Erikson Arne, Tufto Ingunn, Bjønnum Anne Berit, Bruland Øyvind S, Davies Catharina de Lange
Department of Physics, Norwegian University of Science and Technology, H-gskoleringen 5, 7491 Trondheim.
Anticancer Res. 2008 Nov-Dec;28(6A):3557-66.
The extracellular matrix represents a major barrier for drug delivery. This work compares the effects of collagenase and hyaluronidase on tumour uptake and distribution of two differently sized therapeutic molecules, IgG and liposomal doxorubicin.
The enzymes were injected i.v. prior to the therapeutic molecules, and uptake and distribution were studied by confocal laser scanning microscopy. The therapeutic molecules were colocalized with the vasculature and collagen network visualized by the second harmonic signal.
Hyaluronidase increased the uptake of liposomal doxorubicin to a small extent, whereas collagenase had no effect. Collagenase increased, but hyaluronidase reduced the uptake of IgG. Neither of the enzymes induced changes in the collagen network measured by the second harmonic signal.
Degradation of the collagen network improves delivery of molecules with the size of IgG, whereas degradation of the gel of glycosaminoglycans has a higher impact on the distribution of small drugs such as doxorubicin.
细胞外基质是药物递送的主要障碍。本研究比较了胶原酶和透明质酸酶对两种不同大小治疗性分子(免疫球蛋白G和脂质体阿霉素)肿瘤摄取和分布的影响。
在注射治疗性分子之前静脉注射酶,通过共聚焦激光扫描显微镜研究摄取和分布情况。利用二次谐波信号使治疗性分子与脉管系统和胶原网络共定位。
透明质酸酶在一定程度上增加了脂质体阿霉素的摄取,而胶原酶无此作用。胶原酶增加了免疫球蛋白G的摄取,但透明质酸酶降低了其摄取。两种酶均未引起通过二次谐波信号测量的胶原网络变化。
胶原网络的降解改善了免疫球蛋白G大小分子的递送,而糖胺聚糖凝胶的降解对阿霉素等小分子药物的分布影响更大。