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Construction of an In-house Database by Modifying Formulary's Data 通过修改Formulary的数据构建内部数据库
Pub Date : 1994-06-20 DOI: 10.5649/JJPHCS1975.20.253
Takako Kaneda, Tougen Masauji, Noriko Satoh, M. Nakata
We have constructed an in-house database by using a method that employs the commercial application software called “The CARD” . This was done after modifying the formulary data using the word processor program “Ichitaro” . The derived database offers selected information which permits the retrieval of such specifics as drug names, dosages, indications, contraindications, adverse reactions, drug interactions, and precautions.
我们利用商业应用软件“the CARD”的方法构建了一个内部数据库。这是在使用文字处理程序“一aro”修改公式数据后完成的。衍生的数据库提供了选定的信息,允许检索诸如药物名称,剂量,适应症,禁忌症,不良反应,药物相互作用和注意事项等细节。
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引用次数: 0
Preparation of Liposomal-encapsulated SOD and Serum Pharmacokinetics after Intravenous Administration 脂质体囊化SOD的制备及静脉给药后血清药代动力学
Pub Date : 1994-02-20 DOI: 10.5649/JJPHCS1975.20.1
I. Hirata, S. Tanaka, M. Ashihara, S. Tsukamoto, N. Sugioka, H. Kishimoto, T. Yoshikawa, T. Tanigawa, Y. Naito, M. Kondo, Kazuto Nosaka
Liposomal-encapsulated superoxide dismutase (L-SOD) was prepared with a view to prolonging the half-life and pharmacodynamic action time. Presome® was adopted as a phospholipid in the preparation of L-SOD.L-SOD was sterilized through polycarbonate membrane filters having pore diameters of 0.2 μm and 0.4μm. The liposomal particle size, as measured by the dynamic light scattering method, was 198±40 nm. Effective SOD encapsulation efficiency was approximately 25.8%.Immediately after the i.v. injection of L-SOD into rats, blood levels of SOD decreased in a bi-exponential manner; the half-lives of the α-and β-phases were 16.6 minutes and 7.8 hours, respectively.AUC and MRT increased as compared with the i. v. injection of r-hSOD (free SOD), The SOD-activity in plasma was on a low level.These results suggested that still more L-SOD was trapped in the reticulo-endothelial system (RES), involving such organs as in the liver and spleen.In an effect to increase the SOD activity in plasma and prolong the circulation time of liposomes in blood, we prepared L-SOD modified with polyethyleneglycol derivatives (L-SOD/PEG. DOPE; L-SOD/PEG·DMG).After the i. v. injection of L-SOD/PEG·DOPE and L-SOD/PEG·DMG into rats, the SOD activity in plasma became higher and also the circulation time of liposomes in blood became longer as compared with the L-SOD i. v. injection.
制备了脂质体包封超氧化物歧化酶(L-SOD),以延长其半衰期和药效作用时间。采用Presome®作为磷脂制备L-SOD。采用孔径分别为0.2 μm和0.4μm的聚碳酸酯膜过滤器对L-SOD进行灭菌。动态光散射法测得的脂质体粒径为198±40 nm。SOD有效包封率约为25.8%。大鼠静脉注射L-SOD后,血液中SOD水平呈双指数下降;α相和β相的半衰期分别为16.6 min和7.8 h。与静脉注射r-hSOD(游离SOD)相比,AUC和MRT升高,血浆SOD活性处于低水平。这些结果表明,更多的L-SOD被困在网状内皮系统(RES)中,累及肝脏和脾脏等器官。为了提高血浆中SOD的活性,延长脂质体在血液中的循环时间,我们制备了聚乙二醇衍生物修饰的L-SOD (L-SOD/PEG)。涂料;L-SOD /挂钩·DMG)。大鼠注射L-SOD/PEG·DOPE和L-SOD/PEG·DMG后,与注射L-SOD相比,血浆SOD活性升高,血脂质体循环时间延长。
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引用次数: 0
Quantitative Determinations of Phenobarbital and Carbamazepine in Serum by Nephelometric Immunoassay 浊度免疫分析法定量测定血清中苯巴比妥和卡马西平
Pub Date : 1993-10-20 DOI: 10.5649/JJPHCS1975.19.464
H. Muro, T. Tatsuhara, K. Otsubo
An automated rate nephelometric assay (Beckman Array 360 System) for phenobarbital (PB) and carbamazepine (CBZ) was evaluated. The assay offers measuring ranges of 5-120μg/ml serum for PB and 2-40μg/ml for CBZ. The coefficients of variation for within-run and between-run precision for both PB and CBZ were< 5.0%. Test results were not significantly affected by bilirubin-unconjugated (up to 19.2 mg/ dl), bilirubin-conjugated (21.3 mg/dl), hemoglobin (540 mg/dl), turbidity (2070 units), or other antiepileptic drugs. The method produced satisfactory results in dilution tests. Quantitative results obtained by the Array 360 assay on serum samples from patients were compared with those obtained by the fluorescence polarization immunoassay (FPIA) and homogeneous enzyme immunoassay (EMIT) methods. The results correlated well with FPIA (r=0.996 and 0.981 for PB and CBZ, respectively) and EMIT (r=0.994 and 0.983). The Array 360 assay was concluded to be an appropriate and quick method for PB and CBZ determination.
