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PUBMED FOR HANDHELDS

Journal Abstract Search

211 related items for PubMed ID: 7076345

  • 1. The bioavailability of diazepam from uncoated tablets in humans--Part I: correlation with the dissolution rates of the tablets.
    Ogata H, Aoyagi N, Kaniwa N, Koibuchi M, Shibazaki T, Ejima A, Tsuji S, Kawazu Y.
    Int J Clin Pharmacol Ther Toxicol; 1982 Apr; 20(4):159-65. PubMed ID: 7076345
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  • 3. Bioavailability of nalidixic acid from uncoated tablets in humans--Part I: Correlation with the dissolution rates of the tablets.
    Ogata H, Aoyagi N, Kaniwa K, Shibazaki T, Ejima A, Takasugi N, Mafune E, Hayashi T, Suwa K.
    Int J Clin Pharmacol Ther Toxicol; 1984 Apr; 22(4):175-83. PubMed ID: 6715086
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  • 4. Correlation of the bioavailability of diazepam from uncoated tablets in beagle dogs with its dissolution rate and bioavailability in humans.
    Ogata H, Aoyagi N, Kaniwa N, Koibuchi M, Shibazaki T, Ejima A, Shimamoto T, Yashiki T, Ogawa Y, Uda Y, Nishida Y.
    Int J Clin Pharmacol Ther Toxicol; 1982 Dec; 20(12):576-81. PubMed ID: 6818163
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  • 5. Discrepancy among dissolution rates of commercial tablets as a function of dissolution method. Part 5: In vitro/in vivo correlation for chlorpromazine hydrochloride tablets.
    Ammar HO, Khalil RM, Omar SM.
    Pharmazie; 1993 Dec; 48(12):932-5. PubMed ID: 8115438
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  • 7. In vivo/in vitro correlations for four differently dissolving ketorolac tablets.
    Gordon MS, Chowhan Z.
    Biopharm Drug Dispos; 1996 Aug; 17(6):481-92. PubMed ID: 8866039
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  • 13. Correlation between in vitro and in vivo parameters of commercial paracetamol tablets.
    Babalola CP, Oladimeji FA, Femi-Oyewo MN.
    Afr J Med Med Sci; 2001 Dec; 30(4):275-80. PubMed ID: 14510103
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  • 15. Discrepancy among dissolution rates of commercial tables as a function of the dissolution method. Part 7: Aspirin.
    Ammar HA, el-Nahhas SA, Emara LH, Ghorab MM, Salama HA.
    Pharmazie; 1997 Feb; 52(2):145-9. PubMed ID: 9122273
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  • 16. Comparison of two marketed nifedipine modified-release formulations: an exploratory clinical food interaction study.
    Wonnemann M, Schug B, Anschütz M, Brendel E, De Nucci G, Blume H.
    Clin Ther; 2008 Jan; 30(1):48-58. PubMed ID: 18343242
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  • 17. Development of a dissolution medium for nimodipine tablets based on bioavailability evaluation.
    He Z, Zhong D, Chen X, Liu X, Tang X, Zhao L.
    Eur J Pharm Sci; 2004 Mar; 21(4):487-91. PubMed ID: 14998579
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  • 18. Bioavailability of quinidine in slow-release form. A comparison between two preparations containing quinidine bisulphate as the active constituent.
    Regårdh CG, Johnsson G, Lundborg P, Perrson BA.
    Arzneimittelforschung; 1977 Mar; 27(9):1716-8. PubMed ID: 21671
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  • 19. 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
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  • 20. Bioavailability of different brands of griseofulvin tablets and its correlation to dissolution data.
    Khalafalla N, Elgholmy ZA, Khalil SA.
    Pharmazie; 1980 Aug; 35(8):482-4. PubMed ID: 7433499
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