132 related articles for article (PubMed ID: 38670472)
1. A framework for the in silico assessment of the robustness of an MPC in a CDC line in function of process variability.
Waeytens R; Van Hauwermeiren D; Grymonpré W; Nopens I; De Beer T
Int J Pharm; 2024 Jun; 658():124137. PubMed ID: 38670472
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Continuous Feeding and Blending Demonstration with Co-Processed Drug Substance.
Erdemir D; Gawel J; Yohannes B; Yates P; Tang D; Ha K; Breza B; DiMaso E; Abebe A; Zombek J
J Pharm Sci; 2023 Aug; 112(8):2046-2056. PubMed ID: 36462708
[TBL] [Abstract][Full Text] [Related]
5. System-wide hybrid MPC-PID control of a continuous pharmaceutical tablet manufacturing process via direct compaction.
Singh R; Ierapetritou M; Ramachandran R
Eur J Pharm Biopharm; 2013 Nov; 85(3 Pt B):1164-82. PubMed ID: 23523542
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Deep learning for continuous manufacturing of pharmaceutical solid dosage form.
Roggo Y; Jelsch M; Heger P; Ensslin S; Krumme M
Eur J Pharm Biopharm; 2020 Aug; 153():95-105. PubMed ID: 32535045
[TBL] [Abstract][Full Text] [Related]
8. Cleaning of direct compression continuous manufacturing equipment through displacement of API residues by excipients.
Patel DS; Méndez R; Romañach RJ
Int J Pharm; 2024 Mar; 652():123849. PubMed ID: 38266938
[TBL] [Abstract][Full Text] [Related]
9. Manufacturing process transfer to a 30 kg/h continuous direct compression line with real-time composition monitoring.
Waněk A; Menarini L; Giatti F; Kubelka T; Consoli F; Funaro C; Stasiak P; Štěpánek F
Int J Pharm; 2024 May; 656():124100. PubMed ID: 38609059
[TBL] [Abstract][Full Text] [Related]
10. Continuous direct compression of a commercially batch-manufactured tablet formulation with two different processing lines.
Lyytikäinen J; Stasiak P; Kubelka T; Bogaerts I; Wanek A; Stynen B; Holman J; Ketolainen J; Ervasti T; Korhonen O
Eur J Pharm Biopharm; 2024 Jun; 199():114278. PubMed ID: 38583787
[TBL] [Abstract][Full Text] [Related]
11. Comparison between integrated continuous direct compression line and batch processing - The effect of raw material properties.
Karttunen AP; Wikström H; Tajarobi P; Fransson M; Sparén A; Marucci M; Ketolainen J; Folestad S; Korhonen O; Abrahmsén-Alami S
Eur J Pharm Sci; 2019 May; 133():40-53. PubMed ID: 30862514
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Effects of process parameters on tablet critical quality attributes in continuous direct compression: a case study of integrating data-driven statistical models and mechanistic compaction models.
Huang Z; Galbraith SC; Cha B; Liu H; Park S; Flamm MH; Metzger M; Tantuccio A; Yoon S
Pharm Dev Technol; 2020 Dec; 25(10):1204-1215. PubMed ID: 32808839
[TBL] [Abstract][Full Text] [Related]
14. Pharmaceutical excipients properties and screw feeder performance in continuous processing lines: a Quality by Design (QbD) approach.
Santos B; Carmo F; Schlindwein W; Muirhead G; Rodrigues C; Cabral L; Westrup J; Pitt K
Drug Dev Ind Pharm; 2018 Dec; 44(12):2089-2097. PubMed ID: 30113219
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Reduction of tablet weight variability by optimizing paddle speed in the forced feeder of a high-speed rotary tablet press.
Peeters E; De Beer T; Vervaet C; Remon JP
Drug Dev Ind Pharm; 2015 Apr; 41(4):530-9. PubMed ID: 24502268
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Assessment of blend uniformity in a continuous tablet manufacturing process.
Sierra-Vega NO; Román-Ospino A; Scicolone J; Muzzio FJ; Romañach RJ; Méndez R
Int J Pharm; 2019 Apr; 560():322-333. PubMed ID: 30763679
[TBL] [Abstract][Full Text] [Related]
20. Integrating sensors for monitoring blend content in a pharmaceutical continuous manufacturing plant.
Panikar S; Li J; Rane V; Gillam S; Callegari G; Kurtyka B; Lee S; Muzzio F
Int J Pharm; 2021 Sep; 606():120085. PubMed ID: 33737095
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
