“…If further clinical studies support the safety and efficacy of an aerosolized 1 -PI, and it is approved for treatment of cystic fibrosis, the demand for therapeutic 1 -PI preparations could be significantly increased. Dowd et al, 1995;Esnault, 1997;Griffith et al, 1996Panniculitis Chowdhury et al, 2002Gross et al, 2009;Kjus et al, 2002;Smith et al, 1987;Valverde et al, 2008Fibromyalgia Ablin et al, 2009Blanco et al, 2004;Blanco et al, 2010Asthma Blanco et al, 2008Blanco et al, 2011;Eden et al, 1997Pancreatitis Rabassa et al, 1995Needlham & Stockley, 2004Renal Szönyi et al, 2006Ting et., 2008Diabetes Kalis et al, 2010Lisowska-Myjak et al, 2006;Cancer Li et al, 2011;Lindor et al, 2010;Topic et al, 2011Rheumatoid arthritis Grimstein et al, 2010Grimstein et al, 2011Atherosclerosis Stakisaitis et al, 2001Talmud et al, 2003; Acute anterior uveitis Fearnley et al, 1988;Saari et al, 1986 Chronic rhinosinusitis Kilty et al, 2008Kilty et al, , 2010Maune et al, 1995 (Cantin et al, 2002b). According to their data, the site-specific conjugation with either 20 or 40 kD PEG at Cys 232 of nonglycosylated r- 1 -PI (human) results in an active inhibitor with extended in vivo stability.…”