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Modified perfusion bioreactor enhances proliferation of MC3T3-E1 seeded on PLGA/Β-TCP/PCL scaffold

عنوان مقاله: Modified perfusion bioreactor enhances proliferation of MC3T3-E1 seeded on PLGA/Β-TCP/PCL scaffold
شناسه ملی مقاله: ITERMED01_346
منتشر شده در اولین کنگره بین المللی مهندسی بافت و پزشکی بازساختی ایران در سال 1397
مشخصات نویسندگان مقاله:

Fatemeh Mokhtari-Jafari - School of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran
Ghassem Amoabediny - Department of Biomedical Engineering, Research Center for New Technologies in Life Science Engineering, University of Tehran, Tehran, Iran
Mohammad Mehdi Dehghan - Department of Surgery and Radiology, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
Marco N. Helder - Department of Oral and Maxillofacial Surgery, VU University Medical Center, Amsterdam Movement Sciences, Amsterdam, Netherlands

خلاصه مقاله:
IntroductionBone tissue engineering, an important field in contemporary clinical practices, aims to repair or replace bone defects using cells, scaffolds, and bioreactors. This study investigated whether modified perfusion bioreactor at 5 ml/min flow rate enhances proliferation, distribution and extracellular matrix formation of MC3T3-E1 cells cultured on a porous PLGA/β-TCP which PCL porous hollow fibers was embedded in.MethodsMC3T3-E1 pre-osteoblastic cells were seeded onto the porous PLGA/β-TCP/PCL scaffolds (2 cm in diameter and 1 cm in thickness) by adding 200 μl of cell suspension media with 1×106 cells to each scaffold in a dropwise manner and incubated for 2 hr (200 μl of culture medium were added to each scaffold every 30 min). After 2 hr, 10 ml of culture medium was added to each scaffold and incubated in a humidified atmosphere at 37 °C and 5% CO2. After an overnight static culture, scaffolds were transferred to the modified perfusion bioreactors (one scaffold for each bioreactor) with flow rates 5 ml/min.ResultsOur data showed that this new designed perfusion bioreactor with flow rate of 5 ml/min increased proliferation 1.8-fold after 5 days of dynamic culture. The homogeneous cell distribution and extracellular matrix formation within the PLGA/β-TCP scaffolds were demonstrated through DAPI staining and Alizarin red staining, respectively.ConclusionIn conclusion, modified perfusion bioreactor promotes cell proliferation, cell distribution and extracellular matrix formation in bone tissue-engineered constructs which is a promising approach to treat patients with large bone defects.

کلمات کلیدی:
Bone, Modified perfusion bioreactor, proliferation, Cell distribution, Extracellular matrix

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/905846/