146 related articles for article (PubMed ID: 37279742)
1. Analytical Quality by Design-Driven RP-HPLC Method Conditions to Concomitantly Determine Cinnarizine and Morin Hydrate in Combined Drug Solution and Dual Drug-Loaded Formulations.
Goswami A; Rahman SNR; Pawde DM; Shunmugaperumal T
J AOAC Int; 2023 Sep; 106(5):1154-1164. PubMed ID: 37279742
[TBL] [Abstract][Full Text] [Related]
2. Application of Design of Experiments® Approach-Driven Artificial Intelligence and Machine Learning for Systematic Optimization of Reverse Phase High Performance Liquid Chromatography Method to Analyze Simultaneously Two Drugs (Cyclosporin A and Etodolac) in Solution, Human Plasma, Nanocapsules, and Emulsions.
Rahman SNR; Katari O; Pawde DM; Boddeda GSB; Goswami A; Mutheneni SR; Shunmugaperumal T
AAPS PharmSciTech; 2021 May; 22(4):155. PubMed ID: 33987739
[TBL] [Abstract][Full Text] [Related]
3. Analytical Quality-by-Design-Based Systematic Optimization of RP-HPLC Method Conditions to Analyze Simultaneously Chloroquine Phosphate and Flavopiridol in Stress-Induced Combined Drug Solution and Pharmaceutical Emulsions.
Pawde DM; Rahman SNR; Ponneganti S; Goswami A; Borkar RM; Shunmugaperumal T
J Chromatogr Sci; 2023 Aug; 61(7):665-677. PubMed ID: 36355561
[TBL] [Abstract][Full Text] [Related]
4. QbD-steered development and validation of an RP-HPLC method for quantification of ferulic acid: Rational application of chemometric tools.
Saini S; Sharma T; Patel A; Kaur R; Tripathi SK; Katare OP; Singh B
J Chromatogr B Analyt Technol Biomed Life Sci; 2020 Oct; 1155():122300. PubMed ID: 32771967
[TBL] [Abstract][Full Text] [Related]
5. DoE-Based Analytical Failure Modes Critical Effect Analysis (AFMCEA) to a Multipurpose-RP-HPLC Method for the Estimation of Multiple FDC Products of Metformin Hydrochloride Using an Analytical Quality by Design Approach.
Prajapati PB; Mistry KY; Shah SA
J AOAC Int; 2022 Jun; 105(4):986-998. PubMed ID: 35176154
[TBL] [Abstract][Full Text] [Related]
6. Application of DoE-Based Analytical QRM to Development of the Multipurpose RP-HPLC Method for Estimation of Multiple FDC Products of Telmisartan Using Enhanced AQbD Approach.
Prajapati P; Patel A; Shah S
J Chromatogr Sci; 2022 Jul; 60(6):525-537. PubMed ID: 34121125
[TBL] [Abstract][Full Text] [Related]
7. QbD-Based Stability-Indicating RP-HPLC Method Development and Validation for the Estimation of Favipiravir-An Eco-Friendly Approach.
Chandana M S; K S; A A; Narendra P; K S
J AOAC Int; 2024 May; 107(3):377-386. PubMed ID: 38318977
[TBL] [Abstract][Full Text] [Related]
8. DoE-Based Analytical-FMCEA for Enhanced AQbD Approach to MEER-RP-HPLC Method for Synchronous Estimation of 15 Anti-Hypertensive Pharmaceutical Dosage Forms.
Prajapati PB; Patel AS; Shah SA
J AOAC Int; 2022 Feb; 105(1):34-45. PubMed ID: 34293098
[TBL] [Abstract][Full Text] [Related]
9. Analytical method development and validation of reverse-phase high-performance liquid chromatography (RP-HPLC) method for simultaneous quantifications of quercetin and piperine in dual-drug loaded nanostructured lipid carriers.
