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一种用于测量唾液中睾酮的时间分辨荧光免疫测定法:用布西睾酮监测睾酮替代疗法。

A time-resolved fluorescence immunoassay for the measurement of testosterone in saliva: monitoring of testosterone replacement therapy with testosterone buciclate.

作者信息

Tschöp M, Behre H M, Nieschlag E, Dressendörfer R A, Strasburger C J

机构信息

AG Neuroendokrinologie, Medizinische Klinik, Klinikum Innenstadt der Ludwig Maximilians Universität München, München, Germany.

出版信息

Clin Chem Lab Med. 1998 Apr;36(4):223-30. doi: 10.1515/CCLM.1998.038.

Abstract

Monitoring of testosterone replacement therapy requires a reliable method for testosterone measurement. Determination of salivary testosterone, which reflects the hormone's biologically active plasma fraction, is a superior technique for this purpose. The aim of the present study was to establish a new sensitive time-resolved fluorescence immunoassay for the accurate measurement of testosterone levels in saliva and to validate it by monitoring testosterone replacement therapy in eight hypogonadal men. A clinical phase I-study with the new ester testosterone buciclate was performed to search for new testosterone preparations to produce constant serum levels in the therapy of male hypogonadism. After two control examinations eight male patients with primary hypogonadism were randomly assigned to two treatment groups (n = 2 x 4) and given single doses of either 200 mg (group I) or 600 mg (group II) testosterone buciclate intramuscularly. Saliva and blood samples were obtained 1, 2, 3, 5 and 7 days post injection and then weekly for three months. The time-resolved fluorescence immunoassay for salivary testosterone shows a detection limit of 16 pmol/l, an intra-assay CV of 8.9% (at a testosterone concentration of 302 pmol/l), an inter-assay CV of 8.7% (at a testosterone concentration of 305 pmol/l) and a good correlation with an established radioimmunoassay of r = 0.89. The sample volume required by this method is only 180 microliters for extraction and duplicate determination. The assay procedure requires no more than three hours. In group I (200 mg) testosterone did not increase to normal levels either in saliva or in serum. However, in group II, androgen levels increased significantly and were maintained in the normal range for up to 12 weeks with maximal salivary testosterone levels of 303 +/- 18 pmol/l (mean +/- SE) and maximal testosterone levels of 13.1 +/- 0.9 nmol/l (mean +/- SE) in serum in study week 6 and 7. The time-resolved fluorescence immunoassay for salivary testosterone provides a useful tool for monitoring androgen status in men and women and is well suited for the follow-up of testosterone replacement therapy on an outpatient basis. The long-acting ester testosterone buciclate is a promising agent for substitution therapy of male hypogonadism and in combination with testosterone monitoring in saliva offers an interesting new perspective for male contraception.

摘要

睾酮替代疗法的监测需要一种可靠的睾酮测量方法。测定唾液睾酮可反映激素的生物活性血浆部分,是用于此目的的一种优越技术。本研究的目的是建立一种新的灵敏时间分辨荧光免疫分析法,用于准确测量唾液中的睾酮水平,并通过监测八名性腺功能减退男性的睾酮替代疗法对其进行验证。进行了一项关于新的布西睾酮酯的临床I期研究,以寻找新的睾酮制剂,以便在男性性腺功能减退治疗中产生恒定的血清水平。在两次对照检查后,八名原发性性腺功能减退男性患者被随机分为两个治疗组(n = 2×4),分别肌肉注射单剂量200mg(I组)或600mg(II组)布西睾酮。在注射后1、2、3、5和7天采集唾液和血液样本,然后在三个月内每周采集一次。唾液睾酮的时间分辨荧光免疫分析法检测限为16pmol/l,批内变异系数为8.9%(睾酮浓度为302pmol/l时),批间变异系数为8.7%(睾酮浓度为305pmol/l时),与已建立的放射免疫分析法相关性良好,r = 0.89。该方法提取和重复测定所需样本体积仅为180微升。测定过程不超过三小时。在I组(200mg)中,唾液和血清中的睾酮均未升高至正常水平。然而,在II组中,雄激素水平显著升高,并在长达12周的时间内维持在正常范围内,在研究第6周和第7周时,唾液中睾酮最高水平为303±18pmol/l(平均值±标准误),血清中睾酮最高水平为13.1±0.9nmol/l(平均值±标准误)。唾液睾酮的时间分辨荧光免疫分析法为监测男性和女性的雄激素状态提供了一种有用的工具,非常适合在门诊对睾酮替代疗法进行随访。长效酯类布西睾酮是男性性腺功能减退替代疗法的一种有前景的药物,结合唾液睾酮监测为男性避孕提供了一个有趣的新视角。

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