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      Biomaterial strategies for the application of reproductive tissue engineering

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          Abstract

          Human reproductive organs are of vital importance to the life of an individual and the reproduction of human populations. So far, traditional methods have a limited effect in recovering the function and fertility of reproductive organs and tissues. Thus, aim to replace and facilitate the regrowth of damaged or diseased tissue, various biomaterials are developed to offer hope to overcome these difficulties and help gain further research progress in reproductive tissue engineering. In this review, we focus on the biomaterials and their four main applications in reproductive tissue engineering: in vitro generation and culture of reproductive cells; development of reproductive organoids and models; in vivo transplantation of reproductive cells or tissues; and regeneration of reproductive tissue. In reproductive tissue engineering, designing biomaterials for different applications with different mechanical properties, structure, function, and microenvironment is challenging and important, and deserves more attention.

          Graphical abstract

          In this review, we mainly focus on the biomaterial strategies for three main applications in reproductive tissue engineering including in-vitro germ cell generation and culture, the biomaterials for repairing reproductive organs, and developing reproductive organoids.

          Highlights

          • Various biomaterials have been developed and used in reproductive tissue engineering.

          • 3D culture systems can lead to better cell-cell interactions for in vitro production of reproductive cells.

          • Reproductive organoids and models are formed by biomaterials to simulate the environment of natural reproductive organs.

          • Biomaterials should promote vascular regeneration and resist inflammation for in-situ reproductive tissue regeneration.

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          Most cited references126

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          Designing hydrogels for controlled drug delivery

          Hydrogel delivery systems can leverage therapeutically beneficial outcomes of drug delivery and have found clinical use. Hydrogels can provide spatial and temporal control over the release of various therapeutic agents, including small-molecule drugs, macromolecular drugs and cells. Owing to their tunable physical properties, controllable degradability and capability to protect labile drugs from degradation, hydrogels serve as a platform in which various physiochemical interactions with the encapsulated drugs control their release. In this Review, we cover multiscale mechanisms underlying the design of hydrogel drug delivery systems, focusing on physical and chemical properties of the hydrogel network and the hydrogel-drug interactions across the network, mesh, and molecular (or atomistic) scales. We discuss how different mechanisms interact and can be integrated to exert fine control in time and space over the drug presentation. We also collect experimental release data from the literature, review clinical translation to date of these systems, and present quantitative comparisons between different systems to provide guidelines for the rational design of hydrogel delivery systems.
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            Multivascular networks and functional intravascular topologies within biocompatible hydrogels

            Solid organs transport fluids through distinct vascular networks that are biophysically and biochemically entangled, creating complex three-dimensional (3D) transport regimes that have remained difficult to produce and study. We establish intravascular and multivascular design freedoms with photopolymerizable hydrogels by using food dye additives as biocompatible yet potent photoabsorbers for projection stereolithography. We demonstrate monolithic transparent hydrogels, produced in minutes, comprising efficient intravascular 3D fluid mixers and functional bicuspid valves. We further elaborate entangled vascular networks from space-filling mathematical topologies and explore the oxygenation and flow of human red blood cells during tidal ventilation and distension of a proximate airway. In addition, we deploy structured biodegradable hydrogel carriers in a rodent model of chronic liver injury to highlight the potential translational utility of this materials innovation.
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              An organoid platform for ovarian cancer captures intra- and interpatient heterogeneity

              Ovarian cancer (OC) is a heterogeneous disease usually diagnosed at a late stage. Experimental in vitro models that faithfully capture the hallmarks and tumor heterogeneity of OC are limited and hard to establish. We present a protocol that enables efficient derivation and long-term expansion of OC organoids. Utilizing this protocol, we have established 56 organoid lines from 32 patients, representing all main subtypes of OC. OC organoids recapitulate histological and genomic features of the pertinent lesion from which they were derived, illustrating intra- and interpatient heterogeneity, and can be genetically modified. We show that OC organoids can be used for drug-screening assays and capture different tumor subtype responses to the gold standard platinum-based chemotherapy, including acquisition of chemoresistance in recurrent disease. Finally, OC organoids can be xenografted, enabling in vivo drug-sensitivity assays. Taken together, this demonstrates their potential application for research and personalized medicine.
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                Author and article information

                Contributors
                Journal
                Bioact Mater
                Bioact Mater
                Bioactive Materials
                KeAi Publishing
                2452-199X
                20 December 2021
                August 2022
                20 December 2021
                : 14
                : 86-96
                Affiliations
                [a ]National Engineering Research Centre for Tissue Restoration and Reconstruction and School of Material Science and Engineering, South China University of Technology, Guangzhou, 510640, PR China
                [b ]School of Biomedical Science and Engineering, South China University of Technology, Guangzhou, 510640, PR China
                [c ]School of Chemical Engineering and Light Industry, Guangdong University of Technology, Guangzhou, 510006, PR China
                [d ]First Affiliated Hospital of Shenzhen University, Reproductive Medicine Centre, Shenzhen Second People's Hospital, Shenzhen, 518035, PR China
                [e ]Key Laboratory of Biomedical Engineering of Guangdong Province, South China University of Technology, Guangzhou, 510006, PR China
                Author notes
                []Corresponding author. National Engineering Research Centre for Tissue Restoration and Reconstruction and School of Material Science and Engineering, South China University of Technology, Guangzhou, 510640, PR China. shxt@ 123456scut.edu.cn
                [∗∗ ]Corresponding author. gaoliang@ 123456gdut.edu.cn
                [1]

                Contributed equally to this work.

                Article
                S2452-199X(21)00551-X
                10.1016/j.bioactmat.2021.11.023
                8892081
                35310354
                f2a2a43f-bc9f-4322-95a9-b45eb4ec0af5
                © 2021 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 8 July 2021
                : 13 November 2021
                : 22 November 2021
                Categories
                Article

                biomaterials,reproductive tissue engineering,organoids and models

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