Chaudhari VS; Borkar RM; Murty US; Banerjee S
J Pharm Biomed Anal; 2020 Jul; 186():113325. PubMed ID: 32380356
[TBL] [Abstract][Full Text] [Related]
10. Formulation of Cinnarizine for Stabilization of Its Physiologically Generated Supersaturation.
Maghsoodi M; Nokhodchi A; Oskuei MA; Heidari S
AAPS PharmSciTech; 2019 Mar; 20(3):139. PubMed ID: 30868302
[TBL] [Abstract][Full Text] [Related]
11. Utilization of ionotropic gelation technique for bioavailability enhancement of cinnarizine: in-vitro optimization and in-vivo performance in human.
Abouelatta SM; Aboelwafa AA; Khalil RM; El-Gazayerly ON
Drug Deliv; 2016 Oct; 23(8):2736-2746. PubMed ID: 26165421
[TBL] [Abstract][Full Text] [Related]
12. Implementation of DoE and Risk-Based Enhanced Analytical Quality by Design Approach to Stability-Indicating RP-HPLC Method for Stability Study of Bosutinib.
Prajapati PB; Bagul N; Kalyankar G
J AOAC Int; 2021 Dec; 104(6):1742-1753. PubMed ID: 34100929
[TBL] [Abstract][Full Text] [Related]
13. Developing a Validated HPLC Method for Quantification of Ceftazidime Employing Analytical Quality by Design and Monte Carlo Simulations.
Kaur R; Saini S; Patel A; Sharma T; Kaur R; Katare OP; Singh B
J AOAC Int; 2021 Jun; 104(3):620-632. PubMed ID: 33528003
[TBL] [Abstract][Full Text] [Related]
14. Understanding the generation and maintenance of supersaturation during the dissolution of amorphous solid dispersions using modulated DSC and
Baghel S; Cathcart H; O'Reilly NJ
Int J Pharm; 2018 Jan; 536(1):414-425. PubMed ID: 29183857
[TBL] [Abstract][Full Text] [Related]
15. Multivariate Analysis and Response Surface Modeling to Green Analytical Chemistry-Based RP-HPLC-PDA Method for Chromatographic Analysis of Vildagliptin and Remogliflozin Etabonate.
Prajapati P; Prajapati B; Pulusu VS; Shah S
J AOAC Int; 2023 May; 106(3):601-612. PubMed ID: 36651669
[TBL] [Abstract][Full Text] [Related]
16. Application of Principal Component Analysis and DoE-Driven Green Analytical Chemistry Concept to Liquid Chromatographic Method for Estimation of Co-formulated Anti-Hypertensive Drugs.
Prajapati P; Jariwala H; Prajapati B; Salunkhe M; Pulusu VS; Shah S
J AOAC Int; 2023 Jul; 106(4):1087-1097. PubMed ID: 36655771
[TBL] [Abstract][Full Text] [Related]
17. Simultaneous Estimation of Telmisartan, Chlorthalidone, Amlodipine Besylate and Atorvastatin by RP-HPLC Method for Synchronous Assay of Multiple FDC Products Using Analytical FMCEA-Based AQbD Approach.
Prajapati P; Patel A; Shah S
J Chromatogr Sci; 2023 Feb; 61(2):160-171. PubMed ID: 35446938
[TBL] [Abstract][Full Text] [Related]
18. DoE-assisted development and validation of a stability-indicating HPLC-DAD method for simultaneous determination of five cannabinoids in Cannabis sativa L. based on analytical quality by design (AQbD) concept.
de Souza MR; Koetz M; Limberger RP; Henriques AT
Phytochem Anal; 2022 Oct; 33(7):999-1017. PubMed ID: 35733081
[TBL] [Abstract][Full Text] [Related]
19. Development of a validated liquid chromatographic method for quantification of sorafenib tosylate in the presence of stress-induced degradation products and in biological matrix employing analytical quality by design approach.
Sharma T; Khurana RK; Jain A; Katare OP; Singh B
Biomed Chromatogr; 2018 May; 32(5):e4169. PubMed ID: 29244215
[TBL] [Abstract][Full Text] [Related]
20. Development of a Unified Reversed-Phase HPLC Method for Efficient Determination of EP and USP Process-Related Impurities in Celecoxib Using Analytical Quality by Design Principles.
Tome T; Časar Z; Obreza A
Molecules; 2020 Feb; 25(4):. PubMed ID: 32069880
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]