2021
DOI: 10.1016/j.addr.2021.113840
|View full text |Cite
|
Sign up to set email alerts
|

A review of emerging technologies enabling improved solid oral dosage form manufacturing and processing

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
19
0
1

Year Published

2021
2021
2024
2024

Publication Types

Select...
7
1
1

Relationship

0
9

Authors

Journals

citations
Cited by 61 publications
(21 citation statements)
references
References 238 publications
0
19
0
1
Order By: Relevance
“…Conventionally, quality control (QC) tests used in large-scale manufacturing processes on Earth aim to establish shelf-life and identify by-products by accelerating abiotic degradation processes, such as hydrolysis, oxidation and photolysis ( EMA, 2003 ). Analysis typically involves multiple techniques including gas chromatography – mass spectrometry (GC/MS), infra-red spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), and elemental analysis techniques ( Sohail Arshad et al, 2021 ). These help to identify the presence of any impurities, such as heavy metals and leachable, and degradation products due to drug instability.…”
Section: Ensuring Efficacy and Safety: On-site Drug Analysismentioning
confidence: 99%
“…Conventionally, quality control (QC) tests used in large-scale manufacturing processes on Earth aim to establish shelf-life and identify by-products by accelerating abiotic degradation processes, such as hydrolysis, oxidation and photolysis ( EMA, 2003 ). Analysis typically involves multiple techniques including gas chromatography – mass spectrometry (GC/MS), infra-red spectroscopy (IR), nuclear magnetic resonance spectroscopy (NMR), and elemental analysis techniques ( Sohail Arshad et al, 2021 ). These help to identify the presence of any impurities, such as heavy metals and leachable, and degradation products due to drug instability.…”
Section: Ensuring Efficacy and Safety: On-site Drug Analysismentioning
confidence: 99%
“…In the pharmaceutical industry, solid dosage forms are most commonly prescribed and preferred by most medical practitioners, due to their accurate dosing, superior stability, and high precision [ 22 , 23 ]. For instance, the Therapeutic Goods Administration (TGA), Australia approved 59 solid dosage form products in October 2015 containing A. paniculata [ 24 ].…”
Section: Conventional Dosage Formsmentioning
confidence: 99%
“…In addition, the synergistic use of shellac and other functional excipients, such as taste-masking agents, dissolution enhancers, release-rate modifiers, and mucosal adhesives, may also add specific properties to shellac-based matrix tablets. Thus, shellac-based coprocessed excipients and ready-to-use excipients that can be used for continuous manufacturing need to be further developed to expand the application and market value of shellac-based matrix tablets . Advanced technologies also need to be introduced for the further development of shellac-based matrix tablets.…”
Section: Shellac-based Delivery Systemsmentioning
confidence: 99%
“…Thus, shellac-based coprocessed excipients and ready-to-use excipients that can be used for continuous manufacturing need to be further developed to expand the application and market value of shellac-based matrix tablets. 92 Advanced technologies also need to be introduced for the further development of shellacbased matrix tablets. Three-dimensional (3D) printing technology has become a popular additive manufacturing technology in recent years.…”
Section: Shellac-based Delivery Systemsmentioning
confidence: 99%