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Biomaterials for Tissue Engineering

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Cover of 'Biomaterials for Tissue Engineering'

Table of Contents

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    Book Overview
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    Chapter 1 Engineering Citric Acid-Based Porous Scaffolds for Bone Regeneration
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    Chapter 2 Multifunctional Self-Assembling Peptide-Based Nanostructures for Targeted Intracellular Delivery: Design, Physicochemical Characterization, and Biological Assessment
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    Chapter 3 Electrospinning Functionalized Polymers for Use as Tissue Engineering Scaffolds
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    Chapter 4 Low-Temperature Deposition Modeling of β-TCP Scaffolds with Controlled Bimodal Porosity
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    Chapter 5 Three-Dimensional Hydrogel-Based Culture to Study the Effects of Toxicants on Ovarian Follicles
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    Chapter 6 Layer-by-Layer Engineered Polymer Capsules for Therapeutic Delivery
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    Chapter 7 Controlling Fibrin Network Morphology, Polymerization, and Degradation Dynamics in Fibrin Gels for Promoting Tissue Repair
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    Chapter 8 Biofunctionalization of Poly(acrylamide) Gels
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    Chapter 9 Synthetic PEG Hydrogel for Engineering the Environment of Ovarian Follicles
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    Chapter 10 Engineering Human Neural Tissue by 3D Bioprinting
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    Chapter 11 High-Throughput Formation of Mesenchymal Stem Cell Spheroids and Entrapment in Alginate Hydrogels
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    Chapter 12 Crimped Electrospun Fibers for Tissue Engineering
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    Chapter 13 In Vitro Model of Macrophage-Biomaterial Interactions
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    Chapter 14 Synthesis of Self-Assembling Peptide-Based Hydrogels for Regenerative Medicine Using Solid-Phase Peptide Synthesis
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    Chapter 15 H2S Delivery from Aromatic Peptide Amphiphile Hydrogels
Attention for Chapter 5: Three-Dimensional Hydrogel-Based Culture to Study the Effects of Toxicants on Ovarian Follicles
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Chapter title
Three-Dimensional Hydrogel-Based Culture to Study the Effects of Toxicants on Ovarian Follicles
Chapter number 5
Book title
Biomaterials for Tissue Engineering
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7741-3_5
Pubmed ID
Book ISBNs
978-1-4939-7739-0, 978-1-4939-7741-3
Authors

Hong Zhou, Ariella Shikanov, Zhou, Hong, Shikanov, Ariella

Abstract

Various toxicants, such as drugs and their metabolites, can cause potential ovarian toxicity. As the functional units of the ovary, ovarian follicles are susceptible to this type of damage at all developmental stages. Studying the effects of toxicants on ovarian follicles is an important task. Three-dimensional (3D) hydrogels, such as fibrin alginate interpenetrating networks (FA-IPNs), can support ovarian follicle culture in vitro for extended periods of time and serve as a suitable tool for studying ovotoxicity. Growing follicles encapsulated in the FA-IPN can proteolytically degrade the fibrin component in the FA-IPN. The degradation of fibrin mirrors the follicle growth and serves as a surrogate reporter for follicle health. The speed of fibrin degradation can be further controlled by aprotinin, a small molecule that inhibits plasmin-driven proteolytic degradation, which further expands the application of the described system. In this chapter, we describe methods to (1) isolate and encapsulate mouse ovarian follicles in FA-IPN, (2) follow follicle growth and development in vitro, and (3) evaluate the effects of toxicants on folliculogenesis using fibrin degradation.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 15 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 15 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 5 33%
Unspecified 2 13%
Student > Master 2 13%
Student > Bachelor 1 7%
Researcher 1 7%
Other 1 7%
Unknown 3 20%
Readers by discipline Count As %
Chemical Engineering 2 13%
Unspecified 2 13%
Biochemistry, Genetics and Molecular Biology 2 13%
Medicine and Dentistry 2 13%
Neuroscience 1 7%
Other 1 7%
Unknown 5 33%