Evidence map›Paper›PMID 37059242›Full record

SynthesisInternational journal of pharmaceutics2023

Meta-analysis of material properties influencing nanoparticle plasma pharmacokinetics.

Briana Macedo, Manthan Patel, Michael H Zaleski, Parth Mody, Xiaonan Ma, Patrick Mei, Jacob W Myerson, Jacob S Brenner, Patrick M Glassman

Abstract readMeta-Analysis
In one paragraph

Synthesis in International journal of pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Whole-body distribution of threeAntimicrobial agents and chemotherapy · 2026
    Article
  5. 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

9 authors.

Briana MacedoDepartment of Computer Science, Princeton University, Princeton, NJ, USA.
Manthan PatelDepartment of Chemical and Biological Engineering, Drexel University, Philadelphia, USA.
Michael H ZaleskiDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, USA.
Parth ModyDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, USA.
Xiaonan MaDivision of Pulmonary and Critical Care Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Patrick MeiDivision of Pulmonary and Critical Care Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Jacob W MyersonDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, USA.
Jacob S BrennerDepartment of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, USA; Division of Pulmonary and Critical Care Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: jacob.brenner@pennmedicine.upenn.edu.
Patrick M GlassmanDepartment of Pharmaceutical Sciences, Temple University School of Pharmacy, Philadelphia, PA, USA. Electronic address: patrick.glassman@temple.edu.

Funding

Controlling complement to unleash nanomedicine for acute critical illnessesR01HL160694 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRENNER, JACOB, MUZYKANTOV, VLADIMIR R · 2022 to 2025
$2.7M
Nanomedicine for ARDS: A new paradigm to target drugs to multiple cell types within alveolar capillariesR01HL153510 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRENNER, JACOB · 2020 to 2024
$2.0M
FcRn-enabling strategies for improved thrombolytic therapyR00HL153696 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI GLASSMAN, PATRICK MCKENNA · 2022 to 2024
$747k
Nanonscale drug carriers for the treatment of acute respiratory distress syndromeK08HL138269 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI BRENNER, JACOB · 2017 to 2021
$746k
RBC-mediated mopping of cytokines for the treatment of pneumoniaR21AI166778 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI BRENNER, JACOB · 2021 to 2022
$447k
NHLBI NIH HHS K08 HL138269NHLBI NIH HHS R00 HL153696NHLBI NIH HHS R01 HL153510NHLBI NIH HHS R01 HL160694NIAID NIH HHS R21 AI166778
6 · The paper itself

Abstract

Thorough characterization of the plasma pharmacokinetics (PK) is a critical step in clinical development of novel therapeutics and is routinely performed for small molecules and biologics. However, there is a paucity of even basic characterization of PK for nanoparticle-based drug delivery systems. This has led to untested generalizations about how nanoparticle properties govern PK. Here, we present a meta-analysis of 100 nanoparticle formulations following IV administration in mice to identify any correlations between four PK parameters derived by non-compartmental analysis (NCA) and four cardinal properties of nanoparticles: PEGylation, zeta potential, size, and material. There was a statistically significant difference between the PK of particles stratified by nanoparticle properties. However, single linear regression between these properties and PK parameters showed poor predictability (r

Indexed as

NanoparticlesAnimalsDrug CompoundingMicePharmacokineticsMeta-analysisNanoparticlesNon-compartmental analysisPharmacokinetics

Identifiers

PMID37059242
PMCPMC10362388

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.