采用贝克曼阵列360系统(Beckman Array 360 System)对苯巴比妥(PB)和卡马西平(CBZ)的自动速率比浊法进行了评价。测定范围PB为5 ~ 120μg/ml, CBZ为2 ~ 40μg/ml。PB和CBZ的运行内和运行间精度变异系数均< 5.0%。未结合胆红素(高达19.2 mg/dl)、结合胆红素(21.3 mg/dl)、血红蛋白(540 mg/dl)、浊度(2070单位)或其他抗癫痫药物对试验结果没有显著影响。该方法的稀释试验结果令人满意。将Array 360法与荧光偏振免疫法(FPIA)和均相酶免疫法(EMIT)对患者血清样品的定量结果进行比较。结果与PB和CBZ的FPIA (r分别为0.996和0.981)和EMIT (r分别为0.994和0.983)具有良好的相关性。结果表明,阵列360法是测定铅和CBZ的一种简便易行的方法。
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引用次数: 0
Correlation between Accuracy of Dividing Weight and Physical Properties of the Drugs on Automatic Pre-packing Machine 自动预包装机分装精度与药品物性的关系
Pub Date : 1993-03-20 DOI: 10.5649/JJPHCS1975.19.129
Eriko Matsubara, Yuichiro Kosugi, Kimiko Kano, Yusuke Matsumoto, H. Shimodaira, Y. Uchida, H. Yuasa, Y. Kanaya
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引用次数: 0
Prediction and Evaluation of Penetration of Drugs into Cerebrospinal Fluid in Human 药物对人脑脊液渗透的预测与评价
Pub Date : 1992-08-20 DOI: 10.5649/JJPHCS1975.18.349
J. Hamada, Y. Sawada, Kouichi Nakamura, Yasuhiko Yamada, T. Iga
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引用次数: 1
Sensitivity of Clinical Isolates of Bacterial Strains to Antibiotics and the Amount of Antibiotics Used for Inpatients 临床分离菌株对抗生素的敏感性及住院患者抗生素用量
Pub Date : 1992-03-20 DOI: 10.5649/JJPHCS1975.18.153
H. Hashimoto, Osamu Kitamura, Reiko Muramatsu, Yumi Sano, Y. Akaike, T. Goto
We investigated the sensitivity of clinical isolates of bacterial strains to antibiotics and the amount of antibiotics dispensed for inpatients in each ward of our hospital.In the surgery ward, Bacteroides sp., E.coli, P.aeruginosa and S.aureus were frequently isolated, and cephem antibiotics and piperacillin sodium (PIPC) were mainly used, while many isolates were resistant to PIPC.In the neurosurgery ward, frequent isolates were S.aureus, P.aeruginosa, S.epidermidis. In the internal and cardiovascular medicine ward, P.aeruginosa, S.aureus, K.pneumoniae and S.epidermidis were frequent isolates.In these wards, imipenem/cilastatin sodium (IPM/CS) and cephem antibiotics were mainly used, although most isolates of S.aureus were resistant to these drugs.In the urology ward, Enterococcus sp.and P.aeruginosa were fre quently isolated, whereas cephem antibiotics which were ineffective to these isolates were mainly used.The frequent isolates which were resistant to cephem drugs or IPM/CS probably resulted from the frequent use of these drugs.Considering the present results, choice of antibiotics should be more discussed.
