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离子抑制色谱法测定维U颠茄铝胶囊(Ⅲ)中阿托品的含量

离子抑制色谱法测定维U颠茄铝胶囊(Ⅲ)中阿托品的含量

离子抑制色谱法测定维U颠茄铝胶囊(Ⅲ)中阿托品的含量张国柱;任海燕;王仕宝;屈小娟;李晓琳【摘要】目的建立维U颠茄铝胶囊(Ⅲ)中阿托品含量的离子抑制色谱测定方法.方法采用C18柱(150 mm×4.6 mm,5μm);流动相为磷酸三乙胺溶液(取三乙胺4 mL,加水1 000mL,用磷酸调节pH至7.5)-乙腈(85:15);检测波长为206nm.结果阿托品质量浓度在4~200 mg·L-1范围内线性关系良好(r=0.999 9).平均回收率为98.9%,RSD为1.2%.结论方法简便、快速、经济,结果准确,适用于维U颠茄铝胶囊(Ⅲ)的质量控制.【期刊名称】《西北药学杂志》【年(卷),期】2009(024)004【总页数】3页(P246-248)【关键词】维U颠茄铝胶囊(Ⅲ);离子抑制色谱;阿托品;含量测定【作者】张国柱;任海燕;王仕宝;屈小娟;李晓琳【作者单位】汉中市药品检验所,陕西,汉中,723000;汉中市药品检验所,陕西,汉中,723000;汉中市职业技术学院医学院,陕西,汉中,723000;汉中市职业技术学院医学院,陕西,汉中,723000;汉中市药品检验所,陕西,汉中,723000【正文语种】中文【中图分类】R927.2维U颠茄铝胶囊(Ⅲ)收载于《中国药品标准化学药品地方标准上升国家标准第十五册》[1],处方中每千粒含10 g颠茄流浸膏,但药品标准未对颠茄提取物作质量控制。

颠茄流浸膏中主要活性物质阿托品属莨菪碱类生物碱,药理作用剧烈,《药品管理法》将其列为毒性药品进行严格管理,因此准确测定其含量,进行质量控制,对提高药品质量,保障用药安全具有重要的意义。

有文献建议用HPLC法对维U颠茄铝胶囊中阿托品含量进行限度检测[2]。

一些文献对阿托品的测定主要采用离子对色谱[3,4],方法中使用较贵的离子对试剂使其应用受到一定程度的限制;亦有文献采用正相色谱方法测定含阿托品制剂中阿托品的含量,但均未见维U颠茄铝胶囊(Ⅲ)中阿托品含量测定的报道。

乙酰胆碱酯酶试剂盒说明书

乙酰胆碱酯酶试剂盒说明书

乙酰胆碱酯酶试剂盒说明书人胆碱乙酰化酶(CHAc)ELISA试剂盒说明书本试剂盒仅供体外研究使用!预期应用ELISA法定量测定人血清、血浆或其它相关生物液体中CHAc含量。

实验原理用纯化的抗体包被微孔板,制成固相载体,往包被抗CHAc抗体的微孔中依次加入标本或标准品、生物素化的抗CHAc抗体、HRP标记的亲和素,经过彻底洗涤后用底物TMB显色。

TMB在过氧化物酶的催化下转化成蓝色,并在酸的作用下转化成最终的黄色。

颜色的深浅和样品中的CHAc呈正相关。

用酶标仪在450nm波长下测定吸光度(OD值),计算样品浓度。

试剂盒组成及试剂配制1. 酶联板:一块(96孔)2. 标准品(冻干品): 2瓶,每瓶临用前以样品稀释液稀释至1ml,盖好后静置10分钟以上,然后反复颠倒/搓动以助溶解,其浓度为10 ng/ml,做系列倍比稀释(注:不要直接在板中进行倍比稀释)后,分别稀释成10 ng/ml,5 ng/ml,2.5ng/ml,1.25 ng/ml,0.625 ng/ml,0.312 ng/ml,0.156 ng/ml,样品稀释液直接作为标准浓度0 ng/ml,临用前15分钟内配制。

如配制5 ng/ml标准品:取0.5ml (不要少于0.5ml ) 10 ng/ml的上述标准品加入含有0.5ml样品稀释液的Eppendorf管中,混匀即可,其余浓度以此类推。

3. 样品稀释液:1×20ml。

4. 检测稀释液A:1×10ml。

5. 检测稀释液B:1×10ml。

6. 检测溶液A:1×120μl(1:100)临用前以检测稀释液A 1:100稀释,稀释前根据预先计算好的每次实验所需的总量配制(100μl/孔),实际配制时应多配制0.1-0.2ml。

如10μl检测溶液A加990μl检测稀释液A的比例配制,轻轻混匀,在使用前一小时内配制。

7. 检测溶液B:1×120μl/瓶(1:100)临用前以检测稀释液B 1:100稀释。

依达拉奉资料参考翻1

依达拉奉资料参考翻1

Ⅱ.有关名称的项目1.商品名(1)和名:Radicut注射用30mgRadicut静脉点滴用30mg (袋装输液)(2)洋名:RADICUT BAG for I.V. Infusion30mg(3)名称的由来:因本品可清除自由基而得名。

2.通用名(1)和名(命名法):依达拉奉(日本※)※1997年5月在日本将本品原来的名称Meferaven(Meferaven)变更为依达拉奉(Edaravone)。

(2)洋名(命名法):Edaravone(日本※,INN)※1997年5月在日本将本品原来的名称Meferaven(Meferaven)变更为依达拉奉(Edaravone)。

(3)起源:不明3.结构式或示性式4.分子式及分子量分子式:C10H10N2O分子量:174.205.化学名(命名法)3-甲基-1-苯基-2-吡唑啉-5-酮6.惯用名,别名,缩写,记号药物号:MCI-186(MY-7906)别名:meferaven7.CAS登录号89-25-8Ⅲ.有关有效成分的项目1.物理化学的性质(1)外观・性状:本品为白色~微黄白色的结晶或结晶性的粉末。

(2)溶解性:※溶解依达拉奉1g(3)吸湿性:在室温下约0%相对湿度,约64%相对湿度,约93%相对湿度及在40℃下,75%相对湿度的条件下保存38日,均未见重量的变化,表明本品没有吸湿性。

(4)熔点(分解点),沸点,凝固点:熔点:127~131℃(5)酸碱解离常数:pKa=7.0(6)分配系数:(7)其他的主要示性值:吸光度2.有效成分在各种条件下的稳定性试验项目:性状,确认试验,pH,熔点,纯度试验,干燥减量,含量3.有效成分的确认试验法(1)紫外可见吸光度测定法(2)红外吸收光谱法测定法(溴化钾片剂法)4.有效成分的定量法电位差滴定法Ⅳ.有关制剂的项目1.剂形(1)剂形的区别,规格及性状:(2)溶液及溶解时的pH,渗透压比,粘度,比重,稳定的pH域等:*1.对生理盐水之比(3)注射剂的容器中的特殊的气体的有无及种类:Radicut注射用30mg:氮Radicut静脉点滴用(袋装输液):氮2.制剂的组成(1)有效成分(活性成分)的含量:(2)添加物:参照上记(1)项(3)电解质的浓度:没有相关资料。

人参皂苷治疗骨性关节炎的研究进展

人参皂苷治疗骨性关节炎的研究进展

特产研究163Special Wild Economic Animal and Plant ResearchDOI:10.16720/ki.tcyj.2023.093人参皂苷治疗骨性关节炎的研究进展郭校妍1,张伟东1,张扬1※(吉林大学药学院,吉林长春130021)摘要:人参在防治关节软骨损伤退变及参与体外培养软骨细胞修复关节软骨缺损中具有较好治疗前景。

