Literature DB >> 36056225

Continuous Manufacturing and Molecular Modeling of Pharmaceutical Amorphous Solid Dispersions.

Amritha G Nambiar1, Maan Singh1, Abhishek R Mali1, Dolores R Serrano2, Rajnish Kumar1, Anne Marie Healy3, Ashish Kumar Agrawal1, Dinesh Kumar4.   

Abstract

Amorphous solid dispersions enhance solubility and oral bioavailability of poorly water-soluble drugs. The escalating number of drugs with poor aqueous solubility, poor dissolution, and poor oral bioavailability is an unresolved problem that requires adequate interventions. This review article highlights recent solubility and bioavailability enhancement advances using amorphous solid dispersions (ASDs). The review also highlights the mechanism of enhanced dissolution and the challenges faced by ASD-based products, such as stability and scale-up. The role of process analytical technology (PAT) supporting continuous manufacturing is highlighted. Accurately predicting interactions between the drug and polymeric carrier requires long experimental screening methods, and this is a space where computational tools hold significant potential. Recent advancements in data science, computational tools, and easy access to high-end computation power are set to accelerate ASD-based research. Hence, particular emphasis has been given to molecular modeling techniques that can address some of the unsolved questions related to ASDs. With the advancement in PAT tools and artificial intelligence, there is an increasing interest in the continuous manufacturing of pharmaceuticals. ASDs are a suitable option for continuous manufacturing, as production of a drug product from an ASD by direct compression is a reality, where the addition of multiple excipients is easy to avoid. Significant attention is necessary for ongoing clinical studies based on ASDs, which is paving the way for the approval of many new ASDs and their introduction into the market.
© 2022. The Author(s), under exclusive licence to American Association of Pharmaceutical Scientists.

Entities:  

Keywords:  amorphous solid dispersions; bioavailability; continuous manufacturing; dissolution; melt extrusion; molecular modeling; solubility; spray drying

Mesh:

Substances:

Year:  2022        PMID: 36056225     DOI: 10.1208/s12249-022-02408-4

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   4.026


  109 in total

1.  Influence of solvent evaporation rate and formulation factors on solid dispersion physical stability.

Authors:  Jian X Wu; Mingshi Yang; Frans van den Berg; Jari Pajander; Thomas Rades; Jukka Rantanen
Journal:  Eur J Pharm Sci       Date:  2011-10-17       Impact factor: 4.384

2.  Structural development of self nano emulsifying drug delivery systems (SNEDDS) during in vitro lipid digestion monitored by small-angle X-ray scattering.

Authors:  Dimitrios G Fatouros; G Roshan Deen; Lise Arleth; Bjorn Bergenstahl; Flemming Seier Nielsen; Jan Skov Pedersen; Anette Mullertz
Journal:  Pharm Res       Date:  2007-04-26       Impact factor: 4.200

Review 3.  Drug delivery strategies for poorly water-soluble drugs.

Authors:  Alfred Fahr; Xiangli Liu
Journal:  Expert Opin Drug Deliv       Date:  2007-07       Impact factor: 6.648

Review 4.  Formulation design for poorly water-soluble drugs based on biopharmaceutics classification system: basic approaches and practical applications.

Authors:  Yohei Kawabata; Koichi Wada; Manabu Nakatani; Shizuo Yamada; Satomi Onoue
Journal:  Int J Pharm       Date:  2011-08-30       Impact factor: 5.875

Review 5.  Expanding the Application and Formulation Space of Amorphous Solid Dispersions with KinetiSol®: a Review.

Authors:  Daniel J Ellenberger; Dave A Miller; Robert O Williams
Journal:  AAPS PharmSciTech       Date:  2018-05-30       Impact factor: 3.246

Review 6.  Characterization of supersaturatable formulations for improved absorption of poorly soluble drugs.

Authors:  Ping Gao; Yi Shi
Journal:  AAPS J       Date:  2012-07-14       Impact factor: 4.009

7.  Pharmaceutical salts.

Authors:  S M Berge; L D Bighley; D C Monkhouse
Journal:  J Pharm Sci       Date:  1977-01       Impact factor: 3.534

Review 8.  Cyclodextrins and their pharmaceutical applications.

Authors:  Thorsteinn Loftsson; Dominique Duchêne
Journal:  Int J Pharm       Date:  2006-11-09       Impact factor: 5.875

9.  Mechanistic Design of Chemically Diverse Polymers with Applications in Oral Drug Delivery.

Authors:  Laura I Mosquera-Giraldo; Carlos H Borca; Xiangtao Meng; Kevin J Edgar; Lyudmila V Slipchenko; Lynne S Taylor
Journal:  Biomacromolecules       Date:  2016-10-07       Impact factor: 6.988

10.  The effect of drug loading on the properties of abiraterone-hydroxypropyl beta cyclodextrin solid dispersions processed by solvent free KinetiSol® technology.

Authors:  Urvi H Gala; Dave A Miller; Yongchao Su; Angela Spangenberg; Robert O Bill Williams
Journal:  Eur J Pharm Biopharm       Date:  2021-05-09       Impact factor: 5.571

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.