• Journal of Dental Anesthesia and Pain Medicine
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• 제16권4호
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• pp.303-307
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• 2016

Background: In dental intravenous sedation, continuous intravenous infusion of a low-dose drug requires an infusion pump such as a syringe pump. To develop a new syringe pump for clinical use, the functions of the pump must meet certain international standards. Various safety and efficacy tests must be performed on the syringe pump, as stipulated by these standards, and an approval must be received from the approving agency based on such test results. Methods: The authors of the present study developed a novel syringe pump and performed efficacy evaluation by testing its infusion speed at 1 and 25 ml/h, and infusion performance testing at 2 and 24 h. Moreover, performance evaluation was conducted by comparing the novel pump to an existing pump with the infusion speed varied from 1 to 5 ml/h. Results: In the efficacy testing on the newly developed syringe pump, infusion with the infusion speed initially set to 1 ml/h resulted in infusion speeds of 1.00 and 0.99 ml/h in the 2- and 24-h assessment, respectively. Changing the infusion speed setting to 25 ml/h resulted in an infusion speed of 25.09 and 23.92 ml/h in the 2- and 24-h assessment, respectively. These results show no significant differences when compared with other commercially available pumps. Conclusions: The efficacy testing of the newly developed syringe pump showed the accuracy to be within tolerance. Based on these findings, we believe that the newly developed syringe pump is suitable for clinical use.

• 대한전기학회논문지:전기물성ㆍ응용부문C
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• 제50권6호
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• pp.307-313
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• 2001

A micro syringe which can be attached to the end of a micro intravascular endoscope for drug injection is fabricated and its characteristic is tested. The syringe consists of a drug chamber and an actuator chamber which are separated by a silicone rubber membrane. The drug chamber is filled with liquid drug by the membrance actuation caused by the vaporization and condensation of the working liquid in the actuator chamber. The liquid drug is ejected by the electrolysis of the working liquid. The membrane deflection by each actuation method has been measured. The liquid ejection image has been captured during the electrolysis of the electrolyte. Also, the successful operation of the micro syringe under the normal blood pressure was verified.

• International Journal of Advanced Culture Technology
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• 제10권4호
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• pp.23-244
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• 2022

The Pulpose of this systematic review is aimed to establish the procedure of the injection with saftey and efficiency in the pre-hospital cardiac arrest patient performing the cardiopulmonary resuscitation (CPR), compared with traditional medication administration using Ampoule and medication administration with Prefilled Syringe. Databases were searched for CPR, heart arrest, resuscitation, Pre-filled Syringe, and Ampoule by the electronic data research including Pubmed, EMBASE and Cochran Library of Konyang University Library: 4 articles were selected by three co-authors using EndNote X20 and Covidence (Covidence.org) and were systematically reviewed. The Result of this study, the medication administration using Pre-fillled Syringe improves the safety of patients and Emergency medical workers by reducing the error in administration dose and administering the drug in safe than the medication adminisrtaion using Ampoule, also, contributes to the increment of survival rate of cardiac arrest and severe patients by decreasing the administration time that prevents the delay of medication administration.

• Journal of Multimedia Information System
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• 제7권2호
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• pp.175-188
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• 2020

The paper focuses on conception and development of complex systems composed mainly by a pump syringe subsystem and an electronically injector that facilitates patients saving data operation for medical staff use. We successfully developed conventional approaches for medical system staff requirements, such as system boundary conditions. Decisions at a given level are studied. We propose a complex system architecture, based mainly on patients collected data and ordered stepper injection parameters. System is successfully simulated and prototyped. Design and implement tests are accomplished, the proposed system ensures both the electric syringe pump and the electric injector operation. In addition, this new system introduces several additional options as patient database development and automation injection operation. Development and software operating tests to create a visualization control interface are validated. The solution performs syringe function and electronic injector. User can manage a syringe in two C modes of technology. We propose a program composed of two linked parts. If an error such radiologist bad target selection is made, an image with lower intrinsic quality emerges. Developed Shoot syringe different electronic cards are simulated and prototyped, in addition, maps are driven, prototype. All tests results are accomplished.

