• Restorative Dentistry and Endodontics
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• 제22권1호
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• pp.1-33
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• 1997

The objective of this study was to analyze the in vitro and in vivo corrosion products of low and high copper amalgams. The four different types of amalgam alloy used in this study were Fine cut, Caulk spherical, Dispersalloy, and Tytin. After each amalgam alloy and Hg were triturated according to the directions of the manufacturer by means of the mechanical amalgamator(Amalgam mixer. Shinhung Co. Korea), the triturated mass was inserted into a cylindrical metal mold which was 12mm in diameter and 10mm in height. The mass was condensed by 150Kg/cm compressive force. The specimen was removed from the mold and aged at room temperature for about seven days. The standard surface preparation was routinely carried out by emery paper polishing under running water. In vitro amalgam specimens were potentiostatically polarized ten times in a normal saline solution at $37^{\circ}C$(potentiostat : HA-301. Hukuto Denko Corp. Japan). Each specimen was subjected to anodic polarization scan within the potential range -1700mV to+400mV(SCE). After corrosion tests, anodic polarization curves and corrosion potentials were obtained. The amount of component elements dissolved from amalgams into solution was measured three times by ICP AES(Inductive Coupled Plasma Atomic Emission Spectrometry: Plasma 40. Perkim Elmer Co. U.S.A.). The four different types of amalgam were filled in occlusal and buccal class I cavities of four human 3rd molars. After about five years the restorations were carefully removed after tooth extraction to preserve the structural details including the deteriorated margins. The occlusal surface, amalgam-tooth interface and the fractured surface of in vivo amalgam corrosion products were analyzed. In vivo and in vitro amalgam specimens were examined and analyzed metallographically by SEM(Scanning Electron Microscope: JSM 840. Jeol Co. Japan) and EDAX(Energy Dispersive Micro X-ray Analyser: JSM 840. Jeol Co. Japan). 1. The following results are obtained from in vitro corrosion tests. 1) Corrosion potentials of all amalgams became more noble after ten times passing through the in vitro corrosion test compared to first time. 2) After times through the test, released Cu concentration in saline solution was almost equal but highest in Fine cut. Ag and Hg ion concentration was highest in Caulk spherical and Sn was highest in Dispersalloy. 3) Analyses of surface corrosion products in vitro reveal the following results. a)The corroded surface of Caulk spherical has Na-Sn-Cl containing clusters of $5{\mu}m$ needle-like crystals and oval shapes of Sn-Cl phase, polyhedral Sn oxide phase. b)In Fine cut, there appeared to be a large Sn containing phase, surrounded by many Cu-Sn phases of $1{\mu}m$ granular shapes. c)Dispersalloy was covered by a thick reticular layer which contained Zn-Cl phase. d)In Tytin, a very thin, corroded layer had formed with irregularly growing Sn-Cl phases that looked like a stack of plates. 2. The following results are obtained by an analysis of in vivo amalgam corrosion products. 1) Occlusal surfaces of all amalgams were covered by thick amorphous layers containing Ca-P elements which were abraded by occlusal force. 2) In tooth-amalgam interface, Ca-P containing products were examined in all amalgams but were most clearly seen in low copper amalgams. 3) Sn oxide appeared as a polyhedral shape in internal space in Caulk spherical and Fine cut. 4) Apical pyramidal shaped Sn oxide and curved plate-like Sn-Cl phases resulted in Dispersalloy. 5) In Tytin, Sn oxide and Sn hydroxide were not seen but polyhedral Ag-Hg phase crystal appeared in internal space which assumed a ${\beta}_l$ phase.

• 한국버섯학회지
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• 제16권2호
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• pp.111-117
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• 2018

