
| licence_EU =
| licence_US =
| DailyMedID =
| pregnancy_AU =
| pregnancy_US =
| pregnancy_category =
| legal_AU =
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration = Intramuscular injection
| CAS_number = 8055-16-1
| CAS_supplemental =
| ATCvet =
| ATC_prefix =
| ATC_suffix =
| ATC_supplemental =
| PubChem = 91824751
| PubChemSubstance =
| IUPHAR_ligand =
| DrugBank =
| ChemSpiderID =
| UNII =
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| synonyms = Estradiol enantate/dihydroxy­progesterone acetophenide; E2-EN/DHPA
}}Estradiol enantate/algestone acetophenide, also known as estradiol enantate/dihydroxyprogesterone acetophenide (E2-EN/DHPA) and sold under the brand names Perlutal and Topasel among others, is a form of combined injectable birth control which is used to prevent pregnancy.[1][2][3] It contains estradiol enantate (E2-EN), an estrogen, and algestone acetophenide (dihydroxyprogesterone acetophenide; DHPA), a progestin.[1][2][3] The medication is given once a month by injection into muscle.[1][2][3]

E2-EN/DHPA is used widely throughout Latin America, is also marketed in Hong Kong, and was previously available in Portugal and Spain as well but was discontinued in these countries.[1][2][3][13]

Medical uses

E2-EN/DHPA is used in combination as a once-monthly combined injectable contraceptive to prevent pregnancy in women in Latin America and Hong Kong.[14][3][4] E2-EN/DHPA has been said to be used by "travestis" (a term for transgender women in some cultures, especially in South America) as a means of feminizing hormone therapy as well.[5]

Available forms

The following forms of E2-EN/DHPA are or have been available for use:[3][6][7][21][8]

  • E2-EN 10 mg and DHPA 150 mg (brand names Perlutal, Topasel, many others)
  • E2-EN 5 mg and DHPA 75 mg (brand names Anafertin, Patector NF, Yectames)
  • E2-EN 10 mg and DHPA 120 mg (brand names Unalmes, Yectuna)
  • E2-EN 10 mg and DHPA 75 mg (brand name Ova Repos; discontinued)

A 6 mg E2-EN and 90 mg DHPA formulation was also studied, but was never marketed.[9][10][11] The combination of E2-EN and DHPA has also been studied at other doses ranging from 5 to 50 mg E2-EN and 75 to 200 mg DHPA.[12]

Pharmacology

Pharmacology

Clinical studies have found that, on the basis of endometrial changes, E2-EN/DHPA appears, at the doses used, to be an estrogen-dominant combination.[27]

Pharmacokinetics

By intramuscular injection, the elimination half-life of E2-EN has been found to be 5.6 to 7.5 days, while the half-life of algestone acetophenide and its metabolites has been found to be 24 days.[13][14][15][2] Following a single injection, E2-EN and DHPA are detectable in the circulation for up to 30 to 60 days.[16][2]

History

E2-EN/DHPA was first studied as a combined injectable contraceptive in 1964.[21] It was developed by Squibb under the developmental code name and tentative brand name Deladroxate for potential use as a combined injectable contraceptive in the United States.[17][18] Due to toxicological findings of DHPA of pituitary hyperplasia in rats, mammary tumors in beagle dogs, and "uterine swellings" in animals, as well as concerns about possible accumulation of DHPA, Squibb discontinued the development of E2-EN/DHPA in the late 1960s.[17][21][19][2] Subsequently, in 1973, a pharmacokinetic study of E2-EN/DHPA in women generated concerns about potential accumulation of E2-EN with once-monthly use as well.[17][21][2] In spite of these concerns however, no toxicity or tumorigenicity has been observed with E2-EN/DHPA in humans in extensive clinical studies, and there are doubts about the relevance of the animal findings to humans.[19][21][2] In addition, only very limited accumulation of E2-EN has been found to occur with the preparation.[2]

