The bioavailability and the clinical usefulness of the P administered by nasal spray were investigated. Ten healthy menopausal women received an IN spray administration (4 doses of an oleic P solution 20 mg/mL, corresponding to nearly 11.2 mg of P) and the circulating P levels were calculated. Sixty minutes after administration, the maximum concentration (CMax, 3.75 +/- 0.214 ng/mL) was reached. High P levels (greater than 2 ng/mL) lasted until 360 minutes, and the AUC 0 to 720 was 1,481.6 +/- 343 ng.h/mL. Progesterone administration by spray formulation has proven to be effective in reaching therapeutic levels and to be acceptable to patients and, probably, clinically safe.
PMID 2065793 2065793 DOI 10.1016/s0015-0282(16)54433-1 10.1016/s0015-0282(16)54433-1
Cite this article
Cicinelli, E., Ragno, G., Cagnazzo, I., Fanelli, F., Vetuschi, C., & Schonauer, S. (1991). Progesterone administration by nasal spray. *Fertility and sterility*, *56*(1), 139-141. https://doi.org/10.1016/s0015-0282(16)54433-1
Cicinelli E, Ragno G, Cagnazzo I, Fanelli F, Vetuschi C, Schonauer S. Progesterone administration by nasal spray. Fertil Steril. 1991;56(1):139-141. doi:10.1016/s0015-0282(16)54433-1
Cicinelli, E., et al. "Progesterone administration by nasal spray." *Fertility and sterility*, vol. 56, no. 1, 1991, pp. 139-141.
Keywords
Absorption, Administration, Intranasal, Biological Availability, Female, Humans, Kinetics, Middle Aged, Progesterone/administration & Dosage/adverse Effects/pharmacokinetics, Progesterone, Americas, Biology, Clinical Research, Contraception, Contraception Research, Developed Countries, Endocrine System, Family Planning, Hormones, North America, Northern America, Physiology, Progestational Hormones, Progesterone--administraction and Dosage, Progesterone--pharmacodynamics, Research Methodology, United States
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