These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
155 related articles for article (PubMed ID: 32496145)
1. Application of chemometric modelling to UV-Vis spectroscopy: development of simultaneous API and critical excipient assay in a liquid solution continuous flow. Angheluta A; Guizani S; Saunier J; Rönnback R Pharm Dev Technol; 2020 Oct; 25(8):919-929. PubMed ID: 32496145 [TBL] [Abstract][Full Text] [Related]
2. In-line ATR-UV and Raman Spectroscopy for Monitoring API Dissolution Process During Liquid-Filled Soft-Gelatin Capsule Manufacturing. Wan B; Zordan CA; Lu X; McGeorge G AAPS PharmSciTech; 2016 Oct; 17(5):1173-81. PubMed ID: 26604007 [TBL] [Abstract][Full Text] [Related]
3. PAT for tableting: inline monitoring of API and excipients via NIR spectroscopy. Wahl PR; Fruhmann G; Sacher S; Straka G; Sowinski S; Khinast JG Eur J Pharm Biopharm; 2014 Jul; 87(2):271-8. PubMed ID: 24705126 [TBL] [Abstract][Full Text] [Related]
4. [Simultaneous quantitative determination of multicomponents in tablets based on terahertz time-domain spectroscopy]. Chen T; Li Z; Mo W; Hu FR Guang Pu Xue Yu Guang Pu Fen Xi; 2013 May; 33(5):1220-5. PubMed ID: 23905323 [TBL] [Abstract][Full Text] [Related]
5. An investigation into the effects of excipient particle size, blending techniques and processing parameters on the homogeneity and content uniformity of a blend containing low-dose model drug. Alyami H; Dahmash E; Bowen J; Mohammed AR PLoS One; 2017; 12(6):e0178772. PubMed ID: 28609454 [TBL] [Abstract][Full Text] [Related]
6. Predictive evaluation of multicomponent direct compress model tablets by integrating sphere UV-Vis spectroscopy and chemometrics. Otsuka Y; Pal S Biomed Mater Eng; 2022; 33(3):183-194. PubMed ID: 34897077 [TBL] [Abstract][Full Text] [Related]
7. Continuous manufacturing of a pharmaceutical cream: Investigating continuous powder dispersing and residence time distribution (RTD). Bostijn N; Van Renterghem J; Vanbillemont B; Dhondt W; Vervaet C; De Beer T Eur J Pharm Sci; 2019 Apr; 132():106-117. PubMed ID: 30831193 [TBL] [Abstract][Full Text] [Related]
8. Why should the pharmaceutical industry claim for the implementation of second-order chemometric models-A critical review. Vignaduzzo SE; Maggio RM; Olivieri AC J Pharm Biomed Anal; 2020 Feb; 179():112965. PubMed ID: 31753531 [TBL] [Abstract][Full Text] [Related]
9. Near InfraRed Spectroscopy homogeneity evaluation of complex powder blends in a small-scale pharmaceutical preformulation process, a real-life application. Storme-Paris I; Clarot I; Esposito S; Chaumeil JC; Nicolas A; Brion F; Rieutord A; Chaminade P Eur J Pharm Biopharm; 2009 May; 72(1):189-98. PubMed ID: 19059338 [TBL] [Abstract][Full Text] [Related]
10. Assessment of powder blend uniformity: Comparison of real-time NIR blend monitoring with stratified sampling in combination with HPLC and at-line NIR Chemical Imaging. Bakri B; Weimer M; Hauck G; Reich G Eur J Pharm Biopharm; 2015 Nov; 97(Pt A):78-89. PubMed ID: 26455421 [TBL] [Abstract][Full Text] [Related]
11. Impact Of Excipient Variability On Drug Product Processing And Performance. Peng Soh JL; Liew CV; Sia Heng PW Curr Pharm Des; 2015; 21(40):5890-9. PubMed ID: 26446469 [TBL] [Abstract][Full Text] [Related]
12. Excipient variability and its impact on dosage form functionality. Dave VS; Saoji SD; Raut NA; Haware RV J Pharm Sci; 2015 Mar; 104(3):906-15. PubMed ID: 25561249 [TBL] [Abstract][Full Text] [Related]
13. A continuous manufacturing concept for a pharmaceutical oral suspension. Bostijn N; Van Renterghem J; Dhondt W; Vervaet C; De Beer T Eur J Pharm Sci; 2018 Oct; 123():576-583. PubMed ID: 30102980 [TBL] [Abstract][Full Text] [Related]
14. Managing active pharmaceutical ingredient raw material variability during twin-screw blend feeding. Stauffer F; Vanhoorne V; Pilcer G; Chavez PF; Schubert MA; Vervaet C; De Beer T Eur J Pharm Biopharm; 2019 Feb; 135():49-60. PubMed ID: 30582959 [TBL] [Abstract][Full Text] [Related]
15. Process analytical technology (PAT): quantification approaches in terahertz spectroscopy for pharmaceutical application. Wu H; Heilweil EJ; Hussain AS; Khan MA J Pharm Sci; 2008 Feb; 97(2):970-84. PubMed ID: 17722101 [TBL] [Abstract][Full Text] [Related]
16. In-line Raman spectroscopic monitoring and feedback control of a continuous twin-screw pharmaceutical powder blending and tableting process. Nagy B; Farkas A; Gyürkés M; Komaromy-Hiller S; Démuth B; Szabó B; Nusser D; Borbás E; Marosi G; Nagy ZK Int J Pharm; 2017 Sep; 530(1-2):21-29. PubMed ID: 28723408 [TBL] [Abstract][Full Text] [Related]
17. Drug-excipient compatibility screening--role of thermoanalytical and spectroscopic techniques. Chadha R; Bhandari S J Pharm Biomed Anal; 2014 Jan; 87():82-97. PubMed ID: 23845418 [TBL] [Abstract][Full Text] [Related]
18. Analytical comparison between batch and continuous direct compression processes for pharmaceutical manufacturing using an innovative UV-Vis reflectance method and chemometrics. Macchietti L; Melucci D; Menarini L; Consoli F; Zappi A Int J Pharm; 2024 May; 656():124090. PubMed ID: 38582101 [TBL] [Abstract][Full Text] [Related]
19. Monitoring the dissolution of Active Pharmaceutical Ingredient and TPGS in real time via IR spectroscopy during the manufacturing of liquid dosage formulation. Šašić S; Palm AS; Tang D J Pharm Biomed Anal; 2012 Nov; 70():273-9. PubMed ID: 22871426 [TBL] [Abstract][Full Text] [Related]
20. Near-infrared spectroscopic applications in pharmaceutical particle technology. Razuc M; Grafia A; Gallo L; Ramírez-Rigo MV; Romañach RJ Drug Dev Ind Pharm; 2019 Oct; 45(10):1565-1589. PubMed ID: 31282753 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]