O'Doherty M J, Thomas S H, Page C J, Blower P J, Bateman N T, Nunan T O
Department of Nuclear Medicine, St. Thomas' Hospital, London, UK.
Nucl Med Commun. 1993 Jan;14(1):8-11. doi: 10.1097/00006231-199301000-00003.
The pulmonary deposition of nebulized pentamidine (300 mg, Respirgard II nebulizer) was measured in seven human immunodeficiency virus (HIV)-positive men using a new radiopharmaceutical, 123I-iodopentamidine. Mean total pulmonary deposition was 15.3 mg or 5.1% of the initial nebulizer dose. Further studies in two of the patients showed that at 24 h, 87% of deposited 123I was retained in the lungs. Small amounts of activity (expressed as a percentage of the initial nebulizer activity) were also detected over the thyroid (0.4%), bladder (1%) and gut (0.7%). The ratio of 123I activity to pentamidine concentration was similar in the nebulizer solution and urine. These results suggest that 123I-pentamidine may be sufficiently stable in vivo to be used to study the biodistribution of inhaled and parenteral pentamidine in humans.
使用一种新型放射性药物123I-碘喷他脒,对7名人类免疫缺陷病毒(HIV)阳性男性进行了雾化喷他脒(300毫克,Respirgard II雾化器)的肺部沉积测量。平均总肺部沉积量为15.3毫克,占初始雾化器剂量的5.1%。对其中两名患者的进一步研究表明,在24小时时,沉积的123I中有87%保留在肺部。在甲状腺(0.4%)、膀胱(1%)和肠道(0.7%)也检测到少量活性(以初始雾化器活性的百分比表示)。雾化器溶液和尿液中123I活性与喷他脒浓度的比值相似。这些结果表明,123I-喷他脒在体内可能足够稳定,可用于研究吸入和胃肠外给药的喷他脒在人体中的生物分布。