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USA 104 , 72417246 (2007)

Qiao Z-S, Min C-Y, Hua Q-X, Weiss MA, Feng Y-M (2003) In vitro refolding of human proinsulin kinetic intermediates, putative disulfide-forming pathway, folding initiation site, and potential role of C-peptide in folding process

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The authors hypothesized that this result was due to the multifunctional design of the nanoplatform, including the tumor-targeting ability of HA, the mitochondrial-targeting capability of the TPP group, and the ROS-responsive cleavability of the thioester (TK) bond, which collectively enhance the photodynamic, gas, and ferroptotic therapeutic effects