我们调查了我院临床分离菌株对抗生素的敏感性及各病房住院患者抗生素的用量。外科病房常见于拟杆菌、大肠杆菌、铜绿假单胞菌和金黄色葡萄球菌,以头孢类抗生素和哌拉西林钠(PIPC)为主,且多株对PIPC耐药。在神经外科病房,常见的分离株为金黄色葡萄球菌、铜绿假单胞菌、表皮葡萄球菌。在内科和心血管内科病房,常见的是铜绿假单胞菌、金黄色葡萄球菌、肺炎假单胞菌和表皮假单胞菌。这些病房主要使用亚胺培南/西司他汀钠(IPM/CS)和头孢类抗生素,尽管大多数金黄色葡萄球菌分离株对这些药物具有耐药性。泌尿外科病房常见肠球菌和铜绿假单胞菌,主要使用对其无效的头孢类抗生素。频繁出现对头孢类药物或IPM/CS耐药的分离株可能与频繁使用这些药物有关。考虑到目前的结果,抗生素的选择需要更多的讨论。
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引用次数: 1
Diagnosis of Drug Allergy by Lymphocyte Stimulation Test with Ethidium Bromide Fluorescence Assay. 溴化乙锭荧光法淋巴细胞刺激试验诊断药物过敏。
Pub Date : 1991-12-01 DOI: 10.5649/JJPHCS1975.17.399
T. Yoshimura, H. Yamada, M. Hayata, H. Nagai
Lymphocyte stimulation test (LST) is one of the useful laboratory tests for identification of allergy to a specific drug.The present study was conducted to examine utility of LST using ethidium bromide (EB) fluorescence assay as a method for diagnosis of drug allergy.In a preliminary experiment, phytohemagglutinin (PHA) was used instead of suspected drugs.PHA at concentrations between 0.001-1.2% caused an activation of lymphocytes with elevation on stimulation index (SI).Interleukin 2 at concentrations between 1-100 ng/ml enhanced PHA-induced activation of lymphocytes. From these results, LST using EB fluorescence assay would be available for diagnosis of drug allergy.At first we carried out LST on 22 cases of suspicious drug-induced hepatitis.As a result, 9 cases were positive and 13 cases were negative.In order to analyze the relationship between background of the patients and LST, we studied transaminase (GOT and GPT) activities in the sera which were obtained from the patients in different states (remission and acute disease states). As a result, when LST was carried out in remission state, relatively high positive incidence (50%) was obtained.When LST was carried out in acute disease state, positive incidence of LST was low (25%).These results indicate that this method is useful for clinical diagnosis of drug allergy, And in the case of the diagnosis of drug-induced hepatitis, LST would be recommended to be carried out in remission state.
淋巴细胞刺激试验(LST)是鉴定对特定药物过敏的有用实验室试验之一。本研究采用溴化乙啶(EB)荧光法检测LST在药物过敏诊断中的应用。在初步实验中,用植物血凝素(PHA)代替可疑药物。浓度在0.001 ~ 1.2%之间的PHA引起淋巴细胞的活化,刺激指数(SI)升高。白细胞介素2浓度在1-100 ng/ml之间时,可增强pha诱导的淋巴细胞活化。结果表明,利用EB荧光法进行LST检测可用于药物过敏的诊断。我们首先对22例可疑药物性肝炎进行LST。结果:阳性9例,阴性13例。为了分析患者背景与LST的关系,我们研究了不同病情(缓解期和急性期)患者血清中转氨酶(GOT和GPT)的活性。因此,在缓解状态下进行LST时,获得了较高的阳性发生率(50%)。在急性疾病状态下进行LST时,LST阳性发生率较低(25%)。提示该方法可用于药物过敏的临床诊断,对于药物性肝炎的诊断,建议在缓解状态下进行LST检查。
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引用次数: 0
Prescription Ordering System in Hokkaido University Hospital (2) : Improvements of On-lined Automatic Tablet Packaging System 北海道大学医院处方订购系统(2):在线自动片剂包装系统的改进
Pub Date : 1991-08-20 DOI: 10.5649/JJPHCS1975.17.270
S. Kawai, T. Oh-E, T. Takashima, O. Ogino, Katsumi Miyazaki, G. Irie, T. Kudo
The prescription ordering system has been on-lined to a fully automatic tablet packaging machine in order to transmit the host data for inpatient periodical prescription.In this time, we tried to improve the method of transmitting the host data for prescription and drug files in the data converter, and also tried to change the operating machine for one dose packaging in order to dispense tablets more automatically.These resulted in the success of the automatic one dose packaging without modifying the host data by hand, even if the amount of drug component or unequal dispensing was inputted to the computer for prescription.Drug files enable to be changed automatically by using the hard disk in case of the partial replacement of tablet cassettes in the fully automatic tablet packaging machine.Moreover, the new operating machine for one dose packaging enables to input the data by hand easier and to record the amount of tablet consumed over all tablets automatically.
