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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

519 related items for PubMed ID: 16603170

  • 1. A stability-indicating high performance liquid chromatographic assay for the determination of orlistat in capsules.
    Mohammadi A, Haririan I, Rezanour N, Ghiasi L, Walker RB.
    J Chromatogr A; 2006 May 26; 1116(1-2):153-7. PubMed ID: 16603170
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  • 2. A stability-indicating high performance liquid chromatographic (HPLC) assay for the simultaneous determination of atorvastatin and amlodipine in commercial tablets.
    Mohammadi A, Rezanour N, Ansari Dogaheh M, Ghorbani Bidkorbeh F, Hashem M, Walker RB.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Feb 01; 846(1-2):215-21. PubMed ID: 17010681
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  • 3. Development and validation of a stability-indicating high performance liquid chromatographic (HPLC) assay for biperiden in bulk form and pharmaceutical dosage forms.
    Mohammadi A, Mehramizi A, Moghaddam FA, Jabarian LE, Pourfarzib M, Kashani HN.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Jul 01; 854(1-2):152-7. PubMed ID: 17466605
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  • 4. A stability-indicating high performance liquid chromatographic method for the determination of diacerein in capsules.
    Rao J, Chauhan K, Mahadik KR, Kadam SS.
    Indian J Pharm Sci; 2009 Jan 01; 71(1):24-9. PubMed ID: 20177451
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  • 5. HPLC analysis of orlistat and its application to drug quality control studies.
    Souri E, Jalalizadeh H, Kebriaee-Zadeh A, Zadehvakili B.
    Chem Pharm Bull (Tokyo); 2007 Feb 01; 55(2):251-4. PubMed ID: 17268098
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  • 7. RP-HPLC method for simultaneous estimation of bisoprolol fumarate and hydrochlorothiazide in tablet formulation.
    Joshi SJ, Karbhari PA, Bhoir SI, Bindu KS, Das C.
    J Pharm Biomed Anal; 2010 Jul 08; 52(3):362-71. PubMed ID: 19926421
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  • 8. Determination of nelfinavir mesylate as bulk drug and in pharmaceutical dosage form by stability indicating HPLC.
    Jing Q, Shen Y, Tang Y, Ren F, Yu X, Hou Z.
    J Pharm Biomed Anal; 2006 Jun 07; 41(3):1065-9. PubMed ID: 16545536
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  • 9. High-performance liquid chromatographic method for the determination of pioglitazone in human plasma using ultraviolet detection and its application to a pharmacokinetic study.
    Sripalakit P, Neamhom P, Saraphanchotiwitthaya A.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Nov 07; 843(2):164-9. PubMed ID: 16815107
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  • 10. A novel validated LC method for quantitation of lopinavir in bulk drug and pharmaceutical formulation in the presence of its potential impurities and degradation products.
    Seshachalam U, Haribabu B, Chandrasekhar K.
    Biomed Chromatogr; 2007 Jul 07; 21(7):716-23. PubMed ID: 17370253
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  • 11. Development and validation of a HPLC method for the analysis of promethazine hydrochloride in hot-melt extruded dosage forms.
    Thumma S, Zhang SQ, Repka MA.
    Pharmazie; 2008 Aug 07; 63(8):562-7. PubMed ID: 18771002
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  • 14. LC and LC-MS/MS study of forced decomposition behavior of anastrozole and establishment of validated stability-indicating analytical method for impurities estimation in low dose anastrozole tablets.
    Reddy YR, Nandan SR, Bharathi DV, Nagaraju B, Reddy SS, Ravindranath LK, Rao VS.
    J Pharm Biomed Anal; 2009 Oct 15; 50(3):397-404. PubMed ID: 19541446
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  • 19. Quantitative determination of insulin entrapment efficiency in triblock copolymeric nanoparticles by high-performance liquid chromatography.
    Xu X, Fu Y, Hu H, Duan Y, Zhang Z.
    J Pharm Biomed Anal; 2006 Apr 11; 41(1):266-73. PubMed ID: 16303273
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  • 20. Stability indicating validated HPLC method for quantification of levothyroxine with eight degradation peaks in the presence of excipients.
    Shah RB, Bryant A, Collier J, Habib MJ, Khan MA.
    Int J Pharm; 2008 Aug 06; 360(1-2):77-82. PubMed ID: 18524511
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