Evidence map›Paper›PMID 36678932›Full record

ArticlePharmaceutics2023

Fractal Kinetic Implementation in Population Pharmacokinetic Modeling.

Woojin Jung, Hyo-Jeong Ryu, Jung-Woo Chae, Hwi-Yeol Yun

Abstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Woojin JungCollege of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.ORCID 0000-0001-7806-597X
Hyo-Jeong RyuCollege of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.ORCID 0000-0002-2317-8894
Jung-Woo ChaeCollege of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.ORCID 0000-0001-6026-7063
Hwi-Yeol YunCollege of Pharmacy, Chungnam National University, Daejeon 34134, Republic of Korea.ORCID 0000-0001-8793-2449

Funding

Artificial Intelligence Convergence Innovation Human Resources Development Center(Chungnam National University) RS-2022-00155857National Research Foundation of Korea (NRF) grant funded by the Korea government(MSIT) 2022R1A5A7085156National Research Foundation of Korea (NRF) grant funded by the Korea government(MSIT) NRF-2022R1A2C1010929The Korea Environmental Industry and Technology Institute (KEITI) through the Core Technology Development Project for Envi-ronmental Diseases Prevention and Management 2021003310001This study was supported by an Institute of Information Communications Technology Planning Evaluation (IITP) grant funded by the Korean government (MSIT) 2020-0-01441
6 · The paper itself

Abstract

Compartment modeling is a widely accepted technique in the field of pharmacokinetic analysis. However, conventional compartment modeling is performed under a homogeneity assumption that is not a naturally occurring condition. Since the assumption lacks physiological considerations, the respective modeling approach has been questioned, as novel drugs are increasingly characterized by physiological or physical features. Alternative approaches have focused on fractal kinetics, but evaluations of their application are lacking. Thus, in this study, a simulation was performed to identify desirable fractal-kinetics applications in conventional modeling. Visible changes in the profiles were then investigated. Five cases of finalized population models were collected for implementation. For model diagnosis, the objective function value (OFV), Akaike's information criterion (AIC), and corrected Akaike's information criterion (AICc) were used as performance metrics, and the goodness of fit (GOF), visual predictive check (VPC), and normalized prediction distribution error (NPDE) were used as visual diagnostics. In most cases, model performance was enhanced by the fractal rate, as shown in a simulation study. The necessary parameters of the fractal rate in the model varied and were successfully estimated between 0 and 1. GOF, VPC, and NPDE diagnostics show that models with the fractal rate described the data well and were robust. In the simulation study, the fractal absorption process was, therefore, chosen for testing. In the estimation study, the rate application yielded improved performance and good prediction-observation agreement in early sampling points, and did not cause a large shift in the original estimation results. Thus, the fractal rate yielded explainable parameters by setting only the heterogeneity exponent, which reflects true physiological behavior well. This approach can be expected to provide useful insights in pharmacological decision making.

Indexed as

biological drugcompartment modelingfractalintramuscular injectionpharmacokineticstransdermal patch

Identifiers

PMID36678932
PMCPMC9867137

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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.