These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

51 related articles for article (PubMed ID: 3234535)

  • 1. HPLC method for quantitative determination of synthetic ceruletide and its impurities.
    Franzoi L; Gioia B; de Castiglione R; Vigevani A; Williamson MJ
    Farmaco Prat; 1988 Oct; 43(10):317-23. PubMed ID: 3234535
    [No Abstract]   [Full Text] [Related]  

  • 2. Quantitative analysis of ceruletide in the drug substance and in the pharmaceutical preparations by high performance liquid chromatography.
    Raja B; de Castiglione R; Vigevani A
    Farmaco Prat; 1981 Feb; 36(2):89-98. PubMed ID: 7215531
    [No Abstract]   [Full Text] [Related]  

  • 3. Selective determination of potential impurities in an active pharmaceutical ingredient using HPLC-SPE-HPLC.
    Yamamoto E; Niijima J; Asakawa N
    J Pharm Biomed Anal; 2013 Oct; 84():41-7. PubMed ID: 23806999
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spectroscopic characterization and quantitative determination of atorvastatin calcium impurities by novel HPLC method.
    Gupta LK
    Spectrochim Acta A Mol Biomol Spectrosc; 2012 Nov; 97():495-501. PubMed ID: 22842103
    [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. Determination of synthetic by-products and an intermediate in the colour additive D&C Orange No. 5 using high-performance liquid chromatography.
    Yang HH; Weisz A
    Food Addit Contam Part A Chem Anal Control Expo Risk Assess; 2012; 29(9):1386-90. PubMed ID: 22779771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Highly efficient, selective, sensitive and stability indicating RP-HPLC-UV method for the quantitative determination of potential impurities and characterization of four novel impurities in eslicarbazepine acetate active pharmaceutical ingredient by LC/ESI-IT/MS/MS.
    Thomas S; Bharti A; Maddhesia PK; Shandilya S; Agarwal A; Dharamvir ; Biswas S; Bhansal V; Gupta AK; Tewari PK; Mathela CS
    J Pharm Biomed Anal; 2012 Mar; 61():165-75. PubMed ID: 22178334
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Development of a novel RP-HPLC method for the efficient separation of aripiprazole and its nine impurities.
    Nikolic K; Filijović ND; Maričić B; Agbaba D
    J Sep Sci; 2013 Oct; 36(19):3165-75. PubMed ID: 23900963
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A validated RP-HPLC method for quantitative determination of related impurities of ursodeoxycholic acid (API) by refractive index detection.
    Peepliwal A; Bonde CG; Bothara KG
    J Pharm Biomed Anal; 2011 Mar; 54(4):845-9. PubMed ID: 21095088
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Simultaneous determination of rocuronium and its eight impurities in pharmaceutical preparation using high-performance liquid chromatography with amperometric detection.
    Błazewicz A; Fijałek Z; Warowna-Grześkiewicz M; Boruta M
    J Chromatogr A; 2007 May; 1149(1):66-72. PubMed ID: 17222417
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Determination of relative response factors of impurities in paclitaxel with high performance liquid chromatography equipped with ultraviolet and charged aerosol detectors.
    Sun P; Wang X; Alquier L; Maryanoff CA
    J Chromatogr A; 2008 Jan; 1177(1):87-91. PubMed ID: 18067905
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of impurities in semi-synthetic vinorelbine bitartrate by HPLC-MS with mass spectrometric shift technique.
    Cao X; Tai Y; Sun C; Wang K; Pan Y
    J Pharm Biomed Anal; 2005 Sep; 39(1-2):39-45. PubMed ID: 16085133
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A stability indicating simultaneous dual wavelength UV-HPLC method for the determination of potential impurities in fampridine active pharmaceutical ingredient.
    Thomas S; Shandilya S; Bharti A; Agarwal A
    J Pharm Biomed Anal; 2012 Jan; 58():136-40. PubMed ID: 22000073
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A validated reversed phase HPLC method for the determination of process-related impurities in almotriptan malate API.
    Kumar AP; Ganesh VR; Rao DV; Anil C; Rao BV; Hariharakrishnan VS; Suneetha A; Sundar BS
    J Pharm Biomed Anal; 2008 Mar; 46(4):792-8. PubMed ID: 18191357
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Development and validation of a HPLC method for the determination of sertraline and three non-chiral related impurities.
    Ferrarini A; Huidobro AL; Pellati F; Barbas C
    J Pharm Biomed Anal; 2010 Oct; 53(2):122-9. PubMed ID: 20138727
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A high pH based reversed-phase high performance liquid chromatographic method for the analysis of aminoglycoside plazomicin and its impurities.
    Tan L; Wlasichuk KB; Schmidt DE; Campbell RL; Hirtzer P; Cheng L; Karr DE
    J Pharm Biomed Anal; 2012 Jul; 66():75-84. PubMed ID: 22459505
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Separation and determination of synthetic impurities of norfloxacin by reversed-phase high performance liquid chromatography.
    Nageswara Rao R; Nagaraju V
    J Pharm Biomed Anal; 2004 Mar; 34(5):1049-56. PubMed ID: 15019038
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evaluation of high pressure liquid chromatography and gas-liquid chromatography for quantitative determination of sugars in foods.
    Iverson JL; Bueno MP
    J Assoc Off Anal Chem; 1981 Jan; 64(1):139-43. PubMed ID: 7204295
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Separation and determination of synthetic impurities of difloxacin by reversed-phase high-performance liquid chromatography.
    Rao RN; Nagaraju V
    J Pharm Biomed Anal; 2004 Nov; 36(4):729-35. PubMed ID: 15533664
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.