• 대한의용생체공학회:의공학회지
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• 제5권1호
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• pp.63-68
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• 1984

The Infusion pump that is widely used in hospital has been designed. This system consists of microcomputer system, stepping motor control part and mechanical part for syringe driving. It has 450mmHg maximum pressure and $\pm$0.5% accuracy, and and especially keep the accent on the electrical and functional safety.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2015년도 제49회 하계 정기학술대회 초록집
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• pp.236.2-236.2
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• 2015

The copper-zinc(Cu-Zn) nanofiber was prepared by electrospinning method. The Cu/PVP (polyvinylpyrrolidone) and Zn/PVP precursor solutions were prepared by dissolution of copper sulfate and zinc acetate in methanol, respectively. The PVP was used to control the viscosity of the precursor solutions. The optimized ratio for the Cu/PVP and Zn/PVP nanofibers was determined separately. Then the suitable ratio of the precursor solutions was applied for fabrication of Cu/Zn/PVP nanofiber. For the electrospinning method, the precursor solutions were filled in a syringe. The distance between metallic needle on the syringe and collector was fixed at 16 cm and the voltage was applied on the tip was 13.0 kV. And the as-spun nanofiber was heated at 353K for removal of residual solvent. Then the heated nanofibers were calcined at 973K to decompose PVP. The obtained Cu, Zn, and Cu-Zn nanofibers were investigated with X-ray photoelectron spectroscopy (XPS) for the chemical properties, scanning electron microscopy (SEM) for the morphologies, and X-ray diffraction (XRD) to characterize the crystallinity and phase of nanofibers.

• Toxicological Research
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• 제23권3호
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• pp.239-244
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• 2007

Respirable particles cause many occupational and environmental diseases of the lung. To study these diseases, laboratory animals are often exposed to these particles. Inhalation and instillation are the well-known techniques for experimental exposures of the lung to respirable particles. Recently, another technique called oropharyngeal aspiration (OPA) has been introduced for exposing the lung to pathogens and/or particles. The conventional OPA technique for the mouse is generally carried out using a micropipette with a fixed slant board. In order to modify the conventional OPA in this study, anesthetized mice were placed on an adjustable slant board, a syringe pump was used to deliver the solution to the oropharynx, and the mice were allowed to recover in vertically positioned tubes for 6 minutes until fully awaked. Most importantly, the whole process of OPA could be carried out simply by an examiner. This modified OPA technique was validated by exposing the mouse lung to Evans Blue dye with a success rate of 95%.

• 대한치과마취과학회지
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• 제6권2호
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• pp.98-102
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• 2006

The purpose of this study was to evaluate the difference on pain intensity and discomfort between pressure-controlled injection system and conventional syringe injection technique from the patients undergoing oral and maxillofacial surgery. In a prospective, randomized, case-controlled study, 60 patients were divided into two groups (n=30 in each). In experimental group, pressure-controlled injection system was applied. In control group, conventional syringe injection system was applied. Pain rating score (PRS) and visual analogue scale (VAS) were assessed. The average of VAS in experimental group ($16.67{\pm}15.07$) was smaller than that of control group ($25.63{\pm}22.21$), though there were no significant differences (P=0.072). In PRS, fifteen patients (50.0%) of experimental group answered that they experienced mild pain. However sixteen patients (53.3%) of control group answered that they experienced intermediate pain. From the results, pressure-controlled injection system may be an effective method to reduce pain during the dental local anesthetic procedure.

• 한국임상약학회지
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• 제8권1호
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• pp.54-58
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• 1998

The stability of ceftriaxone sodium 100 mg/ml in the water for injection was tested at two temperature conditions (refrigerator and room temperature) and two storage containers (vitro and syringe). The stability of each sample was determined by high-performance liquid chromatography while storing for 5 days at room temperature and 27 days at refrigerator. The concentration of ceftriaxone sodium was 100 mg/ml which the hospital usually use as a filling preparation for I.V. push or Y-site injection. There was no significant difference between the storage in vials and syringes. There was no significant difference in the change of concentration until storing the reconstituted ceftriaxone sodium injection for 2 days at room temperature and 14 days at refrigerator. In conclusion, the ceftriaxone sodium 100 mg/ml in the water for injection can be stored in vial or syringe for 2 days at room temperature and 14 days at refrigerator after preparation.

