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These experimental results demonstrate that siPlk1s can be delivered to target cells in the tumor tissues by the as-developed core/shell nano-vehicle with active tumor-targeting capability and knockdown PLK1 protein, inhibit cell proliferation, induce cell apoptosis, and eventually suppress tumor progression

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doi: 10.1039/D1RA00079A

This stability window is comparable to [BPC-157]( and [Thymosin Beta-4]( but shorter than highly stable peptides like [Epithalon]( which can maintain potency for 60+ days post-reconstitution

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