1.Study on contraceptive effects, safety and acceptable of Vietnamese women in using Implanon
Journal of Practical Medicine 2004;472(2):70-72
Implanon contraceptive medicine was used by 120 women aged 18-40 years old from September 2000 to December 2003. There was no case getting pregnancy. Blood pressure and body weight had not changed significantly. The bleeding pattern had changed in comparing with preferable for women were normal bleeding, spare bleeding and amenorrheoa - 88% -. Side effects manifested with low level and most decreased in comparing with that before the study.
Contraception
;
Safety
;
Women
;
Desogestrel
2.Simultaneous determination of gestodene, etonogestrel and ethinylestradiol in plasma by LC-MS/MS following derivatization.
Xiao-Fen LIU ; Cun-Gang DING ; Qing-Hua GE ; Zhen ZHOU ; Xiao-Jin ZHI
Acta Pharmaceutica Sinica 2010;45(1):87-92
To establish a sensitive and specific method for simultaneous determination of gestodene, etonogestrel and ethinylestradiol in plasma by LC-MS/MS, plasma samples were extracted and derivatized before injection. An ESI ion source was used and operated in the positive ion mode with multiple reaction monitoring (MRM). Norgestrel was chosen as internal standard and performed on a C18 (100 mm x 2.1 mm, 5 microm) column. The concentrations of gestodene, etonogestrel and ethinylestradiol were measured, using step-gradient mobile phase and step-gradient flow rate. The method was validated over the concentration range of 0.1-20 ng x mL(-1) for gestodene and etonogestrel and 0.01-2 ng x mL(-1) for ethinylestradiol, and showed excellent linearity. The intra- and inter-assay accuracy and precision were below 10.0% and recovery was 93.6%-110.9% over the three concentration levels evaluated. The method was applied in pharmacokinetic study of the compound gestodene patch and the compound etonogestrel patch in rabbits. The LC-MS/MS method was selective, accurate and sensitive, especially the LOQ were 100 pg x mL(-1) for gestodene and etonogestrel and 10 pg x mL(-1) for ethinylestradiol. The method was successfully applied in pharmacokinetic study for contraceptives.
Animals
;
Chromatography, Liquid
;
Desogestrel
;
blood
;
pharmacokinetics
;
Ethinyl Estradiol
;
blood
;
pharmacokinetics
;
Norpregnenes
;
blood
;
pharmacokinetics
;
Rabbits
;
Sensitivity and Specificity
;
Spectrometry, Mass, Electrospray Ionization
3.Determination of Optimal Imaging Mode for Ultrasonographic Detection of Subdermal Contraceptive Rods: Comparison of Spatial Compound, Conventional, and Tissue Harmonic Imaging Methods.
Sungjun KIM ; Kyung SEO ; Ho Taek SONG ; Jin Suck SUH ; Choon Sik YOON ; Jeong Ah RYU ; Jeong Seon PARK ; Ah Hyun KIM ; Ah Young PARK ; Yaena KIM
Korean Journal of Radiology 2012;13(5):602-609
OBJECTIVE: To determine which mode of ultrasonography (US), among the conventional, spatial compound, and tissue-harmonic methods, exhibits the best performance for the detection of Implanon(R) with respect to generation of posterior acoustic shadowing (PAS). MATERIALS AND METHODS: A total of 21 patients, referred for localization of impalpable Implanon(R), underwent US, using the three modes with default settings (i.e., wide focal zone). Representative transverse images of the rods, according to each mode for all patients, were obtained. The resulting 63 images were reviewed by four observers. The observers provided a confidence score for the presence of PAS, using a five-point scale ranging from 1 (definitely absent) to 5 (definitely present), with scores of 4 or 5 for PAS being considered as detection. The average scores of PAS, obtained from the three different modes for each observer, were compared using one-way repeated measure ANOVA. The detection rates were compared using a weighted least square method. RESULTS: Statistically, the tissue harmonic mode was significantly superior to the other two modes, when comparing the average scores of PAS for all observers (p < 0.00-1). The detection rate was also highest for the tissue harmonic mode (p < 0.001). CONCLUSION: Tissue harmonic mode in uS appears to be the most suitable in detecting subdermal contraceptive implant rods.
