Luftensteiner C P, Schwendenwein I, Eichler H G, Paul B, Wölfl G, Viernstein H
Institute of Pharmaceutical Technology, University of Vienna, Althanstrasse 14, A-1090, Vienna, Austria.
Int J Pharm. 1999 Apr 15;180(2):251-60. doi: 10.1016/s0378-5173(99)00011-3.
Mitoxantrone (MXN) has demonstrated therapeutic efficacy in the intraperitoneal treatment of malignancies. However, severe local toxicity is dose limiting. Therefore, a particulate formulation of MXN, the drug incorporated in albumin microspheres, was evaluated concerning tolerability. Survival rates as well as alterations in body weight, food intake, water intake, urine volume, urine specific gravity, urine protein content, and complete blood count were observed following single or multiple intraperitoneal injections of MXN solution, dispersions containing MXN-loaded microspheres or unloaded microspheres, and the injection vehicle to female and male Sprague-Dawley rats. Applied MXN dosage was equivalent to 30 mg/m2 body surface area. Unloaded microspheres were well tolerated without signs of toxicity. Application of MXN solution or MXN-loaded microspheres resulted in similar survival rates (56% 9 weeks after single injection) and in a comparable bone marrow toxicity (mainly leucopenia). Body weight, food and water intake as well as urine volume were decreased following application of MXN solution, whereas a progressive gain in weight and no remarkable alterations in nutrition and urine excretion were noted after administration of MXN-loaded and unloaded microspheres, or of the injection vehicle. In conclusion, intraperitoneal injection of MXN incorporated in albumin microspheres exhibits in part less toxicity than conventional treatment.
米托蒽醌(MXN)已在恶性肿瘤的腹腔内治疗中显示出治疗效果。然而,严重的局部毒性限制了其剂量。因此,对一种米托蒽醌的微粒制剂(药物包裹在白蛋白微球中)的耐受性进行了评估。在对雌性和雄性Sprague-Dawley大鼠单次或多次腹腔注射米托蒽醌溶液、含有载药微球或未载药微球的分散液以及注射载体后,观察了存活率以及体重、食物摄入量、饮水量、尿量、尿比重、尿蛋白含量和全血细胞计数的变化。应用的米托蒽醌剂量相当于30mg/m²体表面积。未载药微球耐受性良好,无毒性迹象。注射米托蒽醌溶液或载药微球导致相似的存活率(单次注射9周后为56%)和相当的骨髓毒性(主要是白细胞减少)。注射米托蒽醌溶液后,体重、食物和水摄入量以及尿量均下降,而注射载药和未载药微球或注射载体后,体重逐渐增加,营养和尿液排泄无明显变化。总之,腹腔注射包裹在白蛋白微球中的米托蒽醌,其毒性部分低于传统治疗。