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 *

144 related articles for article (PubMed ID: 35521250)

  • 41. Green Simultaneous Chromatographic Separation of Pyridostigmine Bromide and Its Related Substances in Pure Form, Tablets and Spiked Human Plasma.
    Naguib IA; Abdelaleem EA; Emam AA; Abdallah FF
    J Chromatogr Sci; 2019 Aug; 57(7):653-661. PubMed ID: 31204433
    [TBL] [Abstract][Full Text] [Related]  

  • 42. A new validated liquid chromatographic method for the determination of loratadine and its impurities.
    Ramulu G; Ravindra Kumar Y; Vyas K; Suryanarayana MV; Mukkanti K
    Sci Pharm; 2011; 79(2):277-91. PubMed ID: 21773066
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Development of an effective novel validated stability-indicating HPLC method for the resolution of brivaracetam stereoisomeric impurities.
    Baksam V; N S; Pocha VR; Chakka VB; Ummadi RR; Kumar P
    Chirality; 2020 Sep; 32(9):1208-1219. PubMed ID: 32656914
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Chromatographic Determination of Aminoacridine Hydrochloride, Lidocaine Hydrochloride and Lidocaine Toxic Impurity in Oral Gel.
    Bebawy LI; Elghobashy MR; Abbas SS; Shokry RF
    J Chromatogr Sci; 2016 Apr; 54(4):492-9. PubMed ID: 26671412
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Impurity Profile of Bronchodilators used in Asthma: A Critical Review.
    Prajapati KJ; Kothari CS
    Curr Drug Discov Technol; 2018; 15(4):272-304. PubMed ID: 28875855
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Validatibility of a capillary isoelectric focusing method for impurity quantitation.
    Lasdun AM; Kurumbail RR; Leimgruber NK; Rathore AS
    J Chromatogr A; 2001 May; 917(1-2):147-58. PubMed ID: 11403466
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Simple Eco-Friendly RP-LC Method for the Synchronous Separation of Six Widely Used Drugs in the Treatment of Cerebrovascular and Vestibular Disorders: Application for Analysis in Their Single and Combined Drug Products.
    El-Houssini OM; Mohammad MA
    J AOAC Int; 2022 Jun; 105(4):957-963. PubMed ID: 35167683
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Development and validation of a stability-indicating reverse phase ultra performance liquid chromatographic method for the estimation of nebivolol impurities in active pharmaceutical ingredients and pharmaceutical formulation.
    Thummala VR; Lanka MK
    Se Pu; 2015 Oct; 33(10):1051-8. PubMed ID: 26930962
    [TBL] [Abstract][Full Text] [Related]  

  • 49. RP-LC and TLC Densitometric Determination of Paracetamol and Pamabrom in Presence of Hazardous Impurity of Paracetamol and Application to Pharmaceuticals.
    El-Houssini OM
    Anal Chem Insights; 2013; 8():73-81. PubMed ID: 24046511
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Green chromatographic method for analysis of some anti-cough drugs and their toxic impurities with comparison to conventional methods.
    Abdelaleem EA; Abdelwahab NS
    Saudi Pharm J; 2018 Dec; 26(8):1185-1191. PubMed ID: 30532640
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A validated ultra high-pressure liquid chromatography method for separation of candesartan cilexetil impurities and its degradents in drug product.
    Kumar ND; Babu KS; Gosada U; Sharma N
    Pharm Methods; 2012 Jan; 3(1):31-9. PubMed ID: 23781475
    [TBL] [Abstract][Full Text] [Related]  

  • 52. A Validated TLC-Densitometric Method for the Determination of Mesterolone in Bulk Material and in Tablets.
    Dołowy M; Pyka-Pająk A; Filip K; Zagrodzka J
    Biomed Res Int; 2015; 2015():230104. PubMed ID: 26881196
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A validated stability-indicating LC method for the separation of enantiomer and potential impurities of Linezolid using polar organic mode.
    Satyanarayana Raju T; Vishweshwari Kutty O; Ganesh V; Yadagiri Swamy P
    J Pharm Anal; 2012 Aug; 2(4):272-278. PubMed ID: 29403753
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Chromatographic determination of sulfasalazine and its active metabolites: greenness assessment and application to spiked human plasma.
    Abdelrahman MM; Habib NM; Emam AA; Mahmoud HM; Abdelwhab NS
    Biomed Chromatogr; 2020 Apr; 34(4):e4804. PubMed ID: 32012304
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Development and validation of a selective, sensitive and stability indicating UPLC-MS/MS method for rapid, simultaneous determination of six process related impurities in darunavir drug substance.
    A VBR; Yusop Z; Jaafar J; Aris AB; Majid ZA; Umar K; Talib J
    J Pharm Biomed Anal; 2016 Sep; 128():141-148. PubMed ID: 27262107
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Two validated chromatographic determinations of an antifungal drug, its toxic impurities and degradation product: A comparative study.
    Abdelaleem EA; Abdelrahman MM; Ali NW; Emam RA
    Biomed Chromatogr; 2019 Aug; 33(8):e4547. PubMed ID: 30941788
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Stability-Indicating TLC-Densitometric and HPLC Methods for the Simultaneous Determination of Piracetam and Vincamine in the Presence of Their Degradation Products.
    Ahmed AB; Abdelrahman MM; Abdelwahab NS; Salama FM
    J AOAC Int; 2016 Nov; 99(6):1490-1498. PubMed ID: 27569579
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Development of RP UPLC-TOF/MS, stability indicating method for omeprazole and its related substances by applying two level factorial design; and identification and synthesis of non-pharmacopoeial impurities.
    Jadhav SB; Kumar CK; Bandichhor R; Bhosale PN
    J Pharm Biomed Anal; 2016 Jan; 118():370-379. PubMed ID: 26600119
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Stability-Indicating RP-HPLC Method for Simultaneous Estimation of Enrofloxacin and Its Degradation Products in Tablet Dosage Forms.
    Chakravarthy VA; Sailaja BB; Kumar AP
    J Anal Methods Chem; 2015; 2015():735145. PubMed ID: 25705547
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Analytical advances in pharmaceutical impurity profiling.
    Holm R; Elder DP
    Eur J Pharm Sci; 2016 May; 87():118-35. PubMed ID: 26690047
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.