Adult
;
Analysis of Variance
;
Arm/*ultrasonography
;
*Contraceptive Agents, Female
;
*Desogestrel
;
Female
;
Foreign Bodies/*ultrasonography
;
Humans
;
Middle Aged
;
Ultrasonography/*methods
4.Pulmonary embolism in a healthy woman using the oral contraceptives containing desogestrel.
Obstetrics & Gynecology Science 2017;60(2):232-235
Venous thromboembolism is well known as one of the rare but serious adverse effects of combined oral contraceptives (COCs). The COCs with third and fourth generation progestogens were found to have higher risk of venous thrombosis than those with second generation progestogens. We present a case of pulmonary embolism in a 23-year-old nulligravid woman who was using COCs containing the third generation progestogen (desogestrel). At the time of presentation of the adverse effect, she had been using the COCs for 4 months. She had no additional risk factors for thrombosis such as smoking, surgery, tumor as well as genetic factors. This case demonstrates even young women in otherwise good health may be at risk of venous thromboembolism from low-dose formulations of COCs as an over-the-counter drug. We describe this case with a brief review of literatures.
Contraceptives, Oral*
;
Contraceptives, Oral, Combined
;
Desogestrel*
;
Female
;
Humans
;
Progestins
;
Pulmonary Embolism*
;
Risk Factors
;
Smoke
;
Smoking
;
Thrombosis
;
Venous Thromboembolism
;
Venous Thrombosis
;
Young Adult
5.Drug synergistic antifertility effect of combined administration of low-dose gossypol with steroid hormones in rats.
Qing CHANG ; Zhe LIU ; Wen-Zhi MA ; Chang-Chun HEI ; Xin-Sheng SHEN ; Xiao-Jing QIAN ; Zeng-Lu XU
Chinese Medical Journal 2011;124(11):1678-1682
BACKGROUNDOur previous studies suggested that low-dose gossypol combined with steroid hormones has a reversible antifertility role in adult male rats, and the course of treatment was shorter than that of either gossypol or steroid hormones alone. This result suggested that low-dose gossypol and steroid hormones have a drug synergistic effect on antifertility. The aim of the study was to find the target organs of the antifertility synergistic effect of the combined regimen.
METHODSThirty-two adult male rats were divided into four groups randomly: group GH, rats were fed orally with gossypol acetic acid (GA, 12.5 mg×kg(-1)×d(-1)) and desogestrel (DSG, 0.125 mg×kg(-1)×d(-1))/ethinylestradiol (EE, 0.025 mg×kg(-1)×d(-1))/testosterone undecanoate (TU, 100 mg×kg(-1)×d(-1)); group G, a single dose of GA (12.5 mg×kg(-1)×d(-1)) was given; group H, the same dosage of DSG/EE/TU as in group GH were administered; group C, rats were treated with vehicle (1% methyl cellulose) as control. Testes and epididymis were removed at 8 weeks post-treatment for evaluating their weight, volumes, volume fraction, and total volume of testicular tissue structures and the seminiferous tubule diameter using stereological assay. Sperm cell numbers and the motility of epididymal sperm were quantitated by flow cytometry and morphological methods.
RESULTSCompared with group C, spermatogenesis was normal in group G and suppressed in groups H and GH. Similar changes of testicular tissue structures and sperm number were found in groups H and GH. The decreases of epididymal sperm number and motility in group GH were greater than that of the low-dose gossypol or steroid hormones alone group.
CONCLUSIONSThe suppression of spermatogenesis was induced by steroid hormones in the combined regimen, and the epididymis was the target organ of low-dose gossypol. Combined use of low-dose gossypol and steroid hormones played a comprehensive antifertility role in their synergistic effect on reducing the number and motility of epididymal sperm.
Animals ; Desogestrel ; pharmacology ; Epididymis ; drug effects ; Ethinyl Estradiol ; pharmacology ; Flow Cytometry ; Gossypol ; analogs & derivatives ; pharmacology ; Male ; Random Allocation ; Rats ; Sperm Motility ; drug effects ; Spermatogenesis ; drug effects ; Spermatozoa ; drug effects ; Testis ; drug effects ; Testosterone ; analogs & derivatives ; pharmacology