Manufacturers in other countries, including EuroPharma, Farmitalia, and Promeco, resumed development of E2-EN/DHPA following the discontinuation of its development by Squibb, and introduced it for clinical use as a combined injectable contraceptive, under the brand names Perlutal and Topasel, in Spain and Latin America in the 1970s.[17][20][21] It was one of only two combined injectable contraceptives to have been marketed by 1976, and was one of only three combined injectable contraceptives with considerable clinical experience by 1976.[17][20] The others were estradiol valerate/hydroxyprogesterone caproate (EV/OHPC; brand name Injectable No. 1), which had been marketed in China, and estradiol cypionate/medroxyprogesterone acetate (EC/MPA; code name Cyclo-Provera), which was still experimental by 1976 and did not become formally available for clinical use until the 1990s.[20][21] By 1994, at which point EC/MPA (brand names Cyclofem and later Lunelle) and estradiol valerate/norethisterone enantate (EV/NETE; brand name Mesigyna) had been introduced, E2-EN/DHPA had been in use for many years.[20][21]

E2-EN/DHPA and EV/OHPC have been referred to as first-generation combined injectable contraceptives, while EC/MPA and EV/NETE have been referred to as second-generation combined injectable contraceptives.[17]

Society and culture

Brand names

E2-EN has been marketed under a wide variety of brand names.[13][59][60][61][3][63][7][65][21][8][1] It has been marketed in a few different preparations, with varying doses of E2-EN and DHPA.[7][3][63][6][21][8][1] These formulations all have different brand names, which include the following ( = discontinued):[13][59][60][61][6][7][3][63][8][21]

  • E2-EN 10 mg / DHPA 150 mg: Acefil, Agurin, Atrimon, Ciclomes, Ciclovar, Ciclovular, Cicnor, Clinomin, Cycloven, Daiva, Damix, Deprans, Deproxone, Exuna, Ginestest, Ginoplan, Gynomes, Horprotal, Listen, Luvonal, Neogestar, Neolutin, Nomagest, Nonestrol, Normagest, Normensil, Novular, Oterol, Ovoginal, Patector, Patectro, Perludil, Perlumes, Perlutal, Perlutale, Perlutan, Perlutin, Perlutin-Unifarma, Permisil, Preg-Less, Pregnolan, Progestrol, Protegin, Proter, Seguralmes, Synovular, Topasel, Unigalen, Uno-Ciclo, and Vagital.
  • E2-EN 10 mg / DHPA 120 mg: Anafertin, Patector NF, and Yectames.
  • E2-EN 5 mg / DHPA 75 mg: Unalmes and Yectuna.
  • E2-EN 10 mg / DHPA 75 mg: Ova Repos.
  • Unsorted: Evitas, Femineo, and Primyfar.

The combination of E2-EN 10 mg and DHPA 150 mg was developed under the developmental brand name Deladroxate, but this brand name was never used commercially.[21][8]

Availability

DHPA has been marketed in combination with estradiol enantate (E2-EN) as a combined injectable contraceptive in at least 19 countries, mostly in Latin America.[3][22][7][23][24][25][26][27] A few different preparations, with varying doses of E2-EN and DHPA and varying availability, have been introduced.[7][3][22][6][28][8][1] These formulations have the following approval and availability ( = discontinued in this country):[24][25][26][27][6][7][3][22][8]

  • E2-EN 10 mg / DHPA 150 mg: at least 19 countries, including Argentina, Belize, Brazil, Chile, Colombia, Costa Rica, the Dominican Republic, Ecuador, El Salvador, Guatemala, Honduras, Hong Kong, Mexico, Nicaragua, Panama, Paraguay, Peru, Portugal, and Spain.
  • E2-EN 10 mg / DHPA 120 mg: at least 3 countries, including Brazil, Chile, and Paraguay.
  • E2-EN 5 mg / DHPA 75 mg: at least 9 countries, including Costa Rica, the Dominican Republic, El Salvador, Guatemala, Honduras, Mexico, Nicaragua, Panama, and Spain.

