公立大学法人腾博会国际娱乐_腾博会游戏大厅-【官方授权牌照】
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公立大学法人腾博会国际娱乐_腾博会游戏大厅-【官方授权牌照】
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Alginic acid improves artificial bones, study shows

Published on Aug 11, 2021

Research

Osaka City University study shows how alginic acid improves artificial bones in 3 ways

? ? ? ? ? ? ? ? ? ? ?shimatani

Cross sectional microstructures in the set CPC samples (a) without and (b) with alginate (20 wt%). Little porosity was detected in CPC sample without alginate (a1). Adding alginate resulted in the formation of macropores within the bulk materials (b1)

Summary

Researchers show the benefits of mixing alginic acid with calcium phosphate cement (CPC), a common bone replacement material, with in vitro and in vivo studies. The biopolymer is shown to improve the setting time and compressive strength of CPC, as well as help it acquire porosity – which allows cells to enter the defected area and grow new bone.

Research outline

New research shows that mixing low viscosity alginic acid with calcium phosphate cement (CPC), a material commonly used as a bone replacement, confers 3 functional improvements: shorter setting time, increased compressive strength, and acquisition of porosity.?

One reason for the increased use of CPC in recent years is its self-setting nature, allowing it to be injected into a patient for a more non-invasive approach. However, CPCs have a dense microstructure that make it difficult for cells to enter. This lack of pores limits the potential for new bone growth. This study, published in the Journal of Materials Science: Materials in Medicine, explores the effect the naturally derived biopolymer alginic acid has on this issue.?

Previous research has studied other biopolymers, including gelatin, collagen, and chitosan, but this joint study between the Osaka City University (OCU), Graduate School of Medicine and Graduate School of Engineering, has confirmed the positive effects of mixing alginic acid with CPC. In vitro studies showed alginic acid shorten setting time and increase compressive strength of CPC. In addition, in vivo studies showed the biopolymer increase porosity of CPC, allowing cells to enter and new bone to grow.?

Alginic acid has been widely used in the medical field for procedures such as, cell immobilization, drug delivery, and wound dressing. However, there have been limited studies in conjunction with CPC. The degradability and cross-linking characteristics of alginic acid make it a promising additive to improve on the dense and generally poor mechanical properties of CPC.?

This new study evaluated a series of CPC-alginate (the salt form of alginic acid) compounds with increasing amounts of alginic acid. In vitro, a pH meter showed a decrease in pH levels as alginic acid amounts increased, speeding up setting time. Scanning electron microscopy revealed that compounds with increased alginic acid had more pores and less density. In vivo, X-ray and micro-CT analysis showed that femurs injected with CPC compounds of increased amounts of alginic acid had, after 6 weeks, more degradation and bone formation than the control group.?

"Artificial bones can support broken bones, but they do not replace our own bones and remain in the body as a foreign object” said Graduate Student Akiyoshi Shimatani, and first author of the study. Associate Professor Hiromitsu Toyoda of the OCU Dept. of Orthopedic Surgery continued: “To solve this problem, we have developed an artificial bone in collaboration Professor Yoshiyuki Yokogawa and his team from the OCU Faculty of Engineering, which is sticky, hard to break, and replaces the body’s own bone. We hope this becomes a new option for artificial bones."

Funding

Grants-in-Aid for Scientific Research [Project No. 20K05118])

Publication Information

Date of Publication: 22 June, 2021

Journal name:?Journal of Materials Science: Materials in Medicine

Paper Title: A bone replacement-type calcium phosphate cement that becomes more porous in?vivo by incorporating a degradable polymer

Authors:?Akiyoshi Shimatani、Hiromitsu Toyoda、Kumi Orita、Yuta Ibara、Yoshiyuki Yokogawa、Hiroaki Nakamura

URL:?https://doi.org/10.1007/s10856-021-06555-1

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