• 대한치과보철학회지
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• 제31권3호
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• pp.423-446
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• 1993

Titanium and its alloys are finding increasing use in medical devices and dental implants. The strong selling point of titanium is its resistance to the highly corrosive body fluids in which an implant must survive. This corrosion resistance is due to a tenacious passive oxide or film which exists on the metal's surface and renders it passive. Potentiodynamic polarization measurement is one of the most commonly used electro-chemical methods that have been applied to measure corrosion rates. And the potentiodynamic polarization test supplies detailed information such as open circuit, rupture, and passivation potential. Furthermore, it indicates the passive range and sensitivity to pitting corrosion. This study was designed to compare the corrosion resistance of the commonly used dental implant materials such as CP Ti, Ti-6A1-4V, Co-Cr-Mo alloy, and 316L stainless steel. And the effects of galvanic couples between titanium and the dental alloys were assessed for their useful-ness-as. materials for superstructure. The working electrode is the specimen , the reference electrode is a saturated calomel electrode (SCE), and the counter electrode is made of carbon. In $N_2-saturated$ 0.9% NaCl solutions, the potential scanning was performed starting from -800mV (SCE) and the scan rate was 1 mV/sec. At least three different polarization measurements were carried out for each material on separate specimen. The galvanic corrosion measurements were conducted in the zero-shunt ammeter with an implant supraconstruction surface ratio of 1:1. The contact current density was recorded over a 24-hour period. The results were as follows : 1. In potential-time curve, all specimens became increasingly more noble after immersion in the test solution and reached between -70mV and 50mV (SCE) respectively after 12 hours. 2. The Ti and Ti alloy in the saline solution were most resistant to corrosion. They showed the typical passive behavior which was exhibited over the entire experimental range. Therefore no breakdown potentials were observed. 3. Comparing the rupture potentials, Ti and Ti alloy had the high(:st value (because their break-down potentials were not observed in this study potential range ) followed by Co-Cr-Mo alloy and stainless steel (316L). So , the corrosion resistance of titanium was cecellent, Co-Cr-Mo alloy slightly inferior and stainless steel (316L) much less. 4. The contact current density sinks faster than any other galvanic couple in the case of Ti/gold alloy. 5. Ag-Pd alloy coupled with Ti yielded high current density in the early stage. Furthermore, Ti became anodic. 6. Ti/Ni-Cr alloy showed a relatively high galvanic current and a tendency to increase.

• Journal of Pharmaceutical Investigation
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• 제23권1호
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• pp.41-49
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• 1993

The bioequivalence of two omeprazole enteric-coated products was evaluated in 16 normal male volunteers (age 26-32 yr, body weight 57-75 kg) following single oral administration. Test product was enteric-coated KD-182 tablet (Chong Kun Dang Corp., Korea) and reference product was $Rosec^{\circledR}$ capsule containing enteric-coated pellets of omeprazole (Yuhan Corp., Korea). Both products contain 20 mg of omeprazole. One tablet or capsule of the test or the reference product was administered to the volunteers, respectively, by randomized two period cross-over study ($2\;{\times}\;2$ Latin square method). Average drug concetrations at each sampling time and pharmacokinetic parameters calculated were not significantly different between two products(p>0.05); the area under the concentrationtime curve to last sampling time (8 hr) $(AUC_{0-8hr})$ $(1946.5{\pm}675.3\;vs\;2018.3{\pm}761.6\;ng{\cdot}hr/ml)$, AUC from time zero to infinite $(AUC_{o-\infty})$ $(2288.6{\pm}1212.8\;vs\;2264.9{\pm}1001.3\;ng{\cdot}hr/ml)$, maximum plasma concentration $(C_{max})$ $(772.5{\pm}283.3\;vs\;925.8{\pm}187.7\;ng/ml)$, time to maximum plasma concentration $(T_{max})$ $(2.38{\pm}1.06\;vs\;2.34{\pm}1.09\;hr)$, apparent elimination rate constant $(k_{\ell})$ $(0.5339{\pm}0.2687\;vs\;0.5769 {\pm}0.2184\;hr^{-I})$, apparent absorption rate constant $(k_a)$ $(1.1536{\pm}0.5278\;vs\;0.9739{\pm}0.9507 hr^{-1})$ and mean residence time (MRT) $(3.13{\pm}0.73\;vs \;3.41{\pm}1.04\;hr)$. The differences of mean $(AUC_{0-8hr})$, $C_{max}$, $T_{max}$ and MRT between the two products (3.69, 19.83, 1.32 and 8.99%, respectively) were less than 20%. The power $(1-{\beta})$ and treatment difference $(\triangle)$ for $AUC_{o-8hr}$ $C_{max}$ and MRT were more than 0.8 and less than 0.2, respectively. Although the power for $T_{max}$ was under 0.8, $T_{max}$ of the two products was not significantly different each other(p>0.05). These results suggest that the bioavailability of KD-182 tablet is not significantly different from that of $Rosec^{\circledR}$ capsule. Therefore, two products are bioequivalent based on the current results.

