Advantages and Limitations of Current Techniques for Analyzing the Biodistribution of Nanoparticles
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Nanomedicines are typically submicrometer-sized carrier materials (nanoparticles) encapsulating therapeutic and/or imaging compounds that are used for the prevention, diagnosis and treatment of diseases. They are increasingly being used to overcome biological barriers in the body to improve the way we deliver compounds to specific tissues and organs. Nanomedicine technology aims to improve the balance between the efficacy and the toxicity of therapeutic compounds. Nanoparticles, one of the key technologies of nanomedicine, can exhibit a combination of physical, chemical and biological characteristics that determine their in vivo behavior. A key component in the translational assessment of nanomedicines is determining the biodistribution of the nanoparticles following in vivo administration in animals and humans. There are a range of techniques available for evaluating nanoparticle biodistribution, including histology, liquid scintillation counting (LSC), indirectly measuring drug concentrations, in vivo optical imaging, computed tomography (CT), magnetic resonance imaging (MRI), and nuclear medicine imaging. Each technique has its own advantages and limitations, as well as capabilities for assessing real-time, whole-organ and cellular accumulation. This review will address the principles and methodology of each technique and their advantages and limitations for evaluating in vivo biodistribution of nanoparticles.
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Dynamic contrast-enhanced CT has been utilized to evaluate intratumoral perfusion, permeability, and aggregation of CT contrast agent-carrying NPs in tumors in mice.
“However, dynamic contrast-enhanced (DCE)CT has been utilized to evaluate the intratumoral perfusion, permeability, and aggregation of CT contrast agent-carrying NPs in tumors in mice [19,132,133].”
From Approaches to Improve EPR-Based Drug Delivery for Cancer Therapy and Diagnosis (2023) · cites this paper as [133]
The Computed tomography (CT) section (page unavailable) says CT has been used for real-time, in vivo imaging of nanoparticles carrying contrast agents, including repeated imaging in animals. It does not describe dynamic contrast-enhanced CT measuring intratumoral perfusion, permeability, or nanoparticle aggregation in mouse tumors. (LLM, conf=0.85)
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- Authors
- Arms, L., Smith, D. W., Flynn, J., Palmer, W., Martin, A., Woldu, A., & Hua, S.
- Affiliations
- University of Newcastle Australia (AU)
- Hunter Medical Research Institute (AU)
- Corresponding author
- Hua, Susan
- Venue
- Frontiers in Pharmacology
- Publisher
- Frontiers Media SA
- Published
- 2018-08-14
- Volume
- 9
- Pages
- 802-802
- ISSN
- 1663-9812 (ISSN-L)
- PMC
- PMC6102329
- OpenAlex
- W2885328264
- Cited by
- 159
- References
- 166
- Citations by year
- 2026: 15 · 2025: 31 · 2024: 23 · 2023: 18 · 2022: 17 · 2021: 29 · 2020: 18 · 2019: 8
- FWCI
- 0.91
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Frontiers in Pharmacology (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- NOVA (University of Newcastle Australia) (submittedVersion)
- Funders
- Rebecca L. Cooper Medical Research Foundation
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Physical Sciences › Engineering › Biomedical Engineering › Nanotechnology research and applications
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Radiopharmaceutical Chemistry and Applications
- Keywords
- nanoparticle biodistribution, nanomedicine, in vivo imaging, liquid scintillation counting, in vivo optical imaging, computed tomography, magnetic resonance imaging, scintigraphy, histology, nanoparticle accumulation
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