SCOPUS 정보 검색 플랫폼

Volumn 71, Issue 1-2, 2010, Pages 95-100

Stability indicating fast LC for the simultaneous estimation of intermediates and degradants of duloxetine hydrochloride

(4) Reddy, Paluru Rudra Mohan a Sreeramulu, J a Naidu, Petla Y b Reddy, A Rajasekhara b

a SRI KRISHNADEVARAYA UNIVERSITY (India)

b SIPCOT Industrial Park (India)

Author keywords

Drug products; Duloxetine; Liquid chromatography; Stability sample analysis

Indexed keywords

DULOXETINE; PHOSPHATE;

ACCURACY; ARTICLE; CONTROLLED STUDY; DRUG STRUCTURE; ELUTION; FLOW RATE; PRIORITY JOURNAL; REVERSED PHASE LIQUID CHROMATOGRAPHY; SENSITIVITY AND SPECIFICITY;

EID: 74149084551 PISSN: 00095893 EISSN: 16121112 Source Type: Journal
DOI: 10.1365/s10337-009-1397-0 Document Type: Article

Times cited : (10)

References (13)

1
- 0038443005
- Chemoenzymatic synthesis of duloxetine and its enantiomer: Lipase-catalyzed resolution of 3-hydroxy-3-(2-thienyl) propanenitrile
- DOI 10.1016/S0040-4039(03)00945-6
- A Kamal GBR Khanna R Ramu T Krishnaji 2003 Tetrahedron Lett 44 4783 4787 10.1016/S0040-4039(03)00945-6 10.1016/S0040-4039(03)00945-6 1:CAS:528: DC%2BD3sXktVGrtLk%3D (Pubitemid 36647947)
- (2003) Tetrahedron Letters , vol.44 , Issue.25 , pp. 4783-4787
- Kamal, A.¹ Khanna, G.B.R.² Ramu, R.³ Krishnaji, T.⁴

2
- 0031937876
- Characterization of impurities formed by interaction of duloxetine HCl with enteric polymers hydroxypropyl methylcellulose acetate succinate and hydroxypropyl methylcellulose phthalate
- DOI 10.1021/js970133r
- PJ Jansen PL Oren CA Kemp SR Maple SW Baertschi 1998 J Pharm Sci 87 81 85 10.1021/js970133r 10.1021/js970133r 1:CAS:528:DyaK2sXnvVKltLs%3D (Pubitemid 28079266)
- (1998) Journal of Pharmaceutical Sciences , vol.87 , Issue.1 , pp. 81-85
- Jansen, P.J.¹ Oren, P.L.² Kemp, C.A.³ Maple, S.R.⁴ Baertschi, S.W.⁵

3
- 27144509279
- High-performance liquid chromatographic method for the simultaneous estimation of the key intermediates of duloxetine
- DOI 10.1016/j.talanta.2005.04.020, PII S0039914005002055
- P Soni TT Mariappan UC Banerjee 2005 Talanta 67 975 978 10.1016/j.talanta.2005.04.020 10.1016/j.talanta.2005.04.020 1:CAS:528: DC%2BD2MXhtVClu7zL (Pubitemid 41491924)
- (2005) Talanta , vol.67 , Issue.5 , pp. 975-978
- Soni, P.¹ Mariappan, T.T.² Banerjee, U.C.³

4
- 0028238584
- The validation of analytical methods for drug substances and drug products in UK pharmaceutical laboratories
- DOI 10.1016/0731-7085(93)E0018-I
- GS Clarke 1994 J Pharm Biomed Anal 12 643 652 10.1016/0731-7085(93)E0018- I 10.1016/0731-7085(93)E0018-I 1:CAS:528:DyaK2cXks1Glt74%3D (Pubitemid 24194785)
- (1994) Journal of Pharmaceutical and Biomedical Analysis , vol.12 , Issue.5 , pp. 643-652
- Clarke, G.S.¹

5
- 74149086209
- FDA Food and Drug Administration
- FDA (1994) Food and Drug Administration, 1994, Guidance for industry: analytical procedures and methods validation (draft guidance)
- (1994) 1994, Guidance for Industry: Analytical Procedures and Methods Validation (Draft Guidance)

6
- 0003646348
- FDA Food and Drug Administration, Center of Drug Evolution and Research, 1994
- FDA (1994) Food and Drug Administration, Center of Drug Evolution and Research, 1994, Reviewer guidance, validation of chromatographic methods
- (1994) Reviewer Guidance, Validation of Chromatographic Methods

7
- 74149090231
- ICH
- ICH (1994) International conference on harmonization, October 1994, Text on validation of analytical procedures Q2A
- (1994) International Conference on Harmonization, October 1994, Text on Validation of Analytical Procedures Q2A

8
- 74149092412
- ICH
- ICH (1996) International conference on harmonization November 1996, Validation of analytical procedures methodology (Q2B)
- (1996) International Conference on Harmonization November 1996, Validation of Analytical Procedures Methodology (Q2B)

9
- 0003501326
- Marcel Dekker Inc ISBN 978-0-8247-0763-7
- Chow SC, Shao J (2002) Statistics in drug research: methodologies and recent development, Marcel Dekker Inc, pp 31-52. ISBN 978-0-8247-0763-7
- (2002) Statistics in Drug Research: Methodologies and Recent Development , pp. 31-52
- Chow, S.C.¹ Shao, J.²

10
- 74149090963
- ICH
- ICH (1994) International conference on Harmonization October 1994, Harmonized tripartite guideline prepared with in the third international conference on harmonization of technical requirements for the registration of pharmaceuticals for the human use: text on validation of analytical procedures
- (1994) International Conference on Harmonization October 1994, Harmonized Tripartite Guideline Prepared with in the Third International Conference on Harmonization of Technical Requirements for the Registration of Pharmaceuticals for the Human Use: Text on Validation of Analytical Procedures

11
- 0031738199
- Ruggedness testing of chromatographic methods: Selection of factors and levels
- DOI 10.1016/S0731-7085(98)00174-5, PII S0731708598001745
- Y Van der Heyden F Questier DL Massart 1998 J Pharm Biomed Anal 18 43 56 10.1016/S0731-7085(98)00174-5 10.1016/S0731-7085(98)00174-5 (Pubitemid 28529321)
- (1998) Journal of Pharmaceutical and Biomedical Analysis , vol.18 , Issue.1-2 , pp. 43-56
- Vander Heyden, Y.¹ Questier, F.² Massart, L.³

12
- 74149087420
- ICH
- ICH (2003) International conference on harmonization, Geneva 2003, Stability testing of new drug substances and products, Q1AR2
- (2003) International Conference on Harmonization, Geneva 2003, Stability Testing of New Drug Substances and Products, Q1AR2

13
- 28544447730
- 10.1016/0378-5173(92)90065-A 10.1016/0378-5173(92)90065-A
- VP Shah KK Midha S Dighe IJ McGilveray JP Skelly A Yacobi T Layloff CT Viswanathan CE Cook RD McDowall 1992 Int J Pharm 82 1 7 10.1016/0378-5173(92) 90065-A 10.1016/0378-5173(92)90065-A
- (1992) Int J Pharm , vol.82 , pp. 1-7
- Shah, V.P.¹ Midha, K.K.² Dighe, S.³ McGilveray, I.J.⁴ Skelly, J.P.⁵ Yacobi, A.⁶ Layloff, T.⁷ Viswanathan, C.T.⁸ Cook, C.E.⁹ McDowall, R.D.¹⁰

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