147 related articles for article (PubMed ID: 29403737)
1. Development and validation of RP-HPLC and RP-UPLC methods for quantification of erythropoietin formulated with human serum albumin.
Rane SS; Ajameri A; Mody R; Padmaja P
J Pharm Anal; 2012 Apr; 2(2):160-165. PubMed ID: 29403737
[TBL] [Abstract][Full Text] [Related]
2. Development and validation of RP-HPLC and RP-UPLC methods for quantification of parathyroid hormones (1-34) in medicinal product formulated with meta-cresol.
Rane SS; Ajameri A; Mody R; Padmaja P
J Pharm Anal; 2012 Apr; 2(2):136-142. PubMed ID: 29403733
[TBL] [Abstract][Full Text] [Related]
3. Rapid Development and Validation of Improved Reversed-Phase High-performance Liquid Chromatography Method for the Quantification of Mangiferin, a Polyphenol Xanthone Glycoside in
Naveen P; Lingaraju HB; Prasad KS
Pharmacognosy Res; 2017; 9(2):215-219. PubMed ID: 28539748
[TBL] [Abstract][Full Text] [Related]
4. Development and validation of a HPLC method for the determination of voriconazole in pharmaceutical formulation using an experimental design.
Srinubabu G; Raju ChA; Sarath N; Kumar PK; Rao JV
Talanta; 2007 Feb; 71(3):1424-9. PubMed ID: 19071468
[TBL] [Abstract][Full Text] [Related]
5. Validation of a simple RP-HPLC method developed for the quantification of meta-cresol in parathyroid hormones formulation.
Rane SS; Ajameri A; Mody R; Padmaja P
Pharm Methods; 2011 Jul; 2(3):203-8. PubMed ID: 23781457
[TBL] [Abstract][Full Text] [Related]
6. Development and Validation of a Simple and Rapid UPLC-MS Assay for Valproic Acid and Its Comparison With Immunoassay and HPLC Methods.
Zhao M; Li G; Qiu F; Sun Y; Xu Y; Zhao L
Ther Drug Monit; 2016 Apr; 38(2):246-52. PubMed ID: 26488205
[TBL] [Abstract][Full Text] [Related]
7. Method Development and Validation for the Determination of Caffeine: An Alkaloid from
Naveen P; Lingaraju HB; Deepak M; Medhini B; Prasad KS
Pharmacognosy Res; 2018; 10(1):88-91. PubMed ID: 29568193
[TBL] [Abstract][Full Text] [Related]
8. A New Rapid and Sensitive Stability-Indicating UPLC Assay Method for Tolterodine Tartrate: Application in Pharmaceuticals, Human Plasma and Urine Samples.
Yanamandra R; Vadla CS; Puppala U; Patro B; Murthy YL; Ramaiah PA
Sci Pharm; 2012; 80(1):101-14. PubMed ID: 22396907
[TBL] [Abstract][Full Text] [Related]
9. Rapid determination of nitazoxanide in tablets using reversed-phase ultra-performance liquid chromatography (UPLC) and high-performance liquid chromatography.
Sakamoto T; Hiyama Y
Pharmazie; 2008 Jul; 63(7):503-7. PubMed ID: 18717482
[TBL] [Abstract][Full Text] [Related]
10. A Validated Reverse Phase-Ultra-Performance Liquid Chromatography Method for the Determination of Gemifloxacin Mesylate in Bulk and its Pharmaceutical Preparation.
Wagdy HA; Tarek M; Amer A; Gamal M; Elmazar M
Turk J Pharm Sci; 2019 Mar; 16(1):8-13. PubMed ID: 32454688
[TBL] [Abstract][Full Text] [Related]
11. Fast, selective and quantitative protein profiling of adenovirus-vector based vaccines by ultra-performance liquid chromatography.
van Tricht E; de Raadt P; Verwilligen A; Schenning M; Backus H; Germano M; Somsen GW; Sänger-van de Griend CE
J Chromatogr A; 2018 Dec; 1581-1582():25-32. PubMed ID: 30389208
[TBL] [Abstract][Full Text] [Related]
12. A Chromatographic Determination of Aripiprazole using HPLC and UPLC: A Comparative Validation Study.
Thakkar RS; Saravaia HT; Ambasana MA; Kaila HO; Shah AK
Indian J Pharm Sci; 2011 Jul; 73(4):439-43. PubMed ID: 22707830
[TBL] [Abstract][Full Text] [Related]
13. Development and validation of high-performance liquid chromatography and high-performance thin-layer chromatography methods for the quantification of khellin in Ammi visnaga seed.
Kamal A; Khan W; Ahmad S; Ahmad FJ; Saleem K
J Pharm Bioallied Sci; 2015; 7(4):308-13. PubMed ID: 26681890
[TBL] [Abstract][Full Text] [Related]
14. Validation of a LC method for the analysis of oxaliplatin in a pharmaceutical formulation using an experimental design.
Ficarra R; Calabrò ML; Cutroneo P; Tommasini S; Melardi S; Semreen M; Furlanetto S; Ficarra P; Altavilla G
J Pharm Biomed Anal; 2002 Aug; 29(6):1097-103. PubMed ID: 12110395
[TBL] [Abstract][Full Text] [Related]
15. Development and Validation of Liquid Chromatographic Method for Estimation of Naringin in Nanoformulation.
Musmade KP; Trilok M; Dengale SJ; Bhat K; Reddy MS; Musmade PB; Udupa N
J Pharm (Cairo); 2014; 2014():864901. PubMed ID: 26556205
[TBL] [Abstract][Full Text] [Related]
16. RP-HPLC Method Development and Validation for Determination of Eptifibatide Acetate in Bulk Drug Substance and Pharmaceutical Dosage Forms.
Bavand Savadkouhi M; Vahidi H; Ayatollahi AM; Hooshfar S; Kobarfard F
Iran J Pharm Res; 2017; 16(2):490-497. PubMed ID: 28979304
[TBL] [Abstract][Full Text] [Related]
17. Development and validation of a new ultra-performance liquid chromatographic method for vancomycin assay in serum and its application to therapeutic drug monitoring.
Cao Y; Yu J; Chen Y; Zhang J; Wu X; Zhang Y; Li G
Ther Drug Monit; 2014 Apr; 36(2):175-81. PubMed ID: 24216537
[TBL] [Abstract][Full Text] [Related]
18. Development and Validation of RP-HPLC Method for the Simultaneous Estimation of Montelukast Sodium and Ebastine in Tablet Dosage Form.
Rana NS; Rajesh KS; Patel NN; Patel PR; Limbachiya U; Pasha TY
Indian J Pharm Sci; 2013 Sep; 75(5):599-602. PubMed ID: 24403662
[TBL] [Abstract][Full Text] [Related]
19. RP-HPLC method development for the simultaneous determination of timolol maleate and human serum albumin in albumin nanoparticles.
Boiero C; Allemandi D; Longhi M; Llabot JM
J Pharm Biomed Anal; 2015; 111():186-9. PubMed ID: 25890214
[TBL] [Abstract][Full Text] [Related]
20. Development and validation of RP-HPLC method for sildenafil citrate in rat plasma-application to pharmacokinetic studies.
Tripathi AS; Sheikh I; Dewani AP; Shelke PG; Bakal RL; Chandewar AV; Mazumder PM
Saudi Pharm J; 2013 Jul; 21(3):317-21. PubMed ID: 23960848
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