본 연구에서는 시설재배와 토경(매립) 복령의 성분 분석 및 생리활성 비교를 위해 연구하였다. 일반성분 분석 결과 산소가 45~46%로 가장 많이 포함하고 있었으며 다음으로 39~41%의 탄소, 6.06~6.1% 수소, 0.21~0.22% 질소로 나타났다. 그리고 시험을 실시한 복령 모두에서 황 성분은 발견되지 않았다. 시설 및 토경 재배 복령을 ICP 분석법으로 11종의 무기질을 분석한 결과 S, Fe, Mg, Zn의 함유량은 1년차, 2년차 모두 토경 재배 복령이 시설 재배 복령보다 많았으며 특히 Fe와 Zn의 함유량은 각각 약 3.1~4.9배, 3.6~3.9배 높았다. 50% 에탄올 복령 추출물의 DPPH와 ABTS radical 소거활성과 FRAP 방법을 실행하여 항산화 효과를 알아보았다. 복령 추출물 10 mg/ml의 농도에서 시설 및 토경 재배 복령의 DPPH $IC_{50}$ 값은 1년산 시설 재배(8.601mg/mL), 1년산 토경 재배(12.85mg/mL), 2년산 시설 재배(1.23mg/mL), 2년산 토경 재배(1.18 mg/mL)로 나타났으며 ABTS $IC_{50}$값은 1년산 시설 재배(15.85 mg/mL), 1년산 토경 재배(14.59 mg/mL), 2년산 시설 재배(3.9 mg/mL), 2년산 토경 재배(14.92 mg/mL)로 계산되었다. 연구에 사용한 복령의 항산화 활성은 농도 의존적인 증가를 보였고 2년산 시설 재배 복령이 가장 높은 항산화 활성을 나타냈다. FE-SEM을 이용하여 복령 입자의 초미세구조를 관찰한 결과 샘플간의 뚜렷한 차이점은 발견되지 않았다.

• Restorative Dentistry and Endodontics
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• 제25권4호
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• pp.561-574
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• 2000

Poly-P has been used to prevent decomposition of foods and has been shown to have inhibitory effect on the growth of gram positive bacteria. The purpose of this study was to evaluate the effect of poly-P on the growth of Porphyromonas endodontalis, a gram negative obligate anaerobic rod, endodontopathic bacterium. P. endodontalis ATCC 35406 was in BHI broth containing hemin and vitamin K with or without poly-P. Inhibitory effect of each poly-P which was added at the beginning(lag phase) or during(exponential phase) the culture, MIC(minimum inhibitory concentration) was determined by measuring the optical density of the bacterial cell at 540nm. Viable cell counts were measured to determined whether poly-P has a bactericidal effect. Leakage of intracellular nucleotides from P. endodontalis was determined at 260nm and morphological change of P. endodontalis was observed under the TEM(transmission electron microscope). Binding of 32P-labeled poly-P to P. endodontalis was examined. SDS-polyacrylamide gel electrophoresis and zymography were performed to observe the changes in protein and enzyme profiles of P. endodontalis, respectively. The results from this study were as follows : 1. The minimal inhibitory concentration(MIC) of poly-P to P. endodontalis appeared to be 0.04~0.05%. 2. Poly-P added to the P. endodontalis culture during the exponential phase of P. endodontalis was as much effective as poly-P added at the begining of the culture, suggesting that the antibacterial effect of poly-P is not much dependent on the initial inoculum size of P. endodontalis. 3. Poly-P are bactericidal to P. endodontalis, demonstrating the decrease of the viable cell counts. 4. Intracellular nucleotide release from the P. endodontalis, was not increased in the presence of poly-P and was not reversed by the addition of divalent cations like $Ca^{2+}$ and $Mg^{2-}$. 5. Under the TEM, it was observed that fine electro-dense materials were prominent in the poly-P grown P. endodontalis, appearing locally in the cell, and the materials were more abundant and more dispersed in the cell as the incubation time with poly-P increased. In addition, highly electron dense granules accumulated in many poly-P grown cells, most of which were atypical in their shape. 6. Binding of 32P-labeled poly-P to P. endodontalis appeared to be 32.8 and 45.5 and 53.4% at 30 minutes, 1 hours and 2 hours, respectively. 7. In the presence of poly-P. the synthesis of proteins with apparent molecular masses of 25, 27, 35, 45 was lost or drastically decreased whereas expression of a protein with an apparent molecular mass of 75 was elevated. 8. Proteolytic activity of P. endodontalis was decreased by poly-P. The overall results suggest that use of poly-P may affect the growth of P. endodontalis, and the anti-bacterial activity of poly-P seems largely bactericidal. Changes in shape, protein expression, and proteolytic activity of P. endodontalis by poly-P may be directly and indirectly attributed to the antibacterial effect of poly-P. Further studies will be needed to confirm the effect of poly-P.

