Chen Yongping, Shen Yuanyuan, Guo Xin, Zhang Caoshou, Yang Wenjuan, Ma Minglu, Liu Shu, Zhang Maobin, Wen Long-Ping
Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science & Technology of China, Hefei, Anhui 230027, China.
Nat Biotechnol. 2006 Apr;24(4):455-60. doi: 10.1038/nbt1193. Epub 2006 Mar 26.
Efficient transdermal drug delivery of large hydrophilic drugs is challenging. Here we report that the short synthetic peptide, ACSSSPSKHCG, identified by in vivo phage display, facilitated efficient transdermal protein drug delivery through intact skin. Coadministration of the peptide and insulin to the abdominal skin of diabetic rats resulted in elevated systemic levels of insulin and suppressed serum glucose levels for at least 11 h. Significant systemic bioavailability of human growth hormone was also achieved when topically coadministered with the peptide. The transdermal-enhancing activity of the peptide was sequence specific and dose dependent, did not involve direct interaction with insulin and enabled penetration of insulin into hair follicles beyond a depth of 600 microm. Time-lapse studies suggested that the peptide creates a transient opening in the skin barrier to enable macromolecular drugs to reach systemic circulation.
实现大分子亲水性药物的高效透皮给药具有挑战性。在此,我们报告称,通过体内噬菌体展示鉴定出的短合成肽ACSSSPSKHCG促进了蛋白质药物通过完整皮肤的高效透皮递送。将该肽与胰岛素共同施用于糖尿病大鼠的腹部皮肤,导致胰岛素的全身水平升高,并使血清葡萄糖水平至少在11小时内受到抑制。当与该肽局部共同给药时,人生长激素也实现了显著的全身生物利用度。该肽的透皮增强活性具有序列特异性和剂量依赖性,不涉及与胰岛素的直接相互作用,并能使胰岛素穿透至毛囊深处超过600微米。延时研究表明,该肽在皮肤屏障中形成一个短暂的开口,以使大分子药物能够进入体循环。