• Journal of Pharmaceutical Investigation
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• 제34권4호
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• pp.319-325
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• 2004

A bioequivalence of $Etodol^{TM}$ tablets (Yuhan corporation) and $Kuhnillodine^{TM}$ tablets (Kuhnil Pharm. Co., Ltd.) was evaluated according to the guideline of Korea Food and Drug Administration (KFDA). Single 200 mg dose of etodolac of each medicine was administered orally to 24 healthy male volunteers. This study was performed in a $2{\times}2$ crossover design. Concentrations of etodolac in human plasma were monitored by a high-performance liquid chromatography. $AUC_t$ (the area under the plasma concentration-time curve from time zero to 24 hr) was calculated by the linear trapezoidal rule method. $C_{max}$ (maximum plasma drug concentration) and $T_{max}$ (time to reach $C_{max}$) were compiled from the plasma concentration-time data. Analysis of variance was performed using logarithmically transformed $AUC_t$ and $C_{max}$. No significant sequence effect was found for all of the bioavailability parameters. The 90% confidence intervals of the $AUC_t$ ratio and the $C_{max}$ ratio for $Etodol^{TM}/Kuhnillodine^{TM}$ were 1.01-1.10 and 0.87-1.06, respectively. This study demonstrated a bioequivalence of $Etodol^{TM}$ and $Kuhnillodine^{TM}$ with respect to the rate and extent of absorption.

• Journal of Pharmaceutical Investigation
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• 제34권6호
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• pp.505-511
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• 2004

A bioequivalence study of $Bestidine^{TM}$ tablets (Choong Wae Pharma. Corp., Korea) to Dong-A $Gaster^{TM}$ (Dong-A Pharmaceutical Co., Ltd., Korea) tablets was conducted according to the guidelines of Korea Food and Drug Administration (KFDA). Twenty four healthy male Korean volunteers received each medicine at the famotidine dose of 40 mg in a $2{\times}2$ crossover study. There was a one-week wash out period between the doses. Plasma concentrations of famotidine were monitored by a high-performance liquid chromatography for over a period of 12 hours after the administration. $AUC_t$ (the area under the plasma concentration-time curve from time zero to 12 hr) was calculated by the linear trapezoidal rule method. $C_{max}$ (maximum plasma drug concentration) and $T_{max}$ (time to reach $C_{max}$) were compiled from the plasma concentration-time data. Analysis of variance was carried out using logarithmically transformed $AUC_t$ and $C_{max}$. No significant sequence effect was found for all of the bioavailability parameters indicating that the crossover design was properly performed. The 90% confidence intervals of the $AUC_t$ ratio and the Cmax ratio for $Bestidine^{TM}/Gaster^{TM}$ were log 0.90-log 1.06 and log 0.98-log 1.20, respectively. These values were within the acceptable bioequivalence intervals of 0.80-1.25. Thus, our study demonstrated the bioequivalence of $Bestidine^{TM}$ and $Gaster^{TM}$ with respect to the rate and extent of absorption.

