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050 4 |a RS189  |b .S47 2000 
060 4 |a 2001 D-427 
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084 |a JG 08  |2 blsrissc 
245 0 0 |a Separation methods in drug synthesis and purification /  |c edited by Kl�ara Valk�o. 
260 |a Amsterdam ;  |a New York :  |b Elsevier,  |c 2000. 
300 |a 1 online resource (xxi, 589 pages) :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Handbook of analytical separations ;  |v v. 1 
504 |a Includes bibliographical references and index. 
588 0 |a Print version record. 
506 |3 Use copy  |f Restrictions unspecified  |2 star  |5 MiAaHDL 
533 |a Electronic reproduction.  |b [Place of publication not identified] :  |c HathiTrust Digital Library,  |d 2010.  |5 MiAaHDL 
538 |a Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002.  |u http://purl.oclc.org/DLF/benchrepro0212  |5 MiAaHDL 
583 1 |a digitized  |c 2010  |h HathiTrust Digital Library  |l committed to preserve  |2 pda  |5 MiAaHDL 
505 0 |a Front Cover -- Separation Methods in Drug Synthesis and Purification -- Copyright Page -- Contents -- Editor's Preface -- Series Editor's Preface -- List of Contributors -- Chapter 1. Comparison of various modes and phase systems for analytical HPLC -- 1.1 Fundamentals of HPLC -- 1.2 Chromatographic column and column packing particles -- 1.3 Separation modes in HPLC -- 1.4 Method development and optimisation of conditions in isocratic HPLC -- 1.5 Development of gradient-elution separations -- 1.6 Acknowledgements -- 1.7 References -- Chapter 2. Fast generic HPLC methods -- 2.1 Introduction. 
505 8 |a 2.2 Theory -- 2.3 Strategy for production of fast gradients -- 2.4 Fast gradients in practice -- 2.5 References -- Chapter 3. Application of standard methods in capillary electrophoresis for drug analysis -- 3.1 Introduction to capillary electrophoresis -- 3.2 Analysis of pharmaceuticals by CE -- 3.3 Low-pH buffer for analysis of basic drugs -- 3.4 High-pH buffer for analysis of acidic drugs -- 3.5 Micellar electrokinetic chromatography (MEKC) for neutral and/or charged drugs -- 3.6 Microemulsion electrokinetic chromatography (MEEKC) for neutral and/or charged drugs. 
505 8 |a 3.7 Indirect UV detection method for analysis of inorganic anions -- 3.8 Indirect UV detection method for analysis of simple organic acids -- 3.9 Indirect UV detection method for analysis of metal ions -- 3.10 Non-aqueous CE for analysis of acidic and basic drugs -- 3.11 Benefits of adopting standard CE methods -- 3.12 References -- Chapter 4. Capillary electrochromatography (CEC) -- 4.1 Introduction -- 4.2 Basic principles of capillary electrochromatography -- 4.3 Mobile phase composition -- 4.4 Stationary phases used in CEC -- 4.5 Operational characteristics of CEC. 
505 8 |a 4.6 Gradient and pressure-assisted (pseudo) CEC -- 4.7 Conclusions -- 4.8 Glossary of symbols -- 4.9 References -- Chapter 5. Coupled chromatography-mass spectrometry techniques for the analysis of combinatorial libraries -- 5.1 Introduction -- 5.2 LC/MS analysis of high-throughput parallel synthesis libraries -- 5.3 Example for monitoring the rehearsal phase of the synthesis of a solid-phase library -- 5.4 LC/UV/MS as a pre-screen for autoprep-solution phase -- 5.5 Assisted automated LC/MS analysis -- 5.6 The analysis of split-pool combinatorial libraries -- 5.7 Conclusions and future. 
505 8 |a 5.8 References -- Chapter 6. Optimization strategies for HPLC and CZE -- 6.1 Introduction -- 6.2 Responses and response functions -- 6.3 Univariate optimization strategies -- 6.4 Factorial methods -- 6.5 Mixture designs -- 6.6 Robustness/ruggedness -- 6.7 The simplex sequential approach -- 6.8 Automating the whole process: expert systems and knowledge based systems -- 6.9 References -- Chapter 7. Strategies for the development of process chromatography as a unit operation for the pharmaceutical industry -- 7.1 Introduction -- 7.2 The process development cycle. 
520 |a Separation Methods in Drug Synthesis and Purification. 
650 0 |a Drugs  |x Analysis. 
650 0 |a Drug development. 
650 0 |a Separation (Technology) 
650 0 |a Pharmaceutical chemistry. 
650 1 2 |a Chemistry, Pharmaceutical  |x methods  |0 (DNLM)D002626Q000379 
650 2 2 |a Chemistry, Analytical  |x methods 
650 2 2 |a Pharmaceutical Preparations  |x isolation & purification  |0 (DNLM)D004364Q000302 
650 2 |a Chemistry, Pharmaceutical  |0 (DNLM)D002626 
650 6 |a M�edicaments  |x Analyse.  |0 (CaQQLa)201-0036381 
650 6 |a M�edicaments  |x D�eveloppement.  |0 (CaQQLa)201-0306620 
650 6 |a S�eparation (Technologie)  |0 (CaQQLa)201-0000375 
650 6 |a Chimie pharmaceutique.  |0 (CaQQLa)201-0028674 
650 7 |a MEDICAL  |x Drug Guides.  |2 bisacsh 
650 7 |a MEDICAL  |x Pharmacology.  |2 bisacsh 
650 7 |a MEDICAL  |x Pharmacy.  |2 bisacsh 
650 7 |a MEDICAL  |x Nursing  |x Pharmacology.  |2 bisacsh 
650 7 |a Drug development  |2 fast  |0 (OCoLC)fst00898670 
650 7 |a Drugs  |x Analysis  |2 fast  |0 (OCoLC)fst00898769 
650 7 |a Pharmaceutical chemistry  |2 fast  |0 (OCoLC)fst01060115 
650 7 |a Separation (Technology)  |2 fast  |0 (OCoLC)fst01112723 
655 4 |a Internet Resources. 
700 1 |a Valk�o, Kl�ara. 
776 0 8 |i Print version:  |t Separation methods in drug synthesis and purification.  |d Amsterdam ; New York : Elsevier, 2000  |z 0444500073  |z 9780444500076  |w (OCoLC)45486148 
830 0 |a Handbook of analytical separations ;  |v v. 1. 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780444500076  |z Texto completo 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/handbooks/15677192/1  |z Texto completo 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/bookseries/15677192/1  |z Texto completo