| Поиск по каталогу |
|
(строгое соответствие)
|
- Профессиональная
- Научно-популярная
- Художественная
- Публицистика
- Детская
- Искусство
- Хобби, семья, дом
- Спорт
- Путеводители
- Блокноты, тетради, открытки
UV AND HPLC Method Development and Method Validation of Nevirapine. UV AND HPLC Method Development and Validation of Nevirapine in Bulk and Pharmaceutical dosage forms
В наличии
| Местонахождение: Алматы | Состояние экземпляра: новый |
Бумажная
версия
версия
Автор: Tirthankar Choudhury
ISBN: 9786200218094
Год издания: 2019
Формат книги: 60×90/16 (145×215 мм)
Количество страниц: 108
Издательство: LAP LAMBERT Academic Publishing
Цена: 34613 тг
Положить в корзину
| Способы доставки в город Алматы * комплектация (срок до отгрузки) не более 2 рабочих дней |
| Самовывоз из города Алматы (пункты самовывоза партнёра CDEK) |
| Курьерская доставка CDEK из города Москва |
| Доставка Почтой России из города Москва |
Аннотация: This research work focused on UV and RP-HPLC method and method validation of Nevirapine accurately and economically. UV spectrophotometric method and mehod development for Nevirapine obeyed Beer's law as depicted by linearity of the developed method. A reverse phase HPLC (RP-HPLC) method is described for the determination of nevirapine in tablet dosage forms. Chromatography was carried on an ODS column using a mixture of methanol and water (89:11 v/v) as the mobile phase at a flow rate of 1 mL/min with detection at 284 nm. The method was validated by determining its sensitivity, accuracy and precision. The proposed method is simple, economical, fast, accurate and precise, hence can be applied for routine quality control of nevirapine in bulk and tablet dosage forms.
Ключевые слова: Nevirapine, RP-HPLC, UV, Estimation, Tablet dosage forms
Похожие издания
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Suvarna Ningal,Ramesh Kalkotwar and Manoj Kothule RP-HPLC Method Development & Validation for Pregabalin & Aceclofenac. Development & Validation of Stability Indicating RP-HPLC Method For Simultaneous Estimation of Pregabalin & Aceclofenac. 1905 г., 104 стр., мягкий переплет The aim of present work was to perform stability indicating method and validation of Aceclofenac and Pregabalin in bulk drug and solid dosage form. The proposed simultaneous estimation method was found to be simple, precise, accurate and rapid for the determination of Aceclofenac and Pregabalin. The mobile phase is simple to prepare and... | 37113 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Ramana Hechhu,Tamrat Balcha Balla and R. Vasanthi RP-HPLC Method Development and Validation. Estimation of Thiocolchicoside and Lornoxicam in bulk and Pharmaceutical dosage forms. 1905 г., 112 стр., мягкий переплет High performance liquid chromatography is at present one of the most sophisticated tool of the analysis. The estimation of Thiocolchicoside and Lornoxicam was done by RP-HPLC. The Phosphate buffer was pH 3.0 and the mobile phase was optimized with consists of Methanol: Phosphate buffer mixed in the ratio of 70:30 % v/ v. Inertsil C18 column C18... | 34755 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика PRAFULLA KUMAR SAHU HPLC analysis of antihypertensive drugs in combined therapies. A beginner's guide for HPLC method development & validation. 2020 г., 92 стр., мягкий переплет The use of antihypertensive agents in combination is common. To decrease the pill burden, lower the prescription costs and improve patient compliance; combination antihypertensive therapies compile two or more active drugs. Thiazide diuretics are frequently recommended as one of the first-line therapy for the treatment of hypertension in... | 34044 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Rohit Bhatia,Ajay Kumar and Rajat Rana Estimation of Drug Combinations and Food Colorants by UV & HPLC. Method Development, Validation and Photostability Protocols. 2020 г., 180 стр., мягкий переплет Analytical method is the one by which we can easily quantify the drug in its form or in pharmaceutical dosages form. With the growth of pharmaceutical industry during last several years, there has been rapid progress in the field of pharmaceutical analysis to provide simple analytical procedure for complex formulation. For new drugs, sometimes the... | 46153 тг |
 | Отрасли знаний: Общественные науки -> Экономика Ranabir Chanda ANALYSIS OF EPLARESTAT-PRAGABALIN BY RP-HPLC. METHOD DEVELOPMENT AND VALIDATION FOR THE SIMULTANEOUS ESTIMATION OF EPLARESTAT-PRAGABALIN BY RP-HPLC. 2020 г., 100 стр., мягкий переплет A basic, Accurate, exact strategy was produced for the concurrent estimation of the Epalrestat and Pregabalin in Tablet dose shape. Chromatogram was go through Std Kromasil 250 x 4.6 mm, 5m. Portable stage containing Buffer: Acetonitrile taken in the proportion 60:40 was pumped through section at a stream rate of 1 ml/min. Cradle utilized as a... | 34328 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Sana Shamim Interaction Studies. Metal Complexes, RP-HPLC Method development, Analogue Synthesis,Spectroscopy, Antimicrobial and Enzymatic Activity. 