Evidence map›Paper›PMID 40637551›Full record

ReviewACS applied materials & interfaces2025

Coacervate-Based Delivery Systems: Bridging Fundamentals and Applications.

Mohammad Souri, Wonjun Yim, Moumita Halder, Zhicheng Jin, Jesse V Jokerst

Abstract readReview
In one paragraph

Review in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Oligopeptides/DNA Coacervate Droplets as Macromolecular Delivery Microcarriers.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  7. MgChem & bio engineering · 2026
    Article
  8. Article
  9. Review
  10. Review
  11. Dynamic Covalent Boronate Chemistry forJournal of the American Chemical Society · 2026
    Article
  12. Review
  13. Review
  14. Article
  15. Review
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

5 authors.

Mohammad SouriAiiso Yufeng Li Family Department of Chemical and Nano Engineering, University of California San Diego, La Jolla, San Diego, California 92093, United States.ORCID 0000-0001-9509-1336
Wonjun YimDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Moumita HalderAiiso Yufeng Li Family Department of Chemical and Nano Engineering, University of California San Diego, La Jolla, San Diego, California 92093, United States.ORCID 0009-0008-9113-8510
Zhicheng JinDepartment of Chemistry, Georgia State University, Atlanta, Georgia 30303, United States.ORCID 0000-0001-6072-7533
Jesse V JokerstAiiso Yufeng Li Family Department of Chemical and Nano Engineering, University of California San Diego, La Jolla, San Diego, California 92093, United States.ORCID 0000-0003-2829-6408

Funding

New Tools to Image Tau Protein Form and FunctionR21AG091821 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JOKERST, JESSE VINCENT · 2025 to 2025
$437k
NIA NIH HHS R21 AG091821
6 · The paper itself

Abstract

Coacervate-based drug delivery systems, inspired by liquid-liquid phase separation, have emerged as a flexible platform for encapsulating and controlling the release of therapeutic agents such as nucleic acids, proteins, growth factors, and small molecules. Their capacity to react to exogenous and endogenous stimuli, such as pH and temperature, allows for accurate adjustment of the drug release profile and targeted delivery. Nonetheless, despite these advantages, poor stability in biological environments continues to pose a major obstacle, impacting drug retention and the effectiveness of therapies. This instability further complicates large-scale production, as ensuring uniform coacervate characteristics across different batches poses a significant challenge. Recent developments in molecular engineering, such as polyelectrolyte complexation and stimuli-responsive modifications, have significantly improved the stability and functionality of coacervates. This review offers an in-depth examination of the principles behind coacervate formation, their structural classifications, and the physicochemical properties that affect their effectiveness in drug delivery applications. Recent advancements in formulation techniques and the latest trends in combining nanotechnology with computational modeling are examined, emphasizing their potential to enhance coacervate behavior in biomedical applications. Furthermore, this review explores recent developments in gene therapy, regenerative medicine, and targeted drug delivery, highlighting the promising applications of coacervates in future therapeutic innovations. This work points out the essential challenges and opportunities that will drive the future evolution and clinical application of coacervate-based delivery systems by integrating foundational insights with technological progress.

Indexed as

Drug CarriersDrug Delivery SystemsAnimalsGenetic TherapyHumansRegenerative MedicineDrug Carrierscoacervationcontrolled releasedrug deliveryencapsulationstimuli-responsive

Identifiers

PMID40637551
PMCPMC13093891

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.