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The release data of SA and bioavailable silicon from MSNs-ss-SA were analyzed using zero-order (2), first-order (3), Higuchi (4), Ritger-Peppas (5), and Weibull (6) models, respectively [48]: where M t is the amount of SA or bioavailable silicon released at time t
Going beyond this introduces increasing uncertainty about both potency and sterility
This finding suggests the peptide may behave differently in cancer tissue than in normal healing tissue
Live with a constant sensation of racing against time, deadlines, decay, or loss of opportunity
Proc Natl Acad Sci USA 97:817822
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