人参皂苷作为人参的主要药理活性成分,在治疗骨性关节炎的进程中发挥关键作用。

人参皂苷根据不同的结构被分为不同的类型,各类型均含有多种人参皂苷单体成分,其治疗骨性关节炎的机制也各不相同。

本文对不同人参皂苷单体治疗骨性关节炎的研究进行梳理和总结,探讨其治疗骨性关节炎的潜在可能性和作用机制,为后期临床应用提供依据。

关键词:骨性关节炎;人参皂苷;信号通路中图分类号:R285文献标识码:A文章编号:1001-4721(2023)03-0163-06Research Progress of Ginsenosides in the Treatment of OsteoarthritisGUO Xiaoyan1,ZHANG Weidong1,ZHANG Yang1※(School of Pharmaceutical Sciences,Jilin University,Changchun130021,China)Abstract:Ginseng has pharmacological effects such as anti-inflammatory,antioxidant,antidepressant,anti-Alzheimer's and anti-athero-sclerosis.Current studies have found that it has good therapeutic prospects in preventing degeneration of articular cartilage damage and parti-cipating in in vitro culture of chondrocytes to repair articular cartilage defects.Ginsenosides,as the main pharmacological active component of ginseng,also play an important role in the process of treating osteoarthritis.Ginsenosides can be classified into different types because of their different structures,and each type contains a variety of ginsenoside monomer components with different mechanisms for the treatment of osteoarthritis.In this paper,we review the research progress of different ginsenoside monomers in the treatment of osteoarthritis,and ex-plore their potential possibilities and mechanisms for the treatment of osteoarthritis,so as to provide a basis for later clinical application. Key words:osteoarthritis;ginsenosides;signaling pathway骨性关节炎(Osteoarthritis,OA)是一种退行性病变,系由于增龄、肥胖、遗传、劳损、创伤、关节先天性异常和关节畸形等诸多因素引起的关节软骨退化损伤、关节边缘和软骨下骨反应性增生。

非酒精性脂肪性肝病代谢组学研究进展

非酒精性脂肪性肝病代谢组学研究进展

机制尚未完全明确,1998 年Day 等[12]提出“二次打击”学说。 开。同时NAFLD 肝硬化患者与酒精性肝硬化患者也可有效区
随后Tilg 等[13 -14]提出“多重平行打击”理论,包括遗传因素、 分开(AUC =0. 83)。他们认为此方法可作为区分NAFLD 纤维
IR、氧化应激、脂毒性、慢性炎症、纤维化、免疫和肠道菌群等, 化程度及诊断的无创生物标志物,且可以显著减少对肝活检的
黄酯和13 - cisRA 呈正相关。他们在人类组织中首次检测到 验证;单不饱和TAG 的增加可能是NAFLD 和CHB 患者NASH
atRA 的活性代谢物4 - oxo - atRA,表明这种类维生素A 可能 的特异性标志物。
有助于人体类维生素A 的信号传导。肝脏维生素A 的稳态平 2. 3 代谢组学对NAFLD 药物作用与疗效研究的推动作用
录组学、蛋白质组学为代表的系统生物学技术提供了新的技术 展的新学科,代谢组学较为全面的展示了机体的代谢结果,为
与思路。区别于其他组学技术,以内源性小分子代谢物为研究 临床医学提供了新的技术和方法。
对象的代谢组学可以很好的揭示机体变化的最终代谢结果。因 2 非酒精性脂肪性肝病(NAFLD)
收 基 作DO稿 金 者I:日 项 简10期 目 介. 3:::912上 栾研6709)2海究雨/0j.中婷-is医1s(n1药.1-19大090006学1—;修-附)5回,属2女5日第6,.期七主20:人2要210民.2从00医4事-.院01慢42人7-性才1肝7培病养计的划基(础XX与20临19床- 通信作者:顼志兵,xzb6160@ 163. com
和遗传易感密切相关的代谢应激性肝损伤,包括非酒精性单纯 1 代谢组学概述
性肝脂肪变(NAFL)、非酒精性脂肪性肝炎(NASH)、肝硬化和 1. 1 代谢组学含义 代谢组学最初于1999 年由Nicholson

正交函数分光光度法测定安钠咖注射液的含量

正交函数分光光度法测定安钠咖注射液的含量

正交函数分光光度法测定安钠咖注射液的含量
陈爱民;顾春沫
【期刊名称】《农垦医学》
【年(卷),期】1999(021)001
【总页数】3页(P63-65)
【作者】陈爱民;顾春沫
【作者单位】石河子市药品检验所;石河子市药品检验所
【正文语种】中文
【中图分类】R971.7
【相关文献】
1.正交函数分光光度法测定安痛定注射液中氨基比林的含量 [J], 王春英;张兰桐;和悦;张爱华;周月绵;陈汝红;周增学;刘伟娜;张振华
2.正交函数分光光度法测定溴咖合剂中安钠咖的含量 [J], 邓丽琴;朱虬
3.正交函数分光光度法测定溴咖合剂中安钠咖的含量 [J], 朱虬;顾沧一;钱珑已;向金生
4.正交函数分光光度法测定地塞米松磷酸钠注射液的含量 [J], 张庆雨;张玉环
5.乘子罚函数分光光度法测定安钠咖注射液的含量 [J], 周明达;文莉;邓凯佳;刘建华
因版权原因,仅展示原文概要,查看原文内容请购买。

FDA批准的精准医疗诊断体外器械一览表List of Cleared or Approved Companion Diagnostic Devices

List of Cleared or Approved Companion Diagnostic Devices (In Vitro and Imaging Tools)
Drug Trade Name
NDA/BLA
Device Trade Name
PMA
Device Manufacturer
Intended Use (IU)/ Indications for Use (IFU)
(imatinibmesylate)
NDA 021588
The c-KitpharmDxis indicated as an aid in the differential diagnosis of gastrointestinal stromal tumors (GIST). After diagnosis of GIST, results from c-KitpharmDxmay be used as an aid in identifying those patients eligible for treatment withGleevec/Glivec(imatinibmesylate).
(deferasirox)
Gilotrif
NDA 201292
therascreenEGFR RGQ PCR Kit
P120022
QiagenManchester, Ltd.
ThetherascreenEGFR RGQ PCR Kit is a real-time PCR test for the qualitative detection of exon 19 deletions and exon 21 (L858R) substitution mutations of the epidermal growth factor receptor (EGFR) gene in DNA derived from formalin-fixed paraffin-embedded (FFPE) non-small cell lung cancer (NSCLC) tumor tissue. The test is intended to be used to select patients with NSCLC for whom GILOTRIF (afatinib), an EGFR tyrosine kinase inhibitor (TKI), is indicated. Safety and efficacy of GILOTRIF (afatinib) have not been established in patients whose tumors have L861Q, G719X, S768I, exon 20 insertions, and T790M mutations, which are also detected by thetherascreenEGFR RGQ PCR Kit.