• 자원환경지질
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• 제51권4호
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• pp.323-343
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• 2018

본 연구에서는 석개재 지역 하부 막골층 탄산염암을 대상으로 광물조성, 미세구조 및 지화학적 특성을 분석하고 퇴적 환경에 영향을 준 유체의 특성에 대해 고찰해보았다. X-선 회절을 이용한 광물 정량 분석, SEM-BSE를 이용한 미세구조 분석에 근거하여 막골층 최하부와 하부의 탄산염암 미세구조를 4가지 Type으로 분류하고, EPMA 및 LA-ICP-MS를 이용해 각 Type 내 탄산염광물을 대상으로 주원소 및 미량원소를 분석하여 비교하였다. 다양한 크기의 반자형에서 타형의 돌로마이트 결정이 치밀하게 맞물린 구조를 갖는 Type 1과 다양한 크기의 자형에서 반자형의 돌로마이트 결정이 치밀하게 맞물린 구조를 갖는 Type 2의 돌로마이트는 상대적으로 높은 Mg/Ca ratio, 평평한 기울기의 REE 패턴, 낮은 또는 중간 이하의 Fe 함량, 낮은 Mn 함량 특성을 가진다. 돌로마이트가 광범위하고 치밀하게 맞물린 구조로 나타나는 것은 고염수로부터 지속적인 Mg 유입의 가능성을 지시한다. 반면, 세립질의 자형에서 타형의 돌로마이트 결정이 산재된 특성을 보이는 Type 3와 다양한 크기의 자형에서 반자형의 돌로마이트 결정을 갖는 Type 4는 Type 1, 2에 비해 돌로마이트 결정의 미세구조가 덜 치밀하게 맞물린 형태를 가진다. 또한 상대적으로 낮은 Mg/Ca ratio, MREE가 부화된 패턴, 중간 이상의 또는 높은 Fe 및 Mn 함량 특성을 가진다. 부분적인 돌로마이트화와 덜 치밀하게 맞물린 구조가 관찰되는 것은 해수와 염수의 혼합수 환경에서 Mg의 제한적인 유입을 지시한다. 또한 Type 4에서 나타나는 철함유 광물과 돌로마이트 결정에서 관찰되는 재결정화와 상대적으로 높은 Fe, Mn 함량을 갖는 특성은 속성 유체의 영향과 아산화 환경에 노출되면서 돌로마이트가 재결정화 작용을 받았을 가능성을 제시한다. 막골층 최하부와 하부의 주구성광물인 돌로마이트와 방해석의 광물학적, 미세구조적, 지화학적 분석을 종합한 결과, 최하부는 고염분의 대규모 퇴적수 영향을 받았고 하부는 담수와 해수의 혼합수 환경에서 속성 유체 영향을 받았음을 뒷받침한다.

• 치과방사선
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• 제23권2호
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• pp.229-250
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• 1993

This study was performed to investigate the morphological and structural changes of bone tissues and the effects of irradiation on the mandibular bodies of rats which were fed low calcium diets. In order to carry out this experiment, 160 seven-week old Sprague-Dawley strain rats weighing about 150 gm were selected and equally divided into one normal diet group of 80 rats and one low calcium diet group with the remainder. These groups were then subdivided into two groups, 40 were assigned rats for each subdivided group, exposed to radiation. The Group 1 was composed of forty non-irradiated rats with normal diet, Group 2 of forty irradiated rats with normal diet, Group 3 forty non-irradiated rats with low calcium diet, and Group 4 forty irradiated rats with low calcium diet. The two irradiation groups received a single dose of 20 Gy on the jaw area only and irradiated with a cobalt-50 teletherapy unit. The rats with normal and low calcium diet groups were serially terminated by ten on the 3rd, the 7th, the 14th, and the 21st day after irradiation. After termination, both sides of the dead rats mandible were removed and fixed with 10% neutral formalin. The bone density of mandibular body was measured by use of bone mineral densitometer(Model DPX -alpha, Lunar Corp., U.SA). Triga Mark ill nuclear reactor in Korea Atomic Research Institute was used for neutron activation and then calcium contents of mandibular body were measured by using a 4096 multichannel analyzer (EG and G ORTEC 919 MCA, U.SA). Also the mandibular body was radiographed with a soft X-ray apparatus(Hitex Co., Ltd., Japan). Thereafter, the obtained microradiograms were observed by a light microscope and were used for the morphometric analysis using a image analyzer(Leco 2001 System, Leco Co., Canada). The morphometric analysis was performed for parameters such as the total area, the bone area, the inner and outer perimeters of the bone. The obtained results were as follows: 1. In the morphometric analysis, total area and outer perimeter of the mandibular bodies of Group 3 were a little smaller than that of Group 1. The mean bone width and bone area were much smaller than that of Group 1 and the inner perimeter of Group 3 was much longer than that of Group 1. The total area and outer perimeter of Group 2 and Group 4 showed little difference. The mean bone width and bone area of Group 4 were smaller than that of Group 2 and the inner perimeter of Group 4 was longer than that of Group 2. 2. The remarkable decreases of the number and thickness of trabeculae and also the resorption of endosteal surface of cortical bone could be seen in the microradiogram of Group 3, Group 4 since the 3rd day of experiment. On the 21st day of experiment, the above findings could be more clearly seen in Group 4 than in Group 3. 3. The bone mineral density of Group 3 was lesser than that of Group 1 and the bone mineral density of Group 4 was lesser than that of Group 2 on the 7th, 14th, 21st days. The irradiation caused the bone mineral density to be decreased regardless of diet. In the case of Groups with low calcium diet, the bone mineral density was much decreased on the 21st day than on the 3rd day of experiment. 4. The calcium content in mandible of Group 3 was smaller than that of Group 1 throughout the experiment. roup 4 showed the least amount of calcium content. The irradiation caused the calcium content to be decreased regardless of diet. In the case of Groups with low calcium diet, the calcium content was much decreased on the 21st day than on the 3rd day of experiment. In conclusion, the present study demonstrated that morphological changs and decrease of bone mass due to resorption of bone by low calcium diet, and that the resorption of bone could be found in the spongeous bone and endosteal surface of cortical bone. So the problem of resorption of bone must be considered when the old and the postmenopausal women are taken radiotherapy because the irradiation seems to be accelerated the resorption of osteoporotic bone.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2000년도 추계학술발표회 초록집
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• pp.3-4
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• 2000

