324 related articles for article (PubMed ID: 18029132)
1. Development and validation of UPLC method for determination of primaquine phosphate and its impurities.
Dongre VG; Karmuse PP; Rao PP; Kumar A
J Pharm Biomed Anal; 2008 Jan; 46(2):236-42. PubMed ID: 18029132
[TBL] [Abstract][Full Text] [Related]
2. Development and validation of a UPLC method for quality control of rhubarb-based medicine: fast simultaneous determination of five anthraquinone derivatives.
Wang J; Li H; Jin C; Qu Y; Xiao X
J Pharm Biomed Anal; 2008 Aug; 47(4-5):765-70. PubMed ID: 18440751
[TBL] [Abstract][Full Text] [Related]
3. A rapid method for chemical fingerprint analysis of Hoodia species, related genera, and dietary supplements using UPLC-UV-MS.
Avula B; Wang YH; Pawar RS; Shukla YJ; Smillie TJ; Khan IA
J Pharm Biomed Anal; 2008 Nov; 48(3):722-31. PubMed ID: 18718731
[TBL] [Abstract][Full Text] [Related]
4. Stability-indicating UPLC method for determination of Valsartan and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms.
Krishnaiah Ch; Reddy AR; Kumar R; Mukkanti K
J Pharm Biomed Anal; 2010 Nov; 53(3):483-9. PubMed ID: 20646890
[TBL] [Abstract][Full Text] [Related]
5. Characterization and quantitative determination of impurities in piperaquine phosphate by HPLC and LC/MS/MS.
Dongre VG; Karmuse PP; Ghugare PD; Gupta M; Nerurkar B; Shaha C; Kumar A
J Pharm Biomed Anal; 2007 Jan; 43(1):186-95. PubMed ID: 16916594
[TBL] [Abstract][Full Text] [Related]
6. Stability indicating UPLC method for simultaneous determination of atorvastatin, fenofibrate and their degradation products in tablets.
Kadav AA; Vora DN
J Pharm Biomed Anal; 2008 Sep; 48(1):120-6. PubMed ID: 18583084
[TBL] [Abstract][Full Text] [Related]
7. Determination of nelfinavir mesylate as bulk drug and in pharmaceutical dosage form by stability indicating HPLC.
Jing Q; Shen Y; Tang Y; Ren F; Yu X; Hou Z
J Pharm Biomed Anal; 2006 Jun; 41(3):1065-9. PubMed ID: 16545536
[TBL] [Abstract][Full Text] [Related]
8. A novel rapid method for simultaneous determination of eight active compounds in silymarin using a reversed-phase UPLC-UV detector.
Liu H; Du Z; Yuan Q
J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Dec; 877(32):4159-63. PubMed ID: 19939752
[TBL] [Abstract][Full Text] [Related]
9. Validated UPLC method for the fast and sensitive determination of steroid residues in support of cleaning validation in formulation area.
Fekete S; Fekete J; Ganzler K
J Pharm Biomed Anal; 2009 Apr; 49(3):833-8. PubMed ID: 19185442
[TBL] [Abstract][Full Text] [Related]
10. Development and validation of a stability-indicating RP-UPLC method for the quantitative analysis of nabumetone in tablet dosage form.
Sethi N; Anand A; Chandrul KK; Jain G; Srinivas KS
J Chromatogr Sci; 2012 Feb; 50(2):85-90. PubMed ID: 22298755
[TBL] [Abstract][Full Text] [Related]
11. Development and validation of a stability-indicating RP-UPLC method for the quantitative analysis of sparfloxacin.
Gupta H; Aqil M; Khar RK; Ali A; Sharma A; Chander P
J Chromatogr Sci; 2010 Jan; 48(1):1-6. PubMed ID: 20056027
[TBL] [Abstract][Full Text] [Related]
12. A novel and rapid validated stability-indicating UPLC method of related substances for dorzolamide hydrochloride and timolol maleate in ophthalmic dosage form.
Sharma N; Rao SS; Reddy AM
J Chromatogr Sci; 2012 Oct; 50(9):745-55. PubMed ID: 22562819
[TBL] [Abstract][Full Text] [Related]
13. Stability-indicating UPLC method for determination of Imatinib Mesylate and their degradation products in active pharmaceutical ingredient and pharmaceutical dosage forms.
Nageswari A; Reddy KV; Mukkanti K
J Pharm Biomed Anal; 2012 Jul; 66():109-15. PubMed ID: 22502910
[TBL] [Abstract][Full Text] [Related]
14. Validated stability-indicating HPLC method for the determination of dimethyl-4,4'-dimethoxy-5,6,5',6'-dimethylene dioxybiphenyl-2,2'-dicarboxylate (DDB) and its degradation products.
Hadad GM
J Pharm Biomed Anal; 2008 Aug; 47(4-5):695-703. PubMed ID: 18403161
[TBL] [Abstract][Full Text] [Related]
15. Validation of a fast liquid chromatography-UV method for the analysis of drugs used in combined cardiovascular therapy in human plasma.
Iriarte G; Gonzalez O; Ferreirós N; Maguregui MI; Alonso RM; Jiménez RM
J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Oct; 877(27):3045-53. PubMed ID: 19660995
[TBL] [Abstract][Full Text] [Related]
16. Quantification of potential impurities by a stability indicating UV-HPLC method in niacinamide active pharmaceutical ingredient.
Thomas S; Bharti A; Tharpa K; Agarwal A
J Pharm Biomed Anal; 2012 Feb; 60():86-90. PubMed ID: 22115882
[TBL] [Abstract][Full Text] [Related]
17. A validated stability-indicating LC method for acetazolamide in the presence of degradation products and its process-related impurities.
Srinivasu P; Subbarao DV; Vegesna RV; Sudhakar Babu K
J Pharm Biomed Anal; 2010 May; 52(1):142-8. PubMed ID: 20053517
[TBL] [Abstract][Full Text] [Related]
18. Method transfer for fast liquid chromatography in pharmaceutical analysis: application to short columns packed with small particle. Part I: isocratic separation.
Guillarme D; Nguyen DT; Rudaz S; Veuthey JL
Eur J Pharm Biopharm; 2007 Jun; 66(3):475-82. PubMed ID: 17267188
[TBL] [Abstract][Full Text] [Related]
19. Development and validation of a stability-indicating high performance liquid chromatographic (HPLC) assay for biperiden in bulk form and pharmaceutical dosage forms.
Mohammadi A; Mehramizi A; Moghaddam FA; Jabarian LE; Pourfarzib M; Kashani HN
J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Jul; 854(1-2):152-7. PubMed ID: 17466605
[TBL] [Abstract][Full Text] [Related]
20. Ultrafast UPLC-ESI-MS and HPLC with monolithic column for determination of principal flavor compounds in vanilla pods.
Sharma UK; Sharma N; Sinha AK; Kumar N; Gupta AP
J Sep Sci; 2009 Oct; 32(20):3425-31. PubMed ID: 19750505
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