【推荐下载】HPLC法测定养胃软胶囊中厚朴酚、和厚朴酚的含量

HPLC法测定养胃软胶囊中厚朴酚、和厚朴酚的含量 【编者按】医药论文是科技论文的一种是用来进行医药科学研究和描述研究成果的论说性文章。

论文网为您提供医药论文范文参考,以及论文写作指导和格式排版要求,解决您在论文写作中的难题。

 HPLC法测定养胃软胶囊中厚朴酚、和厚朴酚的含量 【摘要】:目的建立测定养胃软胶囊中厚朴酚、和厚朴酚的含量测定方法。

方法高效液相色谱法采用Phenomenex Kromasil C18(250 mm 4.6 mm,5 m)色谱柱,流动相:甲醇-水(22∶78),流速:1.0 mL/min,检测波长294 nm,柱温40 ℃,进样量10 L。

结果厚朴酚线性范围0.058 8~0.882 0 g,r=0.999 9,平均回收率为99.35%,RSD=1.94%;和厚朴酚线性范围0.020 4~0.306 0 g,r=0.999 8,平均回收率为99.21%,RSD=2.10%(n=6)。

结论本法分离好,快速、简便,可作为该产品的质量控制方法。

 【关键词】养胃软胶囊厚朴酚和厚朴酚高效液相色谱法 Abstract:Objective To establish a method for determination of puerarin in Yangwei Soft Capsule. Methods HPLC was used for quantitative ananlysis. The Phenomenex Kromasil C18 (250 mm 4.6 mm, 5 m) column was used, and mobile phase was composed of methanol-water (22∶78). Detection wavelength was at 294 nm, the flow rate was 1.0 mL/min, column temperature was at 40 ℃, the injection volume was 10 L. Results The linear response ranges from 0.058 8~0.882 0 g of magnolol (r=0.999 9, n=6). The average recovery of magnolol is 99.35%, RSD=1.94%. The linear response ranges from 0.020 4~0.306 0 g of honokio (r=0.999 8, n=6). The averagy recovery of honokio is 99.21%, RSD=2.10%. Conclusion The method is simple, accurate, and suitable for the determination of the purarin in compound preparations. Key words:Yangwei Soft Capsule;magnolol;honokio;HPLC 养胃软胶囊是由陈皮、厚朴、茯苓、甘草、广藿香等14味中药组成的复方制剂,为《卫生部药品标准》第7册(1993年)收载品种,具有温中和胃的功效,主治不思饮食、呕吐酸水、胃脘满闷、四肢倦怠等症。