Many researchers are interested in the synthesis and characterization of carbon nitride and diamond-like carbon (DLq because they show excellent mechanical properties such as low friction and high wear resistance and excellent electrical properties such as controllable electical resistivity and good field electron emission. We have deposited amorphous carbon nitride (a-C:N) thin films and DLC thin films by shielded arc ion plating (SAIP) and evaluated the structural and tribological properties. The application of appropriate negative bias on substrates is effective to increase the film hardness and wear resistance. This paper reports on the deposition and tribological OLC films in relation to the substrate bias voltage (Vs). films are compared with those of the OLC films. A high purity sintered graphite target was mounted on a cathode as a carbon source. Nitrogen or argon was introduced into a deposition chamber through each mass flow controller. After the initiation of an arc plasma at 60 A and 1 Pa, the target surface was heated and evaporated by the plasma. Carbon atoms and clusters evaporated from the target were ionized partially and reacted with activated nitrogen species, and a carbon nitride film was deposited onto a Si (100) substrate when we used nitrogen as a reactant gas. The surface of the growing film also reacted with activated nitrogen species. Carbon macropartic1es (0.1 -100 maicro-m) evaporated from the target at the same time were not ionized and did not react fully with nitrogen species. These macroparticles interfered with the formation of the carbon nitride film. Therefore we set a shielding plate made of stainless steel between the target and the substrate to trap the macropartic1es. This shielding method is very effective to prepare smooth a-CN films. We, therefore, call this method "shielded arc ion plating (SAIP)". For the deposition of DLC films we used argon instead of nitrogen. Films of about 150 nm in thickness were deposited onto Si substrates. Their structures, chemical compositions and chemical bonding states were analyzed by using X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy and infrared spectroscopy. Hardness of the films was measured with a nanointender interfaced with an atomic force microscope (AFM). A Berkovich-type diamond tip whose radius was less than 100 nm was used for the measurement. A force-displacement curve of each film was measured at a peak load force of 250 maicro-N. Load, hold and unload times for each indentation were 2.5, 0 and 2.5 s, respectively. Hardness of each film was determined from five force-displacement curves. Wear resistance of the films was analyzed as follows. First, each film surface was scanned with the diamond tip at a constant load force of 20 maicro-N. The tip scanning was repeated 30 times in a 1 urn-square region with 512 lines at a scanning rate of 2 um/ s. After this tip-scanning, the film surface was observed in the AFM mode at a constant force of 5 maicro-N with the same Berkovich-type tip. The hardness of a-CN films was less dependent on Vs. The hardness of the film deposited at Vs=O V in a nitrogen plasma was about 10 GPa and almost similar to that of Si. It slightly increased to 12 - 15 GPa when a bias voltage of -100 - -500 V was applied to the substrate with showing its maximum at Vs=-300 V. The film deposited at Vs=O V was least wear resistant which was consistent with its lowest hardness. The biased films became more wear resistant. Particularly the film deposited at Vs=-300 V showed remarkable wear resistance. Its wear depth was too shallow to be measured with AFM. On the other hand, the DLC film, deposited at Vs=-l00 V in an argon plasma, whose hardness was 35 GPa was obviously worn under the same wear test conditions. The a-C:N films show higher wear resistance than DLC films and are useful for wear resistant coatings on various mechanical and electronic parts.nic parts.

