Tomlinson R V, Spires H R, Kent J S
J Anim Sci. 1984 Jul;59(1):164-9. doi: 10.2527/jas1984.591164x.
Preliminary studies on use of the synthetic prostaglandin, fenprostalene, as an abortifacient had indicated that maximum effectiveness was dependent upon slow delivery. Because both route of administration and formulation control delivery rates, the influences of intramuscular (im) vs subcutaneous (sc) injections, and aqueous acetate buffer (AAB) vs polyethylene glycol-400 (PEG) vehicles on the plasma concentration and urinary excretion of fenprostalene were compared. Feedlot heifers were administered 1 mg injections of [13,14-3H]-fenprostalene. Blood samples and total urine excretion were collected during the following 96 h. The maximum concentration of tritium in plasma occurred at 2 h for AAB-im (.90 ng eq/ml), PEG-im (.75 ng eq/ml) and AAB-sc (.64 ng eq/ml), and then declined throughout 24 h with t 1/2 values of 6.1, 9.4 and 9.2 h, respectively. The peak concentration from PEG-sc was lower (.37 ng eq/ml, P less than .05), observed later (4h, P less than .05) and declined more slowly following peak concentration (t 1/2 = 15.1 h, P less than .05). Consistent with delayed absorption, a smaller fraction (P less than .05) of the total radioactivity excreted in urine was recovered during the first 24 h after injection for PEG-sc (85%) than for PEG-im (95%), AAB-sc (97%) or AAB-im (99%). In a tissue distribution study, plasma, urine and fecal samples were collected and heifers were slaughtered at various times following sc injection of 1 mg of [3H] fenprostalene in PEG. Peak concentrations of tritium in plasma occurred between 4 and 8 h and declined with a t 1/2 of 15.2 h.(ABSTRACT TRUNCATED AT 250 WORDS)
关于使用合成前列腺素芬前列林作为堕胎药的初步研究表明,最大效果取决于缓慢给药。由于给药途径和制剂都会控制给药速率,因此比较了肌肉注射(im)与皮下注射(sc)以及醋酸盐水溶液缓冲液(AAB)与聚乙二醇-400(PEG)载体对芬前列林血浆浓度和尿排泄的影响。在饲养场给小母牛注射1毫克[13,14-3H] - 芬前列林。在接下来的96小时内收集血样和总尿排泄量。血浆中氚的最大浓度在2小时时出现,AAB-im组为0.90纳克当量/毫升,PEG-im组为0.75纳克当量/毫升,AAB-sc组为0.64纳克当量/毫升,然后在24小时内下降,t 1/2值分别为6.1、9.4和9.2小时。PEG-sc组的峰值浓度较低(0.37纳克当量/毫升,P小于0.05),出现较晚(4小时,P小于0.05),且在峰值浓度后下降更缓慢(t 1/2 = 15.1小时,P小于0.05)。与吸收延迟一致,注射后24小时内,PEG-sc组尿中排泄的总放射性中回收的比例较小(P小于0.05),为85%,而PEG-im组为95%,AAB-sc组为97%,AAB-im组为99%。在一项组织分布研究中,皮下注射1毫克PEG中的[3H]芬前列林后,在不同时间收集血浆、尿液和粪便样本,并宰杀小母牛。血浆中氚的峰值浓度在4至8小时之间出现,t 1/2为15.2小时下降。(摘要截断于250字)