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首页> 外文期刊>BJU international >Transdermal testosterone gel: pharmacokinetics, efficacy of dosing and application site in hypogonadal men.
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Transdermal testosterone gel: pharmacokinetics, efficacy of dosing and application site in hypogonadal men.

机译:透皮睾丸激素凝胶:性腺功能减退男性的药代动力学,给药功效和应用部位。

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摘要

Testosterone gels are being increasingly used throughout the world. There is still some controversy associated with their use, but many of the uncertainties are gradually being overcome and explained. The authors from the USA evaluated the pharmacokinetics and the efficacy of dosing and application sites of another such transdermal gel. The arrival of oral agents for treating male erectile dysfunction has made it easier for GPs to treat this condition. The authors from Southampton have examined the safety of sildenafil used in general medical practice in England, finding that it was used safely at this level, with no unexpected events. OBJECTIVE To determine the regimen that would most effectively maintain serum testosterone concentrations in treated hypogonadal men within the normal reference range of 3-11.4 micro g/L. PATIENTS AND METHODS Eighteen men aged 24-69 years with either primary or secondary hypogonadism participated in and 16 completed a randomized, six-treatment regimen, three-period (phase), three-way matrix-type crossover study. A 1% and 2% testosterone gel (CP601, Cellegy Pharmaceuticals, Inc., San Francisco, USA) was administered either once or twice daily transdermally at different body sites to determine optimal dosing, application sites, and its pharmacokinetics and tolerability in hypogonadal men. Treatments A-F included 1 g of 1% and 2% gel that was equivalent to 10 or 20 mg of testosterone, applied once or twice daily to the skin of either the thigh or the upper arm. Six men also participated in a study of 3 g of 2% gel that was equivalent to 60 mg of testosterone applied once daily, half on each thigh. Pharmacokinetic variables were calculated for testosterone for each man in each treatment period and the results analysed by anova. RESULTS In general the higher dose regimens produced higher serum concentrations of testosterone; the 3 g/2% dose was most successful in maintaining serum testosterone within the normal reference range. The average testosterone concentration (C(avg))was 6.52 micro g/L and all men had a C(avg) of > 3.0 micro g/L. The prediction of all men achieving a C(avg) of > 3.0 micro g/L was 96%. The mean minimum concentration (C(min)) was 3.83 micro g/L and half the patients had a C(min) of > 3.0 micro g/L. Most men had serum testosterone levels within the normal reference range throughout the 24 h, and the treatment was well tolerated. CONCLUSIONS The 3 g/2% dose applied to the skin daily resulted in serum testosterone in the normal reference range in most hypogonadal men. Dose adjustments to either a lower or higher dose should shift serum testosterone concentration to the desired range in those who do not achieve this range with this dose.
机译:睾酮凝胶在世界范围内越来越多地被使用。它们的使用仍然存在一些争议,但是许多不确定性正在逐步克服和解释。美国的作者评估了另一种此类透皮凝胶的药代动力学以及给药和应用部位的功效。用于治疗男性勃起功能障碍的口服药物的出现使GP可以更轻松地治疗这种情况。来自南安普敦的作者检查了西地那非在英国普通医疗实践中的安全性,发现西地那非在此水平安全使用,没有发生任何意外事件。目的确定能够最有效地维持性腺功能减退男性患者血清睾丸激素浓度在3-11.4 micro g / L正常参考范围内的方案。患者和方法18名年龄在24-69岁的原发性或继发性性腺功能减退症的男性参加了研究,其中16名完成了一项随机,六种治疗方案,三期(阶段),三效矩阵式交叉研究。在不同的身体部位每天一次或两次经皮施用1%和2%的睾丸激素凝胶(CP601,Cellegy Pharmaceuticals,Inc.,美国旧金山),以确定性腺功能减退男性的最佳剂量,应用部位及其药代动力学和耐受性。处理A-F包括1克1%和2%的凝胶,相当于10或20毫克的睾丸激素,每天应用于大腿或上臂皮肤一次或两次。六名男子还参加了一项3 g 2%凝胶的研究,该凝胶相当于每天60 mg睾丸激素一次,每条大腿一半。计算每个治疗阶段每个人睾丸激素的药代动力学变量,并通过方差分析对结果进行分析。结果一般而言,较高剂量的治疗方案会产生较高的睾丸激素血清浓度。 3 g / 2%的剂量最成功地将血清睾丸激素维持在正常参考范围内。平均睾丸激素浓度(C(avg))为6.52 micro g / L,所有男性的C(avg)> 3.0 micro g / L。所有男性的C(avg)均> 3.0 micro g / L的预测为96%。平均最低浓度(C(min))为3.83 micro g / L,一半患者的C(min)> 3.0 micro g / L。大多数男性在整个24小时内的血清睾丸激素水平均在正常参考范围内,并且治疗耐受性良好。结论在大多数性腺功能减退的男性中,每天3 g / 2%的剂量可导致血清睾丸激素达到正常参考范围。将剂量调整为较低或较高剂量,应在那些未达到该剂量范围的患者中将血清睾丸激素的浓度移至所需范围。

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