Usage

E2-EN/DHPA is the most widely used combined injectable contraceptive in Latin America.[29] It was estimated in 1995 that E2-EN/DHPA was used as a combined injectable contraceptive in Latin America by at least 1 million women.[7] However, combined injectable contraceptives like E2-EN/DHPA are unlikely to constitute a large proportion of contraceptive use in the countries in which they are available.[7]

See also

  • Combined injectable birth control § Available forms
  • Estradiol benzoate butyrate/algestone acetophenide
  • List of combined sex-hormonal preparations

References

1. ^{{cite journal | vauthors = Garza-Flores J | title = Pharmacokinetics of once-a-month injectable contraceptives | journal = Contraception | volume = 49 | issue = 4 | pages = 347–59 | date = April 1994 | pmid = 8013219 | doi = 10.1016/0010-7824(94)90032-9 | url = }}
2. ^{{cite journal | vauthors = Sang GW | title = Pharmacodynamic effects of once-a-month combined injectable contraceptives | journal = Contraception | volume = 49 | issue = 4 | pages = 361–85 | date = April 1994 | pmid = 8013220 | doi = 10.1016/0010-7824(94)90033-7 | url = }}
3. ^10 11 {{cite journal | vauthors = Bagade O, Pawar V, Patel R, Patel B, Awasarkar V, Diwate S | title = Increasing use of long-acting reversible contraception: safe, reliable, and cost-effective birth control | journal = World J Pharm Pharm Sci | volume = 3 | issue = 10 | pages = 364–392 | year = 2014 | issn = 2278-4357 | doi = | url = http://www.wjpps.com/download/article/1412071798.pdf}}
4. ^{{cite journal|last1=Rowlands|first1=S|title=New technologies in contraception|journal=BJOG: An International Journal of Obstetrics & Gynaecology|volume=116|issue=2|year=2009|pages=230–239|issn=1470-0328|doi=10.1111/j.1471-0528.2008.01985.x}}
5. ^{{cite book|author=Don Kulick|title=Travesti: Sex, Gender, and Culture among Brazilian Transgendered Prostitutes|url=https://books.google.com/books?id=jbZyBfio-hcC&pg=PA64|date=12 January 2009|publisher=University of Chicago Press|isbn=978-0-226-46101-4|pages=64–66}}
6. ^{{cite book|author1=IARC Working Group on the Evaluation of Carcinogenic Risks to Humans|author2=World Health Organization|author3=International Agency for Research on Cancer|title=Combined Estrogen-progestogen Contraceptives and Combined Estrogen-progestogen Menopausal Therapy|url=https://books.google.com/books?id=aGDU5xibtNgC&pg=PA431|year=2007|publisher=World Health Organization|isbn=978-92-832-1291-1|pages=431–433,467}}
7. ^{{cite book|author1=IARC Working Group on the Evaluation of Carcinogenic Risks to Humans|author2=International Agency for Research on Cancer|title=Hormonal Contraception and Post-menopausal Hormonal Therapy|date=1 January 1999|publisher=IARC|isbn=978-92-832-1272-0|page=65|url=https://monographs.iarc.fr/wp-content/uploads/2018/06/mono72.pdf#page=76}}
8. ^{{cite journal | vauthors = Newton JR, D'arcangues C, Hall PE | title = A review of "once-a-month" combined injectable contraceptives | journal = J Obstet Gynaecol (Lahore) | volume = 4 Suppl 1 | issue = | pages = S1–34 | year = 1994 | pmid = 12290848 | doi = 10.3109/01443619409027641 | url = }}
9. ^{{cite journal|last1=d’Arcangues|first1=Catherine|last2=Snow|first2=Rachel C.|title=Injectable Contraceptives|year=1999|pages=121–149|doi=10.1007/978-3-642-86696-8_6}}