• 대한치과의료관리학회지
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• 제9권1호
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• pp.32-37
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• 2021

Many approaches to local anesthesia have been studied in dentistry. In this study, we introduce a new local anesthetic method, "Point-Inject Technique (PIT)", and compare it with traditional injection techniques. The PIT method utilizes both the vasoconstrictive and antinociceptive properties of local anesthetics as well as the application of controlled pressure during injection, reducing the time to complete anesthesia. Fifty patients were selected as the experimental group who were anesthetized using PIT, and the other 50 patients were selected as the control group using the direct injection method with a carpool syringe. The PIT group received 0.25 cartridges of 2% lidocaine with 1:100,000 epinephrine. The control group received 1.5~2 cartridges of 2% lidocaine with 1:100,000 epinephrine. Both groups were asked to mark the intensity of the pain caused by anesthesia using the Numeric Pain Rating Scale. The average time to recover from anesthesia was 40 minutes in the experimental group and 90 minutes in the control group. Additionally, 96% of the experimental group reported feeling no pain, while 78% of the control group reported having some form of pain during injection. The PIT method reduced both the reported pain scores of patients as well as time to recover from local anesthesia than the widely-used syringe injection method.

• Journal of Trauma and Injury
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• 제36권4호
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• pp.451-453
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• 2023

We introduce a convenient method of urethrography before catheterization for patients with pelvic trauma that can be used in a resuscitation area. A 10-mL syringe without a needle was used. X-ray contrast medium (Iohexol, 300 mg I/mL) was administered through the urethral orifice using a 10-mL syringe without needle and a simple pelvic anteroposterior film was taken (70 kilovolt [peak], 50 mAs). A 36-year-old soldier with a saddle injury from a gun barrel was taken to a trauma center. He had a pelvic fracture and complained of hematuria. Bedside urethrography above described was performed. The anterior urethra showed nonspecific findings, but dye leaked from the posterior urethra. Bedside Foley catheter insertion was attempted, but the catheter could not be advanced past the membranous urethra. Thereafter, suprapubic catheterization was performed. On the day of the injury, iliac artery embolization was carried out. The dislocated sacroiliac joint was also treated using open reduction and internal fixation. On hospital day 7, guidewire Foley insertion was performed. This bedside urethrography technique is simple and useful for pelvic fractures in which urethral injury is suspected.

• 한국방사선학회논문지
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• 제16권2호
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• pp.95-102
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• 2022

본 연구는 PET(positron emission tomography) 검사를 위해 내원한 환자를 대상으로 방사성의약품 ¹⁸F-FDG 동위원소를 주사 할 때, 주사 방법과 생리식염수의 용량에 따른 주사기의 잔량의 차이를 비교하였다. 조영제를 사용하는 CT 혹은 MRI 검사 후, 3-way를 제거하지 않고, PET 검사를 위해 내원한 40명의 환자를 대상으로 ¹⁸F-FDG를 주사 할 때, 주사기와 3-way에 남게 되는 방사능을 측정하여, 실제 환자에게 투여된 방사능을 확인했다. 이때 20명의 환자들로 나누어 생리식염수의 용량을 달리하였다. 또 다른 주사 방법은 extension을 이용하여 주사 하였을 때, 주사기의 잔량 비교와 생리식염수 용량에 따른 잔량 차이를 비교하였다. ¹⁸F-FDG 를 주사 한 후, 주사기와 3-way 또는 extension에 남아 있는 방사능을 검량기로 측정하여 실제 투여된 용량을 확인 했다. 방사성의약품을 투여하기 전의 주사기의 방사능과 투여한 후 주사기와 3-way 또는 extension 의 방사능을 측정한 결과, 생리식염수 10 cc에 3way 의 주입 방식이 잔류량이 가장 낮았고, 생리식염수 10 cc에 extension, 생리식염수 5 cc에 3way 순으로 잔량이 증가하였다. 5 cc의 생리식염수에 extension 주사 방법이 잔량이 가장 많이 남아 있었다. 잔량이 가장 적게 남은 주사 방법과의 잔량 차이는 0.053 mCi이다. PET 검사 시, 3-way와 extension에 남게 되는 방사능을 감안하고, 생리식염수의 투여 용량을 조절함에 따라, 실제 환자에게 투여하고자 하는 목적 용량을 고안한다면 좀 더 정확하게 환자에게 방사성의약품을 투여할 수 있을 것이다.

