본 연구는 유소년의 골연령에 따른 체력을 평가하는 데 있으며, 골연령에 따른 체력 표준지표 를 통해 유소년들의 균형적인 발달을 위한 기초자료를 제공하는 데 있다. 연구 대상은 골연령 11세∼13세 및 역연령 11세∼13세에 해당하는 730명을 대상으로 하였으며 골연령 산출을 위해 X-ray 필름을 촬영한 후 TW3 방법으로 평가하였다. 체격은 신장, 체중을 신장계(Hanebio, Korea, 2021), Inbody 270(Biospace, Korea, 2019)를 사용하여 총 2개의 체격 요소를 측정하였으며, 체력은 근력(악력), 평형성 (외발서기), 민첩성(플랫테핑), 순발력(제자리멀리뛰기), 유연성(좌전굴), 근지구력(윗몸일으키기), 심폐지구 력(셔틀런)으로 총 7개 체력 요소의 종목을 측정하였다. 자료처리 방법은 SPSS PC/Program(Version 26.0) 을 이용하여 기술통계, 독립표본 t-test 검정을 실시하였으며, p< .05수준에서 유의한 것으로 간주하였다. 본 연구의 결과는 다음과 같다. 첫째, 11세∼13세 골연령과 역연령을 비교한 결과, 체력에서 남자는 근력, 순발력, 근지구력, 심폐지구력에서 유의한 차이가 나타났다. 여자는 근력, 평형성, 민첩성, 순발력, 유연성, 근지구력, 심폐지구력에서 유의한 차이가 나타났다. 둘째, 골연령에 따른 유소년의 성별과 연령(11∼13세) 별로 체력평가의 기초 자료인 골연령 체력 표준지표를 개발하였다.

Wasted meat & bone has generated as byproducts in the slaughtering process of livestock and also faced with demands for its recycling and environmental protection. Many studies have been conducted to recycle byproducts and carried out mainly on the crushing of bones and the vacuum packing technology of products. In this study, the crushing unit, transporting unit, separated unit and packing unit have designed for development of the crushing and packing systems. Also, to confirm the performance of this system, the experimental verification were carried out the working noise and packing weight.

BMP-2 is a well-known TGF-beta related growth factor, having a significant role in bone and cartilage formation. It has been employed to promote bone formation in some clinical trials, and to differentiate mesenchymal stem cells into osteoblasts. However, it is difficult to obtain this protein in its soluble and active form. hBMP-2 is expressed as an inclusion body in the bacterial system. To continuously supply hBMP-2 for research, we optimized the refolding of recombinant hBMP-2 expressed in E. coli, and established an efficient method by using detergent and alkali. Using a heparin column, the recombinant hBMP-2 was purified with the correct refolding. Although combinatorial refolding remarkably enhanced the solubility of the inclusion body, a higher yield of active dimer form of hBMP-2 was obtained from one-step refolding with detergent. The refolded recombinant hBMP-2 induced alkaline phosphatase activity in mouse myoblasts, at ED50 of 300-480ng/ml. Furthermore, the expressions of osteogenic markers were upregulated in hPDLSCs and hDPSCs. Therefore, using the process described in this study, the refolded hBMP-2 might be cost-effectively useful for various differentiation experiments in a laboratory.

Recently, robot-assisted joint replacement surgeries are on the rise. Robot-assisted surgery can make more accurate outcome, and thus it will be more popular. For the accurate result, secure fixation of bone is necessary, but there are numerous difficulties for the secure fixation. Detecting bone motion is necessary to prevent some errors. Currently, optical sensor and location sensor are in use; however, these sensors can cause interventional problem for the friction between mechanical devices. This study shows how to compose the bone motion detecting device using electromagnetic sensor, how to commercialize the bone motion detecting device.

Our objective of current study was to investigate the development of bone and heart in association with diabetes mellitus (DM). DM was induced by administering an intraperitoneal injection of streptozotocin (STZ; 60 mg/kg) to 4‐gweek‐gold Sprague‐gDawley rats. Body weight and blood glucose were monitored, and rats were sacrificed after 2 or 5 weeks. The left ventricle (LV), including the interventricular septum, was weighed, and body weight and tibial bone length were assessed. Young diabetic rats showed reduced growth in terms of tibial length and body weight compared to controls. Moreover, diabetic males showed more significant growth suppression and reduced LV size than diabetic females. Morphometric analysis of tibiae from diabetic rats revealed suppressed bone growth at 2 and 5 weeks, with no difference between genders. STZ‐ginduced diabetes decreased bone growth and retarded pre‐gpubertal heart development. As a result, diabetes may increase cardiovascular risk factors and lead to eventual heart failure. Therefore, new therapeutic approaches are required for diabetic children exhibiting growth retardation. Heart growth factor, exercise, and cardiopulmonary physical therapy may be required to promote heart development and physiological function.