10. ^{{cite journal | vauthors = Coutinho EM, Spinola P, Barbosa I, Gatto M, Tomaz G, Morais K, Yazlle ME, de Souza RN, Pinho Neto JS, Leal Wde B, Leal C, Hippolito SB, Abranches AD | title = Multicenter, double-blind, comparative clinical study on the efficacy and acceptability of a monthly injectable contraceptive combination of 150 mg dihydroxyprogesterone acetophenide and 10 mg estradiol enanthate compared to a monthly injectable contraceptive combination of 90 mg dihydroxyprogesterone acetophenide and 6 mg estradiol enanthate | journal = Contraception | volume = 55 | issue = 3 | pages = 175–81 | date = March 1997 | pmid = 9115007 | doi = 10.1016/S0010-7824(97)00018-8 | url = }}
11. ^{{cite journal | vauthors = Coutinho EM, Spinola P, Tomaz G, Morais K, Nassar de Souza R, Sabino Pinho Neto J, de Barros Leal W, Bomfim Hippolito S, D'Aurea Abranches A | title = Efficacy, acceptability, and clinical effects of a low-dose injectable contraceptive combination of dihydroxyprogesterone acetophenide and estradiol enanthate | journal = Contraception | volume = 61 | issue = 4 | pages = 277–80 | date = April 2000 | pmid = 10899484 | doi = 10.1016/S0010-7824(00)00099-8 | url = }}
12. ^{{cite journal | vauthors = Koetsawang S | title = Once-a-month injectable contraceptives: efficacy and reasons for discontinuation | journal = Contraception | volume = 49 | issue = 4 | pages = 387–98 | date = April 1994 | pmid = 8013221 | doi = 10.1016/0010-7824(94)90034-5 | url = }}
13. ^{{cite web | url = https://consultaremedios.com.br/algestona-acetofenida-enantato-de-estradiol/bula | archive-url = https://web.archive.org/web/20180918105310/https://consultaremedios.com.br/algestona-acetofenida-enantato-de-estradiol/bula | archive-date = 2018-09-18 | title = Bula do Algestona Acetofenida + Enantato de Estradiol | website = Consulta Remédios | accessdate = 2018-09-18 | format = HTML}}
14. ^{{cite journal | vauthors = Wiemeyer JC, Fernandez M, Moguilevsky JA, Sagasta CL | title = Pharmacokinetic studies of estradiol enantate in menopausic women | journal = Arzneimittelforschung | volume = 36 | issue = 11 | pages = 1674–7 | year = 1986 | pmid = 3814225 | doi = | url = }}
15. ^{{cite journal | vauthors = Jarquín González JD, Elda de Aguirre L, Rodríguez C, Abrego de Aguilar M, Carrillo F, León DA, Lima M, Trigueros S, Acosta R | title = Dihydroxyprogesterone acetophenide 150 mg + estradiol enantate 10 mg as monthly injectable contraceptives | journal = Adv Contracept | volume = 12 | issue = 3 | pages = 213–25 | date = September 1996 | pmid = 8910663 | doi = 10.1007/BF01849664 | url = }}
16. ^{{cite journal|last1=Gual|first1=C.|last2=Pérez-Palacios|first2=G.|last3=Pérez|first3=A.E.|last4=Ruiz|first4=M.R.|last5=Solis|first5=J.|last6=Cervantes|first6=A.|last7=Iramain|first7=C.|last8=Schreiber|first8=E.C.|title=Metabolic fate of a long-acting injectable estrogen-progestogen contraceptive 1,2|journal=Contraception|volume=7|issue=4|year=1973|pages=271–287|issn=00107824|doi=10.1016/0010-7824(73)90145-5}}
17. ^{{cite book|author1=J. Bringer|author2=B. Hedon|title=Fertility and Sterility: A Current Overview|url=https://books.google.com/books?id=vZirsEgpXiMC&pg=PA47|date=15 September 1995|publisher=CRC Press|isbn=978-1-85070-694-6|pages=47–}}
18. ^{{cite journal | vauthors = Sang GW | title = Pharmacodynamic effects of once-a-month combined injectable contraceptives | journal = Contraception | volume = 49 | issue = 4 | pages = 361–85 | date = April 1994 | pmid = 8013220 | doi = 10.1016/0010-7824(94)90033-7 | url = }}
