Evidence map›Paper›PMID 38896158›Full record

ArticleJournal of molecular modeling2024

Diffusion of curcumin in PLGA-based carriers for drug delivery: a molecular dynamics study.

Alessandro De Giorgi, Francesco Maria Bellussi, Stefano Parlani, Andrea Lucisano, Emanuele Silvestri, Susmita Aryal, Sanghyo Park, Jaehong Key, Matteo Fasano

Abstract read
In one paragraph

Article in Journal of molecular modeling, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

  1. Article
  2. Computational approaches in bioprinting processes.Nature reviews bioengineering · 2026
    Article
  3. 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.

Alessandro De GiorgiDepartment of Energy, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, Italy.
Francesco Maria BellussiDepartment of Energy, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, Italy.
Stefano ParlaniDepartment of Energy, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, Italy.
Andrea LucisanoDepartment of Energy, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, Italy.
Emanuele SilvestriDepartment of Energy, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, Italy.
Susmita AryalDepartment of Biomedical Engineering, Yonsei University, Wonju, 26493, Gangwon State, Republic of Korea.
Sanghyo ParkDepartment of Biomedical Engineering, Yonsei University, Wonju, 26493, Gangwon State, Republic of Korea.
Jaehong KeyDepartment of Biomedical Engineering, Yonsei University, Wonju, 26493, Gangwon State, Republic of Korea. jkey@yonsei.ac.kr.
Matteo FasanoDepartment of Energy, Politecnico di Torino, Corso Duca degli Abruzzi 24, Torino, 10129, Italy. matteo.fasano@polito.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextThe rapid growth and diversification of drug delivery systems have been significantly supported by advancements in micro- and nano-technologies, alongside the adoption of biodegradable polymeric materials like poly(lactic-co-glycolic acid) (PLGA) as microcarriers. These developments aim to reduce toxicity and enhance target specificity in drug delivery. The use of in silico methods, particularly molecular dynamics (MD) simulations, has emerged as a pivotal tool for predicting the dynamics of species within these systems. This approach aids in investigating drug delivery mechanisms, thereby reducing the costs associated with design and prototyping. In this study, we focus on elucidating the diffusion mechanisms in curcumin-loaded PLGA particles, which are critical for optimizing drug release and efficacy in therapeutic applications.

methodsWe utilized MD to explore the diffusion behavior of curcumin in PLGA drug delivery systems. The simulations, executed with GROMACS, modeled curcumin molecules in a representative volume element of PLGA chains and water, referencing molecular structures from the Protein Data Bank and employing the CHARMM force field. We generated PLGA chains of varying lengths using the Polymer Modeler tool and arranged them in a bulk-like environment with Packmol. The simulation protocol included steps for energy minimization, T and p equilibration, and calculation of the isotropic diffusion coefficient from the mean square displacement. The Taguchi method was applied to assess the effects of hydration level, PLGA chain length, and density on diffusion.

resultsOur results provide insight into the influence of PLGA chain length, hydration level, and polymer density on the diffusion coefficient of curcumin, offering a mechanistic understanding for the design of efficient drug delivery systems. The sensitivity analysis obtained through the Taguchi method identified hydration level and PLGA density as the most significant input parameters affecting curcumin diffusion, while the effect of PLGA chain length was negligible within the simulated range. We provided a regression equation capable to accurately fit MD results. The regression equation suggests that increases in hydration level and PLGA density result in a decrease in the diffusion coefficient.

Indexed as

CurcuminDrug CarriersMolecular Dynamics SimulationPolylactic Acid-Polyglycolic Acid CopolymerDiffusionDrug Delivery SystemsCurcuminDrug CarriersPolylactic Acid-Polyglycolic Acid CopolymerDiffusionMass transferMolecular dynamicsPolymeric carriersWater

Identifiers

PMID38896158
PMCPMC11186890

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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.