BP2015英国药典索引

page numbers in bold type relate to monograph titles Index V-A797IndexPage numbers in bold type relate to monograph titles.Pages–Vol I:i–xxxii,(Preliminaries and Introduction)1–1280,(General Notices and Monographs)Pages–Vol II:i–viii,(Preliminaries)1–1220,(General Notices and Monographs)Pages–Vol III:i–viii,(Preliminaries)1–1238,(General Notices and Monographs)Pages–Vol IV:i–viii,(Preliminaries)1–754,(General Notices and Monographs)Pages–Vol V:i–viii,(Preliminaries)1–34,(General Notices)S1–S144,(Spectra)A1–A796,(Appendices;Supplementary Chapters)AAbacavir,V-S4Abacavir Oral Solution,III-85 Abacavir Sulfate,I-39Abacavir Tablets,III-86 Abbreviated,V-598Adjectives,V-598Anions,V-598Cations,V-598Preparations,V-598Titles of Monographs,V-598 Abbreviated Titles,Status of,I-7,II-7, III-7,IV-7,V-7Abbreviations and symbols,I-30,II-30, III-30,IV-30,V-30Abnormal Toxicity,Test for,V-409 About,definition of,I-5,II-5,III-5,IV-5,V-5Absence of Mycoplasmas,Test forV-487Absolute Ethanol,V-A61Absolute Ethanol R1,V-A62 Absorbent Cotton,IV-743Absorbent Viscose Wadding,IV-744 Absorption spectrophotometry,infrared, V-162Absorption Spectrophotometry, Ultraviolet and Visible,V-169 Acacia,I-41,V-A19Acacia Solution,V-A19Acacia Spray-dried,I-42 Acamprosate Calcium,I-43 Acanthopanax Bark,IV-49 Acarbose,I-44Accuracy,V-674Acebutolol Capsules,III-87 Acebutolol Hydrochloride,I-46,V-S5, V-A19Acebutolol Tablets,III-88 Aceclofenac,I-48Acemetacin,I-50Acenocoumarol,I-52,V-S5 Acenocoumarol Tablets,III-88 Acesulfame Potassium,I-52Acetal,V-A19Acetaldehyde,V-A19Acetaldehyde Ammonia Trimer Trihydrate,V-A20Acetaldehyde Standard Solution(100ppm C2H4O),V-A148 Acetaldehyde Standard Solution(100ppm C2H4O)R1,V-A148 Acetamide,V-A20Acetate Buffer pH2.8,V-A152 Acetate Buffer pH2.45,V-A152 Acetate Buffer pH3.4,V-A152 Acetate Buffer pH3.5,V-A152 Acetate Buffer pH3.7,V-A152 Acetate Buffer pH4.4,V-A152 Acetate Buffer pH4.6,V-A152 Acetate Buffer pH5.0,V-A152 Acetate Buffer pH6.0,V-A152 Acetate Buffer Solution pH4.7R1,V-A153Acetate Buffer Solution pH4.4,see Acetate Buffer pH4.4Acetate Buffer Solution pH4.6,see Acetate Buffer pH4.6Acetate Buffer Solution pH6.0,seeAcetate Buffer pH6.0Acetate Buffer Solution pH4.4,V-A152Acetate Buffer Solution pH4.5,V-A152Acetate Buffer Solution pH4.7,V-A152Acetate Buffer Solution pH5.0,V-A153Acetate Buffer Solution pH6.0,V-A153Acetate–edetate Buffer Solution pH5.5,V-A153Acetates,Reactions of,V-266Acetazolamide,I-54,V-S5Acetazolamide Oral Suspension,III-89Acetazolamide Tablets,III-90Acetic Acid,V-A20Acetic Acid(6per cent),I-56Acetic Acid(33per cent),I-56Acetic Acid,Anhydrous,V-A20Acetic Acid,Deuterated,V-A50Acetic Acid,Dilute,V-A20Acetic Acid,Dilute,see Acetic Acid(6per cent)Acetic Acid,Glacial,I-55,V-A20Acetic Acid in Synthetic Peptides,Determination of,V-299Acetic Acid VS,V-A142Acetic Acid,see Acetic Acid(33per cent)Acetic Anhydride,V-A20Acetic Anhydride Solution R1,V-A20Acetic Anhydride–Dioxan Solution,V-A20Acetic Anhydride–Sulfuric Acid Solution,V-A20Acetic Anhydride–Sulphuric AcidSolution,see Acetic Anhydride–SulfuricAcid SolutionAcetic Bromine Solution,V-A34Acetone,I-57,V-A20Acetone,Deuterated,V-A50Acetone Solution,Buffered,V-A153Acetone-dried Ox Brain,V-A98Acetonitrile,V-A20Acetonitrile for Chromatography,V-A20Acetonitrile R1,V-A20Acetoxyvalerenic Acid,V-A20Acetyl Chloride,V-A20Acetyl Groups,Reactions of,V-266Acetyl Salicylic Acid see AspirinAcetyl Value,Determination of,V-317Acetylacetamide,V-A20Acetylacetone,V-A20Acetylacetone Reagent R1,V-A20Acetylacetone Reagent R2,V-A204-Acetylbiphenyl,V-A20O-Acetyl Groups in PolysaccharideVaccines,V-467N-Acetyl-e-caprolactam,V-A20Acetylcholine Chloride,I-58,V-A20Acetylcysteine,I-59,V-S6Acetylcysteine Eye Drops,III-90Acetylcysteine Injection,III-91Acetyldigoxin,I-61b-Acetyldigoxin see AcetyldigoxinAcetyleugenol,V-A20N-Acetylglucosamine,V-A21Acetyl-11-keto-b-boswellic Acid,V-A21N-Acetyl-L-cysteine,V-A20N-Acetylneuraminic Acid,V-A21Acetylsalicylic Acid Tablets,see AspirinTabletsN-Acetyltryptophan,V-A21N-Acetyltryptophan see AcetyltryptophanAcetyltryptophan,I-63Acetyltyrosine,I-65N-Acetyltyrosine see AcetyltyrosineAcetyltyrosine Ethyl Ester,V-A21Acetyltyrosine Ethyl Ester,0.2M,V-A21Aciclovir,I-67Aciclovir Cream,III-93Aciclovir Eye Ointment,III-94Aciclovir Infusion,III-95Aciclovir Intravenous Infusion,seeAciclovir Infusion,Aciclovir Oral Suspension,III-97Aciclovir Sodium for Infusion,III-95Aciclovir Sodium for IntravenousInfusion,see Aciclovir Sodium forInfusion,Aciclovir Tablets,III-98Aciclovir Tablets,Dispersible,III-99Acid Blue92,V-A21Acid Blue92Solution,V-A21Acid Blue83,V-A21Acid Blue93Solution,V-A21Acid Blue90,V-A21Acid Gentian Mixture,IV-197Acid Gentian Oral Solution,IV-197Acid Potassium IodobismuthateSolution,V-A108Acid Value,V-317Acid/base Indicators,V-789Acid-base titrations,V-788Acidified Chloroform,V-A41Acidified Dichloromethane,V-A52Acidified Methanol,V-A85Acidified Methylene Chloride,seeAcidified DichloromethaneAcid-insoluble Ash,Determination of,V-336Acid-washed Diatomaceous Support,V-A51Acitretin,I-69Acitretin Capsules,III-100Acknowledgements,I-xxviiAcrylamide,V-A21Acrylamide/bisacrylamide(29:1)Solution,30per cent,V-A21Acrylamide/bisacrylamide(36.5:1)Solution,30per cent,V-A21Acrylic Acid,V-A21Actein,V-A21Acteoside,V-A21Action and Use Statement,Status of,I-17,II-17,III-17,IV-17,V-17Activated Acid Aluminium Oxide,V-A23Activated Attapulgite,I-220Activated Charcoal,I-496,V-A40Activated Zinc,V-A140Active Moiety,V-651Adamantane,V-A21Adapalene,I-71Adapalene Cream,III-101Adapalene Gel,III-103Additions,List of,I-xxviiiAdditions,List of Monographs,I-xxiiAdditives,Plastic,V-592Adenine,I-72,V-A21Adenosine,I-73,V-A21Adipic Acid,I-75,V-A21Adrenaline,V-A21Adrenaline/Epinephrine,I-76page numbers in bold type relate to monograph titles Index V-A799Adrenaline Acid Tartrate,V-A21 Adrenaline Acid Tartrate/Epinephrine Acid Tartrate,I-77Adrenaline and Cocaine Intranasal Solution,III-107Adrenaline(Epinephrine),V-S6 Adrenaline Eye Drops,Epinephrine Eye Drops,Neutral,III-104Adrenaline Eye Drops/Epinephrine Eye Drops,III-104Adrenaline Injection,Bupivacaine and, III-220Adrenaline Injection,Dilute(1in10,000),III-106Adrenaline Injection,Lidocaine and,III-751Adrenaline Injection/Epinephrine Injection,III-105Adrenaline Solution/Epinephrine Solution,III-106Adrenaline Tartrate see Adrenaline Acid TartrateAdrenaline TartrateInjection/Epinephrine Tartrate Injection,III-105Adrenaline TartrateSolution/Epinephrine Tartrate Solution,III-106Adrenalone Hydrochloride,V-A21 Adsorbed Diphtheria and Tetanus Vaccine,IV-537Adsorbed Diphtheria and Tetanus Vaccine for Adults and Adolescents, see Adsorbed Diphtheria and Tetanus Vaccine(adsorbed,Reduced Antigen(s) Content)Adsorbed Diphtheria,Tetanus and Pertussis(Acellular Component) Vaccine,IV-541Adsorbed Diphtheria,Tetanus,Pertussis (Acellular Component)and Haemophilus Type b Conjugate Vaccine,IV-545Adsorbed Diphtheria,Tetanus,Pertussis (Acellular Component)and Hepatitis B(rDNA)Vaccine,IV-547 Adsorbed Diphtheria,Tetanus,Pertussis (Acellular Component)and Inactivated Poliomyelitis Vaccine,IV-548Adsorbed Diphtheria Vaccine,IV-534 Adsorbed Diphtheria Vaccine for Adults and Adolescents,see Diphtheria Vaccine (Adsorbed,Reduced Antigen Content) Adsorbed Pertussis Vaccine(Acellular Component),IV-604Adsorbed Pertussis Vaccine(Acellular, Co-purified),IV-605Adsorbed Tetanus Vaccine,IV-633 Adsorbed Vaccines,Aluminium in,V-463Adsorbed Vaccines,Calcium in,V-464 Adsorption,Gas,Specific Surface Area By(2.9.26.)