Poli Gianluigi, Mariotti Fabrizia, Corrado Mario Ermanno, Acerbi Daniela
Chiesi Farmaceutici S.p.A., Pharmacokinetics Department, Parma Italy.
Eur J Drug Metab Pharmacokinet. 2004 Apr-Jun;29(2):145-52. doi: 10.1007/BF03190589.
Disodium clodronate (dichloromethylene bisphosphonic acid, disodium salt; CAS 22560-50-5) is a bisphosphonate that has demonstrated efficacy in patients with a variety of diseases of enhanced bone resorption. Intramuscular clodronate can determine pain at the injection site, it is therefore particularly useful to co-administer a local anaesthetic with clodronate to reduce pain at the injection site. The tolerability and pharmacokinetic of a new formulation of 100 mg disodium clodronate containing 1% lidocaine (test formulation, Chiesi Farmaceutici S.p.A) were investigated in comparison to the same formulation without the local anaesthetic (Clody) and a marketed formulation containing 1% benzyl alcohol (Clasteon). Thirty healthy female volunteers were treated according to a single dose, double-blind, randomised, three-way cross-over design. The local tolerability was investigated by assessing reddening and hardening at the injection site, and plasma CPK levels. Pain intensity was investigated on the VAS (visual analogue scale) and on the VRS (verbal rating score). Urinary clodronic acid concentrations were determined using a validated specific GC/MS/NCI assay. The statistical analysis on pain assessment showed a significant reduction of pain intensity immediately and up to 2 hours after administration of the new formulation compared to the marketed ones. CPK levels and occurrence of hardening at the injection site did not show statistically significant differences between formulations. No local redness was reported. Clodronate urinary excretion during the 48 h collection interval was not statistically different among the formulations and the 95% confidence intervals were inside the bioequivalence acceptance region, demonstrating comparable bioavailability. It was concluded that the investigated new formulation of 100 mg disodium clodronate was better tolerated than the reference marketed formulations.
氯膦酸二钠(二氯亚甲基双膦酸二钠盐;CAS 22560-50-5)是一种双膦酸盐,已在多种骨吸收增强疾病患者中显示出疗效。肌内注射氯膦酸会引起注射部位疼痛,因此将局部麻醉剂与氯膦酸联合使用以减轻注射部位疼痛特别有用。与不含局部麻醉剂的相同制剂(Clody)和含1%苯甲醇的市售制剂(Clasteon)相比,研究了含1%利多卡因的100mg氯膦酸二钠新制剂(试验制剂,Chiesi Farmaceutici S.p.A)的耐受性和药代动力学。30名健康女性志愿者按照单剂量、双盲、随机、三交叉设计进行治疗。通过评估注射部位的发红和硬结以及血浆CPK水平来研究局部耐受性。采用视觉模拟量表(VAS)和语言评定量表(VRS)对疼痛强度进行研究。使用经过验证的特异性气相色谱/质谱/负化学电离法测定尿氯膦酸浓度。疼痛评估的统计分析表明,与市售制剂相比,新制剂给药后即刻至2小时疼痛强度显著降低。各制剂之间CPK水平和注射部位硬结的发生率无统计学显著差异。未报告局部发红情况。各制剂在48小时收集期内的氯膦酸尿排泄无统计学差异,且95%置信区间在生物等效性接受范围内,表明生物利用度相当。结论是,所研究的100mg氯膦酸二钠新制剂的耐受性优于市售对照制剂。