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Injectable Single-Component Peptide Depot: Autonomously Rechargeable Tumor Photosensitization for Repeated Photodynamic Therapy

Authors
Cho, Hong-JunPark, Sung-JunJung, Woo HyukCho, YuriAhn, Dong JuneLee, Yoon-SikKim, Sehoon
Issue Date
24-11월-2020
Publisher
AMER CHEMICAL SOC
Keywords
photodynamic therapy; internalizing RGD (iRGD); activatable photosensitizer; molecular depot; sustained release
Citation
ACS NANO, v.14, no.11, pp.15793 - 15805
Indexed
SCIE
SCOPUS
Journal Title
ACS NANO
Volume
14
Number
11
Start Page
15793
End Page
15805
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/51458
DOI
10.1021/acsnano.0c06881
ISSN
1936-0851
Abstract
The general practice of photodynamic therapy (PDT) comprises repeated multiple sessions, where photosensitizers are repeatedly administered prior to each operation of light irradiation. To address potential problems arising from the total overdose of photosensitizer by such repeated injections, we here introduce an internalizing RGD peptide (iRGD) derivative (Ppa- iRGDC-BK01) that self-aggregates into an injectable single-component supramolecular depot. Ppa-iRGDC-BK01 is designed as an in situ self-implantable photosensitizer so that it forms a depot by itself upon injection, and its molecular functions (cancer cell internalization and photosensitization) are activated by sustained release, tumor targeting, and tumor-selective proteolytic/reductive cleavage of the iRGD segment. The experimental and theoretical studies revealed that when exposed to body temperature, Ppa-iRGDC-BK01 undergoes thermally accelerated self-assembly to form a supramolecular depot through the hydrophobic interaction of the Ppa pendants and the reorganization of the interpeptide hydrogen bonding. It turned out that the self-aggregation of Ppa-iRGDC-BK01 into a depot exerts a multiple-quenching effect on the photosensitivity to effectively prevent nonspecific phototoxicity and protect it from photobleaching outside the tumor, while enabling autonomous tumor rephotosensitization by long sustained release, tumor accumulation, and intratumoral activation over time. We demonstrate that depot formation through a single peritumoral injection and subsequent quintuple laser irradiations at intervals resulted in complete eradication of the tumor. During the repeated PDT, depot-implanted normal tissues around the tumor exhibited no phototoxic damage under laser exposure. Our approach of single-component photosensitizing supramolecular depot, combined with a strategy of tumor-targeted therapeutic activation, would be a safer and more precise operation of PDT through a nonconventional protocol composed of one-time photosensitizer injection and multiple laser irradiations.
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Graduate School > KU-KIST Graduate School of Converging Science and Technology > 1. Journal Articles

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Ahn, Dong June
공과대학 (화공생명공학과)
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