Luo J P, Hubbard J W, Midha K K
College of Pharmacy & Nutrition, University of Saskatchewan, Saskatoon, Canada.
Pharm Res. 1998 Sep;15(9):1485-9. doi: 10.1023/a:1011978327504.
The release and presystemic absorption of fluphenazine and its decanoate ester from intramuscular depots were investigated.
Rats were sacrificed in groups of three at various times after injection of drug or prodrug in sesame oil. Muscle tissues at the injection sites and various lymph nodes were excised. Blood (plasma) was harvested by cardiac puncture.
Following administration of fluphenazine decanoate, the amount of prodrug at the sites of injection declined exponentially (half-life 3.4 days). Highest concentrations of drug and prodrug were found in iliac and hypogastric lymph nodes nearest to injection sites in which both analytes were detectable 28 days post dose. The half-life for the decline of fluphenazine from lymph nodes (4.6 days) was similar to that from plasma (4.3 days). Following administration of fluphenazine base, only 2.8% of the dose remained at the sites of injection after 2 days. Concentrations of drug in iliac and hypogastric lymph nodes were comparable to those in distal lymph nodes. Fluphenazine concentrations in the lymphatic tissues decreased at about the same rate as plasma concentrations.
The rate limiting step appeared to be slow partitioning of the decanoate from oily deposits at the injection site and proximal lymph nodes with subsequent hydrolysis of the ester group.
研究氟奋乃静及其癸酸酯从肌肉注射贮库中的释放及首过吸收情况。
将大鼠以每组三只的方式,在注射药物或前体药物于芝麻油中后的不同时间点处死。切除注射部位的肌肉组织及各种淋巴结。通过心脏穿刺采集血液(血浆)。
给予癸酸氟奋乃静后,注射部位的前体药物量呈指数下降(半衰期3.4天)。在给药后28天,在最靠近注射部位的髂淋巴结和腹下淋巴结中发现药物和前体药物的浓度最高,且两种分析物均可检测到。氟奋乃静从淋巴结下降的半衰期(4.6天)与从血浆下降的半衰期(4.3天)相似。给予氟奋乃静碱后,2天后仅2.8%的剂量残留在注射部位。髂淋巴结和腹下淋巴结中的药物浓度与远端淋巴结中的浓度相当。淋巴组织中氟奋乃静的浓度下降速率与血浆浓度下降速率大致相同。
限速步骤似乎是癸酸酯从注射部位的油性沉积物和近端淋巴结缓慢分配,随后酯基发生水解。