• Journal of Pharmaceutical Investigation
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• 제21권3호
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• pp.155-160
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• 1991

Particulate is the foreign insoluble material in injectable solution inadvertently present in a given product. Considerable efforts have been made to avoid or minimize particulate contamination by pharmaceutical manufacturers during the production of parenteral products. Particulate contamination of the parenteral products can occur mainly during the opening (cutting) the container immediately before clinical use. In this study, particulate contamination generated during the opening process of ampoules (conventional type, 1-point and color-break ampoules) was compared with that of a prefilled injectable container (prefilled syringe). The particles were examined under a microscope after filtration of the total fluids in the containers. Particles having wide range of size distribution were found from all the ampoules tested. The contamination from the I-point ampoule and colorbreak ampoule was much less than from the conventional ampoule. Glass particles generated by cutting the glass-made ampoules seemed a principal source of the particulate contamination. The glass-partiaulte contamination could be improved substantially by replacing the ampoule containers with the prefilled syringe. Prefilled syringe, which can be used without any cutting process. did not generate particulates during the use. Therefore, it was concluded that prefilled syringe is most preferable container for the small volume parenteral (SVP) fluids in terms of particulate contamination.

• 핵의학기술
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• 제14권2호
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• pp.65-76
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• 2010

1994년 PET의 국내 도입 이후, 현재까지 양적으로나 질적으로 많은 발전이 있었다. 하지만 이와 함께 방사성의약품의 사용량 또한 급증하면서 검사에 있어서 가장 중요한 역할을 하는 방사선사의 개인피폭선량이 높아지는 요인으로 작용했던 것이 사실이다. 식품의약품안전청의 피폭선량관리센터에서 발표한 자료에 따르면 2008년도 방사선작업종사자의 전체 평균 피폭선량은 0.67 mSv였고, 방사선사 전체 피폭선량은 1.33 mSv로 해마다 감소하는 것으로 나타났다. 설문결과를 살펴보면 PET 검사 담당자의 평균피폭선량은 1.69 mSv였고, 1.0 mSv를 초과하는 구간에 75.3%의 방사선사가 포함되어 있었다. 이는 고 노출구간에 속한 방사선사의 비율이 높다는 것을 의미하므로, 피폭저감을 위한 노력이 요구된다. 본 연구에서는 설문조사를 통하여 PET 검사 프러시저별 차폐기구의 활용에 따른 방사선 피폭 정도를 TLD 수치를 이용하여 분석하고, 실험을 통하여 각 차폐기구의 차폐율을 측정함으로써, 그 효용성을 입증하고 적합한 차폐방법을 강구하고자 하였다. 방사선 피폭의 위험에 대해서 어느 누구보다 잘 인지하고 있는 방사선사임에도 불구하고 안이하게 생각하는 경향이 있었다. 설문결과를 살펴보면 방사선 피폭의 위험성에 대한 인식도와 피폭선량과는 크게 관련이 없었으며, 차폐기구의 활용도에 따라서는 피폭선량의 차이가 확연하게 나타났다. 프러시저 중 피폭선량에 가장 많은 영향을 미치는 단계는 방사성의약품의 투여였으며, 투여시 차폐방법에 따라 이동시 차폐방법도 달라졌다. 투여 시 차폐기구 사용현황을 보면 Both shield는 58.5%, L-Block은 20%, Syringe shield는 9%, No shield는 12.3%를 차지하였다. TLD 수치에 따른 투여 시 차폐방법은 수치가 낮을수록 Both shield와 L-block을 많이 사용하였으며, 수치가 높을수록 Syringe shield와 차폐를 시행하지 않는 경우가 많았다. 실험결과, 가장 이상적인 차폐방법은 분배 시엔 L-block을 사용하고, 이동시엔 Syringe shield carrier를 사용하며, 투여 시엔 L-block과 Syringe shield를 함께 사용하는 것이다. 환자 포지셔닝 시 Apron의 차폐율은 평균 16.4%로 차폐효과가 있다. PET 검사를 시행함에 있어서 강한 실천의지를 가지고 프러시저별로 차폐기구를 적극 활용한다면 점증하는 방사선사의 피폭 수준을 크게 감소시킬 수 있을 것으로 판단된다.

