Pharmacokinetics and Bioavailability of the GnRH Analogs in the Form of Solution and Zn2+-Suspension After Single Subcutaneous Injection in Female Rats-Reference-Cited by-同舟云学术

Pharmacokinetics and Bioavailability of the GnRH Analogs in the Form of Solution and Zn2+-Suspension After Single Subcutaneous Injection in Female Rats

Published:2016-05-14 Issue:2 Volume:42 Page:251-259
ISSN:0378-7966
Container-title:European Journal of Drug Metabolism and Pharmacokinetics
language:en
Short-container-title:Eur J Drug Metab Pharmacokinet

Author:

Suszka-Świtek Aleksandra,Ryszka Florian,Dolińska Barbara,Dec Renata,Danch Alojzy,Filipczyk Łukasz,Wiaderkiewicz Ryszard

Funder

Śląski Uniwersytet Medyczny (PL)

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Link

http://link.springer.com/content/pdf/10.1007/s13318-016-0342-5.pdf

Reference30 articles.

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2. Nestor JJ, Ho TL, Simpson RA, Horner BL, Jones GH, McRae GI, et al. Synthesis and biological activity of some very hydrophobic superagonist analogues of luteinizing hormone-releasing hormone. J Med Chem. 1982;25(7):795–801.

3. Van Leusden HA. Impact of different GnRH analogs in benign gynecological disorders related to their chemical structure, delivery systems and dose. Gynecol Endocrinol. 1994;8(3):215–22.

4. Kiesel LA, Rody A, Greb RR, Szilágyi A. Clinical use of GnRH analogues. Clin Endocrinol (Oxf). 2002;56(6):677–87.

5. Colin IM, Jameson JL. Estradiol sensitization of rat pituitary cells to gonadotropin-releasing hormone: involvement of protein kinase C-and calcium-dependent signaling pathways. Endocrinology. 1998;139(9):3796–802.

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