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      International Journal of Nanomedicine (submit here)

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      NIR Laser Responsive Nanoparticles for Ovarian Cancer Targeted Combination Therapy with Dual-Modal Imaging Guidance

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          Abstract

          Purpose

          Multifunctional nanoparticles with targeted therapeutic function and diagnostic-imaging are of great interest in the domain of precision therapy. NIR laser responsive nanoparticles (PLGA-PEG-FA encapsulating Bi 2S 3, PFP, and Dox (designed as FBPD NPs)) are synthesized for ovarian cancer targeted combination therapy with CT/PA dual-modal imaging guidance (PA: photoacoustic; CT: X-ray computed tomography).

          Methods and Results

          The FBPD NPS prepared by the double emulsification method revealed excellent dispersity, great stability, outstanding optical properties. The temperature of FBPD NPs increased rapidly after laser irradiation, inducing liquid-to-gas conversion of perfluoropentane (PFP), and promoting the release of Dox up to 86.7%. These FBPD NPs demonstrated their outstanding imaging capability for both PA and CT imaging both in vitro and in vivo, providing the potential for therapeutic guidance and monitoring. Assisted by folic acid, these nanoparticles could highly enrich in ovarian tumor tissue and the accumulation peaked at 3 h after intravenous administration. The desirable photothermal-conversion efficiency of the nanoparticles combined with chemotherapy achieved highly efficient therapy, which was demonstrated both in vitro and in vivo.

          Conclusion

          We successfully constructed multifunctional theranostic FBPD NPs for highly efficient PTT/chemotherapy combined therapy with dual CT/PA imaging guidance/monitoring. The unique nanoparticles with multiple abilities pave an emerging way toward precise treatment of ovarian cancer.

          Most cited references45

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          Tumor‐Targeted Drug and CpG Delivery System for Phototherapy and Docetaxel‐Enhanced Immunotherapy with Polarization toward M1‐Type Macrophages on Triple Negative Breast Cancers

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            Bismuth sulfide nanorods as a precision nanomedicine for in vivo multimodal imaging-guided photothermal therapy of tumor.

            Here, we present a precision cancer nanomedicine based on Bi(2)S(3) nanorods (NRs) designed specifically for multispectral optoacoustic tomography (MSOT)/X-ray computed tomography (CT)-guided photothermal therapy (PTT). The as-prepared Bi(2)S(3) NRs possess ideal photothermal effect and contrast enhancement in MSOT/CT bimodal imaging. These features make them simultaneously act as "satellite" and "precision targeted weapon" for the visual guide to destruction of tumors in vivo, realizing effective tumor destruction and metastasis inhibition after intravenous injection. In addition, toxicity screening confirms that Bi(2)S(3) NRs have well biocompatibility. This triple-modality-nanoparticle approach enables simultaneously precise cancer therapy and therapeutic monitoring.
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              Oral Delivery of Nanoparticles Loaded With Ginger Active Compound, 6-Shogaol, Attenuates Ulcerative Colitis and Promotes Wound Healing in a Murine Model of Ulcerative Colitis

              Background and Aims Oral drug delivery is the most attractive pathway for ulcerative colitis [UC] therapy, since it has many advantages. However, this strategy has encountered many challenges, including the instability of drugs in the gastrointestinal tract [GT], low targeting of disease tissues, and severe adverse effects. Nanoparticles capable of colitis tissue-targeted delivery and site-specific drug release may offer a unique and therapeutically effective system that addresses these formidable challenges. Methods We used a versatile single-step surface-functionalising technique to prepare PLGA/PLA-PEG-FA nanoparticles loaded with the ginger active compound, 6-shogaol [NPs-PEG-FA/6-shogaol]. The therapeutic efficacy of NPs-PEG-FA/6-shogaol was evaluated in the well-established mouse model of dextran sulphate sodium [DSS]-induced colitis. Results NPs-PEG-FA exhibited very good biocompatibility both in vitro and in vivo . Subsequent cellular uptake experiments demonstrated that NPs-PEG-FA could undergo efficient receptor-mediated uptake by colon-26 cells and activated Raw 264.7 macrophage cells. In vivo , oral administration of NPs-PEG-FA/6-shogaol encapsulated in a hydrogel system [chitosan/alginate] significantly alleviated colitis symptoms and accelerated colitis wound repair in DSS-treated mice by regulating the expression levels of pro-inflammatory [TNF-α, IL-6, IL-1β, and iNOS] and anti-inflammatory [Nrf-2 and HO-1] factors. Conclusions Our study demonstrates a convenient, orally administered 6-shogaol drug delivery system that effectively targets colitis tissue, alleviates colitis symptoms, and accelerates colitis wound repair. This system may represent a promising therapeutic approach for treating inflammatory bowel disease [IBD].
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                Author and article information

                Journal
                Int J Nanomedicine
                Int J Nanomedicine
                ijn
                intjnano
                International Journal of Nanomedicine
                Dove
                1176-9114
                1178-2013
                29 June 2021
                2021
                : 16
                : 4351-4369
                Affiliations
                [1 ]Department of Radiology, The First Affiliated Hospital of Chongqing Medical University , Chongqing, People’s Republic of China
                [2 ]Department of Ultrasound, The First Affiliated Hospital of Chongqing Medical University , Chongqing, People’s Republic of China
                [3 ]Department of Intensive Care Unit (ICU), Dianjiang People’s Hospital of Chongqing , Chongqing, People’s Republic of China
                [4 ]Department of Oncology, The First Affiliated Hospital of Chongqing Medical University , Chongqing, People’s Republic of China
                [5 ]Institute of Ultrasound Imaging, The Second Affiliated Hospital of Chongqing Medical University , Chongqing, People’s Republic of China
                Author notes
                Correspondence: Di Zhou Department of Radiology, The First Affiliated Hospital of Chongqing Medical University , Chongqing, 400010, People’s Republic of ChinaTel +8613508329306 Email zhoudi@cqmu.edu.cn
                Author information
                http://orcid.org/0000-0003-0289-6333
                http://orcid.org/0000-0002-7281-5845
                Article
                299376
                10.2147/IJN.S299376
                8254569
                34234430
                f4959088-3672-454d-9cf4-0a8733baefbe
                © 2021 Zhao et al.

                This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License ( http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms ( https://www.dovepress.com/terms.php).

                History
                : 28 December 2020
                : 01 June 2021
                Page count
                Figures: 11, References: 45, Pages: 19
                Funding
                Funded by: National Natural Science Foundation of China Youth Science Foundation Project;
                Funded by: Medical Science Cultivation Fund of the First Affiliated Hospital of Chongqing Medical University;
                Funded by: Chongqing Postgraduate Research and Innovation Project;
                This work was supported by the National Natural Science Foundation of China Youth Science Foundation Project (NO.81801717), Medical Science Cultivation Fund of the First Affiliated Hospital of Chongqing Medical University (PYJJ2018-15) and Chongqing Postgraduate Research and Innovation Project (Grant No: CYS18194).
                Categories
                Original Research

                Molecular medicine
                bismuth sulfide,folic acid,chemotherapy,photothermal therapy
                Molecular medicine
                bismuth sulfide, folic acid, chemotherapy, photothermal therapy

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