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                             44 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A developed and validated stability-indicating reverse-phase high performance liquid chromatographic method for determination of cefdinir in the presence of its degradation products as per International Conference on Harmonization guidelines Hamrapurkar, Purnima
2011
1 p. 15-20
6 p.
artikel
2 A simple and precise method for quantitative analysis of lumefantrine by planar chromatography Hamrapurkar, Purnima
2010
1 p. 44-48
5 p.
artikel
3 Assay of tianeptine sodium in bulk and its marketed formulations by extraction visible spectrophotometry Buridi, Kalyana Ramu
2013
1 p. 30-32
3 p.
artikel
4 A validated HPTLC method for estimation of moxifloxacin hydrochloride in tablets Dhillon, Vandana
2010
1 p. 54-56
3 p.
artikel
5 A validated method for development of atovaquone as API and tablet dosage forms by UV spectroscopy Patel, Kalpesh N.
2010
1 p. 61-64
4 p.
artikel
6 A validated RP-HPLC-UV/DAD method for simultaneous quantitative determination of rosmarinic acid and eugenol in Ocimum sanctum L. Domlur Thyagaraj, Vishruta
2013
1 p. 1-5
5 p.
artikel
7 A validated stability indicating HPTLC method for simultaneous estimation of irbesartan and hydrochlorothiazide Khodke, Amol S.
2010
1 p. 39-43
5 p.
artikel
8 A validated ultra high-pressure liquid chromatography method for separation of candesartan cilexetil impurities and its degradents in drug product Sudhakar Babu, K.
2012
1 p. 31-39
9 p.
artikel
9 Bioanalysis in drug discovery and development Pandey, Saurabh
2010
1 p. 14-24
11 p.
artikel
10 Bioanalytical method validation: An updated review Tiwari, Gaurav
2010
1 p. 25-38
14 p.
artikel
11 Development and validation of reversed phase- high-performance liquid chromatography method for determination of paracetamol and lornoxicam in tablet dosage form Jain, Deepak Kumar
2011
1 p. 42-46
5 p.
artikel
12 Development and validation of the liquid chromatographic method for simultaneous estimation of metformin, pioglitazone, and glimepiride in pharmaceutical dosage forms Pandit, Vinay
2012
1 p. 9-13
5 p.
artikel
13 Development and validation of the simultaneous UV spectrophotometric method for estimation of metoprolol succinate and olmesartan medoxomil in the tablet dosage form Vora, Bindi N.
2012
1 p. 44-47
4 p.
artikel
14 Development and validation of zero and first-order derivative area under curve spectrophotometric methods for the determination of entacapone in bulk material and in tablets Chalikwar, S.S.
2012
1 p. 14-17
4 p.
artikel
15 Development of the UV spectrophotometric method of Olmesartan medoxomil in bulk drug and pharmaceutical formulation and stress degradation studies Patel, Jaydeep
2011
1 p. 36-41
6 p.
artikel
16 Editorial Board 2013
1 p. i-
1 p.
artikel
17 HPTLC validated stability indicating assay method for marketed herbal antihypertensive formulations Deore, Sharada L.
2013
1 p. 11-15
5 p.
artikel
18 Instructions for Authors 2011
1 p. 67-70
4 p.
artikel
19 Introduction to hyphenated techniques and their applications in pharmacy Patel, Kalpesh N.
2010
1 p. 2-13
12 p.
artikel
20 Ion-pair spectrophotometric estimation of gemifloxacin Sahu, Satyabrata
2012
1 p. 26-30
5 p.
artikel
21 Isolation and determination of deoxynivalenol by reversed-phase high-pressure liquid chromatography Gupta, Vikas Kumar
2011
1 p. 25-29
5 p.
artikel
22 Method validation: A complex concept Furey, Ambrose
2011
1 p. 1-2
2 p.
artikel
23 Optimization and validation of spectrophotometric methods for determination of finasteride in dosage and biological forms Amin, Alaa S.
