Gould A R, Sharp P J, Smith D R, Stegink A J, Chase C J, Kovacs J C, Penglis S, Chatterton B E, Bunn C L
Pi2 Limited, PO Box 270, NSW 2120 Thornleigh, Australia.
Arch Dermatol Res. 2003 Nov;295(6):249-54. doi: 10.1007/s00403-003-0425-4. Epub 2003 Sep 9.
The penetration and permeation of the recombinant protein plasminogen activator inhibitor type 2 (PAI-2) in two formulations, one containing a penetration enhancer, into the psoriatic and uninvolved skin of eight patients with plaque-type psoriasis were investigated. Penetration and permeation of PAI-2 were measured by gamma counting and imaging following radiolabelling of a fraction of the applied PAI-2 with (123)I. The feasibility of topical delivery of drug to psoriatic plaques was confirmed by the finding that the permeability of psoriatic plaques to radiolabelled PAI-2 (P=0.007) and free (123)I (P=0.001) was approximately tenfold higher than the permeability of uninvolved skin. The addition of a penetration enhancer improved the permeation of PAI-2 into psoriatic plaques from an average of 35% to 46% (P=0.005). Occlusion decreased the permeation amount of PAI-2 from 46% to 15% due to losses on the occlusive dressing (P=0.001).
研究了重组蛋白纤溶酶原激活物抑制剂2型(PAI-2)在两种制剂中的渗透情况,其中一种含有渗透促进剂,该制剂作用于8例斑块型银屑病患者的银屑病皮损和正常皮肤。在用(123)I对一部分应用的PAI-2进行放射性标记后,通过γ计数和成像测量PAI-2的渗透情况。银屑病斑块对放射性标记的PAI-2(P = 0.007)和游离(123)I(P = 0.001)的通透性比正常皮肤的通透性高约10倍,这一发现证实了药物局部递送至银屑病斑块的可行性。添加渗透促进剂可使PAI-2进入银屑病斑块的渗透率从平均35%提高到46%(P = 0.005)。由于封闭敷料上的损失,封闭使PAI-2的渗透量从46%降至15%(P = 0.001)。