Jiang F N, Richter A M, Jain A K, Levy J G, Smits C
Department of Microbiology, University of British Columbia, Vancouver, Canada.
Biotechnol Ther. 1993;4(1-2):43-61.
Biodistribution of the photosensitizer benzoporphyrin derivative monoacid ring A (BPD) was compared in DBA/2 mice bearing the syngeneic M-1 tumor and nude mice bearing the A549 human squamous cell carcinoma. These studies, using internally labeled 14C-BPD showed that in general, biodistribution between the two strains was equivalent with the exception of two tissues; lymph nodes (BPD levels were higher in nude mice) and tumor (BPD levels were lower in nude mice). Further studies were carried out in A549-tumor-bearing nude mice in which the biodistribution of BPD conjugated to a monoclonal antibody (5E8) with specificity for an antigen on A549 cells was compared to a conjugate prepared with an irrelevant monoclonal antibody (T48). These studies showed that both conjugates had biodistribution characteristics which distinguished them from free BPD in that they remained in the circulation and most tissues for significantly longer times than did free BPD. Also, with the exception of the 5E8-BPD conjugate and A549 tumor tissue, levels in all tissues were highest at the 3-h time point following injection of conjugates. In the case of A549 tumor and the 5E8-BPD conjugate the highest concentration of 14C-labeled material was observed at the 14-h time point following injection. The results reported herein show that the conjugates tested behaved differently from free BPD, indicating that the materials did not become dissociated in vivo and that the specific conjugate (5E8-BPD) demonstrated specificity for the A549 tumor in terms of the kinetics of its accumulation in tumor tissue.
在携带同基因M-1肿瘤的DBA/2小鼠和携带A549人鳞状细胞癌的裸鼠中,比较了光敏剂苯并卟啉衍生物单酸环A(BPD)的生物分布。这些使用内部标记的14C-BPD的研究表明,一般来说,除了两个组织外,两种品系之间的生物分布是相同的;淋巴结(裸鼠中的BPD水平较高)和肿瘤(裸鼠中的BPD水平较低)。在携带A549肿瘤的裸鼠中进行了进一步研究,其中将与对A549细胞上的抗原具有特异性的单克隆抗体(5E8)偶联的BPD的生物分布与用无关单克隆抗体(T48)制备的偶联物进行了比较。这些研究表明,两种偶联物都具有与游离BPD不同的生物分布特征,因为它们在循环和大多数组织中停留的时间比游离BPD长得多。此外,除了5E8-BPD偶联物和A549肿瘤组织外,在注射偶联物后的3小时时间点,所有组织中的水平最高。就A549肿瘤和5E8-BPD偶联物而言,在注射后的14小时时间点观察到14C标记物质的最高浓度。本文报道的结果表明,所测试的偶联物与游离BPD的行为不同,表明这些物质在体内没有解离,并且特定的偶联物(5E8-BPD)在肿瘤组织中的积累动力学方面表现出对A549肿瘤的特异性。