2012
1 p. 48-55
8 p.
artikel
24 Plant metobolomics - A novel method in phytochemical analysis Mueen, Ahmed K.K.
2010
1 p. 65-66
2 p.
artikel
25 Quantitative estimation of diacerein in bulk and in capsule formulation using hydrotropic solubilizing agents by UV-spectrophotometry and the first order derivative using the area under curve method Pandey, Ramchandra
2012
1 p. 4-8
5 p.
artikel
26 Recent updates on codeine Bhandari, Monika
2011
1 p. 3-8
6 p.
artikel
27 Reviewers, 2011 2012
1 p. 56-
1 p.
artikel
28 Reviwers 2010 2011
1 p. 66-
1 p.
artikel
29 Simple spectrophotometric methods for estimation of aceclofenac from bulk and formulations Bose, A.
2010
1 p. 57-60
4 p.
artikel
30 Simultaneous determination of aspirin and esomeprazole magnesium in combined tablets by validated UPLC method Malisetty, Shravan Kumar
2013
1 p. 26-29
4 p.
artikel
31 Simultaneous determination of losartan, losartan acid and amlodipine in human plasma by LC-MS/MS and its application to a human pharmacokinetic study Karra, Vijaya Kumari
2012
1 p. 18-25
8 p.
artikel
32 Simultaneous determination of paracetamol and lornoxicam by RP-HPLC in bulk and tablet formulation Attimarad, Mahesh
2011
1 p. 61-66
6 p.
artikel
33 Simultaneous estimation of amlodipine besylate and nebivolol hydrochloride in tablet dosage forms by reverse phase-high-performance liquid chromatographic using ultraviolet detection Sharma, Deepak
2011
1 p. 9-14
6 p.
artikel
34 Spectrofluorimetric estimation of salbutamol sulphate in différent dosage forms by formation of inclusion complex with β-cyclodextrin Pandya, Harshit Narmadashankar
2010
1 p. 49-53
5 p.
artikel
35 Spectrophotometric estimation of solifenacin succinate in tablet formulations Singh, Lokesh
2011
1 p. 21-24
4 p.
artikel
36 Spectrophotometric estimation of tamsulosin hydrochloride by acid-dye method Shrivastava, Alankar
2011
1 p. 53-60
8 p.
artikel
37 Spectrophotometric simultaneous determination of Tenofovir disoproxil fumarate and Emtricitabine in combined tablet dosage form by ratio derivative, first order derivative and absorbance corrected methods and its application to dissolution study Choudhari, Vishnu P.
2011
1 p. 47-52
6 p.
artikel
38 Stability-indicating stress degradation studies of lafutidine using UV spectrophotometric method Jadhav, Kiran V.
2013
1 p. 21-25
5 p.
artikel
39 Stability of temozolomide in solutions aimed for oral treatment prepared from a commercially available powder for infusion Nygren, Helen
2012
1 p. 1-3
3 p.
artikel
40 Stress degradation studies and development of a validated stability-indicating-assay-method for determination of diacerein in presence of degradation products Hamrapurkar, Purnima
2011
1 p. 30-35
6 p.
artikel
41 Utilization of reversed-phase TLC and topological indices to the lipophilicity investigations of naproxen Pyka, Alina
2013
1 p. 16-20
5 p.
artikel
42 UV-visible spectrophotometric simultaneous estimation of paracetamol and nabumetone by AUC method in combined tablet dosage form Rote, Ambadas R.
2012
1 p. 40-43
4 p.
artikel
43 Validated liquid chromatographic method for quantitative determination of Rufinamide active pharmaceutical ingredient form and its impurities Parashar, Vikas
2013
1 p. 6-10
5 p.
artikel
44 Welcome to Pharmaceutical Methods Furey, Ambrose
2010
1 p. 1-
1 p.
artikel
                             44 gevonden resultaten
 
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