127 related articles for article (PubMed ID: 17691210)
1. Determination of the impurity profile of adenosine by means of ion-pair reversed-phase chromatography.
Kopec S; Almeling S; Holzgrabe U
Pharmeur Sci Notes; 2006 Dec; 2006(2):17-21. PubMed ID: 17691210
[TBL] [Abstract][Full Text] [Related]
2. A liquid chromatographic method using a reversed-phase hybrid stationary phase to control potential impurities of imipramine hydrochloride.
Dixon SP; La Torre F; Lodi A; Miller JH; Skellern GG
Pharmeur Sci Notes; 2006 Dec; 2006(2):35-9. PubMed ID: 17691212
[TBL] [Abstract][Full Text] [Related]
3. Impurity profile of amino acids?
Kopec S; Holzgrabe U
Pharmeur Sci Notes; 2005 Aug; 2005(1):39-45. PubMed ID: 17687893
[TBL] [Abstract][Full Text] [Related]
4. Acceptance criteria for levels of hydrazine in substances for pharmaceutical use and analytical methods for its determination.
Kean T; Miller JH; Skellern GG; Snodin D
Pharmeur Sci Notes; 2006 Dec; 2006(2):23-33. PubMed ID: 17691211
[TBL] [Abstract][Full Text] [Related]
5. Development of an enhanced separation of erythromycin and its related substances by liquid chromatography.
Deubel A; Holzgrabe U
J Pharm Biomed Anal; 2007 Jan; 43(2):493-8. PubMed ID: 16935448
[TBL] [Abstract][Full Text] [Related]
6. Determination of nucleotides, nucleosides and their transformation products in Cordyceps by ion-pairing reversed-phase liquid chromatography-mass spectrometry.
Yang FQ; Li DQ; Feng K; Hu DJ; Li SP
J Chromatogr A; 2010 Aug; 1217(34):5501-10. PubMed ID: 20637470
[TBL] [Abstract][Full Text] [Related]
7. A validated stability indicating ion-pair RP-LC method for zoledronic acid.
Rao BM; Srinivasu MK; Rani ChP; kumar SS; Kumar PR; Chandrasekhar KB; Veerender M
J Pharm Biomed Anal; 2005 Sep; 39(3-4):781-90. PubMed ID: 15922532
[TBL] [Abstract][Full Text] [Related]
8. Reversed phase ion-pair high performance liquid chromatographic gradient separation of related impurities in 2,4-disulfonic acid benzaldehyde di-sodium salt.
Lu B; Jonsson P; Blomberg S
J Chromatogr A; 2006 Jun; 1119(1-2):270-6. PubMed ID: 16378614
[TBL] [Abstract][Full Text] [Related]
9. An efficient separation and method development for the quantifying of two basic impurities of Nicergoline by reversed-phase high performance liquid chromatography using ion-pairing counter ions.
Yalçin G; Yüktaş N
J Pharm Biomed Anal; 2006 Oct; 42(4):434-40. PubMed ID: 16766155
[TBL] [Abstract][Full Text] [Related]
10. Identification and control of impurities in streptomycin sulfate by high-performance liquid chromatography coupled with mass detection and corona charged-aerosol detection.
Holzgrabe U; Nap CJ; Kunz N; Almeling S
J Pharm Biomed Anal; 2011 Sep; 56(2):271-9. PubMed ID: 21665399
[TBL] [Abstract][Full Text] [Related]
11. [Estimation of impurity profiles of drugs and related materials. 20. Methodological problems in the identification and determination of organic impurities].
Görög S
Acta Pharm Hung; 2000; 70(3-6):131-7. PubMed ID: 11379019
[TBL] [Abstract][Full Text] [Related]
12. A validated stability-indicating RP-HPLC method for levofloxacin in the presence of degradation products, its process related impurities and identification of oxidative degradant.
Lalitha Devi M; Chandrasekhar KB
J Pharm Biomed Anal; 2009 Dec; 50(5):710-7. PubMed ID: 19632800
[TBL] [Abstract][Full Text] [Related]
13. A simple and efficient approach to reversed-phase HPLC method screening.
Biswas KM; Castle BC; Olsen BA; Risley DS; Skibic MJ; Wright PB
J Pharm Biomed Anal; 2009 Apr; 49(3):692-701. PubMed ID: 19181471
[TBL] [Abstract][Full Text] [Related]
14. Separation and determination of nimesulide related substances for quality control purposes by micellar electrokinetic chromatography.
Zacharis CK; Tzanavaras PD; Notou M; Zotou A; Themelis DG
J Pharm Biomed Anal; 2009 Feb; 49(2):201-6. PubMed ID: 19062217
[TBL] [Abstract][Full Text] [Related]
15. Simultaneous determination of cations, zwitterions and neutral compounds using mixed-mode reversed-phase and cation-exchange high-performance liquid chromatography.
Li J; Shao S; Jaworsky MS; Kurtulik PT
J Chromatogr A; 2008 Mar; 1185(2):185-93. PubMed ID: 18304563
[TBL] [Abstract][Full Text] [Related]
16. Determination of local anaesthetics and their impurities in pharmaceutical preparations using HPLC method with amperometric detection.
Fijałek Z; Baczyński E; Piwońska A; Warowna-Grześkiewicz M
J Pharm Biomed Anal; 2005 Apr; 37(5):913-8. PubMed ID: 15862666
[TBL] [Abstract][Full Text] [Related]
17. Simultaneous determination of five nucleosides and nucleobases of Rehmannia glutinosa Libosch. by high performance liquid chromatography.
Zhang WM; Fu WW; Sun MY; Sun LX; Jia YR; Liu P
Yao Xue Xue Bao; 2011 Nov; 46(11):1380-4. PubMed ID: 22260034
[TBL] [Abstract][Full Text] [Related]
18. Isolation and characterization of process related impurities and degradation products of bicalutamide and development of RP-HPLC method for impurity profile study.
Nageswara Rao R; Narasa Raju A; Narsimha R
J Pharm Biomed Anal; 2008 Feb; 46(3):505-19. PubMed ID: 18162355
[TBL] [Abstract][Full Text] [Related]
19. Simultaneous separation and determination of coenzyme Q(10) and its process related impurities by NARP-HPLC and atmospheric pressure chemical ionization-mass spectrometry (APCI-MS).
Nageswara Rao R; Kumar Talluri MV; Shinde DD
J Pharm Biomed Anal; 2008 Jun; 47(2):230-7. PubMed ID: 18243624
[TBL] [Abstract][Full Text] [Related]
20. Determination of inorganic pharmaceutical counterions using hydrophilic interaction chromatography coupled with a Corona CAD detector.
Huang Z; Richards MA; Zha Y; Francis R; Lozano R; Ruan J
J Pharm Biomed Anal; 2009 Dec; 50(5):809-14. PubMed ID: 19616396
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]