(5.8.),V-701Aescin,V-A22Aflatoxin B1,V-A22Aflatoxin B,in Herbal Drugs, Determination of,V-341Agar,I-79,V-A22Agarose for Chromatography,V-A22Agarose for Chromatography,Cross-linked,V-A22Agarose for Chromatography R1,Cross-linked,V-A22Agarose for Electrophoresis,V-A22Agarose/Cross-linked Polyacrylamide,V-A22Agarose-DEAE for Ion ExchangeChromatography,V-A22Agnus Castus Fruit,IV-50Agrimony,IV-52Air,Medical,I-78Air,Medicinal see Medical AirAir Permeability,Specific Surface Areaby,V-505Air,Synthetic,I-81Air,Synthetic Medicinal see Synthetic AirAlanine,I-83,V-A22ß-Alanine,see3-Aminopropionic AcidAlbendazole,I-84Albumin,Bovine,V-A22Albumin,Bovine R1,V-A22Albumin,Human,V-A22Albumin Solution,IV-467Albumin Solution,Human,V-A22Albumin Solution R1,Human,V-A22Alchemilla,IV-53Alcohol(20per cent),I-900Alcohol(25per cent),I-900Alcohol(45per cent),I-900Alcohol(50per cent),I-900Alcohol(60per cent),I-900Alcohol(70per cent),I-900Alcohol(80per cent),I-900Alcohol(90per cent),I-900Alcohol,Aldehyde-free,see Ethanol(96%),Aldehyde-freeAlcoholic Calcium Standard Solution(100ppm Ca),V-A149Alcoholic DimethylaminobenzaldehydeSolution,V-A55Alcoholic Hydroxylamine Solution,V-A74Alcoholic Iodine Solution,III-696,V-A75Alcoholic Potassium Hydroxide,2M,V-A108Alcoholic Potassium Hydroxide,seePotassium Hydroxide VS,EthanolicAlcoholic Potassium Hydroxide Solution,V-A108Alcoholic Potassium Hydroxide SolutionR1,V-A108Alcoholic Solution of Sulfuric Acid,V-A128Alcoholic Sulfuric Acid,0.25M,V-A128Alcoholimetric Tables,V-687Alcohol,see Ethanol(96%)Alcuronium Chloride,I-85Aldehyde Dehydrogenase,V-A22Aldehyde Dehydrogenase Solution,V-A22Aldehyde-free alcohol,see Ethanol(96%),Aldehyde-freeAldehyde-free Ethanol(96%),V-A62Aldehyde-free Methanol,V-A85Aldehydes,Determination of,V-321Aldrin,V-A22Alendronate Sodium Tablets,seeAlendronic Acid TabletsAlendronic Acid Tablets,III-109Aleuritic Acid,V-A22Alexandrian Senna Fruit,IV-362Alfacalcidol,I-87Alfadex,I-88Alfentanil Hydrochloride,I-89Alfuzosin,V-S7Alfuzosin Hydrochloride,I-91Alfuzosin Tablets,III-111Alfuzosin Tablets,Prolonged-release,III-112Alginate Antacid Oral Suspension,Compound,III-113Alginate Oral Suspension,Raft-forming,III-114Alginate Raft-forming Oral Suspension,III-114Alginic Acid,I-92Alimemazine,V-S7Alimemazine Oral Solution,Paediatric,III-115Alimemazine Tablets,III-116Alimemazine Tartrate,I-93Alizarin S,V-A22Alizarin S Solution,V-A22Alkaline Corallin Solution,V-A46Alkaline Eye Drops,see Hypromellose EyeDropsAlkaline Gentian Mixture,IV-198Alkaline Gentian Oral Solution,IV-198Alkaline Hydroxylamine Solution,V-A74Alkaline Hydroxylamine Solution R1,V-A74Alkaline Potassium Mercuri-iodideSolution,V-A109Alkaline Potassium TetraiodomercurateSolution,V-A109Alkaline Pyrogallol Solution,V-A111Alkaline Sodium Picrate Solution,V-A124Alkaline Tetrazolium Blue Solution,V-A132Alkali-washed Diatomaceous Support,V-A51Alkaloids,Complete Extraction of,V-335Alkaloids,Reactions of,V-266all--Alpha-Tocopherol,II-1051Allantoin,I-94,V-A23Allergen Products,I-95Allium Sativum for HomoeopathicPreparations,IV-427Allopurinol,I-98Allopurinol Oral Suspension,III-117Allopurinol Tablets,III-118all-rac-Alpha-Tocopheryl Acetate,II-1054all-rac-a-Tocopheryl see all-rac-Alpha-Tocopherylall-rac-Tocopheryl Acetate see all-rac-Alpha-Tocopheryl AcetateAlmagate,I-100Almond Oil Ear Drops,III-119Almond Oil,Refined,I-100Almond Oil,Virgin,I-99Almond Oil see Virgin Almond OilAloes,Barbados,IV-53Aloes,Cape,IV-54Alovudine,V-A23Alovudine(18F)Injection,IV-669V-A800IndexAloxiprin,I-102Aloxiprin Tablets,III-119Alpha Tocopheryl Acetate Concentrate (Powder Form),II-1057Alpha Tocopheryl Hydrogen Succinate, II-1058Alpha Tocopheryl Succinate Tablets,III-1164Alphacyclodextrin see Alfadex Alprazolam,I-103Alprenolol Hydrochloride,I-105 Alprostadil,I-107Alteplase for Injection,I-109 Alternative methods,I-20,II-20,III-20, IV-20,V-20Alternative Methods for Control of Microbiological Quality,V-745 Altizide,I-113Alum,I-114Aluminium,V-A23Aluminium Acetate Ear Drops,III-120 Aluminium Chloride,V-A23 Aluminium Chloride Hexahydrate,I-114 Aluminium Chloride Reagent,V-A23 Aluminium Chloride Solution,III-121, V-A23Aluminium Glycinate,I-115 Aluminium Hydroxide and Magnesium Trisilicate Tablets,Chewable,III-776 Aluminium Hydroxide,Dried,I-115 Aluminium Hydroxide Gel,V-A23 Aluminium Hydroxide,Hydrated for Adsorption,I-114Aluminium Hydroxide Oral Suspension, III-121Aluminium Hydroxide Oral Suspension, Magnesium Hydroxide and,III-401 Aluminium Hydroxide Tablets, Chewable,III-122Aluminium Hydroxide Tablets, Magnesium Hydroxide and,III-402 Aluminium Hydroxide Tablets see Chewable Aluminium Hydroxide Tablets,III-122Aluminium in Adsorbed Vaccines,V-463 Aluminium Magnesium Silicate,I-118 Aluminium Nitrate,V-A23Aluminium Oxide,Activated Acid,V-A23Aluminium Oxide,Anhydrous,V-A23 Aluminium Oxide,Basic,V-A23 Aluminium Oxide,Deactivated,V-A23 Aluminium Oxide G,V-A23 Aluminium Oxide,Neutral,V-A23 Aluminium Paste,Compound,III-120 Aluminium Phosphate Gel,I-120 Aluminium Phosphate,Hydrated see Dried Aluminium Phosphate Aluminium Potassium Sulfate,V-A23 Aluminium Potassium Sulphate,see Aluminium Potassium Sulfate Aluminium Powder,I-121Aluminium Salts,Reactions of,V-266 Aluminium Sodium Silicate,I-122 Aluminium Standard Solution(2ppm Al),V-A148Aluminium Standard Solution(10ppm Al),V-A148Aluminium Standard Solution(100ppm Al),V-A148Aluminium Standard Solution(200ppmAl),V-A148Aluminium Stearate,I-123Aluminium Sulfate,I-125,V-A23Aluminium Sulphate,see AluminiumSulfateAlverine Capsules,III-122Alverine Citrate,I-126,V-S7Amantadine Capsules,III-123Amantadine Hydrochloride,I-127Amantadine Oral Solution,III-124Amantidine,V-S8Amaranth S,V-A23Amaranth Solution,V-A23Ambroxol Hydrochloride,I-128Americium-243Spiking Solution,V-A23Amethocaine Eye Drops,see TetracaineEye DropsAmfetamine Sulfate,I-130Amfetamine Sulphote,see AmfetamineSulfate,I-130Amido Black10B Solution,V-A23Amidohexadecylsilyl Silica Gel forchromatography,V-A115Amidotrizoic Acid Dihydrate,I-130Amikacin,I-132Amikacin Injection,III-124Amikacin Sulfate,I-135Amiloride and Furosemide Tablets,seeCo-amilofruse TabletsAmiloride and Hydrochlorothiazide OralSolution,see Co-amilozide Oral SolutionAmiloride and HydrochlorothiazideTablets,see Co-amilozide TabletsAmiloride Hydrochloride,I-138Amiloride Tablets,III-125Amines,Primary Aromatic,Reactions of,V-266Amino Acid Analysis,V-221Amino Acid Analysis(2.2.56.)