BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 9885304)

  • 21. Use of in vitro release tests for the prediction of the in vivo behavior and the development of flucytosine controlled-release capsules.
    Bonny JD; Kyowa M
    J Pharm Sci; 1995 May; 84(5):619-23. PubMed ID: 7658354
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Lack of effect of multiple dose sucralfate on the pharmacokinetics of of roxatidine acetate.
    Seibert-Grafe M; Pidgen A
    Eur J Clin Pharmacol; 1991; 40(6):637-8. PubMed ID: 1679394
    [No Abstract]   [Full Text] [Related]  

  • 23. Roxatidine acetate. A review of its pharmacodynamic and pharmacokinetic properties, and its therapeutic potential in peptic ulcer disease and related disorders.
    Murdoch D; McTavish D
    Drugs; 1991 Aug; 42(2):240-60. PubMed ID: 1717223
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Effects of roxatidine acetate on 24-hour gastric acidity. Early evening versus bedtime administration in healthy subjects.
    Hemery P; Congard P; Galmiche JP; Bonfils S
    Drugs; 1988; 35 Suppl 3():76-81. PubMed ID: 2905253
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Twenty-four-hour intragastric acidity following early evening or bedtime administration of roxatidine in duodenal ulcer patients.
    Lazzaroni M; Sangaletti O; Bargiggia S; Bensi G; Canali A; Bianchi Porro G
    Aliment Pharmacol Ther; 1996 Apr; 10(2):187-91. PubMed ID: 8730248
    [TBL] [Abstract][Full Text] [Related]  

  • 26. In vitro-in vivo correlation of a modified-release oral form of ketotifen: in vitro dissolution rate specification.
    Humbert H; Cabiac MD; Bosshardt H
    J Pharm Sci; 1994 Feb; 83(2):131-6. PubMed ID: 8169778
    [TBL] [Abstract][Full Text] [Related]  

  • 27. In vitro dissolution and in vivo oral absorption of methylphenidate from a bimodal release formulation in healthy volunteers.
    Wang Y; Lee L; Somma R; Thompson G; Bakhtiar R; Lee J; Rekhi GS; Lau H; Sedek G; Hossain M
    Biopharm Drug Dispos; 2004 Mar; 25(2):91-8. PubMed ID: 14872557
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Biopharmaceutical characterization of sustained release matrix tablets based on novel carbomer polymers: formulation and in vivo investigation.
    Jelena P; Djurić Z; Jovanović M; Ibrić S; Kilibarda V; Jovanović D; Evic IK
    Eur J Drug Metab Pharmacokinet; 2005; 30(1-2):99-104. PubMed ID: 16010868
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pharmacokinetic characteristics of roxatidine.
    Bender W; Brockmeier D
    J Clin Gastroenterol; 1989; 11 Suppl 1():S6-19. PubMed ID: 2572622
    [TBL] [Abstract][Full Text] [Related]  

  • 30. In vitro and in vivo evaluation of single-unit commercial immediate-and sustained-release capsules compared with multiple-unit polystyrene microparticles dosage forms of indomethacin.
    Tamilvanan S; Sa B
    PDA J Pharm Sci Technol; 2008; 62(3):177-90. PubMed ID: 18661867
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Biopredictive In Vitro Comparison of Oral Locally Acting Mesalazine Formulations by a Novel Dissolution Model for Assessing Intraluminal Drug Release in Individual Subjects.
    Karkossa F; Klein S
    J Pharm Sci; 2018 Jun; 107(6):1680-1689. PubMed ID: 29499277
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Preparation and in vitro/in vivo evaluation of sustained-release venlafaxine hydrochloride pellets.
    Liu Y; Sun Y; Sun J; Zhao N; Sun M; He Z
    Int J Pharm; 2012 Apr; 426(1-2):21-28. PubMed ID: 22266529
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Development of level A, B and C in vitro-in vivo correlations for modified-release levosimendan capsules.
    Kortejärvi H; Mikkola J; Bäckman M; Antila S; Marvola M
    Int J Pharm; 2002 Jul; 241(1):87-95. PubMed ID: 12086724
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Biopharmaceutical characterization of carbamazepine immediate release tablets. In vitro-in vivo comparison.
    Homsek I; Parojcic J; Cvetkovic N; Popadic D; Djuric Z
    Arzneimittelforschung; 2007; 57(8):511-6. PubMed ID: 17915636
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Regulatory aspects of modified release dosage forms: special cases of dissolution testing using the flow-through system.
    Möller H; Wirbitzki E
    Boll Chim Farm; 1993 Apr; 132(4):105-15. PubMed ID: 8333916
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Interpretation and optimization of the dissolution specifications for a modified release product with an in vivo-in vitro correlation (IVIVC).
    Hayes S; Dunne A; Smart T; Davis J
    J Pharm Sci; 2004 Mar; 93(3):571-81. PubMed ID: 14762896
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Impact of physical manipulation on in vitro and in vivo release profiles of oxycodone DETERx®: an extended-release, abuse-deterrent formulation.
    Kopecky EA; Fleming AB; Noonan PK; Varanasi RK; Grima M; Saim S; Mayock SP
    J Opioid Manag; 2014; 10(4):233-46. PubMed ID: 25162603
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Floating drug delivery of a locally acting H2-antagonist: an approach using an in situ gelling liquid formulation.
    Rohith G; Sridhar BK; Srinatha A
    Acta Pharm; 2009 Sep; 59(3):345-54. PubMed ID: 19819830
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Circadian aspects of diclofenac gastroduodenopathy and the protective effect of roxatidine].
    Müller P; Jackisch P; Simon B
    Z Rheumatol; 1993; 52(5):297-300. PubMed ID: 7903132
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Differences in the in vitro and in vivo pharmacokinetic profiles of once-daily modified-release methylphenidate formulations in Canada: examination of current bioequivalence criteria.
    Shram MJ; Quinn AM; Chen N; Faulknor J; Luong D; Sellers EM; Endrenyi L
    Clin Ther; 2012 May; 34(5):1170-81. PubMed ID: 22512898
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.