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 |