“…The formulations for this part of the study were prepared in 10 mM Tris buffer (pH 7.4) because the liposome stability is optimal in this buffer, and it has been used for all preclinical and clinical studies with CAF01. 15,23,24 Because of the high temperature coefficient of Tris leading to a pH shift during heating, 25 experiments were only performed at temperatures up to 50 • C. Over the limited temperature range examined, the pH decreases only one unit, a range over which both protein and liposomes have previously been shown to be stable. The peak positions of the spectra monitored at 15 • C in the presence and absence of liposomes were similar for both H56 and H1, approximately 335-340 nm (Fig.…”