Kota Jagannath, Machavaram Krishna K, McLennan Danielle N, Edwards Glenn A, Porter Christopher J H, Charman Susan A
Department of Pharmaceutics, Victorian College of Pharmacy, Monash University, Parkville, VIC, Australia.
Drug Metab Dispos. 2007 Dec;35(12):2211-7. doi: 10.1124/dmd.107.015669. Epub 2007 Sep 17.
The relative contribution of the lymph and blood in the absorption of darbepoetin alfa (DA) from different s.c. injection sites was determined using a central lymph-cannulated sheep model. DA was administered to parallel groups either as a bolus i.v. injection (0.5 mug/kg) into the jugular vein or as a bolus s.c. injection (2 mug/kg) into the interdigital space, the abdomen, or the shoulder. In the lymph-cannulated groups, the thoracic lymph duct was cannulated for continuous collection of central lymph, and blood samples were periodically collected via the jugular vein in all the groups. The concentration of DA in serum and lymph was determined by enzyme-linked immunosorbent assay. The total fraction of the dose reaching the systemic circulation and the fractions absorbed via the lymph and the blood were determined. A pharmacokinetic model was constructed to simultaneously fit the data from all the treatment groups. Absorption was essentially complete for all three injection sites in non-lymph-cannulated s.c. groups, but the rates of absorption differed significantly. Based on the modeling results for the lymph-cannulated groups, the lymphatics represented the predominant absorption route for both the interdigital (90 +/- 1%) and the abdomen (67 +/- 9%) injection sites. Fluorescein isothiocyanate dextran visualization studies revealed that the lymph draining the shoulder injection site entered the thoracic lymph duct distal to the point of cannulation, effectively precluding collection of thoracic lymph from this site. For that reason, the contribution of the lymphatics following injection in the shoulder could not be determined using these cannulation procedures.
采用中心淋巴管插管绵羊模型,确定了淋巴液和血液在不同皮下注射部位对聚乙二醇化重组人促红细胞生成素(DA)吸收的相对贡献。将DA分别以静脉推注(0.5μg/kg)注入颈静脉或皮下推注(2μg/kg)注入指间间隙、腹部或肩部,给予平行组。在淋巴管插管组中,将胸导管插管以持续收集中心淋巴液,并在所有组中通过颈静脉定期采集血样。通过酶联免疫吸附测定法测定血清和淋巴液中DA的浓度。确定了到达体循环的剂量总分数以及通过淋巴液和血液吸收的分数。构建了药代动力学模型以同时拟合所有治疗组的数据。在非淋巴管插管皮下组中,所有三个注射部位的吸收基本完成,但吸收速率差异显著。基于淋巴管插管组的建模结果,淋巴管是指间(90±1%)和腹部(67±9%)注射部位的主要吸收途径。异硫氰酸荧光素葡聚糖可视化研究表明,引流肩部注射部位的淋巴液进入插管点远端的胸导管,有效地排除了从此部位收集胸导管淋巴液的可能性。因此,使用这些插管程序无法确定肩部注射后淋巴管的贡献。