Modderman E S, Huikeshoven H, Zuidema J, Leiker D L, Merkus F W
Int J Clin Pharmacol Ther Toxicol. 1982 Feb;20(2):51-6.
Dapsone is the drug of first choice in the treatment of leprosy. Although the oral route of administration has been mostly used, recent studies of patient compliance revealed that only about 50% of the tables received by the patients are actually taken. It is generally assumed that irregular self-medication favors the development of dapsone resistance. The need for a more reliable route of administration led us to investigate the possibility of an i.m. dapsone depot injection. To achieve effective blood levels for 3-4 weeks, suspensions of large dapsone particles in an aqueous vehicle were made. In a trial with 20 leprosy patients in Nigeria, injection of 900 mg dapsone i.m. as a mixture of particle sizes less than 90 micrometer (20%) and 90-125 micrometer (80%) resulted in a serum level above 0.5 microgram/ml for 18 +/- 5 days with a mean peak concentration of 3.1 +/- 0.9 microgram/ml (n = 10). Injection of 1200 mg of the same particle-size mixture led to peak concentrations of 2.7 +/- 1.0 microgram/ml and maintenance of the level above 0.5 microgram/ml for 25 +/- 3 days (n = 5). After injection of 1200 mg (particle size less than 90 micrometer), serum levels were kept above 0.5 microgram/ml for 21 +/- 5 days with a maximum concentration of 3.9 +/- 1.2 microgram/ml (n = 5). Serum levels were measured using a rapid non-extractive HPLC method. The injections were very well tolerated. Due to these encouraging results, the dosage and formulation will be further optimized.
氨苯砜是治疗麻风病的首选药物。尽管口服给药途径最为常用,但最近关于患者依从性的研究表明,患者实际服用的药片仅约50%。一般认为,不规律的自我用药会促使氨苯砜耐药性的产生。对更可靠给药途径的需求促使我们研究氨苯砜长效肌内注射的可能性。为了在3 - 4周内达到有效的血药浓度,制备了大颗粒氨苯砜在水性载体中的混悬液。在尼日利亚对20例麻风病患者进行的一项试验中,肌内注射900 mg氨苯砜,其颗粒大小小于90微米(20%)和90 - 125微米(80%)的混合物,血清浓度在0.5微克/毫升以上持续18±5天,平均峰值浓度为3.1±0.9微克/毫升(n = 10)。注射1200 mg相同颗粒大小混合物导致峰值浓度为2.7±1.0微克/毫升,血药浓度在0.5微克/毫升以上维持25±3天(n = 5)。注射1200 mg(颗粒大小小于90微米)后,血清浓度在0.5微克/毫升以上保持21±5天,最大浓度为3.9±1.2微克/毫升(n = 5)。血清浓度采用快速非萃取高效液相色谱法测定。这些注射耐受性良好。由于这些令人鼓舞的结果,剂量和制剂将进一步优化。