In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration

© 2017 Trans Tech Publications, Switzerland. Biodegradable scaffold is an accepted and commercialized medical alternative choice for bone regeneration. In this project, we used our new invention, porous starch-Hydroxyapatite (HA) composite for in vivo clinical trial. The products were prepared from...

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Main Authors: Sittiporn Punyanitya, Rungsarit Koonawoot, Anucha Ruksanti, Sakdiphon Thiensem, Anirut Raksujarit, Watchara Sontichai
Format: Book Series
Published: 2018
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Online Access:https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027005538&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/46887
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Institution: Chiang Mai University
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spelling th-cmuir.6653943832-468872018-04-25T07:32:13Z In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration Sittiporn Punyanitya Rungsarit Koonawoot Anucha Ruksanti Sakdiphon Thiensem Anirut Raksujarit Watchara Sontichai Materials Science Agricultural and Biological Sciences © 2017 Trans Tech Publications, Switzerland. Biodegradable scaffold is an accepted and commercialized medical alternative choice for bone regeneration. In this project, we used our new invention, porous starch-Hydroxyapatite (HA) composite for in vivo clinical trial. The products were prepared from medical grade Thai rice starch mixed with high purity ( > 97%) HA powder from fresh cow bone, and already passed in vivo animal biocompatibility test, then processed by freeze-drying. There were 44 volunteers from orthopedic and neurosurgical division, 4 and 40 patients, respectively. The results were assessed by operative surgeons and nurses, pre-and intraoperative period, including size appropriateness, comfort handle, ease of cutting, void space filling, water stability, product weight, shelf storage, package opening, contamination risk and waste removal. All average satisfactory scales were more than 95% rating. For postoperative period, at least 6 months, the soft tissue swellings around surgical areas were resoluted about 3 days as usual healing process. There were no any symptoms or signs of infection or allergic reactions. The follow up of x-ray imaging showed well ossification about 2 months. All patients have gained good functional performance. So porous starch-HA composites biomaterial can be used for human bone and skull regeneration with completely safety and efficacy. 2018-04-25T07:04:02Z 2018-04-25T07:04:02Z 2017-01-01 Book Series 10139826 2-s2.0-85027005538 10.4028/www.scientific.net/KEM.744.480 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027005538&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/46887
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Materials Science
Agricultural and Biological Sciences
spellingShingle Materials Science
Agricultural and Biological Sciences
Sittiporn Punyanitya
Rungsarit Koonawoot
Anucha Ruksanti
Sakdiphon Thiensem
Anirut Raksujarit
Watchara Sontichai
In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration
description © 2017 Trans Tech Publications, Switzerland. Biodegradable scaffold is an accepted and commercialized medical alternative choice for bone regeneration. In this project, we used our new invention, porous starch-Hydroxyapatite (HA) composite for in vivo clinical trial. The products were prepared from medical grade Thai rice starch mixed with high purity ( > 97%) HA powder from fresh cow bone, and already passed in vivo animal biocompatibility test, then processed by freeze-drying. There were 44 volunteers from orthopedic and neurosurgical division, 4 and 40 patients, respectively. The results were assessed by operative surgeons and nurses, pre-and intraoperative period, including size appropriateness, comfort handle, ease of cutting, void space filling, water stability, product weight, shelf storage, package opening, contamination risk and waste removal. All average satisfactory scales were more than 95% rating. For postoperative period, at least 6 months, the soft tissue swellings around surgical areas were resoluted about 3 days as usual healing process. There were no any symptoms or signs of infection or allergic reactions. The follow up of x-ray imaging showed well ossification about 2 months. All patients have gained good functional performance. So porous starch-HA composites biomaterial can be used for human bone and skull regeneration with completely safety and efficacy.
format Book Series
author Sittiporn Punyanitya
Rungsarit Koonawoot
Anucha Ruksanti
Sakdiphon Thiensem
Anirut Raksujarit
Watchara Sontichai
author_facet Sittiporn Punyanitya
Rungsarit Koonawoot
Anucha Ruksanti
Sakdiphon Thiensem
Anirut Raksujarit
Watchara Sontichai
author_sort Sittiporn Punyanitya
title In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration
title_short In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration
title_full In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration
title_fullStr In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration
title_full_unstemmed In vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration
title_sort in vivo clinical trial of porous starch-hydroxyapatite composite biomaterials for bone regeneration
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85027005538&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/46887
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