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613 related items for PubMed ID: 16330261
1. Development and validation of RP-HPLC and ultraviolet spectrophotometric methods of analysis for the quantitative estimation of antiretroviral drugs in pharmaceutical dosage forms. Sarkar M, Khandavilli S, Panchagnula R. J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Jan 18; 830(2):349-54. PubMed ID: 16330261 [Abstract] [Full Text] [Related]
2. Simultaneous quantification of stavudine, lamivudine and nevirapine by UV spectroscopy, reverse phase HPLC and HPTLC in tablets. Anbazhagan S, Indumathy N, Shanmugapandiyan P, Sridhar SK. J Pharm Biomed Anal; 2005 Sep 15; 39(3-4):801-4. PubMed ID: 15950425 [Abstract] [Full Text] [Related]
3. Simultaneous determination of lamivudine and stavudine in antiretroviral fixed dose combinations by first derivative spectrophotometry and high performance liquid chromatography. Kapoor N, Khandavilli S, Panchagnula R. J Pharm Biomed Anal; 2006 Jun 07; 41(3):761-5. PubMed ID: 16464559 [Abstract] [Full Text] [Related]
4. Development and validation of a normal-phase HPTLC method for the simultaneous analysis of lamivudine, stavudine and nevirapine in fixed-dose combination tablets. Shewiyo DH, Kaale E, Ugullum C, Sigonda MN, Risha PG, Dejaegher B, Smeyers-Verbeke J, Vander Heyden Y. J Pharm Biomed Anal; 2011 Feb 20; 54(3):445-50. PubMed ID: 20943338 [Abstract] [Full Text] [Related]
5. Derivative-differential UV spectrophotometry and compensation technique for the simultaneous determination of zidovudine and lamivudine in human serum. Erk N. Pharmazie; 2004 Feb 20; 59(2):106-11. PubMed ID: 15025177 [Abstract] [Full Text] [Related]
6. Development and validation of a HPLC-UV method for the determination in didanosine tablets. de Oliveira AM, Löwen TC, Cabral LM, dos Santos EM, Rodrigues CR, Castro HC, dos Santos TC. J Pharm Biomed Anal; 2005 Jul 15; 38(4):751-6. PubMed ID: 15967304 [Abstract] [Full Text] [Related]
7. Comparison of HPLC & spectrophotometric methods for estimation of antiretroviral drug content in pharmaceutical products. Hemanth Kumar AK, Sudha V, Swaminathan S, Ramachandran G. Indian J Med Res; 2010 Oct 15; 132():390-4. PubMed ID: 20966516 [Abstract] [Full Text] [Related]
9. HPLC method for the determination of carboplatin and paclitaxel with cremophorEL in an amphiphilic polymer matrix. Mittal A, Chitkara D, Kumar N. J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Aug 15; 855(2):211-9. PubMed ID: 17543592 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
11. Development of a highly efficient extraction technique and specific multiplex assay for measuring antiretroviral drug concentrations in breast milk. Rezk NL, Abdel-Megeed MF, Kashuba AD. Ther Drug Monit; 2007 Aug 08; 29(4):429-36. PubMed ID: 17667797 [Abstract] [Full Text] [Related]
12. Development and validation of RP-HPLC method to determine letrozole in different pharmaceutical formulations and its application to studies of drug release from nanoparticles. Mondal N, Pal TK, Ghosal SK. Acta Pol Pharm; 2009 Aug 08; 66(1):11-7. PubMed ID: 19226963 [Abstract] [Full Text] [Related]
13. Development and validation of an analytical method for metformin hydrochloride and its related compound (1-cyanoguanidine) in tablet formulations by HPLC-UV. Al-Rimawi F. Talanta; 2009 Oct 15; 79(5):1368-71. PubMed ID: 19635372 [Abstract] [Full Text] [Related]
14. Validation of uv derivative spectrophotometric method for determination of benazepril hydrochloride in tablets and evaluation of its stability. Stanisz B, Paszun S, Leśniak M. Acta Pol Pharm; 2009 Oct 15; 66(4):343-9. PubMed ID: 19702164 [Abstract] [Full Text] [Related]
15. Development and validation of a HPLC method for the determination of buprenorphine hydrochloride, naloxone hydrochloride and noroxymorphone in a tablet formulation. Mostafavi A, Abedi G, Jamshidi A, Afzali D, Talebi M. Talanta; 2009 Feb 15; 77(4):1415-9. PubMed ID: 19084658 [Abstract] [Full Text] [Related]
16. High throughput LC-MS/MS method for simultaneous quantification of lamivudine, stavudine and nevirapine in human plasma. Mistri HN, Jangid AG, Pudage A, Gomes N, Sanyal M, Shrivastav P. J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Jun 15; 853(1-2):320-32. PubMed ID: 17481969 [Abstract] [Full Text] [Related]
17. Isocratic RP-HPLC method for rutin determination in solid oral dosage forms. Kuntić V, Pejić N, Ivković B, Vujić Z, Ilić K, Mićić S, Vukojević V. J Pharm Biomed Anal; 2007 Jan 17; 43(2):718-21. PubMed ID: 16920326 [Abstract] [Full Text] [Related]
18. Simultaneous determination of stavudine and lamivudine in human plasma by high performance liquid chromatography and its application to a bioavailability study. Wattananat T, Prasanchaimontri IO, Akarawut W. Southeast Asian J Trop Med Public Health; 2010 Mar 17; 41(2):369-77. PubMed ID: 20578520 [Abstract] [Full Text] [Related]
19. HPLC separation technique for analysis of bufuralol enantiomers in plasma and pharmaceutical formulations using a vancomycin chiral stationary phase and UV detection. Hefnawy MM, Sultan MA, Al-Shehri MM. J Chromatogr B Analyt Technol Biomed Life Sci; 2007 Sep 01; 856(1-2):328-36. PubMed ID: 17681871 [Abstract] [Full Text] [Related]
20. Determination of 19 antiretroviral agents in pharmaceuticals or suspected products with two methods using high-performance liquid chromatography. Rebiere H, Mazel B, Civade C, Bonnet PA. J Chromatogr B Analyt Technol Biomed Life Sci; 2007 May 01; 850(1-2):376-83. PubMed ID: 17196448 [Abstract] [Full Text] [Related] Page: [Next] [New Search]