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      Monodispersed Copper(I)‐Based Nano Metal–Organic Framework as a Biodegradable Drug Carrier with Enhanced Photodynamic Therapy Efficacy

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          Abstract

          Photodynamic therapy (PDT) has emerged as an alternative treatment of cancers. However, the therapeutic efficiency of PDT is severely limited by the microenvironment of insufficient oxygen (O 2) supply and overexpression of glutathione (GSH) in the tumor. Herein, a biodegradable O 2‐loaded CuTz‐1@F127 (denoted as CuTz‐1‐O 2@F127) metal–organic framework (MOF) therapeutic platform is presented for enhanced PDT by simultaneously overcoming intracellular hypoxia and reducing GSH levels in the tumor. The Cu(I)‐based MOF is capable of a Fenton‐like reaction to generate OH and O 2 in the presence of H 2O 2 under NIR irradiation. Meanwhile, the CuTz‐1‐O 2@F127 nanoparticles (NPs) can release adsorbed O 2, which further alleviates intracellular hypoxia. In addition, the Cu I in CuTz‐1@F127 can react with intracellular GSH to reduce the excess GSH. In this way, the efficiency of PDT is greatly enhanced. After tail intravenous injection, the NPs show high antitumor efficacy through a synergistic effect under 808 nm laser irradiation. More importantly, the NPs are biodegradable. In vivo biodistribution and excretion experiments demonstrate that a total of nearly 90% of the NPs can be excreted via feces and urine within 30 d, which indicates significant prospects in the clinical treatment of cancers.

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          Perfluorocarbon nanoparticles enhance reactive oxygen levels and tumour growth inhibition in photodynamic therapy

          Photodynamic therapy (PDT) kills cancer cells by converting tumour oxygen into reactive singlet oxygen (1O2) using a photosensitizer. However, pre-existing hypoxia in tumours and oxygen consumption during PDT can result in an inadequate oxygen supply, which in turn hampers photodynamic efficacy. Here to overcome this problem, we create oxygen self-enriching photodynamic therapy (Oxy-PDT) by loading a photosensitizer into perfluorocarbon nanodroplets. Because of the higher oxygen capacity and longer 1O2 lifetime of perfluorocarbon, the photodynamic effect of the loaded photosensitizer is significantly enhanced, as demonstrated by the accelerated generation of 1O2 and elevated cytotoxicity. Following direct injection into tumours, in vivo studies reveal tumour growth inhibition in the Oxy-PDT-treated mice. In addition, a single-dose intravenous injection of Oxy-PDT into tumour-bearing mice significantly inhibits tumour growth, whereas traditional PDT has no effect. Oxy-PDT may enable the enhancement of existing clinical PDT and future PDT design.
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            Nanozyme Decorated Metal–Organic Frameworks for Enhanced Photodynamic Therapy

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              Carbon-Dot-Decorated Carbon Nitride Nanoparticles for Enhanced Photodynamic Therapy against Hypoxic Tumor via Water Splitting.

              Hypoxia, a typical feature of solid tumors, remarkably restricts the efficiency of photodynamic therapy (PDT). Here, a carbon nitride (C3N4)-based multifunctional nanocomposite (PCCN) for light-driven water splitting was used to solve this problem. Carbon dots were first doped with C3N4 to enhance its red region absorption because red light could be used to trigger the in vivo water splitting process. Then, a polymer containing a protoporphyrin photosensitizer, a polyethylene glycol segment, and a targeting Arg-Gly-Asp motif was synthesized and introduced to carbon-dot-doped C3N4 nanoparticles. In vitro study showed that PCCN, thus obtained, could increase the intracellular O2 concentration and improve the reactive oxygen species generation in both hypoxic and normoxic environments upon light irradiation. Cell viability assay demonstrated that PCCN fully reversed the hypoxia-triggered PDT resistance, presenting a satisfactory growth inhibition of cancer cells in an O2 concentration of 1%. In vivo experiments also indicated that PCCN had superior ability to overcome tumor hypoxia. The use of water splitting materials exhibited great potential to improve the intratumoral oxygen level and ultimately reverse the hypoxia-triggered PDT resistance and tumor metastasis.
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                Author and article information

                Contributors
                mlpang@ciac.ac.cn
                jlin@ciac.ac.cn
                Journal
                Adv Sci (Weinh)
                Adv Sci (Weinh)
                10.1002/(ISSN)2198-3844
                ADVS
                Advanced Science
                John Wiley and Sons Inc. (Hoboken )
                2198-3844
                22 May 2019
                07 August 2019
                : 6
                : 15 ( doiID: 10.1002/advs.v6.15 )
                : 1900848
                Affiliations
                [ 1 ] State Key Laboratory of Rare Earth Resource Utilization Changchun Institute of Applied Chemistry Chinese Academy of Sciences Changchun 130022 P. R. China
                [ 2 ] University of Chinese Academy of Sciences Beijing 100049 P. R. China
                [ 3 ] University of Science and Technology of China No. 96, JinZhai Road, Baohe District Hefei Anhui 230026 P. R. China
                Author notes
                Author information
                https://orcid.org/0000-0002-6388-6078
                https://orcid.org/0000-0001-9572-2134
                Article
                ADVS1194
                10.1002/advs.201900848
                6685469
                a4c2071f-8f1c-4d28-a3a0-21d2dac4f243
                © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 April 2019
                Page count
                Figures: 7, Tables: 0, Pages: 11, Words: 7768
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 51720105015
                Award ID: 51828202
                Award ID: 51628201
                Award ID: 51772288
                Award ID: 51572257
                Award ID: 21728101
                Funded by: Chinese Academy of Sciences
                Award ID: YZDY‐SSWJSC018
                Funded by: CAS-Croucher Funding Scheme for Joint Laboratories
                Award ID: CAS18204
                Funded by: Department of Science and Technology of Jilin Province
                Award ID: 20170101187JC
                Award ID: 20170414003GH
                Categories
                Full Paper
                Full Papers
                Custom metadata
                2.0
                advs1194
                August 7, 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.7 mode:remove_FC converted:07.08.2019

                biodegradable,glutathione reduction,hypoxia therapy,metal–organic frameworks,type i photodynamic therapy

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