• 한국콘텐츠학회논문지
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• 제15권4호
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• pp.357-362
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• 2015

본 실험에서는 조영제를 사용하는 CT 혹은 MRI 검사 후, 3-way를 제거하지 않고, Bone scan 검사를 위해 내원한 50명의 환자를 대상으로 방사성 의약품 99mTc-MDP가 표지된 동위원소를 주사 할 때, 주사기와 3-way에 남게 되는 방사능을 측정하여, 실제 환자에게 투여된 방사능을 확인했다. 핵의학과 Bone scan 검사를 위해 내원한 환자 중 CT 혹은 MRI 검사 후 3-way를 유지하고 있는 50명의 환자를 대상으로 3-way를 통해 99mTc-MDP로 표지된 동위원소를 주사 한 후, 주사기와 3-way에 남아있는 방사능을 검량기로 측정하여 실제 투여된 용량을 확인 했다. 방사성의약품을 투여하기 전의 주사기의 방사능과 투여한 후 주사기와 3-way의 방사능을 측정한 결과, 투여 전 주사기의 방사능은 평균 31.75 mCi, 투여 후 주사기에 남은 방사능은 평균 1.22 mCi, 투여 후 3-way에 남은 방사능은 평균 0.95 mCi으로 측정되었다. 실제 환자에게 투여된 방사능은 평균 29.57 mCi로 처음 환자에게 투여하고자 했던 용량보다 평균2.18 mCi 가 환자에게 덜 투여됨을 알 수 있었다. Bone scan 검사 시, 3-way와 실린지에 남게 되는 방사능을 감안하여 투여 용량을 결정한다면, 실제 환자에게 투여하고자 하는 목적 용량을 좀 더 정확하게 투여 할 수 있을 것이다.

• 한국구조물진단유지관리공학회 논문집
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• 제22권6호
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• pp.72-80
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• 2018

본 연구는 기계주입 방식으로 간단히 재충전 할 수 있는 TPS 공법을 사용하여 실제 건설현장에 적용한 후 콘크리트 균열에 미치는 영향을 알아보고자 하였는데, 그 결과를 요약하면 다음과 같다. 먼저, 초음파 속도의 경우 TPS 공법을 사용하였을 시 주사기 공법에 비해 평균 약 36 mm/sec로 초음파가 빠른 속도로 통과하는 것을 알 수 있었고, 주입깊이의 경우 주사기 공법에서는 부분 충전되는 것을 확인하였으나 TPS 공법의 경우 강한 주입 압력으로 모든 배합에서 보수재가 100% 충전되는 우수한 경향을 나타내었다. 또한, 압축강도의 경우는 TPS 공법 사용 시 평균 16.8 % 증가하는 것으로 나타나 구조적으로 우수한 것으로 나타났다. 이상을 종합하면 주사기 공법에 비해 TPS 공법을 사용하였을 시 균열부위에 주입재가 밀실하게 충전되어 강도 증진으로 인한 품질 향상 및 확인창 설치로 인한 균열보수제의 거동이 확인 가능하다. 또한, TPS 공법 시공구간 532 m에 대하여 약 5일의 공사 기간이 단축됨에 따라 시공성이 우수하여 콘크리트 구조물에 균열 보수공법으로 사용성이 확대될 것으로 기대된다.