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[null,"1.","Record Nr.",null,"UNISA990000265490203316"]
[null,null,"Autore",null,"Lowe, John P."]
[null,null,"Titolo",null,"Quantum chemistry / John P. Lowe"]
[null,null,"Pubbl/distr/stampa",null,"San Diego [etc.] : Academic Press, copyr. 1993"]
[null,null,"ISBN",null,"0-12-457555-2"]
[null,null,"Edizione",null,"[2nd ed]"]
[null,null,"Descrizione fisica",null,"XX, 711 p. : ill. ; 23 cm"]
[null,null,"Disciplina",null,"54128"]
[null,null,"Collocazione",null,"541.28 LOW"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,"2.","Record Nr.",null,"UNINA9910350350903321"]
[null,null,"Autore",null,"Maithani Mukesh"]
[null,null,"Titolo",null,"Development of Novel Stability Indicating Methods Using Liquid Chromatography / / by Mukesh Maithani, Parveen Bansal"]
[null,null,"Pubbl/distr/stampa",null,"Singapore : , : Springer Singapore : , : Imprint : Springer, , 2019"]
[null,null,"ISBN",null,"981-13-8723-0"]
[null,null,"Edizione",null,"[1st ed. 2019.]"]
[null,null,"Descrizione fisica",null,"1 online resource (xxii, 101 pages)"]
[null,null,"Disciplina",null,"616.075"]
[null,null,"Soggetti",null,"Diagnosis, Laboratory"]
[{"$nulls":4},"Pharmaceutical technology"]
[{"$nulls":4},"Chromatographic analysis"]
[{"$nulls":4},"Pharmacy"]
[{"$nulls":4},"Laboratory Medicine"]
[{"$nulls":4},"Pharmaceutical Sciences/Technology"]
[{"$nulls":4},"Chromatography"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,"Nota di contenuto",null,"Chapter 1. Introduction -- Chapter 2. Research Envisaged -- Chapter 3. Drug(s) Profile -- Chapter 4. Materials and Methods -- Chapter 5. Results and Discussion -- Chapter 6. Summary and Conclusion.-."]
[null,null,null,"Sommario/riassunto","Reversed-phase high-performance liquid chromatography (RP-HPLC) has become the most widely used method for pharmaceutical analysis, as it ensures accuracy, specificity and reproducibility for the quantification of drugs, while avoiding interference from any of the excipients that are normally present in pharmaceutical dosage forms. This book presents a simple methodology for developing stability-indicating methods and offers a ‘how-to guide’ to creating novel stability-indicating methods using liquid chromatography. It provides the detailed information needed to devise a stability-indicating method for drug substances and drug products that comply with international regulatory guidelines. As such, it is a must-read for anyone engaged in analytical and bioanalytical chemistry: professionals at reference, test, and control laboratories; students and academics at research laboratories, and scientists working for chemical, pharmaceutical, and biotechnology companies."]