配药系统已与全自动片剂包装机联网,以传送住院患者定期配药的主机数据。在此期间,我们尝试改进了数据转换器中传送处方和药品文件主机数据的方法,并尝试将操作机器改为单剂量包装,以提高配片的自动化程度。这使得即使将药物成分的量或不均匀配药输入计算机进行处方,也可以在不手动修改主机数据的情况下成功地进行单剂量自动包装。全自动片剂包装机在部分更换片剂盒式药品时,可使用硬盘自动更换药品文件。此外,新型的单剂量包装操作机可以更方便地手工输入数据,并自动记录所有片剂的片剂用量。
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引用次数: 1
TOXI-LABシステム(急性薬物中毒分析法)の評価 TOXI-LAB系统(急性药物中毒分析法)的评估
Pub Date : 1991-06-20 DOI: 10.5649/jjphcs1975.17.123
大輔 手嶋, 祐滋 上田, 紀子 田中, 二神 幸次郎, 健司 大坪, 駿 樋口, 敏信 青山
Recently, the acute drug poisonings have been increasing in Japan.Therefore, the accurate and rapid screening method of unknown drug caused poisoing has occupied the more important position in acute medicine.Though many kinds of chromatographies and spectrophotometries have been used to screen the unknown drug caused the poisoning, there is no proper method in Japan from the standpoint of utility and rapidity.Therefore, the practical use of the TOXILAB system (Marion) developed in USA was examined this time.Twenty-five drugs caused frequently acute poisoning were selected and added to the serum, urine and artificial gastric fluid.We investigated both the separation and the lower limit of detection of the drugs by TOXI-LAB system.The separative spots obtained on the TOXIGRAMs were compared to the authentic samples by HPLC.Furthermore, we applied the TOXILAB system to the patient sample in the acute poisoning and examined the utility of this system. Seven kinds of drug, i. e. agricultural medicines, theophylline, diphenhydramine and bromvalerylurea, could not be detected.It was confirmed that prednisolone, acetaminophen, phenacetin, hydroxyzine, chlorpromazine, carbamazepine, amobarbital and amitriptyline were detected even at half or a quarter of the lower limit of detection recorded in a TOXI-LAB compendium.Each spot on the TOXI-GRAM was in agreement with the authentic sample in HPLC.TOXI-LAB system is considered to be a very useful screening method if the drug caused acute poisoning could be predicted to some extent.
最近,日本的急性药物中毒呈上升趋势。因此,准确、快速的未知药物中毒筛查方法在急症医学中占有更为重要的地位。虽然已有多种色谱法和分光光度法用于筛选引起中毒的未知药物,但从实用性和快速性的角度来看,在日本尚无合适的方法。因此,这次研究了美国开发的TOXILAB系统(Marion)的实际应用。选取25种常见急性中毒药物,分别加入血清、尿液和人工胃液中。研究了TOXI-LAB系统对两种药物的分离及检测下限。用高效液相色谱法将毒素图上的分离点与正品进行比较。此外,我们将TOXILAB系统应用于急性中毒患者样本,并检验了该系统的实用性。农用药品、茶碱、苯海拉明、溴缬脲等7种药品均未检出。经证实,强的松龙、对乙酰氨基酚、非那西丁、羟嗪、氯丙嗪、卡马西平、阿莫巴比妥和阿米替林的检出率仅为TOXI-LAB纲目中所记录的检出下限的一半或四分之一。TOXI-GRAM上的每个斑点与HPLC上的真品一致。如果能在一定程度上预测药物引起的急性中毒,tox - lab系统被认为是一种非常有用的筛选方法。
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引用次数: 0
Serum Levels of Carbamazepine and Valproic Acid in Pediatric Patients. Influence of Age and Drug Combination Therapy of L/D Ratios. 小儿患者卡马西平和丙戊酸的血清水平。年龄及药物联合治疗对L/D比值的影响。
Pub Date : 1991-02-20 DOI: 10.5649/JJPHCS1975.17.26
Suzuki Akito, 彰人 鈴木, 栄二 湯川, Yukawa Eiji, 健司 大坪, Ohtsubo Kenji, 一郎 家入, Ieiri Ichiro, 大輔 手嶋, Teshima Daisuke, 駿 樋口, Higuchi Shun, 敏信 青山, Aoyama Toshinobu
The influence of age and drug combination therapy on carbamazepine (CBZ) serum level-dose (L/D) ratio and valproic acid (VPA) L/D ratio was investigated in 442 pediatric patients.The CBZ or VPA L/D ratio increased linearly with the increase in the age of pediatric patients (p<0.001).Concomitant administration of antiepileptic drugs affected those L/D ratios, which were significantly reduced in patients on polypharmacy as compared to those on monopharmacy.Therefore, routine monitoring of CBZ and VPA serum levels would be extremely useful, especially in pediatric age group and in patients required combined antiepileptic medication.
研究了442例小儿卡马西平(CBZ)血清水平剂量比(L/D)和丙戊酸(VPA) L/D比的年龄和药物联合治疗的影响。CBZ或VPA L/D比值随患儿年龄的增加呈线性增加(p<0.001)。同时服用抗癫痫药物会影响这些L/D比率,与服用单一药物的患者相比,服用多种药物的患者的L/D比率显著降低。因此,常规监测CBZ和VPA血清水平将非常有用,特别是在儿童年龄组和需要联合抗癫痫药物的患者中。
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引用次数: 1
期刊
Journal of the Nippon Hospital Pharmacists Association
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