• Journal of Pharmaceutical Investigation
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• 제38권2호
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• pp.135-142
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• 2008

The present study describes the evaluation of the bioequivalence of two atorvastatin tablets, Lipitor $Tablet^{(R)}$ (Pfizer, reference drug) and Atorva $Tablet^{(R)}$ (Yuhan, test drug), according to the guidelines of Korea Food and Drug Administration (KFDA). Forty-nine healthy male Korean volunteers received each medicine at the atorvastatin dose of 40 mg in a $2{\times}2$ crossover study with a two weeks washout interval. After drug administration, serial blood samples were collected at a specific time interval from 0-48 hours. The plasma atorvastatin concentrations were monitored by an high performance liquid chromatography -tandem mass spectrometer (LC-MS/MS) employing electrospray ionization technique and operating in multiple reaction monitoring (MRM) and positive ion mode. The total chromatographic run time was 4.5 min and calibration curves were linear over the concentration range of 0.1-100 ng/mL for atorvastatin. The method was validated for selectivity, sensitivity, linearity, accuracy and precision. $AUC_t$ (the area under the plasma concentration-time curve from time zero to 48hr) was calculated by the linear log trapezoidal rule method. $C_{max}$ (maximum plasma drug concentration) and $T_{max}$ (time to reach $C_{max}$) were complied trom the plasma concentration-time data. Analysis of variance was carried out using logarithmically transformed $AUC_t$ and $C_{max}$. No significant sequence effect was found for all of the bioavailability parameters indicating that the crossover design was properly performed. The 90% confidence intervals of the $AUC_t$ ratio and the $C_{max}$ ratio for Atorva $Tablet^{(R)}$ / Lipitor $Tablet^{(R)}$ were ${\log}\;0.9413{\sim}{\log}\;1.0179$ and ${\log}\;0.831{\sim}{\log}\;1.0569$, respectively. These values were within the acceptable bioequivalence intervals of ${\log}\;0.8{\sim}{\log}\;1.25$. Based on these statistical considerations, it was concluded that the test drug, Atorva $Tablet^{(R)}$ was bioequivalent to the reference drug, Lipitor $Tablet^{(R)}$.

• Biomolecules & Therapeutics
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• 제6권2호
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• pp.219-224
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• 1998

The bioequivalence of two clarithromvcin products was evaluated with 16 normal male volunteers (age 23-28 yr, body weight 57.5-75.517g) following single oral dose. Test product was ReYon Clarithromycin tablets (ReYon Pharm. Corp., Korea) and reference product was Klarici $d_{R}$ tablets (Abbott Korea). Both products contain 250 mg of clarithromucin. One tablet of the test or the reference product was administered to the volunteers, respectively, by randomized two period cross-over study (2$\times$2 Latin square method). The determination of clarithromycin was accomplished using a modified agar well diffusion bioassay. As a result of the assay validation, the quantification of clarithromycin in human serum by this technique was possible down to 0.03$\mu$g/ml using 100$\mu$l of serum. The coefficient of variation (C.V.) was less than 10%. Average drug concentrations at each sampling time and pharmacokinetic parameters calculated were not significantly different between two products P>0.05); the area under the curve to last sampling time (24 hr) (AU $Co_{24hr}$ (8.10$\pm$ 1.26 vs 8.22$\pm$ 1.627g . hr/ml), AUC from time zero to infinite (AU $Co_{\infty}$) (8.61 $\pm$ 1.28 vs 8.84$\pm$ 1.71 $\mu$g . hr/ml), maximum plasma concentration ( $C_{msx}$) (0.87$\pm$0.22 vs 0.88$\pm$0.19 $\mu$g/ml) and time to maximum plasma concentration ( $T_{max}$) (2.69 $\pm$0.48 vs 2.56$\pm$ 0.51 hr). The differences of mean AU $Co_{24h}$, $C_{msx}$ and $T_{msx}$ between the two products (1.44, 1.39, and 4.65%, respectively) were less than 20%. The power (1-$\beta$) and treatment difference ($\Delta$) for AU $Co_{24hr}$, and $C_{max}$ were more than 0.8 and less than 0.2, respectivly. Although the power for $T_{max}$ was under 0.8, $T_{max}$. of the two products was not significantly different each other (p>0.05). These results suggest that the bioavailability of ReYon Clarithromycin tablets is not significantly different from that of Klarici $d_{R}$ tablets. Therefore, two products are bioequivalent based on the current results. results.sults.sults.s.s.s.s.s.s.s.