• 대한의용생체공학회:의공학회지
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• 제44권1호
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• pp.92-98
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• 2023

Purpose: To propose a new infusion rate monitoring technique based on the 2D image marker tacking to improve patient safety by preventing syringe pump-related medication accidents due to decreased infusion rate control accuracy. Materials and Methods: The infusion rate of the syringe pump and drug residue in the pump-equipped syringe were monitored in real time by tracking the movement of the 2D image markers attached to the syringe pump. Results: The error rate between the set and the estimated infusion rates was 1.03, 0.66, 1.95, 0.23, and 1.05% when the infusion rate setting was 10, 20, 30, 40, and 50 mL/H, respectively. In addition, the error rate between the actual and the estimated drug residues was 1.04, 0.47, 0.60, 3.66, and 0.00% when the infusion rate setting was 10, 20, 30, 40, and 50 mL/H, respectively. Conclusion: Experimental results demonstrated that the proposed technique can increase the efficiency of the safety management system for seriously ill inpatients by decreasing a possibility of syringe pump-related medication accidents in hospitals.

• The Plant Pathology Journal
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• 제37권5호
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• pp.489-493
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• 2021

Bacterial canker is a devastating disease of kiwifruit caused by the bacterium Pseudomonas syringe pv. actinidiae. Canker disease of kiwifruit in Korea has been controlled using streptomycin for more than two decades. Four streptomycin-resistant strains, belonging to biovar 2, which are found only in Korea, were collected between 2013 and 2014 from different orchards located in Jeju, Korea. The genetic background for streptomycin resistance among P. syringe pv. actinidiae strains were determined by examining the presence of strA-strB or aadA, which are genes frequently found in streptomycin-resistant bacteria, and a point mutation at codon 43 in the rpsL gene. All four streptomycin-resistant strains of P. syringe pv. actinidiae investigated in this study contained strA-strB as a resistant determinant. The presence of the aadA gene and a mutation in codon 43 of the rpsL gene was not identified.

• 과학교육연구지
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• 제37권1호
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• pp.233-243
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• 2013

이 연구의 목적은 기주의 길이와 공명주파수의 관계를 정량 분석할 수 있는 교육용 실험기구를 개발하는 것이다. 일회용 플라스틱 주사기와 분자모형 조립용 플라스틱 구를 이용하여 '머리' 달린 기주 공명 장치를 제작하고 상용화된 소프트웨어를 이용하여 PC 실험시스템을 구성하였다. 연구 결과, PC 실험시스템은 전문가용 장비를 대신할 수 있는 것으로 나타났다. 주사기로 만든 이 실험기구는 '관'이 아닌 '헬름홀쯔 공명기'인 것으로 증명되었다. 실험으로 얻은 자료가 소리공명현상을 증명할 수 있는 것으로 나타났다. 결론적으로, 이 주사기 공명기는 중고등학생을 위한 영재교육이나 대학 음향실험용으로 사용가능한 실험장치이다.

• 한국콘텐츠학회논문지
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• 제20권10호
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• pp.395-400
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• 2020

2019년 10월부터 2020년 1월까지 대구P병원 핵의학과에서 SPECT 검사를 위한 입원환자 중 3-way 주사재료를 장착하고, ^99mTc 표지화합물을 투여하였던 주사기 120EA를 대상으로 하였다. 플라스틱 주사기 사용시 희석 횟수에 따른 평균 투여율은 ^99mTc-ECD가 90.87±11.08로 가장 높았으며, ^99mTc-DMSA가 75.28±7.43으로 가장 낮았다. 놈젝주사기 사용 시 희석횟수에 따른 평균 투여율은 ^99mTcO4가 93.58±7.96으로 가장 높았으며, ^99mTc-DMSA가 91.60±6.07로 가장 낮았다. ^99mTc-DMSA의 플라스틱 주사기와 놈젝주사기의 차이가 나는지 독립표본 t-검정 결과, 유의확률은 0.007로서 플라스틱 주사기와 놈젝 주사기의 평균은 다르므로 통계적으로 매우 유의하게 나타났다(p<0.01). 특히 신장검사에 사용하는 ^99mTc-DMSA는 소아 환자에게 주로 사용되는 방사성의약품으로 정확한 투여량이 중요하여 일반 플라스틱 주사기보다 놈젝 주사기의 사용이 필요하다고 판단된다.