Evidence map›Paper›PMID 36520546›Full record

ReviewACS nano2022

Integration of In Vitro and In Vivo Models to Predict Cellular and Tissue Dosimetry of Nanomaterials Using Physiologically Based Pharmacokinetic Modeling.

Zhoumeng Lin, Santosh Aryal, Yi-Hsien Cheng, Andre J Gesquiere

Abstract readReview
In one paragraph

Review in ACS nano, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  15. Predicting tissue distribution and tumor delivery of nanoparticles in mice using machine learning models.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Article
  16. Antimicrobial activity of metal-based nanoparticles: a mini-review.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2024
    Review
  17. Advancing Toxicity Predictions: A Review onEnvironment & health (Washington, D.C.) · 2024
    Review
  18. Article
  19. Article
  20. An artificial intelligence-assisted physiologically-based pharmacokinetic model to predict nanoparticle delivery to tumors in mice.Journal of controlled release : official journal of the Controlled Release Society · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Zhoumeng LinDepartment of Environmental and Global Health, College of Public Health and Health Professions, University of Florida, Gainesville, Florida 32610, United States.ORCID 0000-0002-8731-8366
Santosh AryalDepartment of Pharmaceutical Sciences and Health Outcomes, The Ben and Maytee Fisch College of Pharmacy, The University of Texas at Tyler, Tyler, Texas 75799, United States.ORCID 0000-0002-7807-6342
Yi-Hsien ChengDepartment of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas 66506, United States.ORCID 0000-0002-4314-9732
Andre J GesquiereDepartment of Chemistry, College of Sciences, University of Central Florida, Orlando, Florida 32816, United States.

Funding

Development of a web-based predictive model of nanoparticle delivery to tumors by integrating physiologically-based pharmacokinetic modeling with artificial intelligenceR01EB031022 · NIBIB · UNIVERSITY OF FLORIDA · PI Zhoumeng Lin · 2021 to 2026
$2.2M
Re-engineering Tumor Cell-Derived Extracellular Vesicles with Exogenous Tags for Downstream AnalysisR15EB030815 · NIBIB · UNIVERSITY OF TEXAS TYLER · PI ARYAL, SANTOSH · 2020 to 2020
$427k
Physiologically based pharmacokinetic modeling and analysis of administration route-dependent tissue distribution of gold nanoparticlesR03EB026045 · NIBIB · UNIVERSITY OF FLORIDA · PI LIN, ZHOUMENG · 2019 to 2020
$152k
NIBIB NIH HHS R01 EB031022NIBIB NIH HHS R03 EB026045NIBIB NIH HHS R15 EB030815
6 · The paper itself

Abstract

Nanomaterials (NMs) have been increasingly used in a number of areas, including consumer products and nanomedicine. Target tissue dosimetry is important in the evaluation of safety, efficacy, and potential toxicity of NMs. Current evaluation of NM efficacy and safety involves the time-consuming collection of pharmacokinetic and toxicity data in animals and is usually completed one material at a time. This traditional approach no longer meets the demand of the explosive growth of NM-based products. There is an emerging need to develop methods that can help design safe and effective NMs in an efficient manner. In this review article, we critically evaluate existing studies on in vivo pharmacokinetic properties, in vitro cellular uptake and release and kinetic modeling, and whole-body physiologically based pharmacokinetic (PBPK) modeling studies of different NMs. Methods on how to simulate in vitro cellular uptake and release kinetics and how to extrapolate cellular and tissue dosimetry of NMs from in vitro to in vivo via PBPK modeling are discussed. We also share our perspectives on the current challenges and future directions of in vivo pharmacokinetic studies, in vitro cellular uptake and kinetic modeling, and whole-body PBPK modeling studies for NMs. Finally, we propose a nanomaterial in vitro to in vivo extrapolation via physiologically based pharmacokinetic modeling (Nano-IVIVE-PBPK) framework for high-throughput screening of target cellular and tissue dosimetry as well as potential toxicity of different NMs in order to meet the demand of efficient evaluation of the safety, efficacy, and potential toxicity of a rapidly increasing number of NM-based products.

Indexed as

NanostructuresAnimalsBiological TransportModels, Biologicalcellular uptakein vitro kinetic modelingin vitro to in vivo extrapolationnanomaterialsnanoparticlesnanotoxicologyphysiologically based pharmacokinetic modelingrisk assessmenttoxicokinetics

Identifiers

PMID36520546
PMCPMC9798869

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.