• 생명과학회지
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• 제17권12호
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• pp.1766-1770
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• 2007

본 증례는 개의 유선에서 발생한 골형성성의 악성 혼합 유선 종양으로 샘포의 암종성 변화를 동반하고 있다. 종양은 12년령 암캐의 좌측 5번째 유선에서 절제되었으며 직경 $2{\sim}2.5cm$의 단단한 mass로 절단 시 경도가 높은 골성의 구조를 가지고 있었다. 현미경학적 관찰 시, 골유사 물질이 미네랄 침착되고 있었으며 다수의 골형성 세포와 일부 파골세포가 골생성 종양 기질 전반에 걸쳐서 관찰되었다. 이러한 골유사 병변은 높은 밀집도를 보이는 근상피 세포와 연접하고 있었으며 이러한 세포들은 수 개의 유사분열상을 나타내고 있었다. 이와 더불어, 유선세관과 샘포의 암종성 변화를 보이는 세포들이 인접 기질로 침습하고 있는 모습이 관찰되었고 이것 역시 증가된 근상피 세포들로 둘러싸여 있었다. 본 증례에서 볼 수 있는 이러한 세포들의 출현은 동시 발생된 악성 종양의 형태를 제시할 수 있으며 종양의 기원은 상피 유래의 암종성 조직과 중간엽 유래의 육종성 연골 및 골 조직으로 구별할 수 있겠다.

• 전기화학회지
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• 제24권4호
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• pp.120-132
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• 2021

기존 LiCoO₂의 고전압 사용의 제약에 따른 용량적 한계와 코발트 원료의 높은 가격을 해결하기 위하여 high-Nickel에 대한 개발이 활발히 진행되고 있지만 Ni 함량의 증가에 따른 구조적 안정성의 저하에 의한 전지 특성의 저하는 상용화를 지연시키는 중요한 원인이 되고 있다. 이에 Ni-rich 삼성분계 양극소재 LiNi_0.6Co_0.2Mn_0.2O₂의 고안정성을 높이고자 전구체에 균일한 이종원소 Ti를 치환을 위해서 나노크기의 TiO₂ 서스펜젼 형태 소스를 사용하여 전구체 Ni_0.6Co_0.2Mn_0.2-x(OH)₂/xTiO₂를 제조하였다. Li₂CO₃와 혼합하고, 열처리 후 양극활물질 LiNi_0.6Co_0.2Mn_0.2-xTi_xO₂ 합성하여 Ti 함량에 따른 물리적 특성을 비교하였다. Field Emission Scanning electron Microscope(FE-SEM) 및 Energy Dispersive Spectroscopy (EDS) mapping 분석을 통해 Ti 치환된 구형의 전구체와 입자 크기 측정을 통해 균일한 입자크기를 가지는 양극 활물질 제조를 확인하였고, 내부치밀도와 강도가 증가함을 확인 하고, X-ray Diffractometry (XRD) 구조 분석과 Inductively Coupled Plasma Mass Spectrometry (ICP-MS) 정량분석을 통해 Ti 치환된 양극활물질 제조 및 고온, 고전압에서 충·방전을 지속하더라도 효과적으로 용량이 유지됨을 확인하였다.