• Journal of Ginseng Research
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• 제43권3호
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• pp.460-474
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• 2019

Background: Ginsenoside compound K (CK) is a promising drug candidate for rheumatoid arthritis. This study examined the impact of polymorphisms in NR1I2, adenosine triphosphate-binding cassette (ABC) transporter genes on the pharmacokinetics of CK in healthy Chinese individuals. Methods: Forty-two targeted variants in seven genes were genotyped in 54 participants using Sequenom MassARRAY system to investigate their association with major pharmacokinetic parameters of CK and its metabolite 20(S)-protopanaxadiol (PPD). Subsequently, molecular docking was simulated using the AutoDock Vina program. Results: ABCC4 rs1751034 TT and rs1189437 TT were associated with increased exposure of CK and decreased exposure of 20(S)-PPD, whereas CFTR rs4148688 heterozygous carriers had the lowest maximum concentration ($C_{max}$) of CK. The area under the curve from zero to the time of the last quantifiable concentration ($AUC_{last}$) of CK was decreased in NR1I2 rs1464602 and rs2472682 homozygous carriers, while $C_{max}$ was significantly reduced only in rs2472682. ABCC4 rs1151471 and CFTR rs2283054 influenced the pharmacokinetics of 20(S)-PPD. In addition, several variations in ABCC2, ABCC4, CFTR, and NR1I2 had minor effects on the pharmacokinetics of CK. Quality of the best homology model of multidrug resistance protein 4 (MRP4) was assessed, and the ligand interaction plot showed the mode of interaction of CK with different MRP4 residues. Conlusion: ABCC4 rs1751034 and rs1189437 affected the pharmacokinetics of both CK and 20(S)-PPD. NR1I2 rs1464602 and rs2472682 were only associated with the pharmacokinetics of CK. Thus, these hereditary variances could partly explain the interindividual differences in the pharmacokinetics of CK.

• Korean Journal of Radiology
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• 제23권11호
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• pp.1078-1088
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• 2022

Objective: To develop and validate a model using radiomics features from apparent diffusion coefficient (ADC) map to diagnose local tumor recurrence in head and neck squamous cell carcinoma (HNSCC). Materials and Methods: This retrospective study included 285 patients (mean age ± standard deviation, 62 ± 12 years; 220 male, 77.2%), including 215 for training (n = 161) and internal validation (n = 54) and 70 others for external validation, with newly developed contrast-enhancing lesions at the primary cancer site on the surveillance MRI following definitive treatment of HNSCC between January 2014 and October 2019. Of the 215 and 70 patients, 127 and 34, respectively, had local tumor recurrence. Radiomics models using radiomics scores were created separately for T2-weighted imaging (T2WI), contrast-enhanced T1-weighted imaging (CE-T1WI), and ADC maps using non-zero coefficients from the least absolute shrinkage and selection operator in the training set. Receiver operating characteristic (ROC) analysis was used to evaluate the diagnostic performance of each radiomics score and known clinical parameter (age, sex, and clinical stage) in the internal and external validation sets. Results: Five radiomics features from T2WI, six from CE-T1WI, and nine from ADC maps were selected and used to develop the respective radiomics models. The area under ROC curve (AUROC) of ADC radiomics score was 0.76 (95% confidence interval [CI], 0.62-0.89) and 0.77 (95% CI, 0.65-0.88) in the internal and external validation sets, respectively. These were significantly higher than the AUROC values of T2WI (0.53 [95% CI, 0.40-0.67], p = 0.006), CE-T1WI (0.53 [95% CI, 0.40-0.67], p = 0.012), and clinical parameters (0.53 [95% CI, 0.39-0.67], p = 0.021) in the external validation set. Conclusion: The radiomics model using ADC maps exhibited higher diagnostic performance than those of the radiomics models using T2WI or CE-T1WI and clinical parameters in the diagnosis of local tumor recurrence in HNSCC following definitive treatment.

• Radiation Oncology Journal
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• 제6권1호
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• pp.1-11
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• 1988

