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      Targeted Delivery of Chlorin e6 via Redox Sensitive Diselenide-Containing Micelles for Improved Photodynamic Therapy in Cluster of Differentiation 44-Overexpressing Breast Cancer

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          Abstract

          The off-target activation of photosensitizers is one of the most well-known obstacles to effective photodynamic therapy (PDT). The selected activation of photosensitizers in cancer cells is highly desired to overcome this problem. We developed a strategy that enabled diselenide bonds to link hyaluronic acid (HA) and photosensitizer chlorin e6 (Ce6) to assemble the micelles (HA-sese-Ce6 NPs) that can target cancer and achieve a redox responsive release of drugs to enhance the PDT efficiency in breast cancer. The HA was used to form a hydrophilic shell that can target cluster of differentiation 44 (CD44) on the cancer cells. The selenium-containing core is easily dissembled in a redox environment to release Ce6. The triggered release of Ce6 in a redox condition and the positive feedback release by activated Ce6 were observed in vitro. In cytotoxicity assays and in vitro cellular uptake assays, the increased PDT efficiency and targeted internalization of HA-sese-Ce6 NPs in the cells were verified, compared to a free Ce6 treated group. Similar results were showed in the therapeutic study and in vivo fluorescence imaging in an orthotopic mammary fat pad tumor model. In addition, a significant inhibition of metastasis was found after the HA-sese-Ce6 NPs treatment. In general, this study promises an ingenious and easy strategy for improved PDT efficiency.

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          Most cited references26

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          Redox compartmentalization in eukaryotic cells.

          Diverse functions of eukaryotic cells are optimized by organization of compatible chemistries into distinct compartments defined by the structures of lipid-containing membranes, multiprotein complexes and oligomeric structures of saccharides and nucleic acids. This structural and chemical organization is coordinated, in part, through cysteine residues of proteins which undergo reversible oxidation-reduction and serve as chemical/structural transducing elements. The central thiol/disulfide redox couples, thioredoxin-1, thioredoxin-2, GSH/GSSG and cysteine/cystine (Cys/CySS), are not in equilibrium with each other and are maintained at distinct, non-equilibrium potentials in mitochondria, nuclei, the secretory pathway and the extracellular space. Mitochondria contain the most reducing compartment, have the highest rates of electron transfer and are highly sensitive to oxidation. Nuclei also have more reduced redox potentials but are relatively resistant to oxidation. The secretory pathway contains oxidative systems which introduce disulfides into proteins for export. The cytoplasm contains few metabolic oxidases and this maintains an environment for redox signaling dependent upon NADPH oxidases and NO synthases. Extracellular compartments are maintained at stable oxidizing potentials. Controlled changes in cytoplasmic GSH/GSSG redox potential are associated with functional state, varying with proliferation, differentiation and apoptosis. Variation in extracellular Cys/CySS redox potential is also associated with proliferation, cell adhesion and apoptosis. Thus, cellular redox biology is inseparable from redox compartmentalization. Further elucidation of the redox control networks within compartments will improve the mechanistic understanding of cell functions and their disruption in disease.
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            Application of hyaluronic acid as carriers in drug delivery

            Abstract Hyaluronic acid has good biocompatibility, biodegradability, and nonimmunogenicity. In addition, it has the ability to recognize specific receptors that are overexpressed on the surface of tumor cells, and cancer drugs can be targeted to the tumor cells to better kill them. Therefore, hyaluronic acid has attracted much attention as drug delivery vehicle. Herein, the application of hyaluronic acid as carrier in drug delivery was analyzed and summarized in detail. It showed that hyaluronic acid would have broad prospects for drug delivery.
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              Hyaluronic acid-based biopharmaceutical delivery and tumor-targeted drug delivery system

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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                16 April 2019
                2019
                : 10
                : 369
                Affiliations
                [1] 1 Cancer Center, Shanghai East Hospital, Tongji University , Shanghai, China
                [2] 2 Department of Chemical Engineering, Northeastern University , Boston, MA, United States
                [3] 3 Pharmacy Department, Shanghai East Hospital, Tongji University , Shanghai, China
                Author notes

                Edited by: Wei Tao, Harvard Medical School, United States

                Reviewed by: Jiang Ouyang, Central South University, China; Yuling Xiao, Wuhan University, China; Tianjiao Ji, Boston Children’s Hospital and Harvard Medical School, United States

                *Correspondence: Yabin Ma, baishecao@ 123456163.com

                This article was submitted to Experimental Pharmacology and Drug Discovery, a section of the journal Frontiers in Pharmacology

                Article
                10.3389/fphar.2019.00369
                6477080
                31057402
                acc53dc3-c2b6-4820-bda1-29af3d843f1d
                Copyright © 2019 Feng, Zhu, Chen, Lu, Liu, Kim, Liang, Zhang, Lin, Ma and Dong.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 20 February 2019
                : 25 March 2019
                Page count
                Figures: 8, Tables: 0, Equations: 1, References: 36, Pages: 9, Words: 5703
                Funding
                Funded by: National Natural Science Foundation of China Regional Project
                Award ID: 81860547
                Funded by: National Natural Science Foundation of China Project
                Award ID: 81573008
                Funded by: Key Cross-cutting Projects of Central Universities
                Award ID: 150721907
                Funded by: Pilot Talent Training Program of Shanghai East Hospital
                Award ID: 201701
                Funded by: Research project of Shanghai Association for Science and Technology
                Award ID: 16441901004
                Funded by: Key Disciplines Group Construction Project of Pudong Health Bureau of Shanghai
                Award ID: PWZxq2017-13
                Categories
                Pharmacology
                Original Research

                Pharmacology & Pharmaceutical medicine
                chlorin e6,redox sensitive,diselenide,photodynamic therapy,cluster of differentiation 44,targeted delivery,breast cancer

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