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Bioengineering
組織工学のためのアルギン酸微粒子と熱ゲルポリ(N-イソプロピルアクリルアミド) - グラフト - コンド...
組織工学のためのアルギン酸微粒子と熱ゲルポリ(N-イソプロピルアクリルアミド) - グラフト - コンド...
JoVE Journal
Bioengineering
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JoVE Journal Bioengineering
Synthesis of Thermogelling Poly(N-isopropylacrylamide)-graft-chondroitin Sulfate Composites with Alginate Microparticles for Tissue Engineering

組織工学のためのアルギン酸微粒子と熱ゲルポリ(N-イソプロピルアクリルアミド) - グラフト - コンドロイチン硫酸複合材料の合成

Full Text
12,520 Views
12:22 min
October 26, 2016

DOI: 10.3791/53704-v

Thomas R. Christiani1, Katelynn Toomer2, Joseph Sheehan2, Angelika Nitzl2, Amanda Branda2, Elizabeth England2, Pamela Graney3, Cristina Iftode2, Andrea J. Vernengo1

1Department of Chemical Engineering,Rowan University, 2Department of Biological Sciences,Rowan University, 3Department of Biomedical Engineering,Drexel University

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Please note that some of the translations on this page are AI generated. Click here for the English version.

Overview

This study presents an injectable tissue engineering scaffold made from a poly(N-isopropylacrylamide)-graft-chondroitin sulfate (PNIPAAm-g-CS)-containing alginate microparticle composite. The research focuses on evaluating the adhesive strength, swelling properties, and in vitro biocompatibility of this novel hydrogel.

Key Study Components

Area of Science

  • Tissue Engineering
  • Biomaterials
  • Hydrogels

Background

  • Thermal reversible hydrogels are crucial for cell encapsulation in tissue engineering.
  • Understanding adhesive properties is essential for developing effective scaffolds.
  • In vitro studies are necessary to assess the biocompatibility of new materials.
  • This research aims to contribute to the field of intervertebral disc tissue engineering.

Purpose of Study

  • To assess the adhesive properties of a hydrogel composite for nucleus pulposus tissue engineering.
  • To evaluate cellular biocompatibility of the proposed hydrogel.
  • To demonstrate the potential of injectable, thermally-sensitive composites.

Methods Used

  • Tensile mechanical tests to evaluate adhesive strength.
  • Cellular viability assays to assess biocompatibility.
  • Synthesis of bioadhesive hydrogel from purified NIPAAm monomer and mCS.
  • In vitro studies to demonstrate the hydrogel's effectiveness.

Main Results

  • The hydrogel demonstrated favorable adhesive properties.
  • In vitro studies indicated good cellular viability.
  • The composite showed potential as a replacement for the nucleus pulposus.
  • Characterization techniques may be applicable to other thermogelling systems.

Conclusions

  • The PNIPAAm-g-CS hydrogel scaffold is promising for tissue engineering applications.
  • Further studies are needed to explore its long-term biocompatibility.
  • This research provides a foundation for future developments in injectable hydrogels.

Frequently Asked Questions

What is the main application of the hydrogel scaffold?
The hydrogel scaffold is designed for intervertebral disc tissue engineering, specifically for the nucleus pulposus.
How does the hydrogel's adhesive property benefit tissue engineering?
The adhesive property allows the hydrogel to effectively bond with surrounding tissues, enhancing integration and functionality.
What methods were used to assess biocompatibility?
Cellular viability assays were conducted to evaluate the biocompatibility of the hydrogel scaffold.
What are the advantages of using thermally-sensitive hydrogels?
Thermally-sensitive hydrogels can be injected in a liquid form and gel upon reaching body temperature, allowing for minimally invasive applications.
Who conducted the biocompatibility assays in the study?
The biocompatibility assays were conducted by students from the departments of Biological Sciences and Biochemistry.
What are the next steps for this research?
Future research will focus on long-term biocompatibility and potential clinical applications of the hydrogel scaffold.

ポリ(N-イソプロピルアクリルアミド) - グラフト - コンドロイチン硫酸からなる注射可能な組織工学足場は、(のPNIPAAm-G-CS)含有アルギン酸微粒子を調製しました。接着強度、膨潤性及び生体適合性、インビトロでは、この研究で分析されています。ここで開発された特性決定技術は、他の熱ゲル化システムにも適用可能です。

この方法論の全体的な目標は、髄核の椎間板組織工学のために提案されたヒドロゲル複合材料の接着特性と細胞生体適合性の両方を評価することです。この方法は、細胞カプセル化のための生体接着特性を持つ熱可逆性ハイドロゲルをどのように設計および調製するかなど、組織工学の分野における重要な質問に答えるのに役立ちます。この技術の主な利点は、注射可能な熱感受性複合材料を使用したinvitro研究を実証して、髄核の潜在的な代替品としての使用を評価できることです。

この現在の研究では、引張力学的試験と細胞生存率アッセイの両方を実行することにより、新しいハイドロゲル足場を評価します。生体適合性アッセイのデモンストレーションは、生物科学部と生化学部の学生であるEmily Schmidt氏、Mark Dittmer氏、Edward Goldschmidt氏、Frantzeska Giginis氏です。生体接着性ヒドロゲルを合成する前に、テキストプロトコルに記載されているように、NIPAAmモノマーとmCSを精製します。

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