방사선 조사 후 발생한 잠재치사손상의 회복(PLDR)에 있어 조사선량 및 시간에 따른 환경변화가 회복의 동적양상에 미치는 영향을 Vero 세포계를 이용하여 실험하였다. 배양액을 교환시키지 않고 배양하여 평형기에 도달한 세포에 동물실험용 세시움 조사기로 $1Gy\~9Gy$의 감마선을 조사하고 각 조사조건에서 $O\~6$ 및 24시간동안 정치시킨 후 Agarose가 포함된 새로운 배양액에서 배양하였다. 16Gy를 조사한 동종의 세포를 feeder세포로 첨가하여 배양액내의 전 체세포수를 일정하게 한 조건에서 형성된 세포집락수에 따라 세포의 생존을 정하였다. 잠재치사손상의 회복은 $2\~4$시간 정치후에 포화수준에 도달한 빠른 회복이었다. 방사선량이 증가함에 따라 회복속도는 증가하였고, 포화수준의 회복량도 증가하였다. Linear-quadratic mode에 의한 "방사선량-생존분획" 분석 결과 잠채치사손상이 회복됨에 따라 일차 비활성계수 $\alpha$는 급속히 감소하여 $\beta$에 접근하였고 이차 비활성계수 $\beta$는 미미하게 증가하여 PLDR은 $\alpha$로 표시되는 손상에 주로 영향을 주었다. Multitarget model에 따라 분석한 결과 Do는 변화가 없고 Dq가 증가하였다. 세포 생존분획 이 높은 3Gy 이하의 저선량 영역에서 dose modifying factor가 높아 잠재 치사손상의 회복에 의한 영향이 저선량 영역에서 상대적으로 크게 나타났다.

• Applied Biological Chemistry
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• 제16권2호
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• pp.99-111
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• 1973

