2012
DOI: 10.1111/j.1748-720x.2012.00709.x
|View full text |Cite
|
Sign up to set email alerts
|

Concepts of Risk in Nanomedicine Research

Abstract: Risk takes center stage in ethical debates over nanomedical technologies. Yet concepts of risk may hold different meanings, and they are embedded within particular political, economic, and social contexts. This article discusses framings of risk in debates over medical innovations such as nanomedicine, and draws attention to organizational and institutional forms of risk which are less visible in bioethical policy debates. While significant, possibly unique risks may exist in specific nano-based products, risk… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
5
0

Year Published

2015
2015
2023
2023

Publication Types

Select...
6
1
1

Relationship

0
8

Authors

Journals

citations
Cited by 11 publications
(5 citation statements)
references
References 25 publications
(14 reference statements)
0
5
0
Order By: Relevance
“…In the case of ADCs, toxicological analyses are typically the first thing that comes to mind when assessing risk, as they are critical for evaluating the safety of these molecules. There is a significant body of literature on toxicological risk analysis for ADCs, and many new methodologies have been developed and published [ 75 , 76 , 77 ]. However, business risk methodologies for the development of these molecules have been less discussed.…”
Section: Challenges and Business Risks In Randd Of Adcsmentioning
confidence: 99%
“…In the case of ADCs, toxicological analyses are typically the first thing that comes to mind when assessing risk, as they are critical for evaluating the safety of these molecules. There is a significant body of literature on toxicological risk analysis for ADCs, and many new methodologies have been developed and published [ 75 , 76 , 77 ]. However, business risk methodologies for the development of these molecules have been less discussed.…”
Section: Challenges and Business Risks In Randd Of Adcsmentioning
confidence: 99%
“…This increased risk has implications for informed consent in clinical trials. [56][57][58][59][60] For example, the occurrence of side effects may be delayed, given that some nanotechnology platforms, such as nanogold, can accumulate in tissues and persist longer than traditional medicines. 61 As a result, some side effects might not be captured during the trial itself or even during the first few years of postapproval long-term safety monitoring.…”
Section: Ethical Considerations In Nanomedicinementioning
confidence: 99%
“…An elevated degree of unpredictability about prospective hazards and true advantages of NPs and nanomedicines, however, created remarkable obstacles along this translational pathway (Resnik and Tinkle, 2007 ). As such, nanotechnological approaches have opened up a few issues with respect to their proper risk assessment and risk minimization (Hogle, 2012 ), with particular emphasis on human and environmental toxicity (Allhoff, 2009 ; Ramachandran et al, 2012 ). Especially compelling in this respect are “first in human” (FIH) trials of nanotechnology medical applications, as they raise the highest degree of unpredictability in all clinical area (Kimmelman and John London, 2011 ).…”
Section: Risk Assessment and Risk Minimization In Nanomedicinementioning
confidence: 99%