2012 г., 260 стр., мягкий переплет The book deals with the metal complexes of Azithromycin, a macrolide and gemifloxacin, fourth generation fluoroquinolone antibacterial which were synthesized characterized and their antimicrobial activities against various Gram negatives, Gram positives and antifungal species were analyzed. Interaction of gemifloxacin with co-administered drugs... | 52747 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Pankaj Sachdeva,Jimish R. Patel and Anil Middha RP-HPLC Method Development in Nitazoxanide. RP-HPLC Method Development & Validation for determination of percentage content in Nitazoxanide. 2012 г., 84 стр., мягкий переплет A simple, fast and precise (RP-HPLC) reversed phase high performance liquid chromatographic method is developed for the determination of Nitazoxanide. The linearity of Nitazoxanide was found in the range of 50 to 150 ?g/ml. The recovery was calculated by standard addition method. The average recovery was found to be 99.81% for our product. The... | 30642 тг |
 | Отрасли знаний: Точные науки -> Математика -> Анализ Anish Pradhan and Bhupendra Shrestha HPLC Method Development. . 2018 г., 84 стр., мягкий переплет Imatinib mesylate is a promising drug used for targeted therapy in chronic myleiodleukemia. As with any other anticancer drugs, this drug too leads to immunosuppression in the patients which may cause severe infectious diseases. Generally preferred antibiotic class in this case is fluoroquinolones and moxifloxacin being one of the advanced new... | 25834 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Somsubhra Ghosh and Sowjanya Bomma RP-HPLC Method Development & Validation of Vilazodone Hydrocholoride. . 2018 г., 64 стр., мягкий переплет Vilazodone is a serotonergic antidepressant developed by Clinical Data for the treatment of major depressive disorder. The chemical compound was originally developed by Merck KGaA (Germany). Vilazodone was approved by the FDA for use in the United States to treat major depressive disorder in January 21, 2011. Vilazodone acts as a serotonin... | 23010 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Somsubhra Ghosh,B. V. V. Ravikumar and Beduin Mohanti HPLC Method Development of Fingolimod. A new RP HPLC method developmental & validation of Fingolimod HCL. 2015 г., 60 стр., мягкий переплет Multiple sclerosis is the most common chronic inflammatory disease of the central nervous system and it is the leading cause of neurological disability in young adults. Fingolimod Hydrochloride is the first oral drug approved by the USFDA for treating multiple sclerosis. Fingolimod is a sphingosine 1-phosphate receptor modulator, which sequesters... | 24982 тг |
 | Отрасли знаний: Точные науки -> Математика -> Анализ Shubhangi Sutar,Shitalkumar Patil and Sachin Pishavikar Degradation Study Of Tenofovir Disoproxil Fumarate. RP-HPLC Method Development. 2014 г., 68 стр., мягкий переплет Stability indicating RP-HPLC method for estimation of Tenofovir Disoproxil Fumarate in the presence of its degradation products during conduction of stability studies on the pure drug which was carried out by using a mobile phase comprising ACN: Water (70:30 v/v), pH adjusted to 4.5with OPA,, at flow rate of 1 ml/min. with UV detection at 260 nm.... | 25266 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Meghal V. Modi Development and Validation of Stability Indicating RP-HPLC Method. Development and Validation of Stability Indicating RP-HPLC Method for Dexibuprofen. 2014 г., 68 стр., мягкий переплет Newly developed and validated reverse phase high performance liquid chromatography (RP-HPLC) method for the quantitative analysis of dexibuprofen. We could also develop and validate stability indicating RP-HPLC methods for dexibuprofen. RP-HPLC method was developed for the determination of dexibuprofen in single dosage forms. Stability... | 28436 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Somsubhra Ghosh First & New RP- HPLC Method Development of Rilpivirine. . 2013 г., 92 стр., мягкий переплет Relpivirine is a noble antiretroviral drug widely used now a days. Quality control of any molecule is very important & difficult task for an analyst. If the molecule is brand new, its adds up even more difficulties. Recently this drug has received USFDA approval, but as of now no single method is available to determine the Drug by using RP -... | 34044 тг |
 | Отрасли знаний: Медицина -> Фармакология и фармацевтика Pratik Mehta Novel Spectrophotometric and HPLC Method Development and Validation. For Multi Ingredient Cough Suppressants and a Haematinic Preparation. 2013 г., 152 стр., мягкий переплет Drug manufacturing control requires high level and intensive analytical and chemical support of all stages to ensure the drug's quality and safety. Highly specific and sensitive analytical techniques hold the key to the design, development, standardization and quality control of medicinal products. The book is focussed on development and... | 38342 тг |
 | Отрасли знаний: Естественные науки -> Химия Ghulam Shabir HPLC Method Development and Validation in Pharmaceutical Analysis. Handbook for Analytical Scientists. 2013 г., 492 стр., мягкий переплет This handbook is concerned with new chromatographic method development and validation using novel systematic approaches for pharmaceutical compounds. The first stage of the research was to study how method development and validation are typically carried out at present and to formulate this into a simple step-by-step approach. Such a template and... | 60988 тг |