2014
DOI: 10.1208/s12249-014-0177-9
|View full text |Cite
|
Sign up to set email alerts
|

Nanomedicine Scale-up Technologies: Feasibilities and Challenges

Abstract: Abstract. Nanomedicine refers to biomedical and pharmaceutical applications of nanosized cargos of drugs/vaccine/DNA therapeutics including nanoparticles, nanoclusters, and nanospheres. Such particles have unique characteristics related to their size, surface, drug loading, and targeting potential. They are widely used to combat disease by controlled delivery of bioactive(s) or for diagnosis of life-threatening problems in their very early stage. The bioactive agent can be combined with a diagnostic agent in a… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

1
136
0
2

Year Published

2015
2015
2024
2024

Publication Types

Select...
7
3

Relationship

0
10

Authors

Journals

citations
Cited by 255 publications
(148 citation statements)
references
References 39 publications
1
136
0
2
Order By: Relevance
“…109,110 Thus, another hurdle in the development and clinical translation of nanomaterials has been adaptation of manufacturing processes and scale-up challenges, mainly due to extensive diversity of properties of new materials. 111,112 It is fundamental to identify and control the critical points during each manufacturing process. Applying concepts of quality by design, such as process analytical technologies (PAT), will ensure an on line/at line quality assessment approach.…”
Section: Risk Assessment and Control Bandingmentioning
confidence: 99%
“…109,110 Thus, another hurdle in the development and clinical translation of nanomaterials has been adaptation of manufacturing processes and scale-up challenges, mainly due to extensive diversity of properties of new materials. 111,112 It is fundamental to identify and control the critical points during each manufacturing process. Applying concepts of quality by design, such as process analytical technologies (PAT), will ensure an on line/at line quality assessment approach.…”
Section: Risk Assessment and Control Bandingmentioning
confidence: 99%
“…Apart from nanotoxicity, another aspect to be taken into consideration while developing nanoparticle-based pharmaceuticals is their synthesis and production in bulk. Different scale-up technologies are being developed for their large-scale synthesis [132]. Cost optimization along with the demands for market supply need to be fulfilled in order to render nanoparticle-based therapeutics more suitable for clinical use.…”
Section: Discussionmentioning
confidence: 99%
“…89 Since materials for the preparation of nanocarrier may be a polymer, lipid, or metal, selection of method depends on the nature of it. In addition, chronic exposure to nanocarriers such as polymeric and metallic nanoparticles may cause toxicity that may be due to their size, shape, and less biodegradability.…”
Section: Formulation Development and Challengesmentioning
confidence: 99%