• 대한화장품학회지
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• 제47권4호
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• pp.361-368
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• 2021

본 연구는 인체 친화적인 소재로 균을 제거하는 기술을 만들기 위해서 진행하였다. 균총 상호 균형에 중요한 역할을 하는 황색포도상구균이 바이오필름을 생성시킬 때 다양한 농도의 인산염 투입시 나타나는 물성변화를 조사하였다. 원자현미경을 이용해서 인산염 5 mM 처리시 황색포도상구균 바이오필름의 크기와 경도가 통계적으로 유의차가 있게 최소값을 가짐을 관찰하였다. 염료 태깅법으로 흡광도를 관찰한 결과 인산염과 함께 성장한 전체 바이오필름의 농도도 감소한 것을 발견하였다. 이것이 카운터 이온으로서 작용하는 염에 의한 영향인지 확인하기 위하여 소금을 같은 조건에서 처리해보았는데 이때는 바이오필름의 농도 감소가 관찰되지 않았고 이를 통해 인산염이 특별한 생리적인 작용에 관여함을 알 수 있었다. 비행시간형 이차이온 질량분석기를 통해서 이온 검출량을 평가하여 바이오필름 구성성분을 분석한 결과 인산염을 투입하기 전과 후의 모든 바이오필름 외곽에서 세균막만 감지되었는데 특별히 인산염 5 mM에서 이 세균막의 농도가 가장 낮음을 확인하였다. 바이오필름 내부에 어떤 물성 변화가 일어났는지 관찰하기 위해서 시어 응력을 조절하는 유변기기로 바이오필름의 점탄성 특징을 측정을 하니 인산염 5 mM에서 바이오필름의 점도는 변화하지 않았으나 탄성률 감소가 일어난 것을 관찰하였다. 이것을 통해 인산염이 5 mM인 환경에서 균은 내부 탄성률 감소를 통해서 세균막을 탈피시키는 것을 알 수 있었다. 인산염 농도 5 mM에서 관찰되는 세균막 농도 감소는 균이 더 많은 성장을 하기 위해 다른 곳으로 이동하기 쉽게 하기 위해서 스스로 표면에서 탈착하는 것과 연관이 있음을 제시하였다. 마침내 인산염을 투입하면 균의 세균막 제거가 유도되어 결론적으로 황색포도상구균이 쉽게 제거될 수 있음을 밝혀내었다.

• 헤리티지:역사와 과학
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• 제57권1호
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• pp.146-159
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• 2024

본 연구에서는 강진 고성사 청동보살좌상을 대상으로 과학적 분석을 통해 불상의 제작기술 및 납 원료산지에 대한 연구를 실시하였다. 불상에서 수습한 극미량의 시료를 대상으로 미세조직 관찰결과 주조 공정을 통해 제작되었음을 알 수 있었다. 이어 SEM-EDS를 통한 합금조성비 분석결과 구리(Cu) 81.26wt% 주석(Sn) 16.42wt%, 납(Pb) 1.72wt%의 삼원계 합금으로 확인되었다. 열이온화질량분석기(TIMS)를 이용한 납동위원소비 분석결과를 한반도 납동위원소비 분포도에 대입한 결과 전라도와 충청도 지역, 경상남·북도 지역에 도시되었다. 불상이 봉안된 강진 고성사는 해당영역의 사이에 위치하고 있다. 이러한 과학적 분석결과를 종합해 볼 때 강진 고성사 청동보살좌상은 구리, 주석, 납을 합금하여 주조하였으며, 불상제작 시 사용된 납 원료는 고성사 인근 지역에서 수급하여 사용한 것으로 판단된다. 이때 주목할 점은 해당 불상이 높이 51cm의 중·대형 불상임에도 불구하고 합금조성비 분석결과 기존 선행연구에서 제시한 소형 청동 및 금동제 불상의 납 함량비와 유사한 경향성을 보이고 있다는 것이다. 이에 불상의 크기와 납 함량비 간의 연관성을 고찰하고자 고성사 청동보살좌상과 조성연대가 유사한 청동 및 금동제 불상의 형태학적 특징 및 합금조성비 등 전반적인 제작기술을 비교분석 하였다. 비교결과 청동 및 금동제 불상의 합금조성비를 결정하는 요인에는 불상의 크기 뿐만 아니라 양식적인 특징, 조성연대 등 다양한 요인이 존재할 수 있으며, 이에 따라 불상을 조성할 당시 합금조성비 또는 주조기술을 적절히 조절하였을 가능성을 확인하였다. 즉, 불상의 제작기술 연구를 위해서는 방사선 투과촬영조사 등을 활용한 내부구조 관찰, 미세조직관찰 및 합금조성비 분석 등의 과학적 분석결과 뿐만 아니라 양식적 특징 및 조성연대에 관한 고고·미술사학적 연구를 함께 진행함으로서 보다 종합적인 불상 제작기술체계에 대한 규명이 이루어져야 할 것으로 판단된다.