首页> 外文期刊>e-Jurnal Medika Udayana >POTENSI APLIKASI GRANULOCYTE-COLONY STIMULATING FACTOR VIA MICROCHIP SUBKUTAN SEBAGAI TERAPI PREVENTIF PADA TRAVELER PASCA INFARK MIOKARDIUM
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POTENSI APLIKASI GRANULOCYTE-COLONY STIMULATING FACTOR VIA MICROCHIP SUBKUTAN SEBAGAI TERAPI PREVENTIF PADA TRAVELER PASCA INFARK MIOKARDIUM

机译:通过微切屑抽吸法对粒细胞集落刺激因子的潜在应用作为预防性治疗在心肌梗塞后旅行者中的应用

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POTENTIAL APPLICATIONS GRANULOCYTE-COLONY STIMULATING FACTOR VIA SUBCUTANEOUS MICROCHIP ON PREVENTIVE THERAPY AFTER TRAVELER MYOCARDIAL INFARCTION Death incidence among travelers with myocardial infarct (MI) highly reported among travelers experiencing previous reperfusion therapy. Pathological remodeling progresivity post MI have a strong corelation with mortality related with cardiac arythmia and heart failure. Cellular cardiomyoplasty considered as one regenerative therapy which capable in preventing post infarct pathological remodeling by applying the multipotency effect of stem cell. Several studies suggest the use of Mesenchymal Stem Cell (MSC) in the term of celluar cardiomyoplasty which focused on endogenous modulation of stem cells. Regarding to those concern, the emerging effectivity of Granulocyte-Colony Stimulating Factor (G-CSF) in modulates MSC endogenously proved to be relevant. From the travel medicine perspective, G-CSF therapy need several considerations including pre travel condition of a patient after reperfusion therapy, risk factors exposure during travel and medical compliance. Therefore, one strategy named microchip drugs delivery system was suggested as a response for the need of increasing drugs efficacy, stable and continuous transfer, high compliance and self-controlled therapy. This review aimed to explore the G-CSF mechanism as MSC modulator, introducing the construction and the mechanism of subcutaneus microchip to facilitate G-CSF therapy, and provide prospective view of G-CSF therapy via subcutaneus microchip among post MI traveler. G-CSF modulates MSC by performing stimulation for MSC mobilization from bone marrow, homing to the infarct zone and regeneration activity. Inside the construction, microchip as a drugs container passed microfabrication process and package into implant capsule. G-CSF release externally controled by radiofrequency signal that induce the microchip membrane degradation followed by drugs release. Furthermore, regarding to the revealed potentiality, G-CSF therapy expected to perform an evidence based preventive therapy for post MI traveler and increase heart functional capacity to adapt with risk exposure during travel. Overall, deep research strongly required.
机译:潜在的应用心肌梗塞后通过皮下微芯片对粒细胞集落刺激因子的预防性治疗在先前接受过再灌注治疗的旅行者中,心肌梗死(MI)旅行者的死亡发生率很高。心肌梗死后的病理重塑进展与与心律失常和心力衰竭有关的死亡率有很强的相关性。细胞心肌成形术被认为是一种再生疗法,能够通过利用干细胞的多能性效应来预防梗塞后病理重塑。多项研究表明,间质干细胞(MSC)在细胞心肌成形术中的应用,其重点在于干细胞的内源性调节。关于这些问题,粒细胞集落刺激因子(G-CSF)在调节内源性MSC方面新兴的有效性被证明是相关的。从旅行医学的角度来看,G-CSF治疗需要考虑几个因素,包括再灌注治疗后患者的旅行前状况,旅行期间的危险因素暴露以及医疗依从性。因此,提出了一种名为微芯片药物输送系统的策略,作为对提高药物功效,稳定和连续转移,高依从性和自我控制疗法的需求的一种回应。这篇综述旨在探讨作为MSC调节剂的G-CSF机制,介绍促进皮下注射的皮下皮微芯片的构建和机理,并为MI后旅行者中通过皮下皮微芯片进行G-CSF治疗提供前瞻性的观点。 G-CSF通过执行刺激以促进MSC从骨髓动员,归巢到梗塞区和再生活性来调节MSC。在建筑内部,作为药物容器的微芯片经过微细加工过程,然后包装到植入物胶囊中。 G-CSF的释放受射频信号的外部控制,该信号引起微芯片膜降解,然后释放药物。此外,关于所揭示的潜力,G-CSF治疗有望为MI后旅行者做出基于证据的预防性治疗,并增加心脏功能以适应旅行过程中的风险暴露。总体而言,强烈需要深入研究。

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