BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

97 related articles for article (PubMed ID: 3832781)

  • 1. Methods for the evaluation of solid state stability and compatibility between drug and excipient.
    Ahlneck C; Lundgren P
    Acta Pharm Suec; 1985; 22(6):305-14. PubMed ID: 3832781
    [No Abstract]   [Full Text] [Related]  

  • 2. Drug-excipient compatibility screening--role of thermoanalytical and spectroscopic techniques.
    Chadha R; Bhandari S
    J Pharm Biomed Anal; 2014 Jan; 87():82-97. PubMed ID: 23845418
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Design and utilization of the drug-excipient chemical compatibility automated system.
    Thomas VH; Naath M
    Int J Pharm; 2008 Jul; 359(1-2):150-7. PubMed ID: 18486368
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Understanding drug-excipient compatibility: oxidation of compound A in a solid dosage form.
    Wu Y; Dali M; Gupta A; Raghavan K
    Pharm Dev Technol; 2009; 14(5):556-64. PubMed ID: 19743950
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Factorial designs in pharmaceutical preformulation studies. II. Studies on drug stability and compatibility in the solid state.
    Ahlneck C; Waltersson JO
    Acta Pharm Suec; 1986; 23(3):139-50. PubMed ID: 3766159
    [No Abstract]   [Full Text] [Related]  

  • 6. Compatibility studies of promethazine hydrochloride with tablet excipients by means of thermal and non-thermal methods.
    Thumma S; Repka MA
    Pharmazie; 2009 Mar; 64(3):183-9. PubMed ID: 19348341
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Compatibility of chewing gum excipients with the amino acid L-cysteine and stability of the active substance in directly compressed chewing gum formulation.
    Kartal A; Björkqvist M; Lehto VP; Juppo AM; Marvola M; Sivén M
    J Pharm Pharmacol; 2008 Sep; 60(9):1131-8. PubMed ID: 18718115
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Solid-state compatibility studies using a high-throughput and automated forced degradation system.
    Wakasawa T; Sano K; Hirakura Y; Toyo'oka T; Kitamura S
    Int J Pharm; 2008 May; 355(1-2):164-73. PubMed ID: 18215480
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Use of mixture design in drug-excipient compatibility determinations: Thymol nanoparticles case study.
    Pires FQ; Angelo T; Silva JK; Sá-Barreto LC; Lima EM; Gelfuso GM; Gratieri T; Cunha-Filho MS
    J Pharm Biomed Anal; 2017 Apr; 137():196-203. PubMed ID: 28131059
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new approach to accelerated drug-excipient compatibility testing.
    Sims JL; Carreira JA; Carrier DJ; Crabtree SR; Easton L; Hancock SA; Simcox CE
    Pharm Dev Technol; 2003; 8(2):119-26. PubMed ID: 12760562
    [TBL] [Abstract][Full Text] [Related]  

  • 11. PharmDE: A new expert system for drug-excipient compatibility evaluation.
    Wang N; Sun H; Dong J; Ouyang D
    Int J Pharm; 2021 Sep; 607():120962. PubMed ID: 34339812
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Differential scanning calorimetry to investigate the compatibility of ciprofloxacin hydrochloride with excipients.
    Fathy M; Hassan MA; Mohamed FA
    Pharmazie; 2002 Dec; 57(12):825-8. PubMed ID: 12561245
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Stability challenges in drug discovery.
    Di L; Kerns EH
    Chem Biodivers; 2009 Nov; 6(11):1875-86. PubMed ID: 19937822
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of HPLC to assess the compatibility of bisoprolol fumarate with selected excipients in mixtures by isothermal stress testing.
    Marothu VK; Yerramothu P; Gorrepati M; Majeti S; Mamidala SK; Nellutla A
    Ann Pharm Fr; 2015 Nov; 73(6):442-51. PubMed ID: 26142745
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Compatibility of sennoside A and B with pharmaceutical excipients.
    Verloop Q; Marais AF; de Villiers MM; Liebenberg W
    Pharmazie; 2004 Sep; 59(9):728-30. PubMed ID: 15497761
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Thermal and non-thermal methods to evaluate compatibility of granisetron hydrochloride with tablet excipients.
    Late SG; Banga AK
    Pharmazie; 2008 Jun; 63(6):453-8. PubMed ID: 18604989
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pharmaceutical excipient development: the need for preclinical guidance.
    Baldrick P
    Regul Toxicol Pharmacol; 2000 Oct; 32(2):210-8. PubMed ID: 11067777
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Use of a screening method to determine excipients which optimize the extent and stability of supersaturated drug solutions and application of this system to solid formulation design.
    Vandecruys R; Peeters J; Verreck G; Brewster ME
    Int J Pharm; 2007 Sep; 342(1-2):168-75. PubMed ID: 17573214
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Calcium sulphate dihydrate: an useful excipient for tablets containing labile actives.
    Eyjolfsson R
    Pharmazie; 2004 Sep; 59(9):725-6. PubMed ID: 15497759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Testings of compatibility between diverse active compounds and excipients for tablets (author's transl)].
    Jacob M; Lai AM; Duru C; Puech A; Mias F
    J Pharm Belg; 1979; 34(2):96-8. PubMed ID: 512824
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.