(5.8.),V-700Amino Acids,Use of Codes for,I-8,II-8,III-8,IV-8,V-8Aminoazobenzene,V-A23Aminobenzoic Acid,I-139,V-A23,V-A244-Aminobenzoic Acid Solution,V-A24(4-Aminobenzoyl)-L-glutamic Acid,V-A244-Aminobutanoic acid,see4-Amino-n-butyric Acid2-Aminobutan-1-ol,V-A24Aminocaproic Acid,I-1402-Amino-5-chlorobenzophenone,V-A24Aminochlorobenzophenone,see2-Amino-5-chlorbenzophenone4-Aminofolic Acid,V-A24Aminoglutethimide,I-141,V-S8Aminoglutethimide Tablets,III-126Aminohexadecylsilyl Silica Gel forChromatography,V-A1156-Aminohexanoic Acid,V-A24p-Aminohippuric Acid,V-A24Aminohippuric Acid Reagent,V-A244-Amino-3-hydroxynaphthalene-1-sulfonic Acid,V-A24Aminohydroxynaphthalenesulfonic AcidSolution,V-A24Aminohydroxynaphthalenesulfonic AcidSolution,Strong,V-A24AminohydroxynaphthalenesulphonicAcid Solution,Strong,seeAminohydroxynaphthalenesulfonic AcidSolution,StrongAminohydroxynaphthalenesulphonicAcid Solution,seeAminohydroxynaphthalenesulfonic AcidSolution4-Amino-3-hydroxynaphthalene-1-sulphonic Acid,see4-Amino-3-hydroxynaphthalene-1-sulfonic AcidAminohydroxynaphthalenesulphonic,Acid,see Aminonaphthalenesulfonic AcidSolution5-Aminoimidazole-4-carboxamideHydrochloride,V-A24cis-Aminoindanol,V-A24Aminomethylalizarindiacetic AcidReagent,V-A24Aminomethylalizarindiacetic AcidSolution,V-A253-Aminomethylalizarin-N,N-diaceticAcid,V-A244-Aminomethylbenzoic acid,V-A253-(Aminomethyl)pyridine,V-A258-Aminonaphthalene-2-sulfonic Acid,V-A25Aminonaphthalenesulfonic AcidSolution,V-A25Aminonaphthalenesulphonic AcidSolution,see AminonaphthalenesulfonicAcid Solution8-Aminonaphthalene-2-sulphonic Acid,see8-Aminonaphthalene-2-sulfonic Acid4-Amino-n-butyric Acid,V-A242-Amino-5-nitrobenzophenone,V-A25Aminonitrobenzophenone,see2-Amino-5-nitrobenzophenone4-Aminophenazone,V-A25Aminophenazone Solution,V-A253-Aminophenol,V-A254-Aminophenol-free Paracetamol,V-A99Aminophylline,I-143Aminophylline Hydrate,I-145Aminophylline Injection,III-128Aminophylline Tablets,III-128Aminophylline Tablets,Prolonged-release,III-129Aminopolyether,V-A253-Aminopropanol,V-A253-Aminopropionic Acid,V-A25Aminopropylmethylsilyl Silica Gel forChromatography,V-A115Aminopropylsilyl Silica Gel forChromatography,V-A115Aminopropylsilyl Silica Gel forChromatography R1,V-A115Aminopyrazolone,see4-AminophenazoneAminopyrazolone Solution,seeAminophenazone Solution3-Aminosalicylic Acid,V-A25Amiodarone,V-S8Amiodarone Concentrate,Sterile,III-130Amiodarone Hydrochloride,I-147Amiodarone Infusion,III-129Amiodarone Intravenous Infusion,seeAmiodarone Infusion,Amiodarone Oral Suspension,III-131Amiodarone Sterile Concentrate,III-130page numbers in bold type relate to monograph titles Index V-A801Amiodarone Tablets,III-132 Amisulpride,I-149,V-S9Amisulpride Oral Solution,III-133 Amisulpride Tablets,III-134 Amitriptyline Embonate,I-150 Amitriptyline Hydrochloride,I-151 Amitriptyline Tablets,III-135 Amlodipine Besilate,I-153 Ammonia,V-A25Ammonia(13N)Injection,IV-672 Ammonia Buffer pH9.5,see Ammonium Chloride Buffer Solution pH9.5 Ammonia Buffer pH10.9,V-A153 Ammonia Buffer pH10.9,Dilute,V-A153Ammonia Buffer pH10.0,V-A153 Ammonia,Chloride-free,V-A25 Ammonia,Concentrated,V-A25 Ammonia,Lead-free,V-A25 Ammonia,Methanolic,V-A25 Ammonia R1,Concentrated,V-A26 Ammonia R1,Dilute,V-A26 Ammonia R2,Dilute,V-A26 Ammonia R3,Dilute,V-A26 Ammonia Solution,Aromatic,III-136 Ammonia Solution,Concentrated see Strong Ammonia SolutionAmmonia Solution,Dilute,III-137 Ammonia Spirit,Aromatic,III-137 Ammoniacal Copper Oxide Solution,V-A46Ammoniacal Silver Nitrate Solution,V-A120Ammoniacal Solution of Copper Tetrammine,V-A46Ammonia-free Water,V-A139 Ammonio Methacrylate Copolymer (Type A),I-155Ammonio Methacrylate Copolymer (Type B),I-1560.5M Ammonium acetate buffer solution pH4.5,see Ammonium acetate buffer pH4.5,0.5M0.01M Ammonium and Cerium Nitrate, see Ammonium Cerium(IV)Nitrate VS 0.1M Ammonium and Cerium Sulfate, see Ammonium Cerium(IV)Sulfate VS Ammonium Acetate,V-A26 Ammonium acetate buffer pH4.5,0.5M, V-A153Ammonium Acetate Solution,V-A26 Ammonium Acetate Solution,Strong,III-137Ammonium and Cerium Nitrate,see Ammonium Cerium(IV)Nitrate Ammonium and Cerium Sulfate,see Ammonium Cerium(IV)Sulfate Ammonium and Cerium Sulphate,see Ammonium and Cerium Sulfate Ammonium Bicarbonate,I-157 Ammonium Bromide,I-158 Ammonium Carbamate,V-A26 Ammonium Carbonate,V-A26 Ammonium Carbonate Buffer Solution pH10.3,0.1M,V-A153Ammonium Carbonate Solution,V-A26 Ammonium Carbonate Solution,Dilute, V-A26Ammonium carbonate solution R1,V-A26Ammonium Cerium(IV)Nitrate,V-A26Ammonium Cerium(IV)Nitrate VS,V-A142Ammonium Cerium(IV)Sulfate,V-A26Ammonium Cerium(IV)Sulfate VS,V-A142Ammonium Cerium(IV)Sulphate VS,seeAmmonium Cerium(IV)Sulfate VSAmmonium Cerium(IV)Sulphate,seeAmmonium Cerium(iv)SulfateAmmonium Chloride,I-159,V-A26Ammonium Chloride Buffer SolutionpH10.0,see Ammonia Buffer pH10.0Ammonium Chloride Buffer SolutionpH10.4,V-A153Ammonium Chloride Buffer SolutionpH10.7,V-A153Ammonium Chloride Buffer SolutionpH9.5,V-A153Ammonium Chloride Buffer SolutionpH10.0,V-A153Ammonium Chloride Mixture,III-137Ammonium Chloride Oral Solution,III-137Ammonium Chloride Solution,V-A26Ammonium Citrate,V-A26Ammonium Citrate Solution,V-A26Ammonium CobaltothiocyanateSolution,V-A26Ammonium DihydrogenOrthophosphate,V-A26Ammonium Formate,V-A26Ammonium Glycyrrhizinate,I-160Ammonium Hexafluorogermanate,V-A26Ammonium Hydrogen Carbonate,V-A26Ammonium Hydrogen Carbonate seeAmmonium BicarbonateAmmonium Ichthosulphonate seeIchthammolAmmonium Iron(II)Sulfate,V-A26Ammonium Iron(II)Sulfate VS,V-A142Ammonium Iron(II)Sulphate VS,seeAmmonium Iron(II)Sulfate VSAmmonium Iron(II)Sulphate,seeAmmonium Iron(ii)SulfateAmmonium Iron(III)Citrate,V-A26Ammonium Iron(III)Sulfate,V-A26Ammonium Iron(III)Sulfate Solution R1,V-A26Ammonium Iron(III)Sulfate Solution R2,V-A26Ammonium Iron(III)Sulfate Solution R5,V-A26Ammonium Iron(III)Sulfate Solution R6,V-A27Ammonium Iron(III)Sulfate VS,V-A142Ammonium Iron(III)Sulphate SolutionR1,see Ammonium Iron(iii)SulfateSolution R1Ammonium Iron(III)Sulphate SolutionR2,see Ammonium Iron(iii)SulfateSolution R2Ammonium Iron(III)Sulphate SolutionR5,see Ammonium Iron(iii)SulfateSolution R5Ammonium Iron(III)Sulphate VS,seeAmmonium Iron(III)Sulfate VSAmmonium Iron(III)Sulphate,seeAmmonium Iron(iii)SulfateAmmonium Mercaptoacetate Solution,V-A27Ammonium Mercurithiocyanate Reagent,V-A27Ammonium Metavanadate,V-A27Ammonium Metavanadate Solution,V-A27Ammonium Molybdate,V-A27Ammonium Molybdate Reagent,V-A27Ammonium Molybdate Reagent R1,V-A27Ammonium Molybdate