scholarly journals Positive effect on spinal fusion by the combination of platelet-rich plasma and collagen-mineral scaffold using lumbar posterolateral fusion model in rats

Author(s):  
Jen-Chung Liao
2021 ◽  
Vol 25 (1) ◽  
Author(s):  
Yuan-Zhe Jin ◽  
Guang-Bin Zheng ◽  
Minjoon Cho ◽  
Jae Hyup Lee

Abstract Background Bone substrates like hydroxyapatite and tricalcium phosphate have been widely used for promoting spinal fusion and reducing the complications caused by autograft. Whitlockite has been reported to promote better bone formation in rat calvaria models compare with them, but no study investigated its effect on spinal fusion yet. Also, the higher osteoinductivity of whitlockite raised concern of ectopic ossification, which was a complication of spinal fusion surgery that should be avoided. Methods In this study, we compared the osteoinductivity of whitlockite, hydroxyapatite, and tricalcium phosphate porous particles with SD rat spine posterolateral fusion model and investigated whether whitlockite could induce ectopic ossification with SD rat abdominal pouch model. Results The micro-CT result from the posterolateral fusion model showed whitlockite had slightly but significantly higher percent bone volume than tricalcium phosphate, though none of the materials formed successful fusion with surrounding bone tissue. The histology results showed the bone formed on the cortical surface of the transverse process but did not form a bridge between the processes. The result from the abdominal pouch model showed whitlockite did not induce ectopic bone formation. Conclusion Whitlockite had a potential of being a better bone substrate hydroxyapatite and tricalcium phosphate in spinal fusion with low risk of inducing ectopic ossification.


2014 ◽  
Vol 4 (1_suppl) ◽  
pp. s-0034-1376692-s-0034-1376692
Author(s):  
G. Kubota ◽  
H. Kamoda ◽  
K. Yamauchi ◽  
S. Orita ◽  
Y. Sakuma ◽  
...  

2021 ◽  
Vol 22 (11) ◽  
pp. 5492
Author(s):  
Dawid Szwedowski ◽  
Joanna Szczepanek ◽  
Łukasz Paczesny ◽  
Jan Zabrzyński ◽  
Maciej Gagat ◽  
...  

Knee osteoarthritis (KOA) represents a clinical challenge due to poor potential for spontaneous healing of cartilage lesions. Several treatment options are available for KOA, including oral nonsteroidal anti-inflammatory drugs, physical therapy, braces, activity modification, and finally operative treatment. Intra-articular (IA) injections are usually used when the non-operative treatment is not effective, and when the surgery is not yet indicated. More and more studies suggesting that IA injections are as or even more efficient and safe than NSAIDs. Recently, research to improve intra-articular homeostasis has focused on biologic adjuncts, such as platelet-rich plasma (PRP). The catabolic and inflammatory intra-articular processes that exists in knee osteoarthritis (KOA) may be influenced by the administration of PRP and its derivatives. PRP can induce a regenerative response and lead to the improvement of metabolic functions of damaged structures. However, the positive effect on chondrogenesis and proliferation of mesenchymal stem cells (MSC) is still highly controversial. Recommendations from in vitro and animal research often lead to different clinical outcomes because it is difficult to translate non-clinical study outcomes and methodology recommendations to human clinical treatment protocols. In recent years, significant progress has been made in understanding the mechanism of PRP action. In this review, we will discuss mechanisms related to inflammation and chondrogenesis in cartilage repair and regenerative processes after PRP administration in in vitro and animal studies. Furthermore, we review clinical trials of PRP efficiency in changing the OA biomarkers in knee joint.


2010 ◽  
Vol 19 (6) ◽  
pp. 940-944 ◽  
Author(s):  
Julio Urrutia ◽  
Jorge Briceno ◽  
Maximiliano Carmona ◽  
Fernando Olavarria ◽  
Felipe Hodgson

2018 ◽  
Vol 24 (5-6) ◽  
pp. 407-417 ◽  
Author(s):  
Byoung Ju Kim ◽  
Yoshie Arai ◽  
Eun-Mi Park ◽  
Sunghyun Park ◽  
Alvin Bello ◽  
...  

2009 ◽  
Vol 9 (10) ◽  
pp. 26S
Author(s):  
William Lloyd ◽  
Michael Larson ◽  
Ronald Hill
Keyword(s):  

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