19. ^{{cite journal | vauthors = Skegg DC | title = Monthly combined injectable contraceptives and neoplasia | journal = Contraception | volume = 49 | issue = 5 | pages = 435–9 | date = May 1994 | pmid = 8045130 | doi = 10.1016/0010-7824(94)90002-7 | url = }}
20. ^{{cite journal | vauthors = Toppozada M | title = The clinical use of monthly injectable contraceptive preparations | journal = Obstet Gynecol Surv | volume = 32 | issue = 6 | pages = 335–47 | date = June 1977 | pmid = 865726 | doi = 10.1097/00006254-197706000-00001 | url = }}
21. ^{{cite journal | vauthors = Gallo MF, Grimes DA, Lopez LM, Schulz KF, d'Arcangues C | title = Combination injectable contraceptives for contraception | journal = Cochrane Database Syst Rev | volume = 3 | issue = | pages = CD004568 | date = 2013 | pmid = 23641480 | doi = 10.1002/14651858.CD004568.pub3 | url = }}
22. ^{{cite book|author1=Pramilla Senanayake|author2=Malcolm Potts|title=Atlas of Contraception, Second Edition|url=https://books.google.com/books?id=7dDKBQAAQBAJ&pg=PA50|date=14 April 2008|publisher=CRC Press|isbn=978-0-203-34732-4|pages=50–}}
23. ^{{cite book|author1=Thomas Rabe|author2=Benno Runnebaum|title=Fertility Control — Update and Trends: Update and Trends|url=https://books.google.com/books?id=zLopBgAAQBAJ&pg=PT183|date=6 December 2012|publisher=Springer Science & Business Media|isbn=978-3-642-86696-8|pages=183–|quote=Two additional monthly, combined injectable methods warrant mention. Deladroxate (commercially labelled as Perlutan, Topasel, Agurin, Horprotal and Uno-Ciclo in various countries), is a combination of 150 mg dihydroxyprogesterone acetophenide and 10 mg estradiol enanthate, and is available in many Latin American countries and Spain. The method is highly effective, without a single pregnancy reported in large clinical trials (Koetsawang 1994). Although available since the 1960s, the method has not been studied as extensively as Cyclofem or Mesigyna. The original manufacturer withdrew support due to toxicological concerns with dihydroxyprogesterone acetophenide, and clinical evaluations continue to be published. A recent dose-finding trial compared the standard available dose of 150/10 with a lower dose of 90/6, and concluded the lower dose was equally effective (Coutinho et al., 1997).}}
24. ^http://www.micromedexsolutions.com/micromedex2/librarian/
25. ^{{cite book |editor=Sweetman, Sean C. |chapter=Sex hormones and their modulators |title=Martindale: The Complete Drug Reference |edition=36th |year=2009 |page=2082 |publisher=Pharmaceutical Press |location=London|isbn=978-0-85369-840-1|url=https://www.medicinescomplete.com/mc/martindale/}}
26. ^https://www.drugs.com/international/algestone.html
27. ^https://www.drugs.com/international/algestone-acetophenide.html
28. ^10 11 {{cite journal | vauthors = Toppozada MK | title = Existing once-a-month combined injectable contraceptives | journal = Contraception | volume = 49 | issue = 4 | pages = 293–301 | date = April 1994 | pmid = 8013216 | doi = 10.1016/0010-7824(94)90029-9 | url = }}
29. ^{{cite book|author1=Leon Speroff|author2=Marc A. Fritz|title=Clinical Gynecologic Endocrinology and Infertility|url=https://books.google.com/books?id=8sIkqPT2gh4C&pg=PA969|year=2005|publisher=Lippincott Williams & Wilkins|isbn=978-0-7817-4795-0|pages=969–}}
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1 : Combined injectable contraceptives

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