Reagent R2,V-A27Ammonium Molybdate Solution,V-A27Ammonium Molybdate Solution R2,V-A27Ammonium Molybdate Solution R3,V-A27Ammonium Molybdate Solution R4,V-A27Ammonium Molybdate Solution R5,V-A27Ammonium Molybdate Solution R6,V-A27Ammonium Molybdate-Sulfuric AcidSolution,V-A27Ammonium Molybdate-Sulphuric AcidSolution,see Ammonium Molybdate-Sulfuric Acid SolutionAmmonium Muriaticum,V-609Ammonium Nitrate,V-A27Ammonium Nitrate R1,V-A27Ammonium Oxalate,V-A27Ammonium Oxalate Solution,V-A27Ammonium Persulfate,V-A27Ammonium Persulphate,see AmmoniumPersulfateAmmonium Phosphate,see DiammoniumHydrogen OrthophosphateAmmonium Polysulfide Solution,V-A27Ammonium Polysulphide Solution,seeAmmonium Polysulfide SolutionAmmonium Pyrrolidinedithiocarbamate,V-A27Ammonium PyrrolidinedithiocarbamateSolution,V-A27Ammonium Reineckate,V-A27Ammonium Reineckate Solution,V-A28Ammonium Salts and Salts of VolatileBases,Reactions of,V-267Ammonium Salts Reactions of,V-266Ammonium Standard Solution(1ppmNH4),V-A148Ammonium Standard Solution(2.5ppmNH4),V-A148Ammonium Standard Solution(3ppmNH4),V-A148Ammonium Standard Solution(100ppmNH4),V-A148Ammonium Sulfamate,V-A28Ammonium Sulfate,V-A28Ammonium Sulfide Solution,V-A28Ammonium Sulphamate,see AmmoniumSulfamateAmmonium Sulphate,see AmmoniumSulfateAmmonium Sulphide Solution,seeAmmonium Sulfide SolutionV-A802IndexAmmonium Thiocyanate,V-A28 Ammonium Thiocyanate Solution,V-A28Ammonium Thiocyanate VS,V-A142 Ammonium Vanadate Solution,V-A28 Ammonium Vanadate,see Ammonium MetavanadateAmobarbital,I-161Amobarbital Sodium,I-162Amomum fruit,IV-56Amorphous Organosilica Polymer, Octadecylsilyl,V-A98Amoxicillin and Potassium Clavulanate Injection,see Co-amoxiclav Injection Amoxicillin and Potassium Clavulanate Oral Suspension,see Co-amoxiclav Oral SuspensionAmoxicillin and Potassium Clavulanate Tablets,Dispersible,see Dispersible Co-amoxiclav TabletsAmoxicillin and Potassium Clavulanate Tablets,see Co-amoxiclav Tablets Amoxicillin Capsules,III-138 Amoxicillin Injection,III-139 Amoxicillin Oral Suspension,III-141 Amoxicillin Sodium,I-163,V-S9 Amoxicillin Sodium for Injection,III-139Amoxicillin Trihydrate,I-165,V-S9,V-A28Ampere,Definition of,I-32,II-32,III-32,IV-32,V-32 Amperometric,Potentiometric and Voltametric Titrations,V-280 Amperometric Titration,V-280 Amphotericin,I-168Amphotericin B see Amphotericin Amphotericin for Infusion,III-142 Amphotericin Lozenges,I-xxix Amphotericin Oral Suspension,I-xxix Ampicillin,I-170Ampicillin Capsules,III-143Ampicillin Capsules,Flucloxacillin and, see Co-fluampicil CapsulesAmpicillin Injection,III-144Ampicillin Oral Suspension,III-146 Ampicillin Oral Suspension, Flucloxacillin and,see Co-fluampicil Oral SuspensionAmpicillin Sodium,I-172,V-S10 Ampicillin Sodium for Injection,III-144 Ampicillin Trihydrate,I-175,V-S10 Amyl Acetate,V-A28Amyl Alcohol,see Isoamyl Alcohola-Amylase,V-A28a-Amylase Solution,V-A28 Amylmetacresol,I-178,V-S10Amylose-derivative Silica Gel for Chromatography,V-A115b-Amyrin,V-A28Anacardium for Homoeopathic Preparations,IV-428Anaesthetic Ether,I-902Analytical Procedures,Validation of,V-673Analytical Sieving,Particle-size Distribution Estimation By,V-503 Anastrozole,I-179cis-Anethole,V-A28Anethum Graveolens L.Sowa Group,seeAnethum Graveolens Sowa Fruit,Anethum Graveolens Sowa Fruit,IV-58Angelica Archangelica Root,IV-59Angelica Dahurica Root,IV-60Angelica Pubescens Root,IV-62Angelica Sinensis Root,IV-63Angelica Sinensis Root,see ProcessedAngelica Sinensis RootAnhydrous Acetic Acid,V-A20Anhydrous Aluminium Oxide,V-A23Anhydrous Ampicilin see AmpicillinAnhydrous Azapropazone,V-S12Anhydrous Beclometasone Dipropionate,I-239Anhydrous Caffeine,see CaffeineAnhydrous Calcipotriol,I-353Anhydrous Calcium Acetate,see CalciumAcetateAnhydrous Calcium Chloride,V-A37Anhydrous Calcium Gluconate,I-372Anhydrous Calcium HydrogenPhosphate,I-377Anhydrous Calcium Lactate,I-378Anhydrous Chlorobutanol,I-518Anhydrous Citric Acid,I-569,V-A45Anhydrous Copper Sulfate,I-647Anhydrous Disodium HydrogenOrthophosphate,V-A59Anhydrous Disodium HydrogenPhosphate,I-788Anhydrous Docetaxel,I-796Anhydrous Ephedrine,I-849Anhydrous Formic Acid,V-A67Anhydrous Glucose,I-1083Anhydrous Iron(III)Chloride,V-A77Anhydrous Lactose,II-66Anhydrous Lithium Metaborate,V-A81Anhydrous Magnesium Citrate,II-166Anhydrous Methanol,V-A85Anhydrous Morphine,V-A91Anhydrous Nevirapine,II-358Anhydrous Niclosamide,II-362Anhydrous Paroxetine Hydrochloride,II-504Anhydrous Phloroglucinol,II-566Anhydrous Pyridine,V-A110Anhydrous Silica Gel,V-A114Anhydrous Silica,HydrophobicColloidal,II-807Anhydrous Sodium Acetate,V-A120Anhydrous Sodium Carbonate,II-830,V-A121,V-A141Anhydrous Sodium DihydrogenOrthophosphate,V-A122Anhydrous Sodium DihydrogenPhosphate,II-839,V-A122Anhydrous Sodium Sulfate,II-872,V-A124Anhydrous Sodium Sulfite,II-873,V-A124Anhydrous Sodium Sulphate seeAnhydrous Sodium SulfateAnhydrous Sodium Sulphite seeAnhydrous Sodium SulfiteAnhydrous Torasemide,II-1066Anhydrous Valaciclovir Hydrochloride,II-1134Aniline,V-A28Aniline Hydrochloride,V-A28Aniline Hydrochloride Solution,V-A28Animal Spongiform EncephalopathyAgents Via Human and VeterinaryMedicinal Products,Minimising theRisk of Transmitting,V-611Animals,Use of,I-15,II-15,III-15,IV-15,V-15Anion Exchange Resin,V-A28Anion Exchange Resin forChromatography,Strongly Basic,V-A28Anion Exchange Resin R1,V-A28Anion Exchange Resin R2,V-A28Anion exchange resin R3,V-A29Anion Exchange Resin,Strongly Basic,V-A28Anion Exchange Resin,Weak,V-A29Anion-exchange Resin forChromatography,Strongly Basic R1,V-A28Anionic Emulsifying Wax,see EmulsifyingWaxAnisaldehyde,V-A29Anisaldehyde Solution,V-A29Anisaldehyde Solution R1,V-A29Anise Ketone,V-A29Anise Oil,IV-71Anise Water,Concentrated,IV-73Aniseed,IV-66Aniseed Oil,see Anise Oilp-Anisidine,V-A29Anisidine Value,V-326Anolyte for Isoelectric Focusing pH3to5,V-A29Antazoline Hydrochloride,I-181Anthracene,V-A29Anthranilic Acid,see2-Aminobenzoic AcidAnthrax,see Anthrax Vaccine for HumanUse(Adsorbed,Prepared from CultureFiltrates)Anthrax Vaccine for Human Use(Adsorbed,Prepared from CultureFiltrates),IV-527Anthrone,V-A29Anthrone Reagent,V-A29Antibiotics,Microbiological Assay of,V-396,V-655Antibiotics,Potency of,I-14,II-14,III-14,IV-14,V-14Anticoagulant and Preservative Solutionsfor Blood,IV-461Anti-D Immunoglobulin for IntravenousUse,IV-497Anti-D(Rh0)Immunoglobulin,IV-496Antimicrobial Preservation,Efficacy of,V-494,V-653Antithrombin III ConcentrateAnticomplimentary activity ofimmunoglobulin,Test for V-427Anti-D immunoglobulin,human,Assayof V-429Anti-D antibodies in humanimmunoglobulin V-431Anti-A and anti-B haemogglutininsV-432Antimicrobial Preservatives,Definition ofSuitable,I-11,II-11,III-11,IV-11,V-11Antimony Compounds,Reactions of,V-267page numbers in bold type relate to monograph titles Index V-A803。

