622 related articles for article (PubMed ID: 31680080)
1. Development and validation of a stability-Indicating RP-HPLC method for simultaneous estimation of sofosbuvir and velpatasvir in fixed dose combination tablets and plasma.
Mehmood Y; Khan IU; Shahzad Y; Khalid SH; Irfan M; Asghar S; Yousaf AM; Hussain T; Khalid I
Pak J Pharm Sci; 2019 Jul; 32(4(Supplementary)):1835-1842. PubMed ID: 31680080
[TBL] [Abstract][Full Text] [Related]
2. Rapid bioanalytical LC-MS/MS method for the simultaneous determination of sofosbuvir and velpatasvir in human plasma-application to a pharmacokinetic study in Egyptian volunteers.
Elkady EF; Aboelwafa AA
J Chromatogr B Analyt Technol Biomed Life Sci; 2018 Dec; 1102-1103():116-124. PubMed ID: 30384188
[TBL] [Abstract][Full Text] [Related]
3. RP-HPLC Method for the Determination and Quantification of Artesunate.
Saeed MA; Ansari MT; Ch BA; Zaman M
J Chromatogr Sci; 2020 Aug; 58(8):695-699. PubMed ID: 32719858
[TBL] [Abstract][Full Text] [Related]
4. Development and validation of a versatile HPLC-DAD method for simultaneous determination of the antiviral drugs daclatasvir, ledipasvir, sofosbuvir and ribavirin in presence of seven potential impurities. Application to assay of dosage forms and dissolution studies.
Baker MM; Hammad SF; Belal TS
Drug Dev Ind Pharm; 2019 Jul; 45(7):1111-1119. PubMed ID: 30929537
[TBL] [Abstract][Full Text] [Related]
5. Development and validation of RP-HPLC method for determination of Lornoxicam in rabbit's plasma.
Shah SNH; Sohail K; Javaid Z; Zaman M; Basheer E
Pak J Pharm Sci; 2019 Jan; 32(1(Supplementary)):333-338. PubMed ID: 30829212
[TBL] [Abstract][Full Text] [Related]
6. Simultaneous determination of domperidone and Itopride in pharmaceuticals and human plasma using RP-HPLC/UV detection: Method development, validation and application of the method in in-vivo evaluation of fast dispersible tablets.
Khan A; Iqbal Z; Khadra I; Ahmad L; Khan A; Khan MI; Ullah Z; Ismail
J Pharm Biomed Anal; 2016 Mar; 121():6-12. PubMed ID: 26773534
[TBL] [Abstract][Full Text] [Related]
7. RP-HPLC method development and validation for quantification of daclatasvir dihydrochloride and its application to pharmaceutical dosage form.
Hussain Shah SS; Nasiri MI; Sarwar H; Ali A; S Naqvi SB; Anwer S; Kashif M
Pak J Pharm Sci; 2021 May; 34(3):951-956. PubMed ID: 34602418
[TBL] [Abstract][Full Text] [Related]
8. Development and validation of a novel stability-indicating HPLC method for the quantitative determination of eleven related substances in ezetimibe drug substance and drug product.
Luo Z; Deng Z; Liu Y; Wang G; Yang W; Hou C; Tang M; Yang R; Zhou H
Talanta; 2015 Jul; 139():67-74. PubMed ID: 25882410
[TBL] [Abstract][Full Text] [Related]
9. Development and validation of LC-MS/MS method for simultaneous determination of sofosbuvir and daclatasvir in human Plasma: Application to pharmacokinetic study.
Abdallah OM; Abdel-Megied AM; Gouda AS
Biomed Chromatogr; 2018 Jun; 32(6):e4186. PubMed ID: 29314090
[TBL] [Abstract][Full Text] [Related]
10. Development of validated stability indicating assay method for simultaneous estimation of metformin hydrochloride and vildagliptin by RP-HPLC.
Satheeshkumar N; Pradeepkumar M; Shanthikumar S; Rao VJ
Drug Res (Stuttg); 2014 Mar; 64(3):124-9. PubMed ID: 24081820
[TBL] [Abstract][Full Text] [Related]
11. Study on fluorescence properties of HCV antiviral (velpatasvir) and its fluorimetric determination in presence of sofosbuvir; application to stability study and human plasma.
Omar MA; Abdel-Lateef MA; Ali R; Derayea SM
Luminescence; 2018 Nov; 33(7):1249-1256. PubMed ID: 30144265
[TBL] [Abstract][Full Text] [Related]
12. Rosiglitazone quantification in rat plasma using high performance liquid chromatography with mass spectrometric detection and its application to pre-clinical pharmacokinetic studies.
Lakshmi KS; Rajesh T
PDA J Pharm Sci Technol; 2011; 65(2):100-8. PubMed ID: 21502071
[TBL] [Abstract][Full Text] [Related]
13. Spectrophotometric assessment of the brand new antiviral combination: Sofosbuvir and velpatasvir in their pure forms and pharmaceutical formulation.
Rezk MR; Monir HH; Marzouk HM
Spectrochim Acta A Mol Biomol Spectrosc; 2019 Apr; 213():159-166. PubMed ID: 30685554
[TBL] [Abstract][Full Text] [Related]
14. Novel determination of sofosbuvir and velpatasvir in human plasma by UPLC-MS/MS method: Application to a bioequivalence study.
Rezk MR; Basalious EB; Badr KA
Biomed Chromatogr; 2018 Nov; 32(11):e4347. PubMed ID: 30047564
[TBL] [Abstract][Full Text] [Related]
15. Development and validation of a reversed-phase ultra-performance liquid chromatographic method for assay of lacidipine and related substances.
Mohan A; Patel HB; Saravanan D
J AOAC Int; 2011; 94(6):1800-6. PubMed ID: 22320087
[TBL] [Abstract][Full Text] [Related]
16. Validated Reversed-Phase Liquid Chromatographic Method with Gradient Elution for Simultaneous Determination of the Antiviral Agents: Sofosbuvir, Ledipasvir, Daclatasvir, and Simeprevir in Their Dosage Forms.
Ezzeldin E; Abo-Talib NF; Tammam MH; Asiri YA; Amr AEE; Almehizia AA
Molecules; 2020 Oct; 25(20):. PubMed ID: 33050433
[TBL] [Abstract][Full Text] [Related]
17. Development and validation of a stability-indicating RP-HPLC method for the determination of febuxostat (a xanthine oxidase inhibitor).
Mukthinuthalapati MA; Bandaru SP; Bukkapatnam V; Mohapatro C
J Chromatogr Sci; 2013; 51(10):931-8. PubMed ID: 23204011
[TBL] [Abstract][Full Text] [Related]
18. Investigation of anti-Hepatitis C virus, sofosbuvir and daclatasvir, in pure form, human plasma and human urine using micellar monolithic HPLC-UV method and application to pharmacokinetic study.
Zidan DW; Hassan WS; Elmasry MS; Shalaby AA
J Chromatogr B Analyt Technol Biomed Life Sci; 2018 Jun; 1086():73-81. PubMed ID: 29660665
[TBL] [Abstract][Full Text] [Related]
19. Fast RP-HPLC Method for the Determination of Bisoprolol.
Panainte AD; Vieriu M; Ţântaru G; Apostu M; Bibire N
Rev Med Chir Soc Med Nat Iasi; 2016; 120(3):720-6. PubMed ID: 30152661
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
