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1.
Korean Journal of Blood Transfusion ; : 209-216, 2021.
Artigo em Inglês | WPRIM | ID: wpr-917535

RESUMO

The blood management act was revised on December 4, 2020, to enhance transfusion management and has been established in accordance with the department of transfusion management in the medical institution. The department of transfusion management is involved in education related to transfusion, transfusion monitoring, and ward rounding. The department of transfusion management is essential for promoting the stability and safety of transfusions. This paper aims to help the department of transfusion management operation by sharing the experience of the department of transfusion management.

2.
Tissue Engineering and Regenerative Medicine ; (6): 568-578, 2016.
Artigo em Inglês | WPRIM | ID: wpr-644842

RESUMO

Rotator cuff tear is a common musculoskeletal disease that often requires surgical repair. Despite of recent advances in surgical techniques, the re-tear rate of the rotator cuff tendon is very high. In this study, a platelet-derived growth factor-BB (PDGF-BB)-immobilized asymmetrically porous membrane was fabricated to investigate the feasibility for enhancing rotator cuff tendon regeneration through the membrane. PDGF-BB is recognized to promote tendon regeneration. The asymmetrically porous membrane was fabricated by polycaprolactone and Pluronic F127 using an immersion precipitation technique, which can allow selective permeability (preventing scar tissue invasion into defect region but allowing permeation of oxygen/nutrients) and incorporation of bioactive molecules (e.g., PDGF-BB) via heparin binding. The PDGF-BB immobilized on the membrane was released in a sustained manner over 42 days. In an animal study using Sprague-Dawley rats, the PDGF-BB-immobilized membrane group showed significantly greater regeneration of rotator cuff tendon in histological and biomechanical analyses compared with the groups of control (suturing) and membrane without PDGF-BB immobilization. The enhancing regeneration of rotator cuff tendon of the PDGF-BB-immobilized membrane may be caused from the synergistic effect of the asymmetrically porous membrane with unique properties (selective permeability and hydrophilicity) as a scaffold for guided tendon regeneration and PDGF-BB sustainedly released from the membrane.


Assuntos
Animais , Cicatriz , Heparina , Imersão , Imobilização , Membranas , Doenças Musculoesqueléticas , Permeabilidade , Poloxâmero , Ratos Sprague-Dawley , Regeneração , Manguito Rotador , Lágrimas , Tendões
3.
Laboratory Animal Research ; : 255-263, 2012.
Artigo em Inglês | WPRIM | ID: wpr-192523

RESUMO

Gangliosides are ubiquitous components of the membranes of mammalian cells that are thought to play important roles in various cell functions such as cell-cell interaction, cell adhesion, cell differentiation, growth control, and signaling. However, the role that gangliosides play in the immune rejection response after xenotransplantation is not yet clearly understood. In this study, the regulatory effects of human leukocytes on ganglioside expression in primary cultured micro-pig aortic endothelial cells (PAECs) were investigated. To determine the impact of human leukocytes on the expression of gangliosides in PAECs, we performed high-performance thin layer chromatography (HPTLC) in PAECs incubated with FBS, FBS containing human leukocytes, human serum containing human leukocytes, and FBS containing TNF-alpha. Both HPTLC and immunohistochemistry analyses revealed that PAECs incubated with FBS predominantly express the gangliosides GM3, GM1, and GD3. However, the expression of GM1 significantly decreased in PAECs incubated for 5 h with TNF-alpha (10 ng/mL), 10% human serum containing human leukocytes, and 10% FBS containing human leukocytes. Taken together, these results suggest that human leukocytes induced changes in the expression profile of ganglioside GM1 similar to those seen upon treatment of PAECs with TNF-alpha. This finding may be relevant for designing future therapeutic strategies intended to prolong xenograft survival.


Assuntos
Humanos , Adesão Celular , Comunicação Celular , Cromatografia em Camada Fina , Células Endoteliais , Gangliosídeos , Imuno-Histoquímica , Leucócitos , Membranas , Rejeição em Psicologia , Transplante Heterólogo , Fator de Necrose Tumoral alfa
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