伯乐1708895系列说明书

Reaction ProtocolIncubate complete reaction mix in a real-time thermal detection system as follows:cDNA synthesis:10 min at 50°CiScript reverse transcriptase inactivation: 5 min at 95°CPCR cycling and detection (30 to 45 cycles):10 to 15 sec at 95°C30 sec at 55°C to 60°C (data collection step) Recommendations for optimal results using the iScript One-Step RT-PCR Kit for ProbesProbe and primers should be designed according to standard qPCR guidelines.Suggested input quantities of template are: 1 pg to 1 µg total RNA; 10 fg to 100 ng polyA(+) RNA.First strand synthesis can be performed between 40°C and 52°C. Optimal results are generally obtained with a 10-minute incubation at 50°C. Incubation at temperatures higher than 50°C can delay or eliminate the detection of some non-specific amplification artifacts. However, this may also delay the C t for detection of specific targets. We also recommend a 5-minute incubation at 95°C to fully inactive the reverse transcriptase prior to PCR cycling.Thaw all components, except the iScript reverse transcriptase, at room temperature. Mix gently, but thoroughly, and then centrifuge at 4°C to collect contents to the bottom of the tube. Chill on ice before using. Centrifuge again briefly at 4°C if needed. Preparation of a reaction cocktail is crucial in quantitative PCR applications to reduce pipetting errors and maximize assay precision and accuracy. Assemble the reaction cocktail with all required components except sample template (total RNA) and dispense equal aliquots into each reaction tube. Add target sample to each reaction as the final step. Addition of sample as 5–10 µl volumes will improve assay precision. Replicate samples should be assembled as a master mix with a single addition of sample template.Reagents and Materials Not SuppliedGene-specific primers and probePipet tips, aerosol barrier tips, such as:Xcluda®Style B, 211-2006Nuclease-free tubes or plates, such as:0.2 ml thin-wall tubes, 223-9473 or plates, 223-9441RNA purification kit, such as:Aurum™total RNA mini kit, 732-6820, orAurum total RNA kit, 2 x 96 well, 732-6800To learn more about Bio-Rad's complete solution for Amplification, visit our website:/genomicsNOTICE TO PURCHASER: LIMITED LICENSEPractice of the patented polymerase chain reaction (PCR) process requires a license. The Bio-Rad real-time detection systems include a licensed thermal cycler and may be used with PCR licenses available from Applied Biosystems. Its use with authorized reagents also provides a limited PCR license in accordance with the label rights accompanying such reagents. Some applications may require licenses from other parties. Aurum, iScript, iTaq, iQ, iCycler,Xcluda, and MyiQ are trademarks of Bio-Rad Laboratories. SYBR Green is a registered trademark of Molecular Probes, Inc. Bio-Rad Laboratories, Inc. is licensed by Molecular Probes, Inc. to sell reagents containing SYBR Green I for use in real-time PCR, for research purposes only.A license to perform the patented 5’ Nuclease Process for research is obtained by the purchase of (i) both Authorized 5’ Nuclease Core Kit and Licensed Probe, (ii) a Licensed5’ Nuclease Kit, or (iii) license rights from Applied Biosystems.This product is an Authorized 5’ Nuclease Core Kit. Use of this product is covered by one or more of the following US patents and corresponding patent claims outside the US: 5,079,352, 5,789,224, 5,618,711, 6,127,155, 5,677,152, (Claims 1-23 only), 5,773,258, (claims 1 and 6 only), 5,407,800, 5,322,770, 5,310,652, 5,210,015, 5,487,972, and claims outside the US corresponding to US Patent No. 4,889,818. The purchase of this product includes a limited, non-transferable immunity from suit under the foregoing patent claims for using only this amount of product for the purchaser’s own internal research. Separate purchase of a Licensed Probe would convey rights under the applicable claims on US Patents Nos. 5,538,848, 5,723,591, 5,876,930, 6,030,787, 6,258,569, 5,804,375 (claims 1-12 only), and 6,214,979, and corresponding claims outside the United States. No right under any other patent claim and no right to perform commercial services of any kind, including without limitation reporting the results of purchaser’s activities for a fee or other commercial consideration, is conveyed expressly, by implication, or by estoppel. This product is for research use only. Diagnostic uses under Roche patents require a separate license from Roche. Further information on purchasing licenses may be obtained from the Director of Licensing, Applied Biosystems, 850 Lincoln Centre Drive, Foster City, California 94404, USA.Bio-Rad Laboratories2000 Alfred Nobel Drive, Hercules, CA 94547510-741-10004106270 Rev C。

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