TRANSDERMAL IONTOPHORESIS OF GONADOTROPIN-RELEASING HORMONE (LHRH) AND 2 ANALOGS

Gonadotropin releasing hormone (GnRH), as well as an antagonist [Ac‐D2Nal, 1 D4ClPhe, 2 D3Pal, 3 NicLys, 5 DNicLys, 6 ILys, 8 DAla10] GnRH · HOAc (1) and a superagonist [DTrp6, Pro9‐NHEt]GnRH (2), have been electrochemically driven across excised hairless mouse skin. Determined by HPLC analysis, the delivery rate from aqueous solution into isotonic saline at 0.5 mA cm−2 was as high as 19 nM cm−2 h−1 for 2. Because of its insolubility in water, analogue 1 could only be delivered from an acidic donor solution. Analogue 2 was also delivered in pulsatile fashion using current on/off cycles. For all three peptides, passive transport was negligible and stability is evident when in contact with the stratum corneum. Slow metabolism occurs when GnRH contacts the dermal side of hairless mouse skin. Copyright © 1990 Wiley‐Liss, Inc., A Wiley Company