전국적(全國的)으로 실시한 삼요소(三要素) 시험중(試驗中) 1967년(年) 51개소(個所) 68년(年)에 32개소(個所)에서 N 8, 10, 12, 14kg/10a 수준(水準)과 $P_2O_5$ 및 $K_2O$ 각(各) 6과 8kg 시비수준(施肥水準)에 대(對)한 삼요소(三要素) 이용율(利用率)을 조사(調査)하였다. 삼요소(三要素) 이용율(利用率)과 수량(收量) 및 건물생산량(乾物生産量), 삼요소(三要素) 및 규산흡수량(珪酸吸收量)과의 아래와 같은 관계에서 무기양분(無機養分)의 생산(生産)에 기여하는 양상(樣相)이 시용(施用)한 P가 1차적(次的)으로 Si흡수(吸收)를 이차적(二次的)으로 Si가 N흡수(吸收)를 조장(助長)하여 기여하는 P형(型)과 시용(施用)한 K가 P흡수(吸收)를, 이차적(二次的)으로 P가 N흡수(吸收)를 조장(助長)하여 기여하는 K형(型)으로 연도별(年度別) 주도형(主導型)을 구분(區分)할 수 있었다. 1. 질소(窒素)는 전포장수(全圃場數)의 4%, 인산(燐酸)은 48%, 가리(加里)는 38%가 0 또는 부(負)의 이용율(利用率)을 보였으며 이용율(利用率)의 발현빈도(發現頻度) 백분분포(百分分布)가 N는 30 내지 40에서 최고빈도(最高頻度)를 보이는 정규분포(正規分布)에 가깝게, P와 K는 0 이하(以下)에서 최고빈도(最高頻度)를 갖고 점차 감소하는 편의 분포(分布)를 갖는다. 2. 삼요소(三要素) 이용율(利用率) (0 이상(以上)만)은 67년(年)에 N는 33(10kg 시비(施肥) 수준이상(水準以上)) P는 27, K는 40이고 68년(年)엔 40, 20, 46%이고 부(負)의 이용율(利用率)을 0으로한 2개년(個年) 평균(平均)은33(8kg 이상(以上)) 13, 27이었다. 3. 이용율(利用率)의 표준편차(漂準偏差)는 P와 K에서 이용율(利用率)보다 크고 P이용율(利用率)의 변이(變異)가 가장 크다. 4. 이용율(利用率)과 수량(收量) 또는 건물생산량(乾物生産量)과의 유의상관(有意相關) 출현빈도(出現頻度)는 N>K>P의 순(順)이며 10kg 수준의 N이용율(利用率)은 67년(年)엔 P이용율(利用率)과만 63년(年)엔 K이용율(利用率)과만 유의상관(有意相關)을 갖는다. 5. P이용율(利用率)은 그것이 높고 K이용율(利用率)이 낮았던 67년(年)에만, 그리고 K이용율(利用率)은 그와 반대였던 68년(年)에만 모든 처리구의 건물생산량(乾物生産量)과 유의상관(有意相關)을 보이고, 유의상관(有意相關)이 없는 해에는 무비구(無肥區) 및 결비구(缺肥區)區에서 부상관계수(負相顯係數)를 보이고 있다. 6. 이용율(利用率)과 수량(收量)과의 상관(相關)은 이용율(利用率)과 건물생산량(乾物生産量)과의 상관(相關)과 경향은 유사하나 유의성이 적어삼요소(三要素) 영양(營養)은 건물생산(乾物生産)에서 잘 표현된다. 7. N이용율(利用率)은 N시비구(施肥區)의 N흡수량(吸收量)과 많은 경우 유의상관(有意相關)을, 무(無)N구(區)의 흡수량(吸收量)과는 유의부상관(有意負相關)을 보이며, N시비구(施肥區)의 P, K또는 Si흡수량(吸收量)과도 여러 경우 유의상관(有意相關)을 보였다. 8. P이용율(利用率)은 그것이 높았던 67년(年)만 모든 처리구에서 Si흡수량(吸收量)과, 그리고 무(無)P구(區)를 제(除)한 모든 처리구의 N 흡수량(吸收量)과 유의상관(有意相關)을 보여 P는 일차적(一次的)으로 Si흡수(吸收)를 돕고 이차적(二次的)으로 Si흡수(吸收)가 N흡수(吸收)를 조장(助長)함을 나타낸다. P이용율(利用率)은 N시비구(施肥區)의 P흡수량(吸收量)과 K흡수량(吸收量)과도 많은 경우 유의상관(有意相關)을 보였다. 9. K이용율(利用率)은 그것이 컸던 68년(年)에 모든 처리구의 P흡수량(吸收量)과 무(無)N구(區)을 제(除)한 모든 처리구의 N흡수량(吸收量)과 그리고 무(無)P구(區)를 제(除)한 모든 처리구의 K흡수량(吸收量)과 유의상관(有意相關)을 보이며 무(無)K구(區)의 K흡수량(吸收量)과는 부상관(負相關)이고 K이용율(利用率)이 적었던 67년(年)에는 무비구(無肥區)나 결비구(缺肥區)의 P흡수량(吸收量)과 유의성(有意性)은 없으나 부상관(負相關)이었다. K이용율(利用率)은 N나 P와는 달리 K흡수량(吸收量)과 보다 수량(收量)이나 건물생산량(乾物生産量)과의 상관(相關)이 더 크며 K이용율(利用率)이 컸던 해에만 Si흡수량(吸收量)과 무(無)N구(區)와 최고시비구(最高施肥區)에서 유의상관(有意相關)을 갖고 무(無)K구(區)에서 유의부상관(有意負相關)을 보였다. 이로서 K는 일차적(一次的)으로 P흡수(吸收)를 돕고 이차적(二次的)으로 P가 N흡수(吸收)를 도와서 생산(生産)에 기여하는 것 같다. 10. N이용율(利用率)과 수량(收量)이나 건물생산량(乾物生産量)과의 상관(相關)이 무(無)P구(區)에서 보다 무(無)K구(區)가 높고 무(無)K구(區)보다 시비구(施肥區)에서 높으며 이러한 경향은 N이용율(利用率)과 N흡수량(吸收量)사이에서도 동일(同一)하였다. 이 사실과, K이용율(利用率)과 건물생산량(乾物生産量)과의 관계는 P가 N흡수(吸收)를 돕고 N나 P가 부족(不足)할 때에는 K가 N흡수(吸收)를 경쟁적으로 억제하여 생산(生産)을 저하(低下)시키는 것을 나타낸다. 11. 삼요소(三要素) 이용율(利用率)은 67년(年)에는 무(無)P구(區)의 상대건물생산량(相對乾物生産量)과, 68년(年)에는 무(無)K구(區)의 상대수량(相對收量)과 유의상관(有意相關)을 갖는다. 이는 P가 분얼 즉 영양생장단계에, K가 곡실형성 즉 생식 생장단계에 더 작용(作用)하였음을 나타내고 있다. 12. 삼요소(三要素) 이용율(利用率)과 결비구(缺肥區)의 상대생산량(相對生産量)이나 무비구(無肥區)의 결비구(缺肥區)에 대(對)한 상대생산량(相對生産量)과의 상관(相關)에서 어느 경우에도 N가 수도생산(水稻生産)에 가장 큰 역할(役割)을 하고 있음을 보였다. 13. 이상의 결과에서 40 내지 50%의 포장(圃場)은 P와 K를 시비(施肥)하지 아니해도 되며 시비량(施肥量)도 연도(年度)및 포장에 따라 변이(變